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Diversity of greek meningococcal serogroup B isolates and estimated coverage of the 4CMenB meningococcal vaccine

BACKGROUND: Serogroup B meningococcal (MenB) isolates currently account for approximately 90% of invasive meningococcal disease (IMD) in Greece with ST-162 clonal complex predominating. The potential of a multicomponent meningococcal B vaccine (4CMenB) recently licensed in Europe was investigated in...

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Autores principales: Tzanakaki, Georgina, Hong, Eva, Kesanopoulos, Konstatinos, Xirogianni, Athanasia, Bambini, Stefania, Orlandi, Luca, Comanducci, Maurizio, Muzzi, Alessandro, Taha, Muhamed-Kheir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4018652/
https://www.ncbi.nlm.nih.gov/pubmed/24779381
http://dx.doi.org/10.1186/1471-2180-14-111
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author Tzanakaki, Georgina
Hong, Eva
Kesanopoulos, Konstatinos
Xirogianni, Athanasia
Bambini, Stefania
Orlandi, Luca
Comanducci, Maurizio
Muzzi, Alessandro
Taha, Muhamed-Kheir
author_facet Tzanakaki, Georgina
Hong, Eva
Kesanopoulos, Konstatinos
Xirogianni, Athanasia
Bambini, Stefania
Orlandi, Luca
Comanducci, Maurizio
Muzzi, Alessandro
Taha, Muhamed-Kheir
author_sort Tzanakaki, Georgina
collection PubMed
description BACKGROUND: Serogroup B meningococcal (MenB) isolates currently account for approximately 90% of invasive meningococcal disease (IMD) in Greece with ST-162 clonal complex predominating. The potential of a multicomponent meningococcal B vaccine (4CMenB) recently licensed in Europe was investigated in order to find whether the aforementioned vaccine will cover the MenB strains circulating in Greece. A panel of 148 serogroup B invasive meningococcal strains was characterized by multilocus sequence typing (MLST) and PorA subtyping. Vaccine components were typed by sequencing for factor H-binding protein (fHbp), Neisserial Heparin Binding Antigen (NHBA) and Neisseria adhesin A (NadA). Their expression was explored by Meningococcal Antigen Typing System (MATS). RESULTS: Global strain coverage predicted by MATS was 89.2% (95% CI 63.5%-98.6%) with 44.6%, 38.5% and 6.1% of strains covered by one, two and three vaccine antigens respectively. NHBA was the antigen responsible for the highest coverage (78.4%), followed by fHbp (52.7%), PorA (8.1%) and NadA (0.7%). The coverage of the major genotypes did not differ significantly. The most prevalent MLST genotype was the ST-162 clonal complex , accounting for 44.6% of the strains in the panel and with a predicted coverage of 86.4%, mainly due to NHBA and fHbp. CONCLUSIONS: 4CMenB has the potential to protect against a significant proportion of Greek invasive MenB strains.
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spelling pubmed-40186522014-05-14 Diversity of greek meningococcal serogroup B isolates and estimated coverage of the 4CMenB meningococcal vaccine Tzanakaki, Georgina Hong, Eva Kesanopoulos, Konstatinos Xirogianni, Athanasia Bambini, Stefania Orlandi, Luca Comanducci, Maurizio Muzzi, Alessandro Taha, Muhamed-Kheir BMC Microbiol Research Article BACKGROUND: Serogroup B meningococcal (MenB) isolates currently account for approximately 90% of invasive meningococcal disease (IMD) in Greece with ST-162 clonal complex predominating. The potential of a multicomponent meningococcal B vaccine (4CMenB) recently licensed in Europe was investigated in order to find whether the aforementioned vaccine will cover the MenB strains circulating in Greece. A panel of 148 serogroup B invasive meningococcal strains was characterized by multilocus sequence typing (MLST) and PorA subtyping. Vaccine components were typed by sequencing for factor H-binding protein (fHbp), Neisserial Heparin Binding Antigen (NHBA) and Neisseria adhesin A (NadA). Their expression was explored by Meningococcal Antigen Typing System (MATS). RESULTS: Global strain coverage predicted by MATS was 89.2% (95% CI 63.5%-98.6%) with 44.6%, 38.5% and 6.1% of strains covered by one, two and three vaccine antigens respectively. NHBA was the antigen responsible for the highest coverage (78.4%), followed by fHbp (52.7%), PorA (8.1%) and NadA (0.7%). The coverage of the major genotypes did not differ significantly. The most prevalent MLST genotype was the ST-162 clonal complex , accounting for 44.6% of the strains in the panel and with a predicted coverage of 86.4%, mainly due to NHBA and fHbp. CONCLUSIONS: 4CMenB has the potential to protect against a significant proportion of Greek invasive MenB strains. BioMed Central 2014-04-29 /pmc/articles/PMC4018652/ /pubmed/24779381 http://dx.doi.org/10.1186/1471-2180-14-111 Text en Copyright © 2014 Tzanakaki et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Tzanakaki, Georgina
Hong, Eva
Kesanopoulos, Konstatinos
Xirogianni, Athanasia
Bambini, Stefania
Orlandi, Luca
Comanducci, Maurizio
Muzzi, Alessandro
Taha, Muhamed-Kheir
Diversity of greek meningococcal serogroup B isolates and estimated coverage of the 4CMenB meningococcal vaccine
title Diversity of greek meningococcal serogroup B isolates and estimated coverage of the 4CMenB meningococcal vaccine
title_full Diversity of greek meningococcal serogroup B isolates and estimated coverage of the 4CMenB meningococcal vaccine
title_fullStr Diversity of greek meningococcal serogroup B isolates and estimated coverage of the 4CMenB meningococcal vaccine
title_full_unstemmed Diversity of greek meningococcal serogroup B isolates and estimated coverage of the 4CMenB meningococcal vaccine
title_short Diversity of greek meningococcal serogroup B isolates and estimated coverage of the 4CMenB meningococcal vaccine
title_sort diversity of greek meningococcal serogroup b isolates and estimated coverage of the 4cmenb meningococcal vaccine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4018652/
https://www.ncbi.nlm.nih.gov/pubmed/24779381
http://dx.doi.org/10.1186/1471-2180-14-111
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