Elemental analysis of the Mycobacterium avium phagosome in Balb/c mouse macrophages

Biochemical and Biophysical Research Communications

Volumn 344, Issue 4, 2006, Pages 1346-1351

  Wagner, Dirk ^a   Maser, Jörg ^b   Moric, Ivana ^b   Vogt, Stefan ^b   Kern, Winfried V ^a   Bermudez, Luiz E ^c  

^a UNIVERSITY OF FREIBURG   (Germany)

^b ARGONNE NATIONAL LABORATORY   (United States)

^c OREGON STATE UNIVERSITY   (United States)

Author keywords

Chlorine; Inbred mice; Iron; Killing; Metals; Mycobacteria; Phagosomes; Potassium channel

Indexed keywords

CALCIUM; CHLORIDE; COPPER; IRON; MANGANESE; NICKEL; PHOSPHORUS; POTASSIUM; POTASSIUM CHANNEL; SULFUR; ZINC;

ANALYTIC METHOD; ANIMAL CELL; ARTICLE; BACTERICIDAL ACTIVITY; BACTERIUM EXAMINATION; BIOACCUMULATION; BRUCELLA ABORTUS; CELLULAR DISTRIBUTION; COMPARATIVE STUDY; CONTROLLED STUDY; DISEASE PREDISPOSITION; ELEMENTAL ANALYSIS; HYPOTHESIS; INFECTION RISK; LEISHMANIA MAJOR; LISTERIA MONOCYTOGENES; MOUSE; MOUSE STRAIN; MYCOBACTERIOSIS; MYCOBACTERIUM AVIUM; NONHUMAN; PERITONEUM MACROPHAGE; PHAGOSOME; PRIORITY JOURNAL; STATISTICAL SIGNIFICANCE; X RAY MICROANALYSIS;

ANIMALS; CALCIUM; CHLORINE; IRON; MACROPHAGES, PERITONEAL; MICE; MICE, INBRED BALB C; MICE, INBRED C57BL; MYCOBACTERIUM AVIUM; PHAGOSOMES; POTASSIUM; TUBERCULOSIS; ZINC;

BRUCELLA MELITENSIS BIOVAR ABORTUS; CORYNEBACTERINEAE; LEISHMANIA MAJOR; LISTERIA MONOCYTOGENES; MYCOBACTERIUM AVIUM; MYCOBACTERIUM TUBERCULOSIS;

EID: 33646197903     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2006.04.048     Document Type: Article

References (45)

1. Boechat N., Lagier-Roger B., Petit S., Bordat Y., Rauzier J., Hance A.J., Gicquel B., and Reyrat J.M. Disruption of the gene homologous to mammalian Nramp1 in Mycobacterium tuberculosis does not affect virulence in mice. Infect. Immun. 70 (2002) 4124-4131
2. De Voss J.J., Rutter K., Schroeder B.G., Su H., Zhu Y., and Barry III C.E. The salicylate-derived mycobactin siderophores of Mycobacterium tuberculosis are essential for growth in macrophages. Proc. Natl. Acad. Sci. USA 97 (2000) 1252-1257
3. Wagner D., Maser J., Lai B., Cai Z., Barry III C.E., Höner zu Bentrup K., Russell D.G., and Bermudez L.E. Elemental analysis of Mycobacterium avium, Mycobacterium tuberculosis and Mycobacterium smegmatis-containing phagosomes indicates pathogen-induced microenvironments within the host cell's endosomal system. J. Immunol. 174 (2005) 1491-1500
4. Wagner D., Maser J., Moric I., Boechat N., Voigt S., Gicquel B., Lai B., Reyrat J.M., and Bermudez L.E. Changes of the Phagosomal Elemental Concentrations by Mycobacterium tuberculosis Mramp. Microbiology 151 (2005) 323-332
5. Govoni G., and Gros P. Macrophage NRAMP1 and its role in resistance to microbial infections. Inflamm. Res. 47 (1998) 277-284
6. Bellamy R., Ruwende C., Corrah T., McAdam K.P., Whittle H.C., and Hill A.V. Variations in the NRAMP1 gene and susceptibility to tuberculosis in West Africans. N. Engl. J. Med. 338 (1998) 640-644
7. Awomoyi A.A., Marchant A., Howson J.M., McAdam K.P., Blackwell J.M., and Newport M.J. Interleukin-10, polymorphism in SLC11A1 (formerly NRAMP1), and susceptibility to tuberculosis. J. Infect. Dis. 186 (2002) 1808-1814
8. Abel L., Sanchez F.O., Oberti J., Thuc N.V., Hoa L.V., Lap V.D., Skamene E., Lagrange P.H., and Schurr E. Susceptibility to leprosy is linked to the human NRAMP1 gene. J. Infect. Dis. 177 (1998) 133-145
9. Zhang W., Shao L., Weng X., Hu Z., Jin A., Chen S., Pang M., and Chen Z.W. Variants of the natural resistance-associated macrophage protein 1 gene (NRAMP1) are associated with severe forms of pulmonary tuberculosis. Clin. Infect. Dis. 40 (2005) 1232-1236
10. Buschman E., and Skamene E. From Bcg/Lsh/Ity to Nramp1: three decades of search and research. Drug. Metab. Dispos. 29 (2001) 471-473
11. Medina E., Rogerson B.J., and North R.J. The Nramp1 antimicrobial resistance gene segregates independently of resistance to virulent Mycobacterium tuberculosis. Immunology 88 (1996) 479-481
12. Vidal S.M., Pinner E., Lepage P., Gauthier S., and Gros P. Natural resistance to intracellular infections: Nramp1 encodes a membrane phosphoglycoprotein absent in macrophages from susceptible (Nramp1 D169) mouse strains. J. Immunol. 157 (1996) 3559-3568
13. Keller C., Lauber J., Blumenthal A., Buer J., and Ehlers S. Resistance and susceptibility to tuberculosis analysed at the transcriptome level: lessons from mouse macrophages. Tuberculosis (Edinb.) 84 (2004) 144-158
14. Medina E., and North R.J. Resistance ranking of some common inbred mouse strains to Mycobacterium tuberculosis and relationship to major histocompatibility complex haplotype and Nramp1 genotype. Immunology 93 (1998) 270-274
15. Mitsos L.M., Cardon L.R., Ryan L., LaCourse R., North R.J., and Gros P. Susceptibility to tuberculosis: a locus on mouse chromosome 19 (Trl-4) regulates Mycobacterium tuberculosis replication in the lungs. Proc. Natl. Acad. Sci. USA 100 (2003) 6610-6615
16. Gangadharam P.R. Beige mouse model for Mycobacterium avium complex disease. Antimicrob. Agents Chemother. 39 (1995) 1647-1654
17. Appelberg R., and Sarmento A.M. The role of macrophage activation and of Bcg-encoded macrophage function(s) in the control of Mycobacterium avium infection in mice. Clin. Exp. Immunol. 80 (1990) 324-331
18. Munder A., Zelmer A., Schmiedl A., Dittmar K.E., Rohde M., Dorsch M., Otto K., Hedrich H.J., Tummler B., Weiss S., and Tschernig T. Murine pulmonary infection with Listeria monocytogenes: differential susceptibility of BALB/c, C57BL/6 and DBA/2 mice. Microbes Infect. (2005)
19. Heinzel F.P., Sadick M.D., Holaday B.J., Coffman R.L., and Locksley R.M. Reciprocal expression of interferon gamma or interleukin 4 during the resolution or progression of murine leishmaniasis. Evidence for expansion of distinct helper T cell subsets. J. Exp. Med. 169 (1989) 59-72
20. Montaraz J.A., and Winter A.J. Comparison of living and nonliving vaccines for Brucella abortus in BALB/c mice. Infect. Immun. 53 (1986) 245-251
21. Sathiyaseelan J., Jiang X., and Baldwin C.L. Growth of Brucella abortus in macrophages from resistant and susceptible mouse strains. Clin. Exp. Immunol. 121 (2000) 289-294
22. Handley S.A., Dube P.H., Revell P.A., and Miller V.L. Characterization of oral Yersinia enterocolitica infection in three different strains of inbred mice. Infect. Immun. 72 (2004) 1645-1656
23. Bermudez L.E., Parker A., and Goodman J.R. Growth within macrophages increases the efficiency of Mycobacterium avium in invading other macrophages by a complement receptor-independent pathway. Infect. Immun. 65 (1997) 1916-1925
24. 4+ T-lymphocyte response. Immunology 91 (1997) 414-420
25. Z. Cai, B. Lai, W. Yun, P. Ilinski, D. Legnini, J. Maser, W. Rodrigues, Proceedings of the VI. International Conference, in: W. Meyer-Ilse, T. Warwick, D. Attwood (Eds.),American Institute of Physics, Berkeley, CA, 1999, pp. 472-477.
26. Maser J., Wagner D., Lai B., Cai Z., Legnini D., Moric I., and Bermudez L. Trace metals and their relation to bacterial infections studied by X-ray microscopy. In: Susini J., Joyeux D., and Polack F. (Eds). 7th International Conference on X-Ray Microscopy (2003), EDP Sciences, Les Ulis Cedex A 283-288
27. S. Vogt, MAPS: a Set of Software Tools for Analysis and Visualization of 3 D X-ray Fluorescence Data Sets, in: J. Susini, D. Joyeux, F. Polack (Eds.), 7th International Conference on X-Ray Microscopy,EDP Sciences, Les Ulis Cedex A, 2003, pp. 635-638.
28. Litwin C.M., and Calderwood S.B. Role of iron in regulation of virulence genes. Clin. Microbiol. Rev. 6 (1993) 137-149
29. Chang C.F., Shuman H., and Somlyo A.P. Electron probe analysis, X-ray mapping, and electron energy-loss spectroscopy of calcium, magnesium, and monovalent ions in log-phase and in dividing Escherichia coli B cells. J. Bacteriol. 167 (1986) 935-939
30. Outten C.E., and O'Halloran T.V. Femtomolar sensitivity of metalloregulatory proteins controlling zinc homeostasis. Science 292 (2001) 2488-2492
31. Heldal M., Scanlan D.J., Norland S., Thingstad F., and Mann N.H. Elemental composition of single cells of various strains of marine Prochlorococcus and Synechococcus using X-ray microanalysis. Limnology and Oceanography 48 (2003) 1732-1743
32. + flux. Nature 416 (2002) 291-297
33. - concentrations and membrane potential in human monocytes. Biochim. Biophys. Acta 905 (1987) 195-204
34. + channel is essential for innate immunity. Nature 427 (2004) 853-858
35. Ponte-Sucre A., Mendoza-Leon A., and Moll H. Experimental leishmaniasis: synergistic effect of ion channel blockers and interferon-gamma on the clearance of Leishmania major by macrophages. Parasitol. Res. 87 (2001) 27-31
36. Ponte-Sucre A., Figarella K., and Moll H. Experimental leishmaniasis: the glibenclamide-triggered decrease in parasite growth correlates with changes in macrophage features. Immunopharmacol. Immunotoxicol. 23 (2001) 477-486
37. Gumy A., Louis J.A., and Launois P. The murine model of infection with Leishmania major and its importance for the deciphering of mechanisms underlying differences in Th cell differentiation in mice from different genetic backgrounds. Int. J. Parasitol. 34 (2004) 433-444
38. Gribble F.M., and Reimann F. Differential selectivity of insulin secretagogues: mechanisms, clinical implications, and drug interactions. J. Diabetes Complications 17 (2003) 11-15
39. Inagaki N., Gonoi T., Clement J.P., Namba N., Inazawa J., Gonzalez G., guilar-Bryan L., Seino S., and Bryan J. Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor. Science 270 (1995) 1166-1170
40. Silva N., Camacho N., Figarella K., and Ponte-Sucre A. Cell differentiation and infectivity of Leishmania mexicana are inhibited in a strain resistant to an ABC-transporter blocker. Parasitology 128 (2004) 629-634
41. Hellmann E., and Sprenger H.U. Brucella suis infections in the dog Berl Munch. Tierarztl. Wochenschr. 91 (1978) 385-387
42. Geng X., Li L., Watkins S., Robbins P.D., and Drain P. The insulin secretory granule is the major site of K(ATP) channels of the endocrine pancreas. Diabetes 52 (2003) 767-776
43. Quesada I., and Soria B. Intracellular location of KATP channels and sulphonylurea receptors in the pancreatic beta-cell: new targets for oral antidiabetic agents. Curr. Med. Chem. 11 (2004) 2707-2716
44. Segal A.W. How neutrophils kill microbes. Annu. Rev. Immunol. 23 (2005) 197-223
45. DeCoursey T.E. During the respiratory burst, do phagocytes need proton channels or potassium channels, or both?. Sci. STKE. (2004) e21