Detection of hepatitis C virus by an improved loop-mediated isothermal amplification assay
Identifieur interne : 000175 ( Pmc/Curation ); précédent : 000174; suivant : 000176Detection of hepatitis C virus by an improved loop-mediated isothermal amplification assay
Auteurs : Jin Yang [République populaire de Chine] ; Mei-Xin Fang [République populaire de Chine] ; Jie Li [République populaire de Chine] ; Guo-Qiang Lou [République populaire de Chine] ; Hang-Jun Lu [République populaire de Chine] ; Nan-Ping Wu [République populaire de Chine]Source :
- Archives of Virology [ 0304-8608 ] ; 2011.
Abstract
An improved, sensitive, specific, and rapid one-step reverse transcription loop-mediated isothermal amplification (LAMP) assay targeting the 5′ untranslated region (UTR) was developed to detect hepatitis C virus (HCV) infection. Based on an accelerating primer (AP), the present assay, named AP-LAMP, has the advantages of rapidity and sensitivity over the routine LAMP method. The possible AP-based amplification pathway during the reaction was revealed by restriction enzyme digestion and eletrophoresis. The detection limit of the AP-LAMP assay was approximately 84 IU/ml, and no cross-detection was observed. The assay was evaluated further with 126 clinical specimens, and the results indicated the suitability and simplicity of the test as a rapid diagnostic tool for detection of HCV RNA.
Url:
DOI: 10.1007/s00705-011-1001-4
PubMed: 21562883
PubMed Central: 7087303
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<front><div type="abstract" xml:lang="en"><p>An improved, sensitive, specific, and rapid one-step reverse transcription loop-mediated isothermal amplification (LAMP) assay targeting the 5′ untranslated region (UTR) was developed to detect hepatitis C virus (HCV) infection. Based on an accelerating primer (AP), the present assay, named AP-LAMP, has the advantages of rapidity and sensitivity over the routine LAMP method. The possible AP-based amplification pathway during the reaction was revealed by restriction enzyme digestion and eletrophoresis. The detection limit of the AP-LAMP assay was approximately 84 IU/ml, and no cross-detection was observed. The assay was evaluated further with 126 clinical specimens, and the results indicated the suitability and simplicity of the test as a rapid diagnostic tool for detection of HCV RNA.</p>
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<pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">Arch Virol</journal-id>
<journal-id journal-id-type="iso-abbrev">Arch. Virol</journal-id>
<journal-title-group><journal-title>Archives of Virology</journal-title>
</journal-title-group>
<issn pub-type="ppub">0304-8608</issn>
<issn pub-type="epub">1432-8798</issn>
<publisher><publisher-name>Springer Vienna</publisher-name>
<publisher-loc>Vienna</publisher-loc>
</publisher>
</journal-meta>
<article-meta><article-id pub-id-type="pmid">21562883</article-id>
<article-id pub-id-type="pmc">7087303</article-id>
<article-id pub-id-type="publisher-id">1001</article-id>
<article-id pub-id-type="doi">10.1007/s00705-011-1001-4</article-id>
<article-categories><subj-group subj-group-type="heading"><subject>Original Article</subject>
</subj-group>
</article-categories>
<title-group><article-title>Detection of hepatitis C virus by an improved loop-mediated isothermal amplification assay</article-title>
</title-group>
<contrib-group><contrib contrib-type="author"><name><surname>Yang</surname>
<given-names>Jin</given-names>
</name>
<xref ref-type="aff" rid="Aff1">1</xref>
<xref ref-type="aff" rid="Aff2">2</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Fang</surname>
<given-names>Mei-xin</given-names>
</name>
<xref ref-type="aff" rid="Aff1">1</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Li</surname>
<given-names>Jie</given-names>
</name>
<xref ref-type="aff" rid="Aff1">1</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Lou</surname>
<given-names>Guo-qiang</given-names>
</name>
<xref ref-type="aff" rid="Aff3">3</xref>
</contrib>
<contrib contrib-type="author"><name><surname>Lu</surname>
<given-names>Hang-jun</given-names>
</name>
<xref ref-type="aff" rid="Aff2">2</xref>
</contrib>
<contrib contrib-type="author" corresp="yes"><name><surname>Wu</surname>
<given-names>Nan-ping</given-names>
</name>
<address><email>flwnp@yahoo.com.cn</email>
</address>
<xref ref-type="aff" rid="Aff1">1</xref>
</contrib>
<aff id="Aff1"><label>1</label>
<institution-wrap><institution-id institution-id-type="GRID">grid.13402.34</institution-id>
<institution-id institution-id-type="ISNI">000000041759700X</institution-id>
<institution>State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, Institute of Infectious Diseases,</institution>
<institution>The First Affiliated Hospital of Zhejiang University, School of Medicine, Zhejiang University,</institution>
</institution-wrap>
Hangzhou, 310022 China</aff>
<aff id="Aff2"><label>2</label>
<institution-wrap><institution-id institution-id-type="GRID">grid.410621.0</institution-id>
<institution>Department of Medicine,</institution>
<institution>Blood Center of Zhejiang Province,</institution>
</institution-wrap>
Hangzhou, 310005 China</aff>
<aff id="Aff3"><label>3</label>
<institution-wrap><institution-id institution-id-type="GRID">grid.460074.1</institution-id>
<institution>Department of Infectious Diseases, School of Medicine,</institution>
<institution>The Affiliated Hospital of Hangzhou Normal University,</institution>
</institution-wrap>
Hangzhou, 310018 China</aff>
</contrib-group>
<pub-date pub-type="epub"><day>12</day>
<month>5</month>
<year>2011</year>
</pub-date>
<pub-date pub-type="ppub"><year>2011</year>
</pub-date>
<volume>156</volume>
<issue>8</issue>
<fpage>1387</fpage>
<lpage>1396</lpage>
<history><date date-type="received"><day>27</day>
<month>12</month>
<year>2010</year>
</date>
<date date-type="accepted"><day>9</day>
<month>4</month>
<year>2011</year>
</date>
</history>
<permissions><copyright-statement>© Springer-Verlag 2011</copyright-statement>
<license><license-p>This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.</license-p>
</license>
</permissions>
<abstract id="Abs1"><p>An improved, sensitive, specific, and rapid one-step reverse transcription loop-mediated isothermal amplification (LAMP) assay targeting the 5′ untranslated region (UTR) was developed to detect hepatitis C virus (HCV) infection. Based on an accelerating primer (AP), the present assay, named AP-LAMP, has the advantages of rapidity and sensitivity over the routine LAMP method. The possible AP-based amplification pathway during the reaction was revealed by restriction enzyme digestion and eletrophoresis. The detection limit of the AP-LAMP assay was approximately 84 IU/ml, and no cross-detection was observed. The assay was evaluated further with 126 clinical specimens, and the results indicated the suitability and simplicity of the test as a rapid diagnostic tool for detection of HCV RNA.</p>
</abstract>
<kwd-group xml:lang="en"><title>Keywords</title>
<kwd>West Nile Virus</kwd>
<kwd>Lamp Assay</kwd>
<kwd>Lamp Reaction</kwd>
<kwd>Loop Primer</kwd>
<kwd>Lamp Method</kwd>
</kwd-group>
<custom-meta-group><custom-meta><meta-name>issue-copyright-statement</meta-name>
<meta-value>© Springer-Verlag 2011</meta-value>
</custom-meta>
</custom-meta-group>
</article-meta>
</front>
</pmc>
</record>
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