Evaluation of the GenoType NTM-DR line probe assay for nontuberculous mycobacteria using whole genome sequences as reference standard
- PMID: 39293318
- DOI: 10.1016/j.diagmicrobio.2024.116526
Evaluation of the GenoType NTM-DR line probe assay for nontuberculous mycobacteria using whole genome sequences as reference standard
Abstract
Pulmonary nontuberculous mycobacteria (NTM) disease is an emerging public health challenge that is especially problematic in people with cystic fibrosis (CF). Effective treatment depends on accurate species and subspecies identification and antimicrobial susceptibility status. We evaluated the GenoType NTM-DR VER 1.0 assay using biobanked NTM isolates with whole genome sequence (WGS) data and control isolates (total n=285). Species and subspecies detection sensitivity and specificity were 100 % for all species and subspecies except for two subspecies of M. intracellulare, that demonstrated a small degree of discrepant identification between M. intracellulare subspecies intracellulare and subspecies chimaera. All antimicrobial resistance markers were identified with 100 % sensitivity and specificity. We conclude that the GenoType NTM-DR assay offers a rapid and accurate option for identifying the most frequently encountered pathogenic NTM taxa and drug resistance markers. SUPPORT: Colorado CF Research Development Program and Colorado CF National Resource Centers funded by the Cystic Fibrosis Foundation, NJH Advanced Diagnostics Laboratories, Colorado Advanced Industries Accelerator Grant.
Keywords: Aminoglycoside; Cystic fibrosis; Diagnostic; ERM(41); GenoType NTM-DR; Genomic drug resistance markers; Line probe assay; Macrolide; Mycobacterium abscessus; Mycobacterium avium complex; NTM; NTM species and subspecies identification; Nontuberculous mycobacteria; RRL; RRS.
Copyright © 2024. Published by Elsevier Inc.
Conflict of interest statement
Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: L. Elaine Epperson reports financial support was provided by Cystic Fibrosis Foundation. L. Elaine Epperson reports financial support was provided by Colorado Advanced Industries. Michael Strong reports financial support was provided by Colorado Advanced Industries. Michael Strong reports financial support was provided by Cystic Fibrosis Foundation. Rebecca M. Davidson reports financial support was provided by Cystic Fibrosis Foundation. Nabeeh A. Hasan reports financial support was provided by Cystic Fibrosis Foundation. If there are other authors, they declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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