Influenza Swine Flu Virus: a Candidate for the Next Pandemic?
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Influenza: Pigs, People & Public Health
National Pork Board | 800-456-7675 | pork.org Public Health Fact Sheet Influenza: Pigs, People & Public Health Authors: Amy L. Vincent, DVM, PhD, USDA-ARS National Animal Disease Center; Marie R. Culhane, DVM, PhD, College of Veterinary Medicine, University of Minnesota; Christopher W. Olsen, DVM PhD, School of Veterinary Medicine and School of Medicine and Public Health, University of Wisconsin-Madison. Reviewers: Jeff B. Bender, DVM MS, University of Minnesota; Andrew Bowman, DVM PhD, The Ohio State University; Todd Davis, PhD, CDC; Ellen Kasari, DVM MS, USDA; Heather Fowler, VMD PhD MPH, National Pork Board Influenza A viruses (IAV) were first isolated from swine in the United States in 1930. Since that time, they remain an economically important cause of respiratory disease in pigs throughout the world and a public health risk. The clinical signs/symptoms of influenza in pigs and people are remarkably similar, with influenza-like illness (ILI) consisting of fever, lethargy, lack of appetite and coughing promi- nent in both species. Influenza viruses can be directly transmitted from pigs to people as “zoonotic” disease agents (pathogens that are transmitted from animals to humans or shared by animals and humans) and cause human infections. Conversely, influenza viruses from people can also infect and cause disease in pigs. These interspecies infections are most likely to occur when people and pigs are in close proximity with one another, such as during livestock exhibits at fairs, live animal markets, swine production barns, and slaughterhouses. Finally, pigs can serve as intermediaries in the generation of novel reassorted influenza viruses since they are also susceptible to infection with avian influenza viruses. -
Swine Influenza Vaccine, H1N1 & H1N2 & H3N2
® DELTA-1 H1N2 CLUSTER-IV-B CLUSTER-IV-A H3N2 H3N2 NOW WITH NOW WITH NOW GAMMA H1N1 U.S. Veterinary License No. 190 Swine Zoetis Inc. Influenza Vaccine, Kalamazoo, MI 49007, USA H1N1 & H1N2 & For use in swine only For vaccination of healthy swine, including pregnant sows and gilts, 3 weeks of age or older as an aid in H3N2 For veterinary use only preventing respiratory disease caused by swine influenza A viruses H1N1, H1N2 and H3N2 and Killed Virus respiratory disease caused by M. hyopneumoniae for a period of 25 weeks. A duration of immunity of at least 10 weeks has been established against swine Mycoplasma influenza A virus H3N2. This product contains the following Influenza A Virus Hyopneumoniae isolates: A/Swine/Iowa/110600/2000 (H1N1); A/Swine/ Oklahoma/0726H/2008 (H1N2); A/Swine/North Carolina/394/2012 (H3N2); and A/Swine/Minnesota/ Bacterin 872/2012 (H3N2). Directions: Shake diluent before use. Aseptically 50-dose vial of vaccine, rehydrate the freeze-dried vaccine with the liquid rehydrate to 100 mL bacterin provided, shake well, and administer 2 mL intramuscularly. Administer a single 2-mL dose to 100-mL vial of liquid bacterin healthy swine 3 weeks of age or older, followed by for use as diluent a single dose of FluSure XP approximately 3 weeks later. In young pigs, vaccinate after maternally derived antibodies to swine influenza A viruses have declined. Semiannual revaccination with a single H1N1 dose is recommended. GAMMA NOW WITH NOW WITH Precautions: Store at 2°–7°C. Do not freeze. Use H1N1 H1N1 H3N2 H3N2 H1N1 GAMMA GAMMA CLUSTER-IV-A CLUSTER-IV-B GAMMA entire contents when first opened or rehydrated. -
Antiviral Agents Active Against Influenza a Viruses
REVIEWS Antiviral agents active against influenza A viruses Erik De Clercq Abstract | The recent outbreaks of avian influenza A (H5N1) virus, its expanding geographic distribution and its ability to transfer to humans and cause severe infection have raised serious concerns about the measures available to control an avian or human pandemic of influenza A. In anticipation of such a pandemic, several preventive and therapeutic strategies have been proposed, including the stockpiling of antiviral drugs, in particular the neuraminidase inhibitors oseltamivir (Tamiflu; Roche) and zanamivir (Relenza; GlaxoSmithKline). This article reviews agents that have been shown to have activity against influenza A viruses and discusses their therapeutic potential, and also describes emerging strategies for targeting these viruses. HXNY In the face of the persistent threat of human influenza A into the interior of the virus particles (virions) within In the naming system for (H3N2, H1N1) and B infections, the outbreaks of avian endosomes, a process that is needed for the uncoating virus strains, H refers to influenza (H5N1) in Southeast Asia, and the potential of to occur. The H+ ions are imported through the M2 haemagglutinin and N a new human or avian influenza A variant to unleash a (matrix 2) channels10; the transmembrane domain of to neuraminidase. pandemic, there is much concern about the shortage in the M2 protein, with the amino-acid residues facing both the number and supply of effective anti-influenza- the ion-conducting pore, is shown in FIG. 3a (REF. 11). virus agents1–4. There are, in principle, two mechanisms Amantadine has been postulated to block the interior by which pandemic influenza could originate: first, by channel within the tetrameric M2 helix bundle12. -
Treatment and Prevention of Pandemic H1N1 Influenza
Annals of Global Health VOL. 81, NO. 5, 2015 ª 2015 The Authors. Published by Elsevier Inc. ISSN 2214-9996 on behalf of Icahn School of Medicine at Mount Sinai http://dx.doi.org/10.1016/j.aogh.2015.08.014 REVIEW Treatment and Prevention of Pandemic H1N1 Influenza Suresh Rewar, Dashrath Mirdha, Prahlad Rewar Rajasthan, India Abstract BACKGROUND Swine influenza is a respiratory infection common to pigs worldwide caused by type Ainfluenza viruses, principally subtypes H1N1, H1N2, H2N1, H3N1, H3N2, and H2N3. Swine influenza viruses also can cause moderate to severe illness in humans and affect persons of all age groups. People in close contact with swine are at especially high risk. Until recently, epidemiological study of influenza was limited to resource-rich countries. The World Health Organization declared an H1N1 pandemic on June 11, 2009, after more than 70 countries reported 30,000 cases of H1N1 infection. In 2015, incidence of swine influenza increased substantially to reach a 5-year high. In India in 2015, 10,000 cases of swine influenza were reported with 774 deaths. METHODS The Centers for Disease Control and Prevention recommend real-time polymerase chain reaction as the method of choice for diagnosing H1N1. Antiviral drugs are the mainstay of clinical treatment of swine influenza and can make the illness milder and enable the patient to feel better faster. FINDINGS Antiviral drugs are most effective when they are started within the first 48 hours after the clinical signs begin, although they also may be used in severe or high-risk cases first seen after this time. -
Swine Influenza a (H1N1 Virus): a Pandemic Disease
Review Article Swine Influenza A (H1N1 Virus): A Pandemic Disease Gangurde HH, Gulecha VS, Borkar VS, Mahajan MS, Khandare RA, Mundada AS Department of Pharmaceutics, SNJB’s SSDJ College of Pharmacy, Neminagar, Chandwad, Nasik, Maharashtra, India ARTICLE INFO ABSTRACT Article history: Swine influenza (SI) is a respiratory disease of pigs caused by type A influenza that regularly Received 9 September 2009 causes pandemics. SI viruses do not normally infect humans; however, human infections with Accepted 18 September 2009 SI do occur, and cases of human-to-human spread of swine flu viruses have been documented. Available online 19 October 2011 Swine influenza also called as swine flu, hog flu, and pig flu that refers to influenza is caused by Keywords: those strains of influenza virus, called SI virus (SIV), that usually infect pigs endemically. As of Coughing 2009, these strains are all found in influenza C virus and subtypes of influenza A virus known as Fever H1N1, H1N2, H3N1, H3N2, and H2N3. The viruses are 80–120 nm in diameter. The transmission of H1N1 SIV from pigs to humans is not common and does not always cause human influenza, often only sore throat resulting in the production of antibodies in the blood. The meat of the animal poses no risk of swine flu swine influenza virus transmitting the virus when properly cooked. If the transmission does cause human influenza, it is called zoonotic swine flu. People who work with pigs, especially people with intense exposures, are at an increased risk of catching swine flu. In the mid-20th century, the identification of influenza subtypes became possible; this allowed accurate diagnosis of transmission to humans. -
Questions & Answers on Influenza
101 Questions & Answers on Influenza101 101 Questions & Answers Prof. Dr. A.D.M.E. (Ab) Osterhaus is David De Pooter is working at Link Inc on professor of virology at Erasmus Medical since 2003, the Antwerp (Belgium) based Centre Rotterdam, and professor of communication consultancy agency, Environmental Virology at the Utrecht specialised in strategic communication University. Fascinated by the ingenious and social marketing. Link Inc is working ways viruses circumvent the immune with the European Scientific working Influenza system of their hosts to multiply and Group on Influenza (ESWI) since 1998 and spread, Osterhaus started his quest at the is taking care of the positioning of the interface of virology and immunology. He group, the strategy and the implementa Ab Osterhaus quickly translated new insights in this tion of the strategy by developing complex field to applications in animal and targeted communication tools. In this human vaccinology. In addition, he started capacity, David De Pooter is a professional David De Pooter his work on virus discovery, not only writer on medical topics and a communi focussing on the identification of a series cation manager of ESWI. As such he has of animal viruses, but also of new human established a fruitful and long standing viruses. collaboration with Prof Ab Osterhaus. (www.linkinc.be) 101 Questions & Answers on Influenza 101 101 Questions & Answers on Influenza Ab Osterhaus David De Pooter Elsevier, Maarssen © Elsevier, Maarssen 2009 Design: Studio Bassa, Culemborg Elsevier is an imprint of Reed Business bv, PO Box 1110, 3600 BC Maarssen, The Netherlands. To order: Elsevier Gezondheidszorg, Marketing dept., Antwoordnummer 2594 (freepost), 3600 VB Maarssen, The Netherlands. -
AJIC-Oseltamivir-Stockpile-Paper.Pdf
American Journal of Infection Control 45 (2017) 303-5 Contents lists available at ScienceDirect American Journal of Infection Control American Journal of Infection Control journal homepage: www.ajicjournal.org Brief Report Oseltamivir for pandemic influenza preparation: Maximizing the use of an existing stockpile Twisha S. Patel PharmD a, Sandro Cinti MD b, Duxin Sun PhD c, Siwei Li PhD c, Ruijuan Luo PhD c, Bo Wen PhD c, Brian A. Gallagher JD d,e, James G. Stevenson PharmD a,c,* a Pharmacy Services, University of Michigan Health System, Ann Arbor, MI b Infectious Diseases, University of Michigan Health System, Ann Arbor, MI c University of Michigan College of Pharmacy, Ann Arbor, MI d Marshall University School of Pharmacy, Huntington, WV e Joan C. Edwards School of Medicine, Huntington, WV With the threat of significant morbidity and mortality following an influenza pandemic, stockpiling of antiviral agents such as oseltamivir is recommended. Shelf-life extension was explored to maximize use of an existing stockpile. This analysis demonstrated that oseltamivir retains potency defined by United States Pharmacopeia acceptance criteria beyond the labeled expiration date. © 2017 Association for Professionals in Infection Control and Epidemiology, Inc. Published by Elsevier Inc. All rights reserved. BACKGROUND hospital employees because up to 35% are expected to become ill even with the institution of optimal infection control practices during Infection with the influenza virus can lead to devastating com- an influenza pandemic.7 Although imperative, this strategy created plications, including mortality.1 The influenza pandemic in 1918 and asignificantfinancialburdenonourinstitution:A5-daytreat- the Asian H5N1 outbreak in 2005 taught our nation a valuable lesson ment course of oseltamivir is considerably expensive ($120/box of about the importance of creating a national preparedness plan to 10 75-mg capsules, University of Michigan Health System, unpub- combat the spread of infection. -
Swine Influenza Viruses Were First Isolated in the United States in 1930
VOL. 2, NO. 6 JANUARY, 2004 PUBLIC FACT SHEET Author: Christopher W. Olsen, DVM PhD, School of Veterinary Medicine, University of Wisconsin-Madison INFLUENZA: Pigs, People and Public Health NATIONAL Summary: Swine influenza viruses were first isolated in the United States in 1930. Since PORK BOARD that time, they have become an economically important cause of respiratory disease in P.O. BOX 9114 pigs throughout the world, and a human public health risk. The clinical signs/symp- DES MOINES, IA 50306 toms of influenza in pigs and people are remarkably similar, with fever, lethargy, lack of 515 223 2600 FAX 515 223 2646 appetite and coughing prominent in both species. Furthermore, influenza viruses can [email protected] be directly transmitted from pigs to people as "zoonotic" disease agents, and vice versa, from people to pigs. These interspecies infections are most likely to occur when people are in close proximity to pigs, such as in swine production barns, livestock exhibits at fairs, and slaughterhouses. Finally, because of their unique susceptibility to infection with influenza viruses of both mammalian and avian species, pigs can serve as intermedi- aries in the transmission of influenza viruses from birds to people. The birds of greatest AMERICAN ASSOCIATION OF SWINE concern are wild waterfowl, because these species provide an immense natural reservoir VETERINARIANS of influenza viruses. Replication of avian influenza viruses in pigs may allow them to adapt to and be able to efficiently infect mammals, and ultimately be transmitted to peo- 902 1ST STREET PERRY, IA 50220 ple. In addition, pigs can serve as hosts in which two (or more) influenza viruses can 515 465 5255 undergo "genetic reassortment." This is a process in which influenza viruses exchange FAX 515 465 3832 genes during replication. -
HHS 2009 H1N1 Influenza Improvement Plan
U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES 2009 H1N1 Influenza Improvement Plan May 29, 2012 TABLE OF CONTENTS Contents STATEMENT BY SECRETARY SEBELIUS.......................................................................... iii EXECUTIVE SUMMARY ......................................................................................................... iv CHAPTER 1: INTRODUCTION................................................................................................ 1 CHAPTER 2: DETECTION AND CHARACTERIZATION OF A FUTURE INFLUENZA PANDEMIC ................................................................................................................................... 5 CHAPTER 3: COMMUNITY MITIGATION MEASURES ................................................... 8 CHAPTER 4: MEDICAL SURGE CAPACITY ..................................................................... 12 CHAPTER 5: MEDICAL COUNTERMEASURES (MCM) FOR INFLUENZA OTHER THAN VACCINES ..................................................................................................................... 17 CHAPTER 6: VACCINE MANUFACTURING, DISTRIBUTION, AND POST- DISTRIBUTION......................................................................................................................... 25 CHAPTER 7: COMMUNICATIONS....................................................................................... 17 CHAPTER 8: CROSS-CUTTING PREPAREDNESS ISSUES............................................ 33 CHAPTER 9: INTERNATIONAL PARTNERSHIPS AND CAPACITY BUILDING ACTIVITIES -
Pandemic Influenza Preparedness and Response Plan March 2020
Pandemic Influenza Preparedness and Response Plan Version 5.1 March 2020 i DocuSign Envelope ID: BBD02F77-9434-4914-8301-5A7E173ACB6B Illinois Pandemic Influenza Preparedness and Response Plan Version 5.1 March 2020 FOREWORD Influenza is an acute viral infection that spreads easily from person-to-person. It causes illnesses, hospitalizations and deaths every year in Illinois. Intermittently over the centuries, changes in the genetic makeup of influenza virus have resulted in new strains to which people have never been exposed. These new strains have the potential to cause a pandemic or worldwide outbreak of influenza, with potentially catastrophic consequences. In Illinois alone, a pandemic of even modest severity could result in thousands of deaths and the sickening of millions, even among previously healthy persons. In 2009, a new strain of influenza virus, 2009A(H1N1)pdm, emerged. The U.S. Centers for Disease Control and Prevention (CDC) worked with manufacturers to develop a vaccine; however, the time it took to develop a vaccine caused a severe shortage in available vaccine during the height of the outbreak. Manufacturers have since developed ample amounts of vaccine to the 2009A(H1N1)pdm influenza strain; still, new genetic strains can arise leading to another pandemic influenza. The Illinois Pandemic Influenza Preparedness and Response Plan was developed: • To identify steps that need to be taken by state government and its partners prior to a pandemic to improve the level of preparedness; and • To coordinate state government-wide response activities in the event a pandemic occurs. These preparedness and response activities are organized according to the six pandemic phases identified by the World Health Organization (WHO). -
Identification, Genetic Analysis, and Pathogenicity of Classical Swine H1N1 and Human-Swine Reassortant H1N1 Influenza Viruses F
viruses Article Identification, Genetic Analysis, and Pathogenicity of Classical Swine H1N1 and Human-Swine Reassortant H1N1 Influenza Viruses from Pigs in China Yafen Song, Yong Zhang, Bing Zhang, Ling Chen, Min Zhang, Jingwen Wang, Ying Jiang, Chenghuai Yang and Taozhen Jiang * Department of Veterinary Culture Collection, China Institute of Veterinary Drug Control, 8 Nandajie, Zhongguancun, Haidian District, Beijing 100081, China; [email protected] (Y.S.); [email protected] (Y.Z.); [email protected] (B.Z.); [email protected] (L.C.); [email protected] (M.Z.); [email protected] (J.W.); [email protected] (Y.J.); [email protected] (C.Y.) * Correspondence: [email protected]; Tel.: +86-010-62103518; Fax: +86-010-61255380 Received: 14 November 2019; Accepted: 31 December 2019; Published: 2 January 2020 Abstract: Swine influenza virus causes a substantial disease burden to swine populations worldwide and poses an imminent threat to the swine industry and humans. Given its importance, we characterized two swine influenza viruses isolated from Shandong, China. The homology and phylogenetic analyses showed that all eight gene segments of A/swine/Shandong/AV1522/2011(H1N1) were closely related to A/Maryland/12/1991(H1N1) circulating in North America. The HA, NA, M, and NS genes of the isolate were also confirmed to have a high homology to A/swine/Hubei/02/2008(H1N1) which appeared in China in 2008, and the virus was clustered into the classical swine lineage. The gene segments of A/swine/Shandong/AV1523/2011(H1N1) were highly homologous to the early human H1N1 and H2N2 influenza viruses, except for the HA gene, and the virus was a reassortant H1N1 virus containing genes from the classical swine (HA) and human (NA, PB2, PB1, PA, NP, M, and NS) lineages. -
Pandemrix, INN-Pandemic Influenza Vaccine (H1N1)
ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS 1 1. NAME OF THE MEDICINAL PRODUCT Pandemrix suspension and emulsion for emulsion for injection. Pandemic influenza vaccine (H1N1)v (split virion, inactivated, adjuvanted) 2. QUALITATIVE AND QUANTITATIVE COMPOSITION After mixing, 1 dose (0.5 ml) contains: Split influenza virus, inactivated, containing antigen* equivalent to: A/California/7/2009 (H1N1)v-like strain (X-179A) 3.75 micrograms** * propagated in eggs ** haemagglutinin This vaccine complies with the WHO recommendation and EU decision for the pandemic. AS03 adjuvant composed of squalene (10.69 milligrams), DL-α-tocopherol (11.86 milligrams) and polysorbate 80 (4.86 milligrams) The suspension and emulsion, once mixed, form a multidose vaccine in a vial. See section 6.5 for the number of doses per vial. Excipients: the vaccine contains 5 micrograms thiomersal For a full list of excipients see section 6.1. 3. PHARMACEUTICAL FORM Suspension and emulsion for emulsion for injection. The suspension is a colourless light opalescent liquid. The emulsion is a whitish homogeneous liquid. 4. CLINICAL PARTICULARS 4.1 Therapeutic indications Prophylaxis of influenza in an officially declared pandemic situation (see sections 4.2 and 5.1). Pandemic influenza vaccine should be used in accordance with Official Guidance. 4.2 Posology and method of administration Posology The dose recommendations take into account available data from on-going clinical studies in healthy subjects who received a single dose of Pandemrix (H1N1) and from clinical studies in healthy subjects who received two doses of a version of Pandemrixcontaining HA derived from A/Vietnam/1194/2004 (H5N1). 2 In some age groups there are limited data (adults aged 60-79 years), very limited data (adults aged 80 years and older, children aged 6 months to 9 years) or no data (children aged less than 6 months or from 10-17 years) with one or both versions of Pandemrix as detailed in sections 4.4, 4.8 and 5.1.