Neisserial Heparin Binding Antigen (NHBA) Contributes to the Adhesion of Neisseria meningitidis to Human Epithelial Cells

PLoS One. 2016 Oct 25;11(10):e0162878. doi: 10.1371/journal.pone.0162878. eCollection 2016.

Abstract

Neisserial Heparin Binding Antigen (NHBA) is a surface-exposed lipoprotein ubiquitously expressed by Neisseria meningitidis strains and an antigen of the Bexsero® vaccine. NHBA binds heparin through a conserved Arg-rich region that is the target of two proteases, the meningococcal NalP and human lactoferrin (hLf). In this work, in vitro studies showed that recombinant NHBA protein was able to bind epithelial cells and mutations of the Arg-rich tract abrogated this binding. All N-terminal and C-terminal fragments generated by NalP or hLf cleavage, regardless of the presence or absence of the Arg-rich region, did not bind to cells, indicating that a correct positioning of the Arg-rich region within the full length protein is crucial. Moreover, binding was abolished when cells were treated with heparinase III, suggesting that this interaction is mediated by heparan sulfate proteoglycans (HSPGs). N. meningitidis nhba knockout strains showed a significant reduction in adhesion to epithelial cells with respect to isogenic wild-type strains and adhesion of the wild-type strain was inhibited by anti-NHBA antibodies in a dose-dependent manner. Overall, the results demonstrate that NHBA contributes to meningococcal adhesion to epithelial cells through binding to HSPGs and suggest a possible role of anti-Bexsero® antibodies in the prevention of colonization.

MeSH terms

  • Antibodies, Bacterial / chemistry
  • Antibodies, Bacterial / genetics*
  • Antibodies, Bacterial / metabolism*
  • Bacterial Adhesion*
  • Bacterial Outer Membrane Proteins / metabolism*
  • Binding Sites
  • Carrier Proteins / metabolism*
  • Cell Line
  • Epithelial Cells / microbiology*
  • Gene Knockout Techniques
  • Heparan Sulfate Proteoglycans / metabolism
  • Heparin / metabolism
  • Humans
  • Lactoferrin / metabolism
  • Membrane Transport Proteins / metabolism
  • Meningococcal Infections / drug therapy*
  • Meningococcal Infections / microbiology
  • Meningococcal Infections / prevention & control
  • Mutation
  • Neisseria meningitidis / immunology
  • Neisseria meningitidis / physiology*
  • Recombinant Proteins / metabolism
  • Serine Endopeptidases / metabolism

Substances

  • Antibodies, Bacterial
  • Bacterial Outer Membrane Proteins
  • Carrier Proteins
  • Heparan Sulfate Proteoglycans
  • LTF protein, human
  • Membrane Transport Proteins
  • NHBA protein, Neisseria meningitidis
  • Recombinant Proteins
  • Heparin
  • Lactoferrin
  • NalP protein, Neisseria meningitidis
  • Serine Endopeptidases

Grants and funding

GSK Vaccines, (formerly Novartis Vaccines) who developed the Bexsero vaccine, provided support in the form of salaries for EDT, AP, SRP, SM, VM, MP, DS, BA, and ID. IV, GG and MDF, have received a GSK graduate fellowship from the University of Bologna (first two) and Siena (third). KLS and MPJ were supported by the Australian National Health and Medical Research Council (project grant 1099278 and Career Development Fellowship 1045235 to KLS; program grant 1071659 to MPJ). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the 'author contributions' section.