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Lack of Acidification in Mycobacterium Phagosomes Produced by Exclusion of the Vesicular Proton-ATPase
Abstract
The success of Mycobacterium species as pathogens depends on their ability to maintain an infection inside the phagocytic vacuole of the macrophage. Although the bacteria are reported to modulate maturation of their intracellular vacuoles, the nature of such modifications is unknown. In this study, vacuoles formed around Mycobacterium avium failed to acidify below pH 6.3 to 6.5. Immunoelectron microscopy of infected macrophages and immunoblotting of isolated phagosomes showed that Mycobacterium vacuoles acquire the lysosomal membrane protein LAMP-1, but not the vesicular proton-adenosine triphosphatase (ATPase) responsible for phagosomal acidification. This suggests either a selective inhibition of fusion with proton-ATPase-containing vesicles or a rapid removal of the complex from Mycobacterium phagosomes.
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“The early phagosome lacks the proton pumping vesicular ATPase (vATPase) and is therefore characterized by a mildly acidic pH of 6–6.5 (21).”
From Macrophage defense mechanisms against intracellular bacteria (2015) · cites this paper as [21]
In the citing paper
“NRAMP1 is a transmembrane transporter expressed in late phagosomes, where it exerts multiple functions including regulation of phagosome acidification, which is, however, exerted mainly by v-ATPase [144] along with pH-dependent shuttling of divalent metals, including Fe, zinc and manganese, across the phagolysosomal membrane [145-147] (Fig 3).”
From The Iron age of host–microbe interactions (2015) · cites this paper as [144]
Citations
Cites
The catalase—peroxidase gene and isoniazid resistance of Mycobacterium tuberculosis
Zhang, Y., Heym, B., Allen, B., Young, D., & Cole, S. (1992) · Nature · doi:10.1038/358591a0 · Cited by 1,299
Schlesinger, L. S., Bellinger-Kawahara, C., Payne, N. R., & Horwitz, M. A. (1990) · The Journal of Immunology · doi:10.4049/jimmunol.144.7.2771 · Cited by 539
Joiner, K. A., Fuhrman, S. A., Miettinen, H. M., Kasper, L. H., & Mellman, I. (1990) · Science · doi:10.1126/science.2200126 · Cited by 447
Chan, J., Fan, X. D., Hunter, S. W., Brennan, P. J., & Bloom, B. R. (1991) · Infection and Immunity · doi:10.1128/iai.59.5.1755-1761.1991 · Cited by 397
Ammonia inhibits phagosome–lysosome fusion in macrophages
Gordon, A., Hart, P. D., & Young, M. R. (1980) · Nature · doi:10.1038/286079a0 · Cited by 345
Crowle, A. J., Dahl, R., Ross, E., & May, M. H. (1991) · Infection and Immunity · doi:10.1128/iai.59.5.1823-1831.1991 · Cited by 302
Parasitophorous vacuoles of Leishmania amazonensis-infected macrophages maintain an acidic pH
Antoine, J. C., Prina, E., Jouanne, C., & Bongrand, P. (1990) · Infection and Immunity · doi:10.1128/iai.58.3.779-787.1990 · Cited by 239
Fréhel, C., de Chastellier, C., Lang, T., & Rastogi, N. (1986) · Infection and Immunity · doi:10.1128/iai.52.1.252-262.1986 · Cited by 228
Proton pumps populate the contractile vacuoles of Dictyostelium amoebae.
Heuser, J., Zhu, Q., & Clarke, M. (1993) · The Journal of Cell Biology · doi:10.1083/jcb.121.6.1311 · Cited by 224
Self-citationNelson, R. D., Guo, X., Masood, K., Brown, D., Kalkbrenner, M., & Gluck, S. L. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.8.3541 · Cited by 207
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Research works printed but not linked: 2
- APPLEBERG, R, IMMUNOLOGY 80: 352 (1993).
- CHEN, J.W., BIOCH SOC S 51: 97 (1986).
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Items 701–800 of 1,000
Nonadherent cultures of human monocytes kill Mycobacterium smegmatis, but adherent cultures do not
Barker, K. A., Fan, H., Carroll, C., Kaplan, G., Barker, J., Hellmann, W., & Cohn, Z. A. (1996) · Infection and Immunity · doi:10.1128/iai.64.2.428-433.1996 · Cited by 28
Pathogenesis ofMycobacterium Bovis
Thoen, C. O., & Barletta, R. G. (2006) · Wiley eBooks · doi:10.1002/9780470344538.ch4 · Cited by 28
Interactions between Naïve and Infected Macrophages Reduce Mycobacterium tuberculosis Viability
Hartman, M. L., & Kornfeld, H. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027972 · Cited by 27
Lipids in infectious diseases – The case of AIDS and tuberculosis
Dumas, F., & Haanappel, E. (2017) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2017.05.007 · Cited by 28
Therapeutic Targeting of Protein Tyrosine Phosphatases from Mycobacterium tuberculosis
Ruddraraju, K. V., Aggarwal, D., & Zhang, Z. (2020) · Microorganisms · doi:10.3390/microorganisms9010014 · Cited by 27
Effect of pH on the antimicrobial activity of the macrophage metabolite itaconate
Duncan, D., Lupien, A., Behr, M. A., & Auclair, K. (2021) · Microbiology · doi:10.1099/mic.0.001050 · Cited by 28
Mycobacterium avium subsp. paratuberculosis Virulence: A Review
Ssekitoleko, J., Ojok, L., Wahed, A. A. E., Erume, J., Amanzada, A., Eltayeb, E., Eltom, K. H., & Okuni, J. B. (2021) · Microorganisms · doi:10.3390/microorganisms9122623 · Cited by 29
Zacharia, V. M., Manzanillo, P. S., Nair, V. R., Marciano, D. K., Kinch, L. N., Grishin, N. V., Cox, J. S., & Shiloh, M. U. (2013) · mBio · doi:10.1128/mbio.00721-13 · Cited by 28
Nepal, R. M., Mampe, S., Shaffer, B., Erickson, A. H., & Bryant, P. W. (2006) · International Immunology · doi:10.1093/intimm/dxl029 · Cited by 27
Doi, T., Yamada, H., Yajima, T., Wajjwalku, W., Hara, T., & Yoshikai, Y. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.6.3806 · Cited by 27
Reyrat, J., Lopez-Ramirez, G. M., Ofredo, C., Gicquel, B., & Winter, N. (1996) · Infection and Immunity · doi:10.1128/iai.64.9.3934-3936.1996 · Cited by 27
Bermudez, L. E., Goodman, J. R., & Petrofsky, M. (1999) · Infection and Immunity · doi:10.1128/iai.67.9.4912-4916.1999 · Cited by 27
Intracellular pathogens in membrane interactions and vacuole biogenesis
Gorvel, J. (2004) · Cited by 27
Cirone, K. M., Lahiri, P., Holani, R., Tan, Y. L., Arrazuria, R., Buck, J. D., Barkema, H. W., & Cobo, E. R. (2019) · Cell and Tissue Research · doi:10.1007/s00441-019-03098-4 · Cited by 26
Steinhäuser, C., Heigl, U., Tchikov, V., Schwarz, J., Gutsmann, T., Seeger, K., Brandenburg, J., Fritsch, J. H., Schroeder, J. A., Wiesmüller, K., et al. (2012) · Traffic · doi:10.1111/tra.12031 · Cited by 26
A systems biology approach to study the phagosomal proteome modulated by mycobacterial infections.
Rao, P., Singh, C. R., Jagannath, C., & Li, Q. (2009) · PubMed Central · Cited by 26
In-Vivo Gene Signatures of Mycobacterium tuberculosis in C3HeB/FeJ Mice
Gautam, U. S., Mehra, S., & Kaushal, D. (2015) · PLoS ONE · doi:10.1371/journal.pone.0135208 · Cited by 27
Poirier, V., & Av‐Gay, Y. (2015) · Microbiology Spectrum · doi:10.1128/microbiolspec.vmbf-0003-2014 · Cited by 29
Jena, P., Mishra, B. B., Leippe, M., Hasilík, A., Griffiths, G. W., & Sonawane, A. (2011) · Peptides · doi:10.1016/j.peptides.2011.03.002 · Cited by 26
Lo‐Man, R., Langeveld, J., Dériaud, E., Jéhanno, M., Rojas, M., Clément, J.-M., Meloen, R. H., Hofnung, M. J., & Leclerc, C. (2000) · Infection and Immunity · doi:10.1128/iai.68.6.3079-3089.2000 · Cited by 26
Antimicrobial mechanisms of macrophages
Shiloh, M. U., & Nathan, C. (1999) · Advances in cellular and molecular biology of membranes and organelles · doi:10.1016/s1874-5172(99)80042-x · Cited by 26
In vitro control of Mycobacterium bovis by macrophages
Aldwell, F. E., Wedlock, D. N., Slobbe, L. J., Griffin, J. F. T., Buddle, B. M., & Buchan, G. S. (2001) · Tuberculosis · doi:10.1054/tube.2000.0280 · Cited by 26
Lagier, B., Pelicic, V., Lecossier, D., Prod’hom, G., Rauzier, J., Guilhot, C., Gicquel, B., & Hance, A. J. (1998) · Molecular Microbiology · doi:10.1046/j.1365-2958.1998.00933.x · Cited by 26
Life on the inside: Probing Mycobacterium tuberculosis gene expression during infection
Triccas, J. A., & Gicquel, B. (2000) · Immunology and Cell Biology · doi:10.1046/j.1440-1711.2000.00934.x · Cited by 26
Draper, P., & Daffé, M. (2004) · Wiley eBooks · doi:10.1128/9781555817657.ch17 · Cited by 26
MicroRNAs as Regulators of Phagocytosis
Gierlikowski, W., & Gierlikowska, B. (2022) · Cells · doi:10.3390/cells11091380 · Cited by 25
Steiger, J., Stephan, A., Inkeles, M. S., Realegeno, S. E., Bruns, H., Kröll, P., Kroner, J. D. C., Sommer, A., Batinica, M., Pitzler, L., et al. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1502407 · Cited by 25
Mekonnen, D. S., Derbie, A., Mihret, A., Yimer, S. A., Tønjum, T., Gelaw, B., Nibret, E., Munshae, A., Waddell, S. J., & Aseffa, A. (2021) · Lipids in Health and Disease · doi:10.1186/s12944-021-01550-5 · Cited by 26
Immunolocalization of Metabolite Transporter Proteins in a Model Cnidarian-Dinoflagellate Symbiosis
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Molecular Mechanisms of Host–Pathogen Interaction: Entry and Survival of Mycobacteria in Macrophages
Gatfield, J., & Pieters, J. (2003) · Advances in immunology · doi:10.1016/s0065-2776(03)81002-7 · Cited by 25
Butler, R. E., Cihlarova, V., & Stewart, G. R. (2010) · Cellular Microbiology · doi:10.1111/j.1462-5822.2010.01463.x · Cited by 25
Syme, R., Spurrell, J. C. L., Ma, L. L., Green, F. H. Y., & Mody, C. H. (2000) · Infection and Immunity · doi:10.1128/.68.11.6147-6153.2000 · Cited by 25
Mechanisms of Action and Resistance of Antimycobacterial Agents
Karakousis, P. C. (2009) · Humana Press eBooks · doi:10.1007/978-1-59745-180-2_24 · Cited by 25
Gidon, A., Åsberg, S. E., Louet, C., Ryan, L., Haug, M., & Flo, T. H. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006551 · Cited by 25
Innate Immune Recognition in Tuberculosis Infection
Tsolaki, A. G. (2009) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-0901-5_13 · Cited by 25
Gierlikowska, B., Gierlikowski, W., & Demkow, U. A. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.01339 · Cited by 25
Culture at High Density Improves the Ability of Human Macrophages to Control Mycobacterial Growth
Boéchat, N., Bouchonnet, F., Bonay, M., Grodet, A., Pelicic, V., Gicquel, B., & Hance, A. J. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.10.6203 · Cited by 25
Cong, L., Sugden, S., Leclair, P., Lim, C. J., Pham, T. N. Q., & Cohen, É. A. (2021) · mBio · doi:10.1128/mbio.01920-21 · Cited by 27
Khoza, L. J., Kumar, P., Dube, A., Demana, P. H., & Choonara, Y. E. (2022) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2022.121893 · Cited by 24
Cross‐presentation of peptides from intracellular pathogens by MHC class I molecules
Blanchard, N., & Shastri, N. (2010) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.05135.x · Cited by 24
Mycobacterium avium interaction with macrophages and intestinal epithelial cells
Sangari, F. J. (1999) · Frontiers in bioscience · doi:10.2741/sangari · Cited by 24
Muthukuru, M., & Cutler, C. W. (2007) · Infection and Immunity · doi:10.1128/iai.00100-07 · Cited by 24
Jenvey, C. J., Shircliff, A. L., Bannantine, J. P., & Reffett, J. K. (2019) · PLoS ONE · doi:10.1371/journal.pone.0217649 · Cited by 24
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Cardona, P., & Amat, I. (2006) · Archivos de Bronconeumología · doi:10.1157/13083277 · Cited by 21
Growth ofBrucella abortusin macrophages from resistant and susceptible mouse strains
Sathiyaseelan, J., Jiang, X., & Baldwin, C. L. (2000) · Clinical & Experimental Immunology · doi:10.1046/j.1365-2249.2000.01295.x · Cited by 24
Components of Eukaryotic-like Protein Signaling Pathways in Mycobacterium tuberculosis
Av‐Gay, Y., & DAVIES, J. E. (1997) · Microbial & Comparative Genomics · doi:10.1089/omi.1.1997.2.63 · Cited by 24
Peteroy-Kelly, M. A., Venketaraman, V., & Connell, N. D. (2001) · Infection and Immunity · doi:10.1128/iai.69.9.5823-5831.2001 · Cited by 24
Recent advances towards identification of new drug targets for Mycobacterium tuberculosis
Sharma, K., Chopra, P., & Singh, Y. P. (2004) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.8.2.79 · Cited by 24
Immunopathogenesis of Mycobacterium avium infection
Cooper, A. M. (1998) · Frontiers in bioscience · doi:10.2741/a287 · Cited by 24
Zhao, B. Y., Czuprynski, C. J., & Collins, M. T. (1999) · Europe PMC (PubMed Central) · Cited by 24
Bermudez, L. E., & Petrofsky, M. (1999) · Infection and Immunity · doi:10.1128/iai.67.6.3108-3111.1999 · Cited by 24
Macrophages Targeted Drug Delivery as a Key Therapy in Infectious Disease
Cătoi, C. (2014) · Cited by 23
Anes, E., Azevedo‐Pereira, J. M., & Pires, D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.726984 · Cited by 23
Abeldenov, S., Talhaoui, I., Zharkov, D. O., Ishchenko, A. A., Ramanculov, E., Saparbaev, M. K., & Khassenov, B. (2015) · DNA repair · doi:10.1016/j.dnarep.2015.05.007 · Cited by 23
Mycobacterial response to an acidic environment: protective mechanisms
Rai, R., Singh, V., Mathew, B. J., Singh, A. K., & Chaurasiya, S. K. (2022) · Pathogens and Disease · doi:10.1093/femspd/ftac032 · Cited by 23
Wang, J., Yao, Y., Xiong, J., Wu, J., Tang, X., & Li, G. (2015) · BioMed Research International · doi:10.1155/2015/658421 · Cited by 23
Chung, W. J., Kornilov, A. M., Brodsky, B. H., Higgins, M. P., Sanchez, T., Heifets, L. B., Cynamon, M. H., & Welch, J. T. (2008) · Tuberculosis · doi:10.1016/j.tube.2008.06.001 · Cited by 23
von Bargen, K., Wohlmann, J., Taylor, G. A., Utermöhlen, O., & Haas, A. (2011) · Infection and Immunity · doi:10.1128/iai.00983-10 · Cited by 24
Otero, J. H., Jacobs, W. R., & Glickman, M. S. (2003) · Applied and Environmental Microbiology · doi:10.1128/aem.69.9.5039-5044.2003 · Cited by 23
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Nunes, P., Guido, D., & Demaurex, N. (2015) · Journal of Visualized Experiments · doi:10.3791/53402 · Cited by 23
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Bertoldo, J. B., Rodrigues, T., Dunsmore, L., Aprile, F. A., Marques, M. C., Rosado, L. A., Boutureira, O., Steinbrecher, T. B., Sherman, W., Corzana, F., et al. (2017) · Chem · doi:10.1016/j.chempr.2017.07.009 · Cited by 25
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Jee, B. (2020) · Central European Journal of Immunology · doi:10.5114/ceji.2020.94711 · Cited by 23
Cheruvu, M., Plikaytis, B. B., & Shinnick, T. M. (2006) · Tuberculosis · doi:10.1016/j.tube.2006.01.021 · Cited by 23
Basu, S. K., Kumar, D., Singh, D. K., Ganguly, N., Siddiqui, Z., Rao, K. V. S., & Sharma, P. (2006) · FEBS Journal · doi:10.1111/j.1742-4658.2006.05543.x · Cited by 24
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Limia, A., Sangari, F. J., Wagner, D., & Bermudez, L. E. (2001) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2001.tb10597.x · Cited by 23
Russell, D. G. (1995) · Methods in cell biology · doi:10.1016/s0091-679x(08)61857-9 · Cited by 23
Self-citationSun, J., Wang, X., Xiao, J., Yang, Q., Huang, X., Yang, Z., Liu, H., Liu, Y., Wang, H., Huang, Z., et al. (2024) · Scientific Reports · doi:10.1038/s41598-024-77909-2 · Cited by 23
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Ngamtrakulpanit, L., Yu, Y., Adjei, A. A., Amoah, G., Gaston, B., & Hunt, J. F. (2010) · Global Journal of Health Science · doi:10.5539/gjhs.v2n1p106 · Cited by 22
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Juarrero, M. G. (2012) · Immunotherapy · doi:10.2217/imt.11.168 · Cited by 22
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Colas, C., Menezes, S., Gutiérrez-Martínez, E., Péan, C. B., Dionne, M., & Guermonprez, P. (2014) · Journal of Immunological Methods · doi:10.1016/j.jim.2014.06.008 · Cited by 22
Bernardo, J., Long, H. J., & Simons, E. R. (2009) · Cytometry Part A · doi:10.1002/cyto.a.20827 · Cited by 22
Russell, D. G., Purdy, G. E., Owens, R. M., Rohde, K. H., & Yates, R. M. (2005) · Cited by 22
Self-citationLi, Q., Karim, A. F., Ding, X., Das, B., Dobrowolski, C. N., Gibson, R. M., Quiñones‐Mateu, M. E., Karn, J., & Rojas, R. E. (2016) · Scientific Reports · doi:10.1038/srep27566 · Cited by 23
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Singh, B., Saqib, M., Gupta, A., Kumar, P., & Bhaskar, S. (2017) · PLoS ONE · doi:10.1371/journal.pone.0189606 · Cited by 22
Sattler, N., Bosmani, C., Barisch, C., Guého, A., Gopaldass, N., Dias, M., Leuba, F., Brückert, F., Cosson, P., & Soldati, T. (2018) · Journal of Cell Science · doi:10.1242/jcs.218040 · Cited by 22
O’Brien, L. M., Roberts, B., & Andrew, P. W. (1996) · Current topics in microbiology and immunology · doi:10.1007/978-3-642-80166-2_5 · Cited by 22
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Lewis, C. J., & Cobb, B. A. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903168 · Cited by 22
Orme, I. M. (1999) · Elsevier eBooks · doi:10.1016/b978-012775390-4/50174-3 · Cited by 22
Antimycobacterial susceptibility testing: Present practices and future trends
Inderlied, C. B. (1994) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/bf02111499 · Cited by 22
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Riley, L. W. (1995) · Trends in Microbiology · doi:10.1016/s0966-842x(00)88865-4 · Cited by 22
Animal and cell-culture models for the study of mycobacterial infections and treatment
Orme, I. M., Roberts, A. D., Furney, S. K., & Skinner, P. S. (1994) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/bf02111500 · Cited by 22
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Mehrotra, J., & Bishai, W. R. (2001) · International Journal of Medical Microbiology · doi:10.1078/1438-4221-00113 · Cited by 22
Buter, J., Heijnen, D., Wan, I. C., Bickelhaupt, F. M., Young, D. C., Otten, E., Moody, D. B., & Minnaard, A. J. (2016) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.6b01332 · Cited by 21
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Rao, L., & Eissa, N. T. (2019) · Journal of Innate Immunity · doi:10.1159/000497414 · Cited by 21
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Chemaly, A. E., & Demaurex, N. (2011) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2011.10.005 · Cited by 21
Phenotypic assays for Mycobacterium tuberculosis infection
Song, O., Deboosère, N., Delorme, V., Queval, C. J., Deloison, G., Werkmeister, E., Lafont, F., Baulard, A. R., Iantomasi, R., & Brodin, P. M. (2017) · Cytometry Part A · doi:10.1002/cyto.a.23129 · Cited by 24
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Lauvau, G. S., & Pamer, E. G. (2001) · The Journal of Experimental Medicine · doi:10.1084/jem.193.10.f35 · Cited by 21
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Devarajan, P. V., Dawre, S., & Dutta, R. (2014) · Advances in delivery science and technology · doi:10.1007/978-3-319-11355-5_3 · Cited by 21
Gordillo, S., Guirado, E., Gil, O., Díaz, J., Amat, I., Molinos, S., Vilaplana, C., Ausina, V., & Cardona, P.-J. (2006) · Scandinavian Journal of Immunology · doi:10.1111/j.1365-3083.2006.01765.x · Cited by 21
Amara, R. R., & Satchidanandam, V. (1996) · Infection and Immunity · doi:10.1128/iai.64.9.3765-3771.1996 · Cited by 21
Probing the microenvironment of intracellular bacterial pathogens
Harb, O. S., & Kwaik, Y. A. (1999) · Microbes and Infection · doi:10.1016/s1286-4579(99)80048-3 · Cited by 21
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Ansari, M. Y., Batra, S. D., Ojha, H., Dhiman, K., Ganguly, A., Tyagi, J. S., & Mande, S. C. (2020) · FEBS Letters · doi:10.1002/1873-3468.13906 · Cited by 20
Mir, M. A., Mir, B., Kumawat, M., Alkhanani, M., & Jan, U. (2022) · Future Microbiology · doi:10.2217/fmb-2022-0026 · Cited by 20
Petit-Jentreau, L., Jouvion, G., Charles, P., Majlessi, L., Gicquel, B., & Tailleux, L. (2015) · Infection and Immunity · doi:10.1128/iai.00418-15 · Cited by 20
Doherty, T. M. (2012) · Immunotherapy · doi:10.2217/imt.12.52 · Cited by 20
Metadata
- Authors
- Sturgill-Koszycki, S., Schlesinger, P. H., Chakraborty, P., Haddix, P. L., Collins, H. L., Fok, A. K., Allen, R. D., Gluck, S. L., Heuser, J., & Russell, D. G.
- Affiliations
- Washington University Medical Center (US)
- University of Hawaiʻi at Mānoa (US)
- ORCID
- Venue
- Science
- Published
- 1994-02-04
- Volume
- 263
- Issue
- 5147
- Pages
- 678-681
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2147251439
- Cited by
- 1,302
- References
- 26
- Citations by year
- 2026: 17 · 2025: 17 · 2024: 15 · 2023: 21 · 2022: 24 · 2021: 37 · 2020: 34 · 2019: 38 · 2018: 25 · 2017: 42 · 2016: 37 · 2015: 39 · 2014: 67 · 2013: 39 · 2012: 45
- FWCI
- 47.28
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (1r01ai034207-01, 5r01ar042370-04, 5r01ai026889-03)
- National Institute of Allergy and Infectious Diseases (AI 26889, AI 34207)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (AR 42370)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Tuberculosis Research and Epidemiology
- Health Sciences › Medicine › Epidemiology › Mycobacterium research and diagnosis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Keywords
- Mycobacterium avium, phagosome acidification, phagosome maturation, macrophages, LAMP1, lysosomal membrane proteins, intracellular bacterial survival, mycobacterial pathogenesis
- MeSH terms
- Animals, Proton-Translocating ATPases, Hydrogen-Ion Concentration, Leishmania mexicana, Macrophages, Membrane Fusion, Membrane Glycoproteins, Mycobacterium avium, Mycobacterium tuberculosis, Phagosomes, Vacuoles, Antigens, CD, Microscopy, Immunoelectron, Mice, Lysosomal Membrane Proteins
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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