4.6 Article

Bacterial Toxins from Staphylococcus aureus and Bordetella bronchiseptica Predispose the Horse's Respiratory Tract to Equine Herpesvirus Type 1 Infection

Journal

VIRUSES-BASEL
Volume 14, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/v14010149

Keywords

mucosal barriers; cell junctions; equine respiratory mucosal explants; EHV-1; alpha-hemolysin toxin; adenylate cyclase toxin; Staphylococcus aureus; Bordetella bronchiseptica

Categories

Funding

  1. Special Research Fund from Ghent University [01D15319]
  2. Research FoundationFlanders (FWO) [GO35920N]

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This study reveals that bacterial exotoxins derived from Staphylococcus aureus and Bordetella bronchiseptica can increase the susceptibility of horses to EHV-1 infection by disrupting the epithelial barrier function. The toxins cause morphological changes in the respiratory mucosa, leading to increased EHV-1 replication in the epithelium.
Respiratory disease in horses is caused by a multifactorial complex of infectious agents and environmental factors. An important pathogen in horses is equine herpesvirus type 1 (EHV-1). During co-evolution with this ancient alphaherpesvirus, the horse's respiratory tract has developed multiple antiviral barriers. However, these barriers can become compromised by environmental threats. Pollens and mycotoxins enhance mucosal susceptibility to EHV-1 by interrupting cell junctions, allowing the virus to reach its basolateral receptor. Whether bacterial toxins also play a role in this impairment has not been studied yet. Here, we evaluated the role of alpha-hemolysin (Hla) and adenylate cyclase (ACT), toxins derived from the facultative pathogenic bacterium Staphylococcus aureus (S. aureus) and the primary pathogen Bordetella bronchiseptica (B. bronchiseptica), respectively. Equine respiratory mucosal explants were cultured at an air-liquid interface and pretreated with these toxins, prior to EHV-1 inoculation. Morphological analysis of hematoxylin-eosin (HE)-stained sections of the explants revealed a decreased epithelial thickness upon treatment with both toxins. Additionally, the Hla toxin induced detachment of epithelial cells and a partial loss of cilia. These morphological changes were correlated with increased EHV-1 replication in the epithelium, as assessed by immunofluorescent stainings and confocal microscopy. In view of these results, we argue that the ACT and Hla toxins increase the susceptibility of the epithelium to EHV-1 by disrupting the epithelial barrier function. In conclusion, this study is the first to report that bacterial exotoxins increase the horse's sensitivity to EHV-1 infection. Therefore, we propose that horses suffering from infection by S. aureus or B. bronchiseptica may be more susceptible to EHV-1 infection.

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