Development of an isothermal recombinase polymerase amplification assay for rapid detection of pseudorabies virus.

Abstract:

:Recombinase polymerase amplification assays using real-time fluorescent detection (real-time RPA assay) and lateral flow dipstick (RPA LFD assay) were developed targeting the gD gene of pseudorabies virus (PRV). Both assays were performed at 39 °C within 20 min. The sensitivity of the real-time RPA assay and the RPA LFD assay was 100 copies per reaction and 160 copies per reaction, respectively. Both assays did not detect DNAs from other virus or PRV negative samples. Therefore, the developed RPA assays provide a rapid, simple, sensitive and specific alternative tool for detection of PRV.

journal_name

Mol Cell Probes

authors

Yang Y,Qin X,Zhang W,Li Z,Zhang S,Li Y,Zhang Z

doi

10.1016/j.mcp.2017.03.005

subject

Has Abstract

pub_date

2017-06-01 00:00:00

pages

32-35

eissn

0890-8508

issn

1096-1194

pii

S0890-8508(17)30030-0

journal_volume

33

pub_type

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