Interplay between autophagy and metacyclogenesis in Trypanosoma cruzi, unravelling the role of TcVps34-Vps15 complex

Autores
Leis, Juan Manuel; Alonso, Guillermo Daniel; Schoijet, Alejandra Cecilia
Año de publicación
2023
Idioma
inglés
Tipo de recurso
documento de conferencia
Estado
versión publicada
Descripción
Autophagy is a ubiquitous eukaryotic process that also occurs in trypanosomatid parasites. Half of the known yeast and mammalian AuTophaGy (ATG) proteins were detected in trypanosomatids, although with low sequence conservation. Interestingly, autophagy is involved in differentiation of T. cruzi from epimastigotes to metacyclic trypomastigotes, a process called metacyclogenesis. In mammals, two kinases differentially regulate the process of autophagy: mTor and a phosphatidylinositol 3-kinase, Vps34, which interact with a regulatory subunit, Vps15. In this work, we demonstrate that parasites overexpressing TcVps34 or TcVps15 proteins enhance both, autophagy and metacyclogenesis. TcVps34 or TcVps15 overexpressing epimastigotes were able to differentiate to metacyclic forms in a higher proportion than wild type cells. Parasites overexpressing these proteins showed a more intense labeling with the autophagosome marker Atg8.1 and higher levels of monodansycadaverine (MDC) staining, a specific in vivo marker for autophagic vacuoles, in the intermediate forms of differentiated parasites, in comparison to control parasites. To extend this study we also performed assays with DQ-BSA, to evaluate degradative compartments. TcVps34 and TcVps15 overexpressing epimastigotes subjected to nutritional stress shown a significant increase in the number of lysosomes, as compared to controls. In addition, treatment with wortmannin, an inhibitor of autophagy, of parasites exposed to differentiation conditions impaired the autophagic response in less measure in overexpressing parasites. Finally, we are performing infection assays with these overexpressing parasites to assess whether this process is affected. Taken together, these data demonstrate the key role of phosphatidylinositol 3-phosphate pathway in autophagy, differentiation and cell cycle progression in T. cruzi.
Fil: Leis, Juan Manuel. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Alonso, Guillermo Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Schoijet, Alejandra Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
XXXIV Reunión Anual de la Sociedad Argentina de Protozoología
La Plata
Argentina
Sociedad Argentina de Protozoología
Materia
AUTOPHAGY
METACYCLOGENESIS
T. CRUZI
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/240510

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network_name_str CONICET Digital (CONICET)
spelling Interplay between autophagy and metacyclogenesis in Trypanosoma cruzi, unravelling the role of TcVps34-Vps15 complexLeis, Juan ManuelAlonso, Guillermo DanielSchoijet, Alejandra CeciliaAUTOPHAGYMETACYCLOGENESIST. CRUZIhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Autophagy is a ubiquitous eukaryotic process that also occurs in trypanosomatid parasites. Half of the known yeast and mammalian AuTophaGy (ATG) proteins were detected in trypanosomatids, although with low sequence conservation. Interestingly, autophagy is involved in differentiation of T. cruzi from epimastigotes to metacyclic trypomastigotes, a process called metacyclogenesis. In mammals, two kinases differentially regulate the process of autophagy: mTor and a phosphatidylinositol 3-kinase, Vps34, which interact with a regulatory subunit, Vps15. In this work, we demonstrate that parasites overexpressing TcVps34 or TcVps15 proteins enhance both, autophagy and metacyclogenesis. TcVps34 or TcVps15 overexpressing epimastigotes were able to differentiate to metacyclic forms in a higher proportion than wild type cells. Parasites overexpressing these proteins showed a more intense labeling with the autophagosome marker Atg8.1 and higher levels of monodansycadaverine (MDC) staining, a specific in vivo marker for autophagic vacuoles, in the intermediate forms of differentiated parasites, in comparison to control parasites. To extend this study we also performed assays with DQ-BSA, to evaluate degradative compartments. TcVps34 and TcVps15 overexpressing epimastigotes subjected to nutritional stress shown a significant increase in the number of lysosomes, as compared to controls. In addition, treatment with wortmannin, an inhibitor of autophagy, of parasites exposed to differentiation conditions impaired the autophagic response in less measure in overexpressing parasites. Finally, we are performing infection assays with these overexpressing parasites to assess whether this process is affected. Taken together, these data demonstrate the key role of phosphatidylinositol 3-phosphate pathway in autophagy, differentiation and cell cycle progression in T. cruzi.Fil: Leis, Juan Manuel. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Alonso, Guillermo Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaFil: Schoijet, Alejandra Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; ArgentinaXXXIV Reunión Anual de la Sociedad Argentina de ProtozoologíaLa PlataArgentinaSociedad Argentina de ProtozoologíaSociedad Argentina de Protozoología2023info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectReuniónJournalhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/240510Interplay between autophagy and metacyclogenesis in Trypanosoma cruzi, unravelling the role of TcVps34-Vps15 complex; XXXIV Reunión Anual de la Sociedad Argentina de Protozoología; La Plata; Argentina; 2023; 81-812953-5751CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://protozoologia.org.ar/wp-content/uploads/PARASITUS-Volumen-2-2023-ISSN-2953-5751.pdfInternacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:00:19Zoai:ri.conicet.gov.ar:11336/240510instacron: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:34982025-09-10 13:00:19.59CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Interplay between autophagy and metacyclogenesis in Trypanosoma cruzi, unravelling the role of TcVps34-Vps15 complex
title Interplay between autophagy and metacyclogenesis in Trypanosoma cruzi, unravelling the role of TcVps34-Vps15 complex
spellingShingle Interplay between autophagy and metacyclogenesis in Trypanosoma cruzi, unravelling the role of TcVps34-Vps15 complex
Leis, Juan Manuel
AUTOPHAGY
METACYCLOGENESIS
T. CRUZI
title_short Interplay between autophagy and metacyclogenesis in Trypanosoma cruzi, unravelling the role of TcVps34-Vps15 complex
title_full Interplay between autophagy and metacyclogenesis in Trypanosoma cruzi, unravelling the role of TcVps34-Vps15 complex
title_fullStr Interplay between autophagy and metacyclogenesis in Trypanosoma cruzi, unravelling the role of TcVps34-Vps15 complex
title_full_unstemmed Interplay between autophagy and metacyclogenesis in Trypanosoma cruzi, unravelling the role of TcVps34-Vps15 complex
title_sort Interplay between autophagy and metacyclogenesis in Trypanosoma cruzi, unravelling the role of TcVps34-Vps15 complex
dc.creator.none.fl_str_mv Leis, Juan Manuel
Alonso, Guillermo Daniel
Schoijet, Alejandra Cecilia
author Leis, Juan Manuel
author_facet Leis, Juan Manuel
Alonso, Guillermo Daniel
Schoijet, Alejandra Cecilia
author_role author
author2 Alonso, Guillermo Daniel
Schoijet, Alejandra Cecilia
author2_role author
author
dc.subject.none.fl_str_mv AUTOPHAGY
METACYCLOGENESIS
T. CRUZI
topic AUTOPHAGY
METACYCLOGENESIS
T. CRUZI
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Autophagy is a ubiquitous eukaryotic process that also occurs in trypanosomatid parasites. Half of the known yeast and mammalian AuTophaGy (ATG) proteins were detected in trypanosomatids, although with low sequence conservation. Interestingly, autophagy is involved in differentiation of T. cruzi from epimastigotes to metacyclic trypomastigotes, a process called metacyclogenesis. In mammals, two kinases differentially regulate the process of autophagy: mTor and a phosphatidylinositol 3-kinase, Vps34, which interact with a regulatory subunit, Vps15. In this work, we demonstrate that parasites overexpressing TcVps34 or TcVps15 proteins enhance both, autophagy and metacyclogenesis. TcVps34 or TcVps15 overexpressing epimastigotes were able to differentiate to metacyclic forms in a higher proportion than wild type cells. Parasites overexpressing these proteins showed a more intense labeling with the autophagosome marker Atg8.1 and higher levels of monodansycadaverine (MDC) staining, a specific in vivo marker for autophagic vacuoles, in the intermediate forms of differentiated parasites, in comparison to control parasites. To extend this study we also performed assays with DQ-BSA, to evaluate degradative compartments. TcVps34 and TcVps15 overexpressing epimastigotes subjected to nutritional stress shown a significant increase in the number of lysosomes, as compared to controls. In addition, treatment with wortmannin, an inhibitor of autophagy, of parasites exposed to differentiation conditions impaired the autophagic response in less measure in overexpressing parasites. Finally, we are performing infection assays with these overexpressing parasites to assess whether this process is affected. Taken together, these data demonstrate the key role of phosphatidylinositol 3-phosphate pathway in autophagy, differentiation and cell cycle progression in T. cruzi.
Fil: Leis, Juan Manuel. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Alonso, Guillermo Daniel. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
Fil: Schoijet, Alejandra Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina
XXXIV Reunión Anual de la Sociedad Argentina de Protozoología
La Plata
Argentina
Sociedad Argentina de Protozoología
description Autophagy is a ubiquitous eukaryotic process that also occurs in trypanosomatid parasites. Half of the known yeast and mammalian AuTophaGy (ATG) proteins were detected in trypanosomatids, although with low sequence conservation. Interestingly, autophagy is involved in differentiation of T. cruzi from epimastigotes to metacyclic trypomastigotes, a process called metacyclogenesis. In mammals, two kinases differentially regulate the process of autophagy: mTor and a phosphatidylinositol 3-kinase, Vps34, which interact with a regulatory subunit, Vps15. In this work, we demonstrate that parasites overexpressing TcVps34 or TcVps15 proteins enhance both, autophagy and metacyclogenesis. TcVps34 or TcVps15 overexpressing epimastigotes were able to differentiate to metacyclic forms in a higher proportion than wild type cells. Parasites overexpressing these proteins showed a more intense labeling with the autophagosome marker Atg8.1 and higher levels of monodansycadaverine (MDC) staining, a specific in vivo marker for autophagic vacuoles, in the intermediate forms of differentiated parasites, in comparison to control parasites. To extend this study we also performed assays with DQ-BSA, to evaluate degradative compartments. TcVps34 and TcVps15 overexpressing epimastigotes subjected to nutritional stress shown a significant increase in the number of lysosomes, as compared to controls. In addition, treatment with wortmannin, an inhibitor of autophagy, of parasites exposed to differentiation conditions impaired the autophagic response in less measure in overexpressing parasites. Finally, we are performing infection assays with these overexpressing parasites to assess whether this process is affected. Taken together, these data demonstrate the key role of phosphatidylinositol 3-phosphate pathway in autophagy, differentiation and cell cycle progression in T. cruzi.
publishDate 2023
dc.date.none.fl_str_mv 2023
dc.type.none.fl_str_mv info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/conferenceObject
Reunión
Journal
http://purl.org/coar/resource_type/c_5794
info:ar-repo/semantics/documentoDeConferencia
status_str publishedVersion
format conferenceObject
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/240510
Interplay between autophagy and metacyclogenesis in Trypanosoma cruzi, unravelling the role of TcVps34-Vps15 complex; XXXIV Reunión Anual de la Sociedad Argentina de Protozoología; La Plata; Argentina; 2023; 81-81
2953-5751
CONICET Digital
CONICET
url http://hdl.handle.net/11336/240510
identifier_str_mv Interplay between autophagy and metacyclogenesis in Trypanosoma cruzi, unravelling the role of TcVps34-Vps15 complex; XXXIV Reunión Anual de la Sociedad Argentina de Protozoología; La Plata; Argentina; 2023; 81-81
2953-5751
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://protozoologia.org.ar/wp-content/uploads/PARASITUS-Volumen-2-2023-ISSN-2953-5751.pdf
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/
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dc.coverage.none.fl_str_mv Internacional
dc.publisher.none.fl_str_mv Sociedad Argentina de Protozoología
publisher.none.fl_str_mv Sociedad Argentina de Protozoología
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
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