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Neisseria meningitidis porA, fetA and fHbp gene distribution in Western Australia 2000 to 2011

BACKGROUND: PorA, fetA and fHbp are three antigen encoding genes useful for meningococcal typing and FHbp is an important component of meningococcal B vaccines. METHODS: We performed sequence analysis of meningococcal porA, fetA and fHbp genes on 128 isolates from Western Australia, relating results...

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Autores principales: Boan, Peter, Metasan, Norhaliza, Tempone, Simone, Harnett, Gerry, Speers, David J, Keil, Anthony D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266217/
https://www.ncbi.nlm.nih.gov/pubmed/25495685
http://dx.doi.org/10.1186/s12879-014-0686-x
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author Boan, Peter
Metasan, Norhaliza
Tempone, Simone
Harnett, Gerry
Speers, David J
Keil, Anthony D
author_facet Boan, Peter
Metasan, Norhaliza
Tempone, Simone
Harnett, Gerry
Speers, David J
Keil, Anthony D
author_sort Boan, Peter
collection PubMed
description BACKGROUND: PorA, fetA and fHbp are three antigen encoding genes useful for meningococcal typing and FHbp is an important component of meningococcal B vaccines. METHODS: We performed sequence analysis of meningococcal porA, fetA and fHbp genes on 128 isolates from Western Australia, relating results to age, gender, race and geographic region. RESULTS: We found predominantly PorA subtypes P1.22,14-16 (n = 23) and P1.7-2,4 (n = 19); FetA subtypes F1-5 (n = 41), F3-6 (n = 11), F5-1 (n = 10), F5-2 (n = 9), F5-5 (n = 8), F3-3 (n = 8); and FHbp variant groups 1 (n = 65) and 2 (n = 44). PorA P1.22,14-16 and FHbp variant group 2 were associated with younger age and aboriginality. CONCLUSIONS: FHbp modular groups of the bivalent recombinant FHbp vaccine and the multicomponent 4CMenB vaccine make up 8.3% and 47.7% respectively of the examined serogroup B isolates from 2000–2011, however to estimate vaccine efficacy requires an account of all vaccine antigens and their levels of expression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-014-0686-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-42662172014-12-16 Neisseria meningitidis porA, fetA and fHbp gene distribution in Western Australia 2000 to 2011 Boan, Peter Metasan, Norhaliza Tempone, Simone Harnett, Gerry Speers, David J Keil, Anthony D BMC Infect Dis Research Article BACKGROUND: PorA, fetA and fHbp are three antigen encoding genes useful for meningococcal typing and FHbp is an important component of meningococcal B vaccines. METHODS: We performed sequence analysis of meningococcal porA, fetA and fHbp genes on 128 isolates from Western Australia, relating results to age, gender, race and geographic region. RESULTS: We found predominantly PorA subtypes P1.22,14-16 (n = 23) and P1.7-2,4 (n = 19); FetA subtypes F1-5 (n = 41), F3-6 (n = 11), F5-1 (n = 10), F5-2 (n = 9), F5-5 (n = 8), F3-3 (n = 8); and FHbp variant groups 1 (n = 65) and 2 (n = 44). PorA P1.22,14-16 and FHbp variant group 2 were associated with younger age and aboriginality. CONCLUSIONS: FHbp modular groups of the bivalent recombinant FHbp vaccine and the multicomponent 4CMenB vaccine make up 8.3% and 47.7% respectively of the examined serogroup B isolates from 2000–2011, however to estimate vaccine efficacy requires an account of all vaccine antigens and their levels of expression. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-014-0686-x) contains supplementary material, which is available to authorized users. BioMed Central 2014-12-12 /pmc/articles/PMC4266217/ /pubmed/25495685 http://dx.doi.org/10.1186/s12879-014-0686-x Text en © Boan et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Article
Boan, Peter
Metasan, Norhaliza
Tempone, Simone
Harnett, Gerry
Speers, David J
Keil, Anthony D
Neisseria meningitidis porA, fetA and fHbp gene distribution in Western Australia 2000 to 2011
title Neisseria meningitidis porA, fetA and fHbp gene distribution in Western Australia 2000 to 2011
title_full Neisseria meningitidis porA, fetA and fHbp gene distribution in Western Australia 2000 to 2011
title_fullStr Neisseria meningitidis porA, fetA and fHbp gene distribution in Western Australia 2000 to 2011
title_full_unstemmed Neisseria meningitidis porA, fetA and fHbp gene distribution in Western Australia 2000 to 2011
title_short Neisseria meningitidis porA, fetA and fHbp gene distribution in Western Australia 2000 to 2011
title_sort neisseria meningitidis pora, feta and fhbp gene distribution in western australia 2000 to 2011
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4266217/
https://www.ncbi.nlm.nih.gov/pubmed/25495685
http://dx.doi.org/10.1186/s12879-014-0686-x
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