Evidence map›Paper›PMID 42286569›Full record

ArticleBMC veterinary research2026

Proteomics- and immunoinformatics-based design of a multi-epitope vaccine ZZ1 against Glaesserella parasuis.

Zesong Wang, Wenbin Wei, Shifan Feng, Chaoying Jia, Jiyang Fu, Yuanyuan Wang, Yancheng Jin, Hongshuo Liu, Huanchun Chen, Xiangru Wang

Abstract read
In one paragraph

Article in BMC veterinary research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Zesong WangNational Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, 430070, PR China.
Wenbin WeiNational Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, 430070, PR China.
Shifan FengNational Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, 430070, PR China.
Chaoying JiaWuhan Keqian Biological Co., Ltd, Wuhan, 430000, PR China.
Jiyang FuWuhan Keqian Biological Co., Ltd, Wuhan, 430000, PR China.
Yuanyuan WangWuhan Keqian Biological Co., Ltd, Wuhan, 430000, PR China.
Yancheng JinNational Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, 430070, PR China.
Hongshuo LiuNational Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, 430070, PR China.
Huanchun ChenNational Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, 430070, PR China.
Xiangru WangNational Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan, 430070, PR China. wangxr228@mail.hzau.edu.cn.

Funding

Fundamental Research Funds for the Central Universities 2662025PY001Major Project for the Development of Agricultural Microbial Industry in Hubei Province of China NYWSWZX2025-2027-03National Key Research and Development Program of China 2021YFD1800800Scientific Research Innovation Capability Support Project for Young Faculty ZYGXQNJSKYCXNLZCXM-A4The earmarked fund for the China Agriculture Research System CARS-35
6 · The paper itself

Abstract

backgroundGlaesserella parasuis (G. parasuis) is a prevalent opportunistic pathogen of the porcine upper respiratory tract, causing substantial economic losses to the global swine industry. Current commercial vaccines exhibit suboptimal heterologous cross-protection and inherent biosafety concerns, highlighting the need for a safe, broadly effective multi-serotype vaccine.

resultsThis study targeted outer membrane proteins (OMPs) with robust cross-serotype immunogenicity from virulent G. parasuis strains. Comparative proteomic analysis of five strains identified highly abundant, co-expressed OMPs, which were screened based on antigenicity and physicochemical properties. Epitope prediction for helper T lymphocytes (HTL), cytotoxic T lymphocytes (CTL), and B-cells was performed on selected OMPs. Immunodominant epitopes were concatenated using flexible linkers and fused with the TLR2 agonist phenol-soluble modulin α4 (PSMα4) to engineer a multi-epitope vaccine, designated ZZ1. Screening yielded eight conserved OMPs with high antigenicity, hydrophilicity, and thermostability, from which 6 HTL, 7 CTL, and 11 B-cell epitopes were predicted. Immunoinformatic evaluations revealed that ZZ1 possesses a high antigenicity score of 1.018 (threshold: 0.4) and is non-allergenic and non-toxic. Following successful expression, in vivo trials demonstrated that recombinant ZZ1 elicited robust, specific IgG antibody responses. Challenge tests in piglets revealed 100% protective efficacy against G. parasuis serotype 4, and 80% against serotypes 5 and 13.

conclusionsThese findings indicate that ZZ1 is a promising candidate capable of conferring broad cross-protection against multiple prevalent G. parasuis serotypes, offering an innovative strategy for next-generation subunit vaccine development.

Indexed as

Bacterial VaccinesHaemophilus InfectionsHaemophilus parasuisSwine DiseasesAnimalsBacterial Outer Membrane ProteinsEpitopesImmunoinformaticsProtein Subunit VaccinesProteomicsSwineBacterial Outer Membrane ProteinsBacterial VaccinesEpitopesProtein Subunit VaccinesGlaesserella parasuis (G. parasuis)ImmunoinformaticsMulti-epitope vaccines (MEVs)Outer membrane proteins (OMPs)Protective efficacyProteomics

Identifiers

PMID42286569
PMCPMC13491728

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.