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Genomic Surveillance of 4CMenB Vaccine Antigenic Variants among Disease-Causing Neisseria meningitidis Isolates, United Kingdom, 2010–2016

In September 2015, 4CMenB meningococcal vaccine was introduced into the United Kingdom infant immunization program without phase 3 trial information. Understanding the effect of this program requires enhanced surveillance of invasive meningococcal disease (IMD) Neisseria meningitidis isolates and co...

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Autores principales: Rodrigues, Charlene M.C., Lucidarme, Jay, Borrow, Ray, Smith, Andrew, Cameron, J. Claire, Moxon, E. Richard, Maiden, Martin C.J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5875271/
https://www.ncbi.nlm.nih.gov/pubmed/29553330
http://dx.doi.org/10.3201/eid2404.171480
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author Rodrigues, Charlene M.C.
Lucidarme, Jay
Borrow, Ray
Smith, Andrew
Cameron, J. Claire
Moxon, E. Richard
Maiden, Martin C.J.
author_facet Rodrigues, Charlene M.C.
Lucidarme, Jay
Borrow, Ray
Smith, Andrew
Cameron, J. Claire
Moxon, E. Richard
Maiden, Martin C.J.
author_sort Rodrigues, Charlene M.C.
collection PubMed
description In September 2015, 4CMenB meningococcal vaccine was introduced into the United Kingdom infant immunization program without phase 3 trial information. Understanding the effect of this program requires enhanced surveillance of invasive meningococcal disease (IMD) Neisseria meningitidis isolates and comparison with prevaccination isolates. Bexsero Antigen Sequence Types (BASTs) were used to analyze whole-genome sequences of 3,073 prevaccine IMD N. meningitidis isolates obtained during 2010−2016. Isolates exhibited 803 BASTs among 31 clonal complexes. Frequencies of antigen peptide variants were factor H binding protein 1, 13.4%; Neisserial heparin-binding antigen 2, 13.8%; Neisseria adhesin A 8, 0.8%; and Porin A-VR2:P1.4,10.9%. In 2015−16, serogroup B isolates showed the highest proportion (35.7%) of exact matches to >1 Bexsero components. Serogroup W isolates showed the highest proportion (93.9%) of putatively cross-reactive variants of Bexsero antigens. Results highlighted the likely role of cross-reactive antigens. BAST surveillance of meningococcal whole-genome sequence data is rapid, scalable, and portable and enables international comparisons of isolates.
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spelling pubmed-58752712018-04-06 Genomic Surveillance of 4CMenB Vaccine Antigenic Variants among Disease-Causing Neisseria meningitidis Isolates, United Kingdom, 2010–2016 Rodrigues, Charlene M.C. Lucidarme, Jay Borrow, Ray Smith, Andrew Cameron, J. Claire Moxon, E. Richard Maiden, Martin C.J. Emerg Infect Dis Research In September 2015, 4CMenB meningococcal vaccine was introduced into the United Kingdom infant immunization program without phase 3 trial information. Understanding the effect of this program requires enhanced surveillance of invasive meningococcal disease (IMD) Neisseria meningitidis isolates and comparison with prevaccination isolates. Bexsero Antigen Sequence Types (BASTs) were used to analyze whole-genome sequences of 3,073 prevaccine IMD N. meningitidis isolates obtained during 2010−2016. Isolates exhibited 803 BASTs among 31 clonal complexes. Frequencies of antigen peptide variants were factor H binding protein 1, 13.4%; Neisserial heparin-binding antigen 2, 13.8%; Neisseria adhesin A 8, 0.8%; and Porin A-VR2:P1.4,10.9%. In 2015−16, serogroup B isolates showed the highest proportion (35.7%) of exact matches to >1 Bexsero components. Serogroup W isolates showed the highest proportion (93.9%) of putatively cross-reactive variants of Bexsero antigens. Results highlighted the likely role of cross-reactive antigens. BAST surveillance of meningococcal whole-genome sequence data is rapid, scalable, and portable and enables international comparisons of isolates. Centers for Disease Control and Prevention 2018-04 /pmc/articles/PMC5875271/ /pubmed/29553330 http://dx.doi.org/10.3201/eid2404.171480 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited.
spellingShingle Research
Rodrigues, Charlene M.C.
Lucidarme, Jay
Borrow, Ray
Smith, Andrew
Cameron, J. Claire
Moxon, E. Richard
Maiden, Martin C.J.
Genomic Surveillance of 4CMenB Vaccine Antigenic Variants among Disease-Causing Neisseria meningitidis Isolates, United Kingdom, 2010–2016
title Genomic Surveillance of 4CMenB Vaccine Antigenic Variants among Disease-Causing Neisseria meningitidis Isolates, United Kingdom, 2010–2016
title_full Genomic Surveillance of 4CMenB Vaccine Antigenic Variants among Disease-Causing Neisseria meningitidis Isolates, United Kingdom, 2010–2016
title_fullStr Genomic Surveillance of 4CMenB Vaccine Antigenic Variants among Disease-Causing Neisseria meningitidis Isolates, United Kingdom, 2010–2016
title_full_unstemmed Genomic Surveillance of 4CMenB Vaccine Antigenic Variants among Disease-Causing Neisseria meningitidis Isolates, United Kingdom, 2010–2016
title_short Genomic Surveillance of 4CMenB Vaccine Antigenic Variants among Disease-Causing Neisseria meningitidis Isolates, United Kingdom, 2010–2016
title_sort genomic surveillance of 4cmenb vaccine antigenic variants among disease-causing neisseria meningitidis isolates, united kingdom, 2010–2016
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5875271/
https://www.ncbi.nlm.nih.gov/pubmed/29553330
http://dx.doi.org/10.3201/eid2404.171480
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