Persistence of Q strain of H2N2 influenza virus in avian species: Antigenic, biological and genetic analysis of avian and human H2N2 viruses
Identifieur interne : 000049 ( Istex/Corpus ); précédent : 000048; suivant : 000050Persistence of Q strain of H2N2 influenza virus in avian species: Antigenic, biological and genetic analysis of avian and human H2N2 viruses
Auteurs : K. Nerome ; Y. Yoshioka ; C. A. Torres ; A. Oya ; P. Bachmann ; K. Ottis ; R. G. WebsterSource :
- Archives of Virology [ 0304-8608 ] ; 1984-09-01.
English descriptors
- Teeft :
- Antigenic, Antigenic analysis, Antigenic heterogeneity, Antigenic relationships, Antiserum, Asian influenza virus, Asian virus, Asian viruses, Avian, Avian influenza, Avian influenza viruses, Avian species, Avian virus, Avian viruses, Cent polyaerylamide, Culture fluids, Different antisera, Early asian viruses, Former virus, Genetic analysis, Genome analysis, Growth characteristics, Hemagglutinating activity, Hemagglutinin, Heterologous antibodies, High temperature, Human asian viruses, Human viruses, Hyperimmune sera, Influenza, Influenza virus, Influenza viruses, Inhibitor, Large oligonueleotides, Late asian viruses, Mdck, Mdck cells, Mdck monolayers, Mfinchen virus, Miinchen virus, Monoclonal antibodies, Monoelonal antibodies, Mtinchen, Mtinchen virus, National institute, Neuraminidase, Neuraminidase activity, Neuraminidase antigen, Neuraminidase antigens, Oligonucleotide mapping, Other hand, Phase variant, Plaque titration, Present study, Virus.
Abstract
Summary: The characteristics of an avian influenza virus were compared in detail with those of human Asian (H2N2) influenza viruses. Antigenic analysis by different antisera against H2N2 viruses and monoclonal antibodies to both the hemagglutinin and neuraminidase antigens showed that an avian isolate, A/duck/München/9/79 contained hemagglutinin and neuraminidase subunits closely related to those of the early human H2N2 viruses which had been prevalent in 1957. However, this avian virus gave low HI titers with absorbed and non-absorbed antisera to different human H2N2 viruses isolated in 1957. Like human Q phase variant, such as A/RI/5−/57 (H2N2), hemagglutination of the above avian strain was not inhibited by the purified non-specific γ-inhibitor from guinea pig serum. Growth behavior at restrictive temperature (42° C) clearly differentiate the avian H2N2 virus from human influenza viruses, showing that the former virus grew well in MDCK cells at 42° C but not the latters. Genomic analysis of these viruses revealed that the oligonucleotide map of H2N2 virus isolated from a duck was quite different from those of human H2N2 viruses from 1957 to 1967. The oligonucleotide mapping also indicated that different H2N2 influenza virus variants had co-circulated in humans in 1957.
Url:
DOI: 10.1007/BF01309996
Links to Exploration step
ISTEX:891FE6F2681838768A8765CFB958262F64A004CBLe document en format XML
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Antigenic analysis by different antisera against H2N2 viruses and monoclonal antibodies to both the hemagglutinin and neuraminidase antigens showed that an avian isolate, A/duck/München/9/79 contained hemagglutinin and neuraminidase subunits closely related to those of the early human H2N2 viruses which had been prevalent in 1957. However, this avian virus gave low HI titers with absorbed and non-absorbed antisera to different human H2N2 viruses isolated in 1957. Like human Q phase variant, such as A/RI/5−/57 (H2N2), hemagglutination of the above avian strain was not inhibited by the purified non-specific γ-inhibitor from guinea pig serum. Growth behavior at restrictive temperature (42° C) clearly differentiate the avian H2N2 virus from human influenza viruses, showing that the former virus grew well in MDCK cells at 42° C but not the latters. Genomic analysis of these viruses revealed that the oligonucleotide map of H2N2 virus isolated from a duck was quite different from those of human H2N2 viruses from 1957 to 1967. 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Nerome</name><affiliations><json:string>Department of Virology and Rickettsiology, National Institute of Health, Shinagawa-ku, Tokyo, Japan</json:string></affiliations></json:item><json:item><name>Y. Yoshioka</name><affiliations><json:string>Department of Virology and Rickettsiology, National Institute of Health, Shinagawa-ku, Tokyo, Japan</json:string></affiliations></json:item><json:item><name>C. A. Torres</name><affiliations><json:string>Department of Virology and Rickettsiology, National Institute of Health, Shinagawa-ku, Tokyo, Japan</json:string></affiliations></json:item><json:item><name>A. Oya</name><affiliations><json:string>Department of Virology and Rickettsiology, National Institute of Health, Shinagawa-ku, Tokyo, Japan</json:string></affiliations></json:item><json:item><name>P. Bachmann</name><affiliations><json:string>Institute for Medical Microbiology, Infectious, and Epidemic Medicine, Veterinary Faculty, University of Munich, Munich, Germany</json:string></affiliations></json:item><json:item><name>K. Ottis</name><affiliations><json:string>Institute for Medical Microbiology, Infectious, and Epidemic Medicine, Veterinary Faculty, University of Munich, Munich, Germany</json:string></affiliations></json:item><json:item><name>R. G. 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However, this avian virus gave low HI titers with absorbed and non-absorbed antisera to different human H2N2 viruses isolated in 1957. Like human Q phase variant, such as A/RI/5−/57 (H2N2), hemagglutination of the above avian strain was not inhibited by the purified non-specific γ-inhibitor from guinea pig serum. Growth behavior at restrictive temperature (42° C) clearly differentiate the avian H2N2 virus from human influenza viruses, showing that the former virus grew well in MDCK cells at 42° C but not the latters. Genomic analysis of these viruses revealed that the oligonucleotide map of H2N2 virus isolated from a duck was quite different from those of human H2N2 viruses from 1957 to 1967. The oligonucleotide mapping also indicated that different H2N2 influenza virus variants had co-circulated in humans in 1957.</abstract><qualityIndicators><score>9.117</score><pdfWordCount>4789</pdfWordCount><pdfCharCount>21882</pdfCharCount><pdfVersion>1.3</pdfVersion><pdfPageCount>12</pdfPageCount><pdfPageSize>476 x 677 pts</pdfPageSize><refBibsNative>false</refBibsNative><abstractWordCount>194</abstractWordCount><abstractCharCount>1292</abstractCharCount><keywordCount>0</keywordCount></qualityIndicators><title>Persistence of Q strain of H2N2 influenza virus in avian species: Antigenic, biological and genetic analysis of avian and human H2N2 viruses</title><pmid><json:string>6477129</json:string></pmid><genre><json:string>research-article</json:string></genre><host><title>Archives of 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Epidemic Medicine, Veterinary Faculty, University of Munich, Munich, Germany</affiliation></author><author xml:id="author-0005"><persName><forename type="first">K.</forename><surname>Ottis</surname></persName><affiliation>Institute for Medical Microbiology, Infectious, and Epidemic Medicine, Veterinary Faculty, University of Munich, Munich, Germany</affiliation></author><author xml:id="author-0006"><persName><forename type="first">R.</forename><surname>Webster</surname></persName><affiliation>St. Jude Children's Research Hospital, Memphis, Tennessee, USA</affiliation></author><idno type="istex">891FE6F2681838768A8765CFB958262F64A004CB</idno><idno type="ark">ark:/67375/1BB-J2X7FNJZ-W</idno><idno type="DOI">10.1007/BF01309996</idno><idno type="article-id">BF01309996</idno><idno type="article-id">Art5</idno></analytic><monogr><title level="j">Archives of Virology</title><title level="j" type="abbrev">Archives of Virology</title><idno type="pISSN">0304-8608</idno><idno type="eISSN">1432-8798</idno><idno type="journal-ID">true</idno><idno type="issue-article-count">19</idno><idno type="volume-issue-count">4</idno><imprint><publisher>Springer-Verlag</publisher><pubPlace>Vienna</pubPlace><date type="published" when="1984-09-01"></date><biblScope unit="volume">81</biblScope><biblScope unit="issue">3-4</biblScope><biblScope unit="page" from="239">239</biblScope><biblScope unit="page" to="250">250</biblScope></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1983-11-07</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>Summary: The characteristics of an avian influenza virus were compared in detail with those of human Asian (H2N2) influenza viruses. Antigenic analysis by different antisera against H2N2 viruses and monoclonal antibodies to both the hemagglutinin and neuraminidase antigens showed that an avian isolate, A/duck/München/9/79 contained hemagglutinin and neuraminidase subunits closely related to those of the early human H2N2 viruses which had been prevalent in 1957. However, this avian virus gave low HI titers with absorbed and non-absorbed antisera to different human H2N2 viruses isolated in 1957. Like human Q phase variant, such as A/RI/5−/57 (H2N2), hemagglutination of the above avian strain was not inhibited by the purified non-specific γ-inhibitor from guinea pig serum. Growth behavior at restrictive temperature (42° C) clearly differentiate the avian H2N2 virus from human influenza viruses, showing that the former virus grew well in MDCK cells at 42° C but not the latters. Genomic analysis of these viruses revealed that the oligonucleotide map of H2N2 virus isolated from a duck was quite different from those of human H2N2 viruses from 1957 to 1967. The oligonucleotide mapping also indicated that different H2N2 influenza virus variants had co-circulated in humans in 1957.</p></abstract><textClass><keywords scheme="Journal Subject"><list><head>Biomedicine</head><item><term>Medical Microbiology</term></item><item><term>Virology</term></item><item><term>Infectious Diseases</term></item></list></keywords></textClass></profileDesc><revisionDesc><change when="1983-11-07">Created</change><change when="1984-09-01">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/ark:/67375/1BB-J2X7FNJZ-W/fulltext.txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="corpus springer-journals not found" wicri:toSee="no header"><istex:xmlDeclaration>version="1.0" encoding="UTF-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//Springer-Verlag//DTD A++ V2.4//EN" 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TocLevels="0"><VolumeIDStart>81</VolumeIDStart><VolumeIDEnd>81</VolumeIDEnd><VolumeIssueCount>4</VolumeIssueCount></VolumeInfo><Issue IssueType="Combined"><IssueInfo TocLevels="0"><IssueIDStart>3</IssueIDStart><IssueIDEnd>4</IssueIDEnd><IssueArticleCount>19</IssueArticleCount><IssueHistory><CoverDate><DateString>1984</DateString><Year>1984</Year><Month>9</Month></CoverDate></IssueHistory><IssueCopyright><CopyrightHolderName>Springer-Verlag</CopyrightHolderName><CopyrightYear>1984</CopyrightYear></IssueCopyright></IssueInfo><Article ID="Art5"><ArticleInfo Language="En" ArticleType="OriginalPaper" NumberingStyle="Unnumbered" TocLevels="0" ContainsESM="No"><ArticleID>BF01309996</ArticleID><ArticleDOI>10.1007/BF01309996</ArticleDOI><ArticleSequenceNumber>5</ArticleSequenceNumber><ArticleTitle Language="En">Persistence of Q strain of H2N2 influenza virus in avian species: Antigenic, biological and genetic analysis of avian and human H2N2 viruses</ArticleTitle><ArticleCategory>Original Papers</ArticleCategory><ArticleFirstPage>239</ArticleFirstPage><ArticleLastPage>250</ArticleLastPage><ArticleHistory><RegistrationDate><Year>2005</Year><Month>2</Month><Day>28</Day></RegistrationDate><Received><Year>1983</Year><Month>11</Month><Day>7</Day></Received><Accepted><Year>1984</Year><Month>2</Month><Day>16</Day></Accepted></ArticleHistory><ArticleCopyright><CopyrightHolderName>Springer-Verlag</CopyrightHolderName><CopyrightYear>1984</CopyrightYear></ArticleCopyright><ArticleGrants Type="Regular"><MetadataGrant Grant="OpenAccess"></MetadataGrant><AbstractGrant Grant="OpenAccess"></AbstractGrant><BodyPDFGrant Grant="Restricted"></BodyPDFGrant><BodyHTMLGrant Grant="Restricted"></BodyHTMLGrant><BibliographyGrant Grant="Restricted"></BibliographyGrant><ESMGrant Grant="Restricted"></ESMGrant></ArticleGrants><ArticleContext><JournalID>705</JournalID><VolumeIDStart>81</VolumeIDStart><VolumeIDEnd>81</VolumeIDEnd><IssueIDStart>3</IssueIDStart><IssueIDEnd>4</IssueIDEnd></ArticleContext></ArticleInfo><ArticleHeader><AuthorGroup><Author AffiliationIDS="Aff1"><AuthorName DisplayOrder="Western"><GivenName>K.</GivenName><FamilyName>Nerome</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff1"><AuthorName DisplayOrder="Western"><GivenName>Y.</GivenName><FamilyName>Yoshioka</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff1"><AuthorName DisplayOrder="Western"><GivenName>C.</GivenName><GivenName>A.</GivenName><FamilyName>Torres</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff1"><AuthorName DisplayOrder="Western"><GivenName>A.</GivenName><FamilyName>Oya</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff2"><AuthorName DisplayOrder="Western"><GivenName>P.</GivenName><FamilyName>Bachmann</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff2"><AuthorName DisplayOrder="Western"><GivenName>K.</GivenName><FamilyName>Ottis</FamilyName></AuthorName></Author><Author AffiliationIDS="Aff3"><AuthorName DisplayOrder="Western"><GivenName>R.</GivenName><GivenName>G.</GivenName><FamilyName>Webster</FamilyName></AuthorName></Author><Affiliation ID="Aff1"><OrgDivision>Department of Virology and Rickettsiology</OrgDivision><OrgName>National Institute of Health</OrgName><OrgAddress><Street>Shinagawa-ku</Street><City>Tokyo</City><Country>Japan</Country></OrgAddress></Affiliation><Affiliation ID="Aff2"><OrgDivision>Institute for Medical Microbiology, Infectious, and Epidemic Medicine, Veterinary Faculty</OrgDivision><OrgName>University of Munich</OrgName><OrgAddress><City>Munich</City><Country>Germany</Country></OrgAddress></Affiliation><Affiliation ID="Aff3"><OrgName>St. Jude Children's Research Hospital</OrgName><OrgAddress><City>Memphis</City><State>Tennessee</State><Country>USA</Country></OrgAddress></Affiliation></AuthorGroup><Abstract ID="Abs1" Language="En"><Heading>Summary</Heading><Para>The characteristics of an avian influenza virus were compared in detail with those of human Asian (H2N2) influenza viruses. Antigenic analysis by different antisera against H2N2 viruses and monoclonal antibodies to both the hemagglutinin and neuraminidase antigens showed that an avian isolate, A/duck/München/9/79 contained hemagglutinin and neuraminidase subunits closely related to those of the early human H2N2 viruses which had been prevalent in 1957. However, this avian virus gave low HI titers with absorbed and non-absorbed antisera to different human H2N2 viruses isolated in 1957. Like human Q phase variant, such as A/RI/5<Superscript>−</Superscript>/57 (H2N2), hemagglutination of the above avian strain was not inhibited by the purified non-specific γ-inhibitor from guinea pig serum. Growth behavior at restrictive temperature (42° C) clearly differentiate the avian H2N2 virus from human influenza viruses, showing that the former virus grew well in MDCK cells at 42° C but not the latters. Genomic analysis of these viruses revealed that the oligonucleotide map of H2N2 virus isolated from a duck was quite different from those of human H2N2 viruses from 1957 to 1967. The oligonucleotide mapping also indicated that different H2N2 influenza virus variants had co-circulated in humans in 1957.</Para></Abstract><ArticleNote Type="Misc"><SimplePara>With 2 Figures</SimplePara></ArticleNote></ArticleHeader><NoBody></NoBody></Article></Issue></Volume></Journal></Publisher></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Persistence of Q strain of H2N2 influenza virus in avian species: Antigenic, biological and genetic analysis of avian and human H2N2 viruses</title></titleInfo><titleInfo type="alternative" contentType="CDATA"><title>Persistence of Q strain of H2N2 influenza virus in avian species: Antigenic, biological and genetic analysis of avian and human H2N2 viruses</title></titleInfo><name type="personal"><namePart type="given">K.</namePart><namePart type="family">Nerome</namePart><affiliation>Department of Virology and Rickettsiology, National Institute of Health, Shinagawa-ku, Tokyo, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Y.</namePart><namePart type="family">Yoshioka</namePart><affiliation>Department of Virology and Rickettsiology, National Institute of Health, Shinagawa-ku, Tokyo, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">C.</namePart><namePart type="given">A.</namePart><namePart type="family">Torres</namePart><affiliation>Department of Virology and Rickettsiology, National Institute of Health, Shinagawa-ku, Tokyo, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">A.</namePart><namePart type="family">Oya</namePart><affiliation>Department of Virology and Rickettsiology, National Institute of Health, Shinagawa-ku, Tokyo, Japan</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">P.</namePart><namePart type="family">Bachmann</namePart><affiliation>Institute for Medical Microbiology, Infectious, and Epidemic Medicine, Veterinary Faculty, University of Munich, Munich, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">K.</namePart><namePart type="family">Ottis</namePart><affiliation>Institute for Medical Microbiology, Infectious, and Epidemic Medicine, Veterinary Faculty, University of Munich, Munich, Germany</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">R.</namePart><namePart type="given">G.</namePart><namePart type="family">Webster</namePart><affiliation>St. Jude Children's Research Hospital, Memphis, Tennessee, USA</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="OriginalPaper" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-1JC4F85T-7">research-article</genre><originInfo><publisher>Springer-Verlag</publisher><place><placeTerm type="text">Vienna</placeTerm></place><dateCreated encoding="w3cdtf">1983-11-07</dateCreated><dateIssued encoding="w3cdtf">1984-09-01</dateIssued><copyrightDate encoding="w3cdtf">1984</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><abstract lang="en">Summary: The characteristics of an avian influenza virus were compared in detail with those of human Asian (H2N2) influenza viruses. Antigenic analysis by different antisera against H2N2 viruses and monoclonal antibodies to both the hemagglutinin and neuraminidase antigens showed that an avian isolate, A/duck/München/9/79 contained hemagglutinin and neuraminidase subunits closely related to those of the early human H2N2 viruses which had been prevalent in 1957. However, this avian virus gave low HI titers with absorbed and non-absorbed antisera to different human H2N2 viruses isolated in 1957. Like human Q phase variant, such as A/RI/5−/57 (H2N2), hemagglutination of the above avian strain was not inhibited by the purified non-specific γ-inhibitor from guinea pig serum. Growth behavior at restrictive temperature (42° C) clearly differentiate the avian H2N2 virus from human influenza viruses, showing that the former virus grew well in MDCK cells at 42° C but not the latters. Genomic analysis of these viruses revealed that the oligonucleotide map of H2N2 virus isolated from a duck was quite different from those of human H2N2 viruses from 1957 to 1967. The oligonucleotide mapping also indicated that different H2N2 influenza virus variants had co-circulated in humans in 1957.</abstract><note>Original Papers</note><relatedItem type="host"><titleInfo><title>Archives of Virology</title></titleInfo><titleInfo type="abbreviated"><title>Archives of Virology</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><originInfo><publisher>Springer</publisher><dateIssued encoding="w3cdtf">1984-09-01</dateIssued><copyrightDate encoding="w3cdtf">1984</copyrightDate></originInfo><subject><genre>Biomedicine</genre><topic>Medical Microbiology</topic><topic>Virology</topic><topic>Infectious Diseases</topic></subject><identifier type="ISSN">0304-8608</identifier><identifier type="eISSN">1432-8798</identifier><identifier type="JournalID">705</identifier><identifier type="IssueArticleCount">19</identifier><identifier type="VolumeIssueCount">4</identifier><part><date>1984</date><detail type="volume"><number>81</number><caption>vol.</caption></detail><detail type="issue"><number>3-4</number><caption>no.</caption></detail><extent unit="pages"><start>239</start><end>250</end></extent></part><recordInfo><recordOrigin>Springer-Verlag, 1984</recordOrigin></recordInfo></relatedItem><identifier type="istex">891FE6F2681838768A8765CFB958262F64A004CB</identifier><identifier type="ark">ark:/67375/1BB-J2X7FNJZ-W</identifier><identifier type="DOI">10.1007/BF01309996</identifier><identifier type="ArticleID">BF01309996</identifier><identifier type="ArticleID">Art5</identifier><accessCondition type="use and reproduction" contentType="copyright">Springer-Verlag, 1984</accessCondition><recordInfo><recordContentSource authority="ISTEX" authorityURI="https://loaded-corpus.data.istex.fr" valueURI="https://loaded-corpus.data.istex.fr/ark:/67375/XBH-3XSW68JL-F">springer</recordContentSource><recordOrigin>Springer-Verlag, 1984</recordOrigin></recordInfo></mods><json:item><extension>json</extension><original>false</original><mimetype>application/json</mimetype><uri>https://api.istex.fr/ark:/67375/1BB-J2X7FNJZ-W/record.json</uri></json:item></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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