Literature DB >> 33414775

Plasmid Dynamics of mcr-1-Positive Salmonella spp. in a General Hospital in China.

Jianzhong Fan1, Linghong Zhang2,3,4, Jintao He2,3,4, Maoying Zhao5, Belinda Loh6, Sebastian Leptihn2,6, Yunsong Yu2,3,4, Xiaoting Hua2,3,4.   

Abstract

Salmonella is an important food pathogen that can cause severe gastroenteritis with more than 600,000 deaths globally every year. Colistin (COL), a last-resort antibiotic, is ineffective in bacteria that carry a functional mcr-1 gene, which is often spread by conjugative plasmids. Our work aimed to understand the prevalence of the mcr-1 gene in clinical isolates of Salmonella, as the frequency of occurrence of the mcr-1 gene is increasing globally. Therefore, we analyzed 689 clinical strains, that were isolated between 2009 and late 2018. The mcr-1 gene was found in six strains, which we analyzed in detail by whole genome sequencing and antibiotic susceptibility testing, while we also provide the clinical information on the patients suffering from an infection. The genomic analysis revealed that five strains had plasmid-encoded mcr-1 gene located in four IncHI2 plasmids and one IncI2 plasmid, while one strain had the chromosomal mcr-1 gene originated from plasmid. Surprisingly, in two strains the mcr-1 genes were inactive due to disruption by insertion sequences (ISs): ISApl1 and ISVsa5. A detailed analysis of the plasmids revealed a multitude of ISs, most commonly IS26. The IS contained genes that meditate broad resistance toward most antibiotics underlining their importance of the mobile elements, also with respect to the spread of the mcr-1 gene. Our study revealed potential reservoirs for the transmission of COL resistance and offers insights into the evolution of the mcr-1 gene in Salmonella.
Copyright © 2020 Fan, Zhang, He, Zhao, Loh, Leptihn, Yu and Hua.

Entities:  

Keywords:  IS; ISApl1; ISVsa5; Salmonella; inactivation; mcr-1

Year:  2020        PMID: 33414775      PMCID: PMC7782425          DOI: 10.3389/fmicb.2020.604710

Source DB:  PubMed          Journal:  Front Microbiol        ISSN: 1664-302X            Impact factor:   5.640


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