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Virulence characteristics of oral treponemes in a murine model

L Kesavalu1, S G Walker, S C Holt

  • 1Department of Periodontics, University of Texas Health Science Center at San Antonio, 78284, USA.

Infection and Immunity
|December 11, 1997
PubMed

Insights

Oral treponemes cause subcutaneous abscesses in mice, with viable cells being essential for infection. Trypsin-like protease activity varies among species but does not influence abscess formation in this murine model.

Area of Science:

  • Microbiology
  • Oral Microbiology
  • Infectious Diseases

Background:

  • Oral treponemes are associated with periodontal diseases.
  • Understanding the virulence factors of oral treponemes is crucial for developing effective treatments.

Purpose of the Study:

  • To investigate the virulence characteristics of Treponema denticola, T. socranskii, T. pectinovorum, and T. vincentii in a murine model.
  • To evaluate the role of trypsin-like protease (TLPase) activity in the abscess-inducing potential of these oral treponemes.

Main Methods:

  • Mice were challenged with different species of oral treponemes to assess abscess formation.
  • Histological examination was performed on skin lesions.
  • Host resistance was modulated using dexamethasone and cyclophosphamide.
  • Trypsin-like protease (TLPase) activity was measured in vitro.

Main Results:

  • All tested oral treponeme species induced dose-dependent subcutaneous abscesses in mice.
  • Only viable treponeme cells were capable of inducing abscesses.
  • TLPase activity was present in T. denticola and varied in T. pectinovorum, but was absent in T. socranskii and T. vincentii.
  • Modulation of host resistance had minimal impact on virulence expression.
  • No correlation was found between TLPase activity and abscess formation.

Conclusions:

  • A murine model is suitable for evaluating the virulence of oral treponemes.
  • TLPase activity is not essential for abscess induction by oral treponemes in this mouse model.
  • Oral treponeme virulence can be studied independently of TLPase activity.

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