Development and application of a triplex real-time PCR assay for simultaneous detection of avian influenza virus, Newcastle disease virus, and duck Tembusu virus

被引:21
作者
Zhang, Xiyu [1 ,2 ]
Yao, Ming [1 ]
Tang, Zhihui [1 ]
Xu, Daning [3 ]
Luo, Yan [4 ]
Gao, Yunfei [5 ]
Yan, Liping [1 ,2 ]
机构
[1] Nanjing Agr Univ, Coll Vet Med, Nanjing 210095, Peoples R China
[2] Nanjing Agr Univ, MOE Joint Int Res Lab Anim Hlth & Food Safety, Nanjing 210095, Peoples R China
[3] Zhongkai Univ Agr & Engn, Guangdong Prov Key Lab Waterfowl Hlth Breeding, Guangzhou 510225, Peoples R China
[4] Shenzhen Ctr Inspect & Testing Agr Prod, Guangdong Prov Key Lab Supervis Edible Agr Prod, Adm Market Regulat, Shenzhen 518000, Peoples R China
[5] Jofunhwa Biotechnol Nanjing Co Ltd, Nanjing 211102, Peoples R China
关键词
Real-time PCR; AIV; NDV; DTMUV; Ducks; Clinical detection; RAPID DETECTION; RT-PCR; MULTIPLEX PCR; A VIRUSES; IDENTIFICATION; H5; DIFFERENTIATION; MICROBIOLOGY; VALIDATION; ELECTRON;
D O I
10.1186/s12917-020-02399-z
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Background Pathogens including duck-origin avian influenza virus (AIV), duck-origin Newcastle disease virus (NDV) and duck Tembusu virus (DTMUV) posed great harm to ducks and caused great economic losses to the duck industry. In this study, we aim to develop a triplex real-time polymerase chain reaction (PCR) assay to detect these three viruses as early as possible in the suspicious duck flocks. Results The detection limit of the triplex real-time PCR for AIV, NDV, and DTMUV was 1 x 10(1)copies/mu L, which was at least 10 times higher than the conventional PCR. In addition, the triplex assay was highly specific, and won't cross-react with other duck pathogens. Besides, the intra-day relative standard deviation and inter-day relative standard deviation were lower than 4.44% for these viruses at three different concentrations. Finally, a total of 120 clinical samples were evaluated by the triplex real-time PCR, the conventional PCR and virus isolation, and the positive rates for these three methods were 20.83, 21.67, 19.17%, respectively. Taking virus isolation as the gold standard, the diagnostic specificity and positive predictive value of the three viruses were all above 85%, while the diagnostic sensitivity and negative predictive value of the three viruses were all 100%. Conclusion The developed triplex real-time PCR is fast, specific and sensitive, and is feasible and effective for the simultaneous detection of AIV, NDV, and DTMUV in ducks.
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页数:12
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