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Differentiation between Mycobacterium farcinogenes and Mycobacterium senegalense Strains Based on 16S-23S Ribosomal DNA Internal Transcribed Spacer Sequences

机译:基于16S-23S核糖体DNA内部转录间隔区序列的分支杆菌分枝杆菌和塞内加尔分枝杆菌菌株的区分

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摘要

16S ribosomal DNA (rDNA) and 16S-23S internal transcribed spacer rDNA sequence analyses were performed on Mycobacterium farcinogenes and M. senegalense strains and 26 strains of other rapidly growing mycobacteria to investigate the phylogenetic structure of bovine farcy mycobacteria within the M. fortuitum complex. M. farcinogenes and M. senegalense were indistinguishable in their 5"-end 16S rDNA but showed both considerable interspecies spacer sequence divergence and a high level of intraspecies sequence stability. A rapid detection assay using PCR and hybridization with species-specific probes was developed. The assay was specific among 46 species other than M. farcinogenes and M. senegalense and correctly identified all M. farcinogenes and M. senegalense strains. PCR- and 16S-23S rDNA sequence-based detection will be a valuable approach for diagnosis of the causal agents of African bovine farcy in cattle.
机译:分别对杆状分枝杆菌和塞内加尔分枝杆菌菌株以及其他26个快速增长的分枝杆菌菌株进行16S核糖体DNA(rDNA)和16S-23S内部转录间隔区rDNA序列分析,以研究牛分枝杆菌复合物中牛毛状分枝杆菌的系统发育结构。 farcinogenes和M. senegalense在其5“-末端16S rDNA中没有区别,但显示出相当大的种间间隔序列差异和很高的种内序列稳定性。开发了一种使用PCR的快速检测方法以及与物种特异性探针杂交的方法。该检测方法对除了产甲烷链球菌和塞内加尔穆尔氏菌以外的46个物种具有特异性,并正确鉴定了所有产甲烷杆菌和塞内加尔氏菌菌株,基于PCR和16S-23S rDNA序列的检测将是诊断病因的有价值的方法非洲牛闹事在牛中的作用。

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