Literature DB >> 17873043

Five genes encoding surface-exposed LPXTG proteins are enriched in hospital-adapted Enterococcus faecium clonal complex 17 isolates.

Antoni P A Hendrickx1, Willem J B van Wamel, George Posthuma, Marc J M Bonten, Rob J L Willems.   

Abstract

Most Enterococcus faecium isolates associated with hospital outbreaks and invasive infections belong to a distinct genetic subpopulation called clonal complex 17 (CC17). It has been postulated that the genetic evolution of CC17 involves the acquisition of various genes involved in antibiotic resistance, metabolic pathways, and virulence. To gain insight into additional genes that may have favored the rapid emergence of this nosocomial pathogen, we aimed to identify surface-exposed LPXTG cell wall-anchored proteins (CWAPs) specifically enriched in CC17 E. faecium. Using PCR and Southern and dot blot hybridizations, 131 E. faecium isolates (40 CC17 and 91 non-CC17) were screened for the presence of 22 putative CWAP genes identified from the E. faecium TX0016 genome. Five genes encoding LPXTG surface proteins were specifically enriched in E. faecium CC17 isolates. These five LPXTG surface protein genes were found in 28 to 40 (70 to 100%) of CC17 and in only 7 to 24 (8 to 26%) of non-CC17 isolates (P < 0.05). Three of these CWAP genes clustered together on the E. faecium TX0016 genome, which may comprise a novel enterococcal pathogenicity island covering E. faecium contig 609. Expression at the mRNA level was demonstrated, and immunotransmission electron microscopy revealed an association of the five LPXTG surface proteins with the cell wall. Minimal spanning tree analysis based on the presence and absence of 22 CWAP genes revealed grouping of all 40 CC17 strains together with 18 hospital-derived but evolutionary unrelated non-CC17 isolates in a distinct CWAP-enriched cluster, suggesting horizontal transfer of CWAP genes and a role of these CWAPs in hospital adaptation.

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Year:  2007        PMID: 17873043      PMCID: PMC2168695          DOI: 10.1128/JB.00664-07

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  45 in total

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Review 3.  Sortase-catalysed anchoring of surface proteins to the cell wall of Staphylococcus aureus.

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9.  Role of Staphylococcus aureus coagulase and clumping factor in pathogenesis of experimental endocarditis.

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  36 in total

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2.  Characterization of the ebp(fm) pilus-encoding operon of Enterococcus faecium and its role in biofilm formation and virulence in a murine model of urinary tract infection.

Authors:  Jouko Sillanpää; Sreedhar R Nallapareddy; Kavindra V Singh; Vittal P Prakash; Timothy Fothergill; Hung Ton-That; Barbara E Murray
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4.  Influence of isolate origin and presence of various genes on biofilm formation by Enterococcus faecium.

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Review 5.  Population biology of Gram-positive pathogens: high-risk clones for dissemination of antibiotic resistance.

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6.  Dogs are a reservoir of ampicillin-resistant Enterococcus faecium lineages associated with human infections.

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7.  Longer intestinal persistence of Enterococcus faecalis compared to Enterococcus faecium clones in intensive-care-unit patients.

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8.  Pyrosequencing-based comparative genome analysis of the nosocomial pathogen Enterococcus faecium and identification of a large transferable pathogenicity island.

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9.  Adherence to host extracellular matrix and serum components by Enterococcus faecium isolates of diverse origin.

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10.  Enterococcal surface protein Esp is not essential for cell adhesion and intestinal colonization of Enterococcus faecium in mice.

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