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Modulation of activation-associated host cell gene expression by the apicomplexan parasite Theileria annulata
Infection of bovine leucocytes by Theileria annulata results in establishment of transformed, infected cells. Infection of the host cell is known to promote constitutive activation of pro-inflammatory transcription factors that have the potential to be beneficial or detrimental. In this study we hav...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532605/ https://www.ncbi.nlm.nih.gov/pubmed/22533473 http://dx.doi.org/10.1111/j.1462-5822.2012.01809.x |
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author | Durrani, Zeeshan Weir, William Pillai, Sreerekha Kinnaird, Jane Shiels, Brian |
author_facet | Durrani, Zeeshan Weir, William Pillai, Sreerekha Kinnaird, Jane Shiels, Brian |
author_sort | Durrani, Zeeshan |
collection | PubMed |
description | Infection of bovine leucocytes by Theileria annulata results in establishment of transformed, infected cells. Infection of the host cell is known to promote constitutive activation of pro-inflammatory transcription factors that have the potential to be beneficial or detrimental. In this study we have compared the effect of LPS activation on uninfected bovine leucocytes (BL20 cells) and their Theileria-infected counterpart (TBL20). Gene expression profiles representing activated uninfected BL20 relative to TBL20 cells were also compared. The results show that while prolonged stimulation with LPS induces cell death and activation of NF-κB in BL20 cells, the viability of Theileria-infected cells was unaffected. Analysis of gene expression networks provided evidence that the parasite establishes tight control over pathways associated with cellular activation by modulating reception of extrinsic stimuli and by significantly altering the expression outcome of genes targeted by infection-activated transcription factors. Pathway analysis of the data set identified novel candidate genes involved in manipulation of cellular functions associated with the infected transformed cell. The data indicate that the T. annulata parasite can irreversibly reconfigure host cell gene expression networks associated with development of inflammatory disease and cancer to generate an outcome thatis beneficial to survival and propagation of the infected leucocyte. |
format | Online Article Text |
id | pubmed-3532605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-35326052013-01-09 Modulation of activation-associated host cell gene expression by the apicomplexan parasite Theileria annulata Durrani, Zeeshan Weir, William Pillai, Sreerekha Kinnaird, Jane Shiels, Brian Cell Microbiol Original Articles Infection of bovine leucocytes by Theileria annulata results in establishment of transformed, infected cells. Infection of the host cell is known to promote constitutive activation of pro-inflammatory transcription factors that have the potential to be beneficial or detrimental. In this study we have compared the effect of LPS activation on uninfected bovine leucocytes (BL20 cells) and their Theileria-infected counterpart (TBL20). Gene expression profiles representing activated uninfected BL20 relative to TBL20 cells were also compared. The results show that while prolonged stimulation with LPS induces cell death and activation of NF-κB in BL20 cells, the viability of Theileria-infected cells was unaffected. Analysis of gene expression networks provided evidence that the parasite establishes tight control over pathways associated with cellular activation by modulating reception of extrinsic stimuli and by significantly altering the expression outcome of genes targeted by infection-activated transcription factors. Pathway analysis of the data set identified novel candidate genes involved in manipulation of cellular functions associated with the infected transformed cell. The data indicate that the T. annulata parasite can irreversibly reconfigure host cell gene expression networks associated with development of inflammatory disease and cancer to generate an outcome thatis beneficial to survival and propagation of the infected leucocyte. Blackwell Publishing Ltd 2012-09 2012-05-23 /pmc/articles/PMC3532605/ /pubmed/22533473 http://dx.doi.org/10.1111/j.1462-5822.2012.01809.x Text en Copyright © 2012 Blackwell Publishing Ltd http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Original Articles Durrani, Zeeshan Weir, William Pillai, Sreerekha Kinnaird, Jane Shiels, Brian Modulation of activation-associated host cell gene expression by the apicomplexan parasite Theileria annulata |
title | Modulation of activation-associated host cell gene expression by the apicomplexan parasite Theileria annulata |
title_full | Modulation of activation-associated host cell gene expression by the apicomplexan parasite Theileria annulata |
title_fullStr | Modulation of activation-associated host cell gene expression by the apicomplexan parasite Theileria annulata |
title_full_unstemmed | Modulation of activation-associated host cell gene expression by the apicomplexan parasite Theileria annulata |
title_short | Modulation of activation-associated host cell gene expression by the apicomplexan parasite Theileria annulata |
title_sort | modulation of activation-associated host cell gene expression by the apicomplexan parasite theileria annulata |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532605/ https://www.ncbi.nlm.nih.gov/pubmed/22533473 http://dx.doi.org/10.1111/j.1462-5822.2012.01809.x |
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