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Probing Host Pathogen Cross-Talk by Transcriptional Profiling of Both Mycobacterium tuberculosis and Infected Human Dendritic Cells and Macrophages
被引:144
作者:
Tailleux, Ludovic
Waddell, Simon J.
Pelizzola, Mattia
Mortellaro, Alessandra
Withers, Michael
Tanne, Antoine
Castagnoli, Paola Ricciardi
Gicquel, Brigitte
Stoker, Neil G.
Butcher, Philip D.
Foti, Maria
Neyrolles, Olivier
机构:
[1] Institut Pasteur, Unit of Mycobacterial Genetics, Paris
[2] Department of Medical Microbiology, Division of Cellular and Molecular Medicine, St. George's University of London, London
[3] Department of Biotechnology and Bioscience, University of Milan-Bicocca, Milan
[4] Department of Pathology and Infectious Diseases, Royal Veterinary College, London
[5] Department of Molecular Mechanisms of Mycobacterial Infections, Institut de Pharmacologie et Biologie Structurale (IPBS), Université Paul Sabatier, Toulouse
[6] Singapore Immunology Network (SIgN), Biomedical Sciences Institutes, Agency for Science, Technology and Research (A STAR), Singapore
来源:
PLOS ONE
|
2008年
/
3卷
/
01期
基金:
英国惠康基金;
关键词:
D O I:
10.1371/journal.pone.0001403
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Background. 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. Methodology/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.
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