Rv3134c/devR/devS operon of Mycobacterium bovis BCG is differentially transcribed under "in vitro" stress conditions

Tuberculosis

Volumn 88, Issue 4, 2008, Pages 273-282

  Rodriguez, Juan Germán ^a   Burbano, Claudia Sofía ^a   Nuñez, Carmen ^b   González, Clara Eugenia ^a   Zambrano, María Mercedes ^a   García, María Jesús ^b   Del Portillo, Patricia ^a  

^a Genomics and Evolution of Communities of Environmental Microorganisms   (Colombia)

^b UNIVERSIDAD AUTÓNOMA DE MADRID   (Spain)

Author keywords

DevR DevS two component system; Dormancy; M. tuberculosis; Mycobacterium bovis

Indexed keywords

AEROBIC METABOLISM; ARTICLE; BACTERIAL GENE; DEVR GENE; DEVS GENE; DORMANCY; GENE EXPRESSION; GENETIC TRANSCRIPTION; HYPOXIA; IN VITRO STUDY; MYCOBACTERIUM BOVIS; NONHUMAN; OPERON; PRIORITY JOURNAL; PROMOTER REGION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; STARVATION; STRESS;

ANIMALS; BACTERIAL PROTEINS; GENE EXPRESSION REGULATION, BACTERIAL; MACROPHAGES; MICE; MYCOBACTERIUM BOVIS; NITRIC OXIDE; OPERON; OXYGEN; POLYMERASE CHAIN REACTION; PROMOTER REGIONS, GENETIC; PROTAMINE KINASE; STRESS, PHYSIOLOGICAL; TRANSCRIPTION, GENETIC;

EID: 45649084477     PISSN: 14729792     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tube.2007.11.011     Document Type: Article

References (38)

1. Dye C., Watt C.J., Bleed D.M., Hosseini S.M., and Raviglione M.C. Evolution of tuberculosis control and prospects for reducing tuberculosis incidence, prevalence, and deaths globally. JA M A 293 (2005) 2767-2775
2. Nuermberger E., Bishai W.R., and Grosset J.H. Latent tuberculosis infection. Semin Respir Crit Care Med 25 (2004) 317-336
3. Neyrolles O., Hernández-Pando R., Pietri-Rouxel F., Forné P., Tailleux L., Barrios J.A., et al. Is adipose tissue a place for Mycobacterium tuberculosis persistence?. PLoS ONE 1 (2006) e43
4. Frothingham R., Stout J.E., and Hamilton C.D. Current issues in global tuberculosis control. Int J Infect Dis 9 (2005) 297-311
5. Gutierrez M.C., Brisse S., Brosch R., Fabre M., Omaïs B., and Marmiesse M. Ancient origin and Gene Mosaicism of the progenitor of Mycobacterium tuberculosis. PLoS Pathogens 1 1 (2005) e5
6. Ulrichs T., Kosmiadi G.A., PradI S.J.L., Tltukhina M., Mishenko V., and Gushina N. Differential organization of the local immune response in patients with active cavitary tuberculosis or with nonprogressive tuberculoma. J Infect Dis 192 (2005) 89-97
7. Manganelli R., Provvedi R., Rodrigue S., Beaucher J., Gaudreau L., and Smith I. Sigma factors and global gene regulation in Mycobacterium tuberculosis. J Bacteriol 186 (2004) 895-902
8. Stock A.M., Robinson V.L., and Goudreau P.N. Two-component signal transduction. Annu Rev Biochem 69 (2000) 183-215
9. Stock J.B., Surette M.G., Levit M., and Park P. Two-component signal transduction systems: structure-function relationships and mechanisms of catalysis. In: Hoch J.A., and Silhavy T.J. (Eds). Two-component signal transduction (1995), American Society for Microbiology, Washington, DC 25-51
10. Shrivastava R., Das D.R., Wiker H.G., and Das A.K. Modelling and docking of the proteins of a unique two-component system from Mycobacterium tuberculosis and the mechanism of phosphotransfer. Biochem Biophys Res Commun 344 (2006) 1327-1333
11. Cole S.T., Brosch R., Parkhill J., et al. Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence. Nature 393 (1998) 537-544
12. Erratum in: Nature 1998;396(6707):190.
13. Morth J.P., Gosmann S., Nowak E., and Tucker P.A. A novel two-component system found in Mycobacterium tuberculosis. FEBS Lett 579 (2005) 4145-4148
14. Saini D.K., Malhotra V., Dey D., Pant N., Das T.K., and Tyagi J.S. DevR-DevS is a bona fide two-component system of Mycobacterium tuberculosis that is hypoxia-responsive in the absence of the DNA-binding domain of DevR. Microbiology 150 (2004) 865-875
15. Dasgupta N., Kapur V., Singh K.K., Das T.K., Sachdeva S., and Jyothisri K. Characterization of a two component system, devR-devS, of Mycobacterium tuberculosis. Tuberc Lung Dis 80 (2000) 141-159
16. Sherman D.R., Voskuil M., Schnappinger D., Liao R., Harrell M.I., and Schoolnik G.K. Regulation of the Mycobacterium tuberculosis hypoxic response gene encoding alpha -crystalline. Proc Natl Acad Sci USA 98 (2001) 7534-7539
17. Boon C., Li R., Qi R., and Dick T. Proteins of Mycobacterium bovis BCG induced in Wayne dormancy model. J Bacteriol 183 (2001) 2672-2676
18. Park H.D., Guinn K.M., Harrell M.I., Liao R., Voskuil M.I., and Tompa M. Rv3133c/devR is a transcription factor that mediates the hypoxic response of Mycobacterium tuberculosis. Mol Microbiol 48 (2003) 833-843
19. Voskuil M.I., Schnappinger D., Visconti K.C., Harrell M.I., Dolganov G.M., and Sherman D.R. Inhibition of respiration by nitric oxide induces a Mycobacterium tuberculosis dormancy program. J Exp Med 198 (2003) 705-713
20. Bagchi G., Chauhan S., Sharma D., and Tyagi J.S. Transcription and autoregulation of the Rv3134cdevR-devS operon of Mycobacterium tuberculosis. Microbiology 151 (2005) 4045-4053
21. Boon C., and Dick T. Mycobacterium bovis response regulator essential for hypoxic dormancy. J Bacteriol 184 (2002) 6760-6767
22. Betts J.C., Lukey P.T., Robb L.C., McAdam R.A., and Duncan K. Evaluation of a nutrient starvation model of Mycobacterium tuberculosis persistence by gene and protein expression profiling. Mol Microbiol 43 (2002) 717-731
23. Menéndez M.C., Rebollo M.J., Nuñez M.C., Cox R.A., and García M.J. Analysis of the precursor rRNA fractions of rapidly growing mycobacteria: quantification by methods that include the use of a promoter (rrn A P1) as a novel standard. J Bacteriol 187 (2005) 534-543
24. Camacho L.R., Constant P., Raynaud C., Laneelle M.A., Triccas J.A., and Gicquel B. Analysis of the phthiocerol dimycocerosate locus of Mycobacterium tuberculosis. J Biol Chem 276 (2001) 19845-19854
25. Rodrigue S., Pravvedi R., Jacques P.E., Gaudreau L., and Manganelli R.T. The sigma factors of Mycobacterium tuberculosis. FEMS Microbiol Rev 30 (2006) 926-941
26. Voskuil M.I., Visconti K.C., and Schoolnik G.K. Mycobacterium tuberculosis gene expression during adaptation to stationary phase and low-oxygen dormancy. Tuberculosis 84 (2004) 218-227
27. Muttucumarua D.G.N., Robertsa G., Hindsb J., Stablerb R.A., and Parish T. Gene expression profile of Mycobacterium tuberculosis in a non-replicating state. Tuberculosis 84 (2004) 239-246
28. Ioanoviciu A., Yukl E.T., Moenne-Loccoz P., and de Montellano P.R. DevS, a heme-containing two-component oxygen sensor of Mycobacterium tuberculosis. Biochemistry 46 (2007) 4250-4260
29. Kendall S.l., Movahedzadeh F., Rison S.C., Wernisch L., Parish T., and Duncan K. The Mycobacterium tuberculosis dosRS two-component system is induced by multiple stresses. Tuberculosis 84 (2004) 247-255
30. Hampshire T., Soneji S., Bacon J., James B.W., Hinds J., and Laing K. Stationary phase gene expression of Mycobacterium tuberculosis following a progressive nutrient depletion: a model for persistent organisms?. Tuberculosis 84 (2004) 228-238
31. Sousa M.C., and McKay D.B. Structure of the universal stress protein of Haemophilus influenzae. Structure 9 (2001) 1135-1141
32. Soncini F.C., Vescovi E.G., and Groisman E.A. Transcriptional autoregulation of the Salmonella typhimurium phoPQ operon. J Bacteriol 177 (1999) 4364-4371
33. Scarlato V., Prugnola A., Arico B., and Rappuoli R. Positive transcriptional feedback at the bvg locus controls expression of virulence factors in Bordetella pertussis. Proc Natl Acad Sci USA 87 (1990) 6753-6757
34. Paul S., Birkey S., Liu W., and Hulett F.M. Autoinduction of Bacillus subtilis phoPR operon transcription results from enhanced transcription from EsA- and EsE-responsive promoters by phosphorylated PhoP. J Bacteriol 186 (2004) 4262-4275
35. Soto C.Y., Menendez M.C., Perez E., Samper S., Gomez A.B., and Garcia M.J. IS6110 mediates increased transcription of the phoP virulence gene in a multidrug-resistant clinical isolate responsible for tuberculosis outbreaks. J Clin Microbiol 42 (2004) 212-219
36. Smith I., Bishai W.R., and Nagaraja V. Control of mycobacterial transcription. In: Cole S.T., Eisenach K.D., McMurray D.N., and Jacobs W.R. (Eds). Tuberculosis and the tubercle bacillus (2005), ASM Press 219-234
37. Saini D.K., Malhotra V., and Tyagi J.S. Cross talk between DevS sensor kinase homologue, Rv2027c and DevR response regulator of Mycobacterium tuberculosis. FEBS Lett 565 (2004) 75-80
38. Washio T., Sasayama J., and Tomita M. Analysis of complete genomes suggests that many prokaryotes do not rely on hairpin formation in transcription termination. Nucl Acid Res 26 (1998) 5456-5463