The C-terminal region of Trypanosoma cruzi MASPs is antigenic and secreted via exovesicles
- Autores
- de Pablos, Luis Miguel; Díaz Lozano, Isabel María; Jercic, Maria Isabel; Quinzada, Markela; Giménez, Maria José; Calabuig, Eva; Espino, Ana Margarita; Schijman, Alejandro Gabriel; Zulantay, Inés; Apt, Werner; Osuna, Antonio
- Año de publicación
- 2016
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Trypanosoma cruzi is the etiological agent of Chagas disease, a neglected and emerging tropical disease, endemic to South America and present in non-endemic regions due to human migration. The MASP multigene family is specific to T. cruzi, accounting for 6% of the parasite´s genome and plays a key role in immune evasion. A common feature of MASPs is the presence of two conserved regions: an N-terminal region codifying for signal peptide and a C-terminal (C-term) region, which potentially acts as GPI-addition signal peptide. Our aim was the analysis of the presence of an immune response against the MASP C-term region. We found that this region is highly conserved, released via exovesicles (EVs) and has an associated immune response as revealed by epitope affinity mapping, IFA and inhibition of the complement lysis assays. We also demonstrate the presence of a fast IgM response in Balb/c mice infected with T. cruzi. Our results reveal the presence of non-canonical secreted peptides in EVs, which can subsequently be exposed to the immune system with a potential role in evading immune system targets in the parasite.
Fil: de Pablos, Luis Miguel. Universidad de Granada; España. University of York; Reino Unido
Fil: Díaz Lozano, Isabel María. Universidad de Granada; España
Fil: Jercic, Maria Isabel. Instituto de Salud Publica; Chile
Fil: Quinzada, Markela. Universidad de Panamá; Panamá
Fil: Giménez, Maria José. Hospital Universitari i Politècnic La Fe; España
Fil: Calabuig, Eva. Hospital Universitari i Politècnic La Fe; España
Fil: Espino, Ana Margarita. Universidad de Puerto Rico; Puerto Rico
Fil: Schijman, Alejandro Gabriel. Universidad de Buenos Aires; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Zulantay, Inés. Universidad de Chile; Chile
Fil: Apt, Werner. Universidad de Chile; Chile
Fil: Osuna, Antonio. Universidad de Granada; España - Materia
-
Trypanosoma Cruzi
Exosomes
Masp Gene Family
Antigen - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/25250
Ver los metadatos del registro completo
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oai:ri.conicet.gov.ar:11336/25250 |
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network_name_str |
CONICET Digital (CONICET) |
spelling |
The C-terminal region of Trypanosoma cruzi MASPs is antigenic and secreted via exovesiclesde Pablos, Luis MiguelDíaz Lozano, Isabel MaríaJercic, Maria IsabelQuinzada, MarkelaGiménez, Maria JoséCalabuig, EvaEspino, Ana MargaritaSchijman, Alejandro GabrielZulantay, InésApt, WernerOsuna, AntonioTrypanosoma CruziExosomesMasp Gene FamilyAntigenhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Trypanosoma cruzi is the etiological agent of Chagas disease, a neglected and emerging tropical disease, endemic to South America and present in non-endemic regions due to human migration. The MASP multigene family is specific to T. cruzi, accounting for 6% of the parasite´s genome and plays a key role in immune evasion. A common feature of MASPs is the presence of two conserved regions: an N-terminal region codifying for signal peptide and a C-terminal (C-term) region, which potentially acts as GPI-addition signal peptide. Our aim was the analysis of the presence of an immune response against the MASP C-term region. We found that this region is highly conserved, released via exovesicles (EVs) and has an associated immune response as revealed by epitope affinity mapping, IFA and inhibition of the complement lysis assays. We also demonstrate the presence of a fast IgM response in Balb/c mice infected with T. cruzi. Our results reveal the presence of non-canonical secreted peptides in EVs, which can subsequently be exposed to the immune system with a potential role in evading immune system targets in the parasite.Fil: de Pablos, Luis Miguel. Universidad de Granada; España. University of York; Reino UnidoFil: Díaz Lozano, Isabel María. Universidad de Granada; EspañaFil: Jercic, Maria Isabel. Instituto de Salud Publica; ChileFil: Quinzada, Markela. Universidad de Panamá; PanamáFil: Giménez, Maria José. Hospital Universitari i Politècnic La Fe; EspañaFil: Calabuig, Eva. Hospital Universitari i Politècnic La Fe; EspañaFil: Espino, Ana Margarita. Universidad de Puerto Rico; Puerto RicoFil: Schijman, Alejandro Gabriel. Universidad de Buenos Aires; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Zulantay, Inés. Universidad de Chile; ChileFil: Apt, Werner. Universidad de Chile; ChileFil: Osuna, Antonio. Universidad de Granada; EspañaNature Publishing Group2016-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/25250de Pablos, Luis Miguel; Díaz Lozano, Isabel María; Jercic, Maria Isabel; Quinzada, Markela; Giménez, Maria José; et al.; The C-terminal region of Trypanosoma cruzi MASPs is antigenic and secreted via exovesicles; Nature Publishing Group; Scientific Reports; 6; 6-2016; 1-12; 272932045-2322CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1038/srep27293info:eu-repo/semantics/altIdentifier/url/https://www.nature.com/articles/srep27293info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:23:39Zoai:ri.conicet.gov.ar:11336/25250instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:23:40.056CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
The C-terminal region of Trypanosoma cruzi MASPs is antigenic and secreted via exovesicles |
title |
The C-terminal region of Trypanosoma cruzi MASPs is antigenic and secreted via exovesicles |
spellingShingle |
The C-terminal region of Trypanosoma cruzi MASPs is antigenic and secreted via exovesicles de Pablos, Luis Miguel Trypanosoma Cruzi Exosomes Masp Gene Family Antigen |
title_short |
The C-terminal region of Trypanosoma cruzi MASPs is antigenic and secreted via exovesicles |
title_full |
The C-terminal region of Trypanosoma cruzi MASPs is antigenic and secreted via exovesicles |
title_fullStr |
The C-terminal region of Trypanosoma cruzi MASPs is antigenic and secreted via exovesicles |
title_full_unstemmed |
The C-terminal region of Trypanosoma cruzi MASPs is antigenic and secreted via exovesicles |
title_sort |
The C-terminal region of Trypanosoma cruzi MASPs is antigenic and secreted via exovesicles |
dc.creator.none.fl_str_mv |
de Pablos, Luis Miguel Díaz Lozano, Isabel María Jercic, Maria Isabel Quinzada, Markela Giménez, Maria José Calabuig, Eva Espino, Ana Margarita Schijman, Alejandro Gabriel Zulantay, Inés Apt, Werner Osuna, Antonio |
author |
de Pablos, Luis Miguel |
author_facet |
de Pablos, Luis Miguel Díaz Lozano, Isabel María Jercic, Maria Isabel Quinzada, Markela Giménez, Maria José Calabuig, Eva Espino, Ana Margarita Schijman, Alejandro Gabriel Zulantay, Inés Apt, Werner Osuna, Antonio |
author_role |
author |
author2 |
Díaz Lozano, Isabel María Jercic, Maria Isabel Quinzada, Markela Giménez, Maria José Calabuig, Eva Espino, Ana Margarita Schijman, Alejandro Gabriel Zulantay, Inés Apt, Werner Osuna, Antonio |
author2_role |
author author author author author author author author author author |
dc.subject.none.fl_str_mv |
Trypanosoma Cruzi Exosomes Masp Gene Family Antigen |
topic |
Trypanosoma Cruzi Exosomes Masp Gene Family Antigen |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.6 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Trypanosoma cruzi is the etiological agent of Chagas disease, a neglected and emerging tropical disease, endemic to South America and present in non-endemic regions due to human migration. The MASP multigene family is specific to T. cruzi, accounting for 6% of the parasite´s genome and plays a key role in immune evasion. A common feature of MASPs is the presence of two conserved regions: an N-terminal region codifying for signal peptide and a C-terminal (C-term) region, which potentially acts as GPI-addition signal peptide. Our aim was the analysis of the presence of an immune response against the MASP C-term region. We found that this region is highly conserved, released via exovesicles (EVs) and has an associated immune response as revealed by epitope affinity mapping, IFA and inhibition of the complement lysis assays. We also demonstrate the presence of a fast IgM response in Balb/c mice infected with T. cruzi. Our results reveal the presence of non-canonical secreted peptides in EVs, which can subsequently be exposed to the immune system with a potential role in evading immune system targets in the parasite. Fil: de Pablos, Luis Miguel. Universidad de Granada; España. University of York; Reino Unido Fil: Díaz Lozano, Isabel María. Universidad de Granada; España Fil: Jercic, Maria Isabel. Instituto de Salud Publica; Chile Fil: Quinzada, Markela. Universidad de Panamá; Panamá Fil: Giménez, Maria José. Hospital Universitari i Politècnic La Fe; España Fil: Calabuig, Eva. Hospital Universitari i Politècnic La Fe; España Fil: Espino, Ana Margarita. Universidad de Puerto Rico; Puerto Rico Fil: Schijman, Alejandro Gabriel. Universidad de Buenos Aires; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina Fil: Zulantay, Inés. Universidad de Chile; Chile Fil: Apt, Werner. Universidad de Chile; Chile Fil: Osuna, Antonio. Universidad de Granada; España |
description |
Trypanosoma cruzi is the etiological agent of Chagas disease, a neglected and emerging tropical disease, endemic to South America and present in non-endemic regions due to human migration. The MASP multigene family is specific to T. cruzi, accounting for 6% of the parasite´s genome and plays a key role in immune evasion. A common feature of MASPs is the presence of two conserved regions: an N-terminal region codifying for signal peptide and a C-terminal (C-term) region, which potentially acts as GPI-addition signal peptide. Our aim was the analysis of the presence of an immune response against the MASP C-term region. We found that this region is highly conserved, released via exovesicles (EVs) and has an associated immune response as revealed by epitope affinity mapping, IFA and inhibition of the complement lysis assays. We also demonstrate the presence of a fast IgM response in Balb/c mice infected with T. cruzi. Our results reveal the presence of non-canonical secreted peptides in EVs, which can subsequently be exposed to the immune system with a potential role in evading immune system targets in the parasite. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-06 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion 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://hdl.handle.net/11336/25250 de Pablos, Luis Miguel; Díaz Lozano, Isabel María; Jercic, Maria Isabel; Quinzada, Markela; Giménez, Maria José; et al.; The C-terminal region of Trypanosoma cruzi MASPs is antigenic and secreted via exovesicles; Nature Publishing Group; Scientific Reports; 6; 6-2016; 1-12; 27293 2045-2322 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/25250 |
identifier_str_mv |
de Pablos, Luis Miguel; Díaz Lozano, Isabel María; Jercic, Maria Isabel; Quinzada, Markela; Giménez, Maria José; et al.; The C-terminal region of Trypanosoma cruzi MASPs is antigenic and secreted via exovesicles; Nature Publishing Group; Scientific Reports; 6; 6-2016; 1-12; 27293 2045-2322 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1038/srep27293 info:eu-repo/semantics/altIdentifier/url/https://www.nature.com/articles/srep27293 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Nature Publishing Group |
publisher.none.fl_str_mv |
Nature Publishing Group |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1844614231906844672 |
score |
13.070432 |