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Intracellular Fate of Mycobacterium Avium: Use of Dual-label Spectrofluorometry to Investigate the Influence of Bacterial Viability and Opsonization on Phagosomal PH and Phagosome-lysosome Interaction

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Journal Infect Immun
Date 1996 Jan 1
PMID 8557358
Citations 47
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Abstract

Mycobacterium avium is a facultative intracellular pathogen that can survive and replicate within macrophages. We tested the hypotheses that survival mechanisms may include alteration of phagosomal pH or inhibition of phagosome-lysosome fusion. M. avium was surface labeled with N-hydroxysuccinimidyl esters of carboxyfluorescein (CF) and rhodamine (Rho) to enable measurement of the pH of individual M. avium-containing phagosomes and the interactions of bacterium-containing phagosomes with labeled secondary lysosomes. CF fluorescence is pH sensitive, whereas Rho is pH insensitive; pH can be calculated from their fluorescence ratios. Surface labeling of M. avium did not affect viability in broth cultures or within J774, a murine macrophage-like cell line. By fluorescence spectroscopy, live M. avium was exposed to an environmental pH of approximately 5.7 at 6 h after phagocytosis, whereas similarly labeled Salmonella typhimurium, zymosan A, or heat-killed M. avium encountered an environmental pH of < 5.0. Video fluorescence and laser scanning confocal microscopy gave consistent pH results and demonstrated the heterogeneity of intracellular fate early in infection. pH became more homogeneous 6 h after infection. M. avium cells were coated with immunoglobulin G (IgG) or opsonized to investigate whether phagocytosis by the corresponding receptors would alter intracellular fate. Opsonized, unopsonized, and IgG-coated M. avium cells entered compartments of similar pH. Finally, the spatial distribution of intracellular bacteria and secondary lysosomes was compared. Only 18% of live fluorescent M. avium cells colocalized with fluorescent lysosomes, while 98% of heat-killed bacteria colocalized. Thus, both inhibition of phagosome-lysosome fusion and alteration of phagosomal pH may contribute to the intracellular survival of M. avium.

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References
1.
Armstrong J, HART P . Phagosome-lysosome interactions in cultured macrophages infected with virulent tubercle bacilli. Reversal of the usual nonfusion pattern and observations on bacterial survival. J Exp Med. 1975; 142(1):1-16. PMC: 2189870. DOI: 10.1084/jem.142.1.1. View

2.
Chapman J, BERNARD J . The tolerances of unclassified mycobacteria. I. Limits of pH tolerance. Am Rev Respir Dis. 1962; 86:582-3. DOI: 10.1164/arrd.1962.86.4.582. View

3.
Kielian M, COHN Z . Intralysosomal accumulation of polyanions. II. Polyanion internalization and its influence on lysosomal pH and membrane fluidity. J Cell Biol. 1982; 93(3):875-82. PMC: 2112131. DOI: 10.1083/jcb.93.3.875. View

4.
Maxfield F . Weak bases and ionophores rapidly and reversibly raise the pH of endocytic vesicles in cultured mouse fibroblasts. J Cell Biol. 1982; 95(2 Pt 1):676-81. PMC: 2112942. DOI: 10.1083/jcb.95.2.676. View

5.
Murphy R, Powers S, Cantor C . Endosome pH measured in single cells by dual fluorescence flow cytometry: rapid acidification of insulin to pH 6. J Cell Biol. 1984; 98(5):1757-62. PMC: 2113196. DOI: 10.1083/jcb.98.5.1757. View