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Induction of protective immunity after escherichia coli bladder infection in primates. Dependence of the globoside-specific P-fimbrial tip adhesin and its cognate receptor.

Abstract
Clinical observations suggest that immune mechanisms affect etiology and course of recurrent cystitis. A primate infection model was used to show that primary bladder infection with a uropathogenic P-fimbriated strain (binding to globoside present in the bladder wall) protects against rechallenge with homologous as well as heterologous Escherichia coli strains for up to 5-6 mo. In contrast, mutant derivatives producing P-fimbriae either lacking the tip adhesin protein or carrying an adhesin for which no bladder receptor was present, were unable to induce protection, even though they generated bladder infections of similar duration as the wild type. Therefore, the protective effect mediated by the adhesin seemed to depend upon the presence of its cognate receptor. Since the wild strain also mediated protection against mutants that lacked the adhesin, our data suggest that the globoside-binding PapG adhesin acts as an adjuvant during infection to enhance a specific response against other bacterial antigens. In fact, the globoside-binding strain DS17, but not the mutant DS17-1, unable to bind to membrane-bound globoside, elicited a secretory IgA response to LPS in urine. These in vivo findings suggest that bacterial adhesin-ligand interactions may have signaling functions of importance for the immune response.
AuthorsM Söderhäll, S Normark, K Ishikawa, K Karlsson, S Teneberg, J Winberg, R Möllby
JournalThe Journal of clinical investigation (J Clin Invest) Vol. 100 Issue 2 Pg. 364-72 (Jul 15 1997) ISSN: 0021-9738 [Print] United States
PMID9218513 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Adhesins, Escherichia coli
  • Globosides
  • Glycosphingolipids
  • PapG protein, E coli
  • Receptors, Immunologic
  • bacterial adhesin receptor
  • Fimbriae Proteins
Topics
  • Adhesins, Escherichia coli (genetics, immunology, metabolism)
  • Animals
  • Cystitis (immunology, microbiology)
  • Escherichia coli (genetics, immunology, pathogenicity)
  • Escherichia coli Infections (immunology, microbiology)
  • Female
  • Fimbriae Proteins
  • Fimbriae, Bacterial (immunology)
  • Globosides (metabolism)
  • Glycosphingolipids (metabolism)
  • Macaca fascicularis
  • Mutation
  • Receptors, Immunologic (metabolism)
  • Urinary Bladder (microbiology)
  • Vagina (microbiology)

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