首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Extensive Within-Host Diversity in Fecally Carried Extended-Spectrum-Beta-Lactamase-Producing Escherichia coli Isolates: Implications for Transmission Analyses
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Extensive Within-Host Diversity in Fecally Carried Extended-Spectrum-Beta-Lactamase-Producing Escherichia coli Isolates: Implications for Transmission Analyses

机译:粪便携带的产生广谱β-内酰胺酶的大肠杆菌分离物中广泛的宿主内多样性:对传播分析的影响。

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摘要

Studies of the transmission epidemiology of antimicrobial-resistant Escherichia coli, such as strains harboring extended-spectrum beta-lactamase (ESBL) genes, frequently use selective culture of rectal surveillance swabs to identify isolates for molecular epidemiological investigation. Typically, only single colonies are evaluated, which risks underestimating species diversity and transmission events. We sequenced the genomes of 16 E. coli colonies from each of eight fecal samples (n = 127 genomes; one failure), taken from different individuals in Cambodia, a region of high ESBL-producing E. coli prevalence. Sequence data were used to characterize both the core chromosomal diversity of E. coli isolates and their resistance/virulence gene content as a proxy measure of accessory genome diversity. The 127 E. coli genomes represented 31 distinct sequence types (STs). Seven (88%) of eight subjects carried ESBL-positive isolates, all containing blaCTX-M variants. Diversity was substantial, with a median of four STs/individual (range, 1 to 10) and wide genetic divergence at the nucleotide level within some STs. In 2/8 (25%) individuals, the same blaCTX-M variant occurred in different clones, and/or different blaCTX-M variants occurred in the same clone. Patterns of other resistance genes and common virulence factors, representing differences in the accessory genome, were also diverse within and between clones. The substantial diversity among intestinally carried ESBL-positive E. coli bacteria suggests that fecal surveillance, particularly if based on single-colony subcultures, will likely underestimate transmission events, especially in high-prevalence settings.
机译:对耐药性大肠埃希菌的传播流行病学的研究,例如带有超广谱β-内酰胺酶(ESBL)基因的菌株,经常使用直肠监测拭子的选择性培养来鉴定用于分子流行病学研究的分离株。通常,仅评估单个菌落,这可能会低估物种多样性和传播事件。我们对八个粪便样本(n = 127个基因组;一个失败)中的每一个样本的16个大肠杆菌菌落的基因组进行了测序,这些样本取自柬埔寨高ESBL患病率地区的不同个体。序列数据用于表征大肠杆菌分离物的核心染色体多样性及其抗性/毒力基因含量,作为辅助基因组多样性的一种度量。 127个大肠杆菌基因组代表31种不同的序列类型(ST)。 8名受试者中有7名(88%)携带ESBL阳性分离株,均含有blaCTX-M变体。多样性是巨大的,每个个体中位数为四个ST(范围为1至10),并且在某些ST的核苷酸水平上存在广泛的遗传差异。在2/8(25%)的个体中,相同的blaCTX-M变体出现在不同的克隆中,和/或不同的blaCTX-M变体出现在同一克隆中。在克隆内部和克隆之间,代表辅助基因组差异的其他抗性基因和常见毒力因子的模式也各不相同。肠内携带的ESBL阳性大肠杆菌细菌之间的大量差异表明,粪便监测(尤其是基于单菌群亚培养的粪便监测)可能会低估传播事件,尤其是在高流行地区。

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