A recombinant iron transport protein from Bordetella pertussis confers protection against Bordetella parapertussis
- Autores
- Álvarez Hayes, Jimena; Oviedo, Juan Marcos; Valdez, Hugo Alberto; Laborde, Juan Martín; Maschi, Fabricio Alejandro; Ayala, Miguel Ángel; Shah, Rohan; Fernandez Lahore, Marcelo; Rodríguez, María Eugenia
- Año de publicación
- 2017
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Whooping cough, which is caused by Bordetella pertussis and B. parapertussis, is a reemerging disease. New protective antigens are needed to improve the efficacy of current vaccines against both species. Using proteomic tools, it was here found that B. parapertussis expresses a homolog of AfuA, a previously reported new vaccine candidate against B. pertussis. It was found that this homolog, named AfuABpp, is expressed during B. parapertussis infection, exposed on the surface of the bacteria and recognized by specific antibodies induced by the recombinant AfuA cloned from B. pertussis (rAfuA). Importantly, the presence of the O-antigen, a molecule that has been found to shield surface antigens on B. parapertussis, showed no influence on antibody recognition of AfuABpp on the bacterial surface. The present study further showed that antibodies induced by immunization with the recombinant protein were able to opsonize B. parapertussis and promote bacterial uptake by neutrophils. Finally, it was shown that this antigen confers protection against B. parapertussis infection in a mouse model. Altogether, these results indicate that AfuA is a good vaccine candidate for acellular vaccines protective against both causative agents of whooping cough.
Facultad de Ciencias Exactas
Facultad de Ciencias Veterinarias (FCV)
Centro de Investigación y Desarrollo en Fermentaciones Industriales (CINDEFI) - Materia
-
Química
Bordetella parapertussis
new antigens
vaccine - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by-nc-sa/4.0/
- Repositorio
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/79424
Ver los metadatos del registro completo
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A recombinant iron transport protein from Bordetella pertussis confers protection against Bordetella parapertussisÁlvarez Hayes, JimenaOviedo, Juan MarcosValdez, Hugo AlbertoLaborde, Juan MartínMaschi, Fabricio AlejandroAyala, Miguel ÁngelShah, RohanFernandez Lahore, MarceloRodríguez, María EugeniaQuímicaBordetella parapertussisnew antigensvaccineWhooping cough, which is caused by Bordetella pertussis and B. parapertussis, is a reemerging disease. New protective antigens are needed to improve the efficacy of current vaccines against both species. Using proteomic tools, it was here found that B. parapertussis expresses a homolog of AfuA, a previously reported new vaccine candidate against B. pertussis. It was found that this homolog, named AfuABpp, is expressed during B. parapertussis infection, exposed on the surface of the bacteria and recognized by specific antibodies induced by the recombinant AfuA cloned from B. pertussis (rAfuA). Importantly, the presence of the O-antigen, a molecule that has been found to shield surface antigens on B. parapertussis, showed no influence on antibody recognition of AfuABpp on the bacterial surface. The present study further showed that antibodies induced by immunization with the recombinant protein were able to opsonize B. parapertussis and promote bacterial uptake by neutrophils. Finally, it was shown that this antigen confers protection against B. parapertussis infection in a mouse model. Altogether, these results indicate that AfuA is a good vaccine candidate for acellular vaccines protective against both causative agents of whooping cough.Facultad de Ciencias ExactasFacultad de Ciencias Veterinarias (FCV)Centro de Investigación y Desarrollo en Fermentaciones Industriales (CINDEFI)2017info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf407-415http://sedici.unlp.edu.ar/handle/10915/79424enginfo:eu-repo/semantics/altIdentifier/doi/10.1111/1348-0421.12532info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-10-15T11:06:24Zoai:sedici.unlp.edu.ar:10915/79424Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-10-15 11:06:24.425SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
A recombinant iron transport protein from Bordetella pertussis confers protection against Bordetella parapertussis |
title |
A recombinant iron transport protein from Bordetella pertussis confers protection against Bordetella parapertussis |
spellingShingle |
A recombinant iron transport protein from Bordetella pertussis confers protection against Bordetella parapertussis Álvarez Hayes, Jimena Química Bordetella parapertussis new antigens vaccine |
title_short |
A recombinant iron transport protein from Bordetella pertussis confers protection against Bordetella parapertussis |
title_full |
A recombinant iron transport protein from Bordetella pertussis confers protection against Bordetella parapertussis |
title_fullStr |
A recombinant iron transport protein from Bordetella pertussis confers protection against Bordetella parapertussis |
title_full_unstemmed |
A recombinant iron transport protein from Bordetella pertussis confers protection against Bordetella parapertussis |
title_sort |
A recombinant iron transport protein from Bordetella pertussis confers protection against Bordetella parapertussis |
dc.creator.none.fl_str_mv |
Álvarez Hayes, Jimena Oviedo, Juan Marcos Valdez, Hugo Alberto Laborde, Juan Martín Maschi, Fabricio Alejandro Ayala, Miguel Ángel Shah, Rohan Fernandez Lahore, Marcelo Rodríguez, María Eugenia |
author |
Álvarez Hayes, Jimena |
author_facet |
Álvarez Hayes, Jimena Oviedo, Juan Marcos Valdez, Hugo Alberto Laborde, Juan Martín Maschi, Fabricio Alejandro Ayala, Miguel Ángel Shah, Rohan Fernandez Lahore, Marcelo Rodríguez, María Eugenia |
author_role |
author |
author2 |
Oviedo, Juan Marcos Valdez, Hugo Alberto Laborde, Juan Martín Maschi, Fabricio Alejandro Ayala, Miguel Ángel Shah, Rohan Fernandez Lahore, Marcelo Rodríguez, María Eugenia |
author2_role |
author author author author author author author author |
dc.subject.none.fl_str_mv |
Química Bordetella parapertussis new antigens vaccine |
topic |
Química Bordetella parapertussis new antigens vaccine |
dc.description.none.fl_txt_mv |
Whooping cough, which is caused by Bordetella pertussis and B. parapertussis, is a reemerging disease. New protective antigens are needed to improve the efficacy of current vaccines against both species. Using proteomic tools, it was here found that B. parapertussis expresses a homolog of AfuA, a previously reported new vaccine candidate against B. pertussis. It was found that this homolog, named AfuABpp, is expressed during B. parapertussis infection, exposed on the surface of the bacteria and recognized by specific antibodies induced by the recombinant AfuA cloned from B. pertussis (rAfuA). Importantly, the presence of the O-antigen, a molecule that has been found to shield surface antigens on B. parapertussis, showed no influence on antibody recognition of AfuABpp on the bacterial surface. The present study further showed that antibodies induced by immunization with the recombinant protein were able to opsonize B. parapertussis and promote bacterial uptake by neutrophils. Finally, it was shown that this antigen confers protection against B. parapertussis infection in a mouse model. Altogether, these results indicate that AfuA is a good vaccine candidate for acellular vaccines protective against both causative agents of whooping cough. Facultad de Ciencias Exactas Facultad de Ciencias Veterinarias (FCV) Centro de Investigación y Desarrollo en Fermentaciones Industriales (CINDEFI) |
description |
Whooping cough, which is caused by Bordetella pertussis and B. parapertussis, is a reemerging disease. New protective antigens are needed to improve the efficacy of current vaccines against both species. Using proteomic tools, it was here found that B. parapertussis expresses a homolog of AfuA, a previously reported new vaccine candidate against B. pertussis. It was found that this homolog, named AfuABpp, is expressed during B. parapertussis infection, exposed on the surface of the bacteria and recognized by specific antibodies induced by the recombinant AfuA cloned from B. pertussis (rAfuA). Importantly, the presence of the O-antigen, a molecule that has been found to shield surface antigens on B. parapertussis, showed no influence on antibody recognition of AfuABpp on the bacterial surface. The present study further showed that antibodies induced by immunization with the recombinant protein were able to opsonize B. parapertussis and promote bacterial uptake by neutrophils. Finally, it was shown that this antigen confers protection against B. parapertussis infection in a mouse model. Altogether, these results indicate that AfuA is a good vaccine candidate for acellular vaccines protective against both causative agents of whooping cough. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017 |
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/10915/79424 |
url |
http://sedici.unlp.edu.ar/handle/10915/79424 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1111/1348-0421.12532 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
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openAccess |
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http://creativecommons.org/licenses/by-nc-sa/4.0/ Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) |
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