通过对病房废水环境和患者进行基因组流行病学和纵向采样,揭示了医院环境中产蓝 KPC-碳青霉烯酶肠杆菌传播动态的复杂性。

IF 3.7 Q2 INFECTIOUS DISEASES JAC-Antimicrobial Resistance Pub Date : 2024-09-03 eCollection Date: 2024-10-01 DOI:10.1093/jacamr/dlae140
N Stoesser, R George, Z Aiken, H T T Phan, S Lipworth, T P Quan, A J Mathers, N De Maio, A C Seale, D W Eyre, A Vaughan, J Swann, T E A Peto, D W Crook, J Cawthorne, A Dodgson, A S Walker
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引用次数: 0

摘要

背景:产碳青霉烯酶肠杆菌(CPE)定植的医疗相关废水和无症状患者蓄水池导致了院内 CPE 的传播,但其特征和动态仍不清楚:我们在 6-12 个月内对 6 个病房的废水处理场所(349 个场所,4488 份样本)和患者(1247 人)进行了系统采样,以了解这些蓄水池中 blaKPC 相关 CPE(KPC-E)的多样性以及在医疗环境中的传播情况。每个样本最多可测序 5 个 KPC-E 阳性分离株(Illumina)。重组调整后的系统发生被用来定义基因相关的菌株;基于组装和映射的方法被用来描述抗菌药耐药性基因、插入序列 (IS) 和 Tn4401 类型/靶点序列。在一些最大的集群和跨越水库的集群中对附属基因组进行了评估:结果:污水点的 KPC-E 阳性率很高[101/349 个点(28.9%);228/5601(4.1%)名培养出的患者]。利用基因组学方法确定了 13 个 KPC-E 物种和 109 个菌株,24% 的废水和 26% 的患者 KPC-E 阳性样本中含有一个或多个菌株。大多数多样性是由个体生态位解释的,这表明局部因素在选择和传播中非常重要。Tn4401 + 侧翼目标位点序列多样性在废水位点中更为显著(与 P 4401 相关的转座/进化。淋浴/洗澡和水槽/拖把相关位点更有可能出现 KPC-E 阳性(调整 OR = 2.69;95% CI:1.44-5.01;P = 0.0019;调整 OR = 2.60;95% CI:1.04-6.52;P = 0.0410)。不同的菌株具有不同的 blaKPC 传播动态:我们发现在医院环境中,KPC-E 在废水处理场所和患者中的定植数量巨大且种类繁多。蓄水池和生态位特异性因素(如微生物相互作用、选择压力)以及不同菌株和移动遗传因子可能会影响传播动态。监测和控制策略应考虑到这一点。
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Genomic epidemiology and longitudinal sampling of ward wastewater environments and patients reveals complexity of the transmission dynamics of bla KPC-carbapenemase-producing Enterobacterales in a hospital setting.

Background: Healthcare-associated wastewater and asymptomatic patient reservoirs colonized by carbapenemase-producing Enterobacterales (CPE) contribute to nosocomial CPE dissemination, but the characteristics and dynamics of this remain unclear.

Methods: We systematically sampled wastewater sites (n = 4488 samples; 349 sites) and patients (n = 1247) across six wards over 6-12 months to understand blaKPC-associated CPE (KPC-E) diversity within these reservoirs and transmission in a healthcare setting. Up to five KPC-E-positive isolates per sample were sequenced (Illumina). Recombination-adjusted phylogenies were used to define genetically related strains; assembly and mapping-based approaches were used to characterize antimicrobial resistance genes, insertion sequences (ISs) and Tn4401 types/target site sequences. The accessory genome was evaluated in some of the largest clusters, and those crossing reservoirs.

Results: Wastewater site KPC-E-positivity was substantial [101/349 sites (28.9%); 228/5601 (4.1%) patients cultured]. Thirteen KPC-E species and 109 strains were identified using genomics, and 24% of wastewater and 26% of patient KPC-E-positive samples harboured one or more strains. Most diversity was explained by the individual niche, suggesting localized factors are important in selection and spread. Tn4401 + flanking target site sequence diversity was greater in wastewater sites (P < 0.001), which might favour Tn4401-associated transposition/evolution. Shower/bath- and sluice/mop-associated sites were more likely to be KPC-E-positive (adjusted OR = 2.69; 95% CI: 1.44-5.01; P = 0.0019; and adjusted OR = 2.60; 95% CI: 1.04-6.52; P = 0.0410, respectively). Different strains had different blaKPC dissemination dynamics.

Conclusions: We identified substantial and diverse KPC-E colonization of wastewater sites and patients in this hospital setting. Reservoir and niche-specific factors (e.g. microbial interactions, selection pressures), and different strains and mobile genetic elements likely affect transmission dynamics. This should be considered in surveillance and control strategies.

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