Bordetella pertussis expresses a functional type III secretion system that subverts protective innate and adaptive immune responses
- Autores
- Fennelly, Neil K.; Sisti, Federico; Higgins, Sarah C.; Ross, Pádraig J.; Van Der Heide, Han; Mooi, Frits R.; Boyd, Aoife; Mills, Kingston H. G.
- Año de publicación
- 2008
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Certain bacteria use a type III secretion system (TTSS) to deliver effector proteins that interfere with cell function into host cells. While transcription of genes encoding TTSS components has been demonstrated, studies to date have failed to identify TTSS effector proteins in Bordetella pertussis. Here we present the first evidence of a functionally active TTSS in B. pertussis. Three known TTSS effectors, Bsp22, BopN, and BopD, were identified as TTSS substrates in B. pertussis 12743. We found expression of Bsp22 in a significant proportion of clinical isolates but not in common laboratory-adapted strains of B. pertussis. We generated a TTSS mutant of B. pertussis 12743 and showed that it induced significantly lower respiratory tract colonization in mice than the wild-type bacteria. Respiratory infection of mice with the mutant bacteria induced significantly greater innate proinflammatory cytokine production in the lungs soon after challenge, and this correlated with significantly higher antigen-specific interleukin-17, gamma interferon, and immunoglobulin G responses later in infection. Our findings suggest that the TTSS subverts innate and adaptive immune responses during infection of the lungs and may be a functionally important virulence factor for B. pertussis infection of humans.
Instituto de Biotecnologia y Biologia Molecular - Materia
-
Ciencias Exactas
Bordetella pertussis
Enfermedades del Sistema Inmune - 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:10915/83054
Ver los metadatos del registro completo
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Bordetella pertussis expresses a functional type III secretion system that subverts protective innate and adaptive immune responsesFennelly, Neil K.Sisti, FedericoHiggins, Sarah C.Ross, Pádraig J.Van Der Heide, HanMooi, Frits R.Boyd, AoifeMills, Kingston H. G.Ciencias ExactasBordetella pertussisEnfermedades del Sistema InmuneCertain bacteria use a type III secretion system (TTSS) to deliver effector proteins that interfere with cell function into host cells. While transcription of genes encoding TTSS components has been demonstrated, studies to date have failed to identify TTSS effector proteins in Bordetella pertussis. Here we present the first evidence of a functionally active TTSS in B. pertussis. Three known TTSS effectors, Bsp22, BopN, and BopD, were identified as TTSS substrates in B. pertussis 12743. We found expression of Bsp22 in a significant proportion of clinical isolates but not in common laboratory-adapted strains of B. pertussis. We generated a TTSS mutant of B. pertussis 12743 and showed that it induced significantly lower respiratory tract colonization in mice than the wild-type bacteria. Respiratory infection of mice with the mutant bacteria induced significantly greater innate proinflammatory cytokine production in the lungs soon after challenge, and this correlated with significantly higher antigen-specific interleukin-17, gamma interferon, and immunoglobulin G responses later in infection. Our findings suggest that the TTSS subverts innate and adaptive immune responses during infection of the lungs and may be a functionally important virulence factor for B. pertussis infection of humans.Instituto de Biotecnologia y Biologia Molecular2008info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf1257-1266http://sedici.unlp.edu.ar/handle/10915/83054enginfo:eu-repo/semantics/altIdentifier/issn/0019-9567info:eu-repo/semantics/altIdentifier/doi/10.1128/IAI.00836-07info: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:UNLP2025-09-29T11:15:41Zoai:sedici.unlp.edu.ar:10915/83054Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:15:41.322SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
Bordetella pertussis expresses a functional type III secretion system that subverts protective innate and adaptive immune responses |
title |
Bordetella pertussis expresses a functional type III secretion system that subverts protective innate and adaptive immune responses |
spellingShingle |
Bordetella pertussis expresses a functional type III secretion system that subverts protective innate and adaptive immune responses Fennelly, Neil K. Ciencias Exactas Bordetella pertussis Enfermedades del Sistema Inmune |
title_short |
Bordetella pertussis expresses a functional type III secretion system that subverts protective innate and adaptive immune responses |
title_full |
Bordetella pertussis expresses a functional type III secretion system that subverts protective innate and adaptive immune responses |
title_fullStr |
Bordetella pertussis expresses a functional type III secretion system that subverts protective innate and adaptive immune responses |
title_full_unstemmed |
Bordetella pertussis expresses a functional type III secretion system that subverts protective innate and adaptive immune responses |
title_sort |
Bordetella pertussis expresses a functional type III secretion system that subverts protective innate and adaptive immune responses |
dc.creator.none.fl_str_mv |
Fennelly, Neil K. Sisti, Federico Higgins, Sarah C. Ross, Pádraig J. Van Der Heide, Han Mooi, Frits R. Boyd, Aoife Mills, Kingston H. G. |
author |
Fennelly, Neil K. |
author_facet |
Fennelly, Neil K. Sisti, Federico Higgins, Sarah C. Ross, Pádraig J. Van Der Heide, Han Mooi, Frits R. Boyd, Aoife Mills, Kingston H. G. |
author_role |
author |
author2 |
Sisti, Federico Higgins, Sarah C. Ross, Pádraig J. Van Der Heide, Han Mooi, Frits R. Boyd, Aoife Mills, Kingston H. G. |
author2_role |
author author author author author author author |
dc.subject.none.fl_str_mv |
Ciencias Exactas Bordetella pertussis Enfermedades del Sistema Inmune |
topic |
Ciencias Exactas Bordetella pertussis Enfermedades del Sistema Inmune |
dc.description.none.fl_txt_mv |
Certain bacteria use a type III secretion system (TTSS) to deliver effector proteins that interfere with cell function into host cells. While transcription of genes encoding TTSS components has been demonstrated, studies to date have failed to identify TTSS effector proteins in Bordetella pertussis. Here we present the first evidence of a functionally active TTSS in B. pertussis. Three known TTSS effectors, Bsp22, BopN, and BopD, were identified as TTSS substrates in B. pertussis 12743. We found expression of Bsp22 in a significant proportion of clinical isolates but not in common laboratory-adapted strains of B. pertussis. We generated a TTSS mutant of B. pertussis 12743 and showed that it induced significantly lower respiratory tract colonization in mice than the wild-type bacteria. Respiratory infection of mice with the mutant bacteria induced significantly greater innate proinflammatory cytokine production in the lungs soon after challenge, and this correlated with significantly higher antigen-specific interleukin-17, gamma interferon, and immunoglobulin G responses later in infection. Our findings suggest that the TTSS subverts innate and adaptive immune responses during infection of the lungs and may be a functionally important virulence factor for B. pertussis infection of humans. Instituto de Biotecnologia y Biologia Molecular |
description |
Certain bacteria use a type III secretion system (TTSS) to deliver effector proteins that interfere with cell function into host cells. While transcription of genes encoding TTSS components has been demonstrated, studies to date have failed to identify TTSS effector proteins in Bordetella pertussis. Here we present the first evidence of a functionally active TTSS in B. pertussis. Three known TTSS effectors, Bsp22, BopN, and BopD, were identified as TTSS substrates in B. pertussis 12743. We found expression of Bsp22 in a significant proportion of clinical isolates but not in common laboratory-adapted strains of B. pertussis. We generated a TTSS mutant of B. pertussis 12743 and showed that it induced significantly lower respiratory tract colonization in mice than the wild-type bacteria. Respiratory infection of mice with the mutant bacteria induced significantly greater innate proinflammatory cytokine production in the lungs soon after challenge, and this correlated with significantly higher antigen-specific interleukin-17, gamma interferon, and immunoglobulin G responses later in infection. Our findings suggest that the TTSS subverts innate and adaptive immune responses during infection of the lungs and may be a functionally important virulence factor for B. pertussis infection of humans. |
publishDate |
2008 |
dc.date.none.fl_str_mv |
2008 |
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http://sedici.unlp.edu.ar/handle/10915/83054 |
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http://sedici.unlp.edu.ar/handle/10915/83054 |
dc.language.none.fl_str_mv |
eng |
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eng |
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