Tracing carriage, acquisition, and transmission of ESBL-producing Escherichia coli over two years in a tertiary care hospital.

IF 10.4 1区 生物学 Q1 GENETICS & HEREDITY
Minh Ngoc Nguyen, Beryl Primrose Gladstone, Giulia De Angelis, Michael Biggel, Basil Britto Xavier, Christine Lammens, Qiang Lin, Sandra Van Puyvelde, Herman Goossens, Samir Kumar-Singh, Youri Glupczynski, Yehuda Carmeli, Evelina Tacconelli, Surbhi Malhotra-Kumar
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引用次数: 0

Abstract

Background: The impact of community carriage on the influx of extended-spectrum beta-lactamase-producing Enterobacterales (ESBL-E) into hospitals remains understudied. In this prospective 2-year single-centre study, we investigate the community ESBL-E influx and trace the colonisation, nosocomial acquisition, transmission, and infection dynamics of ESBL-producing Escherichia coli (ESBL-Ec) in non-ICU wards at a tertiary care hospital.

Methods: This study reports primary and post hoc outcomes of the clinical trial NCT01208519 in which hospitalised patients were screened for rectal carriage of ESBL-E. ESBL-Ec isolates from ≈50% of carriers, including all patients who developed infections, were sequenced and genotyped. Endogenous infection was defined as infection by the same strain (< 10 SNPs distance) as colonizing strain.

Results: Of 3703 screened patients, 456 (12.3%) were ESBL-positive-at-admission (PA-ESBL). Of the 2268 ESBL-negative-at-admission (NA-ESBL) patients with follow-up samples, 240 (10.6%) acquired ESBL-E (HA-ESBL), with an incidence density rate of 7.96 cases/1000 patient-day, notably higher in patients receiving antibiotics (P < 0.001). PA- and HA-ESBL patients developed significantly more ESBL-E infections than ESBL-free patients (P < 0.001). Sequenced ESBL-Ec showed high clonal diversity dominated by the multidrug-resistant and highly virulent ST131 clade, C2/H30-Rx. Among ESBL-Ec infections, 60% (18/30) were endogenous. Direct between-patients transmission clusters (n = 21) involved 23.9% (48/201) of patients and 23.0% (84/366) of ESBL-Ec isolates.

Conclusions: Our data show a high prevalence of nosocomial acquisition of ESBL-E in a non-ICU setting. The study provides genomic evidence that the endogenous reservoir is the main driver of ESBL-Ec infections underscoring the need for wide implementation of antibiotic stewardship programmes to reduce antibiotic pressure.

在一家三级保健医院追踪产生esbls的大肠杆菌携带、获取和传播的时间超过两年。
背景:社区运输对产广谱β -内酰胺酶肠杆菌(ESBL-E)进入医院的影响仍未得到充分研究。在这项为期2年的前瞻性单中心研究中,我们调查了一家三级医院非icu病房中产生ESBL-E的大肠杆菌(ESBL-Ec)的社区流入情况,并追踪其定植、院内获得、传播和感染动态。方法:本研究报告了临床试验NCT01208519的主要和事后结果,在该试验中,住院患者进行了ESBL-E直肠携带筛查。对约50%的携带者(包括所有发生感染的患者)分离的ESBL-Ec进行测序和基因分型。内源性感染被定义为同一菌株的感染(结果:在3703例筛选的患者中,456例(12.3%)入院时为esbl阳性(PA-ESBL)。在随访样本的2268例入院时esbl阴性(NA-ESBL)患者中,240例(10.6%)获得了ESBL-E (HA-ESBL),发生率为7.96例/1000患者日,接受抗生素治疗的患者中发生率明显更高(P)。结论:我们的数据显示,非icu环境中ESBL-E的院内获得率很高。该研究提供了基因组证据,表明内源性储存库是ESBL-Ec感染的主要驱动因素,强调了广泛实施抗生素管理计划以减少抗生素压力的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Genome Medicine
Genome Medicine GENETICS & HEREDITY-
CiteScore
20.80
自引率
0.80%
发文量
128
审稿时长
6-12 weeks
期刊介绍: Genome Medicine is an open access journal that publishes outstanding research applying genetics, genomics, and multi-omics to understand, diagnose, and treat disease. Bridging basic science and clinical research, it covers areas such as cancer genomics, immuno-oncology, immunogenomics, infectious disease, microbiome, neurogenomics, systems medicine, clinical genomics, gene therapies, precision medicine, and clinical trials. The journal publishes original research, methods, software, and reviews to serve authors and promote broad interest and importance in the field.
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