Rapid and Sensitive Recombinase Polymerase Amplification Combined With Lateral Flow Strip for Detecting African Swine Fever Virus

• Published in: Frontiers in microbiology 2019-05, Vol.10, p.1004-1004
• Main Authors: Miao, Faming, Zhang, Jingyuan, Li, Nan, Chen, Teng, Wang, Lidong, Zhang, Fei, Mi, Lijuan, Zhang, Jinxia, Wang, Shuchao, Wang, Ying, Zhou, Xintao, Zhang, Yanyan, Li, Min, Zhang, Shoufeng, Hu, Rongliang
• Format: Article
• Language: English
• Subjects: African swine virus; lateral flow strip; Microbiology; on site detection; recombinase polymerase amplification; RPA-LFD
• ISSN: 1664-302X; 1664-302X
• DOI: 10.3389/fmicb.2019.01004

African swine fever virus (ASFV), the etiological agent of African swine fever (ASF), a hemorrhagic fever of domestic pigs, has devastating consequences for the pig farming industry. More than 1,000,000 pigs have been slaughtered since 3 August 2018 in China. However, vaccines or drugs for ASF have yet to be developed. As such, a rapid test that can accurately detect ASFV on-site is important to the timely implementation of control measures. In this study, we developed a rapid test that combines recombinase polymerase amplification (RPA) of the ASFV p72 gene with lateral flow detection (LFD). Results showed that the sensitivity of recombinase polymerase amplification with lateral flow dipstick (RPA-LFD) for ASFV was 150 copies per reaction within 10 min at 38°C. The assay was highly specific to ASFV and had no cross-reactions with other porcine viruses, including classical swine fever virus (CSFV). A total of 145 field samples were examined using our method, and the agreement of the positive rate between RPA-LFD (10/145) and real-time PCR (10/145) was 100%. Overall, RPA-LFD provides a novel alternative for the simple, sensitive, and specific identification of ASFV and showed potential for on-site ASFV detection.