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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Mammalian-adaptive mutation NP-Q357K in Eurasian H1N1 Swine Influenza viruses determines the virulence phenotype in mice</title><author><name sortKey="Zhu, Wenfei" sort="Zhu, Wenfei" uniqKey="Zhu W" first="Wenfei" last="Zhu">Wenfei Zhu</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Feng, Zhaomin" sort="Feng, Zhaomin" uniqKey="Feng Z" first="Zhaomin" last="Feng">Zhaomin Feng</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Chen, Yongkun" sort="Chen, Yongkun" uniqKey="Chen Y" first="Yongkun" last="Chen">Yongkun Chen</name><affiliation><nlm:aff id="AF3"><institution>School of Public Health (Shenzhen), Sun Yat-sen University</institution>, Guangdong,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Yang, Lei" sort="Yang, Lei" uniqKey="Yang L" first="Lei" last="Yang">Lei Yang</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Liu, Jia" sort="Liu, Jia" uniqKey="Liu J" first="Jia" last="Liu">Jia Liu</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Li, Xiyan" sort="Li, Xiyan" uniqKey="Li X" first="Xiyan" last="Li">Xiyan Li</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Liu, Suli" sort="Liu, Suli" uniqKey="Liu S" first="Suli" last="Liu">Suli Liu</name><affiliation><nlm:aff id="AF3"><institution>School of Public Health (Shenzhen), Sun Yat-sen University</institution>, Guangdong,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Zhou, Lijuan" sort="Zhou, Lijuan" uniqKey="Zhou L" first="Lijuan" last="Zhou">Lijuan Zhou</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Wei, Hejiang" sort="Wei, Hejiang" uniqKey="Wei H" first="Hejiang" last="Wei">Hejiang Wei</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Gao, Rongbao" sort="Gao, Rongbao" uniqKey="Gao R" first="Rongbao" last="Gao">Rongbao Gao</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Wang, Dayan" sort="Wang, Dayan" uniqKey="Wang D" first="Dayan" last="Wang">Dayan Wang</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Shu, Yuelong" sort="Shu, Yuelong" uniqKey="Shu Y" first="Yuelong" last="Shu">Yuelong Shu</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF3"><institution>School of Public Health (Shenzhen), Sun Yat-sen University</institution>, Guangdong,<country>People’s Republic of China</country></nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">31267843</idno><idno type="pmc">6609330</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609330</idno><idno type="RBID">PMC:6609330</idno><idno type="doi">10.1080/22221751.2019.1635873</idno><date when="2019">2019</date><idno type="wicri:Area/Pmc/Corpus">000953</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000953</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Mammalian-adaptive mutation NP-Q357K in Eurasian H1N1 Swine Influenza viruses determines the virulence phenotype in mice</title><author><name sortKey="Zhu, Wenfei" sort="Zhu, Wenfei" uniqKey="Zhu W" first="Wenfei" last="Zhu">Wenfei Zhu</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Feng, Zhaomin" sort="Feng, Zhaomin" uniqKey="Feng Z" first="Zhaomin" last="Feng">Zhaomin Feng</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Chen, Yongkun" sort="Chen, Yongkun" uniqKey="Chen Y" first="Yongkun" last="Chen">Yongkun Chen</name><affiliation><nlm:aff id="AF3"><institution>School of Public Health (Shenzhen), Sun Yat-sen University</institution>, Guangdong,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Yang, Lei" sort="Yang, Lei" uniqKey="Yang L" first="Lei" last="Yang">Lei Yang</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Liu, Jia" sort="Liu, Jia" uniqKey="Liu J" first="Jia" last="Liu">Jia Liu</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Li, Xiyan" sort="Li, Xiyan" uniqKey="Li X" first="Xiyan" last="Li">Xiyan Li</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Liu, Suli" sort="Liu, Suli" uniqKey="Liu S" first="Suli" last="Liu">Suli Liu</name><affiliation><nlm:aff id="AF3"><institution>School of Public Health (Shenzhen), Sun Yat-sen University</institution>, Guangdong,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Zhou, Lijuan" sort="Zhou, Lijuan" uniqKey="Zhou L" first="Lijuan" last="Zhou">Lijuan Zhou</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Wei, Hejiang" sort="Wei, Hejiang" uniqKey="Wei H" first="Hejiang" last="Wei">Hejiang Wei</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Gao, Rongbao" sort="Gao, Rongbao" uniqKey="Gao R" first="Rongbao" last="Gao">Rongbao Gao</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Wang, Dayan" sort="Wang, Dayan" uniqKey="Wang D" first="Dayan" last="Wang">Dayan Wang</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation></author><author><name sortKey="Shu, Yuelong" sort="Shu, Yuelong" uniqKey="Shu Y" first="Yuelong" last="Shu">Yuelong Shu</name><affiliation><nlm:aff id="AF1"><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF2"><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></nlm:aff></affiliation><affiliation><nlm:aff id="AF3"><institution>School of Public Health (Shenzhen), Sun Yat-sen University</institution>, Guangdong,<country>People’s Republic of China</country></nlm:aff></affiliation></author></analytic><series><title level="j">Emerging Microbes & Infections</title><idno type="eISSN">2222-1751</idno><imprint><date when="2019">2019</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><title>ABSTRACT</title><p>It has recently been proposed that the Eurasian avian-like H1N1 (EA H1N1) swine influenza virus (SIV) is one of the most likely zoonotic viruses to cause the next influenza pandemic. Two main genotypes EA H1N1 viruses have been recognized to be infected humans in China. Our study finds that one of the genotypes JS1-like viruses are avirulent in mice. However, the other are HuN-like viruses and are virulent in mice. The molecular mechanism underlying this difference shows that the NP gene determines the virulence of the EA H1N1 viruses in mice. In addition, a single substitution, Q357K, in the NP protein of the EA H1N1 viruses alters the virulence phenotype. This substitution is a typical human signature marker, which is prevalent in human viruses but rarely detected in avian influenza viruses. The NP-Q357K substitution is readily to be occurred when avian influenza viruses circulate in pigs, and may facilitate their infection of humans and allow viruses also carrying NP-357K to circulate in humans. Our study demonstrates that the substitution Q357K in the NP protein plays a key role in the virulence phenotype of EA H1N1 SIVs, and provides important information for evaluating the pandemic risk of field influenza strains.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Castrucci, Mr" uniqKey="Castrucci M">MR Castrucci</name></author><author><name sortKey="Donatelli, I" uniqKey="Donatelli I">I Donatelli</name></author><author><name sortKey="Sidoli, L" uniqKey="Sidoli L">L Sidoli</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Ma, W" uniqKey="Ma W">W Ma</name></author><author><name sortKey="Kahn, Re" uniqKey="Kahn R">RE Kahn</name></author><author><name sortKey="Richt, Ja" uniqKey="Richt J">JA. 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<front><journal-meta><journal-id journal-id-type="nlm-ta">Emerg Microbes Infect</journal-id><journal-id journal-id-type="iso-abbrev">Emerg Microbes Infect</journal-id><journal-id journal-id-type="publisher-id">TEMI</journal-id><journal-id journal-id-type="publisher-id">temi20</journal-id><journal-title-group><journal-title>Emerging Microbes & Infections</journal-title></journal-title-group><issn pub-type="epub">2222-1751</issn><publisher><publisher-name>Taylor & Francis</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">31267843</article-id><article-id pub-id-type="pmc">6609330</article-id><article-id pub-id-type="publisher-id">1635873</article-id><article-id pub-id-type="doi">10.1080/22221751.2019.1635873</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Mammalian-adaptive mutation NP-Q357K in Eurasian H1N1 Swine Influenza viruses determines the virulence phenotype in mice</article-title><alt-title alt-title-type="running-title">Emerging Microbes & Infections</alt-title><alt-title alt-title-type="running-authors">W. Zhu et al.</alt-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Zhu</surname><given-names>Wenfei</given-names></name><xref ref-type="aff" rid="AF1"><sup>a</sup></xref><xref ref-type="aff" rid="AF2"><sup>b</sup></xref><xref ref-type="author-notes" rid="AN1"><sup>*</sup></xref></contrib><contrib contrib-type="author"><name><surname>Feng</surname><given-names>Zhaomin</given-names></name><xref ref-type="aff" rid="AF1"><sup>a</sup></xref><xref ref-type="aff" rid="AF2"><sup>b</sup></xref><xref ref-type="author-notes" rid="AN1"><sup>*</sup></xref></contrib><contrib contrib-type="author"><name><surname>Chen</surname><given-names>Yongkun</given-names></name><xref ref-type="aff" rid="AF3"><sup>c</sup></xref><xref ref-type="author-notes" rid="AN1"><sup>*</sup></xref></contrib><contrib contrib-type="author"><name><surname>Yang</surname><given-names>Lei</given-names></name><xref ref-type="aff" rid="AF1"><sup>a</sup></xref><xref ref-type="aff" rid="AF2"><sup>b</sup></xref><xref ref-type="author-notes" rid="AN1"><sup>*</sup></xref></contrib><contrib contrib-type="author"><name><surname>Liu</surname><given-names>Jia</given-names></name><xref ref-type="aff" rid="AF1"><sup>a</sup></xref><xref ref-type="aff" rid="AF2"><sup>b</sup></xref></contrib><contrib contrib-type="author"><name><surname>Li</surname><given-names>Xiyan</given-names></name><xref ref-type="aff" rid="AF1"><sup>a</sup></xref><xref ref-type="aff" rid="AF2"><sup>b</sup></xref></contrib><contrib contrib-type="author"><name><surname>Liu</surname><given-names>Suli</given-names></name><xref ref-type="aff" rid="AF3"><sup>c</sup></xref></contrib><contrib contrib-type="author"><name><surname>Zhou</surname><given-names>Lijuan</given-names></name><xref ref-type="aff" rid="AF1"><sup>a</sup></xref><xref ref-type="aff" rid="AF2"><sup>b</sup></xref></contrib><contrib contrib-type="author"><name><surname>Wei</surname><given-names>Hejiang</given-names></name><xref ref-type="aff" rid="AF1"><sup>a</sup></xref><xref ref-type="aff" rid="AF2"><sup>b</sup></xref></contrib><contrib contrib-type="author"><name><surname>Gao</surname><given-names>Rongbao</given-names></name><xref ref-type="aff" rid="AF1"><sup>a</sup></xref><xref ref-type="aff" rid="AF2"><sup>b</sup></xref></contrib><contrib contrib-type="author"><name><surname>Wang</surname><given-names>Dayan</given-names></name><xref ref-type="aff" rid="AF1"><sup>a</sup></xref><xref ref-type="aff" rid="AF2"><sup>b</sup></xref><xref ref-type="corresp" rid="cor1"><sup>CONTACT</sup></xref></contrib><contrib contrib-type="author"><name><surname>Shu</surname><given-names>Yuelong</given-names></name><xref ref-type="aff" rid="AF1"><sup>a</sup></xref><xref ref-type="aff" rid="AF2"><sup>b</sup></xref><xref ref-type="aff" rid="AF3"><sup>c</sup></xref><xref ref-type="corresp" rid="cor2"></xref></contrib><aff id="AF1"><label>a</label><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing,<country>People’s Republic of China</country></aff><aff id="AF2"><label>b</label><institution>Key Laboratory for Medical Virology, National Health and Family Planning Commission</institution>, Beijing,<country>People’s Republic of China</country></aff><aff id="AF3"><label>c</label><institution>School of Public Health (Shenzhen), Sun Yat-sen University</institution>, Guangdong,<country>People’s Republic of China</country></aff></contrib-group><author-notes><corresp id="cor1"><label>CONTACT</label> Dayan Wang <email xlink:href="dayanwang@cnic.org.cn">dayanwang@cnic.org.cn</email><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing102206, <country>People’s Republic of China</country></corresp><corresp id="cor2">Yuelong Shu <email xlink:href="shuylong@mail.sysu.edu.cn">shuylong@mail.sysu.edu.cn</email><institution>National Institute for Viral Disease Control and Prevention, Collaboration Innovation Center for Diagnosis and Treatment of Infectious Diseases, Chinese Center for Disease Control and Prevention</institution>, Beijing102206, <country>People’s Republic of China</country></corresp><fn id="AN1"><label>*</label><p>These authors contributed equally to this work.</p></fn></author-notes><pub-date pub-type="collection"><year>2019</year></pub-date><pub-date pub-type="epub"><day>03</day><month>7</month><year>2019</year></pub-date><volume>8</volume><issue>1</issue><fpage seq="96">989</fpage><lpage>999</lpage><history><date date-type="received"><day>14</day><month>4</month><year>2019</year></date><date date-type="rev-recd"><day>13</day><month>6</month><year>2019</year></date><date date-type="accepted"><day>16</day><month>6</month><year>2019</year></date></history><permissions><copyright-statement>© 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd</copyright-statement><copyright-year>2019</copyright-year><copyright-holder>The Author(s)</copyright-holder><license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/"><license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0/">http://creativecommons.org/licenses/by/4.0/</ext-link>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p></license></permissions><self-uri content-type="pdf" xlink:href="temi-8-1635873.pdf"></self-uri><abstract><title>ABSTRACT</title><p>It has recently been proposed that the Eurasian avian-like H1N1 (EA H1N1) swine influenza virus (SIV) is one of the most likely zoonotic viruses to cause the next influenza pandemic. Two main genotypes EA H1N1 viruses have been recognized to be infected humans in China. Our study finds that one of the genotypes JS1-like viruses are avirulent in mice. However, the other are HuN-like viruses and are virulent in mice. The molecular mechanism underlying this difference shows that the NP gene determines the virulence of the EA H1N1 viruses in mice. In addition, a single substitution, Q357K, in the NP protein of the EA H1N1 viruses alters the virulence phenotype. This substitution is a typical human signature marker, which is prevalent in human viruses but rarely detected in avian influenza viruses. The NP-Q357K substitution is readily to be occurred when avian influenza viruses circulate in pigs, and may facilitate their infection of humans and allow viruses also carrying NP-357K to circulate in humans. Our study demonstrates that the substitution Q357K in the NP protein plays a key role in the virulence phenotype of EA H1N1 SIVs, and provides important information for evaluating the pandemic risk of field influenza strains.</p></abstract><kwd-group kwd-group-type="author"><title>KEYWORDS</title><kwd>Eurasian avian-like H1N1 swine influenza viruses</kwd><kwd>NP gene</kwd><kwd>NP-K357Q</kwd><kwd>pathogenicity</kwd><kwd>pandemic potential</kwd></kwd-group><funding-group><award-group><funding-source><named-content content-type="funder-name">National Key R& D Program of China</named-content></funding-source><award-id>2016YFC1200200</award-id><award-id>2016YFD0500208</award-id></award-group><award-group><funding-source><named-content content-type="funder-name">National Science and Technology Major Project of the Ministry of Science and Technology of China</named-content></funding-source><award-id>2017ZX10304402-001-019</award-id></award-group><award-group><funding-source><named-content content-type="funder-name">National Natural Science Foundation of China</named-content><named-content content-type="funder-identifier">10.13039/501100001809</named-content></funding-source><award-id>81601758</award-id><award-id>81525017</award-id><award-id>31761133003</award-id></award-group><funding-statement>This study was supported by the National Natural Science Foundation of China (81601758 and to WFZ), National Key R&D Program of China (2016YFC1200200 to YLS and 2016YFD0500208 to DYW), National Natural Science Foundation of China (81525017 to YLS), National Natural Science Foundation of China (31761133003), and National Science and Technology Major Project of the Ministry of Science and Technology of China (2017ZX10304402-001-019 to RBG).</funding-statement></funding-group><counts><fig-count count="6"></fig-count><table-count count="1"></table-count><equation-count count="0"></equation-count><ref-count count="52"></ref-count><page-count count="11"></page-count></counts></article-meta></front><body><sec id="S001"><title>Introduction</title><p>Pigs are well-known “genetic mixing vessels” for human and avian influenza viruses [<xref rid="CIT0001" ref-type="bibr">1</xref>,<xref rid="CIT0002" ref-type="bibr">2</xref>]. Human and avian influenza viruses can readily infect pigs, since their respiratory tracts contain receptors for both human and avian influenza viruses. It has been suggested that the past four pandemic pathogens, including the 1918 H1N1, 1957 H2N2, 1968 H3N2, and 2009 pdmH1N1, were generated in pigs [<xref rid="CIT0003" ref-type="bibr">3</xref>]. Therefore, the surveillance and research on the viruses circulating in pig populations are very important in the preparedness and responses to the future influenza pandemics.</p><p>Three subtypes of influenza A viruses are currently circulating in pigs globally, the H1N1, H1N2, and H3N2 viruses [<xref rid="CIT0004" ref-type="bibr">4</xref>]. In China, distinct lineages of swine influenza viruses (SIVs), including triple reassortant H1N1 (TR H1N1), Eurasian avian-like H1N1 (EA H1N1), classical swine H1N1 (CS H1N1), and reassortant H3N2 (RA H3N2), are known to co-circulate in pigs [<xref rid="CIT0005" ref-type="bibr">5</xref>,<xref rid="CIT0006" ref-type="bibr">6</xref>]. Since 2005, the EA H1N1 viruses have become dominant [<xref rid="CIT0005" ref-type="bibr">5</xref>,<xref rid="CIT0006" ref-type="bibr">6</xref>]. After the 2009 pdmH1N1 pandemic viruses transmitted back into pigs, they have reassorted continuously with EA H1N1 viruses and generated a series of variants [<xref rid="CIT0006" ref-type="bibr">6–8</xref>]. After their long-term evolution, the EA H1N1 viruses in China have been reported to preferentially bind to human-type receptors, and some of the viruses tested were transmitted in ferrets by respiratory droplets. This suggests that among the influenza viruses currently circulating in animals, the EA H1N1 SIVs pose the greatest pandemic threat [<xref rid="CIT0006" ref-type="bibr">6</xref>].</p><p>Swine influenza viruses could sporadically cross the species barrier and infect humans after the exposure of humans to infected pigs [<xref rid="CIT0009" ref-type="bibr">9</xref>,<xref rid="CIT0010" ref-type="bibr">10</xref>]. In China, the first reported human case of EA H1N1 SIV (A/Jiangsu/1/2011, JS1) infection was detected in 2011 [<xref rid="CIT0011" ref-type="bibr">11</xref>]. Thereafter, six human cases of EA SIV infection were recorded, and another four viruses were isolated: A/Hebei-Yuhua/SWL1250/2012 (HB1) [<xref rid="CIT0012" ref-type="bibr">12</xref>], A/Hunan/42443/2015 (HuN)[<xref rid="CIT0013" ref-type="bibr">13</xref>], A/Yunnan-Longyang/SWL1982/2015 (YN1), and A/Yunnan-Wuhua/SWL1869/2015 (YN2). A full-genome analysis of these viruses showed that they can be divided into two main genotypes, represented by the JS1 and HuN viruses (Supplementary Figure 1). Full genome of JS1-like viruses (JS1 and HB1 viruses) all originated from EA SIVs [<xref rid="CIT0011" ref-type="bibr">11</xref>,<xref rid="CIT0012" ref-type="bibr">12</xref>], whereas the HuN-like viruses (HuN, YN1, and YN2 viruses) are reassortants of EA SIVs (HA, NA, and M genes), 2009 pdmH1N1 (PB2, PB1, PA, and NP genes), and CS H1N1 SIVs (NS gene) [<xref rid="CIT0013" ref-type="bibr">13</xref>].</p><p>Several viral genetic factors are reported to contribute to the transmissibility, virulence, and pandemic potential of the influenza A viruses, or to their ability to cross species barriers. The polymerase complex genes play a critical role in the replication and adaptation of avian influenza viruses. An H5N1 virus that derived its PA or NS gene from the 2009/H1N1 virus became transmissible to guinea pigs [<xref rid="CIT0014" ref-type="bibr">14</xref>]. Various mutations in the polymerase complex are also associated with increased virulence, including PB2-E158G [<xref rid="CIT0015" ref-type="bibr">15</xref>], A271T [<xref rid="CIT0016" ref-type="bibr">16</xref>], PB1-R198K [<xref rid="CIT0017" ref-type="bibr">17–19</xref>], PB1-F2-N66S [<xref rid="CIT0020" ref-type="bibr">20</xref>], PA-I127V [<xref rid="CIT0021" ref-type="bibr">21</xref>], and so on. Of these, the E627K and/or D701N mutations in the PB2 protein are critical in the mammalian adaptation of avian influenza viruses [<xref rid="CIT0022" ref-type="bibr">22</xref>,<xref rid="CIT0023" ref-type="bibr">23</xref>]. Avian viruses with lysine at position 627 in PB2 protein replicate efficiently in human cells [<xref rid="CIT0024" ref-type="bibr">24</xref>,<xref rid="CIT0025" ref-type="bibr">25</xref>] and display higher pathogenicity in mice [<xref rid="CIT0026" ref-type="bibr">26–29</xref>]. 701N in PB2 is involved in the increased lethality of the H5N1, H7N1, and H7N9 viruses in mice [<xref rid="CIT0029" ref-type="bibr">29–33</xref>]. Both of these PB2 mutations also contribute to the transmission of the H5N1 virus in guinea pigs [<xref rid="CIT0027" ref-type="bibr">27</xref>,<xref rid="CIT0034" ref-type="bibr">34–37</xref>].</p><p>In our previous study, we evaluated the replication and virulence of the JS1 and HuN viruses. The HuN viruses were more virulent than the JS1 viruses in a mouse model [<xref rid="CIT0013" ref-type="bibr">13</xref>]. However, the underlying mechanism was not clarified. In this study, we investigate the molecular mechanism underlying this difference in viral virulence.</p></sec><sec id="S002"><title>Materials and methods</title><sec id="S002-S2001"><title>Ethics statement</title><p>The mouse studies were conducted with the approval of the Ethics Committee of the National Institute for Viral Disease Control and Prevention, China CDC (20160226008). All experiments involving live viruses were performed in a biosecurity level 2 laboratory.</p></sec><sec id="S002-S2002"><title>Cells</title><p>Madin–Darby canine kidney cells (MDCK), human type II alveolar epithelial (A549) cells, human embryonic kidney cells (293T), and porcine kidney cells (PK15) were maintained in Dulbecco’s modified Eagle’s medium (DMEM; Invitrogen, Carlsbad, CA, USA) supplemented with 10% foetal bovine serum (FBS; Invitrogen), HEPES (10 mM; Invitrogen), penicillin (100 units/ml), and streptomycin (100 μg/ml; Invitrogen). Cells were incubated in a humidified atmosphere of 5% CO<sub>2</sub> at 37°C.</p></sec><sec id="S002-S2003"><title>Viruses and virus titration</title><p>The Eurasian avian H1N1 viruses, A/Jiangsu/1/2011 (JS1, H1N1) [<xref rid="CIT0011" ref-type="bibr">11</xref>], A/Hebei-Yuhua/SWL1250/2012 (HB1) [<xref rid="CIT0012" ref-type="bibr">12</xref>], A/Hunan/42443/2015 (HuN, H1N1) [<xref rid="CIT0013" ref-type="bibr">13</xref>], A/Yunnan-Longyang/SWL1982/2015 (YN1), and A/Yunnan-Wuhua/SWL1869/2015 (YN2), were isolated from patients during 2011–2015. The viruses were titrated in MDCK cells, and the median tissue culture infective dose (TCID<sub>50</sub>) was calculated with the Reed–Münch formula [<xref rid="CIT0038" ref-type="bibr">38</xref>].</p></sec><sec id="S002-S2004"><title>Plasmid construction and mutagenesis</title><p>All eight gene segments of the JS1 and HuN viruses were amplified with reverse transcription (RT)–PCR and cloned into the vRNA–mRNA bidirectional expression vector pHW2000, which was kindly provided by Professor Yi Guan, Hong Kong University. Mutations were introduced into the NP gene to generate the corresponding mutant segments. The presence of the introduced mutation and the absence of additional unwanted mutations were verified by sequencing.</p></sec><sec id="S002-S2005"><title>Virus rescue</title><p>All the reassortant and mutant viruses were rescued by the co-transfection of the eight reverse-genetic plasmids containing the double-stranded DNA (dsDNA) representing each gene segment into a monolayer of co-cultured 293T and MDCK cells. All the recombinant viruses were sequenced completely to ensure the absence of unwanted mutations.</p></sec><sec id="S002-S2006"><title>Polymerase activity assay</title><p>293T cells were co-transfected with a firefly RNP luciferase reporter plasmid, a <italic>Renilla</italic> luciferase expressing plasmid pRL-TK (as an internal control), and the RNP expression plasmids using SuperFect Transfection Reagent (Qiagen, Valencia, CA, USA), according to the manufacturer’s instructions. Mock transfections were performed using the two reporter constructs only. Luciferase activity was measured at 24 h after transfection, according to the Dual-Luciferase Reporter Assay kit protocol (Promega, Madison, WI, USA). The firefly RNP polymerase activity was normalized against the Renilla activity.</p></sec><sec id="S002-S2007"><title>Virus growth kinetics study</title><p>Confluent A549 and PK15 cells were infected with indicated recombinant viruses at the multiplicity of infection (MOI) of 0.001. The viral inoculums were removed after 1 h of adsorption and incubated at 37°C in infection medium. Supernatants were collected at 0, 12, 24, 36, 48, 60 and 72 h post infection, and viral titres were determined by TCID<sub>50</sub> in MDCK cells.</p></sec><sec id="S002-S2008"><title>Mouse experiments</title><p>In the mouse experiments, 8–10-week-old specific-pathogen-free female C57BL/6J mice (Vital River Laboratories, Beijing, China) were used. To compare viral pathogenicity, the mice (<italic>n</italic> = 5) were anaesthetized with 0.2 ml of pentobarbital sodium and intranasally inoculated with 10<sup>4</sup> or 10<sup>6</sup> TCID<sub>50</sub> of the indicated viruses in 50 μl volumes, or mock inoculated with phosphate-buffered saline (PBS). Body weights were measured daily. Mice that lost more than 30% of their original weight were euthanized for humane reasons.</p><p>To determine the morbidity and mortality in the mice, groups of mice (<italic>n</italic> = 5) were inoculated intranasally with the recombinant viruses at the indicated dose (10<sup>1</sup>∼10<sup>6</sup> TCID<sub>50</sub>) in 50 μl volumes, or inoculated with PBS as the controls. Their body weights were measured daily. At 14 days post inoculation (dpi), serum samples were collected from the surviving mice and treated with a receptor-destroying enzyme (Denka Seiken) for 18 h at 37°C, heat-inactivated at 56°C for 30 min, and then tested for hemagglutinin inhibiting (HI) antibody titres with 0.5% (vol/vol) chicken erythrocytes. Samples with HI titres of > 40 were considered as antibody positive.</p><p>To determine the viral replication in the infected mice, groups of mice were intranasally inoculated with 10<sup>5</sup> TCID<sub>50</sub> of the indicated viruses and three mice in each group were euthanized at 1, 4, and 7 dpi. Respiratory tissues, including the nasal turbinate, tracheal tissue, and lungs were collected and the viral titres were measured with a TCID<sub>50</sub> assay in MDCK cells.</p></sec><sec id="S002-S2009"><title>Phylogenetic analyses</title><p>To determine the distributions of amino acids at position 357 in the NP protein in field strains, a total of 31,614 NP amino acid sequences from the National Center for Biotechnology Information (NCBI) public database were downloaded and analysed. The sequences were first aligned with MAFFT v7.222 [<xref rid="CIT0039" ref-type="bibr">39</xref>] and simplified with the cd-hit-est model. A maximum likelihood (ML) tree was constructed with MEGA 7.0[<xref rid="CIT0040" ref-type="bibr">40</xref>]. The GTR substitution model assuming a gamma distribution (four gamma categories) and invariant sites was selected, and the initial tree was constructed automatically. A graphical view of the phylogenetic tree was generated with FigTree v1.4.3.</p></sec><sec id="S002-S2010"><title>Statistical analysis</title><p>All determinations were performed in triplicate and repeated three times. Data are expressed as means ± SD. Statistical significance was determined using non-parametric tests and the GraphPad Prism 6.0 software package (GraphPad Software Inc., San Diego, CA, USA). A <italic>P</italic>-value <.05 was deemed to indicate statistical significance.</p></sec></sec><sec id="S003"><title>Results</title><sec id="S003-S2001"><title>Different pathogenicity phenotypes of HuN-like and JS1-like EA SIVs in mice</title><p>To compare the pathogenicity of the HuN-like and JS1-like EA SIVs, we infected mice (<italic>n</italic> = 5 per group) with each EA SIV and monitored their survival and weight loss for 14 dpi. When infected with 10<sup>6</sup> TCID<sub>50</sub> viruses, all the mice infected with the HuN-like viruses, including HuN, YN1, and YN2, died during the observation period. When infected with 10<sup>4</sup> TCID<sub>50</sub> of the HuN-like viruses, all the mice survived, except when infected with the YN2 virus, which caused 40% (2/5 mice) mortality (<xref rid="F0001" ref-type="fig">Figure 1</xref>). In contrast, even when infected with the highest dose (10<sup>6</sup> TCID<sub>50</sub>) of JS1-like viruses, including the JS1 and HB1 viruses, the cohorts of mice showed 100% survival during 14 days post inoculation (<xref rid="F0001" ref-type="fig">Figure 1</xref>). These results suggest that these EA SIVs present different pathogenicity phenotypes in mice, and the HuN-like viruses show higher pathogenic to mice than the JS1-like viruses.
<fig id="F0001" orientation="portrait" position="float"><label>Figure 1.</label><caption><p>Survival rates of mice after inoculation with different viruses. Female C57BL/6J mice (8–10 weeks old) were inoculated intranasally with 50 μl of PBS containing 10<sup>4</sup> TCID<sub>50</sub> or 10<sup>6</sup> TCID<sub>50</sub> of virus A/Yunnan-Longyang/SWL1982/2015 (YN1), A/Yunnan-Wuhua/SWL1869/2015 (YN2), A/Hunan/42443/2015 (HuN), A/Jiangsu/1/2011 (JS1), or A/Hebei-Yuhua/SWL1250/2012 (HB1). Mouse bodyweights were measured daily. Mice that lost > 30% of their original bodyweight or died naturally were recorded as “dead.”</p></caption><alternatives><graphic specific-use="web-only" content-type="color" xlink:href="TEMI_A_1635873_F0001_OC"></graphic><graphic specific-use="print-only" content-type="black-white" xlink:href="TEMI_A_1635873_F0001_PB"></graphic></alternatives></fig></p></sec><sec id="S003-S2002"><title>NP gene critically determines the pathogenicity of EA SIVs</title><p>The gene cassettes of the HuN-like and JS1-like viruses differ in their internal genes (Supplementary Figure 1). To identify the genes of the HuN-like viruses responsible for their higher pathogenicity, we cloned all the gene segments of the HuN or JS1 viruses into ambisense expression plasmids and generated reassortant viruses of the HuN-WT (wild type), JS1-WT, and recombinant viruses, carrying seven segments of HuN and one segment of JS1 or seven segments of JS1 and one segment of HuN (virus nos 1–9 and 17–25, respectively, in Supplementary Table 1). Rescued viruses were inoculated into mice at indicated dosages. Both survival situation and body weight loss were recorded for 14 days.</p><p>Compared with the rgHuN-WT virus, the body weight loss in the inoculated mice was lowest in the mice infected with rgHuN-NP<sub>JS1,</sub> which carried the NP gene of JS1 and other genes of HuN (<xref rid="F0002" ref-type="fig">Figure 2</xref>(A,C)), although the HuN viruses carrying either segment from the JS1 virus caused more or less effect on the bodyweight loss in the mice. On the other hand, although all the mice infected with 10<sup>4</sup> TCID<sub>50</sub> of the recombinant viruses survived (<xref rid="F0002" ref-type="fig">Figure 2</xref>(D)), this was not the case when the mice were infected with 10<sup>6</sup> TCID<sub>50</sub> of the recombinant viruses (<xref rid="F0002" ref-type="fig">Figure 2</xref>(B)). All the mice inoculated with the rgHuN-NP<sub>JS1</sub> virus survived, whereas all the mice infected with the other recombinant viruses died, like those infected with the rgHuN-WT virus (<xref rid="F0002" ref-type="fig">Figure 2</xref>(B)). Correspondingly, the NP gene of the HuN virus significantly increased the bodyweight loss and fatality rates caused by the JS1 viruses (Supplementary Figure 2(A–B)). All the mice survived when infected with wild-type (WT) JS1 viruses, whereas they all died when infected with the rgJS1-NP<sub>HuN</sub> virus carrying the NP gene from the HuN virus (Supplementary Figure 2(A–B)). These results demonstrate that the NP gene is the major determinant of the pathogenicity of the HuN-like viruses.
<fig id="F0002" orientation="portrait" position="float"><label>Figure 2.</label><caption><p>Weight changes and survival rates of mice infected with HuN reassortant viruses. The pathogenicity of reassortants was evaluated by inoculating groups of mice (<italic>n</italic> = 5 per group) with 10<sup>6</sup> TCID<sub>50</sub> (A, B) or 10<sup>4</sup> TCID<sub>50</sub> (C, D) of virus in 50 μl of PBS or with PBS only (control). Bodyweight loss (A, C) and death (B, D) were monitored during the 14-day observation period after inoculation. rgHuN-WT, rescued wild-type HuN virus; rgHuN-PB2<sub>JS1</sub>, rescued HuN virus carrying the PB2 gene from JS1 virus; rHuN-PB1<sub>JS1</sub>, rescued HuN virus carrying the PB1 gene from JS1 virus; rgHuN-PA<sub>JS1</sub>, rescued HuN virus carrying the PA gene from JS1 virus; rgHuN-NP<sub>JS1</sub>, rescued HuN virus carrying the NP gene from JS1 virus; rgHuN-HA<sub>JS1</sub>, rescued HuN virus carrying the HA gene from JS1 virus; rgHuN-NA<sub>JS1</sub>, rescued HuN virus carrying the NA gene from JS1 virus; rgHuN-M<sub>JS1</sub>, rescued HuN virus carrying the M gene from JS1 virus; rgHuN-NS<sub>JS1</sub>, rescued HuN virus carrying the NS gene from JS1 virus.</p></caption><alternatives><graphic specific-use="web-only" content-type="color" xlink:href="TEMI_A_1635873_F0002_OC"></graphic><graphic specific-use="print-only" content-type="black-white" xlink:href="TEMI_A_1635873_F0002_PB"></graphic></alternatives></fig></p></sec><sec id="S003-S2003"><title>Substitutions R305K, F313V, and Q357K in the NP protein are mammalian signatures for the influenza A viruses</title><p>To determine the contributions of individual amino acid substitutions in more detail, we compared the NP sequences of the JS1-like and HuN-like viruses. As shown in Supplementary Table 2, a total of 35 amino acid differences were detected. A statistical analysis of the 35 sites that differed between the human, swine, and avian viruses showed that three of them are mammalian signature residues, including 305K, 313V, and 357K. HuN-like viruses have the residues 305K, 313V, and 357K, while the JS1-like viruses have the residues 305R, 313F, and 357Q. According to Supplementary Table 3, 97.8%, 97.5%, and 97.6% of the human influenza viruses carried 305K, 313V/Y, and 357K in the NP protein, respectively. In contrast, 1%, 0.1%, and 0.4% of the avian influenza viruses carried these three residues, respectively. Approximately 98.9%, 99%, 99.5% of the avian viruses encoded the JS1-like resides, 305R, 313F, and 313Q, respectively.</p><p>To estimate the evolutionary selection and origins of these three amino acids in animals, we analysed the NP sequences of a variety of avian and mammalian influenza viruses deposited in the NCBI and Global Initiative on Sharing All Influenza Data (GISAID) databases. As shown in <xref rid="F0003" ref-type="fig">Figure 3</xref>, two major branches were detected, one corresponding to the American lineage and the other to the Eurasian lineage of viruses. The major subclade in the American lineage included the classical swine and human seasonal viruses, and a minor subclade in the American lineage included equine and avian influenza viruses. The Eurasian lineage included avian and avian-like swine influenza viruses.
<fig id="F0003" orientation="portrait" position="float"><label>Figure 3.</label><caption><p>Phylogenetic analysis of NP sequences of influenza A viruses and the prevalence of different amino acids at residues 305, 313, and 357. A maximum likelihood tree of NP sequences of influenza A viruses from different host species was constructed. Clusters were generally classified into Eurasian avian-like SIVs, avian influenza viruses, horse influenza viruses H3N8, human seasonal influenza viruses, 1918 H1N1 viruses, 2009 pdmH1N1 viruses, classical SIVs, and horse influenza virus H7N7 (shown from top to the bottom in <xref rid="F0003" ref-type="fig">Figure 3</xref>). Pie charts indicate the proportions of different amino acids at positions 305, 313, and 357 in the NP proteins in each cluster. Red triangles indicates JS1-like viruses. Red stars indicate HuN-like viruses.</p></caption><alternatives><graphic specific-use="web-only" content-type="color" xlink:href="TEMI_A_1635873_F0003_OC"></graphic><graphic specific-use="print-only" content-type="black-white" xlink:href="TEMI_A_1635873_F0003_PB"></graphic></alternatives></fig></p><p>According to <xref rid="F0003" ref-type="fig">Figure 3</xref>, the distributions of amino acids at residue 305 were lineage specific. Almost all the viruses in the Eurasian lineage contained 305R (99.9%∼100%), whereas almost all those in the American lineage contained 305K (99.9%∼100%). The distributions of amino acids at residues 313 and 357 were host specific. In the avian isolates in both lineages, 313F and 357Q were dominant (<xref rid="F0003" ref-type="fig">Figure 3</xref>). However, in the seasonal human isolates, including subtypes H1N1, H2N2, and H3N2 (<italic>n</italic> = 8991) and the 1918 H1N1 viruses (<italic>n</italic> = 1), amino acids 313Y and 357K occurred at very high frequencies (99.1%–100%). Most of the 2009 pdmH1N1 human isolates (<italic>n</italic> = 5782) contained 313V and 357K (<xref rid="F0003" ref-type="fig">Figure 3</xref>). Intriguingly, the amino acids at residues 313 and 357 of the avian or human influenza viruses were both detected in SIVs. Most SIVs contained 313F and 357K, whereas some classical SIVs and EA-SIVs contained 313V and 357Q. These results suggest that 305K, 313V/Y, and 357K confer advantages on the viruses circulating in humans, and may facilitate the enhanced pathogenicity of the HuN-like viruses in mice.</p></sec><sec id="S003-S2004"><title>Substitution at NP-357 determines the pathogenicity of EA SIVs</title><p>To further investigate the impact of NP-305K, – 313V, and/or – 357K on viral pathogenicity, recombinant viruses were generated (virus nos 10–16 and 26–32 in Supplementary Table 1). Bodyweight losses and survival rates were determined by inoculating mice with 10<sup>4</sup> or 10<sup>6</sup> TCID<sub>50</sub> of the recombinant viruses. When inoculated with 10<sup>6</sup> TCID<sub>50</sub> of the HuN-backbone viruses, body weight of all the mice were dramatically reduced (<xref rid="F0004" ref-type="fig">Figure 4</xref>(A)). Meanwhile, all mice were dead, except for 1/5 mice infected with rgHuN-NP<sub>K357Q</sub> (<xref rid="F0004" ref-type="fig">Figure 4</xref>(B)). When infected with 10<sup>4</sup> TCID<sub>50</sub> of recombinant virus, the mice infected with the wild-type HuN (rgHuN-WT) or rgHuN-NP<sub>K305R+V313F+K357Q</sub> virus showed a reduction in bodyweight of up to 20% by 9 dpi, and 4/5 mice survived the infection (80% survival rate; <xref rid="F0004" ref-type="fig">Figure 4</xref>(C–D)). All the rgHuN-NP<sub>K305R</sub>-, rgHuN-NP<sub>V313F</sub>-, rgHuN-NP<sub>K305R+V313F</sub>-, or rgHuN-NP<sub>V313F+K357Q</sub>-infected mice became severely ill, lost bodyweight from 2 dpi (> 30% from baseline), and eventually died or were humanly euthanized by 12 dpi (0% survival; <xref rid="F0004" ref-type="fig">Figure 4</xref>(C–D)). In contrast, the two cohorts of mice infected with rgHuN-NP<sub>K357Q</sub> or rgHuN-NP<sub>K305R+K357Q</sub> showed 100% survival for 14 dpi, a very modest bodyweight loss (< 10%), and few clinical symptoms (<xref rid="F0004" ref-type="fig">Figure 4</xref>(C–D)). Correspondingly, the mice infected with the wild-type JS1 virus showed no obvious bodyweight loss and no mice died during the whole observation period. However, the introduction of substitution Q357K into JS1 NP resulted in significant bodyweight loss and 4/5 fatalities in the mice (Supplementary Figure 2(C–D)). These results suggest that the mutation of NP-357 enhances the pathogenicity of EA viruses in mice.
<fig id="F0004" orientation="portrait" position="float"><label>Figure 4.</label><caption><p>The pathogenicity of HuN mutants in mice. Mice (<italic>n</italic> = 5 per group) were inoculated with 10<sup>6</sup> TCID<sub>50</sub> (A, B) or 10<sup>4</sup> TCID<sub>50</sub> (C, D) of HuN mutants. Body loss (A, C) and death (B, D) were monitored for the 14 days post-inoculation. rgHuN-WT, wild-type virus carrying NP-305K, – 313V, and – 357K; rgHuN-NP<sub>K305R</sub>, with NP-305R, – 313V, and – 357K; rgHuN-NP<sub>V313F</sub>, with NP-305K, – 313F, and – 357K; rgHuN-NP<sub>K357Q</sub>, with NP-305K, – 313V, and – 357Q; rgHuN-NP<sub>K305R+V313F</sub>, with NP-305R, – 313F, and – 357K; rgHuN-NP<sub>K305R+K357Q</sub>, with NP-305R, – 313V and – 357Q; rgHuN-NP<sub>V313F+K357Q</sub>, with NP-305K, – 313F and – 357Q; rgHuN-NP<sub>K305R+V313F+ K357Q</sub>, with NP-305R, – 313F and – 357Q.</p></caption><alternatives><graphic specific-use="web-only" content-type="color" xlink:href="TEMI_A_1635873_F0004_OC"></graphic><graphic specific-use="print-only" content-type="black-white" xlink:href="TEMI_A_1635873_F0004_PB"></graphic></alternatives></fig></p></sec><sec id="S003-S2005"><title>Substitution NP-K357Q decreases the infectivity, replication, and virulence of EA SIVs</title><p>To evaluate the contribution of substitution NP-Q357K to the virulence and infectivity of EA SIVs in mammals, the 50% mouse infective dose (MID<sub>50</sub>) and 50% mouse lethal dose (MLD<sub>5</sub>) were first determined.</p><p>When inoculated with 10<sup>1</sup>–10<sup>3</sup> TCID<sub>50</sub> of the recombinant rgHuN-WT or rgHuN<sub>K357Q</sub> virus, no mice died and the bodyweight loss was < 20% (<xref rid="F0005" ref-type="fig">Figure 5</xref>(A)). However, when infected with 10<sup>4</sup>–10<sup>6</sup> TCID<sub>50</sub> of virus, the bodyweight loss was dramatically greater in the mice infected with rgHuN-WT (357K in the NP protein) than in those infected with rgHuN<sub>K357Q</sub> (357Q in the NP protein) (<xref rid="F0005" ref-type="fig">Figure 5</xref>(A)). According to antibody tests, the MID<sub>50</sub> value of the rgHuN-WT virus was 10<sup>1.1</sup> TCID<sub>50</sub>, almost 20-fold lower than that of the rgHuN<sub>K357Q</sub> virus (10<sup>2.3</sup> TCID<sub>50</sub>) (<xref rid="T0001" ref-type="table">Table 1</xref>). This result indicated that the substitution NP-K357Q reduced the infectivity of the EA SIVs in mice.
<fig id="F0005" orientation="portrait" position="float"><label>Figure 5.</label><caption><p>Morbidity, mortality, replication, and polymerase activity assays of rgHuN-WT (357K) and rgHuN-NP<sub>K357Q</sub> (357Q) viruses in mice. Female C57BL/6J mice (8–10 weeks old) were inoculated intranasally with 50 μl of PBS containing 10<sup>1</sup> TCID<sub>50</sub>–10<sup>6</sup> TCID<sub>50</sub> of the recombinant virus rgHuN-WT or rgHuN-NP<sub>K357Q</sub>, or with PBS (mock), to evaluate virally induced morbidity (A) and mortality (B). Morbidity was assessed by bodyweight changes over a 14-day period and was graphed as a percentage of the average weight on the day of inoculation (day 0). The average bodyweight change in each group is shown with error bars representing the standard deviations (±). Mortality associated with infection with the recombinant virus rgHuN-WT (357K) or rgHuN-NP<sub>K357Q</sub> (357Q) was also examined. (C) Viral replication efficiency in the respiratory tracts of mice was analysed by inoculating mice (<italic>n</italic> = 3 per group per time point) intranasally with 10<sup>5</sup> TCID<sub>50</sub> of the recombinant viruses. At 1, 4, and 7 days postinoculation, three mice in each group were euthanized. Tissues, including nasal turbinate (NT), tracheal tissue (Tr), and lung (Lu), were collected for virus titration. (D) Polymerase assay was conducted in 293T cells transfected with reporter plasmids pFluc (encoding firefly luciferase flanked by the noncoding regions of the influenza NP segment to produce an artificial influenza-NP-like RNA segment), pRluc (pRL-TK, encoding <italic>Renilla</italic> luciferase, for normalization), and expression plasmids encoding PB2, PB1, PA, and NP. 357K, wild-type virus carrying NP-357K; 357Q, virus carrying NP-357Q. *<italic>p </italic>< .05; **<italic>p </italic>< .01.</p></caption><alternatives><graphic specific-use="web-only" content-type="color" xlink:href="TEMI_A_1635873_F0005_OC"></graphic><graphic specific-use="print-only" content-type="black-white" xlink:href="TEMI_A_1635873_F0005_PB"></graphic></alternatives></fig><table-wrap id="T0001" orientation="portrait" position="float"><label>Table 1</label><caption><title>Hemagglutinin inhibition antibody test of the C57BL/6 mice inoculated with recombinant rgHuN-WT or rgHuN-NP<sub>K357Q</sub> viruses.</title></caption><pmc-comment>OASIS TABLE HERE</pmc-comment><table frame="hsides" rules="groups"><colgroup><col width="1*"></col><col width="1*"></col><col width="1*"></col><col width="1*"></col><col width="1*"></col><col width="1*"></col><col width="1*"></col><col width="1*"></col></colgroup><thead valign="bottom"><tr><th rowspan="2" align="left">Inoculation viruses</th><th rowspan="2" align="center">Inoculation doses (log TCID<sub>50</sub>)</th><th colspan="5" align="center">HI titres</th><th rowspan="2" align="center">MID<sub>50</sub> (log TCID<sub>50</sub>)</th></tr><tr><th align="left">#1</th><th align="center">#2</th><th align="center">#3</th><th align="center">#4</th><th align="center">#5</th></tr></thead><tbody><tr><td rowspan="6" align="left"><bold>rgHuN-WT</bold></td><td align="left">6</td><td align="center">ND</td><td align="center">ND</td><td align="center">ND</td><td align="center">ND</td><td align="center">ND</td><td rowspan="6" align="char" char=".">1.1</td></tr><tr><td align="left">5</td><td align="center">ND</td><td align="center">ND</td><td align="center">ND</td><td align="center">ND</td><td align="center">ND</td></tr><tr><td align="left">4</td><td align="char" char=".">640</td><td align="char" char=".">640</td><td align="char" char=".">640</td><td align="char" char=".">640</td><td align="char" char=".">640</td></tr><tr><td align="left">3</td><td align="char" char=".">160</td><td align="char" char=".">640</td><td align="char" char=".">320</td><td align="char" char=".">320</td><td align="char" char=".">320</td></tr><tr><td align="left">2</td><td align="char" char=".">80</td><td align="char" char=".">640</td><td align="char" char=".">320</td><td align="char" char=".">80</td><td align="char" char=".">160</td></tr><tr><td align="left">1</td><td align="char" char=".">20</td><td align="char" char=".">80</td><td align="char" char=".">20</td><td align="char" char=".">160</td><td align="char" char=".">20</td></tr><tr><td rowspan="6" align="left"><bold>rgHuN-NP<sub>K357Q</sub></bold></td><td align="left">6</td><td align="center">ND</td><td align="center">ND</td><td align="center">ND</td><td align="center">ND</td><td align="center">ND</td><td rowspan="6" align="char" char=".">2.3</td></tr><tr><td align="left">5</td><td align="char" char=".">320</td><td align="char" char=".">640</td><td align="char" char=".">160</td><td align="char" char=".">320</td><td align="char" char=".">640</td></tr><tr><td align="left">4</td><td align="char" char=".">320</td><td align="char" char=".">640</td><td align="char" char=".">320</td><td align="char" char=".">640</td><td align="char" char=".">160</td></tr><tr><td align="left">3</td><td align="char" char=".">320</td><td align="char" char=".">160</td><td align="char" char=".">160</td><td align="char" char=".">80</td><td align="char" char=".">10</td></tr><tr><td align="left">2</td><td align="char" char=".">80</td><td align="char" char=".">10</td><td align="char" char=".">10</td><td align="char" char=".">20</td><td align="char" char=".">80</td></tr><tr><td align="left">1</td><td align="left"><10</td><td align="left"><10</td><td align="left"><10</td><td align="char" char=".">10</td><td align="char" char=".">20</td></tr><tr><td colspan="2" align="left"><bold>PBS</bold></td><td align="left"><10</td><td align="left"><10</td><td align="left"><10</td><td align="left"><10</td><td align="left"><10</td><td align="char" char="."> </td></tr></tbody></table><table-wrap-foot><p>Notes: Serum were collected from each survival mouse (#1 to #5, respectively) at 14 dpi, and were tested for heamagglutination inhibition (HI) titres against the A/Hunan/42443/2015 virus. Median infectious dose (MID50) was determined using the Karber Method [<xref rid="CIT0052" ref-type="bibr">52</xref>]. ND: Not determined due to death of the animal (treated as positive for determination of the MID50). HI titre < 40 was regarded as negative for seroconversion.</p></table-wrap-foot></table-wrap></p><p>As shown in <xref rid="F0005" ref-type="fig">Figure 5</xref>(B), the rgHuN<sub>K357Q</sub> group mice only died when inoculated with 10<sup>6</sup> TCID<sub>50</sub> virus. Therefore, the MLD<sub>50</sub> of the rgHuN<sub>K357Q</sub> virus was 10<sup>5.5</sup> TCID<sub>50</sub>. In the rgHuN-WT group, 5/5, 5/5, and 0/5 mice died when inoculated with 10<sup>6</sup>, 10<sup>5</sup>, and 10<sup>4</sup> TCID<sub>50</sub> virus, respectively, resulting in an MLD<sub>50</sub> value of 10<sup>4.5</sup> TCID<sub>50</sub>. Therefore, the substitution NP-K357Q reduced the virulence of the EA SIVs in mice.</p><p>To assess the contribution of the NP-Q357K substitution to the replication of EA SIVs in the respiratory tracts of mice, we inoculated mice with 10<sup>5</sup> TCID<sub>50</sub> of each virus and analysed the viral titres in the nasal turbinate, tracheal tissue, and lung at various times after inoculation (<xref rid="F0005" ref-type="fig">Figure 5</xref>(C)). The rgHuN viruses with or without the 357K residue in the NP protein both replicated efficiently in the respiratory tracts of the mice. However, the titre of the rgHuN<sub>K357Q</sub> virus was significantly lower than that of the rgHuN-WT virus in the tracheal tissues of mice at 1, 4, and 7 dpi, and lung tissues of mice at 1 and 4 dpi (<italic>p </italic>< .05, <xref rid="F0005" ref-type="fig">Figure 5</xref>(C)). These results indicate that NP-Q357K increases the viral replication of EA SIVs in mice.</p></sec><sec id="S003-S2006"><title>NP-357K viruses exhibited higher polymerase activity and viral growth titres than NP-357Q mutants in human cell lines</title><p>To understand whether Q357K substitution affect the viral polymerase activity or virus replications <italic>in vitro</italic>, we firstly performed polymerase activities assay. The result showed that the polymerase complex containing the NP-357K residue showed RNP activity 1.7-fold higher than that of the polymerase complex containing the NP-357Q residue (<xref rid="F0005" ref-type="fig">Figure 5</xref>(D)).</p><p>We then created two pairs of reverse genetic viruses containing either 357K or 357Q in NP protein in the HuN or JS1 backbone. Based on the growth kinetics in Supplementary Figure 3, back substitution to 357Q in the NP of HuN virus significantly decreased virus replication in human A549 cells (<italic>p </italic>< .05) but not in porcine PK15 cultures. Conversely, introduction of 357K into NP of the JS1 virus enhanced virus replication in human A549 cell lines (48-60 hpi), but this positive effect was not observed in porcine PK15 cells.</p></sec></sec><sec id="S004"><title>Discussion</title><p>EA SIV H1N1 viruses were reported to be the dominantly circulated viruses in pigs in China and have acquired the ability to infect human [<xref rid="CIT0006" ref-type="bibr">6</xref>]. Two genotypes of EA H1N1 SIVs have been detected in humans in China, with the HuN-like viruses displaying significantly higher virulence than the JS1-like viruses (<xref rid="F0001" ref-type="fig">Figure 1</xref>). Many viral genetic factors are reportedly associated with enhanced virulence, especially the polymerase genes [<xref rid="CIT0022" ref-type="bibr">22</xref>,<xref rid="CIT0023" ref-type="bibr">23</xref>]. In this study, we found that the NP gene is the major determinant of the virulence of EA H1N1 SIVs. Furthermore, when compared to that of rgHuN-WT, the occurrence of a single substitution V313F or K305R increased viral pathogenicity in mice, while K357Q obviously reduced the viral pathogenicity. Dual mutations K305R + V313F increased the fatality of the viruses. However, the introduction of the K305R into dual mutation K305R + V313F led to a similar degree of viral pathogenicity as rgHuN-WT (<xref rid="F0004" ref-type="fig">Figure 4</xref>). Thus, the NP-Q357K mutation in the EA SIVs is fully responsible for the enhanced pathogenicity phenotype, and enhanced the polymerase activity, replication, and infectivity of the viruses in mice.</p><p>NP primarily maintains the RNP conformation [<xref rid="CIT0041" ref-type="bibr">41</xref>,<xref rid="CIT0042" ref-type="bibr">42</xref>], interacting with PB1, PB2, and another NP protein, and plays a central role in the life cycles of the influenza viruses. NP molecules contain a head domain, a body domain, and a protruding tail loop [<xref rid="CIT0043" ref-type="bibr">43</xref>,<xref rid="CIT0044" ref-type="bibr">44</xref>]. A previous study found that the substitution of N319K in NP protein was located on the surface at the right-hand side of the nucleoprotein body domain and resulted in an increase of polymerase activity [<xref rid="CIT0045" ref-type="bibr">45</xref>]. NP-357 was located on RNA-binding groove [<xref rid="CIT0046" ref-type="bibr">46</xref>], which contained many basic amino acids and could mediate nucleoprotein–polymerase interactions that are crucial for viral RNA replication [<xref rid="CIT0047" ref-type="bibr">47</xref>,<xref rid="CIT0048" ref-type="bibr">48</xref>] (Supplementary Figure 4). The introduction of neutral amino acid Q to basic amino acid K substitution might increase the binding of NP proteins to RNAs, and may therefore induce the increased polymerase activity and replication properties (<xref rid="F0005" ref-type="fig">Figure 5</xref>(D)) of EA H1N1 viruses. The substitution of NP-Q357K could also enhance pathogenicity of avian H5N1 virus in mice [<xref rid="CIT0049" ref-type="bibr">49</xref>].</p><p>Q357K in the NP protein is also a typical mammalian-adaptive molecular marker in the influenza A viruses (<xref rid="F0003" ref-type="fig">Figure 3</xref> and Supplementary Table 3). Viruses circulating in birds and humans carry NP-357Q and NP-357K, respectively, whereas among the influenza A viruses circulating in pigs, the majority of CS H1N1 viruses contain NP-357K and most EA H1N1 viruses contain NP-357Q. EA SIVs with NP-357K replicated comparably to those with NP-357Q viruses in porcine cell, but exhibited significantly better growth advantages than NP-357Q viruses in human cell lines (Supplementary Figure 3). In addition, the human-like amino acid mutants NP-Q357K was reported to be likely required for transmission of the 1918 precursor virus to humans [<xref rid="CIT0050" ref-type="bibr">50</xref>,<xref rid="CIT0051" ref-type="bibr">51</xref>]. Therefore, the NP-Q357K substitution was already present when the avian influenza viruses circulated in pigs, allowing the viruses to infect humans. Viruses with NP-357K more readily circulate in humans than those with NP-357Q.</p><p>Taken together, our findings suggest that the mutation Q357K in NP is an adaptive signature of the influenza A viruses, allowing them to cross species barriers and altering the viral virulence phenotype in mice (<xref rid="F0006" ref-type="fig">Figure 6</xref>). NP-357Q is prevalent in avian viruses, and mutated to NP-357K in the swine population. Viruses with the NP-357K residue were successfully selected and crossed the species barrier to circulate in humans. The mutation of 357Q to 357K increases viral replication and induces a fatal infection in mice. Therefore, because EA H1N1 SIVs have acquired the trait necessary to cause a human influenza pandemic, EA SIVs with NP-Q357K pose a greater risk than those without NP-Q357K, and is a matter of great concern.
<fig id="F0006" orientation="portrait" position="float"><label>Figure 6.</label><caption><p>Conceptual model of the generalized inferred evolutionary pathways and virulence outcomes of NP-Q357K in influenza A viruses. Avian influenza viruses carrying NP-357Q were transmitted to pigs. The Q357K substitution was introduced into the NP protein during the adaptation of the avian influenza virus to swine. Mutants with NP-357K were selected, then transmitted to and circulated in humans. The Q357K substitution alters the viral phenotype in mice.</p></caption><alternatives><graphic specific-use="web-only" content-type="color" xlink:href="TEMI_A_1635873_F0006_OC"></graphic><graphic specific-use="print-only" content-type="black-white" xlink:href="TEMI_A_1635873_F0006_PB"></graphic></alternatives></fig></p></sec><sec sec-type="supplementary-material"><title>Supplementary Material</title><supplementary-material content-type="local-data" id="SM7113"><caption><title>Supplemental Material</title></caption><media mimetype="application" mime-subtype="zip" xlink:href="TEMI_A_1635873_SM7113.zip" orientation="portrait" id="d37e264" position="anchor"></media></supplementary-material></sec></body><back><sec><title>Acknowledgements</title><p>We were grateful to Dr Yang Cao, from College of Life Sciences, Sichuan University, for kindly improving the quality of our manuscript.</p></sec><sec id="S005"><title>Disclosure statement</title><p>No potential conflict of interest was reported by 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