Microbiology · Mycobacterial and Fungal Diagnostics (NAAT, LPA, Culture, DST, IGRA, Galactomannan)

Why is Xpert MTB/RIF not recommended for assessing treatment response in a patient already on antitubercular therapy?

  • A Its sensitivity falls sharply once therapy has begun
  • B MTB DNA persists after bacillary death, so positivity does not distinguish live from killed organisms
  • C Prior antibiotic exposure permanently abolishes the rpoB signal
  • D Its internal control fails in post-treatment specimens
Correct answer: B. MTB DNA persists after bacillary death, so positivity does not distinguish live from killed organisms

Explanation

NAAT detects DNA regardless of viability, and MTB DNA remains amplifiable for weeks after effective killing begins. A positive Xpert during follow up therefore cannot separate treatment failure from residual dead bacilli. Culture, which grows only viable organisms, remains the reference standard for monitoring, with smear as a practical adjunct. Sensitivity does not fall because of prior therapy, antibiotics do not erase the rpoB target, and the internal control functions normally.

Reference: Mandell, Douglas and Bennett's Principles and Practice of Infectious Diseases, 9th ed.

High-yield for: NEET PGINI-CETNExTFMGEUSMLEPLABMRCP

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