Literature DB >> 2498209

Role of adherence in pathogenesis of Enterococcus faecalis urinary tract infection and endocarditis.

C A Guzmàn1, C Pruzzo, G LiPira, L Calegari.   

Abstract

Enterococcus faecalis strains isolated from urinary tract infections (UTIs) and endocarditis were analyzed for their ability to adhere to urinary tract epithelial cells (ECs) and Girardi heart (GH) and human embryonic kidney (HEK) cell cultures. UTI isolates adhered to urinary tract ECs more efficiently than to the cultured cells, at the same time showing the least affinity for GH cells. In contrast, endocarditis isolates adhered to GH cell cultures more readily than to urinary tract ECs. Moreover, although strains isolated from endocarditis adhered to GH cells more efficiently than those derived from UTI, the latter strains adhered to urinary tract cells better than the former. Studies of the ability of GH and HEK cells to internalize E. faecalis showed that for UTI isolates, 9 to 74% of adhered bacteria were internalized, while for endocarditis isolates, the percentage varied from 76 to 82%. All strains were able to associate with human neutrophils; endocarditis strains, however, associated less efficiently than UTI isolates. Growth in serum raised the adherence of all tested strains by at least 1.5- to 3-fold, with the greatest increase being observed in UTI strain adherence to GH cells (8-fold). In contrast, the association of serum-grown cells with polymorphonuclear leukocytes was reduced by two- to fivefold. In both cases, the observed serum-dependent alterations were cancelled by a few subcultures in brain heart infusion broth. These results indicate that adhesive properties are important virulence factors in the pathogenesis of UTI and endocarditis and also suggest that UTI strains showing the highest invasion and adhesive potential invade the kidneys, cause bacteremia, and, after having expressed the serum-dependent surface modification, colonize the heart.

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Year:  1989        PMID: 2498209      PMCID: PMC313363          DOI: 10.1128/iai.57.6.1834-1838.1989

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  16 in total

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Journal:  N Engl J Med       Date:  1961-02-09       Impact factor: 91.245

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Authors:  A Bøyum
Journal:  Scand J Immunol       Date:  1976-06       Impact factor: 3.487

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Authors:  I Ofek; D Mirelman; N Sharon
Journal:  Nature       Date:  1977-02-17       Impact factor: 49.962

4.  Endocarditis due to group D streptococci. Comparison of disease caused by streptococcus bovis with that produced by the enterococci.

Authors:  R C Moellering; B K Watson; L J Kunz
Journal:  Am J Med       Date:  1974-08       Impact factor: 4.965

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Authors:  G W Jones; L A Richardson; D Uhlman
Journal:  J Gen Microbiol       Date:  1981-12

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Authors:  J N Sipes; R L Thompson; E W Hook
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Journal:  Infect Immun       Date:  1979-04       Impact factor: 3.441

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Journal:  Ann Microbiol (Paris)       Date:  1982 May-Jun

Review 9.  Bacterial adherence: adhesin-receptor interactions mediating the attachment of bacteria to mucosal surface.

Authors:  E H Beachey
Journal:  J Infect Dis       Date:  1981-03       Impact factor: 5.226

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Authors:  C S Edén; L A Hanson; U Jodal; U Lindberg; A S Akerlund
Journal:  Lancet       Date:  1976-09-04       Impact factor: 79.321

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  37 in total

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Authors:  B D Shepard; M S Gilmore
Journal:  Appl Environ Microbiol       Date:  1999-04       Impact factor: 4.792

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Authors:  C R Gentry-Weeks; R Karkhoff-Schweizer; A Pikis; M Estay; J M Keith
Journal:  Infect Immun       Date:  1999-05       Impact factor: 3.441

3.  Pathogenic Mechanisms of Enterococcal Endocarditis.

Authors: 
Journal:  Curr Infect Dis Rep       Date:  2000-08       Impact factor: 3.725

4.  Serological response in Enterococcus faecalis endocarditis determined by enzyme-linked immunosorbent assay.

Authors:  P J Shorrock; P A Lambert; E J Aitchison; E G Smith; I D Farrell; E Gutschik
Journal:  J Clin Microbiol       Date:  1990-02       Impact factor: 5.948

Review 5.  Pathogenicity of Enterococci.

Authors:  Elizabeth Fiore; Daria Van Tyne; Michael S Gilmore
Journal:  Microbiol Spectr       Date:  2019-07

6.  Importance of the ebp (endocarditis- and biofilm-associated pilus) locus in the pathogenesis of Enterococcus faecalis ascending urinary tract infection.

Authors:  Kavindra V Singh; Sreedhar R Nallapareddy; Barbara E Murray
Journal:  J Infect Dis       Date:  2007-04-26       Impact factor: 5.226

7.  Clinical factors associated with shock in bacteremic UTI.

Authors:  Katsumi Shigemura; Kazushi Tanaka; Kayo Osawa; Sochi Arakawa; Hideaki Miyake; Masato Fujisawa
Journal:  Int Urol Nephrol       Date:  2013-04-25       Impact factor: 2.370

8.  High-resolution visualization by field emission scanning electron microscopy of Enterococcus faecalis surface proteins encoded by the pheromone-inducible conjugative plasmid pCF10.

Authors:  S B Olmsted; S L Erlandsen; G M Dunny; C L Wells
Journal:  J Bacteriol       Date:  1993-10       Impact factor: 3.490

9.  The transcriptome of the nosocomial pathogen Enterococcus faecalis V583 reveals adaptive responses to growth in blood.

Authors:  Heidi C Vebø; Lars Snipen; Ingolf F Nes; Dag A Brede
Journal:  PLoS One       Date:  2009-11-04       Impact factor: 3.240

10.  Role of the pheromone-inducible surface protein Asc10 in mating aggregate formation and conjugal transfer of the Enterococcus faecalis plasmid pCF10.

Authors:  S B Olmsted; S M Kao; L J van Putte; J C Gallo; G M Dunny
Journal:  J Bacteriol       Date:  1991-12       Impact factor: 3.490

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