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Subtype identification of the novel A H1N1 and other human influenza A viruses using an oligonucleotide microarray

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Subtype identification of the novel A H1N1 and other human influenza A viruses using an oligonucleotide microarray

Source :

Archives of Virology [ 0304-8608 ] ; 2010.

RBID : ISTEX:DEB10BB1F29DE950FCFE100D158AFB24A4C55A15

Abstract

Abstract: A novel strain of influenza A (H1N1) virus was isolated in Mexico and the US in March and April 2009. This novel virus spread to many countries and regions in a few months, and WHO raised the level of pandemic alert from phase 5 to phase 6 on June 11, 2009. The accurate identification of H1N1 virus and other human seasonal influenza A viruses is very important for further treatment and control of their infections. In this study, we developed an oligonucleotide microarray to subtype human H1N1, H3N2 and H5N1 influenza viruses, which could distinguish the novel H1N1 from human seasonal H1N1 influenza viruses and swine H1N1 influenza viruses. The microarray utilizes a panel of primers for multiplex PCR amplification of the hemagglutinin (HA), neuraminidase (NA) and matrix (MP) genes of human influenza A viruses. The 59-mer oligonucleotides were designed to distinguish different subtypes of human influenza A viruses. With this microarray, we accurately identified and correctly subtyped the reference virus strains. Moreover, we confirmed 4 out of 39 clinical throat swab specimens from suspected cases of novel H1N1.

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https://api.istex.fr/ark:/67375/VQC-Q7ZSRXG8-G/fulltext.pdf

DOI: 10.1007/s00705-009-0545-z

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Le document en format XML

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<author><name sortKey="Li, Yongqiang" sort="Li, Yongqiang" uniqKey="Li Y" first="Yongqiang" last="Li">Yongqiang Li</name>
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<author><name sortKey="Sun, Honghe" sort="Sun, Honghe" uniqKey="Sun H" first="Honghe" last="Sun">Honghe Sun</name>
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<author><name sortKey="Wu, Weili" sort="Wu, Weili" uniqKey="Wu W" first="Weili" last="Wu">Weili Wu</name>
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<author><name sortKey="Liu, Hong" sort="Liu, Hong" uniqKey="Liu H" first="Hong" last="Liu">Hong Liu</name>
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<author><name sortKey="Lin, Fang" sort="Lin, Fang" uniqKey="Lin F" first="Fang" last="Lin">Fang Lin</name>
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<author><name sortKey="Qing, Chenfeng" sort="Qing, Chenfeng" uniqKey="Qing C" first="Chenfeng" last="Qing">Chenfeng Qing</name>
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<author><name sortKey="Chang, Guohui" sort="Chang, Guohui" uniqKey="Chang G" first="Guohui" last="Chang">Guohui Chang</name>
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<author><name sortKey="Zhu, Qingyu" sort="Zhu, Qingyu" uniqKey="Zhu Q" first="Qingyu" last="Zhu">Qingyu Zhu</name>
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<author><name sortKey="Chen, Weijun" sort="Chen, Weijun" uniqKey="Chen W" first="Weijun" last="Chen">Weijun Chen</name>
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<front><div type="abstract" xml:lang="en">Abstract: A novel strain of influenza A (H1N1) virus was isolated in Mexico and the US in March and April 2009. This novel virus spread to many countries and regions in a few months, and WHO raised the level of pandemic alert from phase 5 to phase 6 on June 11, 2009. The accurate identification of H1N1 virus and other human seasonal influenza A viruses is very important for further treatment and control of their infections. In this study, we developed an oligonucleotide microarray to subtype human H1N1, H3N2 and H5N1 influenza viruses, which could distinguish the novel H1N1 from human seasonal H1N1 influenza viruses and swine H1N1 influenza viruses. The microarray utilizes a panel of primers for multiplex PCR amplification of the hemagglutinin (HA), neuraminidase (NA) and matrix (MP) genes of human influenza A viruses. The 59-mer oligonucleotides were designed to distinguish different subtypes of human influenza A viruses. With this microarray, we accurately identified and correctly subtyped the reference virus strains. Moreover, we confirmed 4 out of 39 clinical throat swab specimens from suspected cases of novel H1N1.</div>
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Subtype identification of the novel A H1N1 and other human influenza A viruses using an oligonucleotide microarray

Subtype identification of the novel A H1N1 and other human influenza A viruses using an oligonucleotide microarray

Source :

Abstract

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Links to Exploration step

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