Hemagglutinin and neuraminidase matching patterns of two influenza A virus strains related to the 1918 and 2009 global pandemics
Identifieur interne : 000490 ( Pmc/Curation ); précédent : 000489; suivant : 000491Hemagglutinin and neuraminidase matching patterns of two influenza A virus strains related to the 1918 and 2009 global pandemics
Auteurs : Yonghui Zhang [République populaire de Chine] ; Xiaojing Lin [République populaire de Chine] ; Fengwei Zhang [République populaire de Chine] ; Jia Wu [République populaire de Chine] ; Wenjie Tan [République populaire de Chine] ; Shengli Bi [République populaire de Chine] ; Jianfang Zhou [République populaire de Chine] ; Yuelong Shu [République populaire de Chine] ; Yue Wang [République populaire de Chine]Source :
- Biochemical and Biophysical Research Communications [ 0006-291X ] ; 2009.
Abstract
The current pandemic influenza A (H1N1) virus has revealed a complicated reassortment of various influenza A viruses. The biological study of these viruses, especially of the viral envelope proteins hemagglutinin (HA) and neuraminidase (NA), is urgently needed for the control and prevention of H1N1 viruses. We have generated H1N1-2009 and H1N1-1918 pseudotyped particles (pp) with high infectivity. Combinations of HA1918 + NA2009 and HA2009 + NA1918 also formed infectious H1N1pps, among which the HA2009 + NA1918 combination resulted in the most highly infectious pp. Our study demonstrated that some reassortments of H1N1 viruses may hold the potential to produce higher infectivity than do their ancestors.
Url:
DOI: 10.1016/j.bbrc.2009.07.040
PubMed: 19615337
PubMed Central: 7092934
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<front><div type="abstract" xml:lang="en"><p>The current pandemic influenza A (H1N1) virus has revealed a complicated reassortment of various influenza A viruses. The biological study of these viruses, especially of the viral envelope proteins hemagglutinin (HA) and neuraminidase (NA), is urgently needed for the control and prevention of H1N1 viruses. We have generated H1N1-2009 and H1N1-1918 pseudotyped particles (pp) with high infectivity. Combinations of HA1918 + NA2009 and HA2009 + NA1918 also formed infectious H1N1pps, among which the HA2009 + NA1918 combination resulted in the most highly infectious pp. Our study demonstrated that some reassortments of H1N1 viruses may hold the potential to produce higher infectivity than do their ancestors.</p>
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<title-group><article-title>Hemagglutinin and neuraminidase matching patterns of two influenza A virus strains related to the 1918 and 2009 global pandemics</article-title>
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<contrib-group><contrib contrib-type="author"><name><surname>Zhang</surname>
<given-names>Yonghui</given-names>
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<xref rid="aff1" ref-type="aff">a</xref>
<xref rid="aff2" ref-type="aff">b</xref>
<xref rid="fn1" ref-type="fn">1</xref>
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<given-names>Xiaojing</given-names>
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<xref rid="aff1" ref-type="aff">a</xref>
<xref rid="fn1" ref-type="fn">1</xref>
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<contrib contrib-type="author"><name><surname>Zhang</surname>
<given-names>Fengwei</given-names>
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<xref rid="aff1" ref-type="aff">a</xref>
<xref rid="aff3" ref-type="aff">c</xref>
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<contrib contrib-type="author"><name><surname>Wu</surname>
<given-names>Jia</given-names>
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<xref rid="aff1" ref-type="aff">a</xref>
<xref rid="aff3" ref-type="aff">c</xref>
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<given-names>Wenjie</given-names>
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<xref rid="aff1" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Bi</surname>
<given-names>Shengli</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Zhou</surname>
<given-names>Jianfang</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Shu</surname>
<given-names>Yuelong</given-names>
</name>
<xref rid="aff1" ref-type="aff">a</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Wang</surname>
<given-names>Yue</given-names>
</name>
<email>euy-tokyo@umin.ac.jp</email>
<xref rid="aff1" ref-type="aff">a</xref>
<xref rid="cor1" ref-type="corresp">⁎</xref>
</contrib>
</contrib-group>
<aff id="aff1"><label>a</label>
State Key Laboratory for Molecular Virology and Genetic Engineering, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Yingxin Street 100, Xuanwu District, Beijing 100052, PR China</aff>
<aff id="aff2"><label>b</label>
Institute of Pathogens and Vectors, Dali University, Dali 671003, Yunnan Province, PR China</aff>
<aff id="aff3"><label>c</label>
Wenzhou Medical College, Wenzhou 325000, Zhejiang Province, PR China</aff>
<author-notes><corresp id="cor1"><label>⁎</label>
Corresponding author. Fax: +86 10 63510565. <email>euy-tokyo@umin.ac.jp</email>
</corresp>
<fn id="fn1"><label>1</label>
<p>These two authors contributed equally to this study.</p>
</fn>
</author-notes>
<pub-date pub-type="pmc-release"><day>15</day>
<month>7</month>
<year>2009</year>
</pub-date>
<pmc-comment> PMC Release delay is 0 months and 0 days and was based on .</pmc-comment>
<pub-date pub-type="ppub"><day>18</day>
<month>9</month>
<year>2009</year>
</pub-date>
<pub-date pub-type="epub"><day>15</day>
<month>7</month>
<year>2009</year>
</pub-date>
<volume>387</volume>
<issue>2</issue>
<fpage>405</fpage>
<lpage>408</lpage>
<history><date date-type="received"><day>23</day>
<month>6</month>
<year>2009</year>
</date>
</history>
<permissions><copyright-statement>Copyright © 2009 Elsevier Inc. All rights reserved.</copyright-statement>
<copyright-year>2009</copyright-year>
<copyright-holder>Elsevier Inc.</copyright-holder>
<license><license-p>Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.</license-p>
</license>
</permissions>
<abstract><p>The current pandemic influenza A (H1N1) virus has revealed a complicated reassortment of various influenza A viruses. The biological study of these viruses, especially of the viral envelope proteins hemagglutinin (HA) and neuraminidase (NA), is urgently needed for the control and prevention of H1N1 viruses. We have generated H1N1-2009 and H1N1-1918 pseudotyped particles (pp) with high infectivity. Combinations of HA1918 + NA2009 and HA2009 + NA1918 also formed infectious H1N1pps, among which the HA2009 + NA1918 combination resulted in the most highly infectious pp. Our study demonstrated that some reassortments of H1N1 viruses may hold the potential to produce higher infectivity than do their ancestors.</p>
</abstract>
<kwd-group><title>Keywords</title>
<kwd>Influenza A (H1N1) virus</kwd>
<kwd>HA, hemagglutinin</kwd>
<kwd>NA, neuraminidase</kwd>
<kwd>H1N1pp, H1N1 pseudotyped particle</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
</record>
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