Identification of CD4+ T-cell epitopes on iron-regulated surface determinant B of Staphylococcus aureus. (December 2015)

• Record Type: Journal Article
• Authors: Yu, Simiao; Zhang, Hua; Yao, Di; Liu, Wei; Wang, Xintong; Chen, Xiaoting; Wei, Yuhua; Zhang, Zhenghai; Wang, Jiannan; Yu, Liquan; Sun, Hunan; Wu, Zhijun; Yu, Yongzhong; Song, Baifen; Ma, Jinzhu; Tong, Chunyu; Cui, Yudong
• Is Part Of: Microbial pathogenesis. Volume 89(2015)
• Page Start: 108
• Page End: 113
• Publication Date: 2015-12
• Subjects: Staphylococcus aureus -- IsdB protein -- T-cell epitope; Pathogenic microorganisms -- Periodicals; Pathology, Molecular -- Periodicals; Communicable Diseases -- microbiology -- Periodicals; Communicable Diseases -- parasitology -- Periodicals; Micro-organismes pathogènes -- Périodiques; Pathologie moléculaire -- Périodiques; Electronic journals; 616.9041
• DOI: 10.1016/j.micpath.2015.09.006
• Languages: English
• ISSNs: 0882-4010

Abstract

Abstract: Iron-regulated surface determinant B (IsdB) of Staphylococcus aureus ( S. aureus ) is a highly conserved surface protein that can induce protective CD4 + T-cell immune response. A pivotal role of CD4 + T-cells in effective immunity against S. aureus infection has been proved, but CD4 + T-cell epitopes on the S. aureus IsdB have not been well identified. In this study, MHC binding assay was firstly used to predict CD4 + T-cell epitopes on S. aureus IsdB protein, and six peptides were synthesized to validate the probable epitopes. Two novel IsdB CD4 + T-cell epitopes, P1 (residues 159–178) and P4 (residues 287–306), were for the first time identified using CD4 + T-cells obtained from IsdB-immunized C57BL/6 (H-2 b ) and BALB/c (H-2 d ) mice spleen based on cell proliferation and cytokines response. The results showed that P1 and P4 emulsified in Freund's adjuvant (FA) induced much higher cell proliferation compared with PBS emulsified in FA. CD4 + T-cells stimulated with peptides P1 and P4 secreted significantly higher levels of IFN-γ and IL-17A. However, the level of the cytokine IL-4 almost remained unchanged, suggesting that P1 and P4 preferentially elicited polarized Th1-type responses. In addition, BALB/c mice just respond to P4 not P1, while C57BL/6 mice respond to P1 not P4, implying that epitope P1 and P4 were determined as H-2 b and H-2 d restricted epitope, respectively. Taken together, our data may provide an explanation of the IsdB-induced protection against S. aureus and highlight the possibility of developing the epitope-based vaccine against the S. aureus . Highlights: Two novel Staphylococcus aureus IsdB CD4 + T-cell epitopes were for the first time identified. Our findings are available for further study of epitope-based vaccines. Two T-cell epitopes preferentially elicited polarized Th1-type responses.