Immunology · 2003 · 205 citations · 22 references
Life SciencesImmunologyMicrobiologyBacteriologyMedical MicrobiologyMicrobial PathogenesisBacterial PathogenesisGastrointestinal ImmunologyGut MicrobiotaMucosal Immune SystemMucosal ImmunitySecretory Immunoglobulin AEpithelial-microbe InteractionsEscherichia ColiImmune Exclusion At Mucosal SurfacesIntestinal Secretory Immunoglobulin AMucosal ColonizationMucosal Immunity To BacteriaPathogenesis Of Enteric InfectionsSecretory Immunoglobulin A Responses
It is critical, both for the host and for the long-term benefit of the bacteria that colonize the gut, that bacterial overgrowth with subsequent bacterial translocation, which may lead to sepsis and death of the host, be avoided. Secretory IgA (sIgA) is known to be a key factor in this process, agglutinating bacteria and preventing their translocation in a process termed 'immune exclusion'. To determine whether human sIgA might facilitate the growth of normal enteric bacteria under some conditions, the growth of human enteric bacteria on cultured, fixed human epithelial cells was evaluated in the presence of sIgA or various other proteins. Human sIgA was found to facilitate biofilm formation by normal human gut flora and by Escherichia coli on cultured human epithelial cell surfaces under conditions in which non-adherent bacteria were repeatedly washed away. In addition, the presence of sIgA resulted in a 64% increase in adherence of E. coli to live cultured epithelial cells over a 45-min period. Mucin, another defence factor thought to play a key role in immune exclusion, was found to facilitate biofilm formation by E. coli. Our findings suggest that sIgA may contribute to biofilm formation in the gut.
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A Model of Host-Microbial Interactions in an Open Mammalian Ecosystem
Lynn Bry, Per Falk, Tore Midtvedt et al. · Science · 1996 · 619 citations
Armelle Phalipon, Ana Cardona, Jean-Pierre Kraehenbuhl et al. · Immunity · 2002 · 416 citations · Full text