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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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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. |
format | Online Article Text |
id | pubmed-4266217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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