Proteus mirabilis causing cellulitis in broiler chickens

Matheus Silva Sanches1, Ana Angelita Sampaio Baptista2, Marielen de Souza2

  • 1Department of Microbiology, Laboratory of Bacteriology, Center of Biological Sciences, State University of Londrina, Rodovia Celso Garcia Cid PO-BOX 6001, Londrina, Paraná, 86051-980, Brazil.

Insights

Proteus mirabilis strains isolated from broiler cellulitis possess virulence factors and can cause lesions. Both strains induced cellulitis in chickens within 24 hours post-inoculation.

Area of Science:

  • Veterinary Microbiology
  • Poultry Pathology
  • Bacterial Pathogenesis

Background:

  • Cellulitis is a significant concern in broiler chickens, impacting flock health and economic viability.
  • Understanding the virulence factors of Proteus mirabilis is crucial for managing infections in poultry.
  • Limited data exists on the specific virulence profiles of P. mirabilis strains causing cellulitis in broilers.

Purpose of the Study:

  • To genetically and phenotypically characterize the virulence profiles of two P. mirabilis strains isolated from broiler cellulitis.
  • To evaluate the in vivo capacity of these strains to induce cellulitis lesions in a broiler model.
  • To compare the virulence of a high-virulence strain (LBUEL-A33) with a low-virulence strain (LBUEL-A34).

Main Methods:

  • Genotypic analysis to identify virulence-associated genes (e.g., fimbriae, proteases, hemolysin, siderophore).
  • Phenotypic characterization including biofilm formation, adhesion patterns (Vero cells), and cytotoxicity assays.
  • In vivo experimental inoculation of broiler chickens to induce and assess cellulitis lesions.
  • Histological examination of affected tissues.

Main Results:

  • The high-virulence strain (LBUEL-A33) possessed multiple virulence genes, formed strong biofilms, exhibited aggregative adhesion, and showed cytotoxicity.
  • The low-virulence strain (LBUEL-A34) lacked specific genes (pmfA, ucaA) but still formed strong biofilms and showed aggregative adhesion without cytotoxicity.
  • Both P. mirabilis strains rapidly induced cellulitis lesions within 24 hours post-inoculation, with no significant changes up to 120 hours.
  • Co-inoculation with avian pathogenic E. coli did not alter lesion severity compared to individual P. mirabilis inoculation.
  • Histological analysis confirmed characteristic cellulitis lesions caused by the LBUEL-A33 strain.

Conclusions:

  • Both P. mirabilis strains isolated from broiler cellulitis possess significant virulence factors.
  • These strains are capable of experimentally inducing cellulitis in broiler chickens.
  • Further research into P. mirabilis virulence mechanisms in poultry is warranted for effective disease control.