Simultaneous detection and differentiation of classical Muscovy duck reovirus and goose-origin Muscovy duck reovirus by RT-qPCR assay with high-resolution melting analysis

被引:0
|
作者
Xu, Zhuoran [1 ,2 ]
Liu, Hongwei [1 ,2 ]
Zheng, Xin [2 ]
Cheng, Xiaoxia [1 ,3 ]
Wang, Shao [1 ,3 ]
You, Guangju [1 ,3 ]
Zhu, Xiaoli [1 ,3 ]
Zheng, Min [1 ,3 ]
Dong, Hui [1 ,3 ]
Xiao, Shifeng [1 ,3 ]
Zeng, Li [1 ,3 ]
Zeng, Xiancheng [2 ]
Chen, Shaoying [1 ,3 ]
Chen, Shilong [1 ,3 ]
机构
[1] Fujian Acad Agr Sci, Inst Anim Husb & Vet Med, Fuzhou, Peoples R China
[2] Fujian Agr & Forestry Univ, Coll Anim Sci, Fuzhou, Peoples R China
[3] Fujian Anim Dis Control Technol Dev Ctr, Fuzhou, Peoples R China
关键词
classical Muscovy duck reovirus; goose-origin Muscovy duck reovirus; duplex real-time RT-PCR; high-resolution melting; differential diagnosis; PCR; ANTIBODIES; INFECTION; SEQUENCE; PROTEIN; GENES;
D O I
10.3389/fvets.2024.1459898
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Introduction Classical Muscovy duck reovirus (C-MDRV) and goose-origin Muscovy duck reovirus (Go-MDRV) infections cause "Liver white-spots disease" in Muscovy duckling and gosling. It is difficult to differentiate the infections caused by C-MDRV and Go-MDRV using conventional serological methods.Methods Specific primers were designed and synthesized according to sigma NS and lambda A nucleotide sequences of C-MDRV and Go-MDRV, respectively. The PCR amplified products were cloned into the pMD-18-T vector. The recombinant plasmid DNA was used to establish an SYBR Green & Iukcy; based duplex real-time PCR assay for the simultaneous detection and differentiation of C-MDRV and Go-MDRV using high-resolution melting (HRM) analysis. The specificity, sensitivity, and repeatability of the methodology were examined based on the optimization of the reaction system and amplification conditions.Results C-MDRV and Go-MDRV were identified by their distinctive melting temperatures with 84.50 +/- 0.25 degrees C for C-MDRV and 87.50 +/- 0.20 degrees C for Go-MDRV, respectively. The amplifications were specific, and other non-targeted waterfowl viruses employed in this study did not show normalized melting peaks. The intra- and inter-assay coefficients of variations were between 0.05 and 1.83%, demonstrating good repeatability. The detection limits of this assay were 51.4 copies<middle dot>mu l-1 for C-MDRV and 61.8 copies<middle dot>mu l-1 for Go-MDRV, respectively. A total of 45 clinical samples were tested by RT-qPCR, with positive rates of 15.56% for C-MDRV and 22.22% for Go-MDRV, without co-infections.Discussion These results suggest that this duplex RT-qPCR method is highly sensitive, specific, and reproducible. The HRM assay established in this study provides a powerful tool for the differential detection and epidemiological investigation of C-MDRV and Go-MDRV.
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页数:10
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