{"title":"Mobile genetic elements beyond the VanB-resistance dissemination among hospital-associated enterococci and other Gram-positive bacteria","authors":"Ewa Sadowy","doi":"10.1016/j.plasmid.2021.102558","DOIUrl":null,"url":null,"abstract":"<div><p>An increasing resistance to vancomycin among clinically relevant enterococci, such as <em>Enterococcus faecalis</em> and <em>Enterococcus faecium</em> is a cause of a great concern, as it seriously limits treatment options. The <em>vanB</em> operon is one of most common determinants of this type of resistance. Genes constituting the operon are located in conjugative transposons, such as Tn<em>1549</em>-type transposons or, more rarely, in ICE<em>Efa</em>V583-type structures. Such elements show differences in structure and size, and reside in various sites of bacterial chromosome or, in the case of Tn<em>1549</em>-type transposons, are also occasionally associated with plasmids of divergent replicon types. While conjugative transposition contributes to the acquisition of Tn<em>1549</em>-type transposons from anaerobic gut commensals by enterococci, chromosomal recombination and conjugal transfer of plasmids appear to represent main mechanisms responsible for horizontal dissemination of <em>vanB</em> determinants among hospital <em>E. faecalis</em> and <em>E. faecium</em>.</p><p>This review focuses on diversity of genetic elements harbouring <em>vanB</em> determinants in hospital-associated strains of <em>E. faecium</em> and <em>E. faecalis,</em> the mechanisms beyond <em>vanB</em> spread in populations of these bacteria, and provides an overview of the <em>vanB-</em>MGE distribution among other enterococci and Gram-positive bacteria as potential reservoirs of <em>vanB</em> genes.</p></div>","PeriodicalId":49689,"journal":{"name":"Plasmid","volume":"114 ","pages":"Article 102558"},"PeriodicalIF":1.8000,"publicationDate":"2021-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.plasmid.2021.102558","citationCount":"9","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plasmid","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0147619X21000056","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 9
Abstract
An increasing resistance to vancomycin among clinically relevant enterococci, such as Enterococcus faecalis and Enterococcus faecium is a cause of a great concern, as it seriously limits treatment options. The vanB operon is one of most common determinants of this type of resistance. Genes constituting the operon are located in conjugative transposons, such as Tn1549-type transposons or, more rarely, in ICEEfaV583-type structures. Such elements show differences in structure and size, and reside in various sites of bacterial chromosome or, in the case of Tn1549-type transposons, are also occasionally associated with plasmids of divergent replicon types. While conjugative transposition contributes to the acquisition of Tn1549-type transposons from anaerobic gut commensals by enterococci, chromosomal recombination and conjugal transfer of plasmids appear to represent main mechanisms responsible for horizontal dissemination of vanB determinants among hospital E. faecalis and E. faecium.
This review focuses on diversity of genetic elements harbouring vanB determinants in hospital-associated strains of E. faecium and E. faecalis, the mechanisms beyond vanB spread in populations of these bacteria, and provides an overview of the vanB-MGE distribution among other enterococci and Gram-positive bacteria as potential reservoirs of vanB genes.
期刊介绍:
Plasmid publishes original research on genetic elements in all kingdoms of life with emphasis on maintenance, transmission and evolution of extrachromosomal elements. Objects of interest include plasmids, bacteriophages, mobile genetic elements, organelle DNA, and genomic and pathogenicity islands.