Identification of membrane-associated proteins with pathogenic potential expressed by Corynebacterium pseudotuberculosis grown in animal serum

• Main Authors: José Tadeu Raynal, Bruno Lopes Bastos, Priscilla Carolinne Bagano Vilas-Boas, Thiago de Jesus Sousa, Marcos Costa-Silva, Maria da Conceição Aquino de Sá, Ricardo Wagner Portela, Lília Ferreira Moura-Costa, Vasco Azevedo, Roberto Meyer
• Format: Article
• Language: English
• Published: BMC 2018-01-01
• Series: BMC Research Notes
• Subjects: Corynebacterium pseudotuberculosis; Caseous lymphadenitis; Sheep; Goat; Antigens; Virulence factors
• Online Access: http://link.springer.com/article/10.1186/s13104-018-3180-5

Abstract Objective Previous works defining antigens that might be used as vaccine targets against Corynebacterium pseudotuberculosis, which is the causative agent of sheep and goat caseous lymphadenitis, have focused on secreted proteins produced in a chemically defined culture media. Considering that such antigens might not reflect the repertoire of proteins expressed during infection conditions, this experiment aimed to investigate the membrane-associated proteins with pathogenic potential expressed by C. pseudotuberculosis grown directly in animal serum. Results Its membrane-associated proteins have been extracted using an organic solvent enrichment methodology, followed by LC–MS/MS and bioinformatics analysis for protein identification and classification. The results revealed 22 membrane-associated proteins characterized as potentially pathogenic. An interaction network analysis indicated that the four potentially pathogenic proteins ciuA, fagA, OppA4 and OppCD were biologically connected within two distinct network pathways, which were both associated with the ABC Transporters KEGG pathway. These results suggest that C. pseudotuberculosis pathogenesis might be associated with the transport and uptake of nutrients; other seven identified potentially pathogenic membrane proteins also suggest that pathogenesis might involve events of bacterial resistance and adhesion. The proteins herein reported potentially reflect part of the protein repertoire expressed during real infection conditions and might be tested as vaccine antigens.