Distribution of Neisseria meningitidis serogroup b (NmB) vaccine antigens in meningococcal disease causing isolates in the United States during 2009-2014, prior to NmB vaccine licensure.
Adolescent
Adult
Aged
Aged, 80 and over
Antigens, Viral
/ analysis
Child
Child, Preschool
Female
Genetic Variation
Genotype
Humans
Infant
Infant, Newborn
Male
Meningitis, Meningococcal
/ epidemiology
Middle Aged
Neisseria meningitidis, Serogroup B
/ classification
Prevalence
United States
/ epidemiology
Young Adult
Genetic diversity
Neisseria meningitidis
Serogroup B
Vaccine antigen
Whole genome sequencing
Journal
The Journal of infection
ISSN: 1532-2742
Titre abrégé: J Infect
Pays: England
ID NLM: 7908424
Informations de publication
Date de publication:
11 2019
11 2019
Historique:
received:
19
07
2019
revised:
02
09
2019
accepted:
04
09
2019
pubmed:
11
9
2019
medline:
17
7
2020
entrez:
11
9
2019
Statut:
ppublish
Résumé
Two Neisseria meningitidis serogroup B (NmB) vaccines are licensed in the United States. To estimate their potential coverage, we examined the vaccine antigen diversity among meningococcal isolates prior to vaccine licensure. NmB vaccine antigen genes of invasive isolates collected in the U.S. from 2009 to 2014 were characterized by Sanger or whole-genome sequencing. During 2009-2014, the predominant antigen types have remained similar to those reported in 2000-2008 for NmB and 2006-2008 for NmC, NmY, with the emergence of a few new types. FHbp of subfamily B or variant 1 (B/v1) remained prevalent among NmB whereas FHbp of subfamily A or variant 2 and 3 (A/v2-3) were more prevalent among non-NmB. FHbp peptide 1 (B24/1.1) remains the most prevalent type in NmB. Full-length NadA peptide was detected in 26% of isolates, primarily in NmB and NmW. The greatest diversity of NhbA peptides was detected among NmB, with p0005 as the most prevalent type. The prevalence and diversity of the NmB vaccine antigens have remained stable with common antigen types persisting over time. The data collected prior to NmB vaccine licensure provide the baseline to understand the potential impact of NmB vaccines on antigen diversity and strain coverage.
Identifiants
pubmed: 31505201
pii: S0163-4453(19)30272-5
doi: 10.1016/j.jinf.2019.09.001
pii:
doi:
Substances chimiques
Antigens, Viral
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
426-434Informations de copyright
Published by Elsevier Ltd.