The vaccine potential of Bordetella pertussis biofilm-derived membrane proteins

Autores
De Gouw, Daan; Serra, Diego Omar; Jonge, Marien I. de; Hermans, Peter W. M.; Wessels, Hans J. C. T.; Zomer, Aldert; Yantorno, Osvaldo Miguel; Diavatopoulos, Dimitri A.; Mooi, Frits R.
Año de publicación
2014
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Pertussis is an infectious respiratory disease of humans caused by the gram-negative pathogen Bordetella pertussis. The use of acellular pertussis vaccines (aPs) which induce immunity of relative short duration and the emergence of vaccine-adapted strains are thought to have contributed to the recent resurgence of pertussis in industrialized countries despite high vaccination coverage. Current pertussis vaccines consist of antigens derived from planktonic bacterial cultures. However, recent studies have shown that biofilm formation represents an important aspect of B. pertussis infection, and antigens expressed during this stage may therefore be potential targets for vaccination. Here we provide evidence that vaccination of mice with B. pertussis biofilm-derived membrane proteins protects against infection. Subsequent proteomic analysis of the protein content of biofilm and planktonic cultures yielded 11 proteins which were ≥ three-fold more abundant in biofilms, of which Bordetella intermediate protein A (BipA) was the most abundant, surface-exposed protein. As proof of concept, mice were vaccinated with recombinantly produced BipA. Immunization significantly reduced colonization of the lungs and antibodies to BipA were found to efficiently opsonize bacteria. Finally, we confirmed that bipA is expressed during respiratory tract infection of mice, and that anti-BipA antibodies are present in the serum of convalescent whooping cough patients. Together, these data suggest that biofilm proteins and in particular BipA may be of interest for inclusion into future pertussis vaccines.
Facultad de Ciencias Exactas
Centro de Investigación y Desarrollo en Fermentaciones Industriales
Materia
Ciencias Exactas
Biofilms
BipA
Bordetella pertussis
Proteomics
Vaccination
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-nd/3.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/85128

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network_name_str SEDICI (UNLP)
spelling The vaccine potential of Bordetella pertussis biofilm-derived membrane proteinsDe Gouw, DaanSerra, Diego OmarJonge, Marien I. deHermans, Peter W. M.Wessels, Hans J. C. T.Zomer, AldertYantorno, Osvaldo MiguelDiavatopoulos, Dimitri A.Mooi, Frits R.Ciencias ExactasBiofilmsBipABordetella pertussisProteomicsVaccinationPertussis is an infectious respiratory disease of humans caused by the gram-negative pathogen <i>Bordetella pertussis</i>. The use of acellular pertussis vaccines (aPs) which induce immunity of relative short duration and the emergence of vaccine-adapted strains are thought to have contributed to the recent resurgence of pertussis in industrialized countries despite high vaccination coverage. Current pertussis vaccines consist of antigens derived from planktonic bacterial cultures. However, recent studies have shown that biofilm formation represents an important aspect of <i>B. pertussis</i> infection, and antigens expressed during this stage may therefore be potential targets for vaccination. Here we provide evidence that vaccination of mice with <i>B. pertussis</i> biofilm-derived membrane proteins protects against infection. Subsequent proteomic analysis of the protein content of biofilm and planktonic cultures yielded 11 proteins which were ≥ three-fold more abundant in biofilms, of which Bordetella intermediate protein A (BipA) was the most abundant, surface-exposed protein. As proof of concept, mice were vaccinated with recombinantly produced BipA. Immunization significantly reduced colonization of the lungs and antibodies to BipA were found to efficiently opsonize bacteria. Finally, we confirmed that <i>bipA</i> is expressed during respiratory tract infection of mice, and that anti-BipA antibodies are present in the serum of convalescent whooping cough patients. Together, these data suggest that biofilm proteins and in particular BipA may be of interest for inclusion into future pertussis vaccines.Facultad de Ciencias ExactasCentro de Investigación y Desarrollo en Fermentaciones Industriales2014info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://sedici.unlp.edu.ar/handle/10915/85128enginfo:eu-repo/semantics/altIdentifier/issn/2222-1751info:eu-repo/semantics/altIdentifier/doi/10.1038/emi.2014.58info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-nd/3.0/Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported (CC BY-NC-ND 3.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:16:24Zoai:sedici.unlp.edu.ar:10915/85128Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:16:25.169SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv The vaccine potential of Bordetella pertussis biofilm-derived membrane proteins
title The vaccine potential of Bordetella pertussis biofilm-derived membrane proteins
spellingShingle The vaccine potential of Bordetella pertussis biofilm-derived membrane proteins
De Gouw, Daan
Ciencias Exactas
Biofilms
BipA
Bordetella pertussis
Proteomics
Vaccination
title_short The vaccine potential of Bordetella pertussis biofilm-derived membrane proteins
title_full The vaccine potential of Bordetella pertussis biofilm-derived membrane proteins
title_fullStr The vaccine potential of Bordetella pertussis biofilm-derived membrane proteins
title_full_unstemmed The vaccine potential of Bordetella pertussis biofilm-derived membrane proteins
title_sort The vaccine potential of Bordetella pertussis biofilm-derived membrane proteins
dc.creator.none.fl_str_mv De Gouw, Daan
Serra, Diego Omar
Jonge, Marien I. de
Hermans, Peter W. M.
Wessels, Hans J. C. T.
Zomer, Aldert
Yantorno, Osvaldo Miguel
Diavatopoulos, Dimitri A.
Mooi, Frits R.
author De Gouw, Daan
author_facet De Gouw, Daan
Serra, Diego Omar
Jonge, Marien I. de
Hermans, Peter W. M.
Wessels, Hans J. C. T.
Zomer, Aldert
Yantorno, Osvaldo Miguel
Diavatopoulos, Dimitri A.
Mooi, Frits R.
author_role author
author2 Serra, Diego Omar
Jonge, Marien I. de
Hermans, Peter W. M.
Wessels, Hans J. C. T.
Zomer, Aldert
Yantorno, Osvaldo Miguel
Diavatopoulos, Dimitri A.
Mooi, Frits R.
author2_role author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Ciencias Exactas
Biofilms
BipA
Bordetella pertussis
Proteomics
Vaccination
topic Ciencias Exactas
Biofilms
BipA
Bordetella pertussis
Proteomics
Vaccination
dc.description.none.fl_txt_mv Pertussis is an infectious respiratory disease of humans caused by the gram-negative pathogen <i>Bordetella pertussis</i>. The use of acellular pertussis vaccines (aPs) which induce immunity of relative short duration and the emergence of vaccine-adapted strains are thought to have contributed to the recent resurgence of pertussis in industrialized countries despite high vaccination coverage. Current pertussis vaccines consist of antigens derived from planktonic bacterial cultures. However, recent studies have shown that biofilm formation represents an important aspect of <i>B. pertussis</i> infection, and antigens expressed during this stage may therefore be potential targets for vaccination. Here we provide evidence that vaccination of mice with <i>B. pertussis</i> biofilm-derived membrane proteins protects against infection. Subsequent proteomic analysis of the protein content of biofilm and planktonic cultures yielded 11 proteins which were ≥ three-fold more abundant in biofilms, of which Bordetella intermediate protein A (BipA) was the most abundant, surface-exposed protein. As proof of concept, mice were vaccinated with recombinantly produced BipA. Immunization significantly reduced colonization of the lungs and antibodies to BipA were found to efficiently opsonize bacteria. Finally, we confirmed that <i>bipA</i> is expressed during respiratory tract infection of mice, and that anti-BipA antibodies are present in the serum of convalescent whooping cough patients. Together, these data suggest that biofilm proteins and in particular BipA may be of interest for inclusion into future pertussis vaccines.
Facultad de Ciencias Exactas
Centro de Investigación y Desarrollo en Fermentaciones Industriales
description Pertussis is an infectious respiratory disease of humans caused by the gram-negative pathogen <i>Bordetella pertussis</i>. The use of acellular pertussis vaccines (aPs) which induce immunity of relative short duration and the emergence of vaccine-adapted strains are thought to have contributed to the recent resurgence of pertussis in industrialized countries despite high vaccination coverage. Current pertussis vaccines consist of antigens derived from planktonic bacterial cultures. However, recent studies have shown that biofilm formation represents an important aspect of <i>B. pertussis</i> infection, and antigens expressed during this stage may therefore be potential targets for vaccination. Here we provide evidence that vaccination of mice with <i>B. pertussis</i> biofilm-derived membrane proteins protects against infection. Subsequent proteomic analysis of the protein content of biofilm and planktonic cultures yielded 11 proteins which were ≥ three-fold more abundant in biofilms, of which Bordetella intermediate protein A (BipA) was the most abundant, surface-exposed protein. As proof of concept, mice were vaccinated with recombinantly produced BipA. Immunization significantly reduced colonization of the lungs and antibodies to BipA were found to efficiently opsonize bacteria. Finally, we confirmed that <i>bipA</i> is expressed during respiratory tract infection of mice, and that anti-BipA antibodies are present in the serum of convalescent whooping cough patients. Together, these data suggest that biofilm proteins and in particular BipA may be of interest for inclusion into future pertussis vaccines.
publishDate 2014
dc.date.none.fl_str_mv 2014
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/85128
url http://sedici.unlp.edu.ar/handle/10915/85128
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/issn/2222-1751
info:eu-repo/semantics/altIdentifier/doi/10.1038/emi.2014.58
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-nd/3.0/
Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported (CC BY-NC-ND 3.0)
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-nd/3.0/
Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported (CC BY-NC-ND 3.0)
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instname:Universidad Nacional de La Plata
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instname_str Universidad Nacional de La Plata
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