Adherence of human oral spirochetes by collagen-binding proteins

Microbiol Immunol. 1997;41(12):917-23. doi: 10.1111/j.1348-0421.1997.tb01950.x.

Abstract

The ability of spirochetes to adhere to collagens was compared among three species of human oral treponemes. Immunoblot analysis demonstrated that type I-, IV-, and V-collagen-binding polypeptides (CBPs) were detected in the heated and unheated preparations from both Treponema denticola ATCC 33520 and T. socranskii subsp. buccale ATCC 35534. Few CBPs, however, were detected in the heated and unheated preparations from a recently characterized isolate, T. medium strain G7201. Immunoelectron microscopy using rabbit antisera against the CBPs from the unheated preparations demonstrated that four CBPs, a 27 kDa type V-CBP of T. denticola ATCC 33520, a 95 kDa type IV-CBP and a 110 kDa type I-CBP of T. socranskii subsp. buccale ATCC 35534, and a 95 kDa type IV-CBP of T. medium strain G7201, were located on the outer envelopes of the individual cells. The adherence of T. denticola to the collagen-coated surfaces was significantly greater than that of T. medium, suggesting that the CBPs on the oral spirochetal cells play an important role in their adherence to collagen-rich connective tissues of the host.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Adhesion*
  • Bacterial Outer Membrane Proteins / analysis*
  • Bacterial Outer Membrane Proteins / immunology
  • Bacterial Outer Membrane Proteins / isolation & purification
  • Bacterial Outer Membrane Proteins / metabolism
  • Carrier Proteins / analysis*
  • Carrier Proteins / metabolism
  • Collagen / metabolism*
  • Electrophoresis, Polyacrylamide Gel
  • Hot Temperature
  • Humans
  • Immunoblotting
  • Microscopy, Electron
  • Peptides / analysis
  • Protein Binding
  • Treponema / chemistry*
  • Treponema / immunology
  • Treponema / physiology*

Substances

  • Bacterial Outer Membrane Proteins
  • Carrier Proteins
  • Peptides
  • Collagen