Designing and Evaluation of a Plasmid Encoding Immunogenic Epitopes From Echinococcus granulosus Eg95-1-6, P29, and GST Against Hydatid Cyst in BALB/c Mice

Cystic echinococcosis (CE) is a neglected parasitic infection with a particular impact in humans and livestock. The current investigation was undertaken to design and evaluate a DNA vaccine encoding Echinococcus granulosus Eg95-1 to EG95-6, P29, and GST against hydatid cyst infection in BALB/c mice....

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Main Authors: Sasan Khazaei, Abdolhossein Dalimi, Majid Pirestani, Fatemeh Ghafarifar
Format: Article
Language:English
Published: Wiley 2025-01-01
Series:Journal of Parasitology Research
Online Access:http://dx.doi.org/10.1155/japr/1655679
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author Sasan Khazaei
Abdolhossein Dalimi
Majid Pirestani
Fatemeh Ghafarifar
author_facet Sasan Khazaei
Abdolhossein Dalimi
Majid Pirestani
Fatemeh Ghafarifar
author_sort Sasan Khazaei
collection DOAJ
description Cystic echinococcosis (CE) is a neglected parasitic infection with a particular impact in humans and livestock. The current investigation was undertaken to design and evaluate a DNA vaccine encoding Echinococcus granulosus Eg95-1 to EG95-6, P29, and GST against hydatid cyst infection in BALB/c mice. Initially, B-cell, cytotoxic T-lymphocyte, and helper T-lymphocyte epitopes were forecasted using B-cell epitope prediction server (BCPREDS) and Immune Epitope Database (IEDB) server, respectively, and a vaccine construct incorporating multiple epitopes was rationally designed and comprehensively analyzed through in silico modeling and simulation studies. Next, Escherichia coli TOP10 was transformed by the recombinant pcDNA 3.1 plasmid and mass production, followed by plasmid extraction, was done. The BALB/c mouse immunization was done with 50 and 100 μg concentrations of plasmid combined with IL-12 adjuvant or alone. Mouse sera and splenic lymphocytes were used for the measurement of specific humoral and cellular responses. The candidate vaccine model weighed 37.49 kDa with 338 residues antigenic, while nonallergenic, soluble, stable, highly thermotolerant, and hydrophilic in nature. Expression in HEK-293 cells was successfully achieved, as evidenced by the detection of a 37 kDa protein band in the western blot analysis. Vaccine doses, especially the 100 μg concentration, alone or in combination with an adjuvant, induced a T-helper 1 (Th1)–type immune response. This was evidenced by higher levels of IgG2a antibody and interferon gamma (IFN-γ) along with lower levels of interleukin 4 (IL-4). Although the groups that received the 50-μg dose of vaccine alone or with adjuvant showed a lower immune response, overall, the vaccinated groups showed statistically significant differences compared to the control groups (phosphate-buffered saline (PBS) and pcDNA). The promising results of this vaccine candidate can be further examined using challenges with various parasite genotypes.
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spelling doaj-art-21eaba97860c46d8aa43653b7bed5dff2025-08-20T03:15:47ZengWileyJournal of Parasitology Research2090-00312025-01-01202510.1155/japr/1655679Designing and Evaluation of a Plasmid Encoding Immunogenic Epitopes From Echinococcus granulosus Eg95-1-6, P29, and GST Against Hydatid Cyst in BALB/c MiceSasan Khazaei0Abdolhossein Dalimi1Majid Pirestani2Fatemeh Ghafarifar3Department of ParasitologyDepartment of ParasitologyDepartment of ParasitologyDepartment of ParasitologyCystic echinococcosis (CE) is a neglected parasitic infection with a particular impact in humans and livestock. The current investigation was undertaken to design and evaluate a DNA vaccine encoding Echinococcus granulosus Eg95-1 to EG95-6, P29, and GST against hydatid cyst infection in BALB/c mice. Initially, B-cell, cytotoxic T-lymphocyte, and helper T-lymphocyte epitopes were forecasted using B-cell epitope prediction server (BCPREDS) and Immune Epitope Database (IEDB) server, respectively, and a vaccine construct incorporating multiple epitopes was rationally designed and comprehensively analyzed through in silico modeling and simulation studies. Next, Escherichia coli TOP10 was transformed by the recombinant pcDNA 3.1 plasmid and mass production, followed by plasmid extraction, was done. The BALB/c mouse immunization was done with 50 and 100 μg concentrations of plasmid combined with IL-12 adjuvant or alone. Mouse sera and splenic lymphocytes were used for the measurement of specific humoral and cellular responses. The candidate vaccine model weighed 37.49 kDa with 338 residues antigenic, while nonallergenic, soluble, stable, highly thermotolerant, and hydrophilic in nature. Expression in HEK-293 cells was successfully achieved, as evidenced by the detection of a 37 kDa protein band in the western blot analysis. Vaccine doses, especially the 100 μg concentration, alone or in combination with an adjuvant, induced a T-helper 1 (Th1)–type immune response. This was evidenced by higher levels of IgG2a antibody and interferon gamma (IFN-γ) along with lower levels of interleukin 4 (IL-4). Although the groups that received the 50-μg dose of vaccine alone or with adjuvant showed a lower immune response, overall, the vaccinated groups showed statistically significant differences compared to the control groups (phosphate-buffered saline (PBS) and pcDNA). The promising results of this vaccine candidate can be further examined using challenges with various parasite genotypes.http://dx.doi.org/10.1155/japr/1655679
spellingShingle Sasan Khazaei
Abdolhossein Dalimi
Majid Pirestani
Fatemeh Ghafarifar
Designing and Evaluation of a Plasmid Encoding Immunogenic Epitopes From Echinococcus granulosus Eg95-1-6, P29, and GST Against Hydatid Cyst in BALB/c Mice
Journal of Parasitology Research
title Designing and Evaluation of a Plasmid Encoding Immunogenic Epitopes From Echinococcus granulosus Eg95-1-6, P29, and GST Against Hydatid Cyst in BALB/c Mice
title_full Designing and Evaluation of a Plasmid Encoding Immunogenic Epitopes From Echinococcus granulosus Eg95-1-6, P29, and GST Against Hydatid Cyst in BALB/c Mice
title_fullStr Designing and Evaluation of a Plasmid Encoding Immunogenic Epitopes From Echinococcus granulosus Eg95-1-6, P29, and GST Against Hydatid Cyst in BALB/c Mice
title_full_unstemmed Designing and Evaluation of a Plasmid Encoding Immunogenic Epitopes From Echinococcus granulosus Eg95-1-6, P29, and GST Against Hydatid Cyst in BALB/c Mice
title_short Designing and Evaluation of a Plasmid Encoding Immunogenic Epitopes From Echinococcus granulosus Eg95-1-6, P29, and GST Against Hydatid Cyst in BALB/c Mice
title_sort designing and evaluation of a plasmid encoding immunogenic epitopes from echinococcus granulosus eg95 1 6 p29 and gst against hydatid cyst in balb c mice
url http://dx.doi.org/10.1155/japr/1655679
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