Virulence and transmissibility of H1N2 influenza virus in ferrets imply the continuing threat of triple-reassortant swine viruses

Efficient worldwide swine surveillance for influenza A viruses is urgently needed; the emergence of a novel reassortant pandemic H1N1 (pH1N1) virus in 2009 demonstrated that swine can be the direct source of pandemic influenza and that the pandemic potential of viruses prevalent in swine populations...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 2012-09, Vol.109 (39), p.15900-15905
Hauptverfasser: Pascua, Philippe Noriel Q., Song, Min-Suk, Lee, Jun Han, Baek, Yun Hee, Kwon, Hyeok-il, Park, Su-Jin, Choi, Eun Hye, Lim, Gyo-Jin, Lee, Ok-Jun, Kim, Si-Wook, Kim, Chul-Joong, Sung, Moon Hee, Kim, Myung Hee, Yoon, Sun-Woo, Govorkova, Elena A., Webby, Richard J., Webster, Robert G., Choi, Young-Ki
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container_end_page 15905
container_issue 39
container_start_page 15900
container_title Proceedings of the National Academy of Sciences - PNAS
container_volume 109
creator Pascua, Philippe Noriel Q.
Song, Min-Suk
Lee, Jun Han
Baek, Yun Hee
Kwon, Hyeok-il
Park, Su-Jin
Choi, Eun Hye
Lim, Gyo-Jin
Lee, Ok-Jun
Kim, Si-Wook
Kim, Chul-Joong
Sung, Moon Hee
Kim, Myung Hee
Yoon, Sun-Woo
Govorkova, Elena A.
Webby, Richard J.
Webster, Robert G.
Choi, Young-Ki
description Efficient worldwide swine surveillance for influenza A viruses is urgently needed; the emergence of a novel reassortant pandemic H1N1 (pH1N1) virus in 2009 demonstrated that swine can be the direct source of pandemic influenza and that the pandemic potential of viruses prevalent in swine populations must be monitored. We used the ferret model to assess the pathogenicity and transmissibility of predominant Korean triple-reassortant swine (TRSw) H1N2 and H3N2 influenza viruses genetically related to North American strains. Although most of the TRSw viruses were moderately pathogenic, one [A/Swine/Korea/1204/2009; Sw/1204 (H1N2)] was virulent in ferrets, causing death within 10 d of inoculation, and was efficiently transmitted to naive contact ferrets via respiratory droplets. Although molecular analysis did not reveal known virulence markers, the Sw/1204 virus acquired mutations in hemagglutinin (HA) (Asp-225-Gly) and neuraminidase (NA) (Ser-315-Asn) proteins during the single ferret passage. The contact-Sw/1204 virus became more virulent in mice, replicated efficiently in vitro, extensively infected human lung tissues ex vivo, and maintained its ability to replicate and transmit in swine. Reverse-genetics studies further indicated that the HA₂₂₅G and NA₃₁₅N substitutions contributed substantially in altering virulence and transmissibility. These findings support the continuing threat of some field TRSw viruses to human and animal health, reviving concerns on the capacity of pigs to create future pandemic viruses. Apart from warranting continued and enhanced global surveillance, this study also provides evidence on the emerging roles of HA₂₂₅G and NA₃₁₅N as potential virulence markers in mammals.
doi_str_mv 10.1073/pnas.1205576109
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We used the ferret model to assess the pathogenicity and transmissibility of predominant Korean triple-reassortant swine (TRSw) H1N2 and H3N2 influenza viruses genetically related to North American strains. Although most of the TRSw viruses were moderately pathogenic, one [A/Swine/Korea/1204/2009; Sw/1204 (H1N2)] was virulent in ferrets, causing death within 10 d of inoculation, and was efficiently transmitted to naive contact ferrets via respiratory droplets. Although molecular analysis did not reveal known virulence markers, the Sw/1204 virus acquired mutations in hemagglutinin (HA) (Asp-225-Gly) and neuraminidase (NA) (Ser-315-Asn) proteins during the single ferret passage. The contact-Sw/1204 virus became more virulent in mice, replicated efficiently in vitro, extensively infected human lung tissues ex vivo, and maintained its ability to replicate and transmit in swine. Reverse-genetics studies further indicated that the HA₂₂₅G and NA₃₁₅N substitutions contributed substantially in altering virulence and transmissibility. These findings support the continuing threat of some field TRSw viruses to human and animal health, reviving concerns on the capacity of pigs to create future pandemic viruses. 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We used the ferret model to assess the pathogenicity and transmissibility of predominant Korean triple-reassortant swine (TRSw) H1N2 and H3N2 influenza viruses genetically related to North American strains. Although most of the TRSw viruses were moderately pathogenic, one [A/Swine/Korea/1204/2009; Sw/1204 (H1N2)] was virulent in ferrets, causing death within 10 d of inoculation, and was efficiently transmitted to naive contact ferrets via respiratory droplets. Although molecular analysis did not reveal known virulence markers, the Sw/1204 virus acquired mutations in hemagglutinin (HA) (Asp-225-Gly) and neuraminidase (NA) (Ser-315-Asn) proteins during the single ferret passage. The contact-Sw/1204 virus became more virulent in mice, replicated efficiently in vitro, extensively infected human lung tissues ex vivo, and maintained its ability to replicate and transmit in swine. Reverse-genetics studies further indicated that the HA₂₂₅G and NA₃₁₅N substitutions contributed substantially in altering virulence and transmissibility. These findings support the continuing threat of some field TRSw viruses to human and animal health, reviving concerns on the capacity of pigs to create future pandemic viruses. 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Song, Min-Suk ; Lee, Jun Han ; Baek, Yun Hee ; Kwon, Hyeok-il ; Park, Su-Jin ; Choi, Eun Hye ; Lim, Gyo-Jin ; Lee, Ok-Jun ; Kim, Si-Wook ; Kim, Chul-Joong ; Sung, Moon Hee ; Kim, Myung Hee ; Yoon, Sun-Woo ; Govorkova, Elena A. ; Webby, Richard J. ; Webster, Robert G. ; Choi, Young-Ki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c534t-b8ffb0771e2053c46e62fb6dd4c986f4aa4140024932b6f595b0d39b2474e0fd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Biological Sciences</topic><topic>Cell Line</topic><topic>Disease transmission</topic><topic>Dogs</topic><topic>Ferrets</topic><topic>Ferrets - virology</topic><topic>Gene expression</topic><topic>H3N2 subtype influenza A virus</topic><topic>Hemagglutinin Glycoproteins, Influenza Virus - genetics</topic><topic>Hemagglutinin Glycoproteins, Influenza Virus - metabolism</topic><topic>Humans</topic><topic>Influenza</topic><topic>Influenza A virus</topic><topic>Influenza A Virus, H1N2 Subtype - genetics</topic><topic>Influenza A Virus, H1N2 Subtype - metabolism</topic><topic>Influenza A Virus, H1N2 Subtype - pathogenicity</topic><topic>Lungs</topic><topic>Mice</topic><topic>Molecular structure</topic><topic>Mutation</topic><topic>Orthomyxoviridae</topic><topic>Orthomyxoviridae Infections - genetics</topic><topic>Orthomyxoviridae Infections - transmission</topic><topic>Orthomyxoviridae Infections - veterinary</topic><topic>Pandemics</topic><topic>Proteins</topic><topic>Swine</topic><topic>Swine - virology</topic><topic>Swine Diseases</topic><topic>Swine flu</topic><topic>Virulence</topic><topic>Virulence Factors - genetics</topic><topic>Virulence Factors - metabolism</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pascua, Philippe Noriel Q.</creatorcontrib><creatorcontrib>Song, Min-Suk</creatorcontrib><creatorcontrib>Lee, Jun Han</creatorcontrib><creatorcontrib>Baek, Yun Hee</creatorcontrib><creatorcontrib>Kwon, Hyeok-il</creatorcontrib><creatorcontrib>Park, Su-Jin</creatorcontrib><creatorcontrib>Choi, Eun Hye</creatorcontrib><creatorcontrib>Lim, Gyo-Jin</creatorcontrib><creatorcontrib>Lee, Ok-Jun</creatorcontrib><creatorcontrib>Kim, Si-Wook</creatorcontrib><creatorcontrib>Kim, Chul-Joong</creatorcontrib><creatorcontrib>Sung, Moon Hee</creatorcontrib><creatorcontrib>Kim, Myung Hee</creatorcontrib><creatorcontrib>Yoon, Sun-Woo</creatorcontrib><creatorcontrib>Govorkova, Elena A.</creatorcontrib><creatorcontrib>Webby, Richard J.</creatorcontrib><creatorcontrib>Webster, Robert G.</creatorcontrib><creatorcontrib>Choi, Young-Ki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; 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the emergence of a novel reassortant pandemic H1N1 (pH1N1) virus in 2009 demonstrated that swine can be the direct source of pandemic influenza and that the pandemic potential of viruses prevalent in swine populations must be monitored. We used the ferret model to assess the pathogenicity and transmissibility of predominant Korean triple-reassortant swine (TRSw) H1N2 and H3N2 influenza viruses genetically related to North American strains. Although most of the TRSw viruses were moderately pathogenic, one [A/Swine/Korea/1204/2009; Sw/1204 (H1N2)] was virulent in ferrets, causing death within 10 d of inoculation, and was efficiently transmitted to naive contact ferrets via respiratory droplets. Although molecular analysis did not reveal known virulence markers, the Sw/1204 virus acquired mutations in hemagglutinin (HA) (Asp-225-Gly) and neuraminidase (NA) (Ser-315-Asn) proteins during the single ferret passage. The contact-Sw/1204 virus became more virulent in mice, replicated efficiently in vitro, extensively infected human lung tissues ex vivo, and maintained its ability to replicate and transmit in swine. Reverse-genetics studies further indicated that the HA₂₂₅G and NA₃₁₅N substitutions contributed substantially in altering virulence and transmissibility. These findings support the continuing threat of some field TRSw viruses to human and animal health, reviving concerns on the capacity of pigs to create future pandemic viruses. Apart from warranting continued and enhanced global surveillance, this study also provides evidence on the emerging roles of HA₂₂₅G and NA₃₁₅N as potential virulence markers in mammals.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>23019374</pmid><doi>10.1073/pnas.1205576109</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; JSTOR Archive Collection A-Z Listing; PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry
subjects Animals
Biological Sciences
Cell Line
Disease transmission
Dogs
Ferrets
Ferrets - virology
Gene expression
H3N2 subtype influenza A virus
Hemagglutinin Glycoproteins, Influenza Virus - genetics
Hemagglutinin Glycoproteins, Influenza Virus - metabolism
Humans
Influenza
Influenza A virus
Influenza A Virus, H1N2 Subtype - genetics
Influenza A Virus, H1N2 Subtype - metabolism
Influenza A Virus, H1N2 Subtype - pathogenicity
Lungs
Mice
Molecular structure
Mutation
Orthomyxoviridae
Orthomyxoviridae Infections - genetics
Orthomyxoviridae Infections - transmission
Orthomyxoviridae Infections - veterinary
Pandemics
Proteins
Swine
Swine - virology
Swine Diseases
Swine flu
Virulence
Virulence Factors - genetics
Virulence Factors - metabolism
Viruses
title Virulence and transmissibility of H1N2 influenza virus in ferrets imply the continuing threat of triple-reassortant swine viruses
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