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

Kaikai Jin1Junjie Zhao1,3Huanxin Chen1Zimo Zhang1Zengguo Cao2Zanheng Huang1Hao Li1Yongsai Liu1Lisi Ai1Yufei Liu1Changqi Fan4Yuanyuan Li1Pei Huang1( )Hualei Wang1( )Haili Zhang1( )
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, Changchun 130062, China
Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Center for Biosafety Mega-Science, Chinese Academy of Sciences, Wuhan 430071, China
National/WOAH Reference Laboratory for Classical Swine Fever, China Institute of Veterinary Drug Control, Beijing 100081, China
Zhili College, Tsinghua University, Beijing 100084, China
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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.

References

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Journal of Integrative Agriculture (JIA)
Pages 790-794

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Cite this article:
Jin K, Zhao J, Chen H, et al. On-site visual detection of Nipah virus combining a reverse transcription recombinase-aided amplification with a lateral-flow dipstick assay. Journal of Integrative Agriculture (JIA), 2025, 24(2): 790-794. https://doi.org/10.1016/j.jia.2024.11.018

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Received: 19 April 2024
Accepted: 24 September 2024
Published: 20 February 2025
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