Mahendran Radha, Jeyabaskar Suganya, Sitharaman Gayathri, Michael Rajamani Dinakaran, Paul Agnal Vincent
Department of Bioinformatics, School of Life Sciences, Vels University, Pallavaram, Chennai, Tamil Nadu, India.
Centre for Fish Immunology, School of Life Sciences, Vels University, Pallavaram, Chennai, Tamil Nadu, India.
Drug Des Devel Ther. 2016 May 23;10:1703-14. doi: 10.2147/DDDT.S95691. eCollection 2016.
Edwardsiella tarda and Flavobacterium columnare are two important intracellular pathogenic bacteria that cause the infectious diseases edwardsiellosis and columnaris in wild and cultured fish. Prediction of major histocompatibility complex (MHC) binding is an important issue in T-cell epitope prediction. In a healthy immune system, the T-cells must recognize epitopes and induce the immune response. In this study, T-cell epitopes were predicted by using in silico immunoinformatics approach with the help of bioinformatics tools that are less expensive and are not time consuming. Such identification of binding interaction between peptides and MHC alleles aids in the discovery of new peptide vaccines. We have reported the potential peptides chosen from the outer membrane proteins (OMPs) of E. tarda and F. columnare, which interact well with MHC class I alleles. OMPs from E. tarda and F. columnare were selected and analyzed based on their antigenic and immunogenic properties. The OMPs of the genes TolC and FCOL_04620, respectively, from E. tarda and F. columnare were taken for study. Finally, two epitopes from the OMP of E. tarda exhibited excellent protein-peptide interaction when docked with MHC class I alleles. Five epitopes from the OMP of F. columnare had good protein-peptide interaction when docked with MHC class I alleles. Further in vitro studies can aid in the development of potential peptide vaccines using the predicted peptides.
迟缓爱德华氏菌和柱状黄杆菌是两种重要的细胞内病原菌,可导致野生和养殖鱼类感染爱德华氏菌病和柱状病。主要组织相容性复合体(MHC)结合预测是T细胞表位预测中的一个重要问题。在健康的免疫系统中,T细胞必须识别表位并诱导免疫反应。在本研究中,借助成本较低且不耗时的生物信息学工具,采用计算机免疫信息学方法预测T细胞表位。肽与MHC等位基因之间结合相互作用的这种鉴定有助于发现新的肽疫苗。我们报道了从迟缓爱德华氏菌和柱状黄杆菌的外膜蛋白(OMP)中选择的潜在肽,它们与MHC I类等位基因相互作用良好。基于其抗原性和免疫原性特性,选择并分析了迟缓爱德华氏菌和柱状黄杆菌的OMP。分别选取了迟缓爱德华氏菌和柱状黄杆菌中基因TolC和FCOL_04620的OMP进行研究。最后,迟缓爱德华氏菌OMP中的两个表位与MHC I类等位基因对接时表现出优异的蛋白质 - 肽相互作用。柱状黄杆菌OMP中的五个表位与MHC I类等位基因对接时具有良好的蛋白质 - 肽相互作用。进一步的体外研究有助于利用预测的肽开发潜在的肽疫苗。