Establishment and field validation of a rapid on-site recombinase polymerase amplification–lateral flow assay for BRSV and BVDV
Zhiteng Zhao, Yanbing Guo, Shaoxiong Liu, Liangyu Hao, Xingzhong Sun, Yu Xiang, Nan Wang, Xiangyu Meng, Hongbo Sun, Shuai Yue, Pengtao Gong, Lili Cao

TL;DR
This paper introduces a fast, on-site diagnostic test for two viruses causing bovine respiratory disease, enabling quick detection and treatment decisions.
Contribution
The novel contribution is a rapid, single-tube field test using recombinase amplification and lateral flow for BRSV and BVDV detection.
Findings
The assay detected as few as 10 viral RNA copies with 100% specificity against related pathogens.
Field testing in China showed 10.87% BRSV and 8.70% BVDV positivity in cattle nasal swabs.
Results matched qPCR and were obtained in 30 minutes without lab equipment.
Abstract
Bovine respiratory disease (BRD) is the costliest bovine syndrome worldwide, inflicting annual losses of over one billion USD in North America alone. Transport stress, overcrowding and viral–bacterial synergy can drive mortality to 70%, yet laboratory-based diagnostics delay decisive treatment. We therefore developed pen-side real-time enzymatic recombinase amplification lateral-flow dipsticks (RT-ERA-LFD) assays targeting the two principal viral agents, bovine respiratory syncytial virus (BRSV) and bovine viral diarrhoea virus (BVDV), which enables their separate detection in a single tube. The BRSV nucleoprotein gene and BVDV 5’-UTR were cloned and in-vitro transcribed into quantified RNA standards to calibrate an enzymatic recombinase amplification (ERA) coupled with lateral-flow dipsticks (LFD). After primer/probe optimisation (BRSV-ERA-F1/R4/P2; BVDV-ERA-F1/R4/P1), the 40 °C,…
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Taxonomy
TopicsRespiratory viral infections research · Microbial infections and disease research · Animal Disease Management and Epidemiology
