Institute for Food Safety and Hygiene, Vetsuisse Faculty, University of Zurich, Winterthurerstrasse 272, 8057 Zurich, Switzerland.
Swiss National Center for Enteropathogenic Bacteria and Listeria (NENT), University of Zurich, Winterthurerstrasse 272, 8057 Zurich, Switzerland.
J Antimicrob Chemother. 2021 Jul 15;76(8):2004-2011. doi: 10.1093/jac/dkab119.
Fosfomycin is an important antibiotic for the treatment of MDR Enterobacteriaceae infections. High susceptibility rates are, however, threatened by the spread of plasmids encoding fosfomycin-modifying enzymes. In this study, we sought to characterize the genetic context of fosA in plasmids from Escherichia coli and Klebsiella spp. isolates recovered from food, wastewater and surface water in Switzerland.
E. coli and Klebsiella spp. isolates collected between 2012 and 2019 in Switzerland were screened for fosfomycin resistance. Presence of fosA was verified by PCR and sodium phosphonoformate (PPF) disc potentiation testing, and transferability was tested using conjugation assays. Whole-genome sequences including complete fosA-containing plasmids were determined using long- and short-read sequencing.
In 11 E. coli and two Klebsiella spp. isolates, high-level fosfomycin resistance was mediated by plasmids containing fosA3 (n = 12) or fosA8 (n = 1). Four isolates harboured a near-identical 45 kb IncN plasmid with fosA3, while replicon types varied in the remaining plasmids. The fosA genes were typically embedded in IS26-bounded transposition units and frequently located in the proximity of blaCTX-M transposition units.
Although fosfomycin resistance rates are currently low, the presence of fosA-encoding plasmids circulating in the Enterobacteriaceae population suggests that fosfomycin resistance may rapidly spread upon increased selection pressure. Transposition mobility of fosA and co-location on plasmids with other resistance genes may further promote its dissemination.
磷霉素是治疗多药耐药肠杆菌科感染的重要抗生素。然而,编码磷霉素修饰酶的质粒的传播威胁着高药敏率。在这项研究中,我们试图描述从瑞士食品、废水和地表水回收的大肠杆菌和克雷伯氏菌分离物的质粒中 fosA 的遗传背景。
在瑞士,2012 年至 2019 年间收集的大肠杆菌和克雷伯氏菌分离物进行磷霉素耐药性筛选。通过 PCR 和磷酸钠(PPF)圆盘增效试验验证 fosA 的存在,并通过接合试验测试可转移性。使用长读和短读测序确定包括完整 fosA 质粒在内的全基因组序列。
在 11 株大肠杆菌和 2 株克雷伯氏菌分离物中,高水平磷霉素耐药性由含有 fosA3(n = 12)或 fosA8(n = 1)的质粒介导。4 株分离物携带具有 fosA3 的近 45kb IncN 质粒,而其余质粒的复制子类型则不同。fosA 基因通常嵌入 IS26 结合的转座单元中,并且经常位于 blaCTX-M 转座单元附近。
尽管目前磷霉素耐药率较低,但在肠杆菌科种群中循环的携带 fosA 基因的质粒的存在表明,在选择压力增加的情况下,磷霉素耐药性可能迅速传播。fosA 的转位移动性及其与其他耐药基因在质粒上的共存可能进一步促进其传播。