Literature DB >> 26055565

Real-time RT-PCR Assay for the detection of Tahyna Virus.

Hao Li1, Yu Xi Cao1, Xiao Xia He1, Shi Hong Fu1, Zhi Lyu1, Ying He1, Xiao Yan Gao1, Xiao Yang Gao, Guo Dong Liang1, Huan Yu Wang1, Huang Yu Wang2.   

Abstract

A real-time RT-PCR (RT-qPCR) assay for the detection of Tahyna virus was developed to monitor Tahyna virus infection in field-collected vector mosquito samples. The targets selected for the assay were S segment sequences encoding the nucleocapsid protein from the Tahyna virus. Primers and probes were selected in conserved regions by aligning genetic sequences from various Tahyna virus strains available from GenBank. The sensitivity of the RT-qPCR approach was compared to that of a standard plaque assay in BHK cells. RT-qPCR assay can detect 4.8 PFU of titrated Tahyna virus. Assay specificities were determined by testing a battery of arboviruses, including representative strains of Tahyna virus and other arthropod-borne viruses from China. Seven strains of Tahyna virus were confirmed as positive; the other seven species of arboviruses could not be detected by RT-qPCR. Additionally, the assay was used to detect Tahyna viral RNA in pooled mosquito samples. The RT-qPCR assay detected Tahyna virus in a sensitive, specific, and rapid manner; these findings support the use of the assay in viral surveillance.
Copyright © 2015 The Editorial Board of Biomedical and Environmental Sciences. Published by China CDC. All rights reserved.

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Year:  2015        PMID: 26055565     DOI: 10.3967/bes2015.052

Source DB:  PubMed          Journal:  Biomed Environ Sci        ISSN: 0895-3988            Impact factor:   3.118


  7 in total

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Journal:  Front Cell Infect Microbiol       Date:  2018-10-24       Impact factor: 5.293

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  7 in total

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