Literature DB >> 20946531

A genetic element present on megaplasmids allows Enterococcus faecium to use raffinose as carbon source.

Xinglin Zhang1, Joyce E P Vrijenhoek, Marc J M Bonten, Rob J L Willems, Willem van Schaik.   

Abstract

Enterococcus faecium is a commensal of the gastrointestinal tract of humans and animals. Since the 1990s, it has also emerged as a nosocomial pathogen. Little is known about carbon metabolism of E. faecium even though the ability to utilize different sugars could be an important factor in adapting to different ecological niches. In this study we identify an E. faecium gene cluster that is responsible for the metabolism of the α-galactoside sugar raffinose. Phenotypic testing of seven E. faecium isolates of which the genomes were previously sequenced showed that one isolate (strain E980) could grow on raffinose. Genome analysis identified a gene cluster containing two genes encoding α-galactosidases (termed agaA and agaB) that was uniquely present in E980. The agaA and agaB genes were significantly more frequently found in strains that are phylogenetically related to E980 and were more prevalent in surveillance isolates from hospital and community sources than in isolates from clinical infections. Disruption of the α-galactosidase gene agaB, but not of agaA, disabled growth on raffinose in strain E980. In all strains agaA and agaB are carried on megaplasmids that are between 150 and 300 kb in size. Filter-mating experiments showed that the megaplasmid of E980 can be transferred to a plasmidless recipient which then gains the ability to grow on raffinose. The observation that raffinose utilization by E. faecium is a trait carried by megaplasmids indicates that these megaplasmids can have important roles in shaping the competitive fitness of E. faecium in the environment, for example by expanding the metabolic repertoire of this organism.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20946531     DOI: 10.1111/j.1462-2920.2010.02355.x

Source DB:  PubMed          Journal:  Environ Microbiol        ISSN: 1462-2912            Impact factor:   5.491


  18 in total

1.  Subinhibitory Concentrations of Ciprofloxacin Enhance Antimicrobial Resistance and Pathogenicity of Enterococcus faecium.

Authors:  Clara Sinel; Margherita Cacaci; Pierrick Meignen; François Guérin; Bryan W Davies; Maurizio Sanguinetti; Jean-Christophe Giard; Vincent Cattoir
Journal:  Antimicrob Agents Chemother       Date:  2017-04-24       Impact factor: 5.191

2.  Galacto-oligosaccharides and Colorectal Cancer: Feeding our Intestinal Probiome.

Authors:  Jose M Bruno-Barcena; M Andrea Azcarate-Peril
Journal:  J Funct Foods       Date:  2015-01       Impact factor: 4.451

3.  Genomic analysis of reduced susceptibility to tigecycline in Enterococcus faecium.

Authors:  Vincent Cattoir; Christophe Isnard; Thibaud Cosquer; Arlène Odhiambo; Fiona Bucquet; François Guérin; Jean-Christophe Giard
Journal:  Antimicrob Agents Chemother       Date:  2014-10-27       Impact factor: 5.191

4.  The Two-Component System ChtRS Contributes to Chlorhexidine Tolerance in Enterococcus faecium.

Authors:  Ana M Guzmán Prieto; Jessica Wijngaarden; Johanna C Braat; Malbert R C Rogers; Eline Majoor; Ellen C Brouwer; Xinglin Zhang; Jumamurat R Bayjanov; Marc J M Bonten; Rob J L Willems; Willem van Schaik
Journal:  Antimicrob Agents Chemother       Date:  2017-04-24       Impact factor: 5.191

5.  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

6.  The carbohydrate metabolism signature of lactococcus lactis strain A12 reveals its sourdough ecosystem origin.

Authors:  Delphine Passerini; Michèle Coddeville; Pascal Le Bourgeois; Pascal Loubière; Paul Ritzenthaler; Catherine Fontagné-Faucher; Marie-Line Daveran-Mingot; Muriel Cocaign-Bousquet
Journal:  Appl Environ Microbiol       Date:  2013-07-19       Impact factor: 4.792

7.  The Enterococcus faecium enterococcal biofilm regulator, EbrB, regulates the esp operon and is implicated in biofilm formation and intestinal colonization.

Authors:  Janetta Top; Fernanda L Paganelli; Xinglin Zhang; Willem van Schaik; Helen L Leavis; Miranda van Luit-Asbroek; Tom van der Poll; Masja Leendertse; Marc J M Bonten; Rob J L Willems
Journal:  PLoS One       Date:  2013-05-31       Impact factor: 3.240

8.  Genome-wide identification of ampicillin resistance determinants in Enterococcus faecium.

Authors:  Xinglin Zhang; Fernanda L Paganelli; Damien Bierschenk; Annemarie Kuipers; Marc J M Bonten; Rob J L Willems; Willem van Schaik
Journal:  PLoS Genet       Date:  2012-06-28       Impact factor: 5.917

9.  Enterococcus faecium biofilm formation: identification of major autolysin AtlAEfm, associated Acm surface localization, and AtlAEfm-independent extracellular DNA Release.

Authors:  Fernanda L Paganelli; Rob J L Willems; Pamela Jansen; Antoni Hendrickx; Xinglin Zhang; Marc J M Bonten; Helen L Leavis
Journal:  mBio       Date:  2013-04-16       Impact factor: 7.867

10.  Functional genomic analysis of bile salt resistance in Enterococcus faecium.

Authors:  Xinglin Zhang; Damien Bierschenk; Janetta Top; Iacovos Anastasiou; Marc J M Bonten; Rob J L Willems; Willem van Schaik
Journal:  BMC Genomics       Date:  2013-05-03       Impact factor: 3.969

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.