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The Journal of Immunology, 2005, 174: 1491-1500.
Copyright © 2005 by The American Association of Immunologists

Elemental Analysis of Mycobacterium avium-, Mycobacterium tuberculosis-, and Mycobacterium smegmatis-Containing Phagosomes Indicates Pathogen-Induced Microenvironments within the Host Cell’s Endosomal System1

Dirk Wagner2,*,{dagger}, Jörg Maser2,{ddagger}, Barry Lai{ddagger}, Zhonghou Cai{ddagger}, Clifton E. Barry, III§, Kerstin Höner zu Bentrup5, David G. Russell and Luiz E. Bermudez3,*

* Kuzell Institute for Arthritis and Infectious Diseases, San Francisco, CA 94115; {dagger} Department of Internal Medizin II Infectious Diseases, University of Freiburg, Freiburg, Germany; {ddagger} Experimental Facilities Division, Argonne National Laboratory, Argonne, IL 60439; § Tuberculosis Research Section, Laboratory of Host Defenses, National Institutes of Health, Rockville, MD 20852; and Department of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853

Mycobacterium avium and Mycobacterium tuberculosis are human pathogens that infect and replicate within macrophages. Both organisms live in phagosomes that fail to fuse with lysosomes and have adapted their lifestyle to accommodate the changing environment within the endosomal system. Among the many environmental factors that could influence expression of bacterial genes are the concentrations of single elements within the phagosomes. We used a novel hard x-ray microprobe with suboptical spatial resolution to analyze characteristic x-ray fluorescence of 10 single elements inside phagosomes of macrophages infected with M. tuberculosis and M. avium or with avirulent M. smegmatis. The iron concentration decreased over time in phagosomes of macrophages infected with Mycobacterium smegmatis but increased in those infected with pathogenic mycobacteria. Autoradiography of infected macrophages incubated with 59Fe-loaded transferrin demonstrated that the bacteria could acquire iron delivered via the endocytic route, confirming the results obtained in the x-ray microscopy. In addition, the concentrations of chlorine, calcium, potassium, manganese, copper, and zinc were shown to differ between the vacuole of pathogenic mycobacteria and M. smegmatis. Differences in the concentration of several elements between M. avium and M. tuberculosis vacuoles were also observed. Activation of macrophages with recombinant IFN-{gamma} or TNF-{alpha} before infection altered the concentrations of elements in the phagosome, which was not observed in cells activated following infection. Siderophore knockout M. tuberculosis vacuoles exhibited retarded acquisition of iron compared with phagosomes with wild-type M. tuberculosis. This is a unique approach to define the environmental conditions within the pathogen-containing compartment.


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