Mycobacterium

Pathogenesis of Bacterial Infections in Animals: Fourth Edition

Volumn , Issue , 2010, Pages 113-132

  Olsen, I ^a   Barletta, R G ^b   Thoen, C O ^c  

^a NORWEGIAN VETERINARY INSTITUTE   (Norway)

^b UNIVERSITY OF NEBRASKA LINCOLN   (United States)

^c IOWA STATE UNIVERSITY   (United States)

Author keywords

Covalently attached molecules of cell wall core of mycobacteria peptidoglycan, arabinogalactan, mycolic acid; M. tuberculosis inducing tuberculin skin sensitivity; Mycobacteria pathogenicity multifactorial phenomenon; Mycobacterial proteins, protein complexes important role in pathogenesis; Mycobacterium; Mycobacterium leprae chronic granulomatous disease; Tuberculosis causing death in humans

Indexed keywords

EID: 77956580365     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1002/9780470958209.ch7     Document Type: Chapter

References (125)

1. Aldwell, F. E., D. L. Keen, N. A. Parlane, M. A. Skinner, G. W. de Lisle, and B. M. Buddle. 2003. Oral vaccination with Mycobacterium bovis BCG in a lipid formulation induces resistance to pulmonary tuberculosis in brushtail possums. Vaccine 22:70-76.
2. Alexander, D. C., C. Y. Turenne, and M. A. Behr. 2009. Insertion and deletion events that define the pathogen Mycobacterium avium subsp. paratuberculosis. J. Bacteriol. 191:1018-1025.
3. Andersen, P., D. Askgaard, L. Ljungqvist, J. Bennedsen, and I. Heron. 1991. Proteins released from Mycobacterium tuberculosis during growth. Infect. Immun. 59:1905-1910.
4. Bach, H., J. Sun, Z. Hmama, and Y. Av-Gay. 2006. Mycobacterium avium subsp. paratuberculosis PtpA is an endogenous tyrosine phosphatase secreted during infection. Infect. Immun. 74:6540-6546.
5. Balseiro, A., J. F. Garcia Marin, P. Solano, J. M. Garrido, and J. M. Prieto. 2008. Histopathological classification of lesions observed in natural cases of paratuberculosis in free-ranging fallow deer (Dama dama). J. Comp. Pathol. 138:180-188.
6. Bannantine, J. P., J. F. Huntley, E. Miltner, J. R. Stabel, and L. E. Bermudez. 2003. The Mycobacterium avium subsp. paratuberculosis 35 kDa protein plays a role in invasion of bovine epithelial cells. Microbiol. 149:2061-2069.
7. Bannantine, J. P., and M. L. Paustian. 2006. Identification of diagnostic proteins in Mycobacterium avium subspecies paratuberculosis by a whole genome analysis approach. Methods Mol. Biol. 345:185-196.
8. Bartow, R. A., and D. N. McMurray. 1998. Lymphocytes expressing Fc gamma receptors suppress antigen-induced proliferation in cells from guinea pigs infected with virulent Mycobacterium tuberculosis. Cell Immunol. 184:51-57.
9. Bassey, E. O., and M. T. Collins. 1997. Study of T-lymphocyte subsets of healthy and Mycobacterium avium subsp. paratuberculosis-infected cattle. Infect. Immun. 65:4869-4872.
10. Begara-McGorum, I., L. A. Wildblood, C. J. Clarke, K. M. Connor, K. Stevenson, C. J. McInnes, et al. 1998. Early immunopathological events in experimental ovine paratuberculosis. Vet. Immunol. Immunopathol. 63:265-287.
11. Belisle, J. T., V. D. Vissa, T. Sievert, K. Takayama, P. J. Brennan, and G. S. Besra. 1997. Role of the major antigen of Mycobacterium tuberculosis in cell wall biogenesis. Science 276:1420-1422.
12. Braunstein, M., S. S. Bardarov, and W. R. Jr. Jacobs, 2002. Genetic methods for deciphering virulence determinants of Mycobacterium tuberculosis. Methods Enzymol. 358:67-99.
13. Brosch, R., S. V. Gordon, M. Marmiesse, P. Brodin, C. Buchrieser, K. Eiglmeier, et al. 2002. A new evolutionary scenario for the Mycobacterium tuberculosis complex. Proc. Natl. Acad. Sci. U S A 99:3684-3689.
14. Buddle, B. M., N. A. Parlane, D. L. Keen, F. E. Aldwell, J. M. Pollock, K. Lightbody, et al. 1999. Differentiation between Mycobacterium bovis BCG-vaccinated and M. bovis-infected cattle by using recombinant mycobacterial antigens. Clin. Diagn. Lab. Immunol. 6:1-5.
15. Buddle, B. M., B. J. Wards, F. E. Aldwell, D. M. Collins, and G. W. de Lisle. 2002. Influence of sensitisation to environmental mycobacteria on subsequent vaccination against bovine tuberculosis. Vaccine 20:1126-1133.
16. Buddle, B. M., D. N. Wedlock, M. Denis, and M. A. Skinner. 2005. Identification of immune response correlates for protection against bovine tuberculosis. Vet. Immunol. Immunopathol. 108:45-51.
17. Buddle, B. M., D. N. Wedlock, N. A. Parlane, L. A. Corner, G. W. de Lisle, and M. A. Skinner. 2003. Revaccination of neonatal calves with Mycobacterium bovis BCG reduces the level of protection against bovine tuberculosis induced by a single vaccination. Infect. Immun. 71:6411-6419.
18. Buza, J. J., H. Hikono, Y. Mori, R. Nagata, S. Hirayama, Aodon-geril, et al. 2004. Neutralization of interleukin-10 significantly enhances gamma interferon expression in peripheral blood by stimulation with Johnin purified protein derivative and by infection with Mycobacterium avium subsp. paratuberculosis in experimentally infected cattle with paratuberculosis. Infect. Immun. 72:2425-2428.
19. Chacon, O., L. E. Bermudez, and R. G. Barletta. 2004. Johne's disease, inflammatory bowel disease, and Mycobacterium paratuberculosis. Annu. Rev. Microbiol. 58:329-363.
20. Chakravarty, S. D., G. Zhu, M. C. Tsai, V. P. Mohan, S. Marino, D. E. Kirschner, et al. 2008. Tumor necrosis factor blockade in chronic murine tuberculosis enhances granulomatous inflammation and disorganizes granulomas in the lungs. Infect. Immun. 76:916-926.
21. Chan, J., X. D. Fan, S. W. Hunter, P. J. Brennan, and B. R. Bloom. 1991. Lipoarabinomannan, a possible virulence factor involved in persistence of Mycobacterium tuberculosis within macrophages. Infect. Immun. 59:1755-1761.
22. Chitale, S., S. Ehrt, I. Kawamura, T. Fujimura, N. Shimono, N. Anand, et al. 2001. Recombinant Mycobacterium tuberculosis protein associated with mammalian cell entry. Cell Microbiol. 3:247-254.
23. Cole, S. T., R. Brosch, J. Parkhill, T. Garnier, C. Churcher, D. Harris, et al. 1998. Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence. Nature 393:537-544.
24. Converse, P. J., P. C. Karakousis, L. G. Klinkenberg, A. K. Kesavan, L. H. Ly, S. S. Allen, et al. 2009. Role of the dosR-dosS two-component regulatory system in Mycobacterium tuberculosis virulence in three animal models. Infect. Immun. 77:1230-1237.
25. Danelishvili, L., M. Wu, B. Stang, M. Harriff, S. L. Cirillo, J. D. Cirillo, et al. 2007. Identification of Mycobacterium avium pathogenicity island important for macrophage and amoeba infection. Proc. Natl. Acad. Sci. USA 104:11038-11043.
26. Denis, M., D. N. Wedlock, A. R. McCarthy, N. A. Parlane, P. J. Cockle, H. M. Vordermeier, et al. 2007. Enhancement of the sensitivity of the whole-blood gamma interferon assay for diagnosis of Mycobacterium bovis infections in cattle. Clin. Vaccine Immunol. 14:1483-1489.
27. Deretic, V. 2008. Autophagy, an immunologic magic bullet: Mycobacterium tuberculosis phagosome maturation block and how to bypass it. Future Microbiol. 3:517-524.
28. Deretic, V., S. Singh, S. Master, J. Harris, E. Roberts, G. Kyei, et al. 2006. Mycobacterium tuberculosis inhibition of phagolysosome biogenesis and autophagy as a host defence mechanism. Cell Microbiol. 8:719-727.
29. Deretic, V., I. Vergne, J. Chua, S. Master, S. B. Singh, J. A. Fazio, et al. 2004. Endosomal membrane traffic: convergence point targeted by Mycobacterium tuberculosis and HIV. Cell Microbiol. 6:999-1009.
30. Devulder, G., M. Perouse de Montclos, and J. P. Flandrois. 2005. A multigene approach to phylogenetic analysis using the genus Mycobacterium as a model. Int. J. Syst. Evol. Microbiol. 55:293-302.
31. Dieli, F., M. Troye-Blomberg, J. Ivanyi, J. J. Fournie, A. M. Krensky, M. Bonneville, et al. 2001. Granulysin-dependent killing of intracellular and extracellular Mycobacterium tuberculosis by Vgamma9/Vdelta2 T lymphocytes. J. Infect. Dis. 184:1082-1085.
32. Edwards, K. M., M. H. Cynamon, R. K. Voladri, C. C. Hager, M. S. DeStefano, K. T. Tham, et al. 2001. Iron-cofactored superoxide dismutase inhibits host responses to Mycobacterium tuberculosis. Am. J. Respir. Crit. Care Med. 164:2213-2219.
33. Ehrt, S., and D. Schnappinger. 2007. Mycobacterium tuberculosis virulence: lipids inside and out. Nat. Med. 13:284-285.
34. Esin, S., G. Batoni, M. Pardini, F. Favilli, D. Bottai, G. Maisetta, et al. 2004. Functional characterization of human natural killer cells responding to Mycobacterium bovis bacille Calmette-Guerin. Immunology 112:143-152.
35. Ferrari, G., H. Langen, M. Naito, and J. Pieters. 1999. A coat protein on phagosomes involved in the intracellular survival of mycobacteria. Cell 97:435-447.
36. Fisher, M. A., B. B. Plikaytis, and T. M. Shinnick. 2002. Microarray analysis of the Mycobacterium tuberculosis transcriptional response to the acidic conditions found in phagosomes. J. Bacteriol. 184:4025-4032.
37. Foley-Thomas, E. M., D. L. Whipple, L. E. Bermudez, and R. G. Barletta. 1995. Phage infection, transfection and transformation of Mycobacterium avium complex and Mycobacterium paratuberculosis. Microbiology 141:1173-1181.
38. Garnier, T., K. Eiglmeier, J. C. Camus, N. Medina, H. Mansoor, M. Pryor, et al. 2003. The complete genome sequence of Mycobacterium bovis. Proc. Natl. Acad. Sci. USA 100:7877-7882.
39. George, K. M., D. Chatterjee, G. Gunawardana, D. Welty, J. Hayman, R. Lee, et al. 1999. Mycolactone: a polyketide toxin from Mycobacterium ulcerans required for virulence. Science 283:854-857.
40. Gioffre, A., E. Infante, D. Aguilar, M. P. Santangelo, L. Klepp, A. Amadio, et al. 2005. Mutation in mce operons attenuates Mycobacterium tuberculosis virulence. Microbes. Infect. 7:325-334.
41. Glickman, M. S., J. S. Cox, and W. R. Jr. Jacobs. 2000. A novel mycolic acid cyclopropane synthetase is required for cording, persistence, and virulence of Mycobacterium tuberculosis. Mol. Cell 5:717-727.
42. Goren, M. B., O. Brokl, and P. Roller. 1979. Cord factor (trehalose-6-6'-dimycolate) of in vivo-derived Mycobacterium lepraemurium. Biochim. Biophys. Acta 574:70-78.
43. Guyot-Revol, V., J. A. Innes, S. Hackforth, T. Hinks, and A. Lalvani. 2006. Regulatory T cells are expanded in blood and disease sites in patients with tuberculosis. Am. J. Respir. Crit Care Med. 173:803-810.
44. Harris, N. B. 2006. Molecular techniques: applications in epidemiologic Studies. In Mycobacterium bovis Infection in animals and Humans. C. O. Thoen, J. H. Steele, and M. J. Gilsdorf (eds.). Ames: Blackwell Publishing, pp. 54-62.
45. Harris, N. B., and R. G. Barletta. 2001. Mycobacterium avium subsp. paratuberculosis in Veterinary Medicine. Clin. Microbiol. Rev. 14:489-512.
46. Harris, N. B., Z. Feng, X. Liu, S. L. Cirillo, J. D. Cirillo, and R. G. Barletta. 1999. Development of a transposon mutagenesis system for Mycobacterium avium subsp. paratuberculosis. FEMS Microbiol. Lett. 175:21-26.
47. Harth, G., and M. A. Horwitz. 1999. Export of recombinant Mycobacterium tuberculosis superoxide dismutase is dependent upon both information in the protein and mycobacterial export machinery. A model for studying export of leaderless proteins by pathogenic mycobacteria. J. Biol. Chem. 274:4281-4292.
48. He, H., R. Hovey, J. Kane, V. Singh, and T. C. Zahrt. 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.
49. Hein, W. R., and L. Dudler. 1997. TCR gamma delta+ cells are prominent in normal bovine skin and express a diverse repertoire of antigen receptors. Immunology 91:58-64.
50. Hewinson, R. G., H. M. Vordermeier, N. H. Smith, and S. V. Gordon. 2006. Recent advances in our knowledge of Mycobacterium bovis: a feeling for the organism. Vet. Microbiol. 112:127-139.
51. Hoek, A., V. P. Rutten, J. Kool, G. J. Arkesteijn, R. J. Bouwstra, I. Rhijn Van, et al. 2008. Subpopulations of bovine WC1+ gammadelta T cells rather than CD4+CD25highFoxp3+ T cells act as immune regulatory cells ex vivo. Vet. Res. 40:6.
52. Holt, J. G, N. R. Krieg, P. H. A Sneath, J. T Staley, and S. T Williams. 1994. Bergey's manual of determinative bacteriology. Baltimore: Williams & Wilkins.
53. Hope, J. C., P. Sopp, and C. J. Howard. 2002. NK-like CD8(+) cells in immunologically naive neonatal calves that respond to dendritic cells infected with Mycobacterium bovis BCG. J. Leukoc. Biol. 71:184-194.
54. Hope, J. C., M. L. Thom, P. A. McCormick, and C. J. Howard. 2004. Interaction of antigen presenting cells with mycobacteria. Vet. Immunol. Immunopathol. 100:187-195.
55. Jain, M., C. J. Petzold, M. W. Schelle, M. D. Leavell, J. D. Mougous, C. R. Bertozzi, et al. 2007. Lipidomics reveals control of Mycobacterium tuberculosis virulence lipids via metabolic coupling. Proc. Natl. Acad. Sci. U S A 104:5133-5138.
56. Jungi, T. W., M. Brcic, H. Sager, D. A. Dobbelaere, A. Furger, and I. Roditi. 1997. Antagonistic effects of IL-4 and interferon-gamma (IFN-gamma) on inducible nitric oxide synthase expression in bovine macrophages exposed to gram-positive bacteria. Clin. Exp. Immunol. 109:431-438.
57. Katz, P., H. Jr. Yeager, G. Whalen, M. Evans, R. P. Swartz, and J. Roecklein. 1990. Natural killer cell-mediated lysis of Mycobacterium-avium complex-infected monocytes. J. Clin. Immunol. 10:71-77.
58. Kaushal, D., B. G. Schroeder, S. Tyagi, T. Yoshimatsu, C. Scott, C. Ko, et al. 2002. Reduced immunopathology and mortality despite tissue persistence in a Mycobacterium tuberculosis mutant lacking alternative sigma factor, SigH. Proc. Natl. Acad. Sci. USA 99:8330-8335.
59. Keane, J., S. Gershon, R. P. Wise, E. Mirabile-Levens, J. Kasznica, W. D. Schwieterman, et al. 2001. Tuberculosis associated with infliximab, a tumor necrosis factor alpha-neutralizing agent. N. Engl. J. Med. 345:1098-1104.
60. Kennedy, H. E., M. D. Welsh, D. G. Bryson, J. P. Cassidy, F. I. Forster, C. J. Howard, et al. 2002. Modulation of immune responses to Mycobacterium bovis in cattle depleted of WC1(+) gamma delta T cells. Infect. Immun. 70:1488-1500.
61. Khader, S. A., G. K. Bell, J. E. Pearl, J. J. Fountain, J. Rangel-Moreno, G. E. Cilley, et al. 2007. IL-23 and IL-17 in the establishment of protective pulmonary CD4+ T cell responses after vaccination and during Mycobacterium tuberculosis challenge. Nat. Immunol. 8:369-377.
62. Koets, A., V. Rutten, A. Hoek, F. van Mil, K. Muller, D. Bakker, et al. 2002. Progressive bovine paratuberculosis is associated with local loss of CD4(+) T cells, increased frequency of gamma delta T cells, and related changes in T-cell function. Infect. Immun. 70:3856-3864.
63. Korbel, D. S., B. E. Schneider, and U. E. Schaible. 2008. Innate immunity in tuberculosis: myths and truth. Microbes Infect. 10:995-1004.
64. Kumar, A., M. Bose, and V. Brahmachari. 2003. Analysis of expression profile of mammalian cell entry (mce) operons of Mycobacterium tuberculosis. Infect. Immun. 71:6083-6087.
65. Ladel, C. H., J. Hess, S. Daugelat, P. Mombaerts, S. Tonegawa, and S. H. Kaufmann. 1995. Contribution of alpha/beta and gamma/delta T lymphocytes to immunity against Mycobacterium bovis bacillus Calmette Guerin: studies with T cell receptor-deficient mutant mice. Eur. J. Immunol. 25:838-846.
66. Leung, A. S., V. Tran, Z. Wu, X. Yu, D. C. Alexander, G. F. Gao, et al. 2008. Novel genome polymorphisms in BCG vaccine strains and impact on efficacy. BMC Genomics 9:413.
67. Leveton, C., S. Barnass, B. Champion, S. Lucas, Souza B. De, M. Nicol, et al. 1989. T-cell-mediated protection of mice against virulent Mycobacterium tuberculosis. Infect. Immun. 57:390-395.
68. Li, L., J. P. Bannantine, Q. Zhang, A. Amonsin, B. J. May, D. Alt, et al. 2005. The complete genome sequence of Mycobacterium avium subspecies paratuberculosis. Proc. Natl. Acad. Sci. U S A 102:12344-12349.
69. Liebana, E., R. M. Girvin, M. Welsh, S. D. Neill, and J. M. Pollock. 1999. Generation of CD8(+) T-cell responses to Mycobacterium bovis and mycobacterial antigen in experimental bovine tuberculosis. Infect. Immun. 67:1034-1044.
70. Liebana, E., S. Marsh, J. Gough, A. Nunez, H. M. Vordermeier, A. Whelan, et al. 2007. Distribution and activation of T-lymphocyte subsets in tuberculous bovine lymph-node granulomas. Vet. Pathol. 44:366-372.
71. Liu, X., Z. Feng, N. B. Harris, J. D. Cirillo, H. Bercovier, and R. G. Barletta. 2001. Identification of a secreted superoxide dismutase in Mycobacterium avium ssp. paratuberculosis. FEMS Microbiol. Lett. 202:233-238.
72. Lockhart, E., A. M. Green, and J. L. Flynn. 2006. IL-17 production is dominated by gamma delta T cells rather than CD4 T cells during Mycobacterium tuberculosis infection. J. Immunol. 177:4662-4669.
73. Lybeck, K. R., A. K. Storset, and I. Olsen. 2009. Neutralisation of interleukin-10 from CD14+ monocytes enhances gamma interferon production in peripheral blood mononuclear cells from Mycobacterium avium subsp. paratuberculosis infected goats. Clin. Vaccine Immunol. Epub.
74. MacHugh, N. D., J. K. Mburu, M. J. Carol, C. R. Wyatt, J. A. Orden, and W. C. Davis. 1997. Identification of two distinct subsets of bovine gamma delta T cells with unique cell surface phenotype and tissue distribution. Immunology 92:340-345.
75. Manganelli, R., R. Provvedi, S. Rodrigue, J. Beaucher, L. Gaudreau, and I. Smith. 2004. Sigma factors and global gene regulation in Mycobacterium tuberculosis. J. Bacteriol. 186:895-902.
76. Marsollier, L., R. Robert, J. Aubry, J. P. Saint Andre, H. Kouakou, P. Legras, et al. 2002. Aquatic insects as a vector for Mycobacterium ulcerans. Appl. Environ. Microbiol. 68:4623-4628.
77. Martin, C., A. Williams, R. Hernandez-Pando, P. J. Cardona, E. Gormley, Y. Bordat, et al. 2006. The live Mycobacterium tuberculosis phoP mutant strain is more attenuated than BCG and confers protective immunity against tuberculosis in mice and guinea pigs. Vaccine 24:3408-3419.
78. McNeil, M. R., and P. J. Brennan. 1991. Structure, function and biogenesis of the cell envelope of mycobacteria in relation to bacterial physiology, pathogenesis and drug resistance; some thoughts and possibilities arising from recent structural information. Res. Microbiol. 142:451-463.
79. Meima, A., J. H. Richardus, and J. D. Habbema. 2004. Trends in leprosy case detection worldwide since 1985. Lepr. Rev. 75:19-33.
80. Momotani, E., D. L. Whipple, A. B. Thiermann, and N. F. Cheville. 1988. Role of M cells and macrophages in the entrance of Mycobacterium paratuberculosis into domes of ileal Peyer's patches in calves. Vet. Pathol. 25:131-137.
81. Mueller, U. G., D. Dash, C. Rabeling, and A. Rodrigues. 2008. Coevolution between attine ants and actinomycete bacteria: a reevaluation. Evolution 62:2894-2912.
82. Olsen, I., P. Boysen, S. Kulberg, J. C. Hope, G. Jungersen, and A. K. Storset. 2005. Bovine NK cells can produce gamma interferon in response to the secreted mycobacterial proteins ESAT-6 and MPP14 but not in response to MPB70. Infect. Immun. 73:5628-5635.
83. Olsen, I., L. J. Reitan, G. Holstad, and H. G. Wiker. 2000. Alkyl hydroperoxide reductases C and D are major antigens constitutively expressed by Mycobacterium avium subsp. paratuberculosis. Infect. Immun. 68:801-808.
84. Park, K. T., J. L. Dahl, J. P. Bannantine, R. G. Barletta, J. Ahn, A. J. Allen, et al. 2008. Demonstration of allelic exchange in the slow-growing bacterium Mycobacterium avium subsp. paratuberculosis, and generation of mutants with deletions at the pknG, relA, and lsr2 loci. Appl. Environ. Microbiol. 74:1687-1695.
85. Piddington, D. L., F. C. Fang, T. Laessig, A. M. Cooper, I. M. Orme, and N. A. Buchmeier. 2001. Cu,Zn superoxide dismutase of Mycobacterium tuberculosis contributes to survival in activated macrophages that are generating an oxidative burst. Infect. Immun. 69:4980-4987.
86. Price, S. J., P. Sopp, C. J. Howard, and J. C. Hope. 2007. Workshop cluster 1+ gamma delta T-cell receptor T cells from calves express high levels of interferon-gamma in response to stimulation with interleukin-12 and-18. Immunology 120:57-65.
87. Quinn, K. M., R. S. McHugh, F. J. Rich, L. M. Goldsack, G. W. de Lisle, B. M. Buddle, et al. 2006. Inactivation of CD4+ CD25+ regulatory T cells during early mycobacterial infection increases cytokine production but does not affect pathogen load. Immunol. Cell Biol. 84:467-474.
88. Rhodes, S. G., J. Sawyer, A. O. Whelan, G. S. Dean, M. Coad, K. J. Ewer, et al. 2007. Is interleukin-4delta3 splice variant expression in bovine tuberculosis a marker of protective immunity? Infect. Immun. 75:3006-3013.
89. Riollet, C., D. Mutuel, M. Duonor-Cerutti, and P. Rainard. 2006. Determination and characterization of bovine interleukin-17 cDNA. J. Interferon Cytokine Res. 26:141-149.
90. Rivera-Marrero, C. A., J. D. Ritzenthaler, S. A. Newburn, J. Roman, and R. D. Cummings. 2002. Molecular cloning and expression of a novel glycolipid sulfotransferase in Mycobacterium tuberculosis. Microbiology 148:783-792.
91. Russell, D. G., H. C. Mwandumba, and E. E. Rhoades. 2002. Mycobacterium and the coat of many lipids. J. Cell Biol. 158:421-426.
92. Sassetti, C. M., D. H. Boyd, and E. J. Rubin. 2003. Genes required for mycobacterial growth defined by high density mutagenesis. Mol. Microbiol. 48:77-84.
93. Sassetti, C. M., and E. J. Rubin. 2003. Genetic requirements for mycobacterial survival during infection. Proc. Natl. Acad. Sci. U S A 100:12989-12994.
94. Schlesinger, L. S. 1993. Macrophage phagocytosis of virulent but not attenuated strains of Mycobacterium tuberculosis is mediated by mannose receptors in addition to complement receptors. J. Immunol. 150:2920-2930.
95. Schlesinger, L. S., C. G. Bellinger-Kawahara, N. R. Payne, and M. A. Horwitz. 1990. Phagocytosis of Mycobacterium tuberculosis is mediated by human monocyte complement receptors and complement component C3. J. Immunol. 144:2771-2780.
96. Scriba, T. J., B. Kalsdorf, D. A. Abrahams, F. Isaacs, J. Hofmeister, G. Black, et al. 2008. Distinct, specific IL-17-and IL-22-producing CD4+ T cell subsets contribute to the human anti-mycobacterial immune response. J. Immunol. 180:1962-1970.
97. Seah, G. T., and G. A. Rook. 2001. Il-4 influences apoptosis of mycobacterium-reactive lymphocytes in the presence of TNF-alpha. J. Immunol. 167:1230-1237.
98. Sechi, L. A., G. E. Felis, N. Ahmed, D. Paccagnini, D. Usai, S. Ortu, et al. 2007. Genome and transcriptome scale portrait of sigma factors in Mycobacterium avium subsp. paratuberculosis. Infect. Genet. Evol. 7:424-432.
99. Secott, T. E., T. L. Lin, and C. C. Wu. 2001. Fibronectin attachment protein homologue mediates fibronectin binding by Mycobacterium avium subsp. paratuberculosis. Infect. Immun. 69:2075-2082.
100. Secott, T. E., T. L. Lin, and C. C. Wu. 2002. Fibronectin attachment protein is necessary for efficient attachment and invasion of epithelial cells by Mycobacterium avium subsp. paratuberculosis. Infect. Immun. 70:2670-2675.
101. Sherman, D. R., K. Mdluli, M. J. Hickey, C. E. III Barry, and C. K. Stover. 1999. AhpC, oxidative stress and drug resistance in Mycobacterium tuberculosis. Biofactors 10:211-217.
102. Shin, S. J., C. W. Wu, H. Steinberg, and A. M. Talaat. 2006. Identification of novel virulence determinants in Mycobacterium paratuberculosis by screening a library of insertional mutants. Infect. Immun. 74:3825-3833.
103. Skinner, M. A., B. M. Buddle, D. N. Wedlock, D. Keen, G. W. de Lisle, R. E. Tascon, et al. 2003a. A DNA pńme-Mycobacterium bovis BCG boost vaccination strategy for cattle induces protection against bovine tuberculosis. Infect. Immun. 71:4901-4907.
104. Skinner, M. A., N. Parlane, A. McCarthy, and B. M. Buddle. 2003b. Cytotoxic T-cell responses to Mycobacterium bovis during experimental infection of cattle with bovine tuberculosis. Immunology 110:234-241.
105. Smyth, A. J., M. D. Welsh, R. M. Girvin, and J. M. Pollock. 2001. In vitro responsiveness of γδ T cells from Mycobacterium bovis-infected cattle to mycobacterial antigens: predominant involvement of WC1(+) cells. Infect. Immun. 69:89-96.
106. Soto, C. Y., M. C. Menendez, E. Perez, S. Samper, A. B. Gomez, M. J. Garcia, et al. 2004. IS6110 mediates increased transcription of the phoP virulence gene in a multidrug-resistant clinical isolate responsible for tuberculosis outbreaks. J. Clin. Microbiol. 42:212-219.
107. Stewart, G. R., L. Wernisch, R. Stabler, J. A. Mangan, J. Hinds, K. G. Laing, et al. 2002. Dissection of the heat-shock response in Mycobacterium tuberculosis using mutants and microarrays. Microbiology 148:3129-3138.
108. Sturgill-Koszycki, S., U. E. Schaible, and D. G. Russell. 1996. Mycobacterium-containing phagosomes are accessible to early endosomes and reflect a transitional state in normal phagosome biogenesis. EMBO J. 15:6960-6968.
109. Tailleux, L., S. J. Waddell, M. Pelizzola, A. Mortellaro, M. Withers, A. Tanne, et al. 2008. Probing host pathogen cross-talk by transcriptional profiling of both Mycobacterium tuberculosis and infected human dendritic cells and macrophages. PLoS ONE 3:e1403.
110. Talaat, A. M., P. Hunter, and S. A. Johnston. 2000. Genome-directed primers for selective labeling of bacterial transcripts for DNA microarray analysis. Nat. Biotechnol. 18:679-682.
111. Teitelbaum, R., A. Glatman-Freedman, B. Chen, J. B. Robbins, E. Unanue, A. Casadevall, et al. 1998. A mAb recognizing a surface antigen of Mycobacterium tuberculosis enhances host survival. Proc. Natl. Acad. Sci. U S A 95:15688-15693.
112. Thoen, C. O. 2010. Tuberculosis and other mycobacterial infections. In The Merck veterinary manual. C. Kahn, and S. Line (eds.). Whitehouse Station: Merck & Co Inc. In press.
113. Thoen, C. O., and R. G. Barletta. 2004. Mycobacterium. In Pathogenesis of mycobacterial infections in animals. C. Gyles, J. F. Prescott, J. G. Songer, and C. O. Thoen (eds.). Ames: Blackwell Publishing, pp. 69-76.
114. Thoen, C. O., Karlson, A. G., and Himes, E. M. 1981. Mycobacterial infections in animals. Rev. Infect Dis. 3:960-72.
115. Thoen, C. O., and P. A. LoBue. 2007. Mycobacterium bovis tuberculosis: forgotten, but not gone. Lancet 369:1236-1238.
116. Thoen, C. O., P. A. Lobue, D. A. Enarson, J. B. Kaneene, and I. N. de Kantor. 2009. Tuberculosis: a re-emerging disease in animals and humans. Vet. Ital. 45:135-181.
117. Thoen, C., LoBue, P., and de Kantor, I. 2006. The importance of Mycobacterium bovis as a zoonosis. Vet. Microbiol. 112:339-45.
118. Valheim, M., O. G. Sigurdardottir, A. K. Storset, L. G. Aune, and C. M. Press. 2004. Characterization of macrophages and occurrence of T cells in intestinal lesions of subclinical paratuberculosis in goats. J. Comp. Pathol. 131:221-232.
119. Vankayalapati, R., P. Klucar, B. Wizel, S. E. Weis, B. Samten, H. Safi, et al. 2004. NK cells regulate CD8+ T cell effector function in response to an intracellular pathogen. J. Immunol. 172:130-137.
120. Vesosky, B., O. C. Turner, J. Turner, and I. M. Orme. 2004. Gamma interferon production by bovine gamma delta T cells following stimulation with mycobacterial mycolylarabinogalactan peptidoglycan. Infect. Immun. 72:4612-4618.
121. Villarreal-Ramos, B., M. McAulay, V. Chance, M. Martin, J. Morgan, and C. J. Howard. 2003. Investigation of the role of CD8+ T cells in bovine tuberculosis in vivo. Infect. Immun. 71:4297-4303.
122. Wedlock, D. N., M. Denis, G. F. Painter, G. D. Ainge, H. M. Vordermeier, R. G. Hewinson, et al. 2008. Enhanced protection against bovine tuberculosis after coadministration of Mycobacterium bovis BCG with a mycobacterial protein vaccine-adjuvant combination but not after coadministration of adjuvant alone. Clin. Vaccine Immunol. 15:765-772.
123. Wu, C. W., J. Glasner, M. Collins, S. Naser, and A. M. Talaat. 2006. Whole-genome plasticity among Mycobacterium avium subspecies: insights from comparative genomic hybridizations. J. Bacteriol. 188:711-723.
124. Wu, C. W., S. K. Schmoller, S. J. Shin, and A. M. Talaat. 2007. Defining the stressome of Mycobacterium avium subsp. paratuberculosis in vitro and in naturally infected cows. J. Bacteriol. 189:7877-7886.
125. Wu, C. W., T. M. Schramm, S. Zhou, D. C. Schwartz, and A. M. Talaat. 2009. Optical mapping of the Mycobacterium avium subspecies paratuberculosis genome. BMC Genomics 10:25.