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Phylogenetic barriers to horizontal transfer of antimicrobial peptide resistance genes in the human gut microbiota

机译:在人类肠道菌群中抗菌肽耐药基因水平转移的系统发育障碍

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摘要

The human gut microbiota has adapted to the presence of antimicrobial peptides (AMPs) that are ancient components of immune defence. Despite its medical importance, it has remained unclear whether AMP resistance genes in the gut microbiome are available for genetic exchange between bacterial species. Here we show that AMP- and antibiotic-resistance genes differ in their mobilization patterns and functional compatibilities with new bacterial hosts. First, whereas AMP resistance genes are widespread in the gut microbiome, their rate of horizontal transfer is lower than that of antibiotic resistance genes. Second, gut microbiota culturing and functional metagenomics revealed that AMP resistance genes originating from phylogenetically distant bacteria have only a limited potential to confer resistance in Escherichia coli, an intrinsically susceptible species. Taken together, functional compatibility with the new bacterial host emerges as a key factor limiting the genetic exchange of AMP resistance genes. Finally, our results suggest that AMPs induce highly specific changes in the composition of the human microbiota with implications for disease risks.
机译:人类肠道菌群已经适应了存在于免疫防御中的古老抗菌肽(AMPs)的存在。尽管具有医学重要性,但尚不清楚肠道微生物组中的AMP抗性基因是否可用于细菌物种之间的遗传交换。在这里,我们显示AMP和抗生素抗性基因的动员模式和与新细菌宿主的功能兼容性不同。首先,虽然AMP抗性基因广泛分布在肠道微生物组中,但是它们的水平转移速率却低于抗生素抗性基因。其次,肠道菌群的培养和功能性宏基因组学研究表明,源自系统发育远缘细菌的AMP抗性基因在固有的易感性大肠杆菌中具有有限的潜力。综上所述,与新细菌宿主的功能相容性成为限制AMP抗性基因遗传交换的关键因素。最后,我们的结果表明AMPs会导致人类微生物群组成的高度特异性变化,从而影响疾病风险。

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