Characterization of the SpaCBA Pilus Fibers in the Probiotic Lactobacillus rhamnosus GG

  • Justus Reunanen
    Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland
  • Ingemar von Ossowski
    Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland
  • Antoni P. A. Hendrickx
    Department of Medical Microbiology, University Medical Center Utrecht, Utrecht, Netherlands
  • Airi Palva
    Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland
  • Willem M. de Vos
    Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland

書誌事項

公開日
2012-04
権利情報
  • https://journals.asm.org/non-commercial-tdm-license
DOI
  • 10.1128/aem.07047-11
公開者
American Society for Microbiology

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説明

<jats:title>ABSTRACT</jats:title> <jats:p> <jats:named-content content-type="genus-species">Lactobacillus rhamnosus</jats:named-content> GG is a human intestinal isolate that has been studied intensively because of its probiotic properties. We have previously shown that <jats:named-content content-type="genus-species">L. rhamnosus</jats:named-content> GG produces proteinaceous pili that earlier had been observed only in Gram-positive pathogens (M. Kankainen et al., Proc. Natl. Acad. Sci. U. S. A. <jats:bold>106:</jats:bold> 17193–17198, 2009). These pili were found to be encoded by the <jats:italic>spaCBA</jats:italic> gene cluster, and the pilus-associated SpaC pilin was shown to confer on the cells a mucus-binding ability. In addition to the <jats:italic>spaCBA</jats:italic> cluster, another putative pilus cluster, <jats:italic>spaFED</jats:italic> , was predicted from the <jats:named-content content-type="genus-species">L. rhamnosus</jats:named-content> GG genome sequence. Herein, we show that only SpaCBA pili are produced by <jats:named-content content-type="genus-species">L. rhamnosus</jats:named-content> , and we describe a detailed analysis of cell wall-associated and affinity-purified SpaCBA pili by Western blotting and immunogold electron microscopy. Our results indicate that SpaCBA pili are heterotrimeric protrusions with a SpaA subunit as the shaft-forming major pilin. Only a few SpaB subunits could be observed in pilus fibers. Instead, SpaB pilins were found at pilus bases, as assessed by immunogold double labeling of thin sections of cells, suggesting that SpaB is involved in the termination of pilus assembly. The SpaC adhesin was present along the whole pilus length at numbers nearly equaling those of SpaA. The relative amount and uniform distribution of SpaC within pili not only makes it possible to exert both long-distance and intimate contact with host tissue but also provides mucus-binding strength, which explains the prolonged intestinal residency times observed for <jats:named-content content-type="genus-species">L. rhamnosus</jats:named-content> GG compared to that of nonpiliated lactobacilli. </jats:p>

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