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Modulation of the Host Nuclear Compartment by Trypanosoma cruzi Uncovers Effects on Host Transcription and Splicing Machinery

Host manipulation is a common strategy for invading pathogens. Trypanosoma cruzi, the causative agent of Chagas Disease, lives intracellularly within host cells. During infection, parasite-associated modifications occur to the host cell metabolism and morphology. However, little is known about the e...

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Autores principales: Gachet-Castro, Camila, Freitas-Castro, Felipe, Gonzáles-Córdova, Raul Alexander, da Fonseca, Carol Kobori, Gomes, Marcelo Damário, Ishikawa-Ankerhold, Hellen Cristina, Baqui, Munira Muhammad Abdel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8560699/
https://www.ncbi.nlm.nih.gov/pubmed/34737973
http://dx.doi.org/10.3389/fcimb.2021.718028
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author Gachet-Castro, Camila
Freitas-Castro, Felipe
Gonzáles-Córdova, Raul Alexander
da Fonseca, Carol Kobori
Gomes, Marcelo Damário
Ishikawa-Ankerhold, Hellen Cristina
Baqui, Munira Muhammad Abdel
author_facet Gachet-Castro, Camila
Freitas-Castro, Felipe
Gonzáles-Córdova, Raul Alexander
da Fonseca, Carol Kobori
Gomes, Marcelo Damário
Ishikawa-Ankerhold, Hellen Cristina
Baqui, Munira Muhammad Abdel
author_sort Gachet-Castro, Camila
collection PubMed
description Host manipulation is a common strategy for invading pathogens. Trypanosoma cruzi, the causative agent of Chagas Disease, lives intracellularly within host cells. During infection, parasite-associated modifications occur to the host cell metabolism and morphology. However, little is known about the effect of T. cruzi infection on the host cell nucleus and nuclear functionality. Here, we show that T. cruzi can modulate host transcription and splicing machinery in non-professional phagocytic cells during infection. We found that T. cruzi regulates host RNA polymerase II (RNAPII) in a time-dependent manner, resulting in a drastic decrease in RNAPII activity. Furthermore, host cell ribonucleoproteins associated with mRNA transcription (hnRNPA1 and AB2) are downregulated concurrently. We reasoned that T. cruzi may hijack the host U2AF35 auxiliary factor, a key regulator for RNA processing, as a strategy to affect the splicing machinery activities directly. In support of our hypothesis, we carried out in vivo splicing assays using an adenovirus E1A pre-mRNA splicing reporter, showing that intracellular T. cruzi directly modulates the host cells by appropriating U2AF35. For the first time, our results provide evidence of a complex and intimate molecular relationship between T. cruzi and the host cell nucleus during infection.
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spelling pubmed-85606992021-11-03 Modulation of the Host Nuclear Compartment by Trypanosoma cruzi Uncovers Effects on Host Transcription and Splicing Machinery Gachet-Castro, Camila Freitas-Castro, Felipe Gonzáles-Córdova, Raul Alexander da Fonseca, Carol Kobori Gomes, Marcelo Damário Ishikawa-Ankerhold, Hellen Cristina Baqui, Munira Muhammad Abdel Front Cell Infect Microbiol Cellular and Infection Microbiology Host manipulation is a common strategy for invading pathogens. Trypanosoma cruzi, the causative agent of Chagas Disease, lives intracellularly within host cells. During infection, parasite-associated modifications occur to the host cell metabolism and morphology. However, little is known about the effect of T. cruzi infection on the host cell nucleus and nuclear functionality. Here, we show that T. cruzi can modulate host transcription and splicing machinery in non-professional phagocytic cells during infection. We found that T. cruzi regulates host RNA polymerase II (RNAPII) in a time-dependent manner, resulting in a drastic decrease in RNAPII activity. Furthermore, host cell ribonucleoproteins associated with mRNA transcription (hnRNPA1 and AB2) are downregulated concurrently. We reasoned that T. cruzi may hijack the host U2AF35 auxiliary factor, a key regulator for RNA processing, as a strategy to affect the splicing machinery activities directly. In support of our hypothesis, we carried out in vivo splicing assays using an adenovirus E1A pre-mRNA splicing reporter, showing that intracellular T. cruzi directly modulates the host cells by appropriating U2AF35. For the first time, our results provide evidence of a complex and intimate molecular relationship between T. cruzi and the host cell nucleus during infection. Frontiers Media S.A. 2021-10-19 /pmc/articles/PMC8560699/ /pubmed/34737973 http://dx.doi.org/10.3389/fcimb.2021.718028 Text en Copyright © 2021 Gachet-Castro, Freitas-Castro, Gonzáles-Córdova, da Fonseca, Gomes, Ishikawa-Ankerhold and Baqui https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Gachet-Castro, Camila
Freitas-Castro, Felipe
Gonzáles-Córdova, Raul Alexander
da Fonseca, Carol Kobori
Gomes, Marcelo Damário
Ishikawa-Ankerhold, Hellen Cristina
Baqui, Munira Muhammad Abdel
Modulation of the Host Nuclear Compartment by Trypanosoma cruzi Uncovers Effects on Host Transcription and Splicing Machinery
title Modulation of the Host Nuclear Compartment by Trypanosoma cruzi Uncovers Effects on Host Transcription and Splicing Machinery
title_full Modulation of the Host Nuclear Compartment by Trypanosoma cruzi Uncovers Effects on Host Transcription and Splicing Machinery
title_fullStr Modulation of the Host Nuclear Compartment by Trypanosoma cruzi Uncovers Effects on Host Transcription and Splicing Machinery
title_full_unstemmed Modulation of the Host Nuclear Compartment by Trypanosoma cruzi Uncovers Effects on Host Transcription and Splicing Machinery
title_short Modulation of the Host Nuclear Compartment by Trypanosoma cruzi Uncovers Effects on Host Transcription and Splicing Machinery
title_sort modulation of the host nuclear compartment by trypanosoma cruzi uncovers effects on host transcription and splicing machinery
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8560699/
https://www.ncbi.nlm.nih.gov/pubmed/34737973
http://dx.doi.org/10.3389/fcimb.2021.718028
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