Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0001403
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dc.titleProbing host pathogen cross-talk by transcriptional profiling of both Mycobacterium tuberculosis and infected human dendritic cells and macrophages
dc.contributor.authorTailleux L.
dc.contributor.authorWaddel S.J.
dc.contributor.authorPelizzola M.
dc.contributor.authorMortellaro A.
dc.contributor.authorWithers M.
dc.contributor.authorTanne A.
dc.contributor.authorCastagnoli P.R.
dc.contributor.authorGicquel B.
dc.contributor.authorStoker N.G.
dc.contributor.authorButcher P.D.
dc.contributor.authorFoti M.
dc.contributor.authorNeyrolles O.
dc.date.accessioned2020-03-18T05:53:04Z
dc.date.available2020-03-18T05:53:04Z
dc.date.issued2008
dc.identifier.citationTailleux 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.issn19326203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/165609
dc.description.abstractBackgound. 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.publisherPublic Library of Science
dc.sourceUnpaywall 20200320
dc.subject3' deamino 3' morpholinooxaunomycin
dc.subjectglutathione peroxidase
dc.subjectglutathione peroxidase 3
dc.subjectglycoprotein gp 91
dc.subjectimmunoglobulin enhancer binding protein
dc.subjectimmunoglobulin enhancer binding protein 1
dc.subjectimmunoglobulin enhancer binding protein 2
dc.subjectinterferon regulatory factor
dc.subjectinterferon regulatory factor 4
dc.subjectinterferon regulatory factor 5
dc.subjectJanus kinase 1
dc.subjectmanganese superoxide dismutase
dc.subjectmyeloid differentiation factor 88
dc.subjectprotein p40
dc.subjectprotein p67
dc.subjectRab protein
dc.subjectRac protein
dc.subjectRac1 protein
dc.subjectSTAT3 protein
dc.subjectSTAT4 protein
dc.subjectSTAT5a protein
dc.subjectSTAT5b protein
dc.subjectsuppressor of cytokine signaling 3
dc.subjecttoll like receptor
dc.subjecttoll like receptor 1
dc.subjecttoll like receptor 4
dc.subjecttranscriptome
dc.subjecttumor necrosis factor receptor associated factor 1
dc.subjecttumor necrosis factor receptor associated factor 5
dc.subjectunclassified drug
dc.subjectacidification
dc.subjectadaptation
dc.subjectarticle
dc.subjectbacterial immunity
dc.subjectcell type
dc.subjectcell vacuole
dc.subjectcluster analysis
dc.subjectcontrolled study
dc.subjectdendritic cell
dc.subjecteukaryote
dc.subjectgene expression profiling
dc.subjectgene expression regulation
dc.subjectgene identification
dc.subjecthost cell
dc.subjecthost pathogen interaction
dc.subjecthuman
dc.subjecthuman cell
dc.subjectintracellular transport
dc.subjectmacrophage
dc.subjectMycobacterium tuberculosis
dc.subjectnonhuman
dc.subjectoxidative stress
dc.subjectphagocyte
dc.subjectphagosome
dc.subjectplasticity
dc.subjecttranscription regulation
dc.subjectdendritic cell
dc.subjectgenetic transcription
dc.subjectgenetics
dc.subjectimmunology
dc.subjectmacrophage
dc.subjectmicrobiology
dc.subjectphysiology
dc.subjectEukaryota
dc.subjectMycobacterium tuberculosis
dc.subjectDendritic Cells
dc.subjectGene Expression Profiling
dc.subjectHumans
dc.subjectMacrophages
dc.subjectMycobacterium tuberculosis
dc.subjectTranscription, Genetic
dc.typeArticle
dc.contributor.departmentMICROBIOLOGY AND IMMUNOLOGY
dc.description.doi10.1371/journal.pone.0001403
dc.description.sourcetitlePLoS ONE
dc.description.volume3
dc.description.issue1
dc.description.pagee1403
dc.published.statePublished
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