| Literature DB >> 29987379 |
Ning Shi1, Hao Liu2, Li-Xia Li3, Bo Hu4, Lei Zhang4, Chuan-Fang Zhao4, Xiao-Yu Deng4, Xin-Tong Li4, Xiang-Hong Xue4, Xue Bai4, Hai-Ling Zhang4, Rong-Guang Lu4, Shi-Zhen Lian4, Yang Wang4, Ming-Hao Yan5, Xi-Jun Yan6.
Abstract
Getah virus (GETV), a mosquito-borne virus that mainly infects horses and pigs, has emerged and spread in China. We developed a highly specific and reproducible TaqMan probe-based quantitative reverse transcription PCR (RT-qPCR) assay targeting the non-structural protein 1 of GETV, whose detection limit is 25.5 copies/µL, which is 100-fold higher than that of conventional RT-PCR. RT-qPCR was used to detect GETV RNA in mosquito and animal clinical samples, showing that the accuracy of RT-qPCR was higher than that of conventional RT-PCR. The newly developed RT-qPCR assay may be a useful alternative tool for rapid, simple and specific diagnosis of GETV infection.Entities:
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Year: 2018 PMID: 29987379 DOI: 10.1007/s00705-018-3927-2
Source DB: PubMed Journal: Arch Virol ISSN: 0304-8608 Impact factor: 2.574