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Phospholipase D-neutralization in serodiagnosis of Arcanobacterium haemolyticum and Corynebacterium

B Skalka1, I Literák, P Chalupa

  • 1Department of Microbiology, Masaryk University Medical School, Brno, Czech Republic.

Zentralblatt Fur Bakteriologie : International Journal of Medical Microbiology
|February 13, 1999
PubMed

Insights

Antibodies targeting Phospholipase D (PLD) from Arcanobacterium haemolyticum and Corynebacterium pseudotuberculosis show higher neutralization of their homologous targets. This indicates distinct antigenic properties between PLD-A and PLD-C.

Area of Science:

  • Microbiology
  • Immunology
  • Veterinary Medicine

Background:

  • Phospholipase D (PLD) is an important virulence factor in bacteria like Arcanobacterium haemolyticum and Corynebacterium pseudotuberculosis.
  • Neutralizing antibodies against bacterial PLD can be crucial for developing effective vaccines and diagnostics.

Purpose of the Study:

  • To investigate the antigenic similarities and differences between PLD from A. haemolyticum (PLD-A) and C. pseudotuberculosis (PLD-C).
  • To assess the neutralizing antibody responses in humans, sheep, goats, and mice against homologous and heterologous PLD.

Main Methods:

  • Sera from infected humans, sheep, goats, and experimentally immunized mice were tested for PLD neutralization.
  • PLD-A and PLD-C were used as neutralizing antigens, with neutralization confirmed by inhibition of hemolytic synergism with the equi factor from Rhodococcus equi.

Main Results:

  • Titers of sera neutralizing homologous PLD were significantly higher than those neutralizing heterologous PLD.
  • In sheep, goats, and mice immunized with PLD-A, the proportion of sera neutralizing homologous PLD significantly exceeded those neutralizing heterologous PLD.
  • The antigenic properties of PLD-A and PLD-C were found to be similar but not identical.

Conclusions:

  • PLD from A. haemolyticum and C. pseudotuberculosis possess distinct antigenic epitopes, leading to higher homologous antibody neutralization.
  • The findings suggest that while cross-protection might occur, targeting specific PLD variants could be more effective for therapeutic or prophylactic interventions.

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