Cross-reactive immunogenicity of group A streptococcal vaccines designed using a recurrent neural network to identify conserved M protein linear epitopes.


Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
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

1773-1779

Subventions

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.

Références

Vaccine. 2010 Jul 12;28(31):5017-22
pubmed: 20546830
N Engl J Med. 2017 Aug 24;377(8):713-722
pubmed: 28834488
J Clin Pathol. 1993 Jul;46(7):617-20
pubmed: 8157746
PLoS One. 2018 Jul 2;13(7):e0198658
pubmed: 29965967
Clin Infect Dis. 2005 Oct 15;41(8):1114-22
pubmed: 16163629
J Exp Med. 1979 Oct 1;150(4):862-77
pubmed: 390084
Nat Microbiol. 2016 Sep 05;1(11):16155
pubmed: 27595425
PLoS Pathog. 2013;9(4):e1003323
pubmed: 23637608
J Infect Dis. 2014 Oct 15;210(8):1325-38
pubmed: 24799598
Infect Immun. 2002 Apr;70(4):2171-7
pubmed: 11895984
Emerg Infect Dis. 1995 Jul-Sep;1(3):69-78
pubmed: 8903167
mSphere. 2018 Dec 19;3(6):
pubmed: 30567901
Emerg Microbes Infect. 2016 Jun 22;5:e65
pubmed: 27329850
Vaccine. 1999 Jan;17(2):193-200
pubmed: 9987154
Lancet Infect Dis. 2005 Nov;5(11):685-94
pubmed: 16253886
Vaccine. 2011 Oct 26;29(46):8175-8
pubmed: 21920403
Vaccine. 2020 Feb 5;38(6):1384-1392
pubmed: 31843270
Vaccine. 2017 Jan 3;35(1):19-26
pubmed: 27890396
Vaccine. 2004 Dec 2;23(3):366-71
pubmed: 15530682
Proteins. 2006 Oct 1;65(1):40-8
pubmed: 16894596
JAMA. 2004 Aug 11;292(6):709-15
pubmed: 15304468
J Exp Med. 1986 May 1;163(5):1191-202
pubmed: 2422314
Clin Infect Dis. 2017 Oct 16;65(9):1523-1531
pubmed: 29020160
BMC Bioinformatics. 2007 Sep 26;8:361
pubmed: 17897458
Infect Immun. 2004 May;72(5):2507-12
pubmed: 15102757
J Biol Chem. 2020 Mar 20;295(12):3826-3836
pubmed: 32029479
Infect Immun. 1997 Sep;65(9):3913-23
pubmed: 9284171
Vaccine. 1993 Sep;11(12):1191-8
pubmed: 7504857
J Exp Med. 1987 Sep 1;166(3):647-56
pubmed: 2442284
Clin Microbiol Rev. 2014 Apr;27(2):264-301
pubmed: 24696436
Lancet Infect Dis. 2009 Oct;9(10):611-6
pubmed: 19778763

Auteurs

Jay A Spencer (JA)

Department of Biological Sciences, The University of Alabama in Huntsville, Huntsville, AL 35899, United States.

Tom Penfound (T)

Department of Medicine, Division of Infectious Diseases, University of Tennessee Health Science Center, Memphis, TN 38163, United States.

Sanaz Salehi (S)

Department of Medicine, Division of Infectious Diseases, University of Tennessee Health Science Center, Memphis, TN 38163, United States.

Michelle P Aranha (MP)

Department of Biochemistry and Cellular and Molecular Biology, University of Tennessee, Knoxville, TN 37996, United States; UT/ORNL Center for Molecular Biophysics, Oak Ridge National Laboratory, Oak Ridge, TN 37830, United States.

Lauren E Wade (LE)

Department of Medicine, Division of Infectious Diseases, University of Tennessee Health Science Center, Memphis, TN 38163, United States.

Rupesh Agarwal (R)

Department of Biochemistry and Cellular and Molecular Biology, University of Tennessee, Knoxville, TN 37996, United States; UT/ORNL Center for Molecular Biophysics, Oak Ridge National Laboratory, Oak Ridge, TN 37830, United States.

Jeremy C Smith (JC)

Department of Biochemistry and Cellular and Molecular Biology, University of Tennessee, Knoxville, TN 37996, United States; UT/ORNL Center for Molecular Biophysics, Oak Ridge National Laboratory, Oak Ridge, TN 37830, United States.

James B Dale (JB)

Department of Medicine, Division of Infectious Diseases, University of Tennessee Health Science Center, Memphis, TN 38163, United States.

Jerome Baudry (J)

Department of Biological Sciences, The University of Alabama in Huntsville, Huntsville, AL 35899, United States. Electronic address: jerome.baudry@uah.edu.

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