Stoesser N, Sheppard A E, Moore C E, Golubchik T, Parry C M, Nget P, Saroeun M, Day N P J, Giess A, Johnson J R, Peto T E A, Crook D W, Walker A S
Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom NIHR Biomedical Research Center, University of Oxford/Oxford University Hospitals NHS Trust, Oxford, United Kingdom
NIHR Biomedical Research Center, University of Oxford/Oxford University Hospitals NHS Trust, Oxford, United Kingdom.
J Clin Microbiol. 2015 Jul;53(7):2122-31. doi: 10.1128/JCM.00378-15. Epub 2015 Apr 22.
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.
对抗菌素耐药性大肠杆菌(如携带超广谱β-内酰胺酶(ESBL)基因的菌株)传播流行病学的研究,经常采用直肠监测拭子的选择性培养来鉴定分离株,以便进行分子流行病学调查。通常情况下,仅对单个菌落进行评估,这有可能低估物种多样性和传播事件。我们对来自柬埔寨8份粪便样本(n = 127个基因组;1次失败)中每份样本的16个大肠杆菌菌落进行了基因组测序,这些样本取自不同个体,柬埔寨是产ESBL大肠杆菌患病率较高的地区。序列数据用于表征大肠杆菌分离株的核心染色体多样性及其耐药/毒力基因含量,作为辅助基因组多样性的替代指标。这127个大肠杆菌基因组代表了31种不同的序列类型(STs)。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。多样性很大,个体中STs的中位数为4种(范围为1至10种),并且在某些STs内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。代表辅助基因组差异的其他耐药基因和常见毒力因子的模式,在克隆内部和克隆之间也存在差异。肠道携带的ESBL阳性大肠杆菌之间存在的大量多样性表明,粪便监测,特别是基于单菌落传代培养的监测,可能会低估传播事件,尤其是在高患病率环境中。