Please use this identifier to cite or link to this item:
https://doi.org/10.1371/journal.pone.0001403
DC Field | Value | |
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dc.title | Probing host pathogen cross-talk by transcriptional profiling of both Mycobacterium tuberculosis and infected human dendritic cells and macrophages | |
dc.contributor.author | Tailleux L. | |
dc.contributor.author | Waddel S.J. | |
dc.contributor.author | Pelizzola M. | |
dc.contributor.author | Mortellaro A. | |
dc.contributor.author | Withers M. | |
dc.contributor.author | Tanne A. | |
dc.contributor.author | Castagnoli P.R. | |
dc.contributor.author | Gicquel B. | |
dc.contributor.author | Stoker N.G. | |
dc.contributor.author | Butcher P.D. | |
dc.contributor.author | Foti M. | |
dc.contributor.author | Neyrolles O. | |
dc.date.accessioned | 2020-03-18T05:53:04Z | |
dc.date.available | 2020-03-18T05:53:04Z | |
dc.date.issued | 2008 | |
dc.identifier.citation | Tailleux L., Waddel S.J., Pelizzola M., Mortellaro A., Withers M., Tanne A., Castagnoli P.R., Gicquel B., Stoker N.G., Butcher P.D., Foti M., Neyrolles O. (2008). Probing host pathogen cross-talk by transcriptional profiling of both Mycobacterium tuberculosis and infected human dendritic cells and macrophages. PLoS ONE 3 (1) : e1403. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0001403 | |
dc.identifier.issn | 19326203 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/165609 | |
dc.description.abstract | Backgound. Transcriptional profiling using microarrays provides a unique opportunity to decipher host pathogen cross-talk on the global level. Here, for the first time, we have been able to investigate gene expression changes in both Mycobacterium tuberculosis, a major human pathogen, and its human host cells, macrophages and dendritic cells. Mothodalogy/Principal Findings. In addition to common responses, we could identify eukaryotic and microbial transcriptional signatures that are specific to the cell type involved in the infection process. In particular M. tuberculosis shows a marked stress response when inside dendritic cells, which is in accordance with the low permissivity of these specialized phagocytes to the tubercle bacillus and to other pathogens. In contrast, the mycobacterial transcriptome inside macrophages reflects that of replicating bacteria. On the host cell side, differential responses to infection in macrophages and dendritic cells were identified in genes involved in oxidative stress, intracellular vesicle trafficking and phagosome acidification. Conclusions/Significance. This study provides the proof of principle that probing the host and the microbe transcriptomes simultaneously is a valuable means to accessing unique information on host pathogen interactions. Our results also underline the extraordinary plasticity of host cell and pathogen responses to infection, and provide a solid framework to further understand the complex mechanisms involved in immunity to M. tuberculosis and in mycobacterial adaptation to different intracellular environments. © 2008 Tailleux et al. | |
dc.publisher | Public Library of Science | |
dc.source | Unpaywall 20200320 | |
dc.subject | 3' deamino 3' morpholinooxaunomycin | |
dc.subject | glutathione peroxidase | |
dc.subject | glutathione peroxidase 3 | |
dc.subject | glycoprotein gp 91 | |
dc.subject | immunoglobulin enhancer binding protein | |
dc.subject | immunoglobulin enhancer binding protein 1 | |
dc.subject | immunoglobulin enhancer binding protein 2 | |
dc.subject | interferon regulatory factor | |
dc.subject | interferon regulatory factor 4 | |
dc.subject | interferon regulatory factor 5 | |
dc.subject | Janus kinase 1 | |
dc.subject | manganese superoxide dismutase | |
dc.subject | myeloid differentiation factor 88 | |
dc.subject | protein p40 | |
dc.subject | protein p67 | |
dc.subject | Rab protein | |
dc.subject | Rac protein | |
dc.subject | Rac1 protein | |
dc.subject | STAT3 protein | |
dc.subject | STAT4 protein | |
dc.subject | STAT5a protein | |
dc.subject | STAT5b protein | |
dc.subject | suppressor of cytokine signaling 3 | |
dc.subject | toll like receptor | |
dc.subject | toll like receptor 1 | |
dc.subject | toll like receptor 4 | |
dc.subject | transcriptome | |
dc.subject | tumor necrosis factor receptor associated factor 1 | |
dc.subject | tumor necrosis factor receptor associated factor 5 | |
dc.subject | unclassified drug | |
dc.subject | acidification | |
dc.subject | adaptation | |
dc.subject | article | |
dc.subject | bacterial immunity | |
dc.subject | cell type | |
dc.subject | cell vacuole | |
dc.subject | cluster analysis | |
dc.subject | controlled study | |
dc.subject | dendritic cell | |
dc.subject | eukaryote | |
dc.subject | gene expression profiling | |
dc.subject | gene expression regulation | |
dc.subject | gene identification | |
dc.subject | host cell | |
dc.subject | host pathogen interaction | |
dc.subject | human | |
dc.subject | human cell | |
dc.subject | intracellular transport | |
dc.subject | macrophage | |
dc.subject | Mycobacterium tuberculosis | |
dc.subject | nonhuman | |
dc.subject | oxidative stress | |
dc.subject | phagocyte | |
dc.subject | phagosome | |
dc.subject | plasticity | |
dc.subject | transcription regulation | |
dc.subject | dendritic cell | |
dc.subject | genetic transcription | |
dc.subject | genetics | |
dc.subject | immunology | |
dc.subject | macrophage | |
dc.subject | microbiology | |
dc.subject | physiology | |
dc.subject | Eukaryota | |
dc.subject | Mycobacterium tuberculosis | |
dc.subject | Dendritic Cells | |
dc.subject | Gene Expression Profiling | |
dc.subject | Humans | |
dc.subject | Macrophages | |
dc.subject | Mycobacterium tuberculosis | |
dc.subject | Transcription, Genetic | |
dc.type | Article | |
dc.contributor.department | MICROBIOLOGY AND IMMUNOLOGY | |
dc.description.doi | 10.1371/journal.pone.0001403 | |
dc.description.sourcetitle | PLoS ONE | |
dc.description.volume | 3 | |
dc.description.issue | 1 | |
dc.description.page | e1403 | |
dc.published.state | Published | |
Appears in Collections: | Elements Staff Publications |
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