Abstract

There is limited data on the use of Genotype MTBDRslVersion 1 (MTBDRsl V1) as an initial rapid screening test to rule out XDR-TB and most importantly its performance in various genotypes of Mycobacterium tuberculosis is scarcely studied. A total of 359 MDR-TB isolates were tested for gene mutations representing second line drug resistance, using the MTBDRsl_V.1 and the results were compared with phenotypic method (Bactec MGIT-960 system) for second-line drug (SLD) susceptibility testing. Genetic lineages of all these isolates were also determined using spoligotyping and SITVIT2 WEB database. The MTBDRsl V1 detected mutations in the gyrA, rrs, and emb genes in 108 (30%), 2 (0.5%) and 129 (35.9%) isolates, respectively. Remaining 120 (33.4%) had no second line drug (SLD) resistance. In 17 (4.7%) isolates mutations were detected in both gyrA and rrs genes. Its concordance with MGIT-960 culture drug susceptibility testing (DST) was 97% and 94.1%, 93.5%, 60.5% and 50% for the detection of XDR-TB, pre-XDR, Ethambutol, and Aminoglycosides/Cyclopeptides resistance. The Beijing lineage was predominant (46%) between both the pre-XDR/XDR-TB isolates. We conclude that MTBDRsl is useful for rapid detection of SLD resistance. Also in pre-XDR and XDR-TB isolates the frequency of relevant genetic mutations was significantly higher in the Beijing strains.

Highlights

  • There is limited data on the use of Genotype MTBDRslVersion 1 (MTBDRsl V1) as an initial rapid screening test to rule out XDR-TB and most importantly its performance in various genotypes of Mycobacterium tuberculosis is scarcely studied

  • multi-drug resistant TB (MDR-TB) isolates subjected to second-line drug susceptibility testing (DST), 231 (64.4%) were found to be susceptible to all second line anti-TB drugs, 127 had resistance to FQ

  • The first decade of this century witnessed the emergence of XDR-TB strains for which management is extremely difficult, and this imposed serious concerns for the health care systems around the world[1,5]

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Summary

Introduction

There is limited data on the use of Genotype MTBDRslVersion 1 (MTBDRsl V1) as an initial rapid screening test to rule out XDR-TB and most importantly its performance in various genotypes of Mycobacterium tuberculosis is scarcely studied. Emergence of resistance even to the SLDs is being reported from all parts of the world. This form of TB is known as extensively drug-resistant TB (XDR-TB), which is a more devastating condition with very poor treatment success[4]. It is essential that all suspected cases of MDR-TB must be investigated for susceptibility to second drugs in a timely manner to control the spread of spread of XDR-TB. This has become essential in order to optimize the treatment regimen at the earliest. The conventional culture-based methods are labour intensive and require longer turn around time (TAT) with undesirable treatment outcome and wider window to disease transmission[7,8]

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