Virulence genes of Pasteurella multocida cap B and its potential cross protection in mice

Adam Bashir Tawor1,2, Osman Erganiş3, Aslı Balevi3

  • 1Department of Microbiology, Faculty of Veterinary Medicine, University of SelçUk, Konya, 42110, Turkey. 193146002003@ogr.selcuk.edu.tr.

Insights

This study characterized Pasteurella multocida strains and evaluated a serogroup B vaccine in mice. Subcutaneous vaccination showed superior antibody titers, but no cross-protection against serogroup E was observed.

Area of Science:

  • Veterinary Microbiology
  • Immunology
  • Bacteriology

Background:

  • Pasteurella multocida, a Gram-negative bacterium, commonly colonizes animal respiratory tracts but can cause severe disease.
  • Virulence factors contribute to P. multocida pathogenicity, necessitating characterization for effective disease control.
  • Understanding immune responses to P. multocida vaccines is crucial for developing effective animal health strategies.

Purpose of the Study:

  • To characterize Pasteurella multocida isolates and their virulence genes.
  • To evaluate the immunogenicity of an inactivated P. multocida serogroup B vaccine using subcutaneous and intramuscular administration routes in mice.
  • To assess potential cross-protection against local serogroup E strains.

Main Methods:

  • Isolation and identification of P. multocida from animal samples using blood agar and PCR targeting the kmt1 gene.
  • Screening of 19 virulence-associated genes, including outer membrane, fimbrial, somatic antigen, and iron-binding genes.
  • Immunization of mice with an inactivated P. multocida serogroup B vaccine via subcutaneous and intramuscular routes, followed by antibody titer measurement and statistical analysis (ANOVA, Duncan's test).

Main Results:

  • 27 P. multocida isolates were obtained, with 21 confirmed by PCR.
  • Specific virulence genes (plpB, tadD, gatG, hgbA) were present in serogroup B and E isolates, while others were absent.
  • Subcutaneous vaccination induced significantly higher antibody titers at 3 and 5 weeks compared to intramuscular, which showed a rapid response after boosters.
  • Statistical analysis confirmed significant differences between vaccination routes (p < 0.001).

Conclusions:

  • P. multocida serogroup B, despite having fewer virulence factors, effectively elicits an immune response in mice.
  • Subcutaneous administration of the inactivated serogroup B vaccine is more immunogenic than intramuscular administration in the studied model.
  • The evaluated vaccine does not provide cross-protection against the local P. multocida serogroup E strain.