Detection methods for influenza A H1N1 virus with special reference to biosensors: a review
Identifieur interne : 000D10 ( Pmc/Curation ); précédent : 000D09; suivant : 000D11Detection methods for influenza A H1N1 virus with special reference to biosensors: a review
Auteurs : Anita Dalal ; Hari Mohan ; Minakshi Prasad ; C. S. PundirSource :
- Bioscience Reports [ 0144-8463 ] ; 2020.
Abstract
H1N1 (Swine flu) is caused by influenza A virus, which is a member of
Url:
DOI: 10.1042/BSR20193852
PubMed: 32016385
PubMed Central: 7000365
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Detection methods for influenza A H1N1 virus with special reference to biosensors: a review</title>
<author><name sortKey="Dalal, Anita" sort="Dalal, Anita" uniqKey="Dalal A" first="Anita" last="Dalal">Anita Dalal</name>
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<author><name sortKey="Mohan, Hari" sort="Mohan, Hari" uniqKey="Mohan H" first="Hari" last="Mohan">Hari Mohan</name>
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<author><name sortKey="Prasad, Minakshi" sort="Prasad, Minakshi" uniqKey="Prasad M" first="Minakshi" last="Prasad">Minakshi Prasad</name>
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<author><name sortKey="Pundir, C S" sort="Pundir, C S" uniqKey="Pundir C" first="C. S." last="Pundir">C. S. Pundir</name>
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<series><title level="j">Bioscience Reports</title>
<idno type="ISSN">0144-8463</idno>
<idno type="eISSN">1573-4935</idno>
<imprint><date when="2020">2020</date>
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<front><div type="abstract" xml:lang="en"><title>Abstract</title>
<p>H1N1 (Swine flu) is caused by influenza A virus, which is a member of <italic>Orthomyxoviridae</italic>
family. Transmission of H1N1 occurs from human to human through air or sometimes from pigs to humans. The influenza virus has different RNA segments, which can reassert to make new virus strain with the possibility to create an outbreak in unimmunized people. Gene reassortment is a process through which new strains are emerging in pigs, as it has specific receptors for both human influenza and avian influenza viruses. H1N1 binds specifically with an α-2,6 glycosidic bond, which is present in human respiratory tract cells as well as in pigs. Considering the fact of fast multiplication of viruses inside the living cells, rapid detection methods need an hour. Currently, WHO recommended methods for the detection of swine flu include real-time PCR in specific testing centres that take 3–4 h. More recently, a number of methods such as Antigen–Antibody or RT-LAMP and DNA biosensors have also been developed that are rapid and more sensitive. This review describes the various challenges in the diagnosis of H1N1, and merits and demerits of conventional vis-à-vis latest methods with special emphasis on biosensors.</p>
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</TEI>
<pmc article-type="review-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Biosci Rep</journal-id>
<journal-id journal-id-type="iso-abbrev">Biosci. Rep</journal-id>
<journal-id journal-id-type="publisher-id">bsr</journal-id>
<journal-title-group><journal-title>Bioscience Reports</journal-title>
</journal-title-group>
<issn pub-type="ppub">0144-8463</issn>
<issn pub-type="epub">1573-4935</issn>
<publisher><publisher-name>Portland Press Ltd.</publisher-name>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">32016385</article-id>
<article-id pub-id-type="pmc">7000365</article-id>
<article-id pub-id-type="doi">10.1042/BSR20193852</article-id>
<article-id pub-id-type="publisher-id">BSR20193852</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Diagnostics & Biomarkers</subject>
</subj-group>
<subj-group subj-group-type="heading"><subject>RNA</subject>
</subj-group>
<subj-group subj-group-type="heading"><subject>Virology</subject>
</subj-group>
<subj-group subj-group-type="heading"><subject>Biochemical Techniques & Resources</subject>
</subj-group>
<subj-group subj-group-type="toc-heading"><subject>Review Articles</subject>
</subj-group>
</article-categories>
<title-group><article-title>Detection methods for influenza A H1N1 virus with special reference to biosensors: a review</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Ravina</surname>
<given-names></given-names>
</name>
<xref ref-type="aff" rid="AFF1"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Dalal</surname>
<given-names>Anita</given-names>
</name>
<xref ref-type="aff" rid="AFF2"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Mohan</surname>
<given-names>Hari</given-names>
</name>
<email>harimohansaini@gmail.com</email>
<xref ref-type="aff" rid="AFF1"></xref>
<xref ref-type="corresp" rid="COR1"></xref>
</contrib>
<contrib contrib-type="author"><name><surname>Prasad</surname>
<given-names>Minakshi</given-names>
</name>
<xref ref-type="aff" rid="AFF3"></xref>
</contrib>
<contrib contrib-type="author"><contrib-id contrib-id-type="orcid" authenticated="false">http://orcid.org/0000-0002-9262-4210</contrib-id>
<name><surname>Pundir</surname>
<given-names>C.S.</given-names>
</name>
<email>chandraspundir@gmail.com</email>
<xref ref-type="aff" rid="AFF4"></xref>
<xref ref-type="corresp" rid="COR1"></xref>
</contrib>
</contrib-group>
<aff id="AFF1"><label>1</label>
Centre for Medical Biotechnology, Maharshi Dayanand University, Rohtak, Haryana 124001, India</aff>
<aff id="AFF2"><label>2</label>
DCR University of Science and Technology, Murthal, Sonepat, Haryana 131039, India</aff>
<aff id="AFF3"><label>3</label>
Department of Animal Biotechnology, Lala Lajpat Rai University of Veterinary and Animal Sciences, Hisar, Haryana 125004, India</aff>
<aff id="AFF4"><label>4</label>
Department of Biochemistry, Maharshi Dayanand University, Rohtak, Haryana 124001, India</aff>
<author-notes><corresp id="COR1"><bold>Correspondence:</bold>
Hari Mohan (<email>harimohansaini@gmail.com</email>
) or C.S. Pundir (<email>chandraspundir@gmail.com</email>
)</corresp>
</author-notes>
<pub-date pub-type="collection"><day>28</day>
<month>2</month>
<year>2020</year>
</pub-date>
<pub-date pub-type="epub" iso-8601-date="2020-02-04"><day>04</day>
<month>2</month>
<year>2020</year>
</pub-date>
<volume>40</volume>
<issue>2</issue>
<elocation-id>BSR20193852</elocation-id>
<history><date date-type="received"><day>18</day>
<month>11</month>
<year>2019</year>
</date>
<date date-type="rev-recd"><day>18</day>
<month>11</month>
<year>2019</year>
</date>
<date date-type="accepted"><day>06</day>
<month>1</month>
<year>2020</year>
</date>
<date date-type="accepted-manuscript"><day>06</day>
<month>1</month>
<year>2020</year>
</date>
</history>
<permissions><copyright-statement>© 2020 The Author(s).</copyright-statement>
<copyright-year>2020</copyright-year>
<license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/"><license-p>This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY).</license-p>
</license>
</permissions>
<self-uri xlink:href="bsr-40-bsr20193852.pdf"></self-uri>
<abstract><title>Abstract</title>
<p>H1N1 (Swine flu) is caused by influenza A virus, which is a member of <italic>Orthomyxoviridae</italic>
family. Transmission of H1N1 occurs from human to human through air or sometimes from pigs to humans. The influenza virus has different RNA segments, which can reassert to make new virus strain with the possibility to create an outbreak in unimmunized people. Gene reassortment is a process through which new strains are emerging in pigs, as it has specific receptors for both human influenza and avian influenza viruses. H1N1 binds specifically with an α-2,6 glycosidic bond, which is present in human respiratory tract cells as well as in pigs. Considering the fact of fast multiplication of viruses inside the living cells, rapid detection methods need an hour. Currently, WHO recommended methods for the detection of swine flu include real-time PCR in specific testing centres that take 3–4 h. More recently, a number of methods such as Antigen–Antibody or RT-LAMP and DNA biosensors have also been developed that are rapid and more sensitive. This review describes the various challenges in the diagnosis of H1N1, and merits and demerits of conventional vis-à-vis latest methods with special emphasis on biosensors.</p>
</abstract>
<kwd-group><kwd>A (H1N1)</kwd>
<kwd>DNA biosensors</kwd>
<kwd>Orthomyxoviridae</kwd>
<kwd>Real Time-PCR</kwd>
<kwd>RT-LAMP</kwd>
<kwd>Swine flu</kwd>
</kwd-group>
<counts><page-count count="18"></page-count>
</counts>
</article-meta>
</front>
</pmc>
</record>
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