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Published on: September 11, 2020
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.
Abstract:
A total of 114 Actinobacillus pleuropneumoniae isolates from porcine hemorrhagic necrotic pleuropneumonia were characterized by the examination of biotype, serovar, antibiotic resistance genes, and genes of toxin production. Pulsed-field gel electrophoresis was used to analyze their genetic relationship, which identified 16 clusters. Serovar 2 (50 isolates), serovar 13 (25 isolates), serovar 9 (11 isolates), and serovar 16 (7 isolates) were the most frequent serovars. Serovar 2 formed nine distinguishable clusters; serovar 13 and serovar 16 were less diverse, exhibiting two potentially related subclusters; serovar 9 was represented by a single cluster. Remarkably small differences were seen in the core genome when nine representative isolates of serovar 13 were subjected to whole-genome sequencing. Tetracycline resistance was relatively frequent in the two clusters of serovar 13; one of them was also frequently resistant against beta-lactams. Resistance in other serovars was sporadic. All isolates carried the apxIV gene. The toxin profiles of serovar 2 were characterized by the production of ApxII and ApxIII toxins, except for a small cluster of three isolates: serovar 9 and serovar 16 isolates produced ApxI and ApxII toxins. Serovar 13 carried apxII and apxIBD genes, indicating the production of the ApxII toxin, but not of ApxI or ApxIII. The unusually high frequency and low diversity of serovar 13 are not explained by its virulence properties, but the high frequency of resistance to beta-lactams and tetracyclines may have played a role in its spread. The emergence of serovar 16 may be facilitated by its high virulence, also explaining its high clonality.
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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