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Biochemical and Structural Characterization of the Carbohydrate Transport Substrate-binding-protein SP0092
Published on: October 2, 2017
Identification of vaccine candidate antigens of Staphylococcus pseudintermedius by whole proteome characterization
Natacha Couto1, Joana Martins2, Ana Mafalda Lourenço3
1Antibiotic Resistance Laboratory, CIISA, Faculdade de Medicina Veterinária, Universidade de Lisboa (FMV-UL), Av. da Universidade Técnica, 1300-477 Lisbon, Portugal; Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Av. da República, 2780-157 Oeiras, Portugal.
Abstract:
The recent emergence of methicillin-resistant Staphylococcus pseudintermedius (MRSP) has complicated considerably the treatment of infections caused by these bacteria. Therefore new treatment strategies are urgently needed, namely through the development of vaccines towards the control of bacterial infections. Our study describes an extensive characterization of the proteome of S. pseudintermedius through a 2-DE MALDI-TOF/TOF approach, followed by SERological Proteome Analysis (SERPA) to identify potential vaccine candidate antigens. We were able to identify 361 unique proteins, of which 39 are surface proteins. In order to assess the immunogenic potential of S. pseudintermedius proteins, a Western blot analysis of two-dimensional gels was carried out with serum from healthy dogs, dogs with atopic dermatitis infected and not infected with S. pseudintermedius. Only immunogenic areas detected by ≥ 50% of the dogs with atopic dermatitis infected with S. pseudintermedius sera and by <50% of the healthy dogs sera were excised and identified from Coomassie-colloidal stained gels. The areas identified by IgE were not considered as vaccine targets, because those proteins could induce hypersensitivity. We were able to identify 13 unique proteins after in-gel digestion of selected protein gel spots, with 4 antigenic proteins showing promising features for vaccine development. No specific antibodies were identified in the dogs with atopic dermatitis not infected with S. pseudintermedius sera that could contribute to prevention of infection. The SERPA approach employed in this study revealed novel candidate therapeutic targets for the control of S. pseudintermedius infections.
Insights
New research identifies potential vaccine targets against methicillin-resistant Staphylococcus pseudintermedius (MRSP) infections in dogs. This study characterized S. pseudintermedius proteins to find antigens for novel vaccine development against this resistant bacteria.
Area of Science:
- Veterinary Microbiology
- Bacterial Pathogenesis
- Vaccine Development
Background:
- Methicillin-resistant Staphylococcus pseudintermedius (MRSP) poses a significant challenge in treating canine bacterial infections.
- The emergence of antibiotic resistance necessitates the development of alternative therapeutic strategies, such as vaccines.
Purpose of the Study:
- To identify potential vaccine candidate antigens from the proteome of S. pseudintermedius.
- To characterize immunogenic proteins for the development of novel control strategies against MRSP infections.
Main Methods:
- Proteomic analysis using 2-DE MALDI-TOF/TOF to characterize the S. pseudintermedius proteome.
- SERological Proteome Analysis (SERPA) and Western blot with canine sera to identify immunogenic surface proteins.
- In-gel digestion and protein identification of selected antigenic spots.
Main Results:
- 361 unique proteins, including 39 surface proteins, were identified in S. pseudintermedius.
- Four antigenic proteins were identified as promising candidates for vaccine development based on immunogenicity in infected dogs.
- No specific preventative antibodies were found in dogs with non-infected atopic dermatitis.
Conclusions:
- The SERPA approach successfully identified novel candidate antigens for MRSP vaccine development.
- Targeting these identified proteins may lead to effective vaccines against S. pseudintermedius infections in dogs.
- Further research is warranted to validate these candidates for therapeutic use.
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