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Detection of hepatitis C virus by an improved loop-mediated isothermal amplification assay

Identifieur interne : 000264 ( Ncbi/Checkpoint ); précédent : 000263; suivant : 000265

Detection 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 :

RBID : PMC:7087303

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


Affiliations:


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PMC:7087303

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<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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<affiliations>
<list>
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<li>République populaire de Chine</li>
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<name sortKey="Yang, Jin" sort="Yang, Jin" uniqKey="Yang J" first="Jin" last="Yang">Jin Yang</name>
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<name sortKey="Fang, Mei Xin" sort="Fang, Mei Xin" uniqKey="Fang M" first="Mei-Xin" last="Fang">Mei-Xin Fang</name>
<name sortKey="Li, Jie" sort="Li, Jie" uniqKey="Li J" first="Jie" last="Li">Jie Li</name>
<name sortKey="Lou, Guo Qiang" sort="Lou, Guo Qiang" uniqKey="Lou G" first="Guo-Qiang" last="Lou">Guo-Qiang Lou</name>
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<name sortKey="Wu, Nan Ping" sort="Wu, Nan Ping" uniqKey="Wu N" first="Nan-Ping" last="Wu">Nan-Ping Wu</name>
<name sortKey="Yang, Jin" sort="Yang, Jin" uniqKey="Yang J" first="Jin" last="Yang">Jin Yang</name>
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