Abstract

BackgroundTranscriptional 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 FindingsIn 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/SignificanceThis 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.

Highlights

  • Co-evolution of microbes and the immune system has resulted in the selection of sophisticated mechanisms, which may provide advantages to the host or to the microbe, and result in resistance or susceptibility to infectious disease

  • ¤a Current address: Singapore Immunology Network (SIgN), Biomedical Sciences Institutes, Agency for Science, Technology and Research (A*STAR), IMMUNOS, Singapore, Singapore, ¤b Current address: Departement of Molecular Mechanisms of Mycobacterial Infections, Institut de Pharmacologie et Biologie Structurale (IPBS), Centre National de la Recherche Scientifique (CNRS), Universite Paul Sabatier, UMR 5089, Toulouse, France interactions most likely depends on differential molecular events, a snapshot of which may be measured in the changing transcriptional profiles of Mws and dendritic cells (DCs), which we have investigated here

  • Human monocyte-derived Mws and DCs were infected by M. tuberculosis for 4, 18 or 48 hours, and cellular transcriptomes were analyzed as compared to the reference transcriptome at the time of infection

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Summary

Introduction

Co-evolution of microbes and the immune system has resulted in the selection of sophisticated mechanisms, which may provide advantages to the host or to the microbe, and result in resistance or susceptibility to infectious disease. A detailed comprehension of the common responses is likely to give insight into the basic mechanisms governing hostpathogen cross-talk, whereas genes that are modulated in a cellspecific manner may provide information about specific gene expression programs initiated upon pathogen encounter. These studies will allow the dissection of regulatory networks, which underlie the transcriptional response to infection [1,2,3,4]. Our results 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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