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Molecular Ecology of Tetracycline Resistance: Development and Validation of Primers for Detection of Tetracycline Resistance Genes Encoding Ribosomal Protection Proteins

机译:四环素抗性的分子生态学:用于检测编码核糖体保护蛋白的四环素抗性基因的引物的开发和验证

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摘要

Phylogenetic analysis of tetracycline resistance genes encoding the ribosomal protection proteins (RPPs) revealed the monophyletic origin of these genes. The most deeply branching class, exemplified by tet and otrA, consisted of genes from the antibiotic-producing organisms Streptomyces rimosus and Streptomyces lividans. With a high degree of confidence, the corresponding genes of the other seven classes (Tet M, Tet S, Tet O, Tet W, Tet Q, Tet T, and TetB P) formed phylogenetically distinct separate clusters. Based on this phylogenetic analysis, a set of PCR primers for detection, retrieval, and sequence analysis of the corresponding gene fragments from a variety of bacterial and environmental sources was developed and characterized. A pair of degenerate primers targeted all tetracycline resistance genes encoding RPPs except otrA and tet, and seven other primer pairs were designed to target the specific classes. The primers were used to detect the circulation of these genes in the rumina of cows, in swine feed and feces, and in swine fecal streptococci. Classes Tet O and Tet W were found in the intestinal contents of both animals, while Tet M was confined to pigs and Tet Q was confined to the rumen. The tet(O) and tet(W) genes circulating in the microbiota of the rumen and the gastrointestinal tract of pigs were identical despite the differences in animal hosts and antibiotic use regimens. Swine fecal streptococci uniformly possessed the tet(O) gene, and 22% of them also carried tet(M). This population could be considered one of the main reservoirs of these two resistance genes in the pig gastrointestinal tract. All classes of RPPs except Tet T and TetB P were found in the commercial components of swine feed. This is the first demonstration of the applicability of molecular ecology techniques to estimation of the gene pool and the flux of antibiotic resistance genes in production animals.
机译:编码核糖体保护蛋白(RPPs)的四环素抗性基因的系统发生分析揭示了这些基因的单系起源。以tet和otrA为例,是分支最深的一类,该类来自产生抗生素的生物rimosus和lividans链霉菌的基因。具有高度的置信度,其他七个类别(Tet M,Tet S,Tet O,Tet W,Tet Q,Tet T和TetB P)的相应基因形成了系统发育上不同的单独簇。基于这种系统发育分析,开发并鉴定了一套PCR引物,用于检测,检索和分析来自各种细菌和环境来源的相应基因片段。一对简并引物靶向除otrA和tet外的所有编码RPP的四环素抗性基因,另外七对引物被设计成针对特定类别。引物用于检测这些基因在牛瘤胃,猪饲料和粪便以及猪粪链球菌中的循环。在两只动物的肠内容物中都发现了Tet O和Tet W类,而Tet M只限于猪,Tet Q只限于瘤胃。尽管动物宿主和抗生素使用方案存在差异,但在猪瘤胃和胃肠道微生物群中循环的tet(O)和tet(W)基因相同。猪粪链球菌均具有tet(O)基因,其中22%还携带tet(M)。该种群可被认为是猪胃肠道中这两个抗性基因的主要储库之一。在猪饲料的商业成分中发现了除Tet T和TetB P外的所有RPP类。这是分子生态技术在生产动物中评估基因库和抗生素抗性基因通量的适用性的首次证明。

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