Impaired fitness of Mycobacterium tuberculosis resistant isolates in a cell culture model of murine macrophages

Emma Rey-Jurado, Griselda Tudó, Sònia Borrell, Fernando Alcaide, Pere Coll, Montserrat Español, Núria Martín-Casabona, Virginie Mick, Michel Montemayor, Raquel Moure, Margarita Salvadó, Eva Vicente, Julià González-Martín

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6 Citations (Scopus)

Abstract

Objectives: We analysed the ability of Mycobacterium tuberculosis clinical isolates to penetrate and grow inside murine macrophages as a surrogate of fitness. Methods: Thirty-five drug-resistant and 10 drug-susceptible M. tuberculosis isolates were studied in a murine macrophage model from the J774.2 cell line in a 6 day protocol, performing semi-quantitative counts in Middlebrook 7H11 medium. The mycobacterial penetration index (MPI) after infection and the mycobacterial growth ratio (MGR) inside the macrophages were determined to evaluate the fitness of isolates. Results: Isolates with the katG S315T mutation and multidrug-resistant (MDR) isolates had a significantly lower MGR compared with drug-susceptible isolates. The MPI of the isolates with the katG S315T mutation showed a significant decrease compared with the MPI of those without this mutation. A trend to significantly lower values was also observed on comparing the MPI of the MDR isolates with that of the drug-susceptible isolates and the isolates resistant to isoniazid. Conclusions: The isoniazid-resistant and MDR isolates with mutations in the katG gene showed decreased multiplication inside murine macrophages, suggesting a lower fitness of M. tuberculosis with these resistance patterns. © The Author 2011. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved.
Original languageEnglish
Article numberdkr288
Pages (from-to)2277-2280
JournalJournal of Antimicrobial Chemotherapy
Volume66
Issue number10
DOIs
Publication statusPublished - 1 Oct 2011

Keywords

  • Inha mutation
  • Katg mutation
  • M. tuberculosis
  • Macrophage cultures
  • RpoB mutation

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