Stoesser N, Sheppard A E, Shakya M, Sthapit B, Thorson S, Giess A, Kelly D, Pollard A J, Peto T E A, Walker A S, Crook D W
Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK
NIHR Biomedical Research Centre, University of Oxford/Oxford University Hospitals NHS Trust, Oxford, UK.
J Antimicrob Chemother. 2015 Apr;70(4):1008-15. doi: 10.1093/jac/dku521. Epub 2015 Jan 3.
There are limited data on Enterobacter cloacae outbreaks and fewer describing these in association with NDM-1. With whole-genome sequencing, we tested the hypothesis that a cluster of 16 E. cloacae bacteraemia cases in a Nepali neonatal unit represented a single clonal outbreak, using a wider set of epidemiologically unrelated clinical E. cloacae isolates for comparison.
Forty-three isolates were analysed, including 23 E. cloacae and 3 Citrobacter sp. isolates obtained from blood cultures from 16 neonates over a 3 month period. These were compared with two contemporaneous community-associated drug-resistant isolates from adults, a unit soap dispenser isolate and a set of historical invasive isolates (n=14) from the same geographical locality.
There were two clear neonatal outbreaks and one isolated case in the unit. One outbreak was associated with an NDM-1 plasmid also identified in a historical community-associated strain. The smaller, second outbreak was likely associated with a contaminated soap dispenser. The two community-acquired adult cases and three sets of historical hospital-associated neonatal isolates represented four additional genetic clusters.
E. cloacae infections in this context represent several different transmission networks, operating at the community/hospital and host strain/plasmid levels. Wide sampling frames and high-resolution typing methods are needed to describe the complex molecular epidemiology of E. cloacae outbreaks, which is not appropriately reflected by routine susceptibility phenotypes. Soap dispensers may represent a reservoir for E. cloacae and bacterial strains and plasmids may persist in hospitals and in the community for long periods, sporadically being involved in outbreaks of disease.
关于阴沟肠杆菌暴发的数据有限,而描述其与新德里金属β-内酰胺酶-1(NDM-1)相关的更少。通过全基因组测序,我们检验了这样一个假设:尼泊尔一家新生儿病房的16例阴沟肠杆菌血流感染病例集群代表一次单一的克隆性暴发,并使用一组在流行病学上不相关的临床阴沟肠杆菌分离株进行比较。
分析了43株分离株,包括在3个月期间从16名新生儿血培养中获得的23株阴沟肠杆菌和3株柠檬酸杆菌属分离株。将这些分离株与同期从成人获得的两株社区获得性耐药分离株、一个病房肥皂液器分离株以及一组来自同一地理位置的历史侵袭性分离株(n = 14)进行比较。
该病房有两次明显的新生儿暴发和1例孤立病例。一次暴发与一个也在一株历史社区相关菌株中鉴定出的NDM-1质粒有关。规模较小的第二次暴发可能与一个被污染的肥皂液器有关。两例社区获得性成人病例和三组历史医院相关新生儿分离株代表另外四个基因簇。
在此背景下,阴沟肠杆菌感染代表几种不同的传播网络,在社区/医院以及宿主菌株/质粒水平发挥作用。需要广泛的采样框架和高分辨率分型方法来描述阴沟肠杆菌暴发的复杂分子流行病学,而常规药敏表型无法恰当反映这一点。肥皂液器可能是阴沟肠杆菌的一个储存库,细菌菌株和质粒可能在医院和社区中长期存在,偶尔引发疾病暴发。