Cross-reactive immunogenicity of group A streptococcal vaccines designed using a recurrent neural network to identify conserved M protein linear epitopes.
Bioinformatics
Linear epitopes
M protein
Neural networks
Streptococcus pyogenes (S. pyogenes)
Vaccine development
Journal
Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899
Informations de publication
Date de publication:
19 03 2021
19 03 2021
Historique:
received:
15
11
2020
revised:
27
01
2021
accepted:
30
01
2021
pubmed:
2
3
2021
medline:
25
5
2021
entrez:
1
3
2021
Statut:
ppublish
Résumé
The M protein of group A streptococci (Strep A) is a major virulence determinant and protective antigen. The N-terminal sequence of the protein defines the more than 200 M types of Strep A and also contains epitopes that elicit opsonic antibodies, some of which cross-react with heterologous M types. Current efforts to develop broadly protective M protein-based vaccines are directed at identifying potential cross-protective epitopes located in the N-terminal regions of cluster-related M proteins for use as vaccine antigens. In this study, we have used a comprehensive approach using the recurrent neural network ABCpred and IEDB epitope conservancy analysis tools to predict 16 residue linear B-cell epitopes from 117 clinically relevant M types of Strep A (~88% of global Strep A infections). To examine the immunogenicity of these epitope-based vaccines, nine peptides that together shared ≥60% sequence identity with 37 heterologous M proteins were incorporated into two recombinant hybrid protein vaccines, in which the epitopes were repeated 2 or 3 times, respectively. The combined immune responses of immunized rabbits showed that the vaccines elicited significant levels of antibodies against all nine vaccine epitopes present in homologous N-terminal 1-50 amino acid synthetic M peptides, as well as cross-reactive antibodies against 16 of 37 heterologous M peptides predicted to contain similar epitopes. The epitope-specificity of the cross-reactive antibodies was confirmed by ELISA inhibition assays and functional opsonic activity was assayed in HL-60-based bactericidal assays. The results provide important information for the future design of broadly protective M protein-based Strep A vaccines.
Identifiants
pubmed: 33642159
pii: S0264-410X(21)00129-8
doi: 10.1016/j.vaccine.2021.01.075
pmc: PMC8045747
mid: NIHMS1680445
pii:
doi:
Substances chimiques
Antibodies, Bacterial
0
Antigens, Bacterial
0
Bacterial Outer Membrane Proteins
0
Bacterial Proteins
0
Carrier Proteins
0
Epitopes
0
Streptococcal Vaccines
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
1773-1779Subventions
Organisme : NIAID NIH HHS
ID : R01 AI132117
Pays : United States
Informations de copyright
Copyright © 2021 Elsevier Ltd. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: J.B.D. is the inventor of certain technologies related to the development of Strep A vaccines. The technology has been licensed from the University of Tennessee Research Foundation to Vaxent, LLC, of which J.B.D. is a member and Chief Scientific Officer. All other authors declare that they have no conflicts of interest with the contents of this article.
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