Monkeypox: a Neglected Viral Zoonotic Disease
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Poxvirus and Rabies Branch (PRB) Fact Sheet
Poxvirus & Rabies Branch (PRB) The epidemiologists, laboratory scientists, and public health professionals in PRB are responsible for surveillance, control, and prevention of illness and death due to poxviruses and rabies. Our Work Laboratory Reference, Diagnostics, & Training PRB’s provides laboratory reference, diagnostic services, and trainings to state and local health departments, the Department of Defense (DOD), international organizations, and the Laboratory Response Network (over 150 labs across the U.S. prepared to respond to bioterrorism). PRB collaborates with the private sector to develop and evaluate novel diagnostic assays, therapeutics, and vaccines for rabies and pox-related viruses. The branch maintains high-containment laboratories (BSL3 &4) to safely conduct public health research. Research & Surveillance PRB conducts research studies on the microbiology, molecular biology, pathogenesis (disease process), ecology, and evolution of Our Pathogens poxviruses and rabies. The branch monitors the incidence rates of PRB’s Poxvirus Team provides subject matter these diseases in the U.S. and internationally. expertise on: Expert Consultation Orthopoxviruses, including PRB provides consultation regarding poxvirus and rabies- Smallpox associated diseases and their diagnoses, prevention, control, and Monkeypox treatments. Assistance is offered to healthcare providers, academic Cowpox institutions, state and local health departments, other government Vaccinia Virus agencies, and the general public. PRB collaborates with non- governmental organizations to develop risk communication Parapoxviruses, including tools for disease prevention. The branch provides training on Orf Virus simple surveillance techniques and trains healthcare workers on monkeypox in the Democratic Republic of the Congo (DRC). PRB Pseudocowpox collaborates with the national government of Haiti on a rabies surveillance and control program which includes health education, enhanced diagnostics, surveillance, and an extensive dog vaccination campaign. -
Guide for Common Viral Diseases of Animals in Louisiana
Sampling and Testing Guide for Common Viral Diseases of Animals in Louisiana Please click on the species of interest: Cattle Deer and Small Ruminants The Louisiana Animal Swine Disease Diagnostic Horses Laboratory Dogs A service unit of the LSU School of Veterinary Medicine Adapted from Murphy, F.A., et al, Veterinary Virology, 3rd ed. Cats Academic Press, 1999. Compiled by Rob Poston Multi-species: Rabiesvirus DCN LADDL Guide for Common Viral Diseases v. B2 1 Cattle Please click on the principle system involvement Generalized viral diseases Respiratory viral diseases Enteric viral diseases Reproductive/neonatal viral diseases Viral infections affecting the skin Back to the Beginning DCN LADDL Guide for Common Viral Diseases v. B2 2 Deer and Small Ruminants Please click on the principle system involvement Generalized viral disease Respiratory viral disease Enteric viral diseases Reproductive/neonatal viral diseases Viral infections affecting the skin Back to the Beginning DCN LADDL Guide for Common Viral Diseases v. B2 3 Swine Please click on the principle system involvement Generalized viral diseases Respiratory viral diseases Enteric viral diseases Reproductive/neonatal viral diseases Viral infections affecting the skin Back to the Beginning DCN LADDL Guide for Common Viral Diseases v. B2 4 Horses Please click on the principle system involvement Generalized viral diseases Neurological viral diseases Respiratory viral diseases Enteric viral diseases Abortifacient/neonatal viral diseases Viral infections affecting the skin Back to the Beginning DCN LADDL Guide for Common Viral Diseases v. B2 5 Dogs Please click on the principle system involvement Generalized viral diseases Respiratory viral diseases Enteric viral diseases Reproductive/neonatal viral diseases Back to the Beginning DCN LADDL Guide for Common Viral Diseases v. -
Pt Education-Rubella
Patient Education Healthcare Epidemiology and Infection Control Rubella An illness requiring droplet precautions This handout describes What is Rubella? Rubella and it symptoms. It Rubella (also called German measles, 3-day measles or Rubella virus also explains how this infection) is a viral disease. It can be prevented with a vaccine. disease can be spread and You are not at risk if you have: offers steps to prevent • Had blood tests showing that you are immune due to a history of others from getting it. clinical disease. To learn more about Rubella, • Received 2 doses of the MMR (Mumps, Measles, Rubella) vaccine. visit these Web sites: Rubella is a reportable disease. The health department is notified when a case is diagnosed to protect others who may have come in contact with www.cdc.gov/ncidod/dvrd/ you and are at risk of becoming ill. revb/measles/rubella_index The greatest danger from rubella is to unborn babies. If a woman gets .htm rubella in the early months of her pregnancy, there is an 80% chance that www.cdc.gov/vaccines/vpd her baby will be born with birth defects. Babies may be born deaf or blind. They may have damaged hearts or small brains. Many are mentally -vac/rubella/default.htm retarded. Miscarriages are also common among women who get rubella while they are pregnant. What are the symptoms? The symptoms of Rubella include a slight fever that lasts for about 24 hours, and a rash on the face and neck that lasts 2 or 3 days. The rash is pink or light red spots that may merge to form splotches. -
Where Do We Stand After Decades of Studying Human Cytomegalovirus?
microorganisms Review Where do we Stand after Decades of Studying Human Cytomegalovirus? 1, 2, 1 1 Francesca Gugliesi y, Alessandra Coscia y, Gloria Griffante , Ganna Galitska , Selina Pasquero 1, Camilla Albano 1 and Matteo Biolatti 1,* 1 Laboratory of Pathogenesis of Viral Infections, Department of Public Health and Pediatric Sciences, University of Turin, 10126 Turin, Italy; [email protected] (F.G.); gloria.griff[email protected] (G.G.); [email protected] (G.G.); [email protected] (S.P.); [email protected] (C.A.) 2 Complex Structure Neonatology Unit, Department of Public Health and Pediatric Sciences, University of Turin, 10126 Turin, Italy; [email protected] * Correspondence: [email protected] These authors contributed equally to this work. y Received: 19 March 2020; Accepted: 5 May 2020; Published: 8 May 2020 Abstract: Human cytomegalovirus (HCMV), a linear double-stranded DNA betaherpesvirus belonging to the family of Herpesviridae, is characterized by widespread seroprevalence, ranging between 56% and 94%, strictly dependent on the socioeconomic background of the country being considered. Typically, HCMV causes asymptomatic infection in the immunocompetent population, while in immunocompromised individuals or when transmitted vertically from the mother to the fetus it leads to systemic disease with severe complications and high mortality rate. Following primary infection, HCMV establishes a state of latency primarily in myeloid cells, from which it can be reactivated by various inflammatory stimuli. Several studies have shown that HCMV, despite being a DNA virus, is highly prone to genetic variability that strongly influences its replication and dissemination rates as well as cellular tropism. In this scenario, the few currently available drugs for the treatment of HCMV infections are characterized by high toxicity, poor oral bioavailability, and emerging resistance. -
Imported Monkeypox, Singapore
DISPATCHES Imported Monkeypox, Singapore Sarah Ee Fang Yong, Oon Tek Ng, Zheng Jie Marc Ho, Tze Minn Mak, Kalisvar Marimuthu, Shawn Vasoo, Tsin Wen Yeo, Yi Kai Ng, Lin Cui, Zannatul Ferdous, Po Ying Chia, Bryan Jun Wei Aw, Charmaine Malenab Manauis, Constance Khia Ki Low, Guanhao Chan, Xinyi Peh, Poh Lian Lim, Li Ping Angela Chow, Monica Chan, Vernon Jian Ming Lee, Raymond Tzer Pin Lin, Mok Kwee Derrick Heng, Yee Sin Leo In May 2019, we investigated monkeypox in a traveler and public health management for this case, together from Nigeria to Singapore. The public health response with lessons learned and implications for control. included rapid identification of contacts, use of quaran- tine, and postexposure smallpox vaccination. No sec- The Case ondary cases were identified. Countries should develop On May 8, 2019, monkeypox was laboratory-con- surveillance systems to detect emerging infectious dis- firmed in a 38-year-old man from Nigeria who had eases globally. traveled to Singapore. The man resided in Delta State, Nigeria, but had attended a wedding in Ebonyi State onkeypox is a zoonosis endemic to West and during April 21–23, where he reported ingestion of MCentral Africa; human cases were first report- barbecued bushmeat that might have been contami- ed in 1970 (1). An outbreak ongoing in Nigeria since nated. He did not handle raw meat and had no expo- 2017 is the largest documented (2). Exported cases in sure to wild animals or their products. He held an ad- the United Kingdom and Israel were reported from ministrative job and reported no contact with rodents travelers infected in Nigeria in 2018 (3,4). -
Chronic Viral Infections Vs. Our Immune System: Revisiting Our View of Viruses As Pathogens
Chronic Viral Infections vs. Our Immune System: Revisiting our view of viruses as pathogens Tiffany A. Reese Assistant Professor Departments of Immunology and Microbiology Challenge your idea of classic viral infection and disease • Define the microbiome and the virome • Brief background on persistent viruses • Illustrate how viruses change disease susceptibility – mutualistic symbiosis – gene + virus = disease phenotype – virome in immune responses Bacteria-centric view of the microbiome The microbiome defined Definition of microbiome – Merriam-Webster 1 :a community of microorganisms (such as bacteria, fungi, and viruses) that inhabit a particular environment and especially the collection of microorganisms living in or on the human body 2 :the collective genomes of microorganisms inhabiting a particular environment and especially the human body Virome Ø Viral component of the microbiome Ø Includes both commensal and pathogenic viruses Ø Viruses that infect host cells Ø Virus-derived elements in host chromosomes Ø Viruses that infect other organisms in the body e.g. phage/bacteria Viruses are everywhere! • “intracellular parasites with nucleic acids that are capable of directing their own replication and are not cells” – Roossinck, Nature Reviews Microbiology 2011. • Viruses infect all living things. • We are constantly eating and breathing viruses from our environment • Only a small subset of viruses cause disease. • We even carry viral genomes as part of our own genetic material! Diverse viruses all over the body Adenoviridae Picornaviridae -
Monkeypox Virus Emergence in Wild Chimpanzees Reveals Distinct Clinical Outcomes and Viral Diversity
ARTICLES https://doi.org/10.1038/s41564-020-0706-0 Monkeypox virus emergence in wild chimpanzees reveals distinct clinical outcomes and viral diversity Livia V. Patrono1,6, Kamilla Pléh1,2,6, Liran Samuni2,3, Markus Ulrich1, Caroline Röthemeier1, Andreas Sachse1, Silvia Muschter4, Andreas Nitsche4, Emmanuel Couacy-Hymann5, Christophe Boesch2,3, Roman M. Wittig 2,3, Sébastien Calvignac-Spencer1 and Fabian H. Leendertz 1 ✉ Monkeypox is a viral zoonotic disease on the rise across endemic habitats. Despite the growing importance of monkeypox virus, our knowledge on its host spectrum and sylvatic maintenance is limited. Here, we describe the recent repeated emergence of monkeypox virus in a wild, human-habituated western chimpanzee (Pan troglodytes verus, hereafter chimpanzee) population from Taï National Park, Ivory Coast. Through daily monitoring, we show that further to causing its typical exanthematous syn- drome, monkeypox can present itself as a severe respiratory disease without a diffuse rash. By analysing 949 non-invasively collected samples, we identify the circulation of at least two distinct monkeypox virus lineages and document the shedding of infectious particles in faeces and flies, suggesting that they could mediate indirect transmission. We also show that the carnivo- rous component of the Taï chimpanzees’ diet, mainly consisting of the sympatric monkeys they regularly hunt, did not change nor shift towards rodent consumption (the presumed reservoir) before the outbreaks, suggesting that the sudden emergence of monkeypox virus in this population is probably due to changes in the ecology of the virus itself. Using long-term mortality surveillance data from Taï National Park, we provide evidence of little to no prior viral activity over at least two decades. -
Select Biological Agent and Toxin List
Select Biological Agent and Toxin List HHS Non-Overlap Select Agents and Toxins USDA High Consequence Livestock Pathogens - Crimean-Congo haemorrhagic fever virus and Toxins (Non-Overlap agents and toxins) - Coccidioides posadasii - Akabane virus - Ebola viruses - African swine fever virus - Cercopithecine herpesvirus 1 (Herpes B virus) - African horse sickness virus - Lassa fever virus - Avian influenza virus (highly pathogenic) - Marburg virus - Blue tongue virus (Exotic) - Monkeypox virus - Bovine spongiform encephalopathy agent - Rickettsia prowazekii - Camel pox virus - Rickettsia rickettsii - Classical swine fever virus South American haemorrhagic fever viruses - Cowdria ruminantium (Heartwater) - Junin - Foot and mouth disease virus - Machupo - Goat pox virus - Sabia - Lumpy skin disease virus - Flexal - Japanese encephalitis virus - Guanarito - Malignant catarrhal fever virus (Exotic) Tick-borne encephalitis complex (flavi) viruses - Menangle virus - Central European tick-borne encephalitis - Mycoplasma capricolum/M.F38/M. mycoides capri - Far Eastern tick-borne encephalitis - Mycoplasma mycoides mycoides - Russian spring and summer encephalitis - Newcastle disease virus (VVND) - Kyasanur forest disease - Peste Des Petits Ruminants virus - Omsk hemorrhagic fever - Rinderpest virus - Variola major virus (Smallpox virus) - Sheep pox virus - Variola minor virus (Alastrim) - Swine vesicular disease virus - Yersinia pestis - Vesicular stomatitis virus (Exotic) - Abrin - Conotoxins - Diacetoxyscirpenol Plant Pathogens - Ricin - Liberobacter -
Emergence of Monkeypox — West and Central Africa, 1970–2017
Morbidity and Mortality Weekly Report Emergence of Monkeypox — West and Central Africa, 1970–2017 Kara N. Durski, MPH1; Andrea M. McCollum, PhD2; Yoshinori Nakazawa, PhD2; Brett W. Petersen, MD2; Mary G. Reynolds, PhD2; Sylvie Briand, MD, PhD1; Mamoudou Harouna Djingarey, MD3; Victoria Olson, PhD2; Inger K. Damon, MD, PhD2, Asheena Khalakdina, PhD1 The recent apparent increase in human monkeypox cases Monkeypox is a zoonotic orthopoxvirus with a similar dis- across a wide geographic area, the potential for further spread, ease presentation to smallpox in humans, with the additional and the lack of reliable surveillance have raised the level of distinguishing symptom of lymphdenopathy. After an initial concern for this emerging zoonosis. In November 2017, the febrile prodrome, a centrifugally distributed maculopapular World Health Organization (WHO), in collaboration with rash develops, with lesions often present on the palms of CDC, hosted an informal consultation on monkeypox with the hands and soles of the feet. The infection can last up to researchers, global health partners, ministries of health, and 4 weeks, until crusts separate and a fresh layer of skin is formed. orthopoxvirus experts to review and discuss human monkeypox Sequelae include secondary bacterial infections, respiratory in African countries where cases have been recently detected and distress, bronchopneumonia, gastrointestinal involvement, also identify components of surveillance and response that need dehydration, encephalitis, and ocular infections, which can improvement. Endemic human monkeypox has been reported result in permanent corneal scarring. No specific treatment for from more countries in the past decade than during the previ- a monkeypox virus infection currently exists, and patients are ous 40 years. -
Serological Evidence of Multiple Zoonotic Viral Infections Among Wild Rodents in Barbados
pathogens Article Serological Evidence of Multiple Zoonotic Viral Infections among Wild Rodents in Barbados Kirk Osmond Douglas 1,*, Claire Cayol 2 , Kristian Michael Forbes 3, Thelma Alafia Samuels 4, Olli Vapalahti 5, Tarja Sironen 5 and Marquita Gittens-St. Hilaire 6,7 1 Centre for Biosecurity Studies, The University of the West Indies, Cave Hill, St. Michael BB11000, Barbados 2 Department of Wildlife, Fish, and Environmental Studies, Swedish University of Agricultural Sciences, Skogsmarksgränd 17, 901 83 Umeå, Sweden; [email protected] 3 Department of Biological Sciences, University of Arkansas, Fayetteville, AR 72701, USA; [email protected] 4 Epidemiology Research Unit, Caribbean Institute for Health Research (CAIHR), The University of the West Indies, Mona, Kingston 7, Jamaica; alafi[email protected] 5 Department of Virology, Faculty of Medicine, University of Helsinki, Medicum, Haartmaninkatu 3, 0290 Helsinki, Finland; olli.vapalahti@helsinki.fi (O.V.); tarja.sironen@helsinki.fi (T.S.) 6 Faculty of Medical Sciences, The University of the West Indies, Cave Hill, St. Michael BB11000, Barbados; [email protected] 7 Best–dos Santos Public Health Laboratory, Enmore #6, Lower Collymore Rock, St. Michael BB11155, Barbados * Correspondence: [email protected]; Tel.: +246-417-7468 Abstract: Background: Rodents are reservoirs for several zoonotic pathogens that can cause human infectious diseases, including orthohantaviruses, mammarenaviruses and orthopoxviruses. Evidence exists for these viruses circulating among rodents and causing human infections in the Americas, Citation: Douglas, K.O.; Cayol, C.; but much less evidence exists for their presence in wild rodents in the Caribbean. Methods: Here, Forbes, K.M.; Samuels, T.A.; we conducted serological and molecular investigations of wild rodents in Barbados to determine Vapalahti, O.; Sironen, T.; Gittens-St. -
Health Canada Extends Approval of IMVAMUNE to Immunization Against Monkeypox and Orthopox Viruses
Press Release Health Canada Extends Approval of IMVAMUNE to Immunization against Monkeypox and Orthopox Viruses COPENHAGEN, Denmark, November 12, 2020 – Bavarian Nordic A/S (OMX: BAVA, OTC: BVNRY) announced today that Health Canada has expanded the approval of the Company’s non-replicating smallpox vaccine, IMVAMUNE® to include additional indications – specifically, monkeypox and related orthopoxvirus infections and disease in adults 18 years of age and older determined to be at high risk for exposure. The extended approval was granted following assessment of additional clinical and non-clinical data, generated since IMVAMUNE received approval as a smallpox vaccine by Health Canada in 2013. These data include among others a Phase 3 study which demonstrated that, in terms of efficacy, IMVAMUNE was non-inferior to replicating smallpox vaccines, while also confirming its favorable benefit/risk profile. IMVAMUNE is approved in Canada under the Extraordinary Use New Drugs (EUNDS) Pathway. Paul Chaplin, President and CEO of Bavarian Nordic said. “The extended approval of IMVAMUNE in Canada confirms its potential to prevent infections from a wider range of orthopoxviruses, many of which are naturally occurring. While monkeypox is endemic to certain parts of Africa, orthopoxvirus infections may occur from animals to humans all over the world. Although cases are rare, no vaccine has previously been approved for these indications, and we are pleased to receive this extended approval of IMVAMUNE.” Bavarian Nordic has collaborated with the Canadian authorities since 2008 on supplying IMVAMUNE, initially for the Canadian Department of National Defence. Subsequent to the initial Canadian EUNDS approval in 2013, Bavarian Nordic has also collaborated with the Public Health Agency of Canada for stockpiling of the vaccine for the general population. -
Fact Sheet: Basic Information About Monkeypox
MONKEYPOX FACT SHEET Basic Information about Monkeypox Monkeypox: An Emerging Infectious Disease in North America Monkeypox is a rare viral disease that is found mostly in the rainforest countries of central and west Africa. The disease is called “monkeypox” because it was first discovered in laboratory monkeys in 1958. Blood tests of animals in Africa later found evidence of monkeypox infection in various rodent species. The virus that causes monkeypox was recovered from an African squirrel, which may be the natural host. Laboratory studies showed that the virus could also infect rats, mice, and rabbits. In 1970, monkeypox was identified as the cause of a rash illness in humans in remote African locations. In early June 2003, monkeypox was reported among several residents in the United States who became ill after having contact with sick pet prairie dogs. This is the first evidence of community-acquired monkeypox in the United States. Cause of Monkeypox The disease is caused by Monkeypox virus, which belongs to the orthopoxvirus group of viruses. Other orthopoxviruses that can cause infection in humans include variola (smallpox), vaccinia (used in smallpox vaccine), and cowpox viruses. Signs and Symptoms In humans, the signs and symptoms of monkeypox are similar to those of smallpox, but usually milder. Unlike smallpox, monkeypox causes swollen lymph nodes. The incubation period for monkeypox is about 12 days.The illness begins with fever, headache, muscle aches, backache, swollen lymph nodes, a general feeling of discomfort, and exhaustion. Within 1 to 3 days (sometimes longer) after onset of fever, the patient develops a papular rash (i.e., raised bumps), often first on the face but sometimes initially on other parts of the body.