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Genetic and antigenic characterisation of serotype A FMD viruses from East Africa to select new vaccine strains

Vaccine strain selection for emerging foot-and-mouth disease virus (FMDV) outbreaks in enzootic countries can be addressed through antigenic and genetic characterisation of recently circulating viruses. A total of 56 serotype A FMDVs isolated between 1998 and 2012, from Central, East and North Afric...

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Autores principales: Bari, Fufa D., Parida, Satya, Tekleghiorghis, Tesfaalem, Dekker, Aldo, Sangula, Abraham, Reeve, Richard, Haydon, Daniel T., Paton, David J., Mahapatra, Mana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4194315/
https://www.ncbi.nlm.nih.gov/pubmed/25171846
http://dx.doi.org/10.1016/j.vaccine.2014.08.033
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author Bari, Fufa D.
Parida, Satya
Tekleghiorghis, Tesfaalem
Dekker, Aldo
Sangula, Abraham
Reeve, Richard
Haydon, Daniel T.
Paton, David J.
Mahapatra, Mana
author_facet Bari, Fufa D.
Parida, Satya
Tekleghiorghis, Tesfaalem
Dekker, Aldo
Sangula, Abraham
Reeve, Richard
Haydon, Daniel T.
Paton, David J.
Mahapatra, Mana
author_sort Bari, Fufa D.
collection PubMed
description Vaccine strain selection for emerging foot-and-mouth disease virus (FMDV) outbreaks in enzootic countries can be addressed through antigenic and genetic characterisation of recently circulating viruses. A total of 56 serotype A FMDVs isolated between 1998 and 2012, from Central, East and North African countries were characterised antigenically by virus neutralisation test using antisera to three existing and four candidate vaccine strains and, genetically by characterising the full capsid sequence data. A Bayesian analysis of the capsid sequence data revealed the viruses to be of either African or Asian topotypes with subdivision of the African topotype viruses into four genotypes (Genotypes I, II, IV and VII). The existing vaccine strains were found to be least cross-reactive (good matches observed for only 5.4–46.4% of the sampled viruses). Three bovine antisera, raised against A-EA-2007, A-EA-1981 and A-EA-1984 viruses, exhibited broad cross-neutralisation, towards more than 85% of the circulating viruses. Of the three vaccines, A-EA-2007 was the best showing more than 90% in-vitro cross-protection, as well as being the most recent amongst the vaccine strains used in this study. It therefore appears antigenically suitable as a vaccine strain to be used in the region in FMD control programmes.
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spelling pubmed-41943152014-10-14 Genetic and antigenic characterisation of serotype A FMD viruses from East Africa to select new vaccine strains Bari, Fufa D. Parida, Satya Tekleghiorghis, Tesfaalem Dekker, Aldo Sangula, Abraham Reeve, Richard Haydon, Daniel T. Paton, David J. Mahapatra, Mana Vaccine Article Vaccine strain selection for emerging foot-and-mouth disease virus (FMDV) outbreaks in enzootic countries can be addressed through antigenic and genetic characterisation of recently circulating viruses. A total of 56 serotype A FMDVs isolated between 1998 and 2012, from Central, East and North African countries were characterised antigenically by virus neutralisation test using antisera to three existing and four candidate vaccine strains and, genetically by characterising the full capsid sequence data. A Bayesian analysis of the capsid sequence data revealed the viruses to be of either African or Asian topotypes with subdivision of the African topotype viruses into four genotypes (Genotypes I, II, IV and VII). The existing vaccine strains were found to be least cross-reactive (good matches observed for only 5.4–46.4% of the sampled viruses). Three bovine antisera, raised against A-EA-2007, A-EA-1981 and A-EA-1984 viruses, exhibited broad cross-neutralisation, towards more than 85% of the circulating viruses. Of the three vaccines, A-EA-2007 was the best showing more than 90% in-vitro cross-protection, as well as being the most recent amongst the vaccine strains used in this study. It therefore appears antigenically suitable as a vaccine strain to be used in the region in FMD control programmes. Elsevier Science 2014-10-07 /pmc/articles/PMC4194315/ /pubmed/25171846 http://dx.doi.org/10.1016/j.vaccine.2014.08.033 Text en © 2014 The Authors https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 Unported License (https://creativecommons.org/licenses/by/3.0/) .
spellingShingle Article
Bari, Fufa D.
Parida, Satya
Tekleghiorghis, Tesfaalem
Dekker, Aldo
Sangula, Abraham
Reeve, Richard
Haydon, Daniel T.
Paton, David J.
Mahapatra, Mana
Genetic and antigenic characterisation of serotype A FMD viruses from East Africa to select new vaccine strains
title Genetic and antigenic characterisation of serotype A FMD viruses from East Africa to select new vaccine strains
title_full Genetic and antigenic characterisation of serotype A FMD viruses from East Africa to select new vaccine strains
title_fullStr Genetic and antigenic characterisation of serotype A FMD viruses from East Africa to select new vaccine strains
title_full_unstemmed Genetic and antigenic characterisation of serotype A FMD viruses from East Africa to select new vaccine strains
title_short Genetic and antigenic characterisation of serotype A FMD viruses from East Africa to select new vaccine strains
title_sort genetic and antigenic characterisation of serotype a fmd viruses from east africa to select new vaccine strains
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4194315/
https://www.ncbi.nlm.nih.gov/pubmed/25171846
http://dx.doi.org/10.1016/j.vaccine.2014.08.033
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