Literature DB >> 20951641

A multiresistance megaplasmid pLG1 bearing a hylEfm genomic island in hospital Enterococcus faecium isolates.

Jenny A Laverde Gomez1, Willem van Schaik, Ana R Freitas, Teresa M Coque, Keith E Weaver, Maria Victoria Francia, Wolfgang Witte, Guido Werner.   

Abstract

Enterococcus faecium is considered to be a nosocomial pathogen with increasing medical importance. The putative virulence factor, hyl(Efm), encoding a putative hyaluronidase, is enriched among the hospital-associated polyclonal subpopulation of E. faecium.. The hyl(Efm) gene is described to be part of a genomic island and was recently identified to be plasmid-located. Here, we present a description of the structure, localization, and distribution of the putative pathogenicity factor hyl(Efm) and its putative island among 39 clinical isolates and elucidate the composition and host range of pLG1, a hyl(Efm) multiresistance plasmid of approximately 281.02kb. The hyl(Efm) gene was located within a 17,824-bp element highly similar to the putative genomic island (GI) structure that had been previously described. This genomic region was conserved among 39 hyl(Efm)-positive strains with variation in a specific region downstream of hyl(Efm) in 18 strains. The putative hyl(Efm) was located on large plasmids (150-350kb) in 37 strains. pLG1 could be horizontally transferred into four different E. faecium recipient strains (n=4) but not into E. faecalis (n=3). Sequencing of pLG1 resolved putative plasmid replication, conjugation, and maintenance determinants as well as a pilin gene cluster, carbon uptake and utilization genes, heavy metal and antibiotic resistance clusters. The hyl(Efm) transferable plasmid pLG1 bears additional putative pathogenicity factors and antibiotic resistance genes. These findings suggest horizontal gene transfer of virulence factors and antibiotic resistance gene clusters by a single genetic event (conjugative transfer) which might be triggered by heavy antibiotic use common in health care units where E. faecium is increasingly prevalent. Copyright Â
© 2010 Elsevier GmbH. All rights reserved.

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Year:  2010        PMID: 20951641     DOI: 10.1016/j.ijmm.2010.08.015

Source DB:  PubMed          Journal:  Int J Med Microbiol        ISSN: 1438-4221            Impact factor:   3.473


  34 in total

1.  Green fluorescent protein-labeled monitoring tool to quantify conjugative plasmid transfer between Gram-positive and Gram-negative bacteria.

Authors:  Karsten Arends; Katarzyna Schiwon; Türkan Sakinc; Johannes Hübner; Elisabeth Grohmann
Journal:  Appl Environ Microbiol       Date:  2011-12-02       Impact factor: 4.792

Review 2.  Mobile Genetic Elements Associated with Antimicrobial Resistance.

Authors:  Sally R Partridge; Stephen M Kwong; Neville Firth; Slade O Jensen
Journal:  Clin Microbiol Rev       Date:  2018-08-01       Impact factor: 26.132

Review 3.  The rise of the Enterococcus: beyond vancomycin resistance.

Authors:  Cesar A Arias; Barbara E Murray
Journal:  Nat Rev Microbiol       Date:  2012-03-16       Impact factor: 60.633

4.  Human and swine hosts share vancomycin-resistant Enterococcus faecium CC17 and CC5 and Enterococcus faecalis CC2 clonal clusters harboring Tn1546 on indistinguishable plasmids.

Authors:  Ana R Freitas; Teresa M Coque; Carla Novais; Anette M Hammerum; Camilla H Lester; Marcus J Zervos; Susan Donabedian; Lars B Jensen; Maria Victoria Francia; Fernando Baquero; Luísa Peixe
Journal:  J Clin Microbiol       Date:  2011-01-12       Impact factor: 5.948

5.  PrgK, a multidomain peptidoglycan hydrolase, is essential for conjugative transfer of the pheromone-responsive plasmid pCF10.

Authors:  Jenny A Laverde Gomez; Minny Bhatty; Peter J Christie
Journal:  J Bacteriol       Date:  2013-11-15       Impact factor: 3.490

Review 6.  Human Health Risk Assessment (HHRA) for environmental development and transfer of antibiotic resistance.

Authors:  Nicholas J Ashbolt; Alejandro Amézquita; Thomas Backhaus; Peter Borriello; Kristian K Brandt; Peter Collignon; Anja Coors; Rita Finley; William H Gaze; Thomas Heberer; John R Lawrence; D G Joakim Larsson; Scott A McEwen; James J Ryan; Jens Schönfeld; Peter Silley; Jason R Snape; Christel Van den Eede; Edward Topp
Journal:  Environ Health Perspect       Date:  2013-07-09       Impact factor: 9.031

7.  The hylEfm gene in pHylEfm of Enterococcus faecium is not required in pathogenesis of murine peritonitis.

Authors:  Diana Panesso; Maria C Montealegre; Sandra Rincón; Maria F Mojica; Louis B Rice; Kavindra V Singh; Barbara E Murray; Cesar A Arias
Journal:  BMC Microbiol       Date:  2011-01-25       Impact factor: 3.605

8.  Intra- and interspecies genomic transfer of the Enterococcus faecalis pathogenicity island.

Authors:  Jenny A Laverde Gomez; Antoni P A Hendrickx; Rob J Willems; Janetta Top; Irina Sava; Johannes Huebner; Wolfgang Witte; Guido Werner
Journal:  PLoS One       Date:  2011-04-29       Impact factor: 3.240

9.  Microevolutionary events involving narrow host plasmids influences local fixation of vancomycin-resistance in Enterococcus populations.

Authors:  Ana R Freitas; Carla Novais; Ana P Tedim; María Victoria Francia; Fernando Baquero; Luísa Peixe; Teresa M Coque
Journal:  PLoS One       Date:  2013-03-29       Impact factor: 3.240

10.  Vancomycin-resistant vanB-type Enterococcus faecium isolates expressing varying levels of vancomycin resistance and being highly prevalent among neonatal patients in a single ICU.

Authors:  Guido Werner; Ingo Klare; Carola Fleige; Uta Geringer; Wolfgang Witte; Heinz-Michael Just; Renate Ziegler
Journal:  Antimicrob Resist Infect Control       Date:  2012-05-30       Impact factor: 4.887

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