Cargando…

Toxoplasma gondii Infection Specifically Increases the Levels of Key Host MicroRNAs

BACKGROUND: The apicomplexan parasite Toxoplasma gondii can infect and replicate in virtually any nucleated cell in many species of warm-blooded animals; thus, it has evolved the ability to exploit well-conserved biological processes common to its diverse hosts. Here we have investigated whether Tox...

Descripción completa

Detalles Bibliográficos
Autores principales: Zeiner, Gusti M., Norman, Kara L., Thomson, J. Michael, Hammond, Scott M., Boothroyd, John C.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806928/
https://www.ncbi.nlm.nih.gov/pubmed/20090903
http://dx.doi.org/10.1371/journal.pone.0008742
_version_ 1782176353479557120
author Zeiner, Gusti M.
Norman, Kara L.
Thomson, J. Michael
Hammond, Scott M.
Boothroyd, John C.
author_facet Zeiner, Gusti M.
Norman, Kara L.
Thomson, J. Michael
Hammond, Scott M.
Boothroyd, John C.
author_sort Zeiner, Gusti M.
collection PubMed
description BACKGROUND: The apicomplexan parasite Toxoplasma gondii can infect and replicate in virtually any nucleated cell in many species of warm-blooded animals; thus, it has evolved the ability to exploit well-conserved biological processes common to its diverse hosts. Here we have investigated whether Toxoplasma modulates the levels of host microRNAs (miRNAs) during infection. METHODOLOGY/PRINCIPAL FINDINGS: Using microarray profiling and a combination of conventional molecular approaches we report that Toxoplasma specifically modulates the expression of important host microRNAs during infection. We show that both the primary transcripts for miR-17∼92 and miR-106b∼25 and the pivotal miRNAs that are derived from miR-17∼92 display increased abundance in Toxoplasma-infected primary human cells; a Toxoplasma-dependent up-regulation of the miR-17∼92 promoter is at least partly responsible for this increase. The abundance of mature miR-17 family members, which are derived from these two miRNA clusters, remains unchanged in host cells infected with the closely related apicomplexan Neospora caninum; thus, the Toxoplasma-induced increase in their abundance is a highly directed process rather than a general host response to infection. CONCLUSIONS/SIGNIFICANCE: Altered levels of miR-17∼92 and miR-106b∼25 are known to play crucial roles in mammalian cell regulation and have been implicated in numerous hyperproliferative diseases although the mechanisms driving their altered expression are unknown. Hence, in addition to the implications of these findings on the host-pathogen interaction, Toxoplasma may represent a powerful probe for understanding the normal mechanisms that regulate the levels of key host miRNAs.
format Text
id pubmed-2806928
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-28069282010-01-21 Toxoplasma gondii Infection Specifically Increases the Levels of Key Host MicroRNAs Zeiner, Gusti M. Norman, Kara L. Thomson, J. Michael Hammond, Scott M. Boothroyd, John C. PLoS One Research Article BACKGROUND: The apicomplexan parasite Toxoplasma gondii can infect and replicate in virtually any nucleated cell in many species of warm-blooded animals; thus, it has evolved the ability to exploit well-conserved biological processes common to its diverse hosts. Here we have investigated whether Toxoplasma modulates the levels of host microRNAs (miRNAs) during infection. METHODOLOGY/PRINCIPAL FINDINGS: Using microarray profiling and a combination of conventional molecular approaches we report that Toxoplasma specifically modulates the expression of important host microRNAs during infection. We show that both the primary transcripts for miR-17∼92 and miR-106b∼25 and the pivotal miRNAs that are derived from miR-17∼92 display increased abundance in Toxoplasma-infected primary human cells; a Toxoplasma-dependent up-regulation of the miR-17∼92 promoter is at least partly responsible for this increase. The abundance of mature miR-17 family members, which are derived from these two miRNA clusters, remains unchanged in host cells infected with the closely related apicomplexan Neospora caninum; thus, the Toxoplasma-induced increase in their abundance is a highly directed process rather than a general host response to infection. CONCLUSIONS/SIGNIFICANCE: Altered levels of miR-17∼92 and miR-106b∼25 are known to play crucial roles in mammalian cell regulation and have been implicated in numerous hyperproliferative diseases although the mechanisms driving their altered expression are unknown. Hence, in addition to the implications of these findings on the host-pathogen interaction, Toxoplasma may represent a powerful probe for understanding the normal mechanisms that regulate the levels of key host miRNAs. Public Library of Science 2010-01-15 /pmc/articles/PMC2806928/ /pubmed/20090903 http://dx.doi.org/10.1371/journal.pone.0008742 Text en Zeiner et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zeiner, Gusti M.
Norman, Kara L.
Thomson, J. Michael
Hammond, Scott M.
Boothroyd, John C.
Toxoplasma gondii Infection Specifically Increases the Levels of Key Host MicroRNAs
title Toxoplasma gondii Infection Specifically Increases the Levels of Key Host MicroRNAs
title_full Toxoplasma gondii Infection Specifically Increases the Levels of Key Host MicroRNAs
title_fullStr Toxoplasma gondii Infection Specifically Increases the Levels of Key Host MicroRNAs
title_full_unstemmed Toxoplasma gondii Infection Specifically Increases the Levels of Key Host MicroRNAs
title_short Toxoplasma gondii Infection Specifically Increases the Levels of Key Host MicroRNAs
title_sort toxoplasma gondii infection specifically increases the levels of key host micrornas
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806928/
https://www.ncbi.nlm.nih.gov/pubmed/20090903
http://dx.doi.org/10.1371/journal.pone.0008742
work_keys_str_mv AT zeinergustim toxoplasmagondiiinfectionspecificallyincreasesthelevelsofkeyhostmicrornas
AT normankaral toxoplasmagondiiinfectionspecificallyincreasesthelevelsofkeyhostmicrornas
AT thomsonjmichael toxoplasmagondiiinfectionspecificallyincreasesthelevelsofkeyhostmicrornas
AT hammondscottm toxoplasmagondiiinfectionspecificallyincreasesthelevelsofkeyhostmicrornas
AT boothroydjohnc toxoplasmagondiiinfectionspecificallyincreasesthelevelsofkeyhostmicrornas