Vaccination and immunization strategies to design Aedes aegypti salivary protein based subunit vaccine tackling Flavivirus infection

被引:10
作者
Pandey, Rajan Kumar [1 ]
Dahiya, Surbhi [1 ]
Mahita, Jarjapu [2 ]
Sowdhamini, Ramanathan [2 ]
Prajapati, Vijay Kumar [1 ]
机构
[1] Cent Univ Rajasthan, Sch Life Sci, Dept Biochem, Ajmer 305817, Rajasthan, India
[2] TIFR, NCBS, Bangalore, Karnataka, India
关键词
Flavivirus; Subunit vaccine; Epitopes; Adjuvant; Salivary protein; Aedes mosquito; IMMUNE-RESPONSE; POTENTIAL INHIBITOR; MOLECULAR DOCKING; LEISHMANIA-MAJOR; CELL EPITOPES; MOSQUITO; VIRUS; ANALOGS; PREDICTION; ALGORITHM;
D O I
10.1016/j.ijbiomac.2018.09.071
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Flavivirus causes arthropod-borne severe diseases that sometimes lead to the death. The Flavivirus species including Dengue virus, Zika virus and yellow fever virus are transmitted by the bite of Aedes mosquitoes. All these viral species target the people living in their respective endemic zone causing a high mortality rate. Recent studies show that immune factors present in the Ae. aegypd saliva is the hidden culprit promoting blood meal collection, suppressing host immune molecules and promoting disease establishment. This study was designed to develop a subunit vaccine using Aedes mosquito salivary proteins targeting the aforementioned Flaviviruses. Subunit vaccine was designed very precisely by combining the immunogenic B-cell epitope with CTL and HTL epitopes and also suitable adjuvant and linkers. Immunogenicity, allergenicity and physiochemical characterization were also performed for scientific validation. Molecular docking and molecular dynamics simulations studies were carried out to confirm the stable affinity between the vaccine protein (3D) and TLR3 receptor. At last, in silico cloning was executed to get the subunit vaccine restriction clone into pET28a vectro to express it in microbial expression system. Additionally, this study warrants the experimental evaluation for the validation purposes. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:1203 / 1211
页数:9
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