Spahr Yvonne, Nordmann Patrice, Fernandez Javier E, Poirel Laurent, Endimiani Andrea, Perreten Vincent
Division of Molecular Bacterial Epidemiology and Infectious Diseases, Institute of Veterinary Bacteriology, Vetsuisse Faculty, University of Bern, 3012, Bern, Switzerland.
Swiss National Reference Center for Emerging Antibiotic Resistance (NARA), University of Fribourg, 1700, Fribourg, Switzerland.
J Appl Microbiol. 2025 Aug 4;136(8). doi: 10.1093/jambio/lxaf181.
To determine the genomic relatedness of E. coli (Ec) sequence type (ST) 410 producing the carbapenemase OXA-181 (ST410-OXA-181), which caused an outbreak in a Swiss companion animal (CA) clinic in 2018 with those isolated from humans between 2017 and 2021 in Switzerland, and to characterize complete plasmids harbouring antimicrobial resistance genes (ARGs).
The complete genomes of 31 Ec ST410-OXA-181 (8 from CA, 23 from humans) were obtained by hybrid assembly of reads from Illumina and Nanopore sequencing technologies. The genomes were used for in silico phylogenetic analysis (cgMLST, SNP, ST410 clade analysis), ARG screening and for comparative analysis of complete plasmids. Antimicrobial susceptibility was determined by MIC measurement. All veterinary strains (CA, veterinarian) belonged to the phylogenetic clade ST410-B2 and the human strains to either ST410-B2 or B3. Strains recovered from the veterinary setting were clonal, differing by 0-4 SNPs. A higher genetic distance (>131 SNPs) was observed between the veterinary and the clinical human strains. All veterinary and 15 human strains shared an identical IncX3 plasmid harbouring blaOXA-181. Additional multidrug resistance plasmids were detected in human strains only.
The Ec ST410-B2-OXA-181 lineage was detected in both humans and animals. Strains share the same OXA-181 plasmids, but differed by SNP-based genetic distances and ARG contents indicating broad dissemination potential and independent evolution of strains of this lineage.
确定2018年在瑞士一家伴侣动物诊所引发疫情的产碳青霉烯酶OXA - 181的大肠杆菌(Ec)序列型(ST)410(ST410 - OXA - 181)与2017年至2021年在瑞士从人类中分离出的该菌株的基因组相关性,并对携带抗菌药物耐药基因(ARG)的完整质粒进行特征分析。
通过对Illumina和Nanopore测序技术读取的数据进行混合组装,获得了31株Ec ST410 - OXA - 181(8株来自伴侣动物,23株来自人类)的完整基因组。这些基因组用于计算机系统发育分析(cgMLST、SNP、ST410分支分析)、ARG筛选以及完整质粒的比较分析。通过MIC测量确定抗菌药物敏感性。所有兽医菌株(伴侣动物、兽医)均属于系统发育分支ST410 - B2,而人类菌株属于ST410 - B2或B3。从兽医环境中分离出的菌株是克隆性的,单核苷酸多态性(SNP)差异为0 - 4个。在兽医菌株和临床人类菌株之间观察到更高的遗传距离(>131个SNP)。所有兽医菌株和15株人类菌株共享一个携带blaOXA - 181的相同IncX3质粒。仅在人类菌株中检测到额外的多药耐药质粒。
在人类和动物中均检测到Ec ST410 - B2 - OXA - 181谱系。菌株共享相同的OXA - 181质粒,但基于SNP的遗传距离和ARG含量不同,表明该谱系菌株具有广泛的传播潜力和独立进化。