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Expression and cellular localisation of Trypanosoma cruzi calpains

BACKGROUND: Calpains are present in almost all organisms and comprise a family of calcium-dependent cysteine peptidases implicated in crucial cellular functions. Trypanosoma cruzi, the causative agent of Chagas disease, presents an expansion on this gene family with unexplored biological properties....

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Autores principales: Ennes-Vidal, Vítor, Pitaluga, André Nóbrega, Britto, Constança Felícia De Paoli de Carvalho, Branquinha, Marta Helena, dos Santos, André Luis Souza, Menna-Barreto, Rubem Figueiredo Sadok, d’Avila-Levy, Claudia Masini
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Instituto Oswaldo Cruz, Ministério da Saúde 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7552305/
https://www.ncbi.nlm.nih.gov/pubmed/33053076
http://dx.doi.org/10.1590/0074-02760200142
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author Ennes-Vidal, Vítor
Pitaluga, André Nóbrega
Britto, Constança Felícia De Paoli de Carvalho
Branquinha, Marta Helena
dos Santos, André Luis Souza
Menna-Barreto, Rubem Figueiredo Sadok
d’Avila-Levy, Claudia Masini
author_facet Ennes-Vidal, Vítor
Pitaluga, André Nóbrega
Britto, Constança Felícia De Paoli de Carvalho
Branquinha, Marta Helena
dos Santos, André Luis Souza
Menna-Barreto, Rubem Figueiredo Sadok
d’Avila-Levy, Claudia Masini
author_sort Ennes-Vidal, Vítor
collection PubMed
description BACKGROUND: Calpains are present in almost all organisms and comprise a family of calcium-dependent cysteine peptidases implicated in crucial cellular functions. Trypanosoma cruzi, the causative agent of Chagas disease, presents an expansion on this gene family with unexplored biological properties. OBJECTIVES: Here, we searched for calpains in the T. cruzi genome, evaluated the mRNA levels, calpain activity and the protein expression and determined the cellular localisation in all three parasite life cycle forms. METHODS/FINDINGS: Sixty-three calpain sequences were identified in T. cruzi CL Brener genome, with fourteen domain arrangements. The comparison of calpain mRNA abundance by quantitative polymerase chain reaction (qPCR) revealed seven up-regulated sequences in amastigotes and/or bloodstream trypomastigotes and five in epimastigotes. Western Blotting analysis revealed seven different molecules in the three parasite forms, and one amastigote-specific, while no proteolytic activity could be detected. Flow cytometry assays revealed a higher amount of intracellular calpains in amastigotes and/or trypomastigotes in comparison to epimastigotes. Finally, ultrastructural analysis revealed the presence of calpains in the cytoplasm, vesicular and plasma membranes of the three parasite forms, and in the paraflagellar rod in trypomastigotes. CONCLUSION: Calpains are differentially expressed and localised in the T. cruzi life cycle forms. This study adds data on the calpain occurrence and expression pattern in T. cruzi.
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spelling pubmed-75523052020-10-23 Expression and cellular localisation of Trypanosoma cruzi calpains Ennes-Vidal, Vítor Pitaluga, André Nóbrega Britto, Constança Felícia De Paoli de Carvalho Branquinha, Marta Helena dos Santos, André Luis Souza Menna-Barreto, Rubem Figueiredo Sadok d’Avila-Levy, Claudia Masini Mem Inst Oswaldo Cruz Original Article BACKGROUND: Calpains are present in almost all organisms and comprise a family of calcium-dependent cysteine peptidases implicated in crucial cellular functions. Trypanosoma cruzi, the causative agent of Chagas disease, presents an expansion on this gene family with unexplored biological properties. OBJECTIVES: Here, we searched for calpains in the T. cruzi genome, evaluated the mRNA levels, calpain activity and the protein expression and determined the cellular localisation in all three parasite life cycle forms. METHODS/FINDINGS: Sixty-three calpain sequences were identified in T. cruzi CL Brener genome, with fourteen domain arrangements. The comparison of calpain mRNA abundance by quantitative polymerase chain reaction (qPCR) revealed seven up-regulated sequences in amastigotes and/or bloodstream trypomastigotes and five in epimastigotes. Western Blotting analysis revealed seven different molecules in the three parasite forms, and one amastigote-specific, while no proteolytic activity could be detected. Flow cytometry assays revealed a higher amount of intracellular calpains in amastigotes and/or trypomastigotes in comparison to epimastigotes. Finally, ultrastructural analysis revealed the presence of calpains in the cytoplasm, vesicular and plasma membranes of the three parasite forms, and in the paraflagellar rod in trypomastigotes. CONCLUSION: Calpains are differentially expressed and localised in the T. cruzi life cycle forms. This study adds data on the calpain occurrence and expression pattern in T. cruzi. Instituto Oswaldo Cruz, Ministério da Saúde 2020-10-12 /pmc/articles/PMC7552305/ /pubmed/33053076 http://dx.doi.org/10.1590/0074-02760200142 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License
spellingShingle Original Article
Ennes-Vidal, Vítor
Pitaluga, André Nóbrega
Britto, Constança Felícia De Paoli de Carvalho
Branquinha, Marta Helena
dos Santos, André Luis Souza
Menna-Barreto, Rubem Figueiredo Sadok
d’Avila-Levy, Claudia Masini
Expression and cellular localisation of Trypanosoma cruzi calpains
title Expression and cellular localisation of Trypanosoma cruzi calpains
title_full Expression and cellular localisation of Trypanosoma cruzi calpains
title_fullStr Expression and cellular localisation of Trypanosoma cruzi calpains
title_full_unstemmed Expression and cellular localisation of Trypanosoma cruzi calpains
title_short Expression and cellular localisation of Trypanosoma cruzi calpains
title_sort expression and cellular localisation of trypanosoma cruzi calpains
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7552305/
https://www.ncbi.nlm.nih.gov/pubmed/33053076
http://dx.doi.org/10.1590/0074-02760200142
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