VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.1 Chapter 22: Laboratory Support for the Surveillance of Vaccine-Preventable Diseases Authors: Sandra Roush, MT, MPH; Bernard Beall, PhD; Lesley McGee, PhD; Pam Cassiday, MS; Michael Bowen, PhD; Joe Icenogle, PhD; Steven Oberste, PhD; Daniel Payne, PhD, MSPH; Paul Rota, PhD; Scott Schmid, PhD; Carole Hickman, PhD; Michael Shaw, PhD; Maria Lucia Tondella, PhD; Annemarie Wasley, ScD; Xin Wang, PhD I. Surveillance of Vaccine-Preventable Diseases Surveillance for vaccine-preventable diseases (VPDs) requires close collaboration of clinicians, public health professionals, and laboratorians. Public health surveillance relies on both clinical and laboratory reports of VPDs; therefore, appropriate specimen collection, transport, and laboratory testing are essential. This chapter provides guidelines on specimen collection for each VPD and interpretation of laboratory results. Each public health professional dealing with VPDs should identify sources of laboratory support for his or her clinical and public health practice. Table 1 lists appropriate tests for VPDs and provides names and contact information for laboratories and laboratory personnel. In addition to the guidelines presented in this chapter, state health department personnel can provide additional guidance on specimen collection, transport, and other related information.

Table 1. Contact persons for VPD surveillance laboratory support

Disease Test name Lab name Lab contact/Phone Dr. Lucia Tondella [email protected] 404-639-1239 Culture CDC Pertussis and Diphtheria or Diphtheria Toxigenicity testing Laboratory Pam Cassiday PCR [email protected] 404-639-1231 FAX: 404-718-2098 Culture Dr. Xin Wang Haemophilus Real-time PCR CDC Bacterial Meningitis [email protected] 404-639-5474 influenzae Serotyping slide agglutination Laboratory FAX: 404-639-4421 Molecular typing (WGS) Dr. Saleem Kamili [email protected] Hepatitis A IgM antibody Hepatitis Reference Laboratory 404-639-4431 FAX 404-639-1378 Dr. Saleem Kamili IgM antibody [email protected] Hepatitis B Hepatitis Reference Laboratory 404-639-4431 PCR FAX 404-639-1378 VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.2

Disease Test name Lab name Lab contact/Phone Dr. Stephen Lindstrom Culture/viral isolation Diagnostic Development Team Lead Antigen detection Influenza Division, Surveillance Influenza and Diagnosis Branch, [email protected] RT-PCR/ Diagnostic Development Team Email: [email protected] real-time RT-PCR 404-639-1587 FAX: 404-639-2350 IgM antibody IgG antibody Dr. Paul Rota Viral Vaccine-Preventable [email protected] Measles Virus isolation Diseases Branch 404-639-4181 RT-PCR FAX: 404-639-4187 Viral genotyping

Culture Dr. Xin Wang Meningococcal Real-time PCR CDC Bacterial Meningitis [email protected] disease Laboratory 404-639-5474 Serogrouping slide agglutination FAX: 404-639-4421 Virus isolation IgM antibody Dr. Carole Hickman Vaccine-Preventable [email protected] Mumps IgG antibody Diseases Branch 404-639-3339 RT-PCR FAX: 404-639-4187 Viral genotyping Dr. Lucia Tondella [email protected] 404-639-1239 Culture CDC Pertussis and or Pertussis PCR Diphtheria Laboratory Pamela Cassiday Serology [email protected] 404-639-1231 FAX: 404-718-2198

Culture Dr. Bernard Beall [email protected] PCR 404-639-1237 Susceptibility testing Pneumococcal CDC Streptococcus or Serotyping disease Laboratory Dr. Lesley McGee (conventional or PCR-based) [email protected] Genotyping 404-639-0455 Antibiotic FAX: 404-639-2070

Culture Cara Burns CDC Polio/Picornavirus [email protected] Poliomyelitis Intratypic differentiation Laboratory 404-639-5499 Serology FAX: 404-639-4011 VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.3

Disease Test name Lab name Lab contact/Phone Antigen EIA RT-PCR Dr. Michael Bowen [email protected] Rotavirus qRT-PCR CDC Rotavirus Laboratory 404-639-4922 Genotyping FAX: 404-639-3645 Sequencing IgM antibody IgG antibody Dr. Joe Icenogle CDC MMR & Herpes Virus [email protected] Rubella IgG Avidity Laboratory 404-639-4557 Culture FAX: 404-639-1516 RT-PCR IgM antibody IgG antibody Dr. Joe Icenogle Congenital CDC MMR & Herpes Virus [email protected] rubella Culture Laboratory 404-639-4557 syndrome RT-PCR FAX: 404-639-1516 Serology PCR DFA Dr. Scott Schmid [email protected] Varicella Culture National VZV Laboratory 404-639-0066 Serology FAX: 404-639-4056 Viral typing/strain identification

II. General Guidelines for Specimen Collection and Laboratory Testing Specimen collection and shipping are important steps in obtaining laboratory diagnosis or confirmation for VPDs. Guidelines have been published for specimen collection and handling for viral and microbiologic agents.1–3 Information is also available on using Centers for Disease Control and Prevention (CDC) laboratories as support for reference and disease surveillance;4 this includes ● a central website (https://www.cdc.gov/laboratory/specimen-submission/index.html) for requesting lab testing; ● the form (https://www.cdc.gov/laboratory/specimen-submission/pdf/form-50-34.pdf) required for submitting specimens to CDC (see Appendix 23, CDC Form 50.34); ● information on general requirements for shipment of etiologic agents (Appendix 24 [http://www.cdc. gov/vaccines/pubs/surv-manual/appx/appendix24-etiologic-agent.pdf])—although written to guide specimen submission to CDC, this information may be applicable to the submission of specimens to other laboratories; and ● the CDC Infectious Diseases Laboratories Test Directory that contains not only a list (https://www.cdc. gov/laboratory/specimen-submission/list.html) of orderable tests for that institution, but also detailed information on appropriate specimen types, collection methods, specimen volume, and points of contact. In addition, there are 4 VPD Reference Centers—public health laboratories that perform testing for 7 VPDs using standardized methods developed by CDC. VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.4 III. Disease-specific Guidelines for Specimen Collection and Laboratory Testing This chapter provides a quick reference summary of the laboratory information from Chapters 1–17 of this manual. Confirmatory and other useful tests for surveillance of vaccine-preventable diseases are listed below in Table 2.

Table 2. Confirmatory and other useful tests for the surveillance of vaccine-preventable diseases

Disease Confirmatory tests Other useful tests PCR Culture Diphtheria Serology (antibodies to diphtheria toxin) Toxigenicity testing MALDI-TOF Serotyping slide agglutination or PCR (identification of capsular type of encapsulated strains) Haemophilus Culture influenzae RT-PCR Antigen detection Molecular typing Total anti-HAV; IgG anti-HAV (markers of immunity)

IgM anti-HAV (positive) PCR for HAV RNA (marker of current infection) Hepatitis A IgM anti-HBc (acute infection) Anti-HBs (marker of immunity) Hepatitis B HBsAg (acute or chronic infection)* Total anti-HBc (marker of past or present infection)

PCR for HBV DNA (marker of current infection) Culture

Influenza Antigen detection (EIA, IFA, EM)

RT-PCR IgM IgG

Measles RT-PCR IgG for seroconversion or 4-fold titer rise

Virus isolation Avidity (case classification) Serogrouping

Slide agglutination or PCR Meningococcal Culture (identification of capsular type of encapsulated strains) disease Antigen detection

Molecular typing IgM Virus isolation Mumps IgG for seroconversion or 4-fold titer rise RT-PCR (not recommended for previously vaccinated persons) Culture Pertussis Serology PCR

Pneumococcal Culture WGS-based deduction of all strain features disease PCR (serotype, antimicrobial resistance, MLST genotype) VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.5

Disease Confirmatory tests Other useful tests Intratypic differentiation (wild vs. vaccine type) Culture-from stool, pharynx, Poliomyelitis Paired serology or CSF CSF analysis Rotavirus RT-PCR/qRT-PCR

Paired sera for IgG Rubella Culture IgM

There are no lab findings Tetanus Serology (for immunity testing) characteristic of tetanus. DFA

Culture Varicella PCR Serology

Genotyping Abbreviations: EIA, enzyme-linked immunosorbent assay; IFA, indirect fluorescent antibody; EM, electron microscopy; PCR, polymerase chain reaction; MLST, multilocus sequence typing; PFGE, pulsed field gel electrophoresis; CSF, cerebral spinal fluid; IgG, immunoglobulin G; IgM, immunoglobulin M; HAV, hepatitis A virus; HBV, hepatitis B virus; anti-HBc; hepatitis B core antibody; HBsAg, hepatitis B surface Ag; qRT-PCR, quantitative reverse transcription polymerase chain reaction *Confirmation of HBsAg positive results by HBsAg neutralization assay should be performed as specified in test package insert.

Table 3 summarizes specimen collection procedures for laboratory testing. Because some specimens require different handling procedures, it is essential to check with the diagnostic laboratory prior to shipping. When in doubt about what specimens to collect, timing of specimen collection, or where or how to transport specimens, call the state health department and the state laboratory.

Table 3. Specimen collection for laboratory testing for VPDs

Timing for Specimens to Transport Collection Disease Test name specimen take requirements requirements collection Culture <24 hrs: Amies’ State health Note: ALERT lab or similar Swab of ASAP, when departments may that diphtheria transport Diphtheria nose, throat, diphtheria is call CDC diphtheria is suspected, medium membrane suspected lab at 404-639-1231 so that tellurite- ≥24 hrs: silica or 404-639-1239. containing media gel sachets will be used. PCR State health Note: ALERT lab Swabs (as Take these Swabs, silica departments may that diphtheria above), pieces specimens at gel sachet; or Diphtheria call CDC diphtheria is suspected, of membrane, same time as a sterile dry lab at 404-639-1231 so that specific biopsy tissue those for culture. container at 4°C PCR assay will or 404-639-1239. be used. Transport State health After Toxigenicity medium, such as departments may Isolate from C. diphtheriae Diphtheria testing Amies medium, call CDC diphtheria culture (above) has been (Elek test) or silica gel lab at 404-639-1231 isolated sachets or 404-639-1239. VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.6

Timing for Specimens to Transport Collection Disease Test name specimen take requirements requirements collection Serology (antibodies to diphtheria toxin)

Note: Collect Before Not useful if paired sera, Diphtheria Serum administration of Frozen (-20°C) diphtheria antitoxin taken 2–3 antitoxin was administered. weeks apart.

This test is currently not available at CDC. Culture

Note: Request Blood culture that lab conduct bottles w/broth Collect 3 separate Haemophilus serotyping on Blood ASAP or lysis- samples in a 24-hr influenzae type b any H. influenzae centrifugation period. isolate from tube any normally sterile site. Culture

Note: Request that lab conduct CSF Haemophilus serotyping on Sterile, screw- Other normally ASAP influenzae type b any H. influenzae capped tube sterile site isolate from any normally sterile site. Chocolate Highest priority Haemophilus Serotyping slide slant, frozen, culture isolate are isolates from influenzae type b agglutination lyophilized or persons <15 years. silica gel pack Haemophilus Antigen Sent frozen on CSF ASAP influenzae type b detection blue ice packs PCR for Haemophilus Any normally Sent frozen on identification ASAP influenzae type b sterile site blue ice packs and serotyping All sera to be tested for serologic markers of HAV and HBV infection can be ASAP after kept at ambient Follow standard symptom onset Hepatitis A IgM anti-HAV Serum temperatures, procedures for (detectable up to refrigerated serum separation. 6 months) (<48 hours) for short term. For longer than 48 hours storage, sera should be frozen. VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.7

Timing for Specimens to Transport Collection Disease Test name specimen take requirements requirements collection Samples can be kept at ambient Total anti-HAV temperatures, refrigerated Note: Measures Follow standard (<48 hours) for Hepatitis A both IgM and Serum No time limit procedures for short term. IgG. serum separation. For longer IgG anti-HAV than 48 hours storage, sera should be frozen. ASAP after Follow standard HAV RNA by symptom onset Store and ship Hepatitis A Serum procedures for PCR (detectable up to samples frozen serum separation. 2 weeks) Samples can be kept at ambient temperatures, ASAP after refrigerated Follow standard symptom onset (<48 hours) for Hepatitis B IgM anti-HBc Serum procedures for (detectable up to short term. serum separation. 6 months) For storage longer than 48 hours, sera should be frozen. HBsAg Samples can be Note: HBsAg- kept at ambient positive results temperatures, should be refrigerated Follow standard confirmed ASAP after (<48 hours) for Hepatitis B Serum procedures for by HBsAg symptom onset short term. serum separation. neutralization For longer assay as than 48 hours specified in the storage, sera package insert should be frozen. for each assay. Samples can be kept at ambient temperatures, refrigerated (<48 Follow standard 1–2 months after Hepatitis B Anti-HBs Serum hours) for short procedures for vaccination term. For longer serum separation. than 48 hours storage, sera should be frozen. Transport Nasal wash, specimens at nasopharyngeal 4°C if tests are aspirates, nasal/ Within 72 hours to be performed Culture/viral throat swabs, Influenza of onset of within 72 hours; isolation transtracheal illness otherwise, freeze aspirate, at -70°C until bronchoalveolar tests can be lavage performed. VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.8

Timing for Specimens to Transport Collection Disease Test name specimen take requirements requirements collection Nasal wash, Transport Note: Save an nasopharyngeal specimens at aliquot of the aspirate, nasal/ 4°C if tests are clinical sample Antigen throat swabs, Within 72 hours to be performed for confirmation Influenza detection and gargling fluid, of onset of within 72 hours; and isolation. RT-PCR transtracheal illness otherwise, freeze Viral isolates aspirates, at -70°C until may be further bronchoalveolar tests can be characterized by lavage performed. WHO/CDC. Transport specimens at Collect at same Nasopharyngeal 4°C if tests are time as samples Note: PCR for aspirates, throat to be performed Virus isolation for serology genotypingCollect Measles swabs, urine, within 72 hours; (best within 3 up to 10 days from RT-PCR heparinized otherwise, freeze days of rash rash onset. blood at -70°C until onset) tests can be performed. ASAP after rash Note: IgM is onset and repeat Ship on cold detectable for at Measles IgM antibody Serum 72 hours after pack least 30 days after onset if first rash onset. negative Acute: ASAP after rash onset (7 days at the Measles IgG antibody Paired sera latest) Convalescent: 14−30 days after acute Culture**

Note: Request Blood culture bottles w/broth Meningococcal that lab conduct Blood ASAP or lysis- . disease serogrouping on any centrifugation N. meningitidis tube isolate Culture**

Note: Request CSF Meningococcal that lab conduct Sterile, screw- ASAP disease serogrouping Other normally capped tube on any sterile site N. meningitidis isolate Serogrouping Slant, frozen, Meningococcal Isolate from slide lyophilized or disease culture (above) agglutination silica gel pack VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.9

Timing for Specimens to Transport Collection Disease Test name specimen take requirements requirements collection PCR for Meningococcal Any normally Sent frozen on detection and ASAP disease sterile site blue ice packs serogrouping Meningococcal Antigen Any normally Sent frozen on ASAP disease detection sterile site blue ice packs Transport specimens at Buccal/parotid 4°C if tests are Massage the swabs; CSF Ideally 0–3 days to be performed salivary/parotid Virus isolation only for aseptic after parotitis Mumps within 72 hours; gland area for 30 meningitis; urine onset but up to RT-PCR otherwise, freeze seconds prior to for cases of 11–14 days at -70°C until swab collection. orchitis tests can be performed. Ideally ≥3 days Ship on cold Mumps IgM antibody Serum after parotitis pack onset

Acute: ideally Four-fold rise in titer Paired sera for 0–3 days after not recommended seroconversion parotitis onset Ship on cold Mumps IgG antibody for previously or 4-fold rise Convalescent: pack vaccinated in titer 2 weeks after persons. acute

Use polyester (such as Dacron), rayon or nylon nasopharyngeal Culture swab. Flocked Note: Inoculate Swabs: swabs are selective primary half-strength preferred. Shaft isolation media charcoal horse may be flexible such as charcoal blood agar plastic, aluminum, horse blood Posterior Within the first 2 at 4°C or twisted wire. Pertussis agar or Bordet- nasopharyngeal weeks of cough Aspirates may Swabs in Regan- Gengou as soon swab or aspirate onset be collected Lowe transport as possible. with a syringe Aspirates: in and catheter by A negative saline in capped introducing a culture does syringe at 4°C small amount of NOT rule out saline into the pertussis nasopharyngeal cavity and collecting it in the syringe. VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.10

Timing for Specimens to Transport Collection Disease Test name specimen take requirements requirements collection Use polyester (such as Dacron) Swabs in Regan- rayon, or nylon Lowe transport pharyngeal swab. at 4°C Flocked swabs are preferred. Shaft Aspirates in may be flexible saline in capped PCR plastic, aluminum, syringe at 4°C or twisted wire. Note: PCR Within the first 2 Nasopharyngeal For PCR testing Aspirates may Pertussis should be weeks of cough swab or aspirate only, swab may be collected validated with onset culture when be placed in with a syringe possible. a sterile tube and catheter by and sent at introducing a 4°C (short term small amount of storage) or -20°C saline into the or below (long nasopharyngeal term storage) cavity and collecting it in the syringe. Serologic results are currently not accepted Short term at 2–8 weeks of as laboratory Pertussis Serology Serum 4°C; long-term at cough onset confirmation -20°C or below for purposes of national surveillance. Blood culture bottles w/broth Collect 2 separate As soon as or lysis- blood samples in possible after centrifugation a 24-hr period. Pneumococcal Normally sterile onset of clinical Culture tube or, if from Most other sterile disease site illness but before another sterile specimens administration of site, a sterile, (e.g., CSF) are antibiotics screw-capped collected only once. tube ASAP, soon after Send specimen Pneumococcal Normally sterile administration of PCR frozen on blue PCR disease site antibiotics is a ice packs viable option Culture-negative Pneumococcal PCR deduction Specimen frozen PCR deduction of sterile site disease of serotype immediately serotype specimen Pneumococcal Susceptibility Slant, frozen, or Susceptibility Pure culture disease testing silica packet testing Pneumococcal Slant, frozen, or Serotyping Pure culture Serotyping disease silica packet VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.11

Timing for Specimens to Transport Collection Disease Test name specimen take requirements requirements collection No carrier for stool; saline buffer for swabs. Stool, Sterile, Poliomyelitis Culture pharyngeal Acute screw-capped Note: Maintain swab, CSF container frozen or transport rapidly to lab; avoid desiccation of swab specimens. Note: Maintain frozen or transport Intratypic Isolate from Poliomyelitis rapidly to lab; avoid differentiation culture (above) desiccation of swab specimens. Acute: ASAP

Poliomyelitis Serology Paired sera Convalescent: 3 weeks after acute Bulk stool EIA, RT-PCR, First to fourth Sterile, Keep frozen or Rotavirus qRT-PCR, Stool day of illness screw-capped transport rapidly to gastroenteritis genotyping, optimal container lab on cold packs; sequencing avoid multiple freeze-thaw cycles. No carrier. Rotavirus- Sterile, RT-PCR, ASAP after associated CSF screw-capped Keep frozen; avoid qRT-PCR symptoms begin seizures container multiple freeze- thaw cycles. ASAP, and repeat 96 hours Maintain at 4°C Rubella IgM antibody Serum after onset if first and ship on ice negative Acute: ASAP after rash onset (7 days Serum Maintain at 4°C Paired sera must Rubella IgG antibody at the latest) and ship on ice be run in parallel Paired sera Convalescent: 14–30 days after acute Collect at same time as samples Note: Maintain Nasopharyngeal for serology frozen (except Viral transport swab/wash, (best within 3 urine) or transport Rubella Culture/PCR media; ship throat swab, days of rash rapidly to lab; avoid frozen or on ice urine onset and no desiccation of swab later than 10 specimens. days post onset) Congenital As soon as Maintain at 4°C rubella syndrome IgM antibody Serum possible, within 6 and ship on ice (CRS) months of birth VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.12

Timing for Specimens to Transport Collection Disease Test name specimen take requirements requirements collection Note: Confirmation is by documenting persistence of After 9 months of Congenital serum IgG titer age, but before Maintain at 4°C rubella syndrome IgG antibody Serum beyond the time vaccination with and ship on ice (CRS) expected from MMR vaccine passive transfer of maternal IgG antibody. As soon as possible for confirmation; Note: Maintain to monitor Nasopharyngeal frozen (except Congenital shedding in Viral transport swab/wash, urine) or transport rubella syndrome Culture/PCR positive cases; media; ship urine, blood, rapidly to lab; avoid (CRS) after 3 months, frozen or on ice cataracts desiccation of swab every month specimens. until cultures are repeatedly negative Immune status: Single IgG assay collect anytime is useful to assess except during immune status. acute illness Varicella Serology Serum Paired serum Paired serologic distinguishes diagnosis: acute between recent within 7–10 days primary infection of onset and past infection. Sera should be shipped frozen Varicella VZV IgG avidity on dry ice or refrigerated in cold packs Fluid from vesicles, nasal or throat swabs, Acute illness 2–3 Definitive diagnosis; serum, spinal days after rash Varicella VZV PCR highly sensitive, fluid, urine, onset and fresh specific and rapid bronchial tree vesicles washing or inflamed joints Analysis of vaccine associated SNP Vesicular swabs using realtime PCR and scabs can methods strategies; be shipped From day of availability limited Vaccine Material from dry at ambient rash onset until to specialized labs, Varicella wild type vesicles, scabs, temperature; crusted lesions e.g., CDC, Columbia discrimination saliva saliva shipped resolve University, and frozen on dry ice the Vaccine or refrigerated Preventable on cold pack Disease Reference Centers **Neisseria meningitidis culture cannot be performed on specimens sent to CDC, but CDC is available to provide advice and answer questions on culture methods. VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.13

A. Diphtheria (see Chapter 1 [http://www.cdc.gov/vaccines/pubs/surv-manual/chpt01-dip.html]) Diagnostic tests used to confirm infection include isolation of Corynebacterium diphtheriae by culture and Elek testing of isolates for diphtheria toxin production. Although no other tests for confirming diphtheria are commercially available, CDC can perform a polymerase chain reaction (PCR) test on clinical specimens to confirm infection with a potentially toxigenic strain. PCR can detect nonviableC. diphtheriae organisms from specimens taken after antibiotic therapy has been initiated. PCR for species identification and detection of the diphtheria toxin gene5, as performed by the CDC Pertussis and Diphtheria Laboratory, and MALDI-TOF provide supportive evidence for the diagnosis but do not confirm toxin production. These tests, when used, should always be combined with a test that confirms toxin production, such as the Elek test Isolation of C. diphtheriae by culture Isolation of C. diphtheriae by bacteriological culture is essential for confirming diphtheria. The following should be considered. ● A clinical specimen for culture should be obtained as soon as possible when diphtheria (involving any site) is suspected, even if treatment with antibiotics has already begun. ● Specimens should be taken from the site of diphtheria infection, nose, throat, and, if present, from the diphtheritic membrane; if possible, swabs also should be taken from beneath the membrane. ● Other pathogens can cause a membrane in the throat and over the tonsils, including the pathogens listed below. The patient’s healthcare provider should be encouraged to perform laboratory tests, when appropriate, to rule out these conditions and organisms, which include ◦ Streptococcus spp., ◦ Epstein-Barr virus and cytomegalovirus (both of which cause infectious mononucleosis syndrome), ◦ Arcanobacter hemolyticum, ◦ Candida albicans, and ◦ fusiform bacteria (which can cause Vincent’s angina). ● The laboratory should be alerted to the suspicion of diphtheria because identification of C. diphtheriae is aided by use of special culture media containing tellurite. ● Specimens from the nose and throat (i.e., both a nasopharyngeal and a pharyngeal swab) for culture should be obtained from all patients with suspected diphtheria and their close contacts. ● Isolation of C. diphtheriae from close contacts may confirm the diagnosis of the case, even if the patient’s culture is negative. Biotype testing After C. diphtheriae has been isolated, the biotype (substrain) should be determined. The 4 biotypes are gravis, mitis, intermedius, and belfanti. Toxigenicity testing In addition to determining biotype, toxigenicity testing using the Elek test should be performed to determine if the C. diphtheriae isolate produces toxin. These tests are not readily available in many clinical microbiology laboratories; isolates should be sent to a reference laboratory proficient in performing the tests. Polymerase chain reaction testing Clinical specimens collected for culture testing can also be used for PCR testing at CDC, if indicated. Because isolation of C. diphtheriae is not always possible (many patients have already received several days of antibiotics by the time a diphtheria diagnosis is considered), PCR can provide additional supportive evidence for the diagnosis of diphtheria. The PCR assay allows for detection of the diphtheria toxin gene (tox), identification of C. diphtheriae through detection of a RNA polymerase gene (rpoB), and detection of C. ulcerans and C. pseudotuberculosis, also with a rpoB target. C. ulcerans and C. pseudotuberculosis are not differentiated from each other in this assay. Clinical specimens (swabs, pieces of membrane, biopsy tissue) can be transported to CDC with cold packs in a sterile empty container or in silica gel sachets. VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.14

For detailed information on specimen collection and shipping and to arrange for PCR testing, the state health department may contact the CDC Pertussis and Diphtheria Laboratory at 404-639-1231 or 404-639-1239. MALDI-TOF Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF) is an additional technology that can be used to rapidly identify bacterial species such as C. diphtheriae. The technique requires an isolate to identify the protein composition of microbial cells. However, this form of testing only confirms the bacterial species, does not confirm diphtheria toxin production, and is not available at the CDC Pertussis and Diphtheria Laboratory. Serologic testing Measurement of the patient’s serum antibodies to diphtheria toxin before administration of antitoxin may help in assessing the probability of the diagnosis of diphtheria. High antibody levels may indicate protection against diphtheria, and C. diphtheriae infection is less likely to produce a serious illness. However, if antibody levels are low, diphtheria cannot be accurately ruled out. The state health department or CDC can provide information on laboratories that offer this test; few laboratories have the capability to accurately test antibody levels. Submission of C. diphtheriae isolates All isolates of C. diphtheriae from any anatomical site should be sent to the CDC Pertussis and Diphtheria Laboratory for reference testing. Clinical specimens from patients with suspected diphtheria for whom diphtheria antitoxin has been released for treatment should also be sent to the CDC Pertussis and Diphtheria Laboratory for culture, PCR, and toxigenicity testing. To arrange for shipping of specimens, contact your state health department. B. Haemophilus influenzae type b (Hib) invasive disease (see Chapter 2 [http://www.cdc.gov/vaccines/pubs/surv-manual/chpt02-hib.html]) Presumptive identification by Gram stain or antigen detection The Gram stain is an empirical method for differentiating bacterial species into 2 large groups based on the chemical and physical properties of their cell walls. Gram-positive bacteria retain the primary stain while gram-negative bacteria take the color of the counterstain. A Gram stain can also serve to assess the quality of a clinical specimen. The Gram stain is useful for preliminary identification of likely H. influenzae, although it is not a confirmatory test and cannot distinguish among H. influenzae type b (Hib) serotypes. Because the type b capsular antigen can be detected in body fluids, including urine, blood, and cerebrospinal fluid (CSF) of patients, clinicians often request a rapid antigen detection test for diagnosis of Hib disease. Antigen detection may be used as an adjunct to culture or PCR, particularly in the diagnosis of patients who have received antimicrobial agents before specimens are obtained for culture. The method for antigen detection is latex agglutination, which is a rapid and sensitive method used to detect Hib capsular polysaccharide antigen in CSF; however, false-negative and false-positive reactions can occur. If the Hib antigen is detected in CSF from a patient with meningitis but a positive result is not obtained from culture of sterile site, the patient should be considered as having a probable case of Hib disease and reported as such. Because antigen detection tests can be positive in urine and serum of persons without invasive Hib disease, persons who are identified exclusively by positive antigen tests in urine or serum should not be reported as cases. Confirmation by culture and PCR Confirming a case of Hib disease requires isolating H. influenzae or detecting H. influenzae DNA from a normally sterile body site. Normally, sterile sites for isolation of invasive H. influenzae typically include CSF, blood, joint fluid, pleural effusion, pericardial effusion, peritoneal fluid, subcutaneous tissue fluid, placenta, and amniotic fluid. Most hospital and commercial microbiologic laboratories have the ability to isolate H. influenzae. Isolates of H. influenzae are recommended to be tested for antimicrobial susceptibility to ampicillin, one of the third-generation cephalosporins, chloramphenicol, and meropenem. Further antimicrobial susceptibility testing should be considered for isolates obtained from cases in which a treatment or chemoprophylaxis failure is suspected or in an outbreak setting. VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.15

Although culture is the gold standard for confirming H. influenzae, real-time PCR is an accepted alternative. In recent years, significant improvements have been made in both the sensitivity and specificity of PCR assays used for the detection of H. influenzae. Real-time PCR assays are available to detect H. influenzae DNA and all 6 serotypes in blood, CSF, or other clinical specimens. A major advantage of PCR is that it allows for detection of H. influenzae from clinical samples in which the organism could not be detected by culture methods, such as when a patient has been treated with antibiotics before a clinical specimen is obtained for culture. Even when the organisms are nonviable following antimicrobial treatment, PCR can still detect H. influenzae DNA. Isolation of the bacterium is needed to test for antimicrobial susceptibility. Several commercial multiplex PCR assays capable of simultaneously testing a single specimen for an array of pathogens that cause blood infections or meningitis/encephalitis are now available, primarily for clinical settings (e.g., FilmArray Blood Culture Identification Panel and FilmArray Meningitis/Encephalitis Panel from BioFire Diagnostics and Meningitis/Encephalitis Panel by PCR from ARUP Laboratories).6–10 While such assays can rapidly identify H. influenzae (Hi) and Neisseria meningitidis (Nm) species, most do not determine serotype or serogroup. Therefore, it is important for laboratories using assays that do not determine serotype/serogroup to perform either a simultaneous culture or a reflex culture if Hi or Nm is identified. At a minimum, laboratories should collect and maintain an adequate clinical sample for further testing at a laboratory with a PCR assay that can detect serotype/serogroup. Serotype testing (serotyping) Serotyping distinguishes encapsulated strains, including Hib, from unencapsulated strains, which cannot be serotyped. The 6 encapsulated types (designated a–f) have distinct capsular polysaccharides that can be differentiated by slide agglutination with type-specific antisera. To make public health decisions about chemoprophylaxis, microbiology laboratories should perform serotype testing of H. influenzae isolates and clinical specimens that are positive for H. influenzae in a timely manner.11, 12 Even though Hib disease has declined, laboratories should continue routine serotyping. If serotyping is not available at a laboratory, laboratory personnel should contact the state health department. State health departments with questions about serotyping should contact the CDC Meningitis and Vaccine-Preventable Disease Branch Laboratory at 404-639-3158. Molecular typing Although not widely available, whole genome sequencing (WGS) has been used to type the H. influenzae isolates to assess their genetic similarity. Subtyping the Hib bacterium by pulsed-field gel electrophoresis (PFGE),13–15 multilocus sequence typing (MLST), can also be performed for epidemiologic purposes in settings where WGS is not available. Some subtyping methods, such as outer membrane proteins, lipopolysaccharides, or enzyme electrophoresis, are no longer recommended or performed because they were unreliable or too labor intensive. The state health department may direct questions about subtyping to the CDC Meningitis and Vaccine-Preventable Disease Branch Laboratory at 404-639-3158. C. Hepatitis A (see Chapter 3 [http://www.cdc.gov/vaccines/pubs/surv-manual/chpt03-hepa.html]) Diagnostic tests used to confirm hepatitis A virus (HAV) infection include serologic testing, and occasionally, PCR-based assays to amplify and sequence viral genomes. Serologic testing Serologic testing is required to distinguish hepatitis A from other types of viral hepatitis, since clinical or epidemiologic features overlap. Virtually all patients with hepatitis A have detectable immunoglobulin M (IgM) anti-HAV. Acute HAV infection is confirmed during the acute or early convalescent phase of infection by the presence of IgM anti-HAV in serum. Serum for IgM anti-HAV testing should be obtained as soon as possible after onset of symptoms because IgM anti-HAV generally disappears within 6 months after onset of symptoms. Immunoglobulin G (IgG) anti-HAV appears in the acute or convalescent phase of infection, remains for the lifetime of the person, and confers enduring protection against disease. The antibody test for total anti-HAV VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.16

measures both IgG anti-HAV and IgM anti-HAV. Persons who are total anti-HAV positive and IgM anti-HAV negative are considered immune whether from past infection or vaccination history. Tests for IgG anti-HAV are also available. CDC laboratory special studies Occasionally, molecular virologic methods such as PCR-based assays are used to amplify and sequence viral genomes. Molecular epidemiologic methods have been useful in understanding HAV transmission within networks of persons with similar risk factors. When applied in combination with conventional epidemiologic methods, HAV sequencing has also been useful in the investigation of outbreaks and determining transmission links.16 However, for routine surveillance purposes, detection of serologic markers—total anti-HAV, or IgG anti-HAV, and IgM anti-HAV—is sufficient actionable information. Specimens collected as part of enhanced hepatitis A surveillance in the United States from 2007 through 2013 were sequenced; 472 (62.7%) of 753 available specimens were HAV RNA positive by polymerase chain reaction. Additional specimens from the Food Safety Project A13FBM from 2013–2016 were sequenced: 98 (26.3%) of 373 available specimens were HAV RNA positive. HAV genotypes among these 570 case specimens were: IA (83.2%), IB (16.0%), and IIIA (0.9%) (CDC Division of Viral Hepatitis Laboratory, unpublished data). Providers with questions about molecular virology methods should consult with their local or state health department and the CDC Division of Viral Hepatitis Laboratory Branch. http://intranet.cdc.gov/nchhstp/ dvh/LAB/index.htm D. Hepatitis B (see Chapter 4 [http://www.cdc.gov/vaccines/pubs/surv-manual/chpt04-hepb.html]) Diagnostic testing for confirmation of hepatitis B virus (HBV) infection includes various serologic markers that can distinguish between different stages of infection and molecular testing, which can provide titer, genotype, and escape mutant information in HBV infected individuals. Serologic marker testing Laboratory tests available for evaluation of HBV infection include testing for hepatitis B surface antigen (HBsAg), total antibodies to HBsAg (total anti-HBs), total and IgM antibodies to HBV core antigen (total and IgM anti-HBc), and total antibodies to hepatitis B e antigen (total anti-HBe). All these tests are commercially available on automated platforms for use in clinical laboratories. HBV laboratory testing algorithm is complex, and it is frequently done in stepwise fashion, starting with the HBsAg test. The presence of HBsAg is indicative of ongoing HBV infection and potential infectiousness. In newly infected persons, HBsAg is present in serum 30–60 days after exposure to HBV. Anti-HBc develops in all HBV infections, appearing at onset of symptoms or liver test abnormalities in acute HBV infection, rising rapidly to high levels, and persisting for life. Acute or recently acquired infection can be distinguished by presence of the IgM class of anti-HBc, which persists for approximately 6 months. In persons who recover from HBV infection, HBsAg is eliminated from the blood, usually in 2–3 months, and antibodies to hepatitis B surface antigen (anti-HBs) develop. The presence of anti-HBs antibodies at levels equal to or higher than 10 mIU/ml indicates immunity from HBV infection. Anti-HBs antibodies also develop in persons vaccinated against hepatitis B virus. The difference between immunized and previously infected individuals can be determined based on total antibodies to hepatitis B core (total anti-HBc). After recovery from natural infection, most persons will be positive for both anti-HBs and anti-HBc antibodies, whereas only anti-HBs antibodies develop in persons who are successfully vaccinated against hepatitis B. Persons who do not recover from HBV infection and become chronically infected remain positive for HBsAg (and anti-HBc antibodies), although a small proportion (0.3% per year) of these persons may eventually clear HBsAg and develop anti-HBs antibodies.17 In some cases, anti-HBc antibody is the only serologic marker detected. Isolated anti-HBc antibody can occur after HBV infection in persons who have recovered but whose anti-HBs antibody levels have waned or in persons in whom anti-HBs antibodies failed to develop. Certain chronically infected persons may be positive for anti-HBc antibodies alone, with HBsAg levels that are below levels detectable by commercially VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.17

available tests or undetectable by these tests due to S gene mutations. Infants who are born to HBsAg- positive mothers and who do not become infected may also have detectable anti-HBc antibodies for up to 24 months after birth from passively transferred maternal antibody.18 The diagnosis of acute hepatitis due to hepatitis B virus infection is serologically confirmed by a positive test for IgM antibody to hepatitis B core antigen (IgM anti-HBc). Confirmation of HBsAg-positive results by HBsAg neutralization assay should be done as needed. In addition to acute HBV infection, both perinatal HBV infection and chronic HBV infection are reportable vaccine-preventable conditions. Chronic infection with HBV is confirmed by a positive test for HBsAg accompanied by a negative test for IgM anti-HBc or by 2 positive HBsAg test results that are at least 6 months apart. A diagnosis of perinatal HBV infection is confirmed by a positive test for HBsAg in an infant 1–24 months of age born in the United States or in U.S. territories to an HBsAg-positive mother. Interpretation of hepatitis B serologic test results is summarized in Table 4.

Table 4. Interpretation of hepatitis B serologic tests

Serologic Markers Interpretation HBsAg* Total Anti-HBc † IgM Anti-HBc§ Anti-HBs¶ - - - - Susceptible, never infected, nor immunized + - - - Acute infection, early incubation** + + + - Acute infection - + + - Acute resolving infection - + - + Past infection, recovered and immune + + - - Chronic infection - + - - False positive (i.e., susceptible), past infection, or “low level” chronic infection - - - + Immune if titer is ≥10 mIU/ml * Hepatitis B surface antigen. † Antibody to hepatitis B core antigen. § Immunoglobulin M antibody to hepatitis B core antigen. ¶ Antibody to hepatitis B surface antigen. ** Transient HBsAg positivity (lasting <18 days) might be detected in some patients during vaccination.

Hepatitis B e antigen (HBeAg) positivity in the serum indicates active viral replication.19 HBeAg is a secreted product of the pre-core open reading frame (ORF) and is found in both acutely and chronically infected patients. Spontaneous conversion from HBeAg to antibodies to hepatitis B e antigen (anti-HBe) may indicate lower levels of HBV. HBeAg positive mothers are at an increased risk of transmitting HBV infection to their unborn babies, requiring timely preventative intervention soon after birth.20 Molecular analysis Polymerase chain reaction (PCR) based methods are used for determination of HBV viral load (quantitative tests) and HBV DNA presence (qualitative tests): they are available as both commercial Food and Drug Administration (FDA) approved tests as well as laboratory developed tests (LDTs). HBV DNA testing is most commonly used for evaluating a patient with diagnosed HBV infection who is receiving or being considered for treatment; these tests are not typically used for the initial diagnosis of infection. Genotype determination is also possible through PCR-based technology and is available as LDTs, most commonly based on the S gene sequence.21 PCR-based methods for amplification or deep sequencing of specific regions of the HBV genome, done in conjunction with epidemiologic studies, may be used for investigating common-source outbreaks of hepatitis B infection, as has been shown for HCV.22 Furthermore, HBV quasispecies diversity can be useful in evaluation of disease progression. The pre-S region of the HBV genome has been associated with disease progression to hepatocellular carcinoma.23 In addition, molecular assays are essential for detecting the emergence of vaccine-escape mutants, diagnostic failure mutants, and treatment resistant mutants.24,25 These types of mutants occur at various rates in different HBV genotypes, so knowing genotype information VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.18

is essential for diagnosis and treatment of patients. Detection of HBV vaccine “escape mutants” among vaccinated infants of HBsAg-positive women is important to determine their potential role in vaccine failures.26 Healthcare professionals with questions about molecular virologic methods or those who identify HBsAg-positive events among vaccinated persons should consult with their state health department or the Epidemiology Branch, Division of Viral Hepatitis, CDC. E. Influenza (updated as of October 2017; see Chapter 6 [http://www.cdc.gov/vaccines/pubs/surv-manual/chpt06- influenza.html]) Methods available for the diagnosis of influenza include virus isolation (standard methods and rapid culture assays), molecular detection (reverse transcriptase-polymerase chain reaction [RT-PCR]), detection of viral antigens (enzyme immunoassays [EIA], immunofluorescent antibody [DFA/IFA] testing, and commercially available rapid diagnostic kits), and less frequently use of immunohistochemistry [IHC], electron microscopy and serologic testing using hemagglutination inhibition or microneutralization.27,28 Virus isolation and rapid culture assay Virus isolation is the gold standard for influenza diagnosis. The following guidelines should be considered. ● Appropriate samples include nasal washes, nasopharyngeal aspirates, nasal and throat swabs, transtracheal aspirates, and bronchoalveolar lavage. ● Samples should be taken within 72 hours of onset of illness to maximize the probability of isolating virus. ● Rapid culture assays that use immunologic methods to detect viral antigens in cell culture are available. These assays can provide results in 18–40 hours, compared with an average of 4–5 days to obtain positive results from standard culture. Molecular testing methods RT-PCR, including real-time RT-PCR, can be used to detect the presence of influenza virus in a clinical specimen or to characterize an influenza virus grown in tissue culture or embryonated eggs. This testing can be performed under biosafety level 2 conditions, even for viruses such as avian influenza A(H5N1), which require biosafety level 3 with enhancements for viral culture. Antigen detection assays Several methods exist for the diagnosis of influenza infection directly from clinical material. 1. Cells from the clinical sample can be stained using an immunofluorescent antibody to look for the presence of viral antigen. Nasal washes, nasopharyngeal aspirates, nasal and throat swabs, gargling fluid, transtracheal aspirates, and bronchoalveolar lavage are suitable clinical specimens. 2. Commercially available kits to test for the presence of viral antigens fall into 3 groups: the first detects only influenza type A viruses; while the second detects both influenza type A and B viruses but does not differentiate between virus types; and the third detects both influenza type A and B viruses and distinguishes between the two. Results of these rapid antigen detection tests can be available in less than 1 hour, although these tests are usually less sensitive (generally approximately 50%–70%) than RT-PCR testing. 29–32 3. Other less frequently used methods include immunofluorescence using staining of respiratory specimens with monoclonal antibodies and visualization of viral antigens by electron microscopy. This method and RT-PCR methods may also be used for detection of influenza antigens and nucleic acids, respectively, in postmortem respiratory tissue samples. When direct antigen detection methods are used for the diagnosis of influenza, it is important to collect and reserve an aliquot of the clinical sample for possible further testing. The medium used to store the specimen for some rapid testing methods is inappropriate for viral culture; in this case, it is necessary to collect 2 separate samples. These additional or reserved samples may be used to confirm direct test results by culture and to subtype influenza A isolates. VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.19

Serologic testing Serologic diagnosis of influenza infection requires paired serum specimens. The acute-phase sample should be collected within 1 week of the onset of illness, and the convalescent-phase sample should be collected approximately 2–3 weeks later. Hemagglutination inhibition (HI) tests are the preferred method of serodiagnosis. A positive result is a 4-fold or greater rise in titer between the acute- and convalescent-phase samples when tested at the same time. Serologic test results are usually available in 24 hours. Serologic testing is most useful in special studies; serologic diagnosis of influenza is not used for national surveillance because of the lack of standardized testing methods and interpretation. F. Measles (see Chapter 7 [http://www.cdc.gov/vaccines/pubs/surv-manual/chpt07-measles.html]) Serologic testing Serologic testing for antibodies to measles is widely available. Generally, in a susceptible person exposed to wild-type measles virus, the IgM response begins around the time of rash onset and can be detected for 1–2 months. The IgG response starts more slowly, at about 5–10 days after rash onset, but typically persists for a lifetime. The diagnosis of acute measles infection can be made by detecting IgM antibody to measles in a single serum specimen or by detecting seroconversion—a 4-fold rise in the titer of IgG antibody in 2 serum specimens obtained approximately 2 weeks apart. Uninfected persons are IgM negative, but will either be IgG negative or IgG positive, depending upon their previous disease or vaccination histories. Recommendations for serologic testing for measles ● An EIA test for IgM antibody to measles in a single serum specimen, obtained at the first contact with the suspected measles case-patient, is one of the recommended methods for diagnosing acute measles. ● A single-specimen test for IgG is the most commonly used test for immunity to measles because IgG antibody is long-lasting. ● Testing for IgG along with IgM is recommended for suspected measles cases. ● Paired sera (acute and convalescent) may be tested for seroconversion or a 4-fold rise in IgG antibody to measles to confirm acute measles infection. ● When a patient with suspected measles has been recently vaccinated (6–45 days prior to rash onset), neither IgM nor IgG antibody responses can distinguish measles disease from rash following vaccination. In this instance, a viral throat or nasopharyngeal swab specimen should be obtained so CDC can attempt to distinguish between vaccine virus and wild-type virus (Table 5). Table 5. Interpretation of measles enzyme immunoassay results*

IgM IgG Previous infection history Current infection Comments Result Result Recently received Not vaccinated, no prior Seroconversion. IgG response depends + - or + first dose of measles history of measles on timing of specimen collection. vaccine Seroconversion. Classic clinical measles. Not vaccinated, no prior + - or + Wild-type measles IgG response depends on timing of history of measles specimen collection. Recently received Previously vaccinated, Seroconversion. IgG response depends + - or + second dose of primary vaccine failure on timing of specimen collection. measles vaccine Recently received - + Previously vaccinated, IgG+ second dose of IgG level may stay the same or may boost. measles vaccine May have few or no symptoms + + Previously vaccinated, IgG+ Wild-type measles (e.g., no fever or rash). VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.20

IgM IgG Previous infection history Current infection Comments Result Result Cannot distinguish between vaccine Exposed to wild- + + Recently vaccinated or wild-type virus; evaluate on type measles epidemiologic grounds.† Distant history of - + Vaccine IgG level may stay the same or may boost. natural measles Distant history of + + Wild-type measles May have few or no symptoms. natural measles * These results are those expected when using the capture IgM and indirect IgG enzyme immunoassays and may not apply to different assays due to different techniques and sensitivities/specificities. † However, in this circumstance, IgM testing will be helpful. If negative, it could rule out wild-type measles infection.

Tests for IgM antibody. Although multiple possible methods exist for testing for IgM antibody, EIA is the most consistently accurate test and is therefore the recommended method. There are 2 formats for IgM tests. The first and most widely available is the indirect format, which requires a specific step to remove IgG antibodies. Problems with removal of IgG antibodies can lead to false-positive33 or, less commonly, false-negative results. The second format, IgM capture, does not require the removal of IgG antibodies. This is the preferred reference test for measles. EIA tests for measles are often positive on the day of rash onset. However, in the first 72 hours after rash onset, up to 30% of tests for IgM may give false-negative results. Tests that are negative in the first 72 hours after rash onset should be repeated; serum should be obtained for repeat testing 72 hours after rash onset. IgM is detectable for at least 28 days after rash onset and frequently longer.34 When a laboratory IgM test result is suspected of being false-positive, additional tests may be performed. False-positive IgM results for measles may be due to the presence of rheumatoid factor in serum specimens. Serum specimens from patients with other rash illness, such as parvovirus B19, rubella, and roseola, have been observed to yield false-positive reactions in some IgM tests for measles. False-positive tests may be suspected when thorough surveillance reveals no source or spread of cases, when the case does not meet the clinical case definition, or when the IgG result is positive within 3 days of rash onset. In these situations, confirmatory tests may be done at the state public health laboratory or at CDC. IgM results by tests other than EIA can be validated with EIA. Indirect EIA tests may be validated with capture EIA. Tests for IgG antibody. Because tests for IgG require 2 serum specimens and a confirmed diagnosis cannot be made until the second specimen is obtained, IgM tests are generally preferred. However, if the IgM tests remain inconclusive, a second (convalescent-phase) serum specimen, collected 14–30 days after the first (acute-phase) specimen, can be used to test for an increase in the IgG titer. These tests can be performed in the state laboratory or at CDC. A variety of tests for IgG antibodies to measles are available; these include EIA, indirect fluorescent antibody tests, and plaque reduction neutralization. Complement fixation, although widely used in the past, is no longer recommended. The “gold standard” test for serologic evidence of recent measles virus infection is plaque reduction neutralization test of IgG in acute- and convalescent-phase paired sera. Paired IgG testing for laboratory confirmation of measles requires the demonstration of a 4-fold rise in titer of antibody against measles. The tests for IgG antibody should be conducted on both acute- and convalescent-phase specimens at the same time. The same type of test should be used on both specimens. The specific criteria for documenting an increase in titer depend on the test. EIA values are not titers and increases in EIA values do not directly correspond to rises in titer. RT-PCR and Virus isolation Isolation of measles virus in culture or detection of measles virus by RT-PCR in clinical specimens confirms the diagnosis of measles. Since culture can take weeks to perform, RT-PCR is preferred for case confirmation. It is important to note that a negative culture or RT-PCR result does not rule out measles because the tests are greatly affected by the timing of specimen collection and the quality and handling of the clinical specimens. If measles virus is cultured or detected by RT-PCR, the viral genotype can be used for molecular epidemiology and to distinguish between measles disease caused by a wild-type measles virus and a measles vaccine reaction. VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.21

Viral culture and RT-PCR are important for molecular epidemiologic surveillance to help determine: ● the origin of the virus, ● which viral strains are circulating in the United States, and ● whether these viral strains have become endemic in the United States. Specimens (urine, nasopharyngeal aspirates, heparinized blood, or throat swabs) from clinically suspected cases of measles obtained for virus isolation should be shipped to the state public health laboratory or to CDC at the direction of the state health department as soon as measles is confirmed. Specimens should be properly stored while awaiting case confirmation (see Appendix 7). Clinical specimens for virus isolation should be collected at the same time as samples for serologic testing. Because virus is more likely to be isolated when the specimens are collected within 3 days of rash onset, collection of specimens for virus isolation should not be delayed until laboratory confirmation is obtained. Clinical specimens should ideally be obtained within 7 days of rash onset and should not be collected if more than 10 days have passed after rash onset. G. Meningococcal disease, Neisseria meningitiditis (see Chapter 8 [http://www.cdc.gov/vaccines/pubs/surv-manual/chpt08-mening.html]) Identification of N. meningitidis Presumptive identification by Gram stain: The Gram stain is an empirical method for differentiating bacterial species into 2 large groups based on the chemical and physical properties of their cell walls. Gram-positive bacteria retain the primary stain while gram-negative bacteria take the color of the counterstain. A Gram stain can also serve to assess the quality of a clinical specimen. Gram staining for N. meningitidis is commonly used and continues to be a reliable and rapid method for presumptive identification. Intracellular gram-negative diplococci in CSF can be considered meningococci until proven otherwise. Presumptive identification by antigen detection: Latex agglutination can be used for rapid detection of meningococcal capsular polysaccharides in CSF; however, false-negative or false-positive results can occur. Antigen agglutination tests on serum or urine samples are unreliable for the diagnosis of meningococcal disease.35 Immunohistochemistry can be used for meningococcal detection in formalin-fixed tissues. Confirmation by culture and PCR: The case definition for confirmed meningococcal disease requires isolation of N. meningitidis or detection of Nm. DNA from a normally sterile site. Typically, normally sterile sites include blood or CSF, but can also include joint, pleural, or pericardial fluid. Aspirates or skin biopsies of purpura or petechiae can yield meningococci in cases of meningococcemia. The typical media used to grow the organism are chocolate agar or Mueller-Hinton medium in an atmosphere containing 5% carbon dioxide.36 Real-time PCR detects DNA of meningococci in blood, CSF, or other clinical specimens and is an acceptable alternative method for confirming meningococcal cases. Real-time PCR assays are available to detect DNA of N. meningitidis and all 6 serogroups in blood, CSF, or other clinical specimens.6–10 A major advantage of PCR is that it allows for detection of N. meningitidis from clinical samples in which the organism could not be detected by culture methods, such as when a patient has been treated with antibiotics before a clinical specimen is obtained for culture. Even when the organisms are nonviable following antimicrobial treatment, PCR can still detect N. meningitidis DNA.37 Because of the severity of meningococcal disease, it is critical to treat the patient as soon as infection is suspected and not delay obtaining a culture or laboratory results. Several commercial multiplex PCR assays capable of simultaneously testing a single specimen for an array of pathogens that cause blood infections or meningitis/encephalitis are now available, primarily for clinical settings (e.g., FilmArray Blood Culture Identification Panel and FilmArray Meningitis/ Encephalitis Panel from BioFire Diagnostics and Meningitis/Encephalitis Panel by PCR from ARUP Laboratories).9,38,39 While such assays can rapidly identify Hi and Nm species, most do not determine serotype or serogroup. Therefore, it is important for laboratories using assays that do not determine VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.22

serotype/serogroup to perform either a simultaneous culture or a reflex culture if Hi or Nm is identified. At a minimum, laboratories should collect and maintain an adequate clinical sample for further testing at a laboratory with a PCR assay that can detect serotype/serogroup. Serogroup testing Serogrouping distinguishes encapsulated meningococcal strains from unencapsulated strains, which do not express any capsule on cell surface and cannot be serogrouped. The 12 encapsulated groups (A, B, C, W, X, Y, etc.) have distinct capsular polysaccharides that can be differentiated by slide agglutination with specific antisera or PCR. Microbiology laboratories should perform serogroup testing of meningococcal isolates and clinical specimens that are positive for N. meningitidis in a timely manner. If serogrouping is not available at a laboratory, laboratory personnel should contact the state health department. State health departments with questions about serogrouping should contact the CDC Meningitis and Vaccine Preventable Disease Branch Laboratory at 404-639-3158. Susceptibility testing Routine antimicrobial susceptibility testing of meningococcal isolates is not recommended. N. meningitidis strains with decreased susceptibility to penicillin G have been identified sporadically from several regions of the United States, Europe, and Africa.40 Most of these isolates with reduced penicillin susceptibility remain moderately susceptible (minimum penicillin inhibitory concentration of between 0.12 µg/mL and 1.0 µg/mL). High-dose penicillin G remains an effective treatment against moderately susceptible meningococci. Surveillance of susceptibility patterns in populations should be conducted to monitor trends in N. meningitidis susceptibility. Molecular typing during outbreaks Phenotypic and genotypic methods are used to investigate meningococcal diversity. Capsular polysaccharide (serogroup), porin protein PorB (serotype), and porin protein PorA (serosubtype) are all phenotypic characteristics that can be used to distinguish meningococci from one another.41 Outbreaks of meningococcal disease are usually caused by the same or closely related strains.42 Molecular genotyping techniques such as PFGE, 16S rRNA gene sequencing, or MLST are used for subtype characterization of an outbreak clone.43,44 This subtyping helps to better define the extent of the outbreak. It is crucial to have rapid and reliable results in determining the meningococcal serogroup in an outbreak because public health response will differ for vaccine-preventable or non-vaccine–preventable disease. Molecular genotyping provides important tools for understanding the overall epidemiology of meningococcal disease, but different methods may be more useful in certain settings. PFGE or 16S rRNA gene typing seem to be most useful for outbreak and short-time-period epidemiology, whereas MLST has become the “gold standard” for long-term, global tracing of meningococcal population changes. H. Mumps (see Chapter 9 [http://www.cdc.gov/vaccines/pubs/surv-manual/chpt09-mumps.html]) Mumps can occur in persons who are fully vaccinated, although vaccinated persons are at much lower risk for mumps and mumps complications. Recent outbreaks have most commonly occurred among fully vaccinated groups of people who have prolonged, close contact exposures, such as sharing water bottles or cups, kissing, practicing sports together or living in close quarters with a person who has mumps. Laboratory confirmation of mumps can be more challenging among vaccinated populations because the viral load may be lower and less easily detected and the IgM response may be absent, delayed, or short- lived compared with unvaccinated people. Successful detection of mumps virus by reverse transcription polymerase chain reaction (RT-PCR) or a mumps IgM response is dependent upon proper collection (parotid massage), timing of collection, and proper transport and storage of specimens. Failure to detect mumps virus RNA by RT-PCR or to detect IgM in serum in samples from a person with clinically compatible mumps does not rule out mumps as a diagnosis. Efforts to train providers in proper collection, storage and shipment of specimens have improved mumps detection.45,46Acute mumps infection can be confirmed by the detection of mumps virus RNA, by RT-PCR, or by isolation of mumps virus from a clinical specimen. A clinically compatible case VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.23

with a positive mumps RT-PCR result or positive virus isolation is classified as confirmed. Maximal viral shedding occurs 1–3 days prior to onset and through day 5 following onset of parotitis. Early collection (0 to 3 days since parotitis onset) of a buccal or oral swab provides the best means of laboratory confirmation, particularly among persons with a history of vaccination since virus titers are lower and virus may be cleared more rapidly than in unvaccinated persons.47–49 If mumps RNA is detected in buccal/oral swab samples, the samples can be submitted for sequence analysis to determine the viral genotype. Analysis of sequence data can help to monitor viral transmission. Additionally, in cases of suspected vaccine reactions (i.e., patients with suspected mumps who were recently vaccinated), it is necessary to collect buccal/oral swab samples for virus detection and genotyping. Since serologic tests cannot differentiate between an exposure to vaccine and an exposure to wild-type mumps virus, genotyping must be used to confirm detection of vaccine strain or wild-type virus. Buccal or oral swab specimens should be obtained by massaging the parotid gland area for 30 seconds prior to swabbing the area around Stensen’s duct. A commercial product designed for the collection of throat specimens or a flocked polyester fiber swab can be used. Synthetic swabs are preferred over cotton swabs, which may contain substances that are inhibitory to enzymes used in RT-PCR. Flocked synthetic swabs appear to be more absorbent and elute samples more efficiently. See the CDC mumps laboratory website for information on viral transport medium, specimen storage, and shipment recommendations. The presence of serum mumps IgM can also be used to aid in the diagnosis of mumps infection but is not confirmatory. Detection of mumps IgM is improved if serum specimens are collected greater than 3 days after parotitis onset.45,50,51 A clinically compatible case with a positive serum anti-mumps immunoglobulin M (IgM) antibody result is classified as probable. Specimen Collection Appropriate timing and collection of specimens is important to improve the sensitivity of laboratory testing. A provider job-aid is available here. ● The parotid should be massaged for 30 seconds prior to buccal swab collection. For instructions on how to appropriately collect a buccal swab for mumps testing, a video is provided here. ● If it has been ≤3 days since parotitis onset, collect a buccal swab specimen for RT-PCR. ● If it has been >3 days since parotitis onset, collect a buccal swab specimen for RT-qPCR and a serum specimen for IgM detection. ● If the patient has orchitis/oophoritis, mastitis, pancreatitis, hearing loss, meningitis or encephalitis and does not have parotitis, collect a buccal swab specimen for RT-qPCR, a urine specimen for RT-qPCR, and a serum specimen for IgM detection regardless of the days since symptom onset. For sporadic cases that have negative laboratory results for mumps consider testing for other etiologies such as influenza virus (influenza A virus subtype H3N2), parainfluenza virus types 1–3, Epstein-Barr virus, human herpesviruses 6A and 6B, herpes simplex viruses 1 and 2, coxsackievirus A, adenovirus, parvovirus B19, echovirus, lymphocytic choriomeningitis virus, HIV, or bacteria including Staphylococcus aureus and alpha hemolytic streptococcus. Virus Isolation and RT-PCR To provide state and local jurisdictions with enhanced surveillance testing capacity for 7 VPDs―including mumps, measles, rubella, varicella zoster virus, Bordetella pertussis, Haemophilus influenzae, and VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.24

Neisseria meningitidis—CDC, in collaboration with the Association of Public Health Laboratories (APHL) and the Council of State and Territorial Epidemiologists (CSTE), in 2013 established 4 Vaccine Preventable Disease Reference Centers (VPD-RCs). These VPDs are typically detected by laboratory testing such as quantitative reverse transcription polymerase chain reaction (RT-PCR) assay of clinical specimens. The VPD-RCs provide state and local health departments with surge capacity for large outbreaks, testing for jurisdictions without RT-PCR capabilities, and genotyping. Since their establishment, VPD-RCs have received and tested the majority of the mumps clinical specimens. Mumps is laboratory confirmed by (RT-PCR), real time RT-PCR (RT-qPCR), or viral culture from buccal or urine specimens. Collect oral or buccal swab samples as soon as mumps disease is suspected. RT-PCR has the greatest diagnostic sensitivity when samples are collected ≤3 days of parotitis onset. Urine is not the optimal specimen for RT-PCR and is not preferred as a specimen for patients with parotitis, even for those patients presenting more than 3 days since symptom onset.46, 52–57 Testing urine during an outbreak does not significantly increase diagnostic yield and can negatively impact testing resources. However, in patients presenting with mumps complications (orchitis, oophoritis, nephritis, encephalitis, meningitis) without parotitis or other salivary gland swelling collecting a urine specimen in addition to an oral specimen might help to confirm mumps infection. At the onset of a suspected mumps outbreak, patients suspected to have mumps should be tested by RT-PCR to confirm mumps and rule out other possible etiologies. However, once a mumps outbreak is confirmed, jurisdictions should consider alternate strategies to reduce testing to conserve public health resources. Molecular Typing Molecular epidemiologic surveillance makes it possible to build a sequence database that will help monitor any changes in the genotype prevalence over time and help track transmission of mumps strains circulating in the United States. Collecting and submitting specimens for sequencing is important for molecular surveillance and informing public health. Specimens for molecular typing should be obtained as soon as possible after the onset of parotitis, ideally from the day of onset to 3 days later (not more than 10 days after parotitis). Molecular typing is the only test that can discriminate vaccine reactions from wild-type infections. Specific instructions for specimen collection and shipping may be obtained from CDC by referring to the CDC mumps laboratory website. CDC and the VPD-RCs can perform mumps genotyping on RT-PCR–positive specimens. The nucleotide sequence of the entire mumps short hydrophobic (SH) gene is used to assign mumps viruses to one of 12 recognized genotypes.58 In some circumstances, a genotype has been associated with endemic circulation of mumps virus in a country; however, routine genotype surveillance for mumps is limited to only a few countries. The genetic information from circulating mumps viruses is used to track the transmission pathways of the virus and can be used to suggest epidemiologic links, or lack thereof, between cases and outbreaks.59 CDC has detected mostly genotype G among people with mumps in the United States since we initiated routine genotype surveillance for mumps in 2006.60 Mumps outbreaks are typically associated with only one genotype. There are no differences in the genotypes detected in vaccinated and unvaccinated people who have gotten mumps in the United States. Public health laboratories are encouraged to send patient samples from RT-PCR positive sporadic cases of mumps, as well as select specimens from an outbreak, (for more information on which specimens, see Guidance for Optimizing Mumps Testing) to CDC or the VPD-RC’s. If the outbreak spreads to another community, an effort should be made to obtain a genotype on initial positive specimens from the new outbreak. Molecular surveillance of mumps outbreaks ● To monitor ongoing established outbreaks, a maximum of 5 specimens per week from these outbreaks should be sent to a VPD-RC or CDC for sequencing ● Obtain an SH sequence for cases at the beginning of an outbreak, during each epidemiologic week of the outbreak, and if/when the outbreak spreads to a new area or community VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.25

● In an outbreak, obtaining a sequence on every specimen is not necessary especially when linkages between cases are well understood ● Obtaining sequences from sporadic cases is important because they help us monitor transmission patterns of mumps virus ● Identifying travel and/or a potential source for mumps cases will help us understand the global distribution of mumps genotypes ● Jurisdictions that perform mumps RT-PCR testing at their state or local public health laboratories should also send RT-PCR positive specimens to monitor new or ongoing outbreaks ● Global virologic surveillance for mumps is not as robust as for measles or rubella, so the true diversity of genotypes is not known Priority patients for sequencing ● Patients with parotitis, salivary gland swelling, oophoritis, or orchitis who are not epidemiologically linked to a confirmed or probable mumps case-patient (sporadic cases) ● Patients with aseptic meningitis, encephalitis, hearing loss, mastitis, or pancreatitis in the absence of parotitis, salivary gland swelling, oophoritis, or orchitis (severe mumps complications) ● Patients who traveled internationally during their likely incubation period (12–25 days prior to onset) ● Patients with recurrent parotitis (submit samples from both occurrences when possible) ● Patient who received ≥3 doses of MMR more than 28 days before symptom onset Serologic Testing for IgM Antibody Vaccination status and timing of specimen collection affect the ability to detect IgM in persons infected with mumps. In general, the percentage of specimens with a positive IgM result is highest in unvaccinated persons, intermediate in one-dose vaccine recipients, and lowest in 2-dose vaccine recipients. Specimens collected greater than 3 days post-parotitis onset are more likely to have a positive IgM result. IgM test methods and kits vary considerably in sensitivity and specificity with some indirect EIA and immunofluorescent assays detecting as few as 12%–15% of confirmed mumps cases.45 IgM capture ELISA is the most sensitive serologic method detecting 46%–71% of RT- PCR confirmed cases.45 The local or state health department can provide guidance on available laboratory services and preferred tests. Failure to detect mumps IgM in previously vaccinated persons who are infected with mumps has been well documented. People with a history of mumps vaccination may not have detectable mumps IgM antibody regardless of timing of specimen collection. ● Enzyme immunoassay— EIA is a highly specific test for diagnosing acute mumps infection. Commercial immunofluorescence (IFA) and indirect EIA tests are less sensitive than capture IgM assays.45 At the direction of the state health department, healthcare providers and state and local health departments may send serum specimens from persons with suspected mumps cases to the CDC Viral Vaccine-Preventable Diseases Branch for IgM detection by their in-house Capture EIA. ● Immunofluorescence assays— IFAs have the advantage of being relatively inexpensive and simple. The reading of IFA IgM tests requires considerable skill and experience since nonspecific staining may cause false-positive readings. IFA and indirect EIA may be susceptible to interference by high levels of IgG. Treatment of serum to remove IgM may be necessary to avoid false-positive results. Note: Commercially available IFA antibody assays and EIA kits for detection of mumps IgM are currently not approved by the U.S. Food and Drug Administration. Each laboratory must validate these tests independently.

Serum collection and timing of the mumps IgM response ● Unvaccinated persons— IgM antibody is detectable within 5 days after onset of symptoms, reaches a maximum level about a week after onset, and remains elevated for several weeks or months.61,62 Most IgM detection assays work well in unvaccinated persons although false negative results may occur if collected too early.1 If an acute-phase serum sample collected ≤3 days after parotitis onset is negative for IgM and negative by RT-PCR, testing a second serum sample collected on day 5 or later after symptom onset is recommended as the IgM response may require more time to reach a detectable level. VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.26

● Vaccinated persons— Patients that mount a secondary immune response to mumps, as seen in most previously vaccinated persons, may not have an IgM response or it may be absent, delayed or short-lived depending on the timing of specimen collection.61 Because of this, a high number of false-negative results may occur in previously vaccinated individuals if specimens are collected ≤3 days. False-positive IgM results can also occur and appear to be more prevalent with certain IgM test formats, such as the IFA. Collecting specimens >3 days after parotitis onset improves the ability to detect IgM. During outbreaks, 13–46% of serum samples collected from patients less than 3 days after symptom onset were positive compared with 71% of serum samples collected >3 days.45 However, persons with a history of mumps vaccination may not have detectable mumps IgM antibody regardless of the timing of specimen collection and failure to detect mumps IgM in serum in samples from a person with clinically compatible mumps does not rule out mumps as a diagnosis. Serologic Testing for IgG Antibody A variety of tests for IgG antibodies to mumps are available and include EIA, IFA, and plaque reduction neutralization. The specific criteria for documenting the presence of mumps IgG antibody or an increase in titer depends on the test. Adults born in 1957 or later or persons with no history of mumps illness or vaccination may have detectable mumps IgG due to a previous asymptomatic infection. ● Diagnosis of mumps with IgG— Documentation of seroconversion from IgG negative to IgG positive by EIA or a 4-fold rise in IgG titer using paired specimens as measured in plaque-reduction neutralization assays or similar quantitative assays can be used to aid in the diagnosis of mumps. Tests for IgG antibody should be conducted on both acute- and convalescent-phase specimens at the same time, and the same type of test should be used on both specimens. EIA values are not titers and increases in EIA values do not directly correspond to rises in titer results. ● Unvaccinated persons— In unvaccinated persons, IgG antibody increases rapidly after onset of symptoms and is typically long lasting. IgG may be present in the acute-phase sample depending on the timing of sample collection. ● Vaccinated persons— In vaccinated persons, the IgG will likely already be elevated in the acute-phase blood sample, which frequently prevents detection of a 4-fold rise in IgG titer in the convalescent serum specimen. For this reason, detection of a 4-fold rise in IgG is not recommended for use among previously vaccinated persons. Presumptive Laboratory Evidence of Immunity The presence of mumps-specific IgG, as detected using a serologic assay (EIA or IFA), is considered evidence of prior exposure to mumps vaccine or mumps virus but does not necessarily predict the presence of neutralizing antibodies or protection from mumps disease. I. Pertussis (see Chapter 10 [http://www.cdc.gov/vaccines/pubs/surv-manual/chpt10-pertussis.html]) Culture Isolation of B. pertussis by bacterial culture remains the gold standard for diagnosing pertussis. It is also required for antimicrobial susceptibility testing and molecular typing. Although bacterial culture is specific for the diagnosis, it is relatively insensitive. Under optimal conditions 80% of suspected cases in outbreak investigations can be confirmed by culture; in most clinical situations isolation rates are much lower.63 The timing of specimen collection can affect the isolation rate, as can inadequately collected specimens and concurrent use of effective antimicrobial agents. Because patients can remain culture positive even while taking effective antibiotics (e.g., when strains are resistant to the antibiotic), nasopharyngeal swab for culture should be obtained regardless of concurrent use of an antibiotic. Fastidious growth requirements make B. pertussis difficult to isolate. Isolation of the organism using direct plating is most successful during the catarrhal stage (i.e., first 1–2 weeks of cough). All persons with suspected pertussis disease should have a nasopharyngeal aspirate or swab obtained from the posterior nasopharynx for culture. Recovery rates of B. pertussis from nasopharyngeal aspirates are similar to or higher than rates of recovery from nasopharyngeal swabs;63–66 rates of recovery from VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.27

throat and anterior nasal swabs are unacceptably low. Therefore, specimens should be obtained from the posterior nasopharynx, not the throat (Figure 1), by using a polyester (such as Dacron) or nylon flocked nasopharyngeal swabs. Cotton-tipped swabs are not acceptable as residues present in these materials inhibit growth of B. pertussis. Specimens should be plated directly onto selective culture medium or placed in transport medium. Regan-Lowe agar or Bordet-Gengou agar are generally used for culture; half- strength Regan-Lowe should be used as the transport medium. Success in isolating the organism declines if the patient has received prior antibiotic therapy effective against susceptible B. pertussis (erythromycin or trimethoprim-sulfamethoxazole), if there is a delay in specimen collection beyond the first 2 weeks of illness, or if the patient has been vaccinated. A positive culture for B. pertussis confirms the diagnosis of pertussis. For this reason, access to a microbiology laboratory that is prepared to perform this service for no cost or for limited cost to the patient is a key component of pertussis surveillance.

Figure 1: Proper technique for obtaining a nasopharyngeal specimen for isolation of B. pertussis

Polymerase chain reaction PCR is an important tool for timely diagnosis of pertussis and is widely available to clinicians. PCR is a molecular technique used to detect DNA sequences of the Bordetella pertussis bacterium, and unlike culture, does not require viable (live) bacteria present in the specimen.67,68 PCR testing of nasopharyngeal swabs or aspirates can be a rapid, sensitive, and specific method for diagnosing pertussis;68,69 however, false-positive results may be obtained because of contamination in the laboratory or during specimen collection.69,70 Although early signs and symptoms of pertussis are often non-specific, only patients with signs and symptoms consistent with pertussis should be tested. Asymptomatic contacts of confirmed cases should not be tested and testing of contacts should not be used for postexposure prophylaxis decisions. Since its inclusion in the case definition in 1997, the proportion of cases confirmed by PCR has increased substantially, and many laboratories now use only PCR to confirm pertussis.71 However, the assay varies among laboratories and is not standardized69 and assay procedures, as well as sensitivity and specificity, can vary greatly between laboratories. Thus, interpretation criteria for diagnosis vary. Interpretation of PCR results, especially those with high cycle threshold (Ct) values should be done in conjunction with an evaluation of signs and symptoms and available epidemiological information. For more information about interpretation of PCR Ct values, see Best Practices for Health Care Professionals on the use of Polymerase Chain Reaction (PCR) for Diagnosing Pertussis.72 While PCR is increasingly used as the sole diagnostic test for pertussis, CDC recommends that PCR be used in conjunction with culture when feasible, rather than as an alternative test. Direct comparison with culture is necessary for validation, and the use of multiple targets is recommended to distinguish B. pertussis from other Bordetella species.73 Even if a laboratory has validated its PCR method, isolation of B. pertussis by culture should be attempted when possible. B. pertussis isolates can then be evaluated for azithromycin and erythromycin susceptibility and by molecular typing methods, which can help define the molecular epidemiology of strains circulating in the United States. VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.28

The timing of PCR testing for pertussis can significantly affect its ability to accurately diagnose the disease. PCR has optimal sensitivity during the first 3 weeks of cough when bacterial DNA is still present in the nasopharynx. After the fourth week of cough, the amount of bacterial DNA rapidly diminishes, which increases the risk of obtaining falsely negative results. Collection methods for PCR are similar to those for culture, and often the same sample can be used for both tests. However, calcium alginate swabs cannot be used to collect nasopharyngeal specimens for PCR. Swabs used solely for PCR (and not culture) testing may be placed in a dry, sterile tube for transport to the laboratory. Use of liquid transport media is discouraged due to the risk of specimen contamination. Serologic testing Although serologic testing has proved useful in clinical studies and outbreak investigations, it is not yet standardized. Also, the lack of association between antibody levels and immunity to pertussis makes results of serologic testing difficult to interpret. Even though serology is not part of the clinical case definition, commercial clinics and manufacturers still provide serologic assays and serology kits for pertussis diagnosis. No serologic assay is FDA approved and very little is understood about the clinical accuracy of these commercially available serologic assays. Cutoff points for diagnostic values of immunoglobulin (Ig)G antibody to pertussis toxin (PT) have not been established, and current IgA and IgM assays lack adequate sensitivity and specificity. In the absence of recent immunization, an elevated serum IgG antibody to PT after 2 weeks of cough onset is suggestive of recent B. pertussis infection. An increasing titer or a single IgG anti-PT value of approximately 100 IU/ mL or greater (using standard reference sera as a comparator) can be used for diagnosis. Only in Massachusetts, where the state utilizes its own clinically validated assay, is serology used for clinical diagnosis and reporting for patients 11 years of age and older.74 CDC, together with the FDA, validated an IgG anti-PT ELISA that has proven useful for diagnosis in adolescents and adults during the later phases of the disease.75–77 The assay is currently performed at the Minnesota Department of Health Public Health Laboratory to support other state health departments, as part of the “Vaccine Preventable Diseases Reference Centers Program External”.74 Elsewhere, with few exceptions, it is not known if serologic testing has been appropriately validated or standardized. Therefore, serologic testing should not be relied upon to confirm cases for national reporting purposes. Cases meeting the clinical case definition that are serologically positive, but not culture positive or PCR positive, should be reported as probable cases. Direct fluorescent antibody testing DFA testing of nasopharyngeal secretions, which is sometimes used to screen for pertussis, is not recommended as a test for diagnosing pertussis. A positive DFA result may increase the probability that the patient has pertussis, but it has limited specificity (frequent false-positive results) and is not a confirmatory test. A monoclonal DFA test is available, but the sensitivity and specificity are variable. Elevated white blood cell count An elevated white blood cell count with a lymphocytosis (i.e., increase in lymphocyte count) is usually present in cases of pertussis. The absolute lymphocyte count can reach 20,000/mm3 or higher. However, there may be no lymphocytosis in very young infants, vaccinated children, or adults with mild cases of pertussis. The white blood cell count is not a test of confirmation. Pulsed-field gel electrophoresis PFGE is a type of DNA fingerprinting. This technique has been a useful tool for distinguishing epidemiologically related strains (e.g., strains from the same household or small community), while showing diversity within larger geographic areas such as cities, counties, and states.78, 79 Multi-locus variable-number tandem repeat analysis Multi-locus variable-number tandem repeat analysis (MLVA) is a molecular typing method that compares genomic regions of direct repeats (variable-number tandem repeats, or VNTRs) between strains;80 it demonstrates less diversity of strains than PFGE. MLVA has the advantage of being applicable to both cultures and directly to nucleic acid extracted from clinical specimens.81 VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.29

Multi-locus sequence typing Multi-locus sequence typing (MLST) is another typing method that analyzes nucleotide variation in a predetermined set of genes or gene fragments.82 MLST methods vary between bacterial species. Although an MLST method for B. pertussis is not standardized, many laboratories analyze fragments of 3 genes and promoter regions encoding virulence factors that are included in several acellular pertussis vaccines.83,84 State health departments with questions regarding isolation, PCR detection, serology, or other test methods for B. pertussis should contact the CDC Pertussis and Diphtheria Laboratory at 404-639-1231.

J. Pneumococcal infection (see Chapter 11 [http://www.cdc.gov/vaccines/pubs/surv-manual/chpt11-pneumo.html]) Culture Streptococcus pneumoniae is a gram-positive, lancet-shaped diplococcus that commonly inhabits the throat as normal flora. S. pneumoniae commonly causes lower and upper respiratory diseases, including pneumonia, meningitis, and acute otitis media. Diagnosis of invasive pneumococcal infection is confirmed by culture and isolation of S. pneumoniae from a normally sterile body site (e.g., blood, CSF, pleural fluid, peritoneal fluid). Alternatively, diagnosis can be confirmed from culture-negative specimens from normally sterile sites using real-time PCR. Antibiotic resistance The Clinical Laboratory Standards Institute (CLSI) recommends that clinical laboratories test all isolates of S. pneumoniae from CSF for resistance to penicillin, cefotaxime or ceftriaxone, meropenem, and vancomycin.85 For organisms from other sources, laboratories should consider testing for resistance to erythromycin, penicillin, trimethoprim-sulfamethoxazole, clindamycin, cefepime, cefotaxime or ceftriaxone, a fluoroquinolone, meropenem, tetracycline, and vancomycin. Pneumococci resistant to vancomycin have never been described. Linezolid-resistance is extremely rare and has been associated with mutations within the rplD-encoded ribosomal protein L4.86 For vancomycin, a strain is considered non-susceptible if it has a minimum inhibitory concentration of >1 μg/ml or greater or zone diameter less than <17 mm. For linezolid, nonsusceptible strains are those with a minimum inhibitory concentration (MIC) of >2 μg/ml or zone diameter <21 mm. Strains found to be nonsusceptible to vancomycin or linezolid should be submitted to a reference laboratory for confirmatory testing, and if resistant, reported to the state health department. Because pneumococci are fastidious organisms, some susceptibility testing methods used for other organisms are not appropriate for pneumococci; see the CLSI document for testing recommendations.85 The CDC’s Antibiotic Resistance Laboratory Network (ARLN) is available to assist state public health laboratories with susceptibility testing of IPD isolates. States can request testing for select IPD isolates. Contact [email protected] for information on this program. Additionally, isolates with unusual resistance features can be sent to the CDC Streptococcus Laboratory for phenotypic verification and genomic analysis employing their specialized bioinformatics pipeline for detecting resistance determinants.87 Contact [email protected] for additional information. State health department laboratories that obtain penicillin binding protein gene sequencing information may consider using the CDC Streptococcus Laboratory database for deducing β-lactam antibiotic MICs (https://www.cdc.gov/ streplab/pneumococcus/mic.html).88 Serotyping Current pneumococcal vaccines are based upon capsular polysaccharides. There are currently >91 known capsular serotypes. Since only subsets of capsular serotypes are included in pneumococcal vaccines, serotyping allows the measurement of vaccine efficacy and can provide data for development of expanded- serotype vaccines.89 CDC and its partners perform active, population-based surveillance for invasive pneumococcal serotypes in specific areas that represent about 30 million people in the United States. Serotyping is currently performed in only a limited number of state public health laboratories, academic centers, or at CDC. State public health laboratories may consider adopting a PCR-based technique for determining capsular serotypes, http://www.cdc.gov/vaccines/pubs/surv-manual/chpt22-lab-support. html#92.90–93 The CDC Streptococcus Laboratory provides numerous protocols and references for state health departments and clinical labs to identify pneumococcal serotypes using PCR (https://www.cdc. gov/streplab/pcr.html). If states are unable to perform PCR serotyping, the CDC’s ARLN and VPD VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.30

programs can provide serotyping assistance for select IPD isolates or specimens. Contact [email protected] for serotyping assistance. The CDC Streptococcus Laboratory will conduct serotyping of pneumococcal isolates from blood, CSF, or other sterile sites in outbreak settings, and when appropriate will perform whole genome sequence analysis to determine strain features and relatedness between isolates from disease clusters. Contact [email protected] for outbreak assistance. Serotypes are deduced through the same bioinformatics pipeline used to determine MLST types and resistance features.87 K. Poliomyelitis (see Chapter 12 [http://www.cdc.gov/vaccines/pubs/surv-manual/chpt12-polio.html]) Virus isolation The likelihood of poliovirus isolation is highest from stool specimens, intermediate from pharyngeal swabs, and very low from blood or spinal fluid. Poliovirus is present in the stool in the highest concentration and for the longest time of any specimen, and therefore remains the most critical specimen for diagnosis. Because cell culture is extremely sensitive for the detection of poliovirus, it remains as sensitive, or more sensitive, than most molecular assays. A negative pan-enterovirus PCR result cannot rule out poliovirus infection. Isolation of poliovirus from stool specimens contributes to the diagnostic evaluation but does not constitute proof of a causal association between the isolated viruses and paralytic poliomyelitis.94 Isolation of virus from CSF is diagnostic but is rarely accomplished. To increase the probability of poliovirus isolation, at least 2 stool specimens and 2 throat swabs should be obtained 24 hours apart from patients with suspected poliomyelitis as early in the course of the disease as possible (i.e., immediately after poliomyelitis is considered as a possible differential diagnosis), but ideally within the first 14 days after onset of paralytic disease. Specimens should be sent to the state or other reference laboratories for primary isolation. Laboratories should forward isolates to CDC for intratypic differentiation to determine whether the poliovirus isolate is wild or vaccine-derived. CDC can assist with culture if it is not otherwise readily available. Isolation of wild poliovirus constitutes a public health emergency, and appropriate control efforts must be immediately initiated (in consultation among healthcare providers, the state and local health departments, and CDC). Type 2 poliovirus has been declared eradicated; type 2 infectious and potentially infectious materials should be handled only in a proper containment facility. As of August 1, 2016, all type 2 poliovirus isolates must be referred to a WHO-accredited polio sequencing laboratory for detailed characterization. Serologic testing Serology may be helpful in supporting or ruling out the diagnosis of paralytic poliomyelitis. An acute-phase serum specimen should be obtained as early in the course of disease as possible, and a convalescent-phase specimen should be obtained at least 3 weeks later. A 4-fold rise in titer between the acute- and convalescent-phase specimens suggests poliovirus infection. Nondetectable antibody titers in both specimens may help rule out poliomyelitis but may be falsely negative in immunocompromised persons, who are also at highest risk for paralytic poliomyelitis. In addition, neutralizing antibodies appear early and may be at high levels by the time the patient is hospitalized, so that a 4-fold rise may not be demonstrated. Vaccinated persons would also be expected to have measurable titers; therefore, vaccination history is important for interpretation of serologic tests. One of the limitations of serology is the inability to distinguish between antibody induced by vaccine-related poliovirus and antibody induced by wild virus. Serologic assays to detect anti-poliovirus antibodies are available in most commercial and state public health laboratories. L. Rotavirus (see Chapter 13 [http://www.cdc.gov/vaccines/pubs/surv-manual/chpt13-rotavirus.html]) Laboratory testing is necessary to confirm group A rotavirus infection and to ensure reliable surveillance and clinical therapy. Because rotavirus is shed in such high concentrations in stool, fecal specimens are preferred for diagnosis of rotavirus. Methods available to diagnose rotavirus infection include detection of viral antigens (EIA, immunochromatography, electron microscopy, and immunostaining) and molecular detection by RT-PCR/quantitative reverse transcription PCR (qRT-PCR) and genomic sequencing.95–97 VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.31

Detection of viral antigens The most widely available method of antigen detection in stool is EIA, which detects an antigen common to all group A rotaviruses.95 Several inexpensive commercial EIA kits are available and provide rapid and highly sensitive results (90%–100%). Because EIA is rapid, inexpensive, and highly sensitive, it is the most appropriate method for clinical diagnosis and surveillance. Another less frequently used method more appropriate for a research setting is visualization of viral particles by electron microscopy. Molecular detection Molecular methods can be used to detect rotavirus infection in clinical specimens and to characterize the virus. Molecular methods for detection of viral RNA include RT-PCR, qRT-PCR, and genomic sequencing.96, 97 Multiplexed, semi-nested RT-PCR genotyping and genomic sequencing are widely used to identify the most common and several uncommon rotavirus G and P genotypes.96, 97 Genomic sequencing has been used extensively to identify uncommon strains and genetic variants that cannot be identified by RT-PCR genotyping and to confirm the results of genotyping methods.96, 97 Virus isolation Rotavirus can be isolated directly from fecal specimens by inoculation of cell cultures in the presence of trypsin-containing growth medium, but this procedure is labor-intensive and more appropriate for research laboratories. M. Rubella (see Chapter 14 [http://www.cdc.gov/vaccines/pubs/surv-manual/chpt14-rubella.html]) Clinical diagnosis of rubella is unreliable; therefore, cases must be laboratory confirmed. Virus detection and serologic testing can be used to confirm acute or recent rubella infection. Serologic tests can also be used to screen for rubella immunity. Virus detection (real-time RT-PCR, RT-PCR) Rubella virus can be detected from nasal, throat, urine, blood, and CSF specimens from persons with rubella (see Appendix 15 at https://www.cdc.gov/vaccines/pubs/surv-manual/appx/appendix15-rubella.pdf). The best results are achieved with throat swabs. CSF specimens should be reserved for persons with suspected rubella encephalitis. Efforts should be made to obtain clinical specimens for virus detection from all case-patients at the time of the initial investigation. Virus may be detected from 1 week before to 2 weeks after rash onset. However, maximum viral shedding occurs up to day 4 after rash onset. Real-time RT-PCR and RT-PCR can be used to detect rubella virus and has been extensively evaluated for its usefulness in detecting rubella virus in clinical specimens.84, 85 Clinical specimens obtained for virus detection and sent to CDC are routinely screened by these techniques. Molecular typing is recommended because it provides important epidemiologic information to track the epidemiology of rubella in the United States now that rubella virus no longer continuously circulates in this country. By comparing virus sequences obtained from new case-patients with other virus sequences, the origin of particular virus types in this country can be tracked.100 Furthermore, this information may help in documenting the maintenance of the elimination of endemic transmission. In addition, genotyping methods are available to distinguish wild-type rubella virus from vaccine virus. Serologic testing The serologic tests available for laboratory confirmation of rubella infections and immunity vary among laboratories. The state health department can provide guidance on available laboratory services and preferred tests. EIAs are the most commonly used and widely available diagnostic test for rubella IgG and IgM antibodies and are sensitive and relatively easy to perform. EIA is the preferred testing method for IgM, using the capture technique, although indirect assays are also acceptable. Latex agglutination tests appear to be sensitive and specific for screening when performed by experienced laboratory personnel. Other tests in limited use to detect rubella-specific IgM include HI and IFA. VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.32

Detection of IgM antibody Rubella-specific IgM can usually be detected 4–30 days after onset of illness, and often for longer. Sera should be collected as early as possible after onset of illness. However, IgM antibodies may not be detectable before day 5 after rash onset. In case of a rubella IgM-negative result in specimens taken before day 5, serologic testing should be repeated on a specimen collected after day 5. Because rubella incidence is low, a high proportion of IgM-positive tests will likely be false positive. False-positive serum rubella IgM tests may occur due to the presence of rheumatoid factors (indicating rheumatologic disease) or cross-reacting IgM, or infection with other viruses.101,102 Avidity testing (see below) and detection of wild-type rubella virus can be used to resolve uncertainties in the serologic evaluation of suspected cases. Particular care should be taken when rubella IgM is detected in a pregnant woman with no history of illness or contact with a rubella-like illness. Although this is not recommended, many pregnant women with no known exposure to rubella are tested for rubella IgM as part of their prenatal care. If rubella test results are IgM-positive for persons who have no or low risk of exposure to rubella, additional laboratory evaluation should be conducted. Laboratory evaluation is similar to that described in the IgM-positive section of Figure 2. Figure 2. Algorithm for serologic evaluation of pregnant women exposed to rubella

IgM and IgG at the time of first visit (Save sera)

IgM+/IgG+ IgM+/IgG- IgM-/IgG- IgM- /IgG+

Acute infection or false Susceptible Immune IgM positive

Repeat IgM/IgG 3–4 weeks Collect 2nd serum 5–10 days later. from suspected exposure IgM, IgG, and avidity testing to be conducted (Test concurrently with first specimen)

High avidity, no rise in Low avidity, rise IgG titers in IgG titers Positive Negative (tested together with (tested together with IgM+, IgG+ first serum) first serum) Likely false positive Acute Infection Repeat IgM/IgG in 6 weeks if risk of exposure continues to exist (Test concurrently with first specimen)

Discuss options for Acute Positive Negative pregnancy infection IgM+, IgG+ outcome

Infection discarded

Detection of IgG antibody (significant rise or avidity) for diagnostictesting To detect a significant rise in rubella-specific IgG concentration, the first serum specimen should be obtained as soon as possible after onset of illness and the second serum sample should be collected about 7–21 days after the first specimen. In most rubella cases, rubella IgG is detectable by 8 days after rash onset.103 Tests for IgG antibody should be conducted on both acute-and convalescent-phase specimens at the same time with the same test. Assays for IgG avidity are useful to distinguish the difference between recent and past rubella infections. Low avidity is associated with recent primary rubella infection, whereas high avidity is associated with past infection or reinfection. Avidity tests are not routine tests and should be performed in reference laboratories. A number of avidity assays have been described.104, 105 VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.33

Detection of IgG antibody to screen for rubella immunity A single serologic IgG test may be used to determine the rubella immune status of persons whose history of rubella disease or vaccination is unknown. The presence of serum IgG rubella-specific antibodies indicates immunity to rubella. N. Congenital rubella syndrome (see Chapter 15 [http://www.cdc.gov/vaccines/pubs/surv-manual/chpt15-crs.html]) Diagnostic tests used to confirm CRS include virus detection and serologic assays. Virus detection (real-time RT-PCR, RT-PCR) Rubella virus can be detected from nasal, throat, urine, and blood specimens from infants with CRS. Efforts should be made to obtain clinical specimens for virus isolation from infants at the time of the initial investigation (see Appendix 15, https://www.cdc.gov/vaccines/pubs/surv-manual/appx/appendix15- rubella.pdf). However, because infants with CRS may shed virus from the throat and urine for a prolonged period (a year or longer), specimens obtained later may also yield rubella virus. As with rubella infection, molecular typing is recommended because it provides important epidemiologic information to track the epidemiology of rubella in the United States now that rubella virus no longer continuously circulates in this country. By comparing virus sequences from new case-patients with virus sequences from other cases, the origin of particular virus types in this country can be tracked.106 Furthermore, this information may help in documenting the maintenance of the elimination of endemic rubella virus transmission. Specimens for molecular typing should be obtained from patients with CRS as soon as possible after diagnosis. Appropriate specimens include throat swabs, urine, and cataracts from surgery. Specimens for virus detection and molecular typing should be sent to CDC as directed by the state health department. Serologic testing The serologic tests available for laboratory confirmation of CRS infections vary among laboratories. EIAs are the most commonly used and widely available diagnostic test for rubella IgG and IgM antibodies. EIAs are sensitive and relatively easy to perform. EIA is the preferred testing method for IgM, using the capture technique, although indirect assays are also acceptable. In infants with CRS, IgM antibody can be detected in the infant’s cord blood or serum and persists for about 6–12 months. Suspect CRS cases that are IgM negative at birth should have this result confirmed at one month of age.

O. Varicella (see Chapter 17 [http://www.cdc.gov/vaccines/pubs/surv-manual/chpt17-varicella.html]) Laboratory confirmation of varicella has become more important due to the common vaccine-modified presentation of the disease, and more limited experience by physicians with unmodified disease. In addition, vaccine wild-type discrimination testing is important for the confirmation of vaccine-associated disease. Because varicella is the most common disease confused with smallpox, rapid laboratory confirmation of varicella zoster virus (VZV) diagnosis is required in cases of vesicular/pustular rash illness that fall into the category of “moderate risk” for smallpox according to the CDC algorithm. Diagnostic tests used to confirm recent varicella infection include detection and characterization of viral DNA. Serologic tests have limited value in confirming VZV etiology, except for IgG avidity, which can distinguish between primary and past infection. Rapid varicella zoster virus identification Realtime PCR techniques are the gold standard for confirming VZV infection. Viral DNA may also be detected in CSF in cases of neurologic disease and vasculopathies associated with VZV infection. If PCR results on CSF are negative, a VZV IgG intrathecal antibody assay may yield a positive result as this method may be used to implicate VZV as much as one month after disease onset. Viral DNA is less frequently detected if more than 10 days post-onset of symptoms. Suitable samples for PCR testing include vesicular swabs, scabs from crusted lesions, saliva, CSF, and biopsy or autopsy samples from cases of suspected disseminated VZV disease. Other direct detection methods such as DFA are generally not recommended due to limitations in both sensitivity and specificity. VPD Surveillance Manual 22 Laboratory Support for the Surveillance of Vaccine-Preventable Diseases: Chapter 22.34

PCR is a powerful technique that permits the rapid amplification of specific sequences of viral DNA that would otherwise be present in clinical specimens at concentrations well below detectable limits. Carefully designed primers that target selected small stretches of viral DNA can be used to replicate small quantities of viral DNA extracted from clinical samples. If a PCR product of the expected size is produced, it is evidence that the virus was present in the lesion. This technique has been extended for VZV by amplifying pieces of varicella DNA that include a mutation in the base sequence that distinguishes the vaccine strain from wild-type varicella strains. Techniques have been developed that can distinguish vaccine markers from wild type in real time, making it possible to complete a test in a single day. Postvaccination situations for which specimens should be tested include: 1) rash with more than 50 lesions occurring 7 or more days after vaccination, 2) suspected secondary transmission of the vaccine virus, 3) herpes zoster in a vaccinated person, or 4) any serious adverse event. The National VZV Laboratory at CDC has the capacity to distinguish wild-type VZV from Oka strain using both conventional and real-time PCR methods. Call the National VZV Laboratory at 404-639-0066, 404-639-2192, or email [email protected] or [email protected] for details about collection and submission of specimens for testing. The Vaccine Preventable Disease Reference Centers located in the state laboratories of California, Wisconsin, New York, and Minnesota are also capable of discriminating varicella vaccine from wild-type VZV. Virus culture Virus culture for VZV is no longer recommended because of the time required to obtain a result and the relative insensitivity of this approach compared with PCR. Serologic testing Serologic tests are available for IgG (acute and convalescent) and IgM antibodies to VZV for confirmation of disease. Testing using commercial kits for IgM antibody is not recommended since available methods lack sensitivity and specificity; false-positive IgM results are common in the presence of high IgG levels. VZV IgM can confirm recent active VZV infection but may not always confirm primary infection. In addition, IgM methods may be prone to producing false positive results. Although not widely available, VZV IgG avidity can distinguish between primary VZV infection and past infection (reactivation of VZV will drive the transient expression of IgM, just as in a primary response). The National VZV Laboratory at CDC has developed a reliable IgM capture assay. Call 404-639-0066, 404-639-2192, or email dds1@cdc. gov or [email protected] for details about collection and submission of specimens for testing.

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