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Published on: September 8, 2021
Staphylococccus pseudintermedius surface proteins SpsD and SpsO mediate adherence to ex vivo canine corneocytes
Jeanette Bannoehr1, Jeremy K Brown, Darren J Shaw
1Dermatology Unit, The Roslin Institute and The Royal (Dick) School of Veterinary Studies, The University of Edinburgh, Easter Bush Veterinary Centre, Roslin, Midlothian EH25 9RG, UK. jeanette.bannoehr@vetsuisse.unibe.ch
Abstract:
The Gram-positive bacterium Staphylococcus pseudintermedius is regarded as the major cause of canine bacterial pyoderma. Despite its clinical importance, there is only very limited knowledge about the pathogenesis of S. pseudintermedius infection and the specific bacterial virulence factors involved in causing disease. Using a whole-genome approach, we have previously identified 18 predicted cell-wall-anchored surface proteins representing possible virulence factors in a clinical isolate of S. pseudintermedius (strain ED99). They were designated S. pseudintermedius surface proteins A-R (SpsA-SpsR). The present study tested three of the putative Sps proteins (SpsD, SpsL and SpsO) for their ability to mediate adherence of bacteria to canine corneocytes. The three proteins were expressed on the surface of the nonpathogenic surrogate host Lactococcus lactis, a Gram-positive bacterium that does not adhere to canine corneocytes. Adherence assays were performed using corneocytes from different healthy canine donors (n = 5), and bacterial cells were quantified using computerized image analysis. Two of the proteins, SpsD and SpsO, mediated adherence of L. lactis to canine corneocytes, suggesting that they contribute to S. pseudintermedius pathogenesis and may represent novel therapeutic targets to combat infection.
Insights
Two Staphylococcus pseudintermedius surface proteins, SpsD and SpsO, were found to mediate bacterial adherence to canine skin cells. These findings offer potential new therapeutic targets for treating canine pyoderma.
Area of Science:
- Veterinary Microbiology
- Bacterial Pathogenesis
- Molecular Biology
Background:
- Staphylococcus pseudintermedius is a primary cause of canine pyoderma.
- Limited understanding exists regarding the specific bacterial virulence factors contributing to canine pyoderma.
- Previous genomic analysis identified 18 potential cell-wall-anchored surface proteins (SpsA-SpsR) in S. pseudintermedius.
Purpose of the Study:
- To investigate the role of three specific S. pseudintermedius surface proteins (SpsD, SpsL, SpsO) in bacterial adherence to canine corneocytes.
- To identify potential virulence factors that contribute to canine pyoderma pathogenesis.
Main Methods:
- Expressed SpsD, SpsL, and SpsO on the surface of Lactococcus lactis, a non-adherent surrogate host.
- Performed adherence assays using corneocytes from five healthy canine donors.
- Quantified bacterial adherence via computerized image analysis.
Main Results:
- SpsD and SpsO significantly mediated the adherence of L. lactis to canine corneocytes.
- SpsL did not demonstrate a significant role in adherence under the tested conditions.
- These results highlight SpsD and SpsO as key factors in S. pseudintermedius adherence.
Conclusions:
- SpsD and SpsO are identified as crucial bacterial virulence factors involved in canine pyoderma.
- These proteins represent promising novel therapeutic targets for combating Staphylococcus pseudintermedius infections in dogs.
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