Establishment and Application Prospect of Reverse Transcriptase Recombinase-Aided Amplification Assay for Subgroup C Avian Metapneumovirus

Author:

Bai Yuhang12345,Wu Xiuhong12345,Liu Jiajia6,Wang Zhanxin6,Dong Mengyue12345,Li Tong12345,Dai Zhenkai12345,Li Hongxin12345,Xie Qingmei12345,Zhang Xinheng12345ORCID

Affiliation:

1. State Key Laboratory of Swine and Poultry Breeding Industry & Heyuan Branch, Guangdong Provincial Laboratory of Lingnan Modern Agricultural Science and Technology, College of Animal Science, South China Agricultural University, Guangzhou 510642, China

2. Guangdong Engineering Research Center for Vector Vaccine of Animal Virus, Guangzhou 510642, China

3. South China Collaborative Innovation Center for Poultry Disease Control and Product Safety, Guangzhou 510642, China

4. Key Laboratory of Animal Health Aquaculture and Environmental Control, Guangzhou 510642, China

5. Guangdong Provincial Key Laboratory of AgroAnimal Genomics and Molecular Breeding, College of Animal Science, South China Agricultural University, Guangzhou 510642, China

6. Guangdong Wen’s Foodstuffs Group Co., Ltd., Yunfu 527439, China

Abstract

Among broilers, the main pathogen that leads to swollen head syndrome (SHS) is the subgroup C avian metapneumovirus (aMPV-C). The aMPV-C infection can lead to an upsurge in the rate of soft-shell eggs, resulting in reduced egg production and seriously affecting the economy of the livestock industry. Therefore, a rapid method for aMPV-C detection needs to be invented. According to the N gene of aMPV-C, we designed the specific probe and primer and created a reverse transcription recombinase-aided amplification assay (RT-RAA) for the detection of aMPV-C. aMPV-C could be detected quickly and specifically by this method at 41 °C for 30 min. The sensitivity assay inferred that the minimum detection threshold of RT-RAA was 3.38 × 101 copies/μL. A specificity assay showed that the RT-RAA method did not cross-react with other subgroups (aMPV-A, aMPV-B, aMPV-D) or other viruses (H9N2, NDV, IBV, IBDV). Forty samples of known clinical background were tested by RT-RAA and RT-qPCR. The two approaches had a 100% correlation rate. In conclusion, this research successfully created an RT-RAA assay for aMPV-C.

Funder

Guangdong Basic and Applied Basic Research Foundation

Heyuan Branch, Guangdong Laboratory for Lingnan Modern Agriculture Project

Natural Science Foundation of Guangzhou

China Agriculture Research System of MOF and MARA

Guangdong Provincial Key R&D Program

construction project of modern agricultural science and technology innovation alliance in Guangdong province

Special Project of National Modern Agricultural Industrial Technology System

Science and Technology Program of Guangdong province, China

Provincial Science and Technology Special Fund Project for Zhongshan City

Publisher

MDPI AG

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