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An in vitro chicken gut model demonstrates transfer of a multidrug resistance plasmid from Salmonella to commensal Escherichia coli

机译:体外鸡肠道模型证明沙门氏菌有多重耐药质粒转移到大肠杆菌中

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摘要

The chicken gastrointestinal tract is richly populated by commensal bacteria that fulfill various beneficial roles for the host, including helping to resist colonization by pathogens. It can also facilitate the conjugative transfer of multidrug resistance (MDR) plasmids between commensal and pathogenic bacteria which is a significant public and animal health concern as it may affect our ability to treat bacterial infections. We used an in vitro chemostat system to approximate the chicken cecal microbiota, simulate colonization by an MDR Salmonella pathogen, and examine the dynamics of transfer of its MDR plasmid harboring several genes, including the extended-spectrum beta-lactamase blaCTX-M1 We also evaluated the impact of cefotaxime administration on plasmid transfer and microbial diversity. Bacterial community profiles obtained by culture-independent methods showed that Salmonella inoculation resulted in no significant changes to bacterial community alpha diversity and beta diversity, whereas administration of cefotaxime caused significant alterations to both measures of diversity, which largely recovered. MDR plasmid transfer from Salmonella to commensal Escherichia coli was demonstrated by PCR and whole-genome sequencing of isolates purified from agar plates containing cefotaxime. Transfer occurred to seven E. coli sequence types at high rates, even in the absence of cefotaxime, with resistant strains isolated within 3 days. Our chemostat system provides a good representation of bacterial interactions, including antibiotic resistance transfer in vivo It can be used as an ethical and relatively inexpensive approach to model dissemination of antibiotic resistance within the gut of any animal or human and refine interventions that mitigate its spread before employing in vivo studies.IMPORTANCE The spread of antimicrobial resistance presents a grave threat to public health and animal health and is affecting our ability to respond to bacterial infections. Transfer of antimicrobial resistance via plasmid exchange is of particular concern as it enables unrelated bacteria to acquire resistance. The gastrointestinal tract is replete with bacteria and provides an environment for plasmid transfer between commensals and pathogens. Here we use the chicken gut microbiota as an exemplar to model the effects of bacterial infection, antibiotic administration, and plasmid transfer. We show that transfer of a multidrug-resistant plasmid from the zoonotic pathogen Salmonella to commensal Escherichia coli occurs at a high rate, even in the absence of antibiotic administration. Our work demonstrates that the in vitro gut model provides a powerful screening tool that can be used to assess and refine interventions that mitigate the spread of antibiotic resistance in the gut before undertaking animal studies.
机译:鸡胃肠道中富含共生细菌,这些共生细菌对宿主具有多种有益作用,包括帮助抵抗病原体的定殖。它还可以促进共生细菌和病原细菌之间的多药耐药性(MDR)质粒的共轭转移,这是公共和动物健康的重要问题,因为它可能会影响我们治疗细菌感染的能力。我们使用了体外化学恒温器系统来近似鸡盲肠菌群,模拟由MDR沙门氏菌病原菌定殖的情况,并检查了其MDR质粒包含多个基因(包括广谱β-内酰胺酶blaCTX-M1)的转移动力学。头孢噻肟给药对质粒转移和微生物多样性的影响。通过不依赖培养的方法获得的细菌群落概况表明,接种沙门氏菌不会导致细菌群落的α多样性和β多样性发生显着变化,而头孢噻肟的施用对两种多样性的测量结果均产生了显着变化,并在很大程度上得到了恢复。通过PCR和从含有头孢噻肟的琼脂平板纯化的分离株的全基因组测序证实了MDR质粒从沙门氏菌到共生大肠埃希菌的转移。即使在没有头孢噻肟的情况下,也可以高速率转移至7种大肠杆菌序列类型,并在3天内分离出耐药菌株。我们的化学恒温器系统很好地代表了细菌相互作用,包括体内的抗生素耐药性转移。它可以作为一种道德且相对便宜的方法来模拟抗生素抗性在任何动物或人类肠道中的传播,并完善可减轻其传播的干预措施重要信息抗菌素耐药性的传播对公共健康和动物健康构成了严重威胁,并正在影响我们对细菌感染的反应能力。通过质粒交换转移抗药性耐药性尤其令人关注,因为它使无关的细菌获得耐药性。胃肠道充满细菌,并为质粒在病原体和病原体之间的转移提供了环境。在这里,我们以鸡肠道菌群为例来模拟细菌感染,抗生素施用和质粒转移的影响。我们表明,从人畜共患病病原体沙门氏菌到共生大肠埃希菌的多药耐药质粒转移发生率很高,即使没有抗生素施用也是如此。我们的工作表明,体外肠道模型提供了一个强大的筛选工具,可用于评估和改进干预措施,以减轻动物肠道中抗生素耐药性在肠道中的扩散。

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