Previous Article | Next Article 
Clinical Microbiology Reviews, July 2003, p. 463-496, Vol. 16, No. 3
0893-8512/03/$08.00+0 DOI: 10.1128/CMR.16.3.463-496.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
Mycobacterium tuberculosis Pathogenesis and Molecular Determinants of Virulence
Issar Smith*
TB Center, Public Health Research Institute, International Center for Public Health, Newark, New Jersey 07103-3535
Tuberculosis (TB), one of the oldest known human diseases. is still is one of the major causes of mortality, since two million people die each year from this malady. TB has many manifestations, affecting bone, the central nervous system, and many other organ systems, but it is primarily a pulmonary disease that is initiated by the deposition of Mycobacterium tuberculosis, contained in aerosol droplets, onto lung alveolar surfaces. From this point, the progression of the disease can have several outcomes, determined largely by the response of the host immune system. The efficacy of this response is affected by intrinsic factors such as the genetics of the immune system as well as extrinsic factors, e.g., insults to the immune system and the nutritional and physiological state of the host. In addition, the pathogen may play a role in disease progression since some M. tuberculosis strains are reportedly more virulent than others, as defined by increased transmissibility as well as being associated with higher morbidity and mortality in infected individuals. Despite the widespread use of an attenuated live vaccine and several antibiotics, there is more TB than ever before, requiring new vaccines and drugs and more specific and rapid diagnostics. Researchers are utilizing information obtained from the complete sequence of the M. tuberculosis genome and from new genetic and physiological methods to identify targets in M. tuberculosis that will aid in the development of these sorely needed antitubercular agents.
* Mailing address: TB Center, Public Health Research Institute, International Center for Public Health, 225 Warren St., Newark NJ 07103-3535. Phone: (973) 854 3260. Fax: (973) 854 3261. E-mail:
smitty{at}phri.org.
Clinical Microbiology Reviews, July 2003, p. 463-496, Vol. 16, No. 3
0893-8512/03/$08.00+0 DOI: 10.1128/CMR.16.3.463-496.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
This article has been cited by other articles:
-
Ghosh, J., Larsson, P., Singh, B., Pettersson, B. M. F., Islam, N. M., Sarkar, S. N., Dasgupta, S., Kirsebom, L. A.
(2009). Sporulation in mycobacteria. Proc. Natl. Acad. Sci. USA
106: 10781-10786
[Abstract]
[Full Text]
-
Rampini, S. K., Selchow, P., Keller, C., Ehlers, S., Bottger, E. C., Sander, P.
(2008). LspA inactivation in Mycobacterium tuberculosis results in attenuation without affecting phagosome maturation arrest. Microbiology
154: 2991-3001
[Abstract]
[Full Text]
-
Veyrier, F., Said-Salim, B., Behr, M. A.
(2008). Evolution of the Mycobacterial SigK Regulon. J. Bacteriol.
190: 1891-1899
[Abstract]
[Full Text]
-
Nakata, N., Fujiwara, N., Naka, T., Yano, I., Kobayashi, K., Maeda, S.
(2008). Identification and Characterization of Two Novel Methyltransferase Genes That Determine the Serotype 12-Specific Structure of Glycopeptidolipids of Mycobacterium intracellulare. J. Bacteriol.
190: 1064-1071
[Abstract]
[Full Text]
-
Wong, K. C., Leong, W. M., Law, H. K. W., Ip, K. F., Lam, J. T. H., Yuen, K. Y., Ho, P. L., Tse, W. S., Weng, X. H., Zhang, W. H., Chen, S., Yam, W. C.
(2007). Molecular Characterization of Clinical Isolates of Mycobacterium tuberculosis and Their Association with Phenotypic Virulence in Human Macrophages. CVI
14: 1279-1284
[Abstract]
[Full Text]
-
Turcotte, K., Gauthier, S., Malo, D., Tam, M., Stevenson, M. M., Gros, P.
(2007). Icsbp1/IRF-8 Is Required for Innate and Adaptive Immune Responses against Intracellular Pathogens. J. Immunol.
179: 2467-2476
[Abstract]
[Full Text]
-
Becq, J., Gutierrez, M. C., Rosas-Magallanes, V., Rauzier, J., Gicquel, B., Neyrolles, O., Deschavanne, P.
(2007). Contribution of Horizontally Acquired Genomic Islands to the Evolution of the Tubercle Bacilli. Mol Biol Evol
24: 1861-1871
[Abstract]
[Full Text]
-
Chitlaru, T., Gat, O., Grosfeld, H., Inbar, I., Gozlan, Y., Shafferman, A.
(2007). Identification of In Vivo-Expressed Immunogenic Proteins by Serological Proteome Analysis of the Bacillus anthracis Secretome. Infect. Immun.
75: 2841-2852
[Abstract]
[Full Text]
-
Srivastava, V., Rouanet, C., Srivastava, R., Ramalingam, B., Locht, C., Srivastava, B. S.
(2007). Macrophage-specific Mycobacterium tuberculosis genes: identification by green fluorescent protein and kanamycin resistance selection. Microbiology
153: 659-666
[Abstract]
[Full Text]
-
Rodrigue, S., Brodeur, J., Jacques, P.-E., Gervais, A. L., Brzezinski, R., Gaudreau, L.
(2007). Identification of Mycobacterial {sigma} Factor Binding Sites by Chromatin Immunoprecipitation Assays. J. Bacteriol.
189: 1505-1513
[Abstract]
[Full Text]
-
Fujiwara, N., Nakata, N., Maeda, S., Naka, T., Doe, M., Yano, I., Kobayashi, K.
(2007). Structural Characterization of a Specific Glycopeptidolipid Containing a Novel N-Acyl-Deoxy Sugar from Mycobacterium intracellulare Serotype 7 and Genetic Analysis of Its Glycosylation Pathway. J. Bacteriol.
189: 1099-1108
[Abstract]
[Full Text]
-
Kurtz, S., McKinnon, K. P., Runge, M. S., Ting, J. P.-Y., Braunstein, M.
(2006). The SecA2 Secretion Factor of Mycobacterium tuberculosis Promotes Growth in Macrophages and Inhibits the Host Immune Response. Infect. Immun.
74: 6855-6864
[Abstract]
[Full Text]
-
Rao, N. A., Saraswathy, S., Smith, R. E.
(2006). Tuberculous Uveitis: Distribution of Mycobacterium tuberculosis in the Retinal Pigment Epithelium. Arch Ophthalmol
124: 1777-1779
[Full Text]
-
Mathema, B., Kurepina, N. E., Bifani, P. J., Kreiswirth, B. N.
(2006). Molecular Epidemiology of Tuberculosis: Current Insights. Clin. Microbiol. Rev.
19: 658-685
[Abstract]
[Full Text]
-
Cosma, C. L., Klein, K., Kim, R., Beery, D., Ramakrishnan, L.
(2006). Mycobacterium marinum Erp Is a Virulence Determinant Required for Cell Wall Integrity and Intracellular Survival.. Infect. Immun.
74: 3125-3133
[Abstract]
[Full Text]
-
Chitlaru, T., Gat, O., Gozlan, Y., Ariel, N., Shafferman, A.
(2006). Differential Proteomic Analysis of the Bacillus anthracis Secretome: Distinct Plasmid and Chromosome CO2-Dependent Cross Talk Mechanisms Modulate Extracellular Proteolytic Activities.. J. Bacteriol.
188: 3551-3571
[Abstract]
[Full Text]
-
Dainese, E., Rodrigue, S., Delogu, G., Provvedi, R., Laflamme, L., Brzezinski, R., Fadda, G., Smith, I., Gaudreau, L., Palu, G., Manganelli, R.
(2006). Posttranslational Regulation of Mycobacterium tuberculosis Extracytoplasmic-Function Sigma Factor {sigma}L and Roles in Virulence and in Global Regulation of Gene Expression. Infect. Immun.
74: 2457-2461
[Abstract]
[Full Text]
-
He, H., Hovey, R., Kane, J., Singh, V., Zahrt, T. C.
(2006). MprAB Is a Stress-Responsive Two-Component System That Directly Regulates Expression of Sigma Factors SigB and SigE in Mycobacterium tuberculosis. J. Bacteriol.
188: 2134-2143
[Abstract]
[Full Text]
-
Casali, N., White, A. M., Riley, L. W.
(2006). Regulation of the Mycobacterium tuberculosis mce1 Operon. J. Bacteriol.
188: 441-449
[Abstract]
[Full Text]
-
Park, J. S., Tamayo, M. H., Gonzalez-Juarrero, M., Orme, I. M., Ordway, D. J.
(2006). Virulent clinical isolates of Mycobacterium tuberculosis grow rapidly and induce cellular necrosis but minimal apoptosis in murine macrophages. J. Leukoc. Biol.
79: 80-86
[Abstract]
[Full Text]
-
Smith, I., Nathan, C., Peavy, H. H.
(2005). Progress and New Directions in Genetics of Tuberculosis: An NHLBI Working Group Report. Am. J. Respir. Crit. Care Med.
172: 1491-1496
[Abstract]
[Full Text]
-
Li, L., Bannantine, J. P., Zhang, Q., Amonsin, A., May, B. J., Alt, D., Banerji, N., Kanjilal, S., Kapur, V.
(2005). The complete genome sequence of Mycobacterium avium subspecies paratuberculosis. Proc. Natl. Acad. Sci. USA
102: 12344-12349
[Abstract]
[Full Text]
-
Yang, Z., Yang, D., Kong, Y., Zhang, L., Marrs, C. F., Foxman, B., Bates, J. H., Wilson, F., Cave, M. D.
(2005). Clinical Relevance of Mycobacterium tuberculosis plcD Gene Mutations. Am. J. Respir. Crit. Care Med.
171: 1436-1442
[Abstract]
[Full Text]
-
Rao, V., Fujiwara, N., Porcelli, S. A., Glickman, M. S.
(2005). Mycobacterium tuberculosis controls host innate immune activation through cyclopropane modification of a glycolipid effector molecule. JEM
201: 535-543
[Abstract]
[Full Text]
-
Kreiner, T., Buck, K. T.
(2005). Moving toward whole-genome analysis: A technology perspective. Am J Health Syst Pharm
62: 296-305
[Abstract]
[Full Text]
-
Daniel, J., Deb, C., Dubey, V. S., Sirakova, T. D., Abomoelak, B., Morbidoni, H. R., Kolattukudy, P. E.
(2004). Induction of a Novel Class of Diacylglycerol Acyltransferases and Triacylglycerol Accumulation in Mycobacterium tuberculosis as It Goes into a Dormancy-Like State in Culture. J. Bacteriol.
186: 5017-5030
[Abstract]
[Full Text]
-
Fortune, S. M., Solache, A., Jaeger, A., Hill, P. J., Belisle, J. T., Bloom, B. R., Rubin, E. J., Ernst, J. D.
(2004). Mycobacterium tuberculosis Inhibits Macrophage Responses to IFN-{gamma} through Myeloid Differentiation Factor 88-Dependent and -Independent Mechanisms. J. Immunol.
172: 6272-6280
[Abstract]
[Full Text]
-
Kocincova, D., Sonden, B., Bordat, Y., Pivert, E., de Mendonca-Lima, L., Gicquel, B., Reyrat, J.-M.
(2004). The Hydrophobic Domain of the Mycobacterial Erp Protein Is Not Essential for the Virulence of Mycobacterium tuberculosis. Infect. Immun.
72: 2379-2382
[Abstract]
[Full Text]