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Transfer and Persistence of a Multi-Drug Resistance Plasmid in situ of the Infant Gut Microbiota in the Absence of Antibiotic Treatment

机译:缺乏抗生素治疗的婴儿肠道菌群多药耐药质粒的原位转移和持久性

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摘要

The microbial ecosystem residing in the human gut is believed to play an important role in horizontal exchange of virulence and antibiotic resistance genes that threatens human health. While the diversity of gut-microorganisms and their genetic content has been studied extensively, high-resolution insight into the plasticity, and selective forces shaping individual genomes is scarce. In a longitudinal study, we followed the dynamics of co-existing Escherichia coli lineages in an infant not receiving antibiotics. Using whole genome sequencing, we observed large genomic deletions, bacteriophage infections, as well as the loss and acquisition of plasmids in these lineages during their colonization of the human gut. In particular, we captured the exchange of multidrug resistance genes, and identified a clinically relevant conjugative plasmid mediating the transfer. This resistant transconjugant lineage was maintained for months, demonstrating that antibiotic resistance genes can disseminate and persist in the gut microbiome; even in absence of antibiotic selection. Furthermore, through in vivo competition assays, we suggest that the resistant transconjugant can persist through a fitness advantage in the mouse gut in spite of a fitness cost in vitro. Our findings highlight the dynamic nature of the human gut microbiota and provide the first genomic description of antibiotic resistance gene transfer between bacteria in the unperturbed human gut. These results exemplify that conjugative plasmids, harboring resistance determinants, can transfer and persists in the gut in the absence of antibiotic treatment.
机译:据信,存在于人类肠道中的微生物生态系统在威胁人类健康的毒力和抗生素抗性基因的水平交换中起着重要作用。尽管对肠道微生物的多样性及其遗传含量进行了广泛研究,但对可塑性和形成单个基因组的选择力的高分辨率见解却很少。在一项纵向研究中,我们追踪了未接受抗生素的婴儿中共存的大肠杆菌谱系的动态。使用全基因组测序,我们观察到大的基因组缺失,噬菌体感染以及这些谱系在人类肠道定居过程中质粒的丢失和获取。特别是,我们捕获了多药耐药基因的交换,并鉴定了介导转移的临床相关缀合质粒。这种抗性转导结合谱系可以维持数月,这表明抗生素抗性基因可以在肠道微生物组中传播并持续存在。即使没有选择抗生素。此外,通过体内竞争试验,我们认为尽管体外适应性成本高,但抗性转结合剂仍可通过小鼠肠道的适应性优势而持续存在。我们的发现突出了人类肠道菌群的动态特性,并首次在不受干扰的人类肠道细菌之间进行了抗生素抗性基因转移的基因组描述。这些结果表明,在没有抗生素治疗的情况下,带有抗性决定簇的结合质粒可以转移并在肠道中持续存在。

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