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Real-Time PCR for Quantitative Analysis of Human Commensal Escherichia coli Populations Reveals a High Frequency of Subdominant Phylogroups

机译:实时PCR定量分析人类共生大肠埃希氏菌种群揭示高频率的主要Phylogroups。

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Escherichia coli is divided into four main phylogenetic groups, which each exhibit ecological specialization. To understand the population structure of E. coli in its primary habitat, we directly assessed the relative proportions of these phylogroups from the stools of 100 healthy human subjects using a new real-time PCR method, which allows a large number of samples to be studied. The detection threshold for our technique was 0.1% of the E. coli population, i.e., 10~(5) CFU/g of feces; in other methods based on individual colony analysis, the threshold is 10%. One, two, three, or four phylogenetic groups were simultaneously found in 21%, 48%, 21%, and 8% of the subjects, respectively. Phylogroups present at a threshold of less than 10% of the population were found in 40% of the subjects, revealing high within-individual diversity. Phylogroups A and B2 were detected in 74% and 70% of the subjects, respectively; phylogroups B1 and D were detected in 36% and 32%, respectively. When phylogroup B2 was dominant, it tended not to cooccur with other phylogroups. In contrast, other phylogroups were present when phylogroup A was dominant. These data indicate a complex pattern of interactions between the members of a single species within the human gut and identify a reservoir of clones that are present at a low frequency. The presence of these minor clones could explain the fluctuation in the composition of the E. coli microbiota within single individuals that may be seen over time. They could also constitute reservoirs of virulent and/or resistant strains.
机译:大肠杆菌分为四个主要的系统发育类别,每个类别均具有生态专长。为了了解大肠杆菌在其主要生境中的种群结构,我们使用新的实时PCR方法直接从100名健康人的粪便中评估了这些系统群的相对比例,该方法可以研究大量样品。我们技术的检测阈值为大肠埃希菌的0.1%,即10〜(5)CFU / g粪便;在其他基于个体菌落分析的方法中,阈值为10%。在21%,48%,21%和8%的受试者中同时发现了一个,两个,三个或四个系统发育组。在40%的受试者中发现了少于种群总数10%阈值的菌群,表明个体内部多样性高。分别在74%和70%的受试者中检测到Phylogroups A和B2;系统群B1和D分别检出36%和32%。当系统群B2占优势时,它倾向于不与其他系统群同时发生。相反,当系统群A占优势时,则存在其他系统群。这些数据表明人类肠道内单个物种的成员之间相互作用的复杂模式,并鉴定出以低频率存在的克隆库。这些微小克隆的存在可以解释随着时间的流逝,单个个体中大肠杆菌微生物群组成的波动。它们也可能构成有毒力和/或抗性菌株的库。

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