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A multiple genome analysis of Mycobacterium tuberculosis reveals specific novel genes and mutations associated with pyrazinamide resistance

  • Patricia Sheen
  • , David Requena
  • , Eduardo Gushiken
  • , Robert H. Gilman
  • , Ricardo Antiparra
  • , Bryan Lucero
  • , Pilar Lizárraga
  • , Basilio Cieza
  • , Elisa Roncal
  • , Louis Grandjean
  • , Arnab Pain
  • , Ruth McNerney
  • , Taane G. Clark
  • , David Moore
  • , Mirko Zimic
  • Universidad Peruana Cayetano Heredia
  • Johns Hopkins Bloomberg School of Public Health
  • University College London
  • King Abdullah University of Science and Technology
  • London School of Hygiene and Tropical Medicine

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

33 Citas (Scopus)

Resumen

Background: Tuberculosis (TB) is a major global health problem and drug resistance compromises the efforts to control this disease. Pyrazinamide (PZA) is an important drug used in both first and second line treatment regimes. However, its complete mechanism of action and resistance remains unclear. Results: We genotyped and sequenced the complete genomes of 68 M. tuberculosis strains isolated from unrelated TB patients in Peru. No clustering pattern of the strains was verified based on spoligotyping. We analyzed the association between PZA resistance with non-synonymous mutations and specific genes. We found mutations in pncA and novel genes significantly associated with PZA resistance in strains without pncA mutations. These included genes related to transportation of metal ions, pH regulation and immune system evasion. Conclusions: These results suggest potential alternate mechanisms of PZA resistance that have not been found in other populations, supporting that the antibacterial activity of PZA may hit multiple targets.

Idioma originalInglés
Número de artículo769
PublicaciónBMC Genomics
Volumen18
N.º1
DOI
EstadoPublicada - 11 oct. 2017

ODS de las Naciones Unidas

Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible

  1. ODS 3: Salud y bienestar
    ODS 3: Salud y bienestar

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