Tuberc Respir Dis.  2012 Jun;72(6):475-480.

pncA Mutations in the Specimens from Extrapulmonary Tuberculosis

Affiliations
  • 1Jeju National University School of Medicine, Jeju, Korea. yomust7@cheju.ac.kr
  • 2Department of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, Korea.
  • 3Department of Biomedical Science, Faculty of Medicine and Health Sciences, University Putra Malaysia, Selangor Darul Ehsan, Malaysia.

Abstract

BACKGROUND
Pyrazinamide (PZA) is an effective antitubercular drug that becomes toxic to Mycobacterium tuberculosis when converted to pyrazinoic acid by pyrazinamidase (PZase), encoded by mycobacterial pncA. A strong association was noted between the loss of PZase activity and PZA resistance. The causative organisms in extrapulmonary tuberculosis are rarely cultured and isolated. To detect pncA mutations in specimens from extrapulmonary tuberculosis as confirmative diagnosis of mycobacterial infection and alternative susceptibility test to PZA.
METHODS
Specimens were collected from clinically proven extrapulmonary tuberculosis. pncA was sequenced and compared with wild-type pncA.
RESULTS
pncA from 30 specimens from 23 donors were successfully amplified (56.6% in specimens, 59% in donors). Six mutations in pncA were detected (20.0% in amplified specimens, 26.1% in specimen donors) at nucleotide positions of 169, 248 and 419. The mutation at position 169 results in substitution of aspartic acid for histidine, a possible allelic variation of M. bovis that have intrinsic PZA resistance. The mutation at position 248 changes proline into arginine and that at position 419, arginine into histidine.
CONCLUSION
DNA-based diagnosis using pncA may be simultaneously useful for the early diagnosis of mycobacterial infection and the rapid susceptibility to PZA in extrapulmonary tuberculosis. A potential implication of pncA allelic variation at 169 might be suggested as a rapid diagnostic test for M. bovis infection or Bacille Calmette-Guerin (BCG) reactivation.

Keyword

Antitubercular Agents; Pyrazinamide; Tuberculosis; Amidohydrolases; Mycobacterium bovis

MeSH Terms

Amidohydrolases
Antitubercular Agents
Arginine
Aspartic Acid
Diagnostic Tests, Routine
Early Diagnosis
Histidine
Humans
Mycobacterium bovis
Mycobacterium tuberculosis
Proline
Pyrazinamide
Tissue Donors
Tuberculosis
Amidohydrolases
Antitubercular Agents
Arginine
Aspartic Acid
Histidine
Proline
Pyrazinamide

Figure

  • Figure 1 Genomic DNA sequences of pncA encoding pyrazinamidase in Mycobacterium tuberculosis. The mutation spots in pncA in pyrazinamide (PZA)-resistant isolates previously reported in the reference 6-8,11 among South Koreans were underlined. Three mutations from extrapulmonary tuberculosis detected in this study were marked in bold. Nucleotides were numbered from start codon of pncA. This figure is modified from those of the reference7,11.


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