Department of Clinical Laboratory Medicine, Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China; Department of Microbiology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, 510080, China; Key Laboratory of Tropical Diseases Control (Sun Yat-sen University), Ministry of Education, Guangzhou, 510080, China.
Department of Clinical Laboratory Medicine, Third Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Int J Med Microbiol. 2021 May;311(4):151501. doi: 10.1016/j.ijmm.2021.151501. Epub 2021 Apr 1.
Previous studies reported the prevalence of mcr-1 among clinical infected Salmonella isolates in China. However, the transmission dynamics of mcr-1 in different ecological niches were not well investigated. Our objective is to exhibit the transmission dynamics of mcr-1 in Salmonella.
598 Salmonella isolates were recovered from ten hospitals; besides 936 pig faces and 167 pork samples were collected from January 2015 to December 2017 in Guangzhou, China. PCR and sequencing were used to identify mcr-1-positive Salmonella. Antimicrobial susceptibility testing was performed with 16 antimicrobials. Conjugation, S1-PFGE, and Southern blot were used to determine the transferability and location of mcr-1. Whole-genome sequencing was used to investigate pangenome, phylogeny, plasmid, and transposon.
Eleven mcr-1-positive Salmonella isolates were identified from patients with infectious diarrhea. Five pig fecal samples and three pork samples contained mcr-1-positive Salmonella isolates. All isolates were multi-drug resistant. The mcr-1 genes were located on ∼210-250 kb IncHI2-pST3 plasmids, and 12 mcr-1 genes were transferable. All isolates were assigned to ST34 or its genetically closed STs. The distribution of the core-genome network was significantly correlated with source distributions. The accessory genes-based network demonstrated that the diverse clonal complexes could share highly similar accessory genomes.
The prevalence of mcr-1-positive Salmonella among different sources was low. Clonal transmission could not be the main reason for the expansion of mcr-1-positive Salmonella, but be attributed to the horizontal transfer of IncHI2-pST3 plasmid. Continuous surveillance on Salmonella should be performed to investigate the response of colistin banning in food-producing animals by mcr-1-positive Salmonella populations.
先前的研究报告了中国临床感染沙门氏菌分离株中 mcr-1 的流行情况。然而,mcr-1 在不同生态位中的传播动态尚未得到很好的研究。我们的目的是展示 mcr-1 在沙门氏菌中的传播动态。
从十家医院中回收了 598 株沙门氏菌;此外,2015 年 1 月至 2017 年 12 月,在中国广州还从 936 个猪脸和 167 个猪肉样本中采集了沙门氏菌。使用 PCR 和测序来鉴定 mcr-1 阳性沙门氏菌。使用 16 种抗生素进行药敏试验。通过接合、S1-PFGE 和 Southern blot 来确定 mcr-1 的可转移性和位置。全基因组测序用于调查泛基因组、系统发育、质粒和转座子。
从感染性腹泻患者中鉴定出 11 株 mcr-1 阳性沙门氏菌。5 个猪粪便样本和 3 个猪肉样本中含有 mcr-1 阳性沙门氏菌。所有分离株均为多药耐药。mcr-1 基因位于约 210-250 kb IncHI2-pST3 质粒上,可转移的 mcr-1 基因有 12 个。所有分离株均被分配到 ST34 或其遗传上紧密相关的 STs。核心基因组网络的分布与来源分布显著相关。基于附加基因的网络表明,不同的克隆复合体可以共享高度相似的附加基因组。
不同来源的 mcr-1 阳性沙门氏菌的流行率较低。克隆传播可能不是 mcr-1 阳性沙门氏菌扩张的主要原因,而是归因于 IncHI2-pST3 质粒的水平转移。应继续对沙门氏菌进行监测,以调查 mcr-1 阳性沙门氏菌对食品动物中黏菌素禁用的反应。