Associations between Pleurisy and the Main Bacterial Pathogens of the Porcine Respiratory Diseases Complex (PRDC)

Fernando Antônio Moreira Petri1, Geovana Coelho Ferreira1, Laíza Pinto Arruda1

  • 1School of Agricultural and Veterinarian Sciences, São Paulo State University (Unesp), Jaboticabal 14884-900, SP, Brazil.

Insights

Porcine Respiratory Diseases Complex (PRDC) in pigs is linked to several bacterial pathogens. This study used qPCR on carcass samples, finding correlations between lesion severity and specific bacteria, aiding PRDC surveillance.

Area of Science:

  • Veterinary Medicine
  • Animal Pathology
  • Molecular Diagnostics

Background:

  • Porcine Respiratory Diseases Complex (PRDC) is a significant economic concern in swine production.
  • PRDC involves multiple bacterial pathogens, including *Mycoplasma hyopneumoniae*, *Actinobacillus pleuropneumoniae*, *Pasteurella multocida*, *Glaesserella parasuis*, and *Streptococcus suis*.
  • Pleurisy lesions caused by PRDC can lead to carcass condemnation, impacting the pork industry.

Purpose of the Study:

  • To evaluate the utility of slaughterhouse-based diagnostics for identifying PRDC pathogens.
  • To correlate the severity of respiratory lesions with the presence of specific bacterial agents using qPCR.
  • To assess the potential of qPCR as a surveillance tool for PRDC.

Main Methods:

  • Selection of 1015 pig carcasses from three commercial farms.
  • Evaluation of respiratory conditions using the Slaughterhouse Pleurisy Evaluation System (SPES).
  • Collection of 106 pleural and lung fragments for quantitative Polymerase Chain Reaction (qPCR) analysis to detect five key bacterial pathogens.

Main Results:

  • Moderate correlations were observed between lesion severity and the presence of *Pasteurella multocida* (R=0.38) and *Actinobacillus pleuropneumoniae* (R=0.28) in pleural samples.
  • Lung lesion severity showed moderate correlations with *Pasteurella multocida* (R=0.43) and *Mycoplasma hyopneumoniae* (R=0.35).
  • A strong correlation (R=0.82) was found between *Pasteurella multocida* and *Mycoplasma hyopneumoniae* in pleural tissues.

Conclusions:

  • qPCR is a valuable tool for identifying and quantifying PRDC causative agents in field surveillance.
  • The study highlights the complex interplay between bacterial pathogens and lesion development in PRDC.
  • Slaughterhouse diagnostics combined with molecular methods can provide comprehensive insights into PRDC prevalence and impact.

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