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Systems approach to design multi-epitopic peptide vaccine candidate against fowl adenovirus structural proteins for Gallus gallus domesticus.
Mugunthan, Susithra Priyadarhni; Venkatesan, Divyadharshini; Govindasamy, Chandramohan; Selvaraj, Dhivya; Harish, Mani Chandra.
Afiliação
  • Mugunthan SP; Department of Biotechnology, Thiruvalluvar University, Vellore, Tamil Nadu, India.
  • Venkatesan D; Department of Biotechnology, Thiruvalluvar University, Vellore, Tamil Nadu, India.
  • Govindasamy C; Department of Community Health Sciences, College of Applied Medical Sciences, King Saud University, Riyadh, Saudi Arabia.
  • Selvaraj D; Artificial Intelligence Laboratory, School of Computer Information and Communication Engineering, Kunsan National University, Gunsan, Republic of Korea.
  • Harish MC; Department of Biotechnology, Thiruvalluvar University, Vellore, Tamil Nadu, India.
Front Cell Infect Microbiol ; 14: 1351303, 2024.
Article em En | MEDLINE | ID: mdl-38881736
ABSTRACT

Introduction:

Fowl adenovirus (FAdV) is a significant pathogen in poultry, causing various diseases such as hepatitis-hydropericardium, inclusion body hepatitis, and gizzard erosion. Different serotypes of FAdV are associated with specific conditions, highlighting the need for targeted prevention strategies. Given the rising prevalence of FAdV-related diseases globally, effective vaccination and biosecurity measures are crucial. In this study, we explore the potential of structural proteins to design a multi-epitope vaccine targeting FAdV.

Methods:

We employed an in silico approach to design the multi-epitope vaccine. Essential viral structural proteins, including hexon, penton, and fiber protein, were selected as vaccine targets. T-cell and B-cell epitopes binding to MHC-I and MHC-II molecules were predicted using computational methods. Molecular docking studies were conducted to validate the interaction of the multi-epitope vaccine candidate with chicken Toll-like receptors 2 and 5.

Results:

Our in silico methodology successfully identified potential T-cell and B-cell epitopes within the selected viral structural proteins. Molecular docking studies revealed strong interactions between the multi-epitope vaccine candidate and chicken Toll-like receptors 2 and 5, indicating the structural integrity and immunogenic potential of the designed vaccine.

Discussion:

The designed multi-epitope vaccine presents a promising approach for combating FAdV infections in chickens. By targeting essential viral structural proteins, the vaccine is expected to induce a robust immunological response. The in silico methodology utilized in this study provides a rapid and cost-effective means of vaccine design, offering insights into potential vaccine candidates before experimental validation. Future studies should focus on in vitro and in vivo evaluations to further assess the efficacy and safety of the proposed vaccine.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças das Aves Domésticas / Galinhas / Infecções por Adenoviridae / Epitopos de Linfócito T / Epitopos de Linfócito B / Vacinas de Subunidades Antigênicas / Simulação de Acoplamento Molecular Limite: Animals Idioma: En Revista: Front Cell Infect Microbiol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças das Aves Domésticas / Galinhas / Infecções por Adenoviridae / Epitopos de Linfócito T / Epitopos de Linfócito B / Vacinas de Subunidades Antigênicas / Simulação de Acoplamento Molecular Limite: Animals Idioma: En Revista: Front Cell Infect Microbiol Ano de publicação: 2024 Tipo de documento: Article