首页> 外文期刊>Antonie van Leeuwenhoek >Transferability of a tetracycline resistance gene from probiotic Lactobacillus reuteri to bacteria in the gastrointestinal tract of humans
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Transferability of a tetracycline resistance gene from probiotic Lactobacillus reuteri to bacteria in the gastrointestinal tract of humans

机译:四环素抗性基因从益生菌罗伊氏乳杆菌到人类胃肠道细菌的转移性

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摘要

The potential of Lactobacillus reuteri as a donor of antibiotic resistance genes in the human gut was investigated by studying the transferability of the tetracycline resistance gene tet(W) to faecal enterococci, bifidobacteria and lactobacilli. In a double-blind clinical study, seven subjects consumed L. reuteri ATCC 55730 harbouring a plasmid-encoded tet(W) gene (tet(W)-reuteri) and an equal number of subjects consumed L. reuteri DSM 17938 derived from the ATCC 55730 strain by the removal of two plasmids, one of which contained the tet(W) gene. Faecal samples were collected before, during and after ingestion of 5 × 108 CFU of L. reuteri per day for 14 days. Both L. reuteri strains were detectable at similar levels in faeces after 14 days of intake but neither was detected after a two-week wash-out period. After enrichment and isolation of tetracycline resistant enterococci, bifidobacteria and lactobacilli from each faecal sample, DNA was extracted and analysed for presence of tet(W)-reuteri using a real-time PCR allelic discrimination method developed in this study. No tet(W)-reuteri signal was produced from any of the DNA samples and thus gene transfer to enterococci, bifidobacteria and lactobacilli during intestinal passage of the probiotic strain was non-detectable under the conditions tested, although transfer at low frequencies or to the remaining faecal bacterial population cannot be excluded. Keywords Allelic discrimination - Gene transferability - Human gut - Lactobacillus reuteri - Tetracycline resistance - tet(W) gene
机译:通过研究四环素抗性基因tet(W)对粪便肠球菌,双歧杆菌和乳杆菌的转移能力,研究了罗伊氏乳杆菌作为人类肠道抗药性基因供体的潜力。在一项双盲临床研究中,七名受试者摄入了带有质粒编码的tet(W)基因(tet(W)-reuteri)的罗伊氏乳杆菌ATCC 55730,同等数量的受试者食用了源自ATCC的罗伊氏乳杆菌DSM 17938通过除去两个质粒(其中一个包含tet(W)基因)来去除55730菌株。每天摄入5×10 8 罗伊氏乳杆菌14天之前,之中和之后收集粪便样品。摄入14天后,两种罗伊氏乳杆菌菌株在粪便中的检出水平相似,但经过两周的冲洗后均未检出。从每个粪便样品中富集和分离出四环素抗性肠球菌,双歧杆菌和乳杆菌后,使用本研究开发的实时PCR等位基因鉴别方法提取DNA并分析tet(W)-reuteri的存在。没有从任何DNA样品中产生tet(W)-reuteri信号,因此在测试条件下无法检测到益生菌肠通过过程中向肠球菌,双歧杆菌和乳酸杆菌的基因转移,尽管在低频或低频率下转移。不能排除剩余的粪便细菌种群。关键词等位基因歧视-基因转移性-人肠-罗伊氏乳杆菌-四环素抗性-tet(W)基因

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