Evidence map›Paper›PMID 40723326›Full record

ArticleBiology2025

Design of a Multi-Epitope Vaccine Candidate Against Infectious Laryngotracheitis Virus Affecting Poultry by Computational Approaches.

Periyasamy Ponnusamy, Kuppannan Sukumar, Angamuthu Raja, Sellappan Saravanan, Palani Srinivasan, Kalaivanan Ramya, Mani Selvaraju, Ramasamy Saravanan

Abstract read
In one paragraph

Article in Biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Periyasamy PonnusamyDepartment of Veterinary Microbiology, Veterinary College and Research Institute, Namakkal 637002, Tamil Nadu, India.ORCID 0000-0003-2326-2559
Kuppannan SukumarDepartment of Veterinary Microbiology, Veterinary College and Research Institute, Namakkal 637002, Tamil Nadu, India.
Angamuthu RajaDepartment of Animal Biotechnology, Madras Veterinary College, Chennai 600007, Tamil Nadu, India.ORCID 0000-0002-5477-2730
Sellappan SaravananDepartment of Veterinary Microbiology, Veterinary College and Research Institute, Namakkal 637002, Tamil Nadu, India.
Palani SrinivasanDepartment of Veterinary Pathology, Veterinary College and Research Institute, Namakkal 637002, Tamil Nadu, India.
Kalaivanan RamyaDepartment of Veterinary Microbiology, Veterinary College and Research Institute, Namakkal 637002, Tamil Nadu, India.ORCID 0000-0001-5853-1638
Mani SelvarajuVeterinary College and Research Institute, Namakkal 637002, Tamil Nadu, India.
Ramasamy SaravananDepartment of Animal Genetics and Breeding, Veterinary College and Research Institute, Tamil Nadu Veterinary and Animal Sciences University, Namakkal 637002, Tamil Nadu, India.ORCID 0000-0003-2409-0357

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Infectious laryngotracheitis (ILT) is a severe upper respiratory disease highly contagious in chickens that causes a huge economic impact on the poultry industry all over the world. The current study aimed to design a multi-epitope-based vaccine candidate using envelope glycoprotein B and glycoprotein D of the ILT virus using an immune informatics approach. The glycoproteins B and D are crucial for attachment as well as entry of ILT virus inside the cell, which makes them a potential option for designing vaccine candidates. The prediction of epitopes, viz. helper T lymphocyte, cytotoxic T lymphocyte and interferon-gamma producing epitopes, was performed and high-scoring predicted epitopes were joined in an organized manner using suitable linkers to design the final vaccine candidate. The avian beta-defensin 1 was included as an adjuvant in the amino-terminal of the vaccine design that possesses antimicrobial activity and histidine residues at the carboxy-terminal for the purpose of purification. The final vaccine candidate was evaluated for its physicochemical characteristics, solubility, antigenicity, stability, and allergenicity and validated for its modeling. Molecular docking, binding affinity, and interacting residues between the vaccine candidate and immune receptors, viz. TLR 3, MHC Class I and Class II were assessed. Further, to assess the immune response profile generated by the final vaccine design, an insilico immune simulation study was also performed. The findings of this study revealed that the final vaccine candidate was antigenic, nonallergenic, stable, interacted with immune receptors, and able to produce antibodies as well as cellular immune responses against ILTV infection.

Indexed as

avian beta-defensin 1glycoprotein Bglycoprotein Dimmunoinformaticsinfectious laryngotracheitis virusmulti-epitope vaccine

Identifiers

PMID40723326
PMCPMC12292712

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Registered trials

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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.