Literature DB >> 6114036

Binding specificity of piliated strains of Escherichia coli and Salmonella typhimurium to epithelial cells, saccharomyces cerevisiae cells, and erythrocytes.

T K Korhonen, H Leffler, C Svanborg Edén.   

Abstract

The binding to mammalian cells of piliated enteric bacteria and the inhibition of the binding by antibodies to purified pili were studied. The target cells were epithelial cells from human bucca and human and rat urinary tracts, erythrocytes from various species, and Saccharomyces cerevisiae cells. The strains were selected to represent the two main agglutination patterns of enteric bacteria: mannose-resistant agglutination of human and other erythrocytes and mannose-sensitive agglutination of guinea pig and other erythrocytes. Escherichia coli 3669 caused only mannose-resistant agglutination, E. coli 6013 caused only mannose-sensitive agglutination, and E. coli 3048 caused both types of agglutination simultaneously. Salmonella typhimurium SH6749 exhibited only mannose-sensitive hemagglutination and was included to allow comparison of its pili with those of E. coli strains. The range of epithelial cells to which the bacteria adhered was related to their agglutination patterns. All four strains attached to human buccal cells. Only E. coli strains 3669 and 3048, which caused mannose-resistant agglutination, adhered to human urinary tract epithelial cells, and only those strains that caused mannose-sensitive agglutination adhered to rat urinary tract epithelial cells. The binding of S. typhimurium SH6749, but not of the other strains with mannose-sensitive agglutination, was significantly inhibited by d-mannose. Globotetraosylceramide, a glycolipid present in the human urinary tract epithelium, inhibited attachment to human uroepithelial cells of the two strains with mannose-resistant hemagglutination. As tested by the enzyme-linked immunosorbent assay, cross-reactions between type 1 pili of the E. coli strains were strong, but those between S. typhimurium and E. coli mannose-sensitive pili were weak. The two pili that induced mannose-resistant hemagglutination on E. coli did not cross-react. Significant inhibition of adhesion of all four strains was obtained with the homologous anti-pilus antiserum. The binding of bacteria to mammalian cells may thus be mediated by several types of bacterial pili reacting with different receptors on mammalian cells.

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Year:  1981        PMID: 6114036      PMCID: PMC351515          DOI: 10.1128/iai.32.2.796-804.1981

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


  18 in total

1.  Location of binding sites on common type 1 fimbriae from Escherichia coli.

Authors:  G Sweeney; J H Freer
Journal:  J Gen Microbiol       Date:  1979-06

2.  Enzyme-linked immunosorbent assay, Elisa. 3. Quantitation of specific antibodies by enzyme-labeled anti-immunoglobulin in antigen-coated tubes.

Authors:  E Engvall; P Perlmann
Journal:  J Immunol       Date:  1972-07       Impact factor: 5.422

3.  Antigens of the type-1 fimbriae of salmonellae and other enterobacteria.

Authors:  J P Duguid; I Campbell
Journal:  J Med Microbiol       Date:  1969-11-04       Impact factor: 2.472

4.  The function of bacterial fimbriae.

Authors:  J P Duguid
Journal:  Arch Immunol Ther Exp (Warsz)       Date:  1968       Impact factor: 4.291

Review 5.  The structure, function, synthesis and genetic control of bacterial pili and a molecular model for DNA and RNA transport in gram negative bacteria.

Authors:  C C Brinton
Journal:  Trans N Y Acad Sci       Date:  1965-06

6.  New Method for isolation of immunologically pure pili from Escherichia coli.

Authors:  T K Korhonen; E L Nurmiaho; H Ranta; C S Edén
Journal:  Infect Immun       Date:  1980-02       Impact factor: 3.441

7.  Structures of ceramide tetrasaccharides from various sources: uniqueness of rat kidney ceramide tetrasaccharide.

Authors:  B Siddiqui; J Kawanami; Y T Li; S Hakomori
Journal:  J Lipid Res       Date:  1972-09       Impact factor: 5.922

8.  Adhesion, hemagglutination, and virulence of Escherichia coli causing urinary tract infections.

Authors:  L Hagberg; U Jodal; T K Korhonen; G Lidin-Janson; U Lindberg; C Svanborg Edén
Journal:  Infect Immun       Date:  1981-02       Impact factor: 3.441

9.  Comparison of Escherichia coli fimbrial antigen F7 with type 1 fimbriae.

Authors:  I Orskov; F Orskov; A Birch-Andersen
Journal:  Infect Immun       Date:  1980-02       Impact factor: 3.441

10.  Characterization of type 1 pili of Salmonella typhimurium LT2.

Authors:  T K Korhonen; K Lounatmaa; H Ranta; N Kuusi
Journal:  J Bacteriol       Date:  1980-11       Impact factor: 3.490

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  28 in total

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Authors:  Laurence Nachin; Ulf Nannmark; Thomas Nyström
Journal:  J Bacteriol       Date:  2005-09       Impact factor: 3.490

Review 2.  Escherichia coli in extra-intestinal infections.

Authors:  I Orskov; F Orskov
Journal:  J Hyg (Lond)       Date:  1985-12

3.  Type 1 fimbria-mediated adhesion of enteric bacteria to grass roots.

Authors:  K Haahtela; E Tarkka; T K Korhonen
Journal:  Appl Environ Microbiol       Date:  1985-05       Impact factor: 4.792

4.  Binding characteristics of Escherichia coli adhesins in human urinary bladder.

Authors:  R Virkola; B Westerlund; H Holthöfer; J Parkkinen; M Kekomäki; T K Korhonen
Journal:  Infect Immun       Date:  1988-10       Impact factor: 3.441

Review 5.  P-fimbriae, bacterial adhesion, and pyelonephritis.

Authors:  J Winberg
Journal:  Arch Dis Child       Date:  1984-02       Impact factor: 3.791

6.  P-antigen-recognizing fimbriae from human uropathogenic Escherichia coli strains.

Authors:  T K Korhonen; V Väisänen; H Saxén; H Hultberg; S B Svenson
Journal:  Infect Immun       Date:  1982-07       Impact factor: 3.441

7.  Lesions in two Escherichia coli type 1 pilus genes alter pilus number and length without affecting receptor binding.

Authors:  P W Russell; P E Orndorff
Journal:  J Bacteriol       Date:  1992-09       Impact factor: 3.490

8.  Interaction of Saccharomyces boulardii with Salmonella enterica serovar Typhimurium protects mice and modifies T84 cell response to the infection.

Authors:  Flaviano S Martins; Guillaume Dalmasso; Rosa M E Arantes; Anne Doye; Emmanuel Lemichez; Patricia Lagadec; Veronique Imbert; Jean-François Peyron; Patrick Rampal; Jacques R Nicoli; Dorota Czerucka
Journal:  PLoS One       Date:  2010-01-27       Impact factor: 3.240

9.  Uropathogenic Escherichia coli triggers oxygen-dependent apoptosis in human neutrophils through the cooperative effect of type 1 fimbriae and lipopolysaccharide.

Authors:  Robert Blomgran; Limin Zheng; Olle Stendahl
Journal:  Infect Immun       Date:  2004-08       Impact factor: 3.441

10.  Mechanism of interaction of Salmonella and Schistosoma species.

Authors:  R F Melhem; P T LoVerde
Journal:  Infect Immun       Date:  1984-05       Impact factor: 3.441

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