| Literature DB >> 32037037 |
Ritu Singhal1, Divya Anthwal2, Gavish Kumar3, Grish Sah3, Max Salfinger4, Sangeeta Choudhury5, Jyoti Arora3, Manpreet Bhalla3, Vithal P Myneedu3, Rohit Sarin6, Sagarika Haldar7.
Abstract
In GenoType MTBDRplus assay [line probe assay (LPA)], when Mycobacterium tuberculosis (M. tuberculosis) sample DNA fails to hybridize to at least 1 rpoB wild-type probe and any mutation probe, it is inferred as rifampin (RIF)-resistant. In this study, we sought to identify such 'inferred' mutations in M. tuberculosis isolates (n = 203) by rpoB gene sequencing and determined their association with phenotypic resistance. D516Y, H526N, L511P mutations were associated with both phenotypically sensitive (59%, n = 38/64) and resistant (23.7%, n = 33/139) antimicrobial susceptibility testing (AST) results, whereas S531W mutation was associated with only RIF-resistant isolates (33%, n = 46/139). These results demonstrated that, at standard drug concentrations, some 'inferred' mutations may be missed by RIF-AST (phenotypically sensitive). The use of LPA permits identification of these RIF-resistant isolates, and incorporation of additional mutation probes (e.g., S531W) could further increase LPA specificity. Further studies are needed to establish the significance of the type of 'inferred' mutation with clinical/treatment outcomes.Entities:
Keywords: GenoType MTBDRplus; Inferred mutations; Mycobacterium tuberculosis; RIF-AST; Rifampin; Sequencing
Year: 2020 PMID: 32037037 DOI: 10.1016/j.diagmicrobio.2020.114995
Source DB: PubMed Journal: Diagn Microbiol Infect Dis ISSN: 0732-8893 Impact factor: 2.803