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Main Authors: Liu, Xinxin, Sun, Yun, He, Zikai, Li, Bo, Song, Wenye, Liu, Hongli, Wei, Caoying, Wu, Ying, Cao, Zhenjie, Zhang, Chen, Zhou, Yongcan
Format: Artículo científico
Language:en
Published: Developmental and comparative immunology 2026
Subjects:
Online Access:https://pubmed.ncbi.nlm.nih.gov/41687983/
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author Liu, Xinxin
Sun, Yun
He, Zikai
Li, Bo
Song, Wenye
Liu, Hongli
Wei, Caoying
Wu, Ying
Cao, Zhenjie
Zhang, Chen
Zhou, Yongcan
author_facet Liu, Xinxin
Sun, Yun
He, Zikai
Li, Bo
Song, Wenye
Liu, Hongli
Wei, Caoying
Wu, Ying
Cao, Zhenjie
Zhang, Chen
Zhou, Yongcan
Liu, Xinxin
Sun, Yun
He, Zikai
Li, Bo
Song, Wenye
Liu, Hongli
Wei, Caoying
Wu, Ying
Cao, Zhenjie
Zhang, Chen
Zhou, Yongcan
collection PubMed - marine biology
contents Immune and protective effects of recombinant multi-epitopes vaccine against infectious spleen and kidney necrosis virus in pearl gentian grouper (♀Epinephelus fuscoguttatus × ♂Epinephelus lanceolatus). Liu, Xinxin Sun, Yun He, Zikai Li, Bo Song, Wenye Liu, Hongli Wei, Caoying Wu, Ying Cao, Zhenjie Zhang, Chen Zhou, Yongcan Animals Fish Diseases Viral Vaccines DNA Virus Infections Iridoviridae Epitopes, T-Lymphocyte Bass Vaccination Capsid Proteins Epitopes, B-Lymphocyte Vaccines, Synthetic Immunity, Humoral Immunity, Cellular Antibodies, Viral Protein Subunit Vaccines The capsid protein (CP), the primary structural component and key antigen of infectious spleen kidney necrosis virus (ISKNV), remains poorly characterized in terms of its antigenic epitopes. These epitopes, typically ∼20 amino acid residues in length, are specific chemical groups determining antigenic specificity. To address this gap, we employed immunoinformatics to analyze CP epitopes. Subsequently, a multi-epitope vaccine targeting ISKNV (MEV) was designed, constructed, and screened. Immune response evaluation revealed that the predicted three T lymphocyte and five B lymphocyte epitopes exhibited antigenicity, non-toxicity, and non-allergenicity. Fusion of these epitopes yielded the MEV vaccine. In grouper trials, MEV vaccination significantly upregulated mRNA expression of immune-related genes (IL-1β, TNF-α, CD4, CD8α, MHC-Iα, MHC-IIα) and markedly increased total IgM levels, indicating induction of both cellular and humoral immunity. Crucially, MEV conferred significantly higher resistance against ISKNV challenge compared to CP immunization, achieving 85.33% survival rate. Furthermore, MEV vaccination significantly reduced viral loads in the spleen and head kidney. This study presents an economical, rapid, safe, and effective strategy for aquatic vaccine development, positioning MEV as a highly promising candidate for preventing infectious spleen kidney necrosis disease.
format Artículo científico
id pubmed_41687983
institution PubMed
language en
publishDate 2026
publisher Developmental and comparative immunology
record_format pubmed
spellingShingle Immune and protective effects of recombinant multi-epitopes vaccine against infectious spleen and kidney necrosis virus in pearl gentian grouper (♀Epinephelus fuscoguttatus × ♂Epinephelus lanceolatus).
Liu, Xinxin
Sun, Yun
He, Zikai
Li, Bo
Song, Wenye
Liu, Hongli
Wei, Caoying
Wu, Ying
Cao, Zhenjie
Zhang, Chen
Zhou, Yongcan
Animals
Fish Diseases
Viral Vaccines
DNA Virus Infections
Iridoviridae
Epitopes, T-Lymphocyte
Bass
Vaccination
Capsid Proteins
Epitopes, B-Lymphocyte
Vaccines, Synthetic
Immunity, Humoral
Immunity, Cellular
Antibodies, Viral
Protein Subunit Vaccines
Immune and protective effects of recombinant multi-epitopes vaccine against infectious spleen and kidney necrosis virus in pearl gentian grouper (♀Epinephelus fuscoguttatus × ♂Epinephelus lanceolatus). Liu, Xinxin Sun, Yun He, Zikai Li, Bo Song, Wenye Liu, Hongli Wei, Caoying Wu, Ying Cao, Zhenjie Zhang, Chen Zhou, Yongcan Animals Fish Diseases Viral Vaccines DNA Virus Infections Iridoviridae Epitopes, T-Lymphocyte Bass Vaccination Capsid Proteins Epitopes, B-Lymphocyte Vaccines, Synthetic Immunity, Humoral Immunity, Cellular Antibodies, Viral Protein Subunit Vaccines The capsid protein (CP), the primary structural component and key antigen of infectious spleen kidney necrosis virus (ISKNV), remains poorly characterized in terms of its antigenic epitopes. These epitopes, typically ∼20 amino acid residues in length, are specific chemical groups determining antigenic specificity. To address this gap, we employed immunoinformatics to analyze CP epitopes. Subsequently, a multi-epitope vaccine targeting ISKNV (MEV) was designed, constructed, and screened. Immune response evaluation revealed that the predicted three T lymphocyte and five B lymphocyte epitopes exhibited antigenicity, non-toxicity, and non-allergenicity. Fusion of these epitopes yielded the MEV vaccine. In grouper trials, MEV vaccination significantly upregulated mRNA expression of immune-related genes (IL-1β, TNF-α, CD4, CD8α, MHC-Iα, MHC-IIα) and markedly increased total IgM levels, indicating induction of both cellular and humoral immunity. Crucially, MEV conferred significantly higher resistance against ISKNV challenge compared to CP immunization, achieving 85.33% survival rate. Furthermore, MEV vaccination significantly reduced viral loads in the spleen and head kidney. This study presents an economical, rapid, safe, and effective strategy for aquatic vaccine development, positioning MEV as a highly promising candidate for preventing infectious spleen kidney necrosis disease.
title Immune and protective effects of recombinant multi-epitopes vaccine against infectious spleen and kidney necrosis virus in pearl gentian grouper (♀Epinephelus fuscoguttatus × ♂Epinephelus lanceolatus).
topic Animals
Fish Diseases
Viral Vaccines
DNA Virus Infections
Iridoviridae
Epitopes, T-Lymphocyte
Bass
Vaccination
Capsid Proteins
Epitopes, B-Lymphocyte
Vaccines, Synthetic
Immunity, Humoral
Immunity, Cellular
Antibodies, Viral
Protein Subunit Vaccines
url https://pubmed.ncbi.nlm.nih.gov/41687983/