NHC Key Laboratory of Food Safety Risk Assessment, Food Safety Research Unit (2019RU014) of Chinese Academy of Medical Science, China National Center for Food Safety Risk Assessment, Beijing, China.
UCD-Centre for Food Safety, School of Public Health, Physiotherapy and Population Science, University College Dublin, Belfield, Dublin, Ireland.
J Antimicrob Chemother. 2021 Jun 18;76(7):1776-1785. doi: 10.1093/jac/dkab090.
This study aimed to characterize the genomic features of a Salmonella enterica serovar Typhimurium ST34 isolate, CFSA629, which carried a novel mcr-1 variant, designated as mcr-1.19, mapped to an ESBL-encoding IncHI2 plasmid.
Antimicrobial susceptibility assays as well as WGS were carried out on isolate CFSA629. The complete closed genome was obtained and then explored to obtain genomic features. Plasmid sequence comparison was performed for pCFSA629 with similar plasmids and the mcr-1 genetic environment was analysed.
S. Typhimurium ST34 CFSA629 expressed an MDR phenotype to six classes of compound and consisted of a single circular chromosome and one plasmid. It possessed 11 resistance genes including 2 ESBL genes that mapped to the chromosome and the plasmid; an IS26-flanked composite-like transposon was identified. A novel mcr-1 variant (mcr-1.19) was identified, which had a unique SNP (G1534A) that gave rise to a novel MCR-1 protein containing a Val512Ile amino acid substitution. Plasmid pCFSA629 possessed a conjugative plasmid transfer gene cluster as well as an antimicrobial resistance-encoding gene cluster-containing region that contained two IS26 composite-like transposonal modules, but was devoid of any plasmid-mediated quinolone resistance genes. The background of mcr-1.19 consisted of an ISApl1-mcr-1-PAP2-ter module.
We report on an MDR S. Typhimurium ST34 CFSA629 isolate cultured from egg in China, harbouring an mcr-1.19 variant mapped to an IncHI2 plasmid. This highlights the importance of surveillance to mitigate dissemination of mcr-encoding genes among foodborne Salmonella. Improved surveillance is important for tackling the dissemination of mcr genes among foodborne Salmonella around the world.
本研究旨在对携带新型 mcr-1 变体 mcr-1.19 的肠炎沙门氏菌血清型 Typhimurium ST34 分离株 CFSA629 的基因组特征进行描述,该变体位于一个 ESBL 编码 IncHI2 质粒上。
对分离株 CFSA629 进行药敏试验和 WGS。获得完整的闭合基因组,然后进行探索以获得基因组特征。对 pCFSA629 与类似质粒进行质粒序列比较,并分析 mcr-1 遗传环境。
肠炎沙门氏菌血清型 Typhimurium ST34 CFSA629 对六类化合物表现出 MDR 表型,由一个单一的圆形染色体和一个质粒组成。它拥有 11 个耐药基因,包括 2 个位于染色体和质粒上的 ESBL 基因;鉴定出一个 IS26 侧翼复合样转座子。发现了一种新型 mcr-1 变体(mcr-1.19),它具有一个独特的 SNP(G1534A),导致 MCR-1 蛋白发生 Val512Ile 氨基酸取代。质粒 pCFSA629 具有一个可转移的质粒转移基因簇以及一个包含两个 IS26 复合样转座子模块的抗菌药物耐药基因编码基因簇,但不含有任何质粒介导的喹诺酮耐药基因。mcr-1.19 的背景由 ISApl1-mcr-1-PAP2-ter 模块组成。
我们报告了在中国从鸡蛋中培养的 MDR 肠炎沙门氏菌血清型 Typhimurium ST34 CFSA629 分离株,携带位于 IncHI2 质粒上的 mcr-1.19 变体。这凸显了对食源性病原体沙门氏菌中 mcr 编码基因传播进行监测的重要性。提高监测水平对于在全球范围内解决食源性病原体沙门氏菌中 mcr 基因的传播至关重要。