On-site visual detection of Nipah virus combining a reverse transcription recombinase-aided amplification with a lateral-flow dipstick assay

被引:0
|
作者
Kaikai Jin [1 ]
Junjie Zhao [1 ,2 ]
Huanxin Chen [1 ]
Zimo Zhang [1 ]
Zengguo Cao [3 ]
Zanheng Huang [1 ]
Hao Li [1 ]
Yongsai Liu [1 ]
Lisi Ai [1 ]
Yufei Liu [1 ]
Changqi Fan [4 ]
Yuanyuan Li [1 ]
Pei Huang [1 ]
Hualei Wang [1 ]
Haili Zhang [1 ]
机构
[1] State Key Laboratory for Diagnosis and Treatment of Severe Zoonotic Infectious Diseases/Key Laboratory for Zoonosis Research of the Ministry of Education/Institute of Zoonosis, College of Veterinary Medicine, Jilin University
[2] National/WOAH Reference Laboratory for Classical Swine Fever, China Institute of Veterinary Drug Control
[3] Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences
[4] Zhili College, Tsinghua
关键词
D O I
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中图分类号
S852.65 [家畜病毒学];
学科分类号
摘要
<正>Highlights The RT-RAA-VF assay developed for the NiV P gene can perform rapid detection of NiV within 20 min at 42°C with high specificity.This assay is capable of attaining sensitivity to a single copy of NiV RNA transcripts.This assay effectively avoids false positives caused by aerosol contamination with a sealed disposable nucleic acid visualization test paper device.
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收藏
页码:790 / 794
页数:5
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