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Novel Insights into Selection for Antibiotic Resistance in Complex Microbial Communities

机译:对复杂微生物群落中抗生素耐药性选择的新见解

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ABSTRACT Recent research has demonstrated that selection for antibiotic resistance occurs at very low antibiotic concentrations in single-species experiments, but the relevance of these findings when species are embedded in complex microbial communities is unclear. We show that the strength of selection for naturally occurring resistance alleles in a complex community remains constant from low subinhibitory to above clinically relevant concentrations. Selection increases with antibiotic concentration before reaching a plateau where selection remains constant over a 2-order-magnitude concentration range. This is likely to be due to cross protection of the susceptible bacteria in the community following rapid extracellular antibiotic degradation by the resistant population, shown experimentally through a combination of chemical quantification and bacterial growth experiments. Metagenome and 16S rRNA analyses of sewage-derived bacterial communities evolved under cefotaxime exposure show preferential enrichment for bla _(CTX-M)genes over all other beta-lactamase genes, as well as positive selection and co-selection for antibiotic resistant, opportunistic pathogens. These findings have far-reaching implications for our understanding of the evolution of antibiotic resistance, by challenging the long-standing assumption that selection occurs in a dose-dependent manner. IMPORTANCE Antibiotic resistance is one of the greatest global issues facing society. Still, comparatively little is known about selection for resistance at very low antibiotic concentrations. We show that the strength of selection for clinically important resistance genes within a complex bacterial community can remain constant across a large antibiotic concentration range (wide selective space). Therefore, largely understudied ecological compartments could be just as important as clinical environments for selection of antibiotic resistance.
机译:摘要最近的研究表明,在单物种实验中,对抗生素耐药性的选择发生在非常低​​的抗生素浓度下,但是当物种被嵌入复杂的微生物群落中时,这些发现的相关性还不清楚。我们表明,从低亚抑制作用到高于临床相关浓度,对于复杂社区中天然存在的抗性等位基因的选择强度保持恒定。在达到高原(在2数量级浓度范围内保持不变)之前,抗生素浓度随选择的增加而增加。通过化学定量和细菌生长实验相结合的实验表明,这是由于耐药菌群迅速引起细胞外抗生素降解后,社区中易感细菌的交叉保护所致。头孢噻肟暴露下进化的污水来源细菌群落的元基因组和16S rRNA分析显示,bla _(CTX-M)基因比其他所有β-内酰胺酶基因优先富集,并对抗生素抗性,机会病原体进行正选择和共选择。通过挑战长期以来的假设,即选择以剂量依赖性方式进行,这些发现对我们对抗生素耐药性演变的理解具有深远的意义。重要事项抗生素耐药性是社会面临的最大的全球性问题之一。但是,关于在非常低的抗生素浓度下选择抗药性的了解还很少。我们表明,在复杂的细菌群落中具有重要临床意义的抗性基因的选择强度可以在较大的抗生素浓度范围(较宽的选择性空间)内保持恒定。因此,对于抗生素抗性的选择,在很大程度上未被研究的生态区隔可能与临床环境一样重要。

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