In silico cloning and B/T cell epitope prediction of triosephosphate isomerase from Echinococcus granulosus

Fen Wang1, Bin Ye2,3

  • 1Department of Pathogenic Biology, Chongqing Medical University, Chongqing, 400016, China.

Parasitology Research
|June 11, 2016
PubMed

Insights

Researchers identified potential vaccine targets for cystic echinococcosis by analyzing the Echinococcus granulosus triosephosphate isomerase gene. This study predicts key epitopes for developing a new anti-hydatidosis vaccine.

Area of Science:

  • Parasitology
  • Vaccinology
  • Bioinformatics

Background:

  • Cystic echinococcosis, a global zoonosis caused by Echinococcus granulosus, faces diagnostic and treatment limitations.
  • The need for novel vaccine strategies against hydatidosis is critical.

Purpose of the Study:

  • To identify potential target proteins for a new anti-hydatidosis vaccine.
  • To in silico clone the triosephosphate isomerase (EgTIM) gene of E. granulosus.
  • To predict B cell and T cell epitopes for vaccine development.

Main Methods:

  • In silico cloning of the E. granulosus triosephosphate isomerase gene.
  • Bioinformatic prediction of B cell and T cell epitopes.
  • Analysis of cDNA and deduced amino acid sequences.

Main Results:

  • The EgTIM cDNA sequence comprises 1094 base pairs with a 753 base pair open reading frame.
  • The deduced amino acid sequence consists of 250 amino acids.
  • Five cross-reactive epitopes were identified at specific amino acid positions (21-35, 43-57, 94-107, 115-129, and 164-183).

Conclusions:

  • The identified epitopes are potential candidates for developing a vaccine against Echinococcus granulosus.
  • These findings provide a foundation for gene cloning, recombinant expression, and anti-hydatidosis vaccine design.

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