Detection of Mycobacterium tuberculosis complex in pulmonary and extrapulmonary samples with the FluoroType MTBDR assay.

Abstract

OBJECTIVES\nRifampicin (RIF) and isoniazid (INH) are the two most effective first-line antibiotic drugs for the treatment of tuberculosis (TB). The new FluoroType MTBDR (FT-MTBDR) real-time PCR is intended to detect INH and RIF resistance mutations as a second step following a primary Mycobacterium tuberculosis complex (MTBC) PCR. Here we evaluate the feasibility of the FT-MTBDR assay to detect simultaneously MTBC specific DNA as well as to detect potential INH and RIF resistance through analysing inhA promotor, katG and rpoB sequences in one PCR reaction.\n\n\nMETHODS\nWe analysed 3,885 consecutive primary samples with FT-MTBDR and compared the results with microscopy and culture: 978 were from sputum, 2,007 from other respiratory tract locations plus gastric lavages, and 875 from extrapulmonary locations, respectively.\n\n\nRESULTS\nOverall, 176 samples were MTBC culture positive and 139 FT-MTBDR positive, providing a FT-MTBDR sensitivity of 0.714 (95% confidence interval 0.640 - 0.779) and specificity of 0,996 (0.994 -0.998), respectively. For the 978 sputum, 96 were MTBC culture positive and 89 FT MTBDR positive, sensitivity 0.854 (0.764 - 0.915) and specificity 0.992 (0.983 - 0.997). Of the 139 MTBC positive, 99 (71%) had interpretable genotypic resistance results for at least one drug, 92 (66%) for both drugs.\n\n\nCONCLUSIONS\nThe ability of FT-MTBDR to detect MTBC is adequate with the significant added feature of simultaneous genotypic resistance detection of both INH and RIF in a single PCR reaction.