Mechanisms of pyrazinamide action and resistance

Ying Zhang, Wanliang Shi, Wenhong Zhang, Denis Mitchison

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Pyrazinamide (PZA), a nicotinamide analogue (Fig. 1), was first chemically synthesized in 1936 (1), but its antituberculosis (anti-TB) potential was not recognized until 1952 (2). Its discovery as a TB drug was based on a serendipitous observation that nicotinamide had certain activity against mycobacteria in animal models (3). Subsequent synthesis of nicotinamide analogues and direct testing in the mouse model of TB infection without in vitro testing led to the identification of PZA as an active agent (4, 5). Before the 1970s, PZA was mainly used as a second-line TB drug for the treatment of drug-resistant TB or in treatment of relapsed TB because of the hepatic toxicity caused by a higher PZA dosage (3.0 g daily) and longer treatment used in earlier clinical studies. However, largely encouraged by the impressive mouse studies by McDermott and colleagues that demonstrated high sterilizing activity of PZA in combination with isoniazid (INH) (6), the British Medical Research Council conducted clinical trials in East Africa with lower PZA doses (1.5 to 2.0 g daily), which are not significantly hepatotoxic. PZA was found to be almost as effective as rifampin (RIF) as a sterilizing drug, as judged by more frequent sputum conversion at 2 months and by the relapse rates. Subsequent clinical studies showed that the effects of RIF and PZA were synergistic. These studies showed that treatment could be shortened from 12 months or more to 9 months if either RIF or PZA was added to the regimen, and to 6 months if both were included (7). PZA has since been used as a first-line agent for treatment of drug-susceptible TB with RIF, INH, and ethambutol, which is currently the best TB therapy. PZA is also an integral component of treatment regimens for multidrug-resistant (MDR) TB (8) and of any new regimens in conjunction with new TB drug candidates in clinical trials (9).

Original languageEnglish (US)
Title of host publicationMolecular Genetics of Mycobacteria
Publisherwiley
Pages479-491
Number of pages13
ISBN (Electronic)9781683671008
ISBN (Print)9781555818838
DOIs
StatePublished - Oct 22 2015

Keywords

  • Multidrug-resistant tuberculosis
  • Prototype model persister drug
  • Pyrazinamide resistance
  • Pyrazinoic acid
  • Tuberculosis therapy

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)

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