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Rapid Diagnosis of Avian Influenza Virus in Wild Birds: Use of a Portable rRT-PCR and Freeze-dried Reagents in the Field
Published on: August 2, 2011
Loop-mediated isothermal amplification combined with a Pyrococcus furiosus argonaute system for the rapid detection
Fosheng Yang1, Zhong Liu1, Jianqiang Ye2
1Nanchang Key Laboratory of Novel Prevention and Control Agents for Animal Infectious Diseases, Institute of Animal Disease Prevention and Control, Jiangxi Agricultural University, College of Animal Science and Technology, Jiangxi Agricultural University, Nanchang, Jiangxi 330045, China; Jiangxi Provincial Engineering Technology Center for Animal Disease Prevention and Control Agents, Nanchang, Jiangxi 330045, China.
Abstract:
Goose astrovirus (GAstV) is a newly emerged viral pathogen in goose, characterized by a high incidence and significant mortality rates. This etiology has repeatedly occurred in coastal areas of China, rapidly spreading to inland provinces in recent decade, and thus imposed huge economic losses on China's goose industry. Therefore, it is essential to establish a rapid, accurate and sensitive method for GAstV diagnosis. In this study, we employed reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay combined with a Pyrococcus furiosus Argonaute (PfAgo) system, providing a simple and precise approach for GAstV. Specific primers and guide DNA (gDNA) were designed to target conserved regions of the GAstV genome. The assay achieved a detection limit of 10 copies/μL in preliminary validation assays when targeting conserved regions of the viral genome with optimized reaction conditions. Importantly, the assay exhibited no cross-reactivity with other viruses, including Goose parvovirus (GPV), Goose circovirus (GoCV), Tembusu Virus (TMUV), Muscovy Duck Reovirus (MDRV), and Escherichia coli (E. coli). Detection results from 59 clinical samples demonstrated complete concordance in positive rates between the LAMP-PfAgo and qPCR methods.
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