Identification of a novel bacterial outer membrane interleukin-1Β-binding protein from Aggregatibacter actinomycetemcomitans

PLoS One. 2013 Jul 31;8(7):e70509. doi: 10.1371/journal.pone.0070509. Print 2013.

Abstract

Aggregatibacter actinomycetemcomitans is a gram-negative opportunistic oral pathogen. It is frequently associated with subgingival biofilms of both chronic and aggressive periodontitis, and the diseased sites of the periodontium exhibit increased levels of the proinflammatory mediator interleukin (IL)-1β. Some bacterial species can alter their physiological properties as a result of sensing IL-1β. We have recently shown that this cytokine localizes to the cytoplasm of A. actinomycetemcomitans in co-cultures with organotypic gingival mucosa. However, current knowledge about the mechanism underlying bacterial IL-1β sensing is still limited. In this study, we characterized the interaction of A. actinomycetemcomitans total membrane protein with IL-1β through electrophoretic mobility shift assays. The interacting protein, which we have designated bacterial interleukin receptor I (BilRI), was identified through mass spectrometry and was found to be Pasteurellaceae specific. Based on the results obtained using protein function prediction tools, this protein localizes to the outer membrane and contains a typical lipoprotein signal sequence. All six tested biofilm cultures of clinical A. actinomycetemcomitans strains expressed the protein according to phage display-derived antibody detection. Moreover, proteinase K treatment of whole A. actinomycetemcomitans cells eliminated BilRI forms that were outer membrane specific, as determined through immunoblotting. The protein was overexpressed in Escherichia coli in both the outer membrane-associated form and a soluble cytoplasmic form. When assessed using flow cytometry, the BilRI-overexpressing E. coli cells were observed to bind 2.5 times more biotinylated-IL-1β than the control cells, as detected with avidin-FITC. Overexpression of BilRI did not cause binding of a biotinylated negative control protein. In a microplate assay, soluble BilRI bound to IL-1β, but this binding was not specific, as a control protein for IL-1β also interacted with BilRI. Our findings suggest that A. actinomycetemcomitans expresses an IL-1β-binding surface-exposed lipoprotein that may be part of the bacterial IL-1β-sensing system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aggregatibacter actinomycetemcomitans / genetics
  • Aggregatibacter actinomycetemcomitans / metabolism*
  • Aggregatibacter actinomycetemcomitans / physiology
  • Amino Acid Sequence
  • Bacterial Outer Membrane Proteins / genetics
  • Bacterial Outer Membrane Proteins / metabolism*
  • Bacterial Outer Membrane Proteins / physiology
  • Biofilms
  • Cell Membrane / metabolism
  • Cytosol / metabolism
  • Electrophoresis, Polyacrylamide Gel
  • Electrophoretic Mobility Shift Assay
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Humans
  • Immunoblotting
  • Interleukin-1beta / metabolism*
  • Molecular Sequence Data
  • Pasteurellaceae Infections / microbiology
  • Protein Binding
  • Protein Sorting Signals / genetics
  • Recombinant Proteins / metabolism*

Substances

  • Bacterial Outer Membrane Proteins
  • Interleukin-1beta
  • Protein Sorting Signals
  • Recombinant Proteins

Grants and funding

This work was supported by the grants form the Academy of Finland (http://www.aka.fi/en-GB/A/), the Paulo Foundation (http://www.paulo.fi/in-english), The Ella and Georg Ehrnrooth Foundation (http://www.ellageorg.fi/en/about), and the Finnish Dental Society Apollonia (http://www.apollonia.fi/Apollonia/www5.nsf/sp?open&cid=home) to RI, Biocenter Finland (http://www.biocenter.fi/) to UL and ML, and Erasmus to IN. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.