AI Article Synopsis

  • Recent studies highlight the role of secretory IgA (SIgA) and mucin in biofilm formation by gut bacteria, especially E. coli.
  • Research found that the type 1 pilus is crucial for SIgA-mediated biofilm formation; while stable expression aids this process in lab strains, transient expression only works for environmental strains.
  • The findings suggest that mucin has a lower threshold for biofilm formation compared to SIgA, indicating different functions in gut biofilm development, and introduce methods for studying bacterial biofilms on live epithelial cells.

Article Abstract

Recent studies suggest the importance of secretory IgA (SIgA) and mucin in the mediation of biofilm formation by commensal bacteria within the mammalian gut. Studies using a variety of strains of Escherichia coli have indicated that the interaction between E. coli and SIgA is dependent on the type 1 pilus. In this study, the importance of the pilus in SIgA-mediated biofilm formation by a laboratory strain (MG1655) and environmental (fecal) strains of E. coli was evaluated. Transient expression of the type 1 pilus by the laboratory strain of E. coli failed to facilitate SIgA-mediated biofilm formation, whereas constitutive expression of the type 1 pilus by the laboratory strain was sufficient. In contrast, transient expression of the type 1 pilus was sufficient to facilitate SIgA-mediated biofilm formation by environmental isolates. The "threshold" for mucin-mediated biofilm formation appeared to be lower than that for SIgA-mediated biofilm formation, perhaps reflecting disparate roles of mucin and SIgA in mediating biofilm formation in the gut. These studies also provide the first procedures for the growth of bacterial biofilms on live epithelial cells in vitro, an important development that may facilitate future studies on the effects of bacterial biofilms on epithelial cells.

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http://dx.doi.org/10.1016/j.molimm.2005.02.013DOI Listing

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