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Streptococcus pluranimalium 2N12 Exerts an Antagonistic Effect Against the Swine Pathogen Actinobacillus pleuropneumoniae by Producing Hydrogen Peroxide

Actinobacillus pleuropneumoniae is the causal agent of porcine pleuropneumonia, a highly contagious and often deadly respiratory disease that causes major economic losses in the swine industry worldwide. The aim of the present study was to investigate the hydrogen peroxide (H(2)O(2))-dependent antag...

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Detalles Bibliográficos
Autores principales: Vaillancourt, Katy, Frenette, Michel, Gottschalk, Marcelo, Grenier, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8692661/
https://www.ncbi.nlm.nih.gov/pubmed/34957284
http://dx.doi.org/10.3389/fvets.2021.787241
Descripción
Sumario:Actinobacillus pleuropneumoniae is the causal agent of porcine pleuropneumonia, a highly contagious and often deadly respiratory disease that causes major economic losses in the swine industry worldwide. The aim of the present study was to investigate the hydrogen peroxide (H(2)O(2))-dependent antagonistic activity of Streptococcus pluranimalium 2N12 (pig nasal isolate) against A. pleuropneumoniae. A fluorimetric assay showed that S. pluranimalium produces H(2)O(2) dose- and time-dependently. The production of H(2)O(2) increased in the presence of exogenous lactate, suggesting the involvement of lactate oxidase. All 20 strains of A. pleuropneumoniae tested, belonging to 18 different serovars, were susceptible to H(2)O(2), with minimal inhibitory concentrations and minimal bactericidal concentrations ranging from 0.57 to 2.3 mM. H(2)O(2), as well as a culture supernatant of S. pluranimalium, killed planktonic cells of A. pleuropneumoniae. Treating the culture supernatant with catalase abolished its bactericidal property. H(2)O(2) was also active against a pre-formed biofilm-like structure of A. pleuropneumoniae albeit to a lesser extent. A checkerboard assay was used to show that there were antibacterial synergistic interactions between H(2)O(2) and conventional antibiotics, more particularly ceftiofur. Based on our results and within the limitations of this in vitro study, the production of H(2)O(2) by S. pluranimalium could be regarded as a potential protective mechanism of the upper respiratory tract against H(2)O(2)-sensitive pathogens such as A. pleuropneumoniae.