Visual Detection of Norovirus Genogroup II by Reverse Transcription Loop-Mediated Isothermal Amplification with Hydroxynaphthol Blue Dye

A simple, rapid, specific, and sensitive colorimetric reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay with hydroxynaphthol blue dye (HNB) was established, targeting RNA-dependent RNA polymerase and capsid protein gene for the detection of the dominant norovirus genogroup...

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Veröffentlicht in:Food and environmental virology 2014-09, Vol.6 (3), p.196-201
Hauptverfasser: Luo, Jianming, Xu, Ziqian, Nie, Kai, Ding, Xiong, Guan, Li, Wang, Ji, Xian, Yuying, Wu, Xiyang, Ma, Xuejun
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Sprache:eng
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Zusammenfassung:A simple, rapid, specific, and sensitive colorimetric reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay with hydroxynaphthol blue dye (HNB) was established, targeting RNA-dependent RNA polymerase and capsid protein gene for the detection of the dominant norovirus genogroup in China—NoV GII. The assay was carried out at 65 °C for 60 min with no cross-reactivity with other common gastroenteritis viruses. The sensitivity of this assay was 10 3 copies per reaction which is equivalent to the conventional RT-PCR test. The clinical test showed 94.83 % coincidence rate for NoV genogroup II detection compared with the results, confirmed by the Department of Viral Diarrhea of Chinese Center for Disease Control and Prevention via conventional RT-PCR. The HNB dye-based RT-LAMP could be a novel rapid screening method for prevalent norovirus genogroup II in China, especially in those resource-limited hospitals and rural local clinics.
ISSN:1867-0334
1867-0342
DOI:10.1007/s12560-014-9142-8