Author:
Poirier Valérie,Av-Gay Gal,Av-Gay Yossef
Abstract
AbstractAlveolar macrophages serve as the first line of defence against microbial infection, yet provide a unique niche for the growth ofMycobacterium tuberculosis. To better understand the evasive nature of the tubercle bacilli and its molecular manifest on the macrophage response to infection, we conducted a global quantitative proteomic profile of infected macrophages. By examining four independent controlled infection experiments, we detected 42,007 peptides resulting in the characterization of 4,868 distinct proteins. Of these, we identified 845 macrophage proteins whose expression is modulated upon infection in all replicates. We showed that the macrophage’s response toM. tuberculosisinfection includes simultaneous and concerted upregulation of selected proteins. Using a number of statistical methods, we identified 27 proteins whose expression levels are significantly regulated outside of a 90% confidence interval about the mean. These host proteins represent the macrophage transcriptional, translational, and innate immune response to infection as well as its signaling capacity. The contribution of PtpA, anM. tuberculosissecreted virulence factor, modulated the expression levels of 11 host macrophage proteins, as categorized by RNA metabolism, translation, and cellular respiration.
Publisher
Cold Spring Harbor Laboratory
Reference76 articles.
1. Global tuberculosis incidence and mortality during 1990-2000;W. H. O. Bull,1994
2. Mycobacterial manipulation of the host cell;FEMS Microbiol. Rev,2005
3. Mycobacterium tuberculosis modulators of the macrophage’s cellular events;Microbes Infect,2012
4. Mycobacterium tuberculosis Virulence Is Mediated by PtpA Dephosphorylation of Human Vacuolar Protein Sorting 33B
5. Dishevelled interacts with the DIX domain polymerization interface of Axin to interfere with its function in down-regulating β-catenin