Literature DB >> 30790106

Multiplex one-step real-time PCR assay for rapid simultaneous detection of velogenic and mesogenic Newcastle disease virus and H5-subtype avian influenza virus.

Zhujun Zhang1,2,3, Dong Liu1,2,3, Jiao Hu1,2,3, Wenqiang Sun1,2,3, Kaituo Liu1,2,3, Juan Li1,2,3, Haixu Xu1,2,3, Jing Liu1,2,3, Lihong He1,2,3, Daxiu Jiang1,2,3, Min Gu1,2,3, Shunlin Hu1,2,3, Xiaoquan Wang1,2,3, Xiaowen Liu1,2,3, Xiufan Liu4,5,6.   

Abstract

H5 avian influenza virus (AIV) and velogenic Newcastle disease virus (v-NDV) are pathogens listed in the OIE Terrestrial Animal Health Code and are considered key pathogens to be eliminated in poultry production. Molecular techniques for rapid detection of H5 AIV and v-NDV are required to investigate their transmission characteristics and to guide prevention. Traditional virus isolation, using embryonated chicken eggs, is time-consuming and cannot be used as a rapid diagnostic technology. In this study, a multiplex real-time RT-PCR (RRT-PCR) detection method for six H5 AIV clades, three v-NDV subtypes, and one mesogenic NDV subtype was successfully established. The detection limit of our multiplex NDV and H5 AIV RRT-PCR was five copies per reaction for each pathogen, with good linearity and efficiency (y = -3.194x + 38.427 for H5 AIV and y = -3.32x + 38.042 for NDV). Multiplex PCR showed good intra- and inter-assay reproducibility, with coefficient of variance (CV) less than 1%. Furthermore, using the RRT-PCR method, H5 AIV and NDV detection rates in clinical samples were higher overall than those obtained using the traditional virus isolation method. Therefore, our method provides a promising technique for surveillance of various H5 AIV clades and multiple velogenic and mesogenic NDV subtypes in live-poultry markets.

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Year:  2019        PMID: 30790106     DOI: 10.1007/s00705-019-04180-6

Source DB:  PubMed          Journal:  Arch Virol        ISSN: 0304-8608            Impact factor:   2.574


  4 in total

1.  Rapid differential detection of subtype H1 and H3 swine influenza viruses using a TaqMan-MGB-based duplex one-step real-time RT-PCR assay.

Authors:  Kaibiao Chen; Ming Kong; Jiao Liu; Jun Jiao; Zixiong Zeng; Liwei Shi; Xinxin Bu; Yayao Yan; Yu Chen; Ruyi Gao; Xiaowen Liu; Xiaoquan Wang; Jiao Hu; Shunlin Hu; Xinan Jiao; Xiufan Liu; Min Gu
Journal:  Arch Virol       Date:  2021-06-06       Impact factor: 2.574

2.  Establishment of reverse transcription recombinase-aided amplification-lateral-flow dipstick and real-time fluorescence-based reverse transcription recombinase-aided amplification methods for detection of the Newcastle disease virus in chickens.

Authors:  Wenjing Wang; Chunguang Wang; Yun Bai; Peng Zhang; Shanshan Yao; Jingru Liu; Tie Zhang
Journal:  Poult Sci       Date:  2020-04-15       Impact factor: 3.352

3.  Cysteamine-Gold Coated Carboxylated Fluorescent Nanoparticle Mediated Point-of-Care Dual-Modality Detection of the H5N1 Pathogenic Virus.

Authors:  Kaliannan Durairaj; Duc Duong Than; Anh Thi Viet Nguyen; Hak Sung Kim; Seon-Ju Yeo; Hyun Park
Journal:  Int J Mol Sci       Date:  2022-07-19       Impact factor: 6.208

4.  Development of a Multiplex RT-qPCR for the Detection of Different Clades of Avian Influenza in Poultry.

Authors:  Tran Bac Le; Hye Kwon Kim; Woonsung Na; Van Phan Le; Min-Suk Song; Daesub Song; Dae Gwin Jeong; Sun-Woo Yoon
Journal:  Viruses       Date:  2020-01-15       Impact factor: 5.048

  4 in total

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