Actinomyces Species: Clinical Aspects and Diagnostic Possibilities

Total Page:16

File Type:pdf, Size:1020Kb

Actinomyces Species: Clinical Aspects and Diagnostic Possibilities © by author ESCMID Online Lecture Library Actinomyces species: Clinical aspects and diagnostic possibilities © by author Willem Manson ESCMID Online Lecture Library Prof. dr. John Degener, dr. Willem Manson University Medical Center Groningen UMCG AIM OF THIS PRESENTATION, to gain knowledge of: • the clinical importance of Actinomyces spp. • Clinical pitfalls. • Basic bacteriological properties of Actinomyces spp. • Methods of isolation and identification. • Recent taxonomic changes. • Antimicrobial susceptibility and therapeutc options. © by author ESCMID Online Lecture Library • A 41 year old man complains since some weeks of fever, malaise and weight loss • Since 2 days pain in the left chest • Moderately ill, dyspnea • Temp 38 C, • Friction rub. • BSE 67 mm L 15.5 • X –thorax: infiltrate left • CTscan: diminished© perfusionby author • DIAGNOSIS: lung embolism ESCMID Online Lecture Library • Intravenous heparin was administered and after 10 days the patient was discharged • Symptoms of malaise, weight loss and periods of fever persisted • BSE 127 mm, L 19.0, T 37.5 • Sputum cultures didn’t reveal any pathogenic microorganism. ZN negative • Gram stain pleural fluid: L+++, no micro-organisms, culture neg • No diagnosis was© made by and author the patient was discharged again ESCMID Online Lecture Library • Clinical condition deteriorated and 15 weeks after the first admission the patient was admitted for the third time. • Because of a suspicion of a malignancy a thoracotomy was performed. • PATHOLOGY: a inflammatory infiltrate neutrophils. Clusters of branched bacteria. No malignacy • Microbiology: Gram© Lby +++, author sporadic branched Gram positive rods ESCMID Online Lecture Library • Culture: Actinomyces species Treatment with i.v.penicillin G for 2 months followed by oral doxycyclin for 6 months At follow-up 12 months after starting therapy the patient was in a good condition without pulmonary complaints. It was© noted by howeverauthor that his dental status was poor and he was advised to visit his ESCMIDdentist for sanitation. Online Lecture Library • Actinomycosis presenting as carcinoma. Hinnie J, Jaques BC, Bell E, Hansell DT, Milroy R. • Pulmonary actinomycosis resembling an anterior mediastinal tumor Sato T, Takada N,Dobashi Y, Suzuki M, Ouchi M,Abe Y • Cervical actinomycosis. A rare differential diagnosis of parotid tumor Lang-Roth R, Schippers C, Eckel HE. • Abdominal actinomycosis presenting as a malignant tumor--report of a case and review of the literature Molnar T, Nagy A, Ligeti E, Gyulai C, Marton J, Nagy F. • Endobronchial actinomycosis simulating endobronchial tuberculosis: a case report. Lee SH, Shim JJ, Kang EY, Lee© SYby, Jo JYauthor, In KH, Yoo SH, Kang KH. • Abdominal actinomycosis misdiagnosed as a secondary bladder tumor: a case report. KawaharaESCMID M, Kawahara Online K, Goto T, Yamamoto Lecture S, Fuchinoue Library S, Matsumoto T ACTINOMYCES / NOCARDIA Bacteria that masquerade as fungi or cancer C. Sullivan, S. Chapman. Proc.Am. Thorac. Soc. 2010. 7: 216-221 Order Actinomycetales: Aerobic: Nocardia, Gordona,Tsukamurella,Streptomyces, Rhodococcus, Corynebacteria © by author Anaerobic: Actinomyces,Arachnia,Rothia, Bifidobacterium ESCMID Online Lecture Library ACTINOMYCOSE • 1877 infections in cattle (Bollinger) • 1878 Actinomyces was found during an obduction (Israel) • 1879 oral-cervicofacial abscess (Ponflick) • 1891 isolation of Actinomyces by Israel & Wolf • 1898 Actinomyces© by author israelii ESCMID Online Lecture Library Deep Actinomyces infections are rare 1 : 100.000-300.000 • CERVICOFACIAL 60% • ABDOMINAL 20% • THORACAL 15% • OTHERS 5% © by author ESCMID Online Lecture Library CERVICAL ACTINOMYCOSIS © by author ESCMID Online Lecture Library ACTINOMYCOSE OF THE LUNG © by author ESCMID Online Lecture Library ACTINOMYCOSE OF THE LUNG © by author ESCMID Online Lecture Library SECTION OF LESION IN THE LONG, CAUSED BY ACTINOMYCES © by author ESCMID Online Lecture Library Brain abscess due to a combined Actinomyces- Actinobacillus actinomycetemcomitans infection. Zijlstra EE, Swart GR, Godfroy FJM, DegenerJE. J. Infection 1992. 25:83-87. © by author ESCMID Online Lecture Library Actinomycosis of 54 years' duration Clin. Infect Dis 1998: 27:889 • 72 years old man was wounded at the 6th of june 1944 at the hand. After some weeks a purulent discharge appeared with yellow-white granula • Actinomyces israelii • Treatment with courses© by of erythromycin,author oral penicillins, tetracyclines and clindamycin all gave only temporarily resolution of symptoms ESCMID Online Lecture Library • The disease persisted for 54 years ACTINOMYCETES: • Heterogeneous group Gram pos. mo • Grampositive rods, often branched • Sulphur granula • (facultative) anaerobe mo • molar like aspect • Motility: - • catalase - ( excl. A.viscosus en A.neuii) • indole - © by author ESCMID Online Lecture Library © by author ESCMID Online Lecture Library © by author ESCMID Online Lecture Library © by author ESCMID Online Lecture Library Actinomyces • Sulphur granules- purulent discharge originating from Actinomyces infection © by author ESCMID Online Lecture Library © by author ESCMID Online Lecture Library © by author ESCMID Online Lecture Library Actinomyces • Grows slowly in culture- should be observed for up to 21 days • Selective medium- MMBA • Molar tooth colonies © by author ESCMID Online Lecture Library © by author ESCMID Online Lecture Library ISOLATION - IDENTIFICATION • SELECTIVE MEDIA: • Cadmium Fluoride Acriflavin Tellurite agar • Mupirocin Metronidazole Blood Agar (MMBA) (Columbia agar with 128 mg/L mupirocin en 2.5 mg/L metronidazole) • Colony morphology • GLC © by author • PHENOTYPIC • ESCMIDSEQUENCE (16s RNA) Online Lecture Library • Malditof 97% correct id Online Lecture Library Slide withheld at request© byof author author ESCMID Online Lecture Library Online Lecture Library Slide withheld at request© byof author author ESCMID Online Lecture Library ACTINOMYCES ( presently 42 species, 2 subsp) • A. israelii • A. europaeus • A. naeslundii • A. neuii • A. viscosus • A. radinga • A. odontolyticus • A. turicensis • A. georgiae • A. cardiffensis • A. meyeri • A. houstonensis • A. gerencseriae • A. hongkongensis • A. graevenitzii © by author• A. funkei ESCMID Online Lecture Library taxonomic changes among Actinomyces and closely related genera from human sources Year current name previous or source taxonomic position 1994 A. neuii supsp anitratus CDC gr 1 coryneform abscess, blood 1994 A. neuii subsp neuii CDC gr 1 like coryneform abscess, blood 1995 A. radingae A. pyogenes - like polymicrobial 1995 A. turicensis A. pyogenes - like polymocrobial 1995 A. europaeus new abscess 1997 A. graevenitzii new resp.tract 2000 A. radicidentis new oral cavity 2000 A. urogenitalis new urogenital 2001 A. funkii new blood 1997 Actinobaculum schaalii ©new by author blood 1997 Arcanobacterium bernardiae A. bernardiae abscess, blood 1998 Arcanobacterium pyogenes A. pyogenes polymicrobial ESCMID Online Lecture Library Sarkonen, et al. J.Clin. Microbiol(2001) Online Lecture Library Slide withheld at request© byof author author ESCMID Online Lecture Library Phenotypic identification of Actinomyces, obsolete? © by author ESCMID Online Lecture Library IDENTIFICATION OF ACTINOMYCES BY AMPLIFIED 16S RIBOSOMAAL DNA Val Hall et al. J.Clin. Microbiol 39: 3555 (2001) 475 clinical Actinomyces isolates 331 (70%) Actinomyces species 44(9%) no Actinomyces 113 A. meyeri : 21 A. meyeri 63 A. turicensis 7 other Actinomycetes 22 not identified© by author ESCMID Online Lecture Library SUSCEPTIBILITY OF ACTINOMYCES • All Actinomyces spp are susceptible to penicillins, cefalosporins, linezolid • Most of the Actinomyces spp are resistant against ciprofloxacin • A. turicensis is less susceptible to tetracycline • A. europaeus is less susceptible to erythromycin and clindamycin © by author ESCMID Online Lecture Library Smith et al. J. Antimicrobiol. Chemother. (2005) THERAPY FOR ACTINOMYCOSIS • SURGIGAL THERAPY • ANTIBIOTIC THERAPY 12 – 24 ME i.v. Penicillin G 2 – 6 weeks 6 (3) – 12 months oral therapy © by author Alternatives 1: clindamycin, erythromycin, doxycycline AlternativesESCMID 2: Online ceftriaxone, Lecture imipenem Library Medical management of pulmonary actinomycosis: data from 49 consecutive cases, co-morbidity 70% 46 patients iv antibiotics 21.5 days 43 patients oral antibiotics 115 days (penicillins, doxycyclin, macrolide) 16 patients side effects 5 patients lost for follow up 41 patients follow-up for 27 months 35 patients were cured (85%) 6 recurrence “Pulmonary actinomycosis with duration of AB treatment © by author adequate antibiotic treatment 5/6 recurrence treatment < 3 month (p<0.001 compared with 35 patients with uneventful follow-up)has an excellent prognosis” KolditzESCMID et al. (JAC 2009. 4: 839-841) Online Lecture Library OPTIMAL DURATION OF IV AND ORAL ANTIBIOTICS IN THE TREATMENT OF THORACIC ACTINOMYCOSIS _______________________________________________ n= 28 IV antibiotc PO antibiotic days days _______________________________________________ Surgical (n=13) 8 (3 – 17) 150 (0 – 534) Medical (n= 15) 2 (0 – 18) 167 (76 -412) _______________________________________________© by author NoESCMID disease recurrence Online with Lecturea short treatment Library regimen Choi et al. Chest (2005) Human Pathology (2006) Volume: 37, Issue: 1, Pages: 61-67 © by author ESCMID Online Lecture Library Online Lecture Library Slide withheld at request© byof author author ESCMID Online Lecture Library Online Lecture Library Slide withheld at request© byof author author ESCMID Online Lecture Library .
Recommended publications
  • Leprae by Means of Cytoplasmic Antigens
    Bull. Org. mond. Santt 1972, 46, 509-513 Bull. Wld Hlth Org. Immunological determination of Mycobacterium leprae by means of cytoplasmic antigens J. B. G. KWAPINSKI,1 J. 0. DE ALMEIDA,2 & E. H. KWAPINSKI 3 Mycobacterium leprae was isolated and purified from lepromas, the spleen, and the liver of leprosy patients. An immunodiffusion analysis of the cytoplasms obtained from four lots of M. leprae and M. lepraemurium, 295 strains of different actinomycetales, and 12 other bacteria was performed with the use ofthe cytoplasm antisera. Immunological relationships were revealed between the cytoplasms of M. leprae, M. lepraemurium, M. avium, M. gallinarum, M. tuberculosis, M. simiae, M. kansasii, M. chitae, M. cap- sulatum, Actinomyces israelii, A. naeslundii, and some strains of saprophytic myco- bacteria. These studies led to the proposed concept of the immunological evolution of M. leprae and M. lepraemurium and an Actinomyces-like progenitor through M. avium- M. gallinarum and to a proposal for the polyvalent vaccine currently being developed by this research group. Most of the past immunological research on lep- help to elucidate the immunogenicity of M. leprae rosy dealt with the skin or serum reactions of leprosy and would be useful for the preparation of an anti- patients with different mycobacterial antigen prepa- leprosy vaccine. rations. Almost all of these data were critically re- viewed by Bechelli (1971) and by de Almeida.4 More recently, the cross-reactions given by polysaccharide- MATERIALS AND METHODS protein complexes purified from M. leprae with the Sources of M. leprae and M. lepraemurium sera obtained from human leprosy, tuberculosis, and nocardiosis were revealed by Estrada-Parra (1970).
    [Show full text]
  • A Case of Disseminated Infection Due to Actinomyces Meyeri Involving
    Case Report Infection & http://dx.doi.org/10.3947/ic.2014.46.4.269 Infect Chemother 2014;46(4):269-273 Chemotherapy ISSN 2093-2340 (Print) · ISSN 2092-6448 (Online) A Case of Disseminated Infection due to Actinomyces meyeri Involving Lung and Brain Hyun Jung Park1, Ki-Ho Park3, Sung-Han Kim1, Heungsup Sung2, Sang-Ho Choi1, Yang Soo Kim1, Jun Hee Woo1, and Sang-Oh Lee1 Departments of 1Internal Medicine and 2Laboratory Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul; 3Department of Internal Medicine, Kyung Hee University School of Medicine, Seoul, Korea Actinomyces meyeri is rarely isolated in cases of actinomycosis. The identification of A. meyeri had historically been difficult and unreliable. With the recent development of 16S ribosomal RNA (16S rRNA) sequencing, Actinomyces species such as A. meyeri can be isolated much more reliably. A. meyeri often causes disseminated disease, which can be secondary to frequent pulmonary infections. A penicillin-based regimen is the mainstay of A. meyeri treatment, with a prolonged course usually re- quired. Here, we report a case of pulmonary actinomycosis with brain abscess caused by A. meyeri that was initially thought to represent lung cancer with brain metastasis. Key Words: Actinomyces; Sequence analysis, RNA; Brain abscess Introduction cies to cause similar clinical disease is largely unknown [2]. Recent developments in microbiological identification tech- Actinomycosis is a chronic infection caused by organisms in niques, especially 16S ribosomal RNA (16S rRNA) sequencing, the genus Actinomyces, with Actinomyces israelii being the have identified other Actinomyces species such as A. meyeri, most common etiologic agent [1].
    [Show full text]
  • Common Commensals
    Common Commensals Actinobacterium meyeri Aerococcus urinaeequi Arthrobacter nicotinovorans Actinomyces Aerococcus urinaehominis Arthrobacter nitroguajacolicus Actinomyces bernardiae Aerococcus viridans Arthrobacter oryzae Actinomyces bovis Alpha‐hemolytic Streptococcus, not S pneumoniae Arthrobacter oxydans Actinomyces cardiffensis Arachnia propionica Arthrobacter pascens Actinomyces dentalis Arcanobacterium Arthrobacter polychromogenes Actinomyces dentocariosus Arcanobacterium bernardiae Arthrobacter protophormiae Actinomyces DO8 Arcanobacterium haemolyticum Arthrobacter psychrolactophilus Actinomyces europaeus Arcanobacterium pluranimalium Arthrobacter psychrophenolicus Actinomyces funkei Arcanobacterium pyogenes Arthrobacter ramosus Actinomyces georgiae Arthrobacter Arthrobacter rhombi Actinomyces gerencseriae Arthrobacter agilis Arthrobacter roseus Actinomyces gerenseriae Arthrobacter albus Arthrobacter russicus Actinomyces graevenitzii Arthrobacter arilaitensis Arthrobacter scleromae Actinomyces hongkongensis Arthrobacter astrocyaneus Arthrobacter sulfonivorans Actinomyces israelii Arthrobacter atrocyaneus Arthrobacter sulfureus Actinomyces israelii serotype II Arthrobacter aurescens Arthrobacter uratoxydans Actinomyces meyeri Arthrobacter bergerei Arthrobacter ureafaciens Actinomyces naeslundii Arthrobacter chlorophenolicus Arthrobacter variabilis Actinomyces nasicola Arthrobacter citreus Arthrobacter viscosus Actinomyces neuii Arthrobacter creatinolyticus Arthrobacter woluwensis Actinomyces odontolyticus Arthrobacter crystallopoietes
    [Show full text]
  • INTERNATIONAL BULLETIN of BACTERIOLOGICAL NOMENCLATURE and TAXONOMY Vol
    INTERNATIONAL BULLETIN OF BACTERIOLOGICAL NOMENCLATURE AND TAXONOMY Vol. 15, No. 3 July 15, 1965 pp. 143-163 THE CLASSIFICATION AND PHYLOGENETIC RELATIONSHIPS OF THE ACTINOMYCETALES ' Leo Pine and Lucille Georg Communicable Disease Center, Public Health Service, U. S. Department of Health, Education, and Welfare, Atlanta, Georgia SUMMARY. The taxonomic and phylogenetic re- lationships of members of the order Actino- mycetales have been examined. On the basis of cellular and colony morphology, cell wall composition, fermentation products, and cer- tain physiological characteristics, the taxa within the family Actinomycetaceae were divided into two groups. Each group was closely related to members of the family -Lactobacillaceae. One group consisted of Actinomyces israelii, -A. naeslundii, ,A. pro- pionicus, Nocardia dentocariosus and Odonto- myces viscosis ("hamster organism"). The second group consisted of bovis, ,A. erik- sonii, and Lactobacillus bifidusA. type 11 (k parabifidus). This latter organism was re- named Actinomyces pa.rabifidus nov. comb. because its morphological, physiological and biochemical characteristics related it to the members of both groups of the genus Actino- myces. The families Streptomycetaceae and Mycobacteriaceae appeared more closely re- lated to the family Corynebacteriaceae than to the family Actinomycetaceae. The use of certain criteria for classification and deter- mination of phylogenetic relationships was discussed. We have stressed those areas in which necessasy information is lacking. A report to
    [Show full text]
  • Actinomycetes (Branching Bacteria ): Dr.Jawad K
    College of Medicine Microbiology Medical bacteriology Actinomycetes (branching bacteria ): Dr.Jawad K. Al-Khafaji ----------------------------------------------------------------------------------------- Actinomycete (fungus-like bacteria) resembles fungus as it forms mycelia and resemble bacteria as it has not true nucleus. Important properties: 1. Actinomycetes for many years were classified as fungi because the actinomycetes are form long branching filaments that resemble the hyphae of fungi .But they are reclassified as bacteria since they are thin, possesses cell wall containing muramic acid, it has prokaryotic nuclei and susceptible to bacterial antibiotic agents. 2. Actinomycetes are common in soil .There are two medically important organisms, Actinomyces israelii and Nocardia asteroids . A.israelii is anaerobe that forms part of normal flora of oral cavity. N.asteroides is aerobe and is found in environment, particularly in the soil. 3. They are gram-positive bacilli. Many isolates of N.asteroides are weakly acid fast stain. 4. The A israelii is strict anaerobic; whereas N.asteroides is grow under strict aerobic conditions. Transmission : A.israelii infection is acquired endogenously, from normal oral flora. There is no person to person spread. Infection of N.asteroides is acquired from soil by airborne route. Actinomycetes infections are not transmitted from person to person ( the diseases are not communicable ). Pathogenesis : Actinomycetes are responsible for three human infections. 1. Actinomycosis is caused by A.israelii in human or by A.bovis in cattle. The disease is chronic suppurative and granulomatous infection that produces pyogenic lesions with interconnecting sinus tract that contain sulfur granules. Three forms are (i)Cervicofacial lesion is most common ,especially among poor dental hygiene and tooth extraction.
    [Show full text]
  • ABSA General Microbiology Fact Sheets
    GENERAL MICROBIOLOGY FACT SHEET Signs & Pathogen Genus species Disease Risk Group Host Range Transmission Symptoms Incubation Fact Micrograph Bacteria Actinomcyces spp. Actinomycosis Humans, cattle, Person-to-person by contact of Opportunistic pathogen. Chronic bacterial variable - days to months. Fatality rate of 5-20% if untreated. Opportuinistic Actinomyces israelii horses mouth, aerosols, fomites. disease localized in jaw, thorax, or pathogen. abdomen. Characterized by persistent swelling, suppuration and formation of 2 abscesses or granulomas. Bacteria Bacillus cereus Food Poisoning Humans Ingestion of foods kept at Opportunistic pathogen; intoxication 1-6 hours, average 4 hours; Infectious dose is greater than 10e6 organisms by ambient conditions after characterized by two forms: an emetic form diarrheal form 6-24 hours ingestion (>10e5 organisms/g of food). cooking; emetic form frequently with severe nausea and vomiting and a (average 17 hours) associated with cooked rice. diarrheal form with abdominal cramps and 2 Not communicable from person diarrhea. Usually mild and self-limiting (24 to person. hrs). Bacteria Bordetella pertussis Whooping Cough Humans Direct contact with discharges Stage 1: Catarrhal: Irritating cough, lasts 1 6-20 days Common in children worldwide; pertussis is among the from respiratory mucous to 2 weeks; Stage 2: Paroxysmal; violent most lethal infant diseases- membranes of infected persons coughs followed by a high pitched Treatment with dTaP(acellular pertussis vaccine, a by the airborne route. inspiratory whoop, lasts 2 to 6 weeks; preventive vaccine) is now available for adults 2 Stage 3: Convalescent; the cough gradually decreases in frequency and severity, lasts several weeks Bacteria Brucella melitensis Brucellosis Humans, swine, Skin or mucous membrane High and protracted (extended) fever.
    [Show full text]
  • Appendix a Bacteria
    Appendix A Complete list of 594 pathogens identified in canines categorized by the following taxonomical groups: bacteria, ectoparasites, fungi, helminths, protozoa, rickettsia and viruses. Pathogens categorized as zoonotic/sapronotic/anthroponotic have been bolded; sapronoses are specifically denoted by a ❖. If the dog is involved in transmission, maintenance or detection of the pathogen it has been further underlined. Of these, if the pathogen is reported in dogs in Canada (Tier 1) it has been denoted by an *. If the pathogen is reported in Canada but canine-specific reports are lacking (Tier 2) it is marked with a C (see also Appendix C). Finally, if the pathogen has the potential to occur in Canada (Tier 3) it is marked by a D (see also Appendix D). Bacteria Brachyspira canis Enterococcus casseliflavus Acholeplasma laidlawii Brachyspira intermedia Enterococcus faecalis C Acinetobacter baumannii Brachyspira pilosicoli C Enterococcus faecium* Actinobacillus Brachyspira pulli Enterococcus gallinarum C C Brevibacterium spp. Enterococcus hirae actinomycetemcomitans D Actinobacillus lignieresii Brucella abortus Enterococcus malodoratus Actinomyces bovis Brucella canis* Enterococcus spp.* Actinomyces bowdenii Brucella suis Erysipelothrix rhusiopathiae C Actinomyces canis Burkholderia mallei Erysipelothrix tonsillarum Actinomyces catuli Burkholderia pseudomallei❖ serovar 7 Actinomyces coleocanis Campylobacter coli* Escherichia coli (EHEC, EPEC, Actinomyces hordeovulneris Campylobacter gracilis AIEC, UPEC, NTEC, Actinomyces hyovaginalis Campylobacter
    [Show full text]
  • Presentation of Pulmonary Tuberculosis and Actinomyces Co-Infection As a Lung Mass: a Literature Review and Unique Case Report
    Monaldi Archives for Chest Disease 2019; volume 89:1180 Presentation of pulmonary tuberculosis and actinomyces co-infection as a lung mass: a literature review and unique case report Evangelos Balis1, Sotirios Kakavas1, Steven Kompogiorgas1, Konstantinos Kotsifas1, Georgios Boulbasakos1 First Pulmonary Department, Evangelismos General Hospital of Athens, Greece or metastatic lung cancer and in some cases, infection and cancer Abstract may even coexist. Actinomycosis occurs in humans worldwide and is usually caused by Actinomyces israelii, an anaerobic or Parenchymal lung infections occasionally present with clinical microaerophilic, non-spore-forming, gram-positive rod. The symptoms and radiological findings similar to lung malignancy. extension of the infection in large bronchi is a rare manifestation Pulmonary actinomycosis is a rare condition of its own right, let of the disease. Most infections with Actinomyces spp. are alone in coexistence with tuberculosis. We report a case of a man polymicrobial [1]. However, cases with concomitant actinomycosis presenting with hemoptysis alongside a chest computed and tuberculosis appear to be rare. We present a case of a tomography compatible with lung cancer. The diagnosis, after Mycobacterium tuberculosis co-infection with actinomycosis that removal of a large endobronchial mass with flexible bronchoscopy presented as a large endobronchial mass. Written consent was and cryon, was a concomitant infection with Mycobacterium obtained from the patient whose personal data were fully tuberculosis and Actinomyces odontoliticus. In the literature, there anonymized to protect theonly identity of the individual. This meets the are few reported cases with concomitant tuberculosis and requirements by the Ethics Committee of Evaggelismos General actinomycosis. To our knowledge, such radical treatment without Hospital that approved the present case report.
    [Show full text]
  • Actinomyces) Propionica
    Br J Ophthalmol: first published as 10.1136/bjo.65.1.10 on 1 January 1981. Downloaded from British Journal of Ophthalmology, 1981, 65, 10-13 Lacrimal canaliculitis due to Arachnia (Actinomyces) propionica D. V. SEAL,1 J. McGILL,2 D. FLANAGAN,2 AND B. PURRIER' From the 'Public Health Laboratory, Southampton, and 2Southampton Eye Hospital SUMMARY The clinical and microbiological findings in a chronic case of lacrimal canaliculitis due to Arachnia propionica are described. Bacterial culture and identification should be performed in the investigation of the disease in order to establish the role of A. propionica and other specific actinomycetes at the acute as well as at the chronic stage. Mycotic canaliculitis has been recognised for many mal duct. A culture of the discharge grew Haemo- years as an uncommon clinical entity which usually philus influenzae, sensitive to gentamicin, while responds to surgery and iodine. 146 cases have been actinomycetes could be neither seen on examination reported from 1854 to 1972, in which a single of pus nor cultured from it. The patient was started canaliculus has usually been involved, the lower in on topical gentamicin and Polyfax (polymyxin B 105 cases and the upper in 41.1 The disease has been and bacitracin). considered in the past as due to streptothrix, The swelling and discharge persisted. After 2 leptothrix, or nocardia organisms but is now thought months the left upper punctum and canaliculus to be due to anaerobic actinomycetes, though the were explored under general anaesthesia. White species involved has not often been identified.23 cheesy material was removed from the canaliculus, Actinomyces propionicus was first isolated from a leaving a cavity 2X 2 mm wide.
    [Show full text]
  • Prosthetic Joint Infection Due to Actinomyces Species: a Case Series and Review of Literature Ramez Dagher1, Talha Riaz1, Aaron J
    J. Bone Joint Infect. 2019, Vol. 4 174 Ivyspring International Publisher Journal of Bone and Joint Infection 2019; 4(4): 174-180. doi: 10.7150/jbji.35592 Research Paper Prosthetic Joint Infection due to Actinomyces species: A case series and review of literature Ramez Dagher1, Talha Riaz1, Aaron J. Tande1, Douglas R. Osmon1, Anil Jagtiani1, James M. Steckelberg1, Tad Mabry2, Elie F. Berbari1 1. Department of Internal Medicine and Division of Infectious Diseases, Mayo Clinic College of Medicine, 200 1st Street SW, Rochester, MN 55905. 2. Department of Orthopedic Surgery, Mayo Clinic College of Medicine, 200 1st Street SW, Rochester, MN 55905. Corresponding author: Elie J. Berbari MD, Division of Infectious Diseases, Mayo Clinic College of Medicine, 200 1st Street SW, Rochester, MN 55905. Email: [email protected], Phone: 507-255-6482, Fax: 507-255-7767 © The author(s). This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. Received: 2019.04.09; Accepted: 2019.06.07; Published: 2019.08.02 Abstract Background: Actinomyces prosthetic joint infections (APJIs) are rare and optimal medical and surgical treatment strategies are unknown. The purpose of our study was to characterize the demographics, risk factors, management and outcomes of patients with PJIs due to Actinomyces spp. Methods: Using a retrospective cohort study design, the medical records of all patients with Actinomyces spp. total hip or knee arthroplasty infection (APJI) seen at a single institution between January 1, 1969 and December 31, 2016 were reviewed.
    [Show full text]
  • Prosthetic Joint Infection Diagnosis Using Conventional Methods
    11/5/2018 Prosthetic Joint Infection Diagnosis Using Conventional Methods HOT TOPIC / 2018 ©MFMER Presenter: Robin Patel, M.D. Professor of Medicine and Microbiology Chair, Division of Clinical Microbiology and the Elizabeth P. and Robert E. Allen Professor of Individualized Medicine Department of Laboratory Medicine and Pathology at Mayo Clinic, Rochester, Minnesota ©MFMER 1 11/5/2018 Disclosures • Dr. Robin Patel has a US patent for a method and an apparatus for sonication, but has foregone her right to personally receive royalties. Funding • National Institutes of Health • Department of Defense • National Science Foundation ©MFMER Total Hip and Knee Replacement Procedures United States1 Total knee Total hip Year ©MFMER 2 11/5/2018 ©MFMER Prosthetic Hip and Knee Infections: United States2 2001‐2020 ©MFMER 3 11/5/2018 Surgical Management of Prosthetic Hip or Knee Infection3 Reprinted with permission from Massachusetts Medical Society. ©MFMER Prosthetic Joint Infection Microbiology4 Hip and Knee Hip Knee Shoulder Elbow All time periods Early Number of joints 2435 637 1979 1427 199 110 Staphylococcus aureus 27 38 13 23 18 42 Coagulase negative staphylococci 27 22 30 23 41 41 Streptococcus species 846644 Enterococcus species 310223 0 Aerobic gram negative bacilli 92475107 Anaerobic bacteria 4395 Cutibacterium acnes 24 1 Other anaerobes 30 Culture negative 14 10 7 11 15 5 Polymicrobial 15 31 14 12 16 3 Other 3 ©MFMER 4 11/5/2018 Unusual Causes of Prosthetic Joint Infection5 Actinomyces israelii Granulicatella adiacens Aspergillus fumigatus
    [Show full text]
  • Oral Actinomyces Species in Health and Disease: Identification, Occurrence and Importance of Early Colonization
    Nanna Sarkonen Oral Actinomyces Species in Health and Disease: Identification, Occurrence and Importance of Early Colonization Publications of the National Public Health Institute A 8/2007 Department of Bacterial and Inflammatory Diseases National Public Health Institute, Helsinki, Finland and Institute of Dentistry, Faculty of Medicine, University of Helsinki, Finland Helsinki 2007 ORAL ACTINOMYCES SPECIES IN HEALTH AND DISEASE: IDENTIFICATION, OCCURRENCE AND IMPORTANCE OF EARLY COLONIZATION Nanna Sarkonen ACADEMIC DISSERTATION To be presented with the permission of the Faculty of Medicine, University of Helsinki, for public examination in the Small Hall, University Main Building, Fabianinkatu 33, on June 15 th, at 12 noon. Department of Bacterial and Inflammatory Diseases National Public Health Institute, Helsinki, Finland and Institute of Dentistry, Faculty of Medicine, University of Helsinki, Finland Helsinki 2007 Publications of the National Public Health Institute KTL A8 / 2007 Copyright National Public Health Institute Julkaisija-Utgivare-Publisher Kansanterveyslaitos (KTL) Mannerheimintie 166 00300 Helsinki Puh. vaihde (09) 474 41, telefax (09) 4744 8408 Folkhälsoinstitutet Mannerheimvägen 166 00300 Helsingfors Tel. växel (09) 474 41, telefax (09) 4744 8408 National Public Health Institute Mannerheimintie 166 FIN-00300 Helsinki, Finland Telephone +358 9 474 41, telefax +358 9 4744 8408 ISBN 951-740-704-5 ISSN 0359-3584 ISBN 951-740-705-2 (pdf) ISSN 1458-6290 (pdf) Edita Prima Oy Helsinki 2007 Supervised by Professor Eija Könönen
    [Show full text]