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Development of a reverse-transcription recombinase polymerase amplification assay with a lateral flow assay for rapid detection of avian orthoavulavirus 1
Author(s) -
Jindai Fan,
Wenxian Chen,
Yuanyuan Zhang,
Zhixiang Liu,
Xiaoming Li,
Hongxing Ding,
Lin Yi,
Jinding Chen,
Mingqiu Zhao
Publication year - 2021
Publication title -
journal of veterinary diagnostic investigation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.529
H-Index - 78
eISSN - 1943-4936
pISSN - 1040-6387
DOI - 10.1177/1040638721990122
Subject(s) - recombinase polymerase amplification , newcastle disease , virology , biology , reverse transcriptase , reverse transcription polymerase chain reaction , virus , polymerase chain reaction , complementary dna , real time polymerase chain reaction , recombinase , microbiology and biotechnology , messenger rna , gene , genetics , recombination
Newcastle disease is an avian infectious disease caused by avian orthoavulavirus 1, also known as Newcastle disease virus (NDV). This disease has caused significant economic losses to the poultry industry worldwide. The rapid and simple detection of NDV infection is crucial to inform the appropriate control measures. We developed a reverse-transcription recombinase polymerase amplification (RT-RPA) assay combined with a lateral flow assay (LFA) for NDV detection. The RPA assay can be completed at 37°C within 20 min, and the RPA result can be visualized by the LFA within 5 min. The NDV RT-RPA-LFA detected NDV specifically with no cross-reactivity with other pathogens. The detection limit of NDV cDNA with our RT-RPA-LFA was 3.34 × 10 -3  ng/μL. Consequently, the RT-RPA-LFA showed good potential for the detection of NDV infection in the field, especially in resource-limited settings.

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