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A voting mechanism-based linear epitope prediction system for the host-specific Iridoviridae family

BACKGROUND: The Iridoviridae family is categorized into five genera and clustered into two subfamilies: Alphairidovirinae includes Lymphocystivirus, Ranavirus (GIV), and Megalocystivirus (TGIV), which infect vertebrate hosts and Betairidovirinae includes Iridovirus and Chloriridovirus, which infect...

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Autores principales: Shih, Tao-Chuan, Ho, Li-Ping, Wu, Jen-Leih, Chou, Hsin-Yiu, Pai, Tun-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509842/
https://www.ncbi.nlm.nih.gov/pubmed/31074372
http://dx.doi.org/10.1186/s12859-019-2736-2
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author Shih, Tao-Chuan
Ho, Li-Ping
Wu, Jen-Leih
Chou, Hsin-Yiu
Pai, Tun-Wen
author_facet Shih, Tao-Chuan
Ho, Li-Ping
Wu, Jen-Leih
Chou, Hsin-Yiu
Pai, Tun-Wen
author_sort Shih, Tao-Chuan
collection PubMed
description BACKGROUND: The Iridoviridae family is categorized into five genera and clustered into two subfamilies: Alphairidovirinae includes Lymphocystivirus, Ranavirus (GIV), and Megalocystivirus (TGIV), which infect vertebrate hosts and Betairidovirinae includes Iridovirus and Chloriridovirus, which infect invertebrate hosts. Clustered Iridoviridae subfamilies possess host-specific characteristics, which can be considered as exclusive features for in-silico prediction of effective epitopes for vaccine development. A voting mechanism-based linear epitope (LE) prediction system was applied to identify and endorse LE candidates with a minimum length requirement for each clustered subfamily RESULTS: The experimental results showed that four conserved epitopes among the Iridovirideae family, one exclusive epitope for invertebrate subfamily and two exclusive epitopes for vertebrate family were predicted. These predicted LE candidates were further validated by ELISA assays for evaluating the strength of antigenicity and cross antigenicity. The conserved LEs for Iridoviridae family reflected high antigenicity responses for the two subfamilies, while exclusive LEs reflected high antigenicity responses only for the host-specific subfamily CONCLUSIONS: Host-specific characteristics are important features and constraints for effective epitope prediction. Our proposed voting mechanism based system provides a novel approach for in silico LE prediction prior to vaccine development, and it is especially powerful for analyzing antigen sequences with exclusive features between two clustered groups.
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spelling pubmed-65098422019-06-05 A voting mechanism-based linear epitope prediction system for the host-specific Iridoviridae family Shih, Tao-Chuan Ho, Li-Ping Wu, Jen-Leih Chou, Hsin-Yiu Pai, Tun-Wen BMC Bioinformatics Research BACKGROUND: The Iridoviridae family is categorized into five genera and clustered into two subfamilies: Alphairidovirinae includes Lymphocystivirus, Ranavirus (GIV), and Megalocystivirus (TGIV), which infect vertebrate hosts and Betairidovirinae includes Iridovirus and Chloriridovirus, which infect invertebrate hosts. Clustered Iridoviridae subfamilies possess host-specific characteristics, which can be considered as exclusive features for in-silico prediction of effective epitopes for vaccine development. A voting mechanism-based linear epitope (LE) prediction system was applied to identify and endorse LE candidates with a minimum length requirement for each clustered subfamily RESULTS: The experimental results showed that four conserved epitopes among the Iridovirideae family, one exclusive epitope for invertebrate subfamily and two exclusive epitopes for vertebrate family were predicted. These predicted LE candidates were further validated by ELISA assays for evaluating the strength of antigenicity and cross antigenicity. The conserved LEs for Iridoviridae family reflected high antigenicity responses for the two subfamilies, while exclusive LEs reflected high antigenicity responses only for the host-specific subfamily CONCLUSIONS: Host-specific characteristics are important features and constraints for effective epitope prediction. Our proposed voting mechanism based system provides a novel approach for in silico LE prediction prior to vaccine development, and it is especially powerful for analyzing antigen sequences with exclusive features between two clustered groups. BioMed Central 2019-05-01 /pmc/articles/PMC6509842/ /pubmed/31074372 http://dx.doi.org/10.1186/s12859-019-2736-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Shih, Tao-Chuan
Ho, Li-Ping
Wu, Jen-Leih
Chou, Hsin-Yiu
Pai, Tun-Wen
A voting mechanism-based linear epitope prediction system for the host-specific Iridoviridae family
title A voting mechanism-based linear epitope prediction system for the host-specific Iridoviridae family
title_full A voting mechanism-based linear epitope prediction system for the host-specific Iridoviridae family
title_fullStr A voting mechanism-based linear epitope prediction system for the host-specific Iridoviridae family
title_full_unstemmed A voting mechanism-based linear epitope prediction system for the host-specific Iridoviridae family
title_short A voting mechanism-based linear epitope prediction system for the host-specific Iridoviridae family
title_sort voting mechanism-based linear epitope prediction system for the host-specific iridoviridae family
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509842/
https://www.ncbi.nlm.nih.gov/pubmed/31074372
http://dx.doi.org/10.1186/s12859-019-2736-2
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