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C 型禽偏肺病毒逆转录酶重组酶介导扩增检测方法的建立及应用前景

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

作者信息

Bai Yuhang, Wu Xiuhong, Liu Jiajia, Wang Zhanxin, Dong Mengyue, Li Tong, Dai Zhenkai, Li Hongxin, Xie Qingmei, Zhang Xinheng

机构信息

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.

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

出版信息

Vet Sci. 2024 Mar 7;11(3):122. doi: 10.3390/vetsci11030122.

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 × 10 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.

摘要

在肉鸡中,导致肿头综合征(SHS)的主要病原体是C亚群禽偏肺病毒(aMPV-C)。aMPV-C感染会导致软壳蛋比率上升,从而使产蛋量减少,并严重影响畜牧业经济。因此,需要发明一种快速检测aMPV-C的方法。根据aMPV-C的N基因,我们设计了特异性探针和引物,并创建了一种用于检测aMPV-C的逆转录重组酶辅助扩增检测法(RT-RAA)。通过该方法可在41℃下30分钟快速、特异性地检测到aMPV-C。敏感性分析推断RT-RAA的最低检测阈值为3.38×10拷贝/μL。特异性分析表明,RT-RAA方法与其他亚群(aMPV-A、aMPV-B、aMPV-D)或其他病毒(H9N2、NDV、IBV、IBDV)无交叉反应。用RT-RAA和RT-qPCR对40份已知临床背景的样本进行检测。两种方法的符合率为100%。总之,本研究成功创建了一种用于检测aMPV-C的RT-RAA检测法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4747/10975772/0d8aae54706b/vetsci-11-00122-g001.jpg

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