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Orthomyxoviruses September 15,16, 2010
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The big pandemic of 1918
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John Hopkins Hospital Bulletin April 1919
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Nature Jan 18, 2007
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The 1918 virus Loo and Gale Nature Jan 18, 2007
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Orthomyxoviridae -ve stranded RNA, segmented Haemagglutinin (HA) and neuraminidase (N) on surface
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Viruses with -ve RNA genomes Paramyxoviridae Rhabdoviridae Orthomyxoviridae Filoviridae Bunyaviridae parainfluenza virus canine distemper virus respiratory syncytial virus rabies virus vesicular stomatitis virus influenzaviruses Ebola virus Haantan virus
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Orthomyxoviridae Influenzavirus A Influenzavirus B Influenzavirus C humans horses pigs birds marine mammals humans pigs dogs cats
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Influenza virions nucleocapsid (RNA fragments wrapped in protein) envelope haemagglutinin and neuraminidase “spikes” In envelope 100 nm
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Haemagglutinin and Neuraminidase receptor binding site active site variable loops variable loops HAN sialic acid on receptor
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Distribution of HA serotypes in nature HA serotypeBirdsHorsesPigsHumans HA1 HA2 HA3 HA4 HA5 HA6 HA7 HA8-16 yes
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Distribution of N serotypes in nature BirdsHorsesPigs N1 N2 N3 N4 N5 N6 N7 N8 yes N9yes Humans yes
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Nomenclature A/equine/Saskatoon/1/90(H3N8) group species location Isolate number year Serotype of HA and N A/equine/Prague/1/56(H7N7) A/fowl/Hong Kong/1/98(H5N1) A/swine/Lincoln/1/86(H1N1)
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Influenzavirus replication HA cleaved by proteases HA binds to receptor virus in phagolysosome lowered pH, HA fuses membranes RNA released virus buds N releases virus
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Cleavage of HA Clara (mucus), extracellular, serum, bacterial proteases HA0 HA1 HA2 binds receptor binds receptor penetrates cell
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Chemotherapy Prevent membrane fusion –Amantidine (Symmetrel) –Remantidine (Flumadine) Neuraminidase inhibitors –Zanamivir (Relenza) –Oseltamivir (Tamiflu)
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Epidemiology of influenza ?
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How do flu viruses change? virus polymerase makes mistakes selection of antigenic and host variants viruses re-assort
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How changes have led to human pandemics 1918 1957 1968 2009 avian H1N1 virus adapts to humans reassortment H2, N2, PB1 from duck rest from human H1N1 H3, PB1 from duck rest from human H2N2 H2N2 H3N2 swine human avian H1N1
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Factors that sustain epizootics/epidemics Antigenic drift Reassortment and antigenic shift Short term immunity Cross species transfer
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Introduction of influenza to horses Before 1950s –A/eq/Prague/1/56(H7N7) 1963 - from birds? –A/eq/Miami/1/63(H3N8) persists today (“Eurasian” “American strains”) 1989 - from birds –A/eq/Jilin/1/89(H3N8) –epizootoics in 1989,90 –none since Extinguished World-wide, except New Zealand, Iceland Extinguished, central Asia ? dogs 2004
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Pathogenesis inhalation (infected animal or fomites) replication in epithelial cells upper RT
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Clinical signs Sudden onset Fever (39-42), biphasic Dry cough Nasal discharge (serous ->mucopurulent)
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Risk factors Current specific antibody levels Time since last vaccination Age Sex
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Other pathogens that cause similar signs influenza equine herpesvirus 1, 4 S. equi equine viral arteritis
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Diagnosis Clinical signs Virus isolation Directagen Flu-A Serological tests –HAI –Single radial haemolysis
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Vaccines Inactivated, H7N7 and H3N8 isolates –Adjuvant –Most -> short lived protection Revaccinate at 6 week intervals Intranasal, cold-adapted Vectored (Recombitek)
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Swine influenza H1N1 - two variants H3N2 Ontario (1989-92) –53% H1N1 –17% H3N2 (similar to human virus) –4% H1N2 (similar to human virus)
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WHO update http://www.who.int/csr/don/2009_09_04/en/index.ht ml
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Avian influenza Highly Pathogenic Avian Influenza (to date H5, H7) –Pennsylvania - 1983 - $65,000,000 –Mexico - 1993-4 - $$? –B.C. 2004 –Saskatchewan 2007 (H7N3) http://www.inspection.gc.ca/english/anima/heasan/disemala/av flu/2007sask/repsaske.shtml Asymptomatic to fatal (HPAI)
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HA cleavage and virulence May ‘94 -> June ‘94 Dec ‘94 -> Jan ‘95 P Q - - R E T R low cleavability low virulence P Q R K R K T R high cleavability high virulence systemic infection respiratory infection ?
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Cleavage of HA Clara (mucus), extracellular, serum, bacterial proteases HA0 HA1 HA2 binds receptor binds receptor penetrates cell
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The 2004 BC outbreak 17 million birds destroyed 1128 claims, 56 million dollars dispensed August 18, 2004 –surveillance indicates highly pathogenic influenza eliminated from BC flocks –all control measured eliminated
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Avian H5N1 disease in cats intra tracheal inoculation in-contact feeding infected chick control or H3N2 virus excretion by cats Kuiken et al. Oct 2004 Science 306:241
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HA and host specificity 2,3 2,6 2,3 2,6 avian gutpig resp. tracthuman resp. tract avian H1-H15 pig H1, H3 H1(1918)H2, H3 human Stevens. Science, March 19, 2004
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Why does avian H5N1spread inefficiently between humans Shinya et al. Nature March 22, 2006 nasal mucosa paranasal sinus bronchus resp. bronchiole alveolus
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Process for human influenza vaccines February meeting –Commonwealth Serum Labs (Australia) –CDC (USA) –Natl. Inst. For Medical Research (UK) –European Inst. For Biological Standardization (EU) –Food and Drug Admin. (USA)
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Process for human influenza vaccines March-April –Genetic and antigenic characterization of approved strains –Distribution by WHO to manufacturers –Production of seed stock –Tests for contaminants (bacteria, mycoplasma, viruses)
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Process for human influenza vaccines April-August –Vaccine production –License application made –Clinical trials (to be submitted before vaccination season)
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Process for human influenza vaccines August-September –Distribution begins
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Human flu vaccine composition for 2008 A/Brisbane/59/2007 (H1N1) A/Brisbane/2007 (H3N2) B/Florida/4/2006
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