Pertussis Vaccine Candidate Based on Outer Membrane Vesicles Derived From Biofilm Culture

Autores
Carriquiriborde, Francisco Pablo; Aispuro, Pablo Martín; Ambrosis, Nicolás Martín; Zurita, María Eugenia; Bottero, Daniela; Gaillard, María Emilia; Castuma, Celina Elisabet; Rudi, Erika; Lodeiro, Aníbal Roberto; Hozbor, Daniela Flavia
Año de publicación
2021
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Outer membrane vesicles (OMV) derived from Bordetella pertussis—the etiologic agent of the resurgent disease called pertussis—are safe and effective in preventing bacterial colonization in the lungs of immunized mice. Vaccine formulations containing those OMV are capable of inducing a mixed Th1/Th2/Th17 profile, but even more interestingly, they may induce a tissue-resident memory immune response. This immune response is recommended for the new generation of pertussis-vaccines that must be developed to overcome the weaknesses of current commercial acellular vaccines (second-generation of pertussis vaccine). The third-generation of pertussis vaccine should also deal with infections caused by bacteria that currently circulate in the population and are phenotypically and genotypically different [in particular those deficient in the expression of pertactin antigen, PRN(-)] from those that circulated in the past. Here we evaluated the protective capacity of OMV derived from bacteria grown in biofilm, since it was observed that, by difference with older culture collection vaccine strains, circulating clinical B. pertussis isolates possess higher capacity for this lifestyle. Therefore, we performed studies with a clinical isolate with good biofilm-forming capacity. Biofilm lifestyle was confirmed by both scanning electron microscopy and proteomics. While scanning electron microscopy revealed typical biofilm structures in these cultures, BipA, fimbria, and other adhesins described as typical of the biofilm lifestyle were overexpressed in the biofilm culture in comparison with planktonic culture. OMV derived from biofilm (OMVbiof) or planktonic lifestyle (OMVplank) were used to formulate vaccines to compare their immunogenicity and protective capacities against infection with PRN(+) or PRN(-) B. pertussis clinical isolates. Using the mouse protection model, we detected that OMVbiof-vaccine was more immunogenic than OMVplank-vaccine in terms of both specific antibody titers and quality, since OMVbiof-vaccine induced antibodies with higher avidity. Moreover, when OMV were administered at suboptimal quantity for protection, OMVbiof-vaccine exhibited a significantly adequate and higher protective capacity against PRN(+) or PRN(-) than OMVplank-vaccine. Our findings indicate that the vaccine based on B. pertussis biofilm-derived OMV induces high protection also against pertactin-deficient strains, with a robust immune response.
Instituto de Biotecnología y Biología Molecular
Materia
Biología
Bordetella pertussis
outer membrane vesicles
biofilm
planktonic
protection
vaccine
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/143071

id SEDICI_1933b7e612f89a85d5fe83cde1584100
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repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling Pertussis Vaccine Candidate Based on Outer Membrane Vesicles Derived From Biofilm CultureCarriquiriborde, Francisco PabloAispuro, Pablo MartínAmbrosis, Nicolás MartínZurita, María EugeniaBottero, DanielaGaillard, María EmiliaCastuma, Celina ElisabetRudi, ErikaLodeiro, Aníbal RobertoHozbor, Daniela FlaviaBiologíaBordetella pertussisouter membrane vesiclesbiofilmplanktonicprotectionvaccineOuter membrane vesicles (OMV) derived from Bordetella pertussis—the etiologic agent of the resurgent disease called pertussis—are safe and effective in preventing bacterial colonization in the lungs of immunized mice. Vaccine formulations containing those OMV are capable of inducing a mixed Th1/Th2/Th17 profile, but even more interestingly, they may induce a tissue-resident memory immune response. This immune response is recommended for the new generation of pertussis-vaccines that must be developed to overcome the weaknesses of current commercial acellular vaccines (second-generation of pertussis vaccine). The third-generation of pertussis vaccine should also deal with infections caused by bacteria that currently circulate in the population and are phenotypically and genotypically different [in particular those deficient in the expression of pertactin antigen, PRN(-)] from those that circulated in the past. Here we evaluated the protective capacity of OMV derived from bacteria grown in biofilm, since it was observed that, by difference with older culture collection vaccine strains, circulating clinical B. pertussis isolates possess higher capacity for this lifestyle. Therefore, we performed studies with a clinical isolate with good biofilm-forming capacity. Biofilm lifestyle was confirmed by both scanning electron microscopy and proteomics. While scanning electron microscopy revealed typical biofilm structures in these cultures, BipA, fimbria, and other adhesins described as typical of the biofilm lifestyle were overexpressed in the biofilm culture in comparison with planktonic culture. OMV derived from biofilm (OMVbiof) or planktonic lifestyle (OMVplank) were used to formulate vaccines to compare their immunogenicity and protective capacities against infection with PRN(+) or PRN(-) B. pertussis clinical isolates. Using the mouse protection model, we detected that OMVbiof-vaccine was more immunogenic than OMVplank-vaccine in terms of both specific antibody titers and quality, since OMVbiof-vaccine induced antibodies with higher avidity. Moreover, when OMV were administered at suboptimal quantity for protection, OMVbiof-vaccine exhibited a significantly adequate and higher protective capacity against PRN(+) or PRN(-) than OMVplank-vaccine. Our findings indicate that the vaccine based on B. pertussis biofilm-derived OMV induces high protection also against pertactin-deficient strains, with a robust immune response.Instituto de Biotecnología y Biología Molecular2021-09-15info: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/10915/143071enginfo:eu-repo/semantics/altIdentifier/issn/1664-3224info:eu-repo/semantics/altIdentifier/doi/10.3389/fimmu.2021.730434info:eu-repo/semantics/altIdentifier/pmid/34603306info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-10-15T11:23:52Zoai:sedici.unlp.edu.ar:10915/143071Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-10-15 11:23:52.984SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Pertussis Vaccine Candidate Based on Outer Membrane Vesicles Derived From Biofilm Culture
title Pertussis Vaccine Candidate Based on Outer Membrane Vesicles Derived From Biofilm Culture
spellingShingle Pertussis Vaccine Candidate Based on Outer Membrane Vesicles Derived From Biofilm Culture
Carriquiriborde, Francisco Pablo
Biología
Bordetella pertussis
outer membrane vesicles
biofilm
planktonic
protection
vaccine
title_short Pertussis Vaccine Candidate Based on Outer Membrane Vesicles Derived From Biofilm Culture
title_full Pertussis Vaccine Candidate Based on Outer Membrane Vesicles Derived From Biofilm Culture
title_fullStr Pertussis Vaccine Candidate Based on Outer Membrane Vesicles Derived From Biofilm Culture
title_full_unstemmed Pertussis Vaccine Candidate Based on Outer Membrane Vesicles Derived From Biofilm Culture
title_sort Pertussis Vaccine Candidate Based on Outer Membrane Vesicles Derived From Biofilm Culture
dc.creator.none.fl_str_mv Carriquiriborde, Francisco Pablo
Aispuro, Pablo Martín
Ambrosis, Nicolás Martín
Zurita, María Eugenia
Bottero, Daniela
Gaillard, María Emilia
Castuma, Celina Elisabet
Rudi, Erika
Lodeiro, Aníbal Roberto
Hozbor, Daniela Flavia
author Carriquiriborde, Francisco Pablo
author_facet Carriquiriborde, Francisco Pablo
Aispuro, Pablo Martín
Ambrosis, Nicolás Martín
Zurita, María Eugenia
Bottero, Daniela
Gaillard, María Emilia
Castuma, Celina Elisabet
Rudi, Erika
Lodeiro, Aníbal Roberto
Hozbor, Daniela Flavia
author_role author
author2 Aispuro, Pablo Martín
Ambrosis, Nicolás Martín
Zurita, María Eugenia
Bottero, Daniela
Gaillard, María Emilia
Castuma, Celina Elisabet
Rudi, Erika
Lodeiro, Aníbal Roberto
Hozbor, Daniela Flavia
author2_role author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Biología
Bordetella pertussis
outer membrane vesicles
biofilm
planktonic
protection
vaccine
topic Biología
Bordetella pertussis
outer membrane vesicles
biofilm
planktonic
protection
vaccine
dc.description.none.fl_txt_mv Outer membrane vesicles (OMV) derived from Bordetella pertussis—the etiologic agent of the resurgent disease called pertussis—are safe and effective in preventing bacterial colonization in the lungs of immunized mice. Vaccine formulations containing those OMV are capable of inducing a mixed Th1/Th2/Th17 profile, but even more interestingly, they may induce a tissue-resident memory immune response. This immune response is recommended for the new generation of pertussis-vaccines that must be developed to overcome the weaknesses of current commercial acellular vaccines (second-generation of pertussis vaccine). The third-generation of pertussis vaccine should also deal with infections caused by bacteria that currently circulate in the population and are phenotypically and genotypically different [in particular those deficient in the expression of pertactin antigen, PRN(-)] from those that circulated in the past. Here we evaluated the protective capacity of OMV derived from bacteria grown in biofilm, since it was observed that, by difference with older culture collection vaccine strains, circulating clinical B. pertussis isolates possess higher capacity for this lifestyle. Therefore, we performed studies with a clinical isolate with good biofilm-forming capacity. Biofilm lifestyle was confirmed by both scanning electron microscopy and proteomics. While scanning electron microscopy revealed typical biofilm structures in these cultures, BipA, fimbria, and other adhesins described as typical of the biofilm lifestyle were overexpressed in the biofilm culture in comparison with planktonic culture. OMV derived from biofilm (OMVbiof) or planktonic lifestyle (OMVplank) were used to formulate vaccines to compare their immunogenicity and protective capacities against infection with PRN(+) or PRN(-) B. pertussis clinical isolates. Using the mouse protection model, we detected that OMVbiof-vaccine was more immunogenic than OMVplank-vaccine in terms of both specific antibody titers and quality, since OMVbiof-vaccine induced antibodies with higher avidity. Moreover, when OMV were administered at suboptimal quantity for protection, OMVbiof-vaccine exhibited a significantly adequate and higher protective capacity against PRN(+) or PRN(-) than OMVplank-vaccine. Our findings indicate that the vaccine based on B. pertussis biofilm-derived OMV induces high protection also against pertactin-deficient strains, with a robust immune response.
Instituto de Biotecnología y Biología Molecular
description Outer membrane vesicles (OMV) derived from Bordetella pertussis—the etiologic agent of the resurgent disease called pertussis—are safe and effective in preventing bacterial colonization in the lungs of immunized mice. Vaccine formulations containing those OMV are capable of inducing a mixed Th1/Th2/Th17 profile, but even more interestingly, they may induce a tissue-resident memory immune response. This immune response is recommended for the new generation of pertussis-vaccines that must be developed to overcome the weaknesses of current commercial acellular vaccines (second-generation of pertussis vaccine). The third-generation of pertussis vaccine should also deal with infections caused by bacteria that currently circulate in the population and are phenotypically and genotypically different [in particular those deficient in the expression of pertactin antigen, PRN(-)] from those that circulated in the past. Here we evaluated the protective capacity of OMV derived from bacteria grown in biofilm, since it was observed that, by difference with older culture collection vaccine strains, circulating clinical B. pertussis isolates possess higher capacity for this lifestyle. Therefore, we performed studies with a clinical isolate with good biofilm-forming capacity. Biofilm lifestyle was confirmed by both scanning electron microscopy and proteomics. While scanning electron microscopy revealed typical biofilm structures in these cultures, BipA, fimbria, and other adhesins described as typical of the biofilm lifestyle were overexpressed in the biofilm culture in comparison with planktonic culture. OMV derived from biofilm (OMVbiof) or planktonic lifestyle (OMVplank) were used to formulate vaccines to compare their immunogenicity and protective capacities against infection with PRN(+) or PRN(-) B. pertussis clinical isolates. Using the mouse protection model, we detected that OMVbiof-vaccine was more immunogenic than OMVplank-vaccine in terms of both specific antibody titers and quality, since OMVbiof-vaccine induced antibodies with higher avidity. Moreover, when OMV were administered at suboptimal quantity for protection, OMVbiof-vaccine exhibited a significantly adequate and higher protective capacity against PRN(+) or PRN(-) than OMVplank-vaccine. Our findings indicate that the vaccine based on B. pertussis biofilm-derived OMV induces high protection also against pertactin-deficient strains, with a robust immune response.
publishDate 2021
dc.date.none.fl_str_mv 2021-09-15
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info:eu-repo/semantics/altIdentifier/doi/10.3389/fimmu.2021.730434
info:eu-repo/semantics/altIdentifier/pmid/34603306
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Creative Commons Attribution 4.0 International (CC BY 4.0)
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