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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...

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Detalles Bibliográficos
Autores principales: Durrani, Zeeshan, Weir, William, Pillai, Sreerekha, Kinnaird, Jane, Shiels, Brian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2012
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.
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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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