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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页数:14
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共 74 条
[31]  
Mangan JA, 2002, METHOD MICROBIOL, V33, P137
[32]   Persistence of Mycobacterium tuberculosis in macrophages and mice requires the glyoxylate shunt enzyme isocitrate lyase [J].
McKinney, JD ;
zu Bentrup, KH ;
Muñoz-Elias, EJ ;
Miczak, A ;
Chen, B ;
Chan, WT ;
Swenson, D ;
Sacchettini, JC ;
Jacobs, WR ;
Russell, DG .
NATURE, 2000, 406 (6797) :735-738
[33]   Interaction of Mycobacterium avium with human monocyte-derived dendritic cells [J].
Mohagheghpour, N ;
van Vollenhoven, A ;
Goodman, J ;
Bermudez, LE .
INFECTION AND IMMUNITY, 2000, 68 (10) :5824-5829
[34]   Reactive oxygen and nitrogen intermediates in the relationship between mammalian hosts and microbial pathogens [J].
Nathan, C ;
Shiloh, MU .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (16) :8841-8848
[35]   Human macrophage activation programs induced by bacterial pathogens [J].
Nau, GJ ;
Richmond, JFL ;
Schlesinger, A ;
Jennings, EG ;
Lander, ES ;
Young, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (03) :1503-1508
[36]   Inducible nitric oxide synthase in pulmonary alveolar macrophages from patients with tuberculosis [J].
Nicholson, S ;
BoneciniAlmeida, MDG ;
Silva, JRLE ;
Nathan, C ;
Xie, QW ;
Mumford, R ;
Weidner, JR ;
Calaycay, J ;
Geng, J ;
Boechat, N ;
Linhares, C ;
Rom, W ;
Ho, JL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (05) :2293-2302
[37]   Entry and survival of Salmonella typhimurium in dendritic cells and presentation of recombinant antigens do not require macrophage-specific virulence factors [J].
Niedergang, F ;
Sirard, JC ;
Blanc, CT ;
Kraehenbuhl, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (26) :14650-14655
[38]   The effects of reactive nitrogen intermediates on gene expression in Mycobacterium tuberculosis [J].
Ohno, H ;
Zhu, GF ;
Mohan, VP ;
Chu, D ;
Kohno, S ;
Jacobs, WR ;
Chan, J .
CELLULAR MICROBIOLOGY, 2003, 5 (09) :637-648
[39]   glnE is an essential gene in Mycobacterium tuberculosis [J].
Parish, T ;
Stoker, NG .
JOURNAL OF BACTERIOLOGY, 2000, 182 (20) :5715-5720
[40]   Rv3133c/dosR is a transcription factor that mediates the hypoxic response of Mycobacterium tuberculosis [J].
Park, HD ;
Guinn, KM ;
Harrell, MI ;
Liao, R ;
Voskuil, MI ;
Tompa, M ;
Schoolnik, GK ;
Sherman, DR .
MOLECULAR MICROBIOLOGY, 2003, 48 (03) :833-843