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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Characterization of a porcine kidney cell line resistant to influenza virus infection.</title><author><name sortKey="Kimura, Y" sort="Kimura, Y" uniqKey="Kimura Y" first="Y" last="Kimura">Y. Kimura</name></author><author><name sortKey="Yokochi, T" sort="Yokochi, T" uniqKey="Yokochi T" first="T" last="Yokochi">T. Yokochi</name></author><author><name sortKey="Miyadai, T" sort="Miyadai, T" uniqKey="Miyadai T" first="T" last="Miyadai">T. Miyadai</name></author><author><name sortKey="Yoshida, K" sort="Yoshida, K" uniqKey="Yoshida K" first="K" last="Yoshida">K. Yoshida</name></author><author><name sortKey="Yokoo, J" sort="Yokoo, J" uniqKey="Yokoo J" first="J" last="Yokoo">J. Yokoo</name></author><author><name sortKey="Matsumoto, K" sort="Matsumoto, K" uniqKey="Matsumoto K" first="K" last="Matsumoto">K. Matsumoto</name></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">3973972</idno><idno type="pmc">254737</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC254737</idno><idno type="RBID">PMC:254737</idno><date when="1985">1985</date><idno type="wicri:Area/Pmc/Corpus">000401</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000401</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Characterization of a porcine kidney cell line resistant to influenza virus infection.</title><author><name sortKey="Kimura, Y" sort="Kimura, Y" uniqKey="Kimura Y" first="Y" last="Kimura">Y. Kimura</name></author><author><name sortKey="Yokochi, T" sort="Yokochi, T" uniqKey="Yokochi T" first="T" last="Yokochi">T. Yokochi</name></author><author><name sortKey="Miyadai, T" sort="Miyadai, T" uniqKey="Miyadai T" first="T" last="Miyadai">T. Miyadai</name></author><author><name sortKey="Yoshida, K" sort="Yoshida, K" uniqKey="Yoshida K" first="K" last="Yoshida">K. Yoshida</name></author><author><name sortKey="Yokoo, J" sort="Yokoo, J" uniqKey="Yokoo J" first="J" last="Yokoo">J. Yokoo</name></author><author><name sortKey="Matsumoto, K" sort="Matsumoto, K" uniqKey="Matsumoto K" first="K" last="Matsumoto">K. Matsumoto</name></author></analytic><series><title level="j">Journal of Virology</title><idno type="ISSN">0022-538X</idno><idno type="eISSN">1098-5514</idno><imprint><date when="1985">1985</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>A mutant cell line of porcine kidney cells that resists the cytopathic effect of influenza virus has been obtained and characterized. These cells, designated ESK-R, were originally obtained by prolonged cultivation of cells surviving influenza B/Kanagawa/73 virus infection. No infectious virus was recovered from ESK-R cells, and no evidence for the presence of virus antigens in the cells was demonstrated by immunofluorescent staining. ESK-R cells also showed a distinct resistance to various other strains of both types A and B influenza viruses. The growth of mumps, Sendai, or Newcastle disease virus was considerably restricted, but the cell line normally supported the replication of vesicular stomatitis virus. ESK-R cells were found to lack specific receptors for influenza virus as determined by fluorescence-activated cell sorter analyses. The membrane barrier of ESK-R cells was successfully overcome by nonspecific endocytosis of calcium-coprecipitated virus particles followed by production of an appreciable amount of progeny virus.</p></div></front></TEI><pmc article-type="research-article"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">J Virol</journal-id><journal-title>Journal of Virology</journal-title><issn pub-type="ppub">0022-538X</issn><issn pub-type="epub">1098-5514</issn></journal-meta><article-meta><article-id pub-id-type="pmid">3973972</article-id><article-id pub-id-type="pmc">254737</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title>Characterization of a porcine kidney cell line resistant to influenza virus infection.</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Kimura</surname><given-names>Y</given-names></name></contrib><contrib contrib-type="author"><name><surname>Yokochi</surname><given-names>T</given-names></name></contrib><contrib contrib-type="author"><name><surname>Miyadai</surname><given-names>T</given-names></name></contrib><contrib contrib-type="author"><name><surname>Yoshida</surname><given-names>K</given-names></name></contrib><contrib contrib-type="author"><name><surname>Yokoo</surname><given-names>J</given-names></name></contrib><contrib contrib-type="author"><name><surname>Matsumoto</surname><given-names>K</given-names></name></contrib></contrib-group><pub-date pub-type="ppub"><month>3</month><year>1985</year></pub-date><volume>53</volume><issue>3</issue><fpage>980</fpage><lpage>983</lpage><abstract><p>A mutant cell line of porcine kidney cells that resists the cytopathic effect of influenza virus has been obtained and characterized. These cells, designated ESK-R, were originally obtained by prolonged cultivation of cells surviving influenza B/Kanagawa/73 virus infection. No infectious virus was recovered from ESK-R cells, and no evidence for the presence of virus antigens in the cells was demonstrated by immunofluorescent staining. ESK-R cells also showed a distinct resistance to various other strains of both types A and B influenza viruses. The growth of mumps, Sendai, or Newcastle disease virus was considerably restricted, but the cell line normally supported the replication of vesicular stomatitis virus. ESK-R cells were found to lack specific receptors for influenza virus as determined by fluorescence-activated cell sorter analyses. The membrane barrier of ESK-R cells was successfully overcome by nonspecific endocytosis of calcium-coprecipitated virus particles followed by production of an appreciable amount of progeny virus.</p></abstract></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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