Cargando…

Immunogenic Consensus Sequence T helper Epitopes for a Pan-Burkholderia Biodefense Vaccine

BACKGROUND: Biodefense vaccines against Category B bioterror agents Burkholderia pseudomallei (BPM) and Burkholderia mallei (BM) are needed, as they are both easily accessible to terrorists and have strong weaponization potential. Burkholderia cepaciae (BC), a related pathogen, causes chronic lung i...

Descripción completa

Detalles Bibliográficos
Autores principales: De Groot, Anne S., Ardito, Matthew, Moise, Leonard, Gustafson, Eric A., Spero, Denice, Tejada, Gloria, Martin, William
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206550/
https://www.ncbi.nlm.nih.gov/pubmed/25346775
http://dx.doi.org/10.4172/1745-7580.1000043
_version_ 1782340846509621248
author De Groot, Anne S.
Ardito, Matthew
Moise, Leonard
Gustafson, Eric A.
Spero, Denice
Tejada, Gloria
Martin, William
author_facet De Groot, Anne S.
Ardito, Matthew
Moise, Leonard
Gustafson, Eric A.
Spero, Denice
Tejada, Gloria
Martin, William
author_sort De Groot, Anne S.
collection PubMed
description BACKGROUND: Biodefense vaccines against Category B bioterror agents Burkholderia pseudomallei (BPM) and Burkholderia mallei (BM) are needed, as they are both easily accessible to terrorists and have strong weaponization potential. Burkholderia cepaciae (BC), a related pathogen, causes chronic lung infections in cystic fibrosis patients. Since BPM, BM and BC are all intracellular bacteria, they are excellent targets for T cell-based vaccines. However, the sheer volume of available genomic data requires the aid of immunoinformatics for vaccine design. Using EpiMatrix, ClustiMer and EpiAssembler, a set of immunoinformatic vaccine design tools, we screened the 31 available Burkholderia genomes and performed initial tests of our selections that are candidates for an epitope-based multi-pathogen vaccine against Burkholderia species. RESULTS: Immunoinformatics analysis of 31 Burkholderia genomes yielded 350,004 9-mer candidate vaccine peptides of which 133,469 had perfect conservation across the 10 BM genomes, 175,722 had perfect conservation across the 11 BPM genomes and 40,813 had perfect conservation across the 10 BC genomes. Further screening with EpiMatrix yielded 54,010 high-scoring Class II epitopes; these were assembled into 2,880 longer highly conserved ‘immunogenic consensus sequence’ T helper epitopes. 100% of the peptides bound to at least one HLA class II allele in vitro, 92.7% bound to at least two alleles, 82.9% to three, and 75.6% of the binding results were consistent with the immunoinformatics analysis. CONCLUSIONS: Our results show it is possible to rapidly identify promiscuous T helper epitopes conserved across multiple Burkholderia species and test their binding to HLA ligands in vitro. The next step in our process will be to test the epitopes ex vivo using peripheral leukocytes from BC, BPM infected humans and for immunogenicity in human HLA transgenic mice. We expect that this approach will lead to development of a licensable, pan-Burkholderia biodefense vaccine.
format Online
Article
Text
id pubmed-4206550
institution National Center for Biotechnology Information
language English
publishDate 2011
record_format MEDLINE/PubMed
spelling pubmed-42065502014-10-22 Immunogenic Consensus Sequence T helper Epitopes for a Pan-Burkholderia Biodefense Vaccine De Groot, Anne S. Ardito, Matthew Moise, Leonard Gustafson, Eric A. Spero, Denice Tejada, Gloria Martin, William Immunome Res Article BACKGROUND: Biodefense vaccines against Category B bioterror agents Burkholderia pseudomallei (BPM) and Burkholderia mallei (BM) are needed, as they are both easily accessible to terrorists and have strong weaponization potential. Burkholderia cepaciae (BC), a related pathogen, causes chronic lung infections in cystic fibrosis patients. Since BPM, BM and BC are all intracellular bacteria, they are excellent targets for T cell-based vaccines. However, the sheer volume of available genomic data requires the aid of immunoinformatics for vaccine design. Using EpiMatrix, ClustiMer and EpiAssembler, a set of immunoinformatic vaccine design tools, we screened the 31 available Burkholderia genomes and performed initial tests of our selections that are candidates for an epitope-based multi-pathogen vaccine against Burkholderia species. RESULTS: Immunoinformatics analysis of 31 Burkholderia genomes yielded 350,004 9-mer candidate vaccine peptides of which 133,469 had perfect conservation across the 10 BM genomes, 175,722 had perfect conservation across the 11 BPM genomes and 40,813 had perfect conservation across the 10 BC genomes. Further screening with EpiMatrix yielded 54,010 high-scoring Class II epitopes; these were assembled into 2,880 longer highly conserved ‘immunogenic consensus sequence’ T helper epitopes. 100% of the peptides bound to at least one HLA class II allele in vitro, 92.7% bound to at least two alleles, 82.9% to three, and 75.6% of the binding results were consistent with the immunoinformatics analysis. CONCLUSIONS: Our results show it is possible to rapidly identify promiscuous T helper epitopes conserved across multiple Burkholderia species and test their binding to HLA ligands in vitro. The next step in our process will be to test the epitopes ex vivo using peripheral leukocytes from BC, BPM infected humans and for immunogenicity in human HLA transgenic mice. We expect that this approach will lead to development of a licensable, pan-Burkholderia biodefense vaccine. 2011-05 /pmc/articles/PMC4206550/ /pubmed/25346775 http://dx.doi.org/10.4172/1745-7580.1000043 Text en © 2011 De Groot et al; licensee Nikolai Petrovsky 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 cited.
spellingShingle Article
De Groot, Anne S.
Ardito, Matthew
Moise, Leonard
Gustafson, Eric A.
Spero, Denice
Tejada, Gloria
Martin, William
Immunogenic Consensus Sequence T helper Epitopes for a Pan-Burkholderia Biodefense Vaccine
title Immunogenic Consensus Sequence T helper Epitopes for a Pan-Burkholderia Biodefense Vaccine
title_full Immunogenic Consensus Sequence T helper Epitopes for a Pan-Burkholderia Biodefense Vaccine
title_fullStr Immunogenic Consensus Sequence T helper Epitopes for a Pan-Burkholderia Biodefense Vaccine
title_full_unstemmed Immunogenic Consensus Sequence T helper Epitopes for a Pan-Burkholderia Biodefense Vaccine
title_short Immunogenic Consensus Sequence T helper Epitopes for a Pan-Burkholderia Biodefense Vaccine
title_sort immunogenic consensus sequence t helper epitopes for a pan-burkholderia biodefense vaccine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4206550/
https://www.ncbi.nlm.nih.gov/pubmed/25346775
http://dx.doi.org/10.4172/1745-7580.1000043
work_keys_str_mv AT degrootannes immunogenicconsensussequencethelperepitopesforapanburkholderiabiodefensevaccine
AT arditomatthew immunogenicconsensussequencethelperepitopesforapanburkholderiabiodefensevaccine
AT moiseleonard immunogenicconsensussequencethelperepitopesforapanburkholderiabiodefensevaccine
AT gustafsonerica immunogenicconsensussequencethelperepitopesforapanburkholderiabiodefensevaccine
AT sperodenice immunogenicconsensussequencethelperepitopesforapanburkholderiabiodefensevaccine
AT tejadagloria immunogenicconsensussequencethelperepitopesforapanburkholderiabiodefensevaccine
AT martinwilliam immunogenicconsensussequencethelperepitopesforapanburkholderiabiodefensevaccine