Veterinary Services Newsletter August 2017
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Reportable Diseases and Conditions
KINGS COUNTY DEPARTMENT of PUBLIC HEALTH 330 CAMPUS DRIVE, HANFORD, CA 93230 REPORTABLE DISEASES AND CONDITIONS Title 17, California Code of Regulations, §2500, requires that known or suspected cases of any of the diseases or conditions listed below are to be reported to the local health jurisdiction within the specified time frame: REPORT IMMEDIATELY BY PHONE During Business Hours: (559) 852-2579 After Hours: (559) 852-2720 for Immediate Reportable Disease and Conditions Anthrax Escherichia coli: Shiga Toxin producing (STEC), Rabies (Specify Human or Animal) Botulism (Specify Infant, Foodborne, Wound, Other) including E. coli O157:H7 Scrombroid Fish Poisoning Brucellosis, Human Flavivirus Infection of Undetermined Species Shiga Toxin (Detected in Feces) Cholera Foodborne Disease (2 or More Cases) Smallpox (Variola) Ciguatera Fish Poisoning Hemolytic Uremic Syndrome Tularemia, human Dengue Virus Infection Influenza, Novel Strains, Human Viral Hemorrhagic Fever (Crimean-Congo, Ebola, Diphtheria Measles (Rubeola) Lassa, and Marburg Viruses) Domonic Acid Poisoning (Amnesic Shellfish Meningococcal Infections Yellow Fever Poisoning) Novel Virus Infection with Pandemic Potential Zika Virus Infection Paralytic Shellfish Poisoning Plague (Specify Human or Animal) Immediately report the occurrence of any unusual disease OR outbreaks of any disease. REPORT BY PHONE, FAX, MAIL WITHIN ONE (1) WORKING DAY Phone: (559) 852-2579 Fax: (559) 589-0482 Mail: 330 Campus Drive, Hanford 93230 Conditions may also be reported electronically via the California -
Coxiella Burnetii
SENTINEL LEVEL CLINICAL LABORATORY GUIDELINES FOR SUSPECTED AGENTS OF BIOTERRORISM AND EMERGING INFECTIOUS DISEASES Coxiella burnetii American Society for Microbiology (ASM) Revised March 2016 For latest revision, see web site below: https://www.asm.org/Articles/Policy/Laboratory-Response-Network-LRN-Sentinel-Level-C ASM Subject Matter Expert: David Welch, Ph.D. Medical Microbiology Consulting Dallas, TX [email protected] ASM Sentinel Laboratory Protocol Working Group APHL Advisory Committee Vickie Baselski, Ph.D. Barbara Robinson-Dunn, Ph.D. Patricia Blevins, MPH University of Tennessee at Department of Clinical San Antonio Metro Health Memphis Pathology District Laboratory Memphis, TN Beaumont Health System [email protected] [email protected] Royal Oak, MI BRobinson- Erin Bowles David Craft, Ph.D. [email protected] Wisconsin State Laboratory of Penn State Milton S. Hershey Hygiene Medical Center Michael A. Saubolle, Ph.D. [email protected] Hershey, PA Banner Health System [email protected] Phoenix, AZ Christopher Chadwick, MS [email protected] Association of Public Health Peter H. Gilligan, Ph.D. m Laboratories University of North Carolina [email protected] Hospitals/ Susan L. Shiflett Clinical Microbiology and Michigan Department of Mary DeMartino, BS, Immunology Labs Community Health MT(ASCP)SM Chapel Hill, NC Lansing, MI State Hygienic Laboratory at the [email protected] [email protected] University of Iowa [email protected] Larry Gray, Ph.D. Alice Weissfeld, Ph.D. TriHealth Laboratories and Microbiology Specialists Inc. Harvey Holmes, PhD University of Cincinnati College Houston, TX Centers for Disease Control and of Medicine [email protected] Prevention Cincinnati, OH om [email protected] [email protected] David Welch, Ph.D. -
Plague (Yersinia Pestis)
Division of Disease Control What Do I Need To Know? Plague (Yersinia pestis) What is plague? Plague is an infectious disease of animals and humans caused by the bacterium Yersinia pestis. Y. pestis is found in rodents and their fleas in many areas around the world. There are three types of plague: bubonic plague, septicemic plague and pneumonic plague. Who is at risk for plague? All ages may be at risk for plague. People usually get plague from being bitten by infected rodent fleas or by handling the tissue of infected animals. What are the symptoms of plague? Bubonic plague: Sudden onset of fever, headache, chills, and weakness and one or more swollen and painful lymph nodes (called buboes) typically at the site where the bacteria entered the body. This form usually results from the bite of an infected flea. Septicemic plague: Fever, chills, extreme weakness, abdominal pain, shock, and possibly bleeding into the skin and other organs. Skin and other tissues, especially on fingers, toes, and the nose, may turn black and die. This form usually results from the bites of infected fleas or from handling an infected animal. Pneumonic plague: Fever, headache, weakness, and a rapidly developing pneumonia with shortness of breath, chest pain, cough, and sometimes bloody or watery mucous. Pneumonic plague may develop from inhaling infectious droplets or may develop from untreated bubonic or septicemic plague after the bacteria spread to the lungs. How soon do symptoms appear? Symptoms of bubonic plague usually occur two to eight days after exposure, while symptoms for pneumonic plague can occur one to six days following exposure. -
Early History of Infectious Disease
© Jones and Bartlett Publishers. NOT FOR SALE OR DISTRIBUTION CHAPTER ONE EARLY HISTORY OF INFECTIOUS 1 DISEASE Kenrad E. Nelson, Carolyn F. Williams Epidemics of infectious diseases have been documented throughout history. In ancient Greece and Egypt accounts describe epidemics of smallpox, leprosy, tuberculosis, meningococcal infections, and diphtheria.1 The morbidity and mortality of infectious diseases profoundly shaped politics, commerce, and culture. In epidemics, none were spared. Smallpox likely disfigured and killed Ramses V in 1157 BCE, although his mummy has a significant head wound as well.2 At times political upheavals exasperated the spread of disease. The Spartan wars caused massive dislocation of Greeks into Athens triggering the Athens epidemic of 430–427 BCE that killed up to one half of the population of ancient Athens.3 Thucydides’ vivid descriptions of this epidemic make clear its political and cultural impact, as well as the clinical details of the epidemic.4 Several modern epidemiologists have hypothesized on the causative agent. Langmuir et al.,5 favor a combined influenza and toxin-producing staphylococcus epidemic, while Morrens and Chu suggest Rift Valley Fever.6 A third researcher, Holladay believes the agent no longer exists.7 From the earliest times, man has sought to understand the natural forces and risk factors affecting the patterns of illness and death in society. These theories have evolved as our understanding of the natural world has advanced, sometimes slowly, sometimes, when there are profound break- throughs, with incredible speed. Remarkably, advances in knowledge and changes in theory have not always proceeded in synchrony. Although wrong theories or knowledge have hindered advances in understanding, there are also examples of great creativity when scientists have successfully pursued their theories beyond the knowledge of the time. -
LIST of REPORTABLE COMMUNICABLE DISEASES in BC July 2009
LIST OF REPORTABLE COMMUNICABLE DISEASES IN BC July 2009 Schedule A: Reportable by all sources, including Laboratories Meningococcal Disease, All Invasive including “Primary Meningococcal Acquired Immune Deficiency Syndrome Pneumonia” and “Primary Meningococcal Anthrax Conjunctivitis” Botulism Mumps Brucellosis Neonatal Group B Streptococcal Infection Chancroid Paralytic Shellfish Poisoning (PSP) Cholera Pertussis (Whooping Cough) Congenital Infections: Plague Toxoplasmosis Poliomyelitis Rubella Rabies Cytomegalovirus Reye Syndrome Herpes Simplex Rubella Varicella-Zoster Severe Acute Respiratory Syndrome (SARS) Hepatitis B Virus Smallpox Listeriosis and any other congenital infection Streptococcus pneumoniae Infection, Invasive Creutzfeldt-Jacob Disease Syphilis Cryptococcal infection Tetanus Cryptosporidiosis Transfusion Transmitted Infection Cyclospora infection Tuberculosis Diffuse Lamellar Keratitis Tularemia Diphtheria: Typhoid Fever and Paratyphoid Fever Cases Waterborne Illness Carriers All causes Encephalitis: West Nile Virus Infection Post-infectious Yellow Fever Subacute sclerosing panencephalitis Vaccine-related Viral Schedule B: Reportable by Laboratories only Foodborne illness: All causes All specific bacterial and viral stool pathogens: Gastroenteritis epidemic: (i) Bacterial: Bacterial Campylobacter Parasitic Salmonella Viral Shigella Genital Chlamydia Infection Yersinia Giardiasis (ii) Viral Gonorrhea – all sites Amoebiasis Group A Streptococcal Disease, Invasive Borrelia burgdorferi infection H5 and H7 strains of the -
AMD Projects: Deadly Disease Databases
CDC’s AMD Program AMD Projects Innovate • Transform • Protect CDC’s Advanced Molecular Detection (AMD) program fosters scientific innovation in genomic sequencing, epidemiology, and bioinformatics to transform public health and protect people from disease threats. AMD Project: Deadly Disease Databases Whole genome analysis and database development for anthrax (Bacillus anthracis), melioidosis (Burkholderia pseudomallei), and Brucellosis (Brucella spp.) Epidemiologists and forensic professionals can use whole genome sequencing – a way of determining an organism’s complete, detailed genome – and large databases to determine the source of dangerous germs. Having a large, accessible collection of disease pathogens could help scientists quickly find out if a certain illness is naturally occurring or the result of bioterrorism. CDC is establishing a public database where scientists from around the world can share information about these potentially deadly CDC is establishing public databases so that diseases. CDC scientists have begun sequencing the organisms that scientists from around the world can share information about deadly diseases like cause anthrax (Bacillus anthracis), brucellosis (Brucella spp.), and anthrax, brucellosis, and melioidosis. melioidosis (Burkholderia pseudomallei), three pathogens that could occur naturally or as the result of bioterrorism. Current methods of determining the genetic structure of these organisms are not standardized and sometimes not effective. Using whole genome sequencing for these pathogens will allow scientists www.cdc.gov/amd Updated: May 2017 to accurately and quickly find the geographic origin of the isolates and will improve overall knowledge and understanding of them. Having a detailed database of these genomes will also ensure quicker and more effective responses to outbreaks. For more information on anthrax, please visit www.cdc.gov/anthrax/index.html. -
The Plague of Thebes, a Historical Epidemic in Sophocles' Oedipus
Oedipus Rex) is placed in the fi rst half of the decade 430– The Plague 420 BC. The play has been labeled an analytical tragedy, meaning that the crucial events which dominate the play of Thebes, a have happened in the past (2,3). Oedipus Rex, apart from the undeniable literary and Historical Epidemic historic value, also presents signifi cant medical interest because the play mentions a plague, an epidemic, which in Sophocles’ was devastating Thebes, the town of Oedipus’ hegemony. Oedipus Rex Several sections, primarily in the fi rst third of the play, refer to the aforementioned plague; the epidemic, however, Antonis A. Kousoulis, is not the primary topic of the tragedy. The epidemic, in Konstantinos P. Economopoulos, fact, is mostly a matter that serves the theatrical economy Effi e Poulakou-Rebelakou, George Androutsos, by forming a background for the evolution of the plot. and Sotirios Tsiodras Given the potential medical interest of Oedipus Rex, we decided to adopt a critical perspective by analyzing the Sophocles, one of the most noted playwrights of the literary descriptions of the plague, unraveling its clinical ancient world, wrote the tragedy Oedipus Rex in the fi rst features, defi ning the underlying cause, and discussing half of the decade 430–420 BC. A lethal plague is described in this drama. We adopted a critical approach to Oedipus possible therapeutic options. The ultimate goals of our Rex in analyzing the literary description of the disease, study were to clarify whether the plague described in unraveling its clinical features, and defi ning a possible Oedipus Rex could refl ect an actual historical event, underlying cause. -
Tick-Borne Disease Working Group 2020 Report to Congress
2nd Report Supported by the U.S. Department of Health and Human Services • Office of the Assistant Secretary for Health Tick-Borne Disease Working Group 2020 Report to Congress Information and opinions in this report do not necessarily reflect the opinions of each member of the Working Group, the U.S. Department of Health and Human Services, or any other component of the Federal government. Table of Contents Executive Summary . .1 Chapter 4: Clinical Manifestations, Appendices . 114 Diagnosis, and Diagnostics . 28 Chapter 1: Background . 4 Appendix A. Tick-Borne Disease Congressional Action ................. 8 Chapter 5: Causes, Pathogenesis, Working Group .....................114 and Pathophysiology . 44 The Tick-Borne Disease Working Group . 8 Appendix B. Tick-Borne Disease Working Chapter 6: Treatment . 51 Group Subcommittees ...............117 Second Report: Focus and Structure . 8 Chapter 7: Clinician and Public Appendix C. Acronyms and Abbreviations 126 Chapter 2: Methods of the Education, Patient Access Working Group . .10 to Care . 59 Appendix D. 21st Century Cures Act ...128 Topic Development Briefs ............ 10 Chapter 8: Epidemiology and Appendix E. Working Group Charter. .131 Surveillance . 84 Subcommittees ..................... 10 Chapter 9: Federal Inventory . 93 Appendix F. Federal Inventory Survey . 136 Federal Inventory ....................11 Chapter 10: Public Input . 98 Appendix G. References .............149 Minority Responses ................. 13 Chapter 11: Looking Forward . .103 Chapter 3: Tick Biology, Conclusion . 112 Ecology, and Control . .14 Contributions U.S. Department of Health and Human Services James J. Berger, MS, MT(ASCP), SBB B. Kaye Hayes, MPA Working Group Members David Hughes Walker, MD (Co-Chair) Adalbeto Pérez de León, DVM, MS, PhD Leigh Ann Soltysiak, MS (Co-Chair) Kevin R. -
KDHE's Notifiable Disease List
REPORTABLE DISEASES IN KANSAS (K.S.A. 65-118, 65-128, 65-6001 - 65-6007, K.A.R. 28-1-2, 28-1-4, and 28-1-18. Changes effective as of 5/11/2018) For 4-hour reportable diseases report to the KDHE Epidemiology Hotline: 877-427-7317. For all other reportable diseases fax a Kansas Reportable Disease Form and any lab results to your local health department or to KDHE: 877-427-7318 within 24 hours or by the next business day. Acute flaccid myelitis Influenza, novel A virus infection Anthrax Legionellosis Anaplasmosis Listeriosis Arboviral disease, neuroinvasive and nonneuroinvasive Lyme disease (including chikungunya virus, dengue virus, La Malaria Crosse, West Nile virus, and Zika virus) Measles (rubeola) Babesiosis Meningococcal disease Blood lead levels (any results) Mumps Botulism Pertussis (whooping cough) Brucellosis Plague (Yersinia pestis) Campylobacteriosis Poliovirus Candida auris Psittacosis Carbapenem-resistant bacterial infection or Q Fever (Coxiella burnetii, acute and chronic) colonization Rabies, human Carbon monoxide poisoning Rabies, animal Chancroid Rubella Chickenpox (varicella) Salmonellosis, including typhoid fever Chlamydia trachomatis infection Severe Acute Respiratory Syndrome-associated Cholera coronavirus (SARS-CoV) Coccidioidomycosis Shiga toxin-producing Escherichia coli (STEC) Cryptosporidiosis Shigellosis Cyclosporiasis Smallpox Diphtheria Spotted fever rickettsiosis Ehrlichiosis Streptococcus pneumoniae, invasive disease Giardiasis Syphilis, all stages, including congenital syphilis Gonorrhea -
Development of Diagnostic Assays for Melioidosis, Tularemia, Plague And
University of Nevada, Reno Development of Diagnostic Assays for Melioidosis, Tularemia, Plague and COVID19 A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Cellular and Molecular Biology By Derrick Hau Dr. David P. AuCoin / Dissertation Advisor December 2020 THE GRADUATE• SCHOOL We recommend that the dissertation prepared under our supervision by entitled be accepted in partial fulfillment of the requirements for the degree of Advisor Committee Member Committee Member Committee Member Graduate School Representative David W. Zeh, Ph.D., Dean Graduate School December 2020 i Abstract Infectious diseases are caused by pathogenic organisms which can be spread throughout communities by direct and indirect contact. Burkholderia pseudomallei, Francisella tularenisis, and Yersinia pestis are the causative agents of melioidosis, tularemia and plague, respectively. These bacteria pertain to the United States of America Federal Select Agent Program as they are associated with high mortality rates, lack of medical interventions and are potential agents of bioterrorism. The novel coronavirus disease (COVID-19) has resulted in a global pandemic due to the highly infectious nature and elevated virulence of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Proper diagnosis of these infections is warranted to administer appropriate medical care and minimize further spreading. Current practices of diagnosing melioidosis, tularemia, plague and COVID-19 are inadequate due to limited resources and the untimely nature of the techniques. Commonly, diagnosing an infectious disease is by the direct detection of the causative agent. Isolation by bacterial culture is the gold standard for melioidosis, tularemia and plague infections; detection of SAR-CoV-2 nucleic acid by real-time polymerase chain reaction (RT-PCR) is the gold standard for diagnosing COVID-19. -
Brucellosis Annual Report 2018
Brucellosis Annual Report 2018 Brucellosis Brucellosis is a Class A Disease. It must be reported to the state within 24 hours by calling the number listed on the website. Brucellosis is a zoonotic infection of domesticated and wild animals, caused by bacteria of the genus Brucella. Humans become infected by ingestion of food products of animal origin (such as undercooked meat or unpasteurized milk or dairy products), direct contact with infected animals, or inhalation of infectious aerosols. Brucella abortus (cattle), B.melitensis (sheep and goats), B.suis (pigs), and B.canis (dogs), are the most common species. The most common etiology in the U.S. is B.melitensis. Marine Brucella (B.ceti and B.pinnipedialis) may also pose a risk to humans who interact with marine animals; people should avoid contact with stranded or dead marine mammals. Infection may cause a range of symptoms, including fever, sweats, malaise, anorexia, headache, joint and muscle pain, and fatigue. Some symptoms may last for prolonged periods of time including recurrent fevers, arthritis, swelling of the testicle and scrotum area, swelling of the heart, swelling of the liver and/or spleen, neurologic symptoms, chronic fatigue, and depression. Treatment consists of antibiotics, but recovery may take a few weeks to several months. Bovine brucellosis caused by B. abortus, is a bacterial infection transmitted through oral exposure to uterine discharges from infected cows at time of calving or abortion. This previously common disease has been eliminated from the state through the cooperation of the cattle industry and state-federal animal health officials. On November 1, 2000, Louisiana was declared free of brucellosis in cattle. -
Tularemia (CFSPH)
Tularemia Importance Tularemia is a zoonotic bacterial disease with a wide host range. Infections are most prevalent among wild mammals and marsupials, with periodic epizootics in Rabbit Fever, lagomorphs and rodents, but clinical cases also occur in sheep, cats and other Deerfly Fever, domesticated species. A variety of syndromes can be seen, but fatal septicemia is Meat-Cutter’s Disease common in some species. In humans, tularemia varies from a localized infection to Ohara Disease, fulminant, life-threatening pneumonia or septicemia. Francis Disease Tularemia is mainly seen in the Northern Hemisphere, where it has recently emerged or re-emerged in some areas, including parts of Europe and the Middle East. A few endemic clinical cases have also been recognized in regions where this disease Last Updated: June 2017 was not thought to exist, such as Australia, South Korea and southern Sudan. In some cases, emergence may be due to increased awareness, surveillance and/or reporting requirements; in others, it has been associated with population explosions of animal reservoir hosts, or with social upheavals such as wars, where sanitation is difficult and infected rodents may contaminate food and water supplies. Occasionally, this disease may even be imported into a country in animals. In 2002, tularemia entered the Czech Republic in a shipment of sick pet prairie dogs from the U.S. Etiology Tularemia is caused by Francisella tularensis (formerly known as Pasteurella tularensis), a Gram negative coccobacillus in the family Francisellaceae and class γ- Proteobacteria. Depending on the author, either three or four subspecies are currently recognized. F. tularensis subsp. tularensis (also known as type A) and F.