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Mycothiol biosynthesis is essential for ethionamide susceptibility in Mycobacterium tuberculosis

Catherine Vilchèze, Yossef Av‐Gay, Rodgoun Attarian and 8 more

Molecular Microbiology · 2008

doi:10.1111/j.1365-2958.2008.06365.x

Abstract

Summary Spontaneous mutants of Mycobacterium tuberculosis that were resistant to the anti‐tuberculosis drugs ethionamide and isoniazid were isolated and found to map to mshA , a gene encoding the first enzyme involved in the biosynthesis of mycothiol, a major low‐molecular‐weight thiol in M. tuberculosis . Seven independent missense or frameshift mutations within mshA were identified and characterized. Precise null deletion mutations of the mshA gene were generated by specialized transduction in three different strains of M. tuberculosis . The mshA deletion mutants were defective in mycothiol biosynthesis, were only ethionamide‐resistant and required catalase to grow. Biochemical studies suggested that the mechanism of ethionamide resistance in mshA mutants was likely due to a defect in ethionamide activation. In vivo , a mycothiol‐deficient strain grew normally in immunodeficient mice, but was slightly defective for growth in immunocompetent mice. Mutations in mshA demonstrate the non‐essentiality of mycothiol for growth in vitro and in vivo , and provide a novel mechanism of ethionamide resistance in M. tuberculosis.

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References 55

  1. 1.

    Banerjee A, Dubnau E, Quemard A, Balasubramanian V, Um KS, Wilson T, et al. inhA, a gene encoding a target for isoniazid and ethionamide in Mycobacterium tuberculosis. Science. 1994;263:227-230.

    Not in our library10.1126/science.8284673

  2. 2.

    Bardarov S, Bardarov S, Pavelka MS, Sambandamurthy V, Larsen M, Tufariello J, et al. Specialized transduction: an efficient method for generating marked and unmarked targeted gene disruptions in Mycobacterium tuberculosis, M. bovis BCG and M. smegmatis. Microbiology. 2002;148:3007-3017.

    Not in our library10.1099/00221287-148-10-3007

  3. 3.

    Baulard AR, Betts JC, Engohang-Ndong J, Quan S, McAdam RA, Brennan PJ, et al. Activation of the pro-drug ethionamide is regulated in mycobacteria. J Biol Chem. 2000;275:28326-28331.

    Not in our library10.1074/jbc.m003744200

  4. 4.

    Buchmeier N, Fahey RC. The mshA gene encoding the glycosyltransferase of mycothiol biosynthesis is essential in Mycobacterium tuberculosis Erdman. FEMS Microbiol Lett. 2006;264:74-79.

    Not in our library10.1111/j.1574-6968.2006.00441.x

  5. 5.

    Buchmeier NA, Newton GL, Koledin T, Fahey RC. Association of mycothiol with protection of Mycobacterium tuberculosis from toxic oxidants and antibiotics. Mol Microbiol. 2003;47:1723-1732.

    Not in our library10.1046/j.1365-2958.2003.03416.x

  6. 6.

    Buchmeier NA, Newton GL, Fahey RC. A mycothiol synthase mutant of Mycobacterium tuberculosis has an altered thiol-disulfide content and limited tolerance to stress. J Bacteriol. 2006;188:6245-6252.

    Not in our library10.1128/jb.00393-06

  7. 7.

    Cardoso RF, Cooksey RC, Morlock GP, Barco P, Cecon L, Forestiero F, et al. Screening and characterization of mutations in isoniazid-resistant Mycobacterium tuberculosis isolates obtained in Brazil. Antimicrob Agents Chemother. 2004;48:3373-3381.

    Not in our library10.1128/aac.48.9.3373-3381.2004

  8. 8.
  9. 9.

    Dessen A, Quemard A, Blanchard JS, Jacobs WR, Sacchettini JC. Crystal structure and function of the isoniazid target of Mycobacterium tuberculosis. Science. 1995;267:1638-1641.

    Not in our library10.1126/science.7886450

  10. 10.

    Dover LG, Alahari A, Gratraud P, Gomes JM, Bhowruth V, Reynolds RC, et al. EthA, a common activator of thiocarbamide-containing drugs acting on different mycobacterial targets. Antimicrob Agents Chemother. 2007;51:1055-1063.

    Not in our library10.1128/aac.01063-06

  11. 11.

    Dubos RJ, Middlebrook G. Media for tubercle bacilli. Am Rev Tuberc. 1947;56:334-345.

    Not in our library

  12. 12.

    Gandhi NR, Moll A, Sturm AW, Pawinski R, Govender T, Lalloo U, et al. Extensively drug-resistant tuberculosis as a cause of death in patients co-infected with tuberculosis and HIV in a rural area of South Africa. Lancet. 2006;368:1575-1580.

    Not in our library10.1016/s0140-6736(06)69573-1

  13. 13.

    Hazbon MH, Brimacombe M, Bobadilla del Valle M, Cavatore M, Guerrero MI, Varma-Basil M, et al. Population genetics study of isoniazid resistance mutations and evolution of multidrug-resistant Mycobacterium tuberculosis. Antimicrob Agents Chemother. 2006;50:2640-2649.

    Not in our library10.1128/aac.00112-06

  14. 14.

    Koledin T, Newton GL, Fahey RC. Identification of the mycothiol synthase gene (mshD) encoding the acetyltransferase producing mycothiol in actinomycetes. Arch Microbiol. 2002;178:331-337.

    Not in our library10.1007/s00203-002-0462-y

  15. 15.

    Larsen MH, Vilcheze C, Kremer L, Besra GS, Parsons L, Salfinger M, et al. Overexpression of inhA, but not kasA, confers resistance to isoniazid and ethionamide in Mycobacterium smegmatis, M. bovis BCG and M. tuberculosis. Mol Microbiol. 2002;46:453-466.

    Not in our library10.1046/j.1365-2958.2002.03162.x

  16. 16.

    Leonardo MR, Dailly Y, Clark DP. Role of NAD in regulating the adhE gene of Escherichia coli. J Bacteriol. 1996;178:6013-6018.

    Not in our library10.1128/jb.178.20.6013-6018.1996

  17. 17.

    Lund O, Nielsen M, Lundegaard C, Worning P. CPHmodels 2.0: X3M a Computer Program to Extract 3D Models. 2002.

    Not in our library

  18. 18.

    Marrakchi H, Laneelle G, Quemard A. InhA, a target of the antituberculous drug isoniazid, is involved in a mycobacterial fatty acid elongation system, FAS-II. Microbiology. 2000;146(Part 2):289-296.

    Not in our library10.1099/00221287-146-2-289

  19. 19.

    Martin A, Morcillo N, Lemus D, Montoro E, Telles MA, Simboli N, et al. Multicenter study of MTT and resazurin assays for testing susceptibility to first-line anti-tuberculosis drugs. Int J Tuberc Lung Dis. 2005;9:901-906.

    Not in our library

  20. 20.

    Middlebrook G. Isoniazid resistance and catalase activity of tubercle bacilli. Am Rev Tuberc. 1954;69:471-472.

    Not in our library10.1164/art.1954.69.3.471

  21. 21.

    Middlebrook G, Cohn ML, Schaefer WB. Studies on isoniazid and tubercle bacilli. III. The isolation, drug-susceptibility, and catalase-testing of tubercle bacilli from isoniazid-treated patients. Am Rev Tuberc. 1954;70:852-872.

    Not in our library10.1164/art.1954.70.5.852

  22. 22.

    Miesel L, Weisbrod TR, Marcinkeviciene JA, Bittman R, Jacobs WR. NADH dehydrogenase defects confer isoniazid resistance and conditional lethality in Mycobacterium smegmatis. J Bacteriol. 1998;180:2459-2467.

    Not in our library10.1128/jb.180.9.2459-2467.1998

  23. 23.

    Morlock GP, Metchock B, Sikes D, Crawford JT, Cooksey RC. ethA, inhA, and katG loci of ethionamide-resistant clinical Mycobacterium tuberculosis isolates. Antimicrob Agents Chemother. 2003;47:3799-3805.

    Not in our library10.1128/aac.47.12.3799-3805.2003

  24. 24.

    Newton GL, Fahey RC. Mycothiol biochemistry. Arch Microbiol. 2002;178:388-394.

    Not in our library10.1007/s00203-002-0469-4

  25. 25.

    Newton GL, Arnold K, Price MS, Sherrill C, Delcardayre SB, Aharonowitz Y, et al. Distribution of thiols in microorganisms: mycothiol is a major thiol in most actinomycetes. J Bacteriol. 1996;178:1990-1995.

    Not in our library10.1128/jb.178.7.1990-1995.1996

  26. 26.

    Newton GL, Unson MD, Anderberg SJ, Aguilera JA, de Oh NNI, Cardayre SB, et al. Characterization of Mycobacterium smegmatis mutants defective in 1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside and mycothiol biosynthesis. Biochem Biophys Res Commun. 1999;255:239-244.

    Not in our library10.1006/bbrc.1999.0156

  27. 27.

    Newton GL, Av-Gay Y, Fahey RC. A novel mycothiol-dependent detoxification pathway in mycobacteria involving mycothiol S-conjugate amidase. Biochemistry. 2000a;39:10739-10746.

    Not in our library10.1021/bi000356n

  28. 28.

    Newton GL, Av-Gay Y, Fahey RC. N-acetyl-1-D-myo-inosityl-2-amino-2-deoxy-alpha-D-glucopyranoside deacetylase (MshB) is a key enzyme in mycothiol biosynthesis. J Bacteriol. 2000b;182:6958-6963.

    Not in our library10.1128/jb.182.24.6958-6963.2000

  29. 29.

    Newton GL, Koledin T, Gorovitz B, Rawat M, Fahey RC, Av-Gay Y. The glycosyltransferase gene encoding the enzyme catalyzing the first step of mycothiol biosynthesis (mshA). J Bacteriol. 2003;185:3476-3479.

    Not in our library10.1128/jb.185.11.3476-3479.2003

  30. 30.

    Newton GL, Ta P, Bzymek KP, Fahey RC. Biochemistry of the initial steps of mycothiol biosynthesis. J Biol Chem. 2006;281:33910-33920.

    Not in our library10.1074/jbc.m604724200

  31. 31.

    Piatek AS, Telenti A, Murray MR, El-Hajj H, Jacobs WR, Kramer FR, Alland D. Genotypic analysis of Mycobacterium tuberculosis in two distinct populations using molecular beacons: implications for rapid susceptibility testing. Antimicrob Agents Chemother. 2000;44:103-110.

    Not in our library10.1128/aac.44.1.103-110.2000

  32. 32.

    Quemard A, Laneelle G, Lacave C. Mycolic acid synthesis: a target for ethionamide in mycobacteria? Antimicrob Agents Chemother. 1992;36:1316-1321.

    Not in our library10.1128/aac.36.6.1316

  33. 33.

    Quemard A, Sacchettini JC, Dessen A, Vilcheze C, Bittman R, Jacobs WR, Blanchard JS. Enzymatic characterization of the target for isoniazid in Mycobacterium tuberculosis. Biochemistry. 1995;34:8235-8241.

    Not in our library10.1021/bi00026a004

  34. 34.

    Ramaswamy SV, Reich R, Dou SJ, Jasperse L, Pan X, Wanger A, et al. Single nucleotide polymorphisms in genes associated with isoniazid resistance in Mycobacterium tuberculosis. Antimicrob Agents Chemother. 2003;47:1241-1250.

    Not in our library10.1128/aac.47.4.1241-1250.2003

  35. 35.

    Rawat M, Kovacevic S, Billman-Jacobe H, Av-Gay Y. Inactivation of mshB, a key gene in the mycothiol biosynthesis pathway in Mycobacterium smegmatis. Microbiology. 2003;149:1341-1349.

    Not in our library10.1099/mic.0.26084-0

  36. 36.

    Rawat M, Johnson C, Cadiz V, Av-Gay Y. Comparative analysis of mutants in the mycothiol biosynthesis pathway in Mycobacterium smegmatis. Biochem Biophys Res Commun. 2007;363:71-76.

    Not in our library10.1016/j.bbrc.2007.08.142

  37. 37.

    Rozwarski DA, Grant GA, Barton DH, Jacobs WR, Sacchettini JC. Modification of the NADH of the isoniazid target (InhA) from Mycobacterium tuberculosis. Science. 1998;279:98-102.

    Not in our library10.1126/science.279.5347.98

  38. 38.

    San KY, Bennett GN, Berrios-Rivera SJ, Vadali RV, Yang YT, Horton E, et al. Metabolic engineering through cofactor manipulation and its effects on metabolic flux redistribution in Escherichia coli. Metab Eng. 2002;4:182-192.

    Not in our library10.1006/mben.2001.0220

  39. 39.

    Sareen D, Newton GL, Fahey RC, Buchmeier NA. Mycothiol is essential for growth of Mycobacterium tuberculosis Erdman. J Bacteriol. 2003;185:6736-6740.

    Not in our library10.1128/jb.185.22.6736-6740.2003

  40. 40.
  41. 41.

    Stover CK, de la Cruz VF, Fuerst TR, Burlein JE, Benson LA, Bennett LT, et al. New use of BCG for recombinant vaccines. Nature. 1991;351:456-460.

    Not in our library10.1038/351456a0

  42. 42.

    Takayama K, Wang L, David HL. Effect of isoniazid on the in vivo mycolic acid synthesis, cell growth, and viability of Mycobacterium tuberculosis. Antimicrob Agents Chemother. 1972;2:29-35.

    Not in our library10.1128/aac.2.1.29

  43. 43.

    Telenti A, Honore N, Bernasconi C, March J, Ortega A, Heym B, et al. Genotypic assessment of isoniazid and rifampin resistance in Mycobacterium tuberculosis: a blind study at reference laboratory level. J Clin Microbiol. 1997;35:719-723.

    Not in our library10.1128/jcm.35.3.719-723.1997

  44. 44.

    Vannelli TA, Dykman A, Ortiz de Montellano PR. The antituberculosis drug ethionamide is activated by a flavoprotein monooxygenase. J Biol Chem. 2002;277:12824-12829.

    Not in our library10.1074/jbc.m110751200

  45. 45.

    Vetting MW, Frantom PA, Blanchard JS. Structural and enzymatic analysis of Msha from Corynebacterium glutamicum: substrate-assisted catalysis. J Biol Chem. 2008;283:15834-15844.

    Not in our library10.1074/jbc.m801017200

  46. 46.

    Vilcheze C, Jacobs WR. aIsolation and analysis of Mycobacterium tuberculosis mycolic acids. 2007a.

    Not in our library10.1002/9780471729259.mc10a03s05

  47. 47.

    Vilcheze C, Jacobs WR. The mechanism of isoniazid killing: clarity through the scope of genetics. Annu Rev Microbiol. 2007b;61:35-50.

    Not in our library10.1146/annurev.micro.61.111606.122346

  48. 48.

    Vilcheze C, Weisbrod TR, Chen B, Kremer L, Hazbon MH, Wang F, et al. Altered NADH/NAD+ ratio mediates coresistance to isoniazid and ethionamide in mycobacteria. Antimicrob Agents Chemother. 2005;49:708-720.

    Not in our library10.1128/aac.49.2.708-720.2005

  49. 49.

    Vilcheze C, Wang F, Arai M, Hazbon MH, Colangeli R, Kremer L, et al. Transfer of a point mutation in Mycobacterium tuberculosis inhA resolves the target of isoniazid. Nat Med. 2006;12:1027-1029.

    Not in our library10.1038/nm1466

  50. 50.

    Wang F, Langley R, Gulten G, Dover LG, Besra GS, Jacobs WR, Sacchettini JC. Mechanism of thioamide drug action against tuberculosis and leprosy. J Exp Med. 2007;204:73-78.

    Not in our library10.1084/jem.20062100

  51. 51.

    Wilming M, Johnsson K. Spontaneous formation of the bioactive form of the tuberculosis drug isoniazid. Angew Chem Int Ed Engl. 1999;38:2588-2590.

    Not in our library10.1002/(sici)1521-3773(19990903)38:17<2588::aid-anie2588>3.0.co;2-8

  52. 52.

    Winder FG, Collins PB. Inhibition by isoniazid of synthesis of mycolic acids in Mycobacterium tuberculosis. J Gen Microbiol. 1970;63:41-48.

    Not in our library10.1099/00221287-63-1-41

  53. 53.

    Winder FG, Collins PB, Whelan D. Effects of ethionamide and isoxyl on mycolic acid synthesis in Mycobacterium tuberculosis BCG. J Gen Microbiol. 1971;66:379-380.

    Not in our library10.1099/00221287-66-3-379

  54. 54.

    Zhang Y, Heym B, Allen B, Young D, Cole S. The catalase-peroxidase gene and isoniazid resistance of Mycobacterium tuberculosis. Nature. 1992;358:591-593.

    Not in our library10.1038/358591a0

  55. 55.

    Zignol M, Hosseini MS, Wright A, Weezenbeek CL, Nunn P, Watt CJ, et al. Global incidence of multidrug-resistant tuberculosis. J Infect Dis. 2006;194:479-485.

    Not in our library10.1086/505877

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