In Silico-Based Vaccine Design Against Hepatopancreatic Microsporidiosis in Shrimp

Authors

  • Sk Injamamul Islam The International Graduate Program of Veterinary Science and Technology, Department of Veterinary Microbiology, Faculty of Veterinary Science and Technology, Chulalongkorn University, Bangkok 10330, Thailand https://orcid.org/0000-0002-0888-6075
  • Moslema Jahan Mou Department of Genetic Engineering and Biotechnology, Faculty of Life and Earth Science, University of Rajshahi, Bangladesh, India
  • Saloa Sanjida Department of Environmental Science and Technology, Faculty of Applied Science and Technology, Jashore University of Science and Technology, Bangladesh 7408, India

DOI:

https://doi.org/10.48048/tis.2022.2679

Keywords:

Enterocytozoon hepatopenaei, Hepatopancreatic microsporidiosis, Vaccine, Epitopes, MD Simulation

Abstract

Enterocytozoon hepatopenaei (EHP) is a spore-forming intracellular parasite that produces an economically devastating disease in farmed shrimp called hepatopancreatic microsporidiosis (HPM), known to slow the growth of hosts in aquaculture. Spore wall proteins are implicated in the recognition of host cells in microsporidia. Many parasites have been demonstrated to detect heparin, a glycosaminoglycan (GAG) molecule present on cell surfaces, as a host. The sequencing and characterization of several EHP strains started to reveal information regarding pathogen biology, pathogenicity, and spore wall proteins must bind to the shrimp cell surface to infect it, and failure to do so results in ineffective infection. Despite these devastating complications, there is still no cure or vaccine for the parasites. In this regard, an immunoinformatics method was used to generate an epitope-based vaccine against this pathogen. The immunodominant T-cell and B-cell epitopes were identified using the spore wall proteins of EHP. The final constructed vaccine sequence was developed to be immunogenic, non-allergenic as well as have better solubility. Molecular dynamics simulation revealed significant binding stability and structural compactness. Finally, using Escherichia coli K12 as a model, codon optimization yielded ideal GC content and a higher CAI value, which was then included in the cloning vector pET2+ (a). Altogether, our outcomes imply that the proposed peptide vaccine may be a good option for HPM prophylaxis.

HIGHLIGHTS

  • Hepatopancreatic microsporidiosis (HPM) is known to slow the growth of shrimp
  • There are approved drugs or vaccines to control this disease
  • In-silico approach and immunoinformatics has some advantage previously in fishes
  • The design vaccine candidate would have some advantages to combat the disease for sustainable shrimp production


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Published

2022-11-01

How to Cite

Islam, S. I., Mou, M. J. ., & Sanjida, S. . (2022). In Silico-Based Vaccine Design Against Hepatopancreatic Microsporidiosis in Shrimp. Trends in Sciences, 19(21), 2679. https://doi.org/10.48048/tis.2022.2679