In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata
Descripción del Articulo
Taenia solium is known to cause human cysticercosis while T. saginata does not. Comparative in vitro and in vivo studies on the oncosphere and the postoncospheral (PO) forms of T. solium and T. saginata may help to elucidate why cysticercosis can occur from one and not the other. The aim of this stu...
Autores: | , , , , , , , , , , , |
---|---|
Formato: | artículo |
Fecha de Publicación: | 2018 |
Institución: | Consejo Nacional de Ciencia Tecnología e Innovación |
Repositorio: | CONCYTEC-Institucional |
Lenguaje: | inglés |
OAI Identifier: | oai:repositorio.concytec.gob.pe:20.500.12390/2776 |
Enlace del recurso: | https://hdl.handle.net/20.500.12390/2776 https://doi.org/10.1371/journal.pntd.0007261 |
Nivel de acceso: | acceso abierto |
Materia: | Public Health Infectious Diseases Environmental and Occupational Health http://purl.org/pe-repo/ocde/ford#4.02.01 |
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dc.title.none.fl_str_mv |
In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata |
title |
In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata |
spellingShingle |
In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata Palma S. Public Health Infectious Diseases Environmental and Occupational Health http://purl.org/pe-repo/ocde/ford#4.02.01 |
title_short |
In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata |
title_full |
In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata |
title_fullStr |
In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata |
title_full_unstemmed |
In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata |
title_sort |
In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata |
author |
Palma S. |
author_facet |
Palma S. Chile N. Carmen-Orozco R.P. Trompeter G. Fishbeck K. Cooper V. Rapoport L. Bernal-Teran E.G. Condori B.J. Gilman R.H. Verastegui M.R. for the Cysticercosis Working Group in Peru |
author_role |
author |
author2 |
Chile N. Carmen-Orozco R.P. Trompeter G. Fishbeck K. Cooper V. Rapoport L. Bernal-Teran E.G. Condori B.J. Gilman R.H. Verastegui M.R. for the Cysticercosis Working Group in Peru |
author2_role |
author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Palma S. Chile N. Carmen-Orozco R.P. Trompeter G. Fishbeck K. Cooper V. Rapoport L. Bernal-Teran E.G. Condori B.J. Gilman R.H. Verastegui M.R. for the Cysticercosis Working Group in Peru |
dc.subject.none.fl_str_mv |
Public Health |
topic |
Public Health Infectious Diseases Environmental and Occupational Health http://purl.org/pe-repo/ocde/ford#4.02.01 |
dc.subject.es_PE.fl_str_mv |
Infectious Diseases Environmental and Occupational Health |
dc.subject.ocde.none.fl_str_mv |
http://purl.org/pe-repo/ocde/ford#4.02.01 |
description |
Taenia solium is known to cause human cysticercosis while T. saginata does not. Comparative in vitro and in vivo studies on the oncosphere and the postoncospheral (PO) forms of T. solium and T. saginata may help to elucidate why cysticercosis can occur from one and not the other. The aim of this study was to use in vitro culture assays and in vivo models to study the differences in the development of the T. solium and T. saginata oncosphere. Furthermore, this study aimed to evaluate the expression of cytokines and metalloproteinases (MMPs) in human peripheral blood mononuclear cells (PBMCs), which were stimulated by these oncospheres and PO antigens. T. solium and T. saginata activated oncospheres (AO) were cultured in INT-407 and HCT-8 intestinal cells for 180 days. The T. solium began to die while the T. saginata grew for 180 days and developed to cysticerci in INT-407 cells. Rats were inoculated intracranially with AO and PO forms of either T. saginata or T. solium. Rats infected with T. solium AO and PO forms developed neurocysticercosis (NCC), while those infected with the T. saginata did not. Human PMBCs were stimulated with antigens of AO and PO forms of both species, and the production of cytokines and metalloproteinases (MMPs) was measured. The T. solium AO antigen stimulated a higher production of IL-4, IL-5, IL-13, IFN-γ, and IL-2 cytokines compared to T. saginata AO. In the PO form, the T. saginata PO antigen increased the production of IL-4, IL-5, IL-13, IFN-γ, IL-1β, IL-6, IL-10, TNF-α and IL-12 cytokines compared to T. solium, suggesting that this global immune response stimulated by different forms could permit survival or destruction of the parasite depending of their life-cycle stage. Regarding MMPs, T. solium AO antigen stimulated a higher production of MMP-9 compared to T. saginata AO antigen, which may be responsible for altering the permeability of intestinal cells and facilitating breakdown of the blood-brain barrier during the process of invasion of host tissue. © 2019 Palma et al. |
publishDate |
2018 |
dc.date.accessioned.none.fl_str_mv |
2024-05-30T23:13:38Z |
dc.date.available.none.fl_str_mv |
2024-05-30T23:13:38Z |
dc.date.issued.fl_str_mv |
2018 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
dc.identifier.uri.none.fl_str_mv |
https://hdl.handle.net/20.500.12390/2776 |
dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.1371/journal.pntd.0007261 |
dc.identifier.scopus.none.fl_str_mv |
2-s2.0-85063951711 |
url |
https://hdl.handle.net/20.500.12390/2776 https://doi.org/10.1371/journal.pntd.0007261 |
identifier_str_mv |
2-s2.0-85063951711 |
dc.language.iso.none.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.none.fl_str_mv |
PLoS Neglected Tropical Diseases |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess |
dc.rights.uri.none.fl_str_mv |
https://creativecommons.org/licenses/by/4.0/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by/4.0/ |
dc.publisher.none.fl_str_mv |
Public Library of Science |
publisher.none.fl_str_mv |
Public Library of Science |
dc.source.none.fl_str_mv |
reponame:CONCYTEC-Institucional instname:Consejo Nacional de Ciencia Tecnología e Innovación instacron:CONCYTEC |
instname_str |
Consejo Nacional de Ciencia Tecnología e Innovación |
instacron_str |
CONCYTEC |
institution |
CONCYTEC |
reponame_str |
CONCYTEC-Institucional |
collection |
CONCYTEC-Institucional |
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Publicationrp07415600rp07254600rp05664600rp05666600rp07416600rp07419600rp07418600rp07257600rp07414600rp00604600rp05775600rp07417600Palma S.Chile N.Carmen-Orozco R.P.Trompeter G.Fishbeck K.Cooper V.Rapoport L.Bernal-Teran E.G.Condori B.J.Gilman R.H.Verastegui M.R.for the Cysticercosis Working Group in Peru2024-05-30T23:13:38Z2024-05-30T23:13:38Z2018https://hdl.handle.net/20.500.12390/2776https://doi.org/10.1371/journal.pntd.00072612-s2.0-85063951711Taenia solium is known to cause human cysticercosis while T. saginata does not. Comparative in vitro and in vivo studies on the oncosphere and the postoncospheral (PO) forms of T. solium and T. saginata may help to elucidate why cysticercosis can occur from one and not the other. The aim of this study was to use in vitro culture assays and in vivo models to study the differences in the development of the T. solium and T. saginata oncosphere. Furthermore, this study aimed to evaluate the expression of cytokines and metalloproteinases (MMPs) in human peripheral blood mononuclear cells (PBMCs), which were stimulated by these oncospheres and PO antigens. T. solium and T. saginata activated oncospheres (AO) were cultured in INT-407 and HCT-8 intestinal cells for 180 days. The T. solium began to die while the T. saginata grew for 180 days and developed to cysticerci in INT-407 cells. Rats were inoculated intracranially with AO and PO forms of either T. saginata or T. solium. Rats infected with T. solium AO and PO forms developed neurocysticercosis (NCC), while those infected with the T. saginata did not. Human PMBCs were stimulated with antigens of AO and PO forms of both species, and the production of cytokines and metalloproteinases (MMPs) was measured. The T. solium AO antigen stimulated a higher production of IL-4, IL-5, IL-13, IFN-γ, and IL-2 cytokines compared to T. saginata AO. In the PO form, the T. saginata PO antigen increased the production of IL-4, IL-5, IL-13, IFN-γ, IL-1β, IL-6, IL-10, TNF-α and IL-12 cytokines compared to T. solium, suggesting that this global immune response stimulated by different forms could permit survival or destruction of the parasite depending of their life-cycle stage. Regarding MMPs, T. solium AO antigen stimulated a higher production of MMP-9 compared to T. saginata AO antigen, which may be responsible for altering the permeability of intestinal cells and facilitating breakdown of the blood-brain barrier during the process of invasion of host tissue. © 2019 Palma et al.Fondo Nacional de Desarrollo Científico y Tecnológico - FondecytengPublic Library of SciencePLoS Neglected Tropical Diseasesinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/4.0/Public HealthInfectious Diseases-1Environmental and Occupational Health-1http://purl.org/pe-repo/ocde/ford#4.02.01-1In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginatainfo:eu-repo/semantics/articlereponame:CONCYTEC-Institucionalinstname:Consejo Nacional de Ciencia Tecnología e 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Thumbnailimage/jpeg6193https://repositorio.concytec.gob.pe/bitstreams/79a017ce-dc0f-4184-b301-ee5e7ae78bb8/downloadc7aea1d7585c45806e50ae441539b5aeMD5320.500.12390/2776oai:repositorio.concytec.gob.pe:20.500.12390/27762025-01-15 22:00:36.892https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessopen accesshttps://repositorio.concytec.gob.peRepositorio Institucional CONCYTECrepositorio@concytec.gob.pe#PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE##PLACEHOLDER_PARENT_METADATA_VALUE#<Publication xmlns="https://www.openaire.eu/cerif-profile/1.1/" id="a30a8352-32d2-46b5-8e7d-63b05515e57e"> <Type xmlns="https://www.openaire.eu/cerif-profile/vocab/COAR_Publication_Types">http://purl.org/coar/resource_type/c_1843</Type> <Language>eng</Language> <Title>In vitro model of postoncosphere development, and in vivo infection abilities of Taenia solium and Taenia saginata</Title> <PublishedIn> <Publication> <Title>PLoS Neglected Tropical Diseases</Title> </Publication> </PublishedIn> <PublicationDate>2018</PublicationDate> <DOI>https://doi.org/10.1371/journal.pntd.0007261</DOI> <SCP-Number>2-s2.0-85063951711</SCP-Number> <Authors> <Author> <DisplayName>Palma S.</DisplayName> <Person id="rp07415" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Chile N.</DisplayName> <Person id="rp07254" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Carmen-Orozco R.P.</DisplayName> <Person id="rp05664" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Trompeter G.</DisplayName> <Person id="rp05666" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Fishbeck K.</DisplayName> <Person id="rp07416" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Cooper V.</DisplayName> <Person id="rp07419" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Rapoport L.</DisplayName> <Person id="rp07418" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Bernal-Teran E.G.</DisplayName> <Person id="rp07257" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Condori B.J.</DisplayName> <Person id="rp07414" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Gilman R.H.</DisplayName> <Person id="rp00604" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>Verastegui M.R.</DisplayName> <Person id="rp05775" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> <Author> <DisplayName>for the Cysticercosis Working Group in Peru</DisplayName> <Person id="rp07417" /> <Affiliation> <OrgUnit> </OrgUnit> </Affiliation> </Author> </Authors> <Editors> </Editors> <Publishers> <Publisher> <DisplayName>Public Library of Science</DisplayName> <OrgUnit /> </Publisher> </Publishers> <License>https://creativecommons.org/licenses/by/4.0/</License> <Keyword>Public Health</Keyword> <Keyword>Infectious Diseases</Keyword> <Keyword>Environmental and Occupational Health</Keyword> <Abstract>Taenia solium is known to cause human cysticercosis while T. saginata does not. Comparative in vitro and in vivo studies on the oncosphere and the postoncospheral (PO) forms of T. solium and T. saginata may help to elucidate why cysticercosis can occur from one and not the other. The aim of this study was to use in vitro culture assays and in vivo models to study the differences in the development of the T. solium and T. saginata oncosphere. Furthermore, this study aimed to evaluate the expression of cytokines and metalloproteinases (MMPs) in human peripheral blood mononuclear cells (PBMCs), which were stimulated by these oncospheres and PO antigens. T. solium and T. saginata activated oncospheres (AO) were cultured in INT-407 and HCT-8 intestinal cells for 180 days. The T. solium began to die while the T. saginata grew for 180 days and developed to cysticerci in INT-407 cells. Rats were inoculated intracranially with AO and PO forms of either T. saginata or T. solium. Rats infected with T. solium AO and PO forms developed neurocysticercosis (NCC), while those infected with the T. saginata did not. Human PMBCs were stimulated with antigens of AO and PO forms of both species, and the production of cytokines and metalloproteinases (MMPs) was measured. The T. solium AO antigen stimulated a higher production of IL-4, IL-5, IL-13, IFN-γ, and IL-2 cytokines compared to T. saginata AO. In the PO form, the T. saginata PO antigen increased the production of IL-4, IL-5, IL-13, IFN-γ, IL-1β, IL-6, IL-10, TNF-α and IL-12 cytokines compared to T. solium, suggesting that this global immune response stimulated by different forms could permit survival or destruction of the parasite depending of their life-cycle stage. Regarding MMPs, T. solium AO antigen stimulated a higher production of MMP-9 compared to T. saginata AO antigen, which may be responsible for altering the permeability of intestinal cells and facilitating breakdown of the blood-brain barrier during the process of invasion of host tissue. © 2019 Palma et al.</Abstract> <Access xmlns="http://purl.org/coar/access_right" > </Access> </Publication> -1 |
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Nota importante:
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).