文献类型： 外文期刊

作者： Lin, Yusheng ¹ ; Jiang, Jinxiu ¹ ; Zhang, Jingpeng ¹ ; You, Wei ¹ ; Hu, Qilin ¹ ;

作者机构： 1.Fujian Acad Agr Sci, Inst Anima Husb & Vet Med, Fuzhou 350013, Fujian, Peoples R China

关键词： Mycoplasma mycoides subsp. capri; TaqMan; Real-time PCR; Detection method

期刊名称：SMALL RUMINANT RESEARCH （ 影响因子：1.611； 五年影响因子：1.813 ）

ISSN： 0921-4488

年卷期： 2019 年 175 卷

页码：

收录情况： SCI

摘要： Background: The purpose of this study was to develop a real-time quantitative fluorescence polymerase chain reaction (QF-PCR) method for the rapid detection of Mycoplasma mycoides subsp. capri (Mmc). Based on the Mmc MLC_1770 gene sequence (No.FQ377874.1) from GenBank, specific primers and a TaqMan probe were designed using Beacon Designer 7.9. The recombinant plasmid of Mmc-1770 was constructed as a positive control for the construction of the standard curve and assessment of the specificity, sensitivity, and repeatability of the method. Results: The results indicated that a sensitivity of 11copies/mu L could be achieved with this detection method, which is 1000 times higher than that of conventional PCR. Cross-reactions with Mycoplasma capricolum subsp. capri pneumoniae (Mccp), Mycoplasma leachii (M. Leachii), Mycoplasma agalactiae (M.agalactiae), Mycoplasma capricolum subsp. capricolum (Mcc), Escherichia coli (E.coli), Pasteurella multocida (Pm), Staphylococcus aureus (SA), Mannheimia haemolytica (Mh), Mycoplasma arginine (M.arginini), Mycoplasma ovipneumoniae (Mo), Mycoplasma bovis (M.bovis), and orf virus (ORFV) were not observed. The intra- and inter-assay coefficients of variation were 0.60-1.52% and 0.49-0.78%, respectively, which indicated the method was highly repeatable. Subsequently, the method was used to test 188 suspected Mmc-infected samples, and Mmc was detected in 27, giving a positive rate of 14.36%. Conclusion: The results of this study demonstrate that the developed QF-PCR method has high sensitivity, specificity, and repeatability, and provides reliable technological support for the detection, prevention, and control of Mmc infection.