Effect of pyrazinamidase activity on pyrazinamide resistance in Mycobacterium tuberculosis.

Patricia Sheen, Patricia Ferrer, Robert H Gilman, Jon López-Llano, Patricia Fuentes, Eddy Valencia, Mirko J Zimic
Author Information
  1. Patricia Sheen: Laboratorio de Enfermedades Infecciosas, Laboratorios de Investigación y Desarrollo, Facultad de Ciencias, Universidad Peruana Cayetano Heredia, San Martín de Porres, Lima, Peru. psheen@jhsph.edu

Abstract

Resistance of Mycobacterium tuberculosis to pyrazinamide is associated with mutations in the pncA gene, which codes for pyrazinamidase. The association between the enzymatic activity of mutated pyrazinamidases and the level of pyrazinamide resistance remains poorly understood. Twelve M. tuberculosis clinical isolates resistant to pyrazinamide were selected based on Wayne activity and localization of pyrazinamidase mutation. Recombinant pyrazinamidases were expressed and tested for their kinetic parameters (activity, k(cat), K(m), and efficiency). Pyrazinamide resistance level was measured by Bactec-460TB and 7H9 culture. The linear correlation between the resistance level and the kinetic parameters of the corresponding mutated pyrazinamidase was calculated. The enzymatic activity and efficiency of the mutated pyrazinamidases varied with the site of mutation and ranged widely from low to high levels close to the corresponding of the wild type enzyme. The level of resistance was significantly associated with pyrazinamidase activity and efficiency, but only 27.3% of its statistical variability was explained. Although pyrazinamidase mutations are indeed associated with resistance, the loss of pyrazinamidase activity and efficiency as assessed in the recombinant mutated enzymes is not sufficient to explain a high variability of the level of pyrazinamide resistance, suggesting that complementary mechanisms for pyrazinamide resistance in M. tuberculosis with mutations in pncA are more important than currently thought.

References

  1. Int J Tuberc Lung Dis. 2006 Mar;10(3):317-22 [PMID: 16562713]
  2. Antimicrob Agents Chemother. 1997 Mar;41(3):540-3 [PMID: 9055989]
  3. J Korean Med Sci. 2001 Oct;16(5):537-43 [PMID: 11641519]
  4. Epidemiol Infect. 2002 Apr;128(2):337-42 [PMID: 12002553]
  5. Int J Tuberc Lung Dis. 2003 Jan;7(1):6-21 [PMID: 12701830]
  6. J Bacteriol. 1998 Nov;180(22):5809-14 [PMID: 9811635]
  7. Front Biosci. 2004 Jan 01;9:975-94 [PMID: 14766424]
  8. Antimicrob Agents Chemother. 2004 Jul;48(7):2736-8 [PMID: 15215139]
  9. J Clin Microbiol. 1991 Nov;29(11):2578-86 [PMID: 1685494]
  10. Biochemistry. 2001 Nov 27;40(47):14166-72 [PMID: 11714269]
  11. Antimicrob Agents Chemother. 1983 Oct;24(4):600-1 [PMID: 6418066]
  12. Antimicrob Agents Chemother. 1999 Sep;43(9):2317-9 [PMID: 10471589]
  13. Tubercle. 1987 Sep;68(3):221-4 [PMID: 3129848]
  14. Antimicrob Agents Chemother. 2000 Mar;44(3):528-32 [PMID: 10681313]
  15. Int J Tuberc Lung Dis. 2004 Apr;8(4):465-72 [PMID: 15141740]
  16. Tubercle. 1985 Sep;66(3):219-25 [PMID: 3931319]
  17. Antimicrob Agents Chemother. 1999 Jul;43(7):1761-3 [PMID: 10390238]
  18. Chest. 1988 Oct;94(4):845-50 [PMID: 3048929]
  19. Antimicrob Agents Chemother. 1981 Oct;20(4):556-7 [PMID: 6805419]
  20. Biochem J. 2001 Feb 1;353(Pt 3):453-8 [PMID: 11171040]
  21. FEBS J. 2008 Feb;275(4):753-62 [PMID: 18201201]
  22. Am Rev Respir Dis. 1967 Mar;95(3):461-9 [PMID: 4225184]
  23. Nat Med. 1996 Jun;2(6):662-7 [PMID: 8640557]
  24. Am Rev Respir Dis. 1974 Jan;109(1):147-51 [PMID: 4203284]
  25. J Antimicrob Chemother. 2003 Nov;52(5):790-5 [PMID: 14563891]
  26. J Infect Dis. 2006 Aug 15;194(4):479-85 [PMID: 16845631]
  27. J Clin Microbiol. 2002 Feb;40(2):501-7 [PMID: 11825963]
  28. Antimicrob Agents Chemother. 1999 Jul;43(7):1764-6 [PMID: 10390239]
  29. J Med Microbiol. 2000 Jul;49(7):651-656 [PMID: 10882091]

Grants

  1. P01 AI051976/NIAID NIH HHS
  2. R03 AI067608/NIAID NIH HHS
  3. U01 AI035894/NIAID NIH HHS
  4. U01 AI035894-07/NIAID NIH HHS

MeSH Term

Amidohydrolases
Antitubercular Agents
Cloning, Molecular
Drug Resistance, Bacterial
Humans
Microbial Sensitivity Tests
Mutation
Mycobacterium tuberculosis
Pyrazinamide
Recombinant Proteins
Sputum

Chemicals

Antitubercular Agents
Recombinant Proteins
Pyrazinamide
Amidohydrolases
PncA protein, Mycobacterium tuberculosis
pyrazinamide deamidase

Word Cloud

Created with Highcharts 10.0.0resistancepyrazinamidaseactivitypyrazinamideleveltuberculosismutatedefficiencyassociatedmutationspyrazinamidasesMycobacteriumpncAenzymaticMmutationkineticparameterscorrespondinghighvariabilityResistancegenecodesassociationremainspoorlyunderstoodTwelveclinicalisolatesresistantselectedbasedWaynelocalizationRecombinantexpressedtestedkcatKmPyrazinamidemeasuredBactec-460TB7H9culturelinearcorrelationcalculatedvariedsiterangedwidelylowlevelsclosewildtypeenzymesignificantly273%statisticalexplainedAlthoughindeedlossassessedrecombinantenzymessufficientexplainsuggestingcomplementarymechanismsimportantcurrentlythoughtEffect

Similar Articles

Cited By