Literature DB >> 12202574

Possible connection between a widely disseminated conjugative gentamicin resistance (pMG1-like) plasmid and the emergence of vancomycin resistance in Enterococcus faecium.

Haruyoshi Tomita1, Carl Pierson, Suk Kyung Lim, Don B Clewell, Yasuyoshi Ike.   

Abstract

A total of 640 vancomycin-resistant Enterococcus faecium (VRE) isolates, which were obtained between 1994 and 1999 from the Medical School Hospital of the University of Michigan, Ann Arbor, were used in this study. Of the 640 strains, 611 and 29 were VanA and VanB VRE, respectively, based on PCR analysis. Four hundred ninety-two (77%) of the strains exhibited resistance to concentrations of gentamicin from 64 micro g/ml (MIC) to more than 1,024 micro g/ml (MIC). The gentamicin resistance of each of 261 (53%) of the 492 gentamicin-resistant strains was transferred to E. faecium at a frequency of about 10(-5) to 10(-6) per donor cell in broth mating. More than 90% of vancomycin resistances of the 261 strains cotransferred with the gentamicin resistances to E. faecium strains by filter mating. The conjugative gentamicin resistance plasmids were identified and were classified into five types (A through E) with respect to their EcoRI restriction profiles. The transfer frequencies of each type of plasmid between E. faecium strains or Enterococcus faecalis strains were around 10(-3) to 10(-5) per donor cell or around 10(-6) to 10(-7) per donor cell, respectively, in broth mating. Type A and type B were the most frequently isolated, at an isolation frequency of about 40% per VRE isolate harboring the gentamicin resistance conjugative plasmid. The plasmids did not show any homology in Southern hybridization with the pheromone-responsive plasmids and broad-host-range plasmids pAMbeta1 and pIP501. The EcoRI or NdeI restriction fragments of each type of plasmids hybridized to the conjugative gentamicin resistance plasmid pMG1 (65.1 kb), which was originally isolated from an E. faecium clinical isolate, and transfer efficiently in broth mating.

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Year:  2002        PMID: 12202574      PMCID: PMC130708          DOI: 10.1128/JCM.40.9.3326-3333.2002

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  39 in total

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Review 2.  Intergeneric and interspecies gene exchange in gram-positive cocci.

Authors:  D R Schaberg; M J Zervos
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3.  Plasmid-mediated resistance to vancomycin and teicoplanin in Enterococcus faecium.

Authors:  R Leclercq; E Derlot; J Duval; P Courvalin
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Review 4.  Bacterial sex pheromone-induced plasmid transfer.

Authors:  D B Clewell
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6.  In vitro susceptibility studies of vancomycin-resistant Enterococcus faecalis.

Authors:  D F Sahm; J Kissinger; M S Gilmore; P R Murray; R Mulder; J Solliday; B Clarke
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9.  Physical and genetic analyses of streptococcal plasmid pAM beta 1 and cloning of its replication region.

Authors:  D J Leblanc; L N Lee
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Authors:  R Leclercq; E Derlot; M Weber; J Duval; P Courvalin
Journal:  Antimicrob Agents Chemother       Date:  1989-01       Impact factor: 5.191

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  35 in total

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Authors:  Sreedhar R Nallapareddy; Kavindra V Singh; Barbara E Murray
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3.  Genetic analysis of transfer-related regions of the vancomycin resistance Enterococcus conjugative plasmid pHTbeta: identification of oriT and a putative relaxase gene.

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4.  Epidemiological link between wastewater and human vancomycin-resistant Enterococcus faecium isolates.

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5.  Partial Diversity Generates Effector Immunity Specificity of the Bac41-Like Bacteriocins of Enterococcus faecalis Clinical Strains.

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Journal:  J Bacteriol       Date:  2016-08-11       Impact factor: 3.490

6.  Toxin-antitoxin systems are ubiquitous and plasmid-encoded in vancomycin-resistant enterococci.

Authors:  Elizabeth M Moritz; Paul J Hergenrother
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8.  Clonal Emergence of Invasive Multidrug-Resistant Staphylococcus epidermidis Deconvoluted via a Combination of Whole-Genome Sequencing and Microbiome Analyses.

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Journal:  J Bacteriol       Date:  2008-01-18       Impact factor: 3.490

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