Detection of influenza A virus from live-bird market poultry swab samples in China by a pan-IAV, one-step reverse-transcription FRET-PCR

被引:12
作者
Luan, Lu [1 ]
Sun, Zhihao [1 ]
Kaltenboeck, Bernhard [2 ]
Huang, Ke [1 ]
Li, Min [1 ]
Peng, Daxin [1 ]
Xu, Xiulong [1 ]
Ye, Jianqiang [1 ]
Li, Jing [1 ]
Guo, Weina [1 ]
Wang, Chengming [1 ,2 ]
机构
[1] Yangzhou Univ, Coll Vet Med, Jiangsu Coinnovat Ctr Prevent & Control Important, Yangzhou, Jiangsu, Peoples R China
[2] Auburn Univ, Coll Vet Med, Auburn, AL USA
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
关键词
MULTIPLEX RT-PCR; EASTERN CHINA; A(H7N9) VIRUS; ASSAY; AMPLIFICATION; TRANSMISSION; SUBTYPES; QPCR; H7N9; H5N1;
D O I
10.1038/srep30015
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The persistent public health threat of animal to human transmission of influenza A virus (IAV) has stimulated interest in rapid and accurate detection of all IAV subtypes in clinical specimens of animal origin. In this study, a new set of primers and probes was designed for one-step pan-IAV reverse-transcription fluorescence resonance energy transfer (FRET)-PCR. The detection limit of one-step pan-IAV RT FRET-PCR was 10 copies of the matrix gene per reaction, and proved to be equivalent or superior to virus isolation in detecting nine IAV subtypes. Application of the pan-IAV RT FRET-PCR to oral-pharyngeal and cloacal swab specimens collected from healthy poultry in 34 live bird markets in 24 provinces of China revealed that 9.2% of the animals (169/1,839) or 6.3% of their oral-pharyngeal or cloacal swabs (233/3,678) were positive for IAV, and 56.8% of IAV-positive samples were of the H9N2 subtype. Paralleling detection of IAV in H9N2-infected SPF chickens and chickens from LBM showed that pan-IAV FRET-PCR had a higher detection limit than virus isolation in eggs while the results by FRET-PCR and virus isolation overall matched. It is expected that this strategy can be useful for facile surveillance for IAV in clinical samples from a variety of sources.
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收藏
页数:9
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