Elton Linzy, Williams Alan, Ali Shanom, Heaphy Jelena, Pang Vicky, Commins Liam, O'Brien Conor, Yetiş Özge, Caine Estelle, Ward Imogen, Muzslay Monika, Yui Samuel, Karia Kush, Shore Ellinor, Rofael Sylvia, Mack Damien J F, McHugh Timothy D, Wey Emmanuel Q
The Centre for Clinical Microbiology, University College London, London, UK.
Department of Infection Sciences, Health Services Laboratories, London, UK.
Ann Clin Microbiol Antimicrob. 2024 Dec 20;23(1):108. doi: 10.1186/s12941-024-00762-8.
Colonisation and infection with Carbapenem-resistant Enterobacterales (CRE) in healthcare settings poses significant risks, especially for vulnerable patients. Genomic analysis can be used to trace transmission routes, supporting antimicrobial stewardship and informing infection control strategies. Here we used genomic analysis to track the movement and transmission of CREs within clinical and environmental samples.
25 isolates were cultured from clinical patient samples or swabs, that tested positive for OXA-48-like variants using the NG-Test® CARBA-5 test and whole genome sequenced (WGS) using Oxford Nanopore Technologies (ONT). 158 swabs and 52 wastewater samples were collected from the ward environment. 60 isolates (matching clinical isolate genera; Klebsiella, Enterobacter, Citrobacter and Escherichia) were isolated from the environmental samples using selective agar. Metagenomic sequencing was undertaken on 36 environmental wastewater and swab samples.
21/25 (84%) clinical isolates had > 1 bla gene and 19/25 (76%) harboured > 1 bla gene. Enterobacterales were most commonly isolated from environmental wastewater samples 27/52 (51.9%), then stick swabs 5/43 (11.6%) and sponge swabs 5/115 (4.3%). 11/60 (18%) environmental isolates harboured > 1 bla gene and 1.9% (1/60) harboured bla. bla genes were found in 2/36 (5.5%) metagenomic environmental samples.
Potential for putative patient-patient and patient-ward transmission was shown. Metagenomic sampling needs optimization to improve sensitivity.
医疗机构中耐碳青霉烯类肠杆菌科细菌(CRE)的定植和感染带来了重大风险,尤其是对脆弱患者而言。基因组分析可用于追踪传播途径,支持抗菌药物管理并为感染控制策略提供信息。在此,我们使用基因组分析来追踪CRE在临床和环境样本中的移动和传播情况。
从临床患者样本或拭子中培养出25株分离菌,这些样本使用NG-Test® CARBA-5检测对OXA-48样变体呈阳性,并使用牛津纳米孔技术(ONT)进行全基因组测序(WGS)。从病房环境中收集了158份拭子和52份废水样本。使用选择性琼脂从环境样本中分离出60株分离菌(与临床分离菌属匹配;克雷伯菌属、肠杆菌属、柠檬酸杆菌属和大肠杆菌属)。对36份环境废水和拭子样本进行了宏基因组测序。
21/25(84%)的临床分离菌有>1个bla基因,19/25(76%)携带>1个bla基因。肠杆菌科细菌最常从环境废水样本中分离出来,为27/52(51.9%),然后是粘拭子5/43(11.6%)和海绵拭子5/115(4.3%)。11/60(18%)的环境分离菌携带>1个bla基因,1.9%(1/60)携带bla。在2/36(5.5%)的宏基因组环境样本中发现了bla基因。
显示了患者与患者之间以及患者与病房之间可能的传播情况。宏基因组采样需要优化以提高敏感性。