Genetic Diversity of Actinobacillus pleuropneumoniae Serovars in Hungary

Gábor Kardos1, Rita Sárközi2, Levente Laczkó1

  • 1Institute of Metagenomics, University of Debrecen, Nagyerdei krt. 94, H-4032 Debrecen, Hungary.

Veterinary Sciences
|October 26, 2022
PubMed

Insights

This study analyzed 114 Actinobacillus pleuropneumoniae isolates, finding serovar 13 common despite low virulence, possibly due to antibiotic resistance. Serovar 16 showed high virulence and clonality.

Area of Science:

  • Veterinary Microbiology
  • Bacterial Pathogenesis
  • Antimicrobial Resistance

Background:

  • Actinobacillus pleuropneumoniae causes significant swine respiratory disease.
  • Understanding the genetic diversity and virulence factors of circulating strains is crucial for disease control.
  • Antibiotic resistance in A. pleuropneumoniae poses a growing threat to animal health and food safety.

Purpose of the Study:

  • To characterize genetic relationships, serovars, toxin production, and antibiotic resistance profiles of A. pleuropneumoniae isolates.
  • To investigate factors contributing to the prevalence and emergence of specific serovars.
  • To assess the genetic diversity within key serovars.

Main Methods:

  • Characterization of 114 A. pleuropneumoniae isolates based on biotype, serovar, antibiotic resistance genes, and toxin gene presence.
  • Pulsed-field gel electrophoresis (PFGE) for genetic relationship analysis.
  • Whole-genome sequencing of representative serovar 13 isolates.

Main Results:

  • Sixteen distinct genetic clusters were identified by PFGE.
  • Serovars 2, 13, 9, and 16 were the most prevalent.
  • Serovar 13 isolates showed high frequency of tetracycline and beta-lactam resistance, with low genetic diversity.
  • All isolates possessed the apxIV gene; toxin profiles varied by serovar (ApxII, ApxIII, ApxI).
  • Serovar 16 exhibited high virulence and clonality.

Conclusions:

  • The high frequency of serovar 13 may be linked to its antibiotic resistance rather than virulence.
  • Antibiotic resistance, particularly to beta-lactams and tetracyclines, likely facilitated the spread of serovar 13.
  • The emergence and clonality of serovar 16 appear to be driven by its high virulence.

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