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Evaluation of the GenoType NTM-DR line probe assay for nontuberculous mycobacteria using whole genome sequences as reference standard
被引:0
|作者:
Epperson, L. Elaine
[1
]
Davidson, Rebecca M.
[1
]
Kammlade, Sara M.
[1
]
Hasan, Nabeeh A.
[1
]
Nick, Sophie E.
[1
]
Machado, Iara M. P.
[2
]
Rodriguez, Valerie H.
[2
]
Appleman, Aaron
[2
]
Helstrom, Niels K.
[2
]
Strong, Michael
[1
]
机构:
[1] Natl Jewish Hlth, Ctr Genes Environm & Hlth, 1600 Jackson St, Denver, CO USA
[2] Natl Jewish Hlth, Adv Diagnost Labs, Denver, CO USA
关键词:
Aminoglycoside;
Cystic fibrosis;
Diagnostic;
ERM(41);
Genomic drug resistance markers;
GenoType NTM-DR;
Line probe assay;
Macrolide;
Mycobacterium abscessus;
Mycobacterium avium complex;
Nontuberculous mycobacteria;
NTM;
NTM species and subspecies identification;
RRL;
RRS;
AVIUM COMPLEX;
CLARITHROMYCIN RESISTANCE;
IDENTIFICATION;
ABSCESSUS;
DISEASE;
GENE;
PREVALENCE;
MUTATIONS;
AMIKACIN;
ERM(41);
D O I:
10.1016/j.diagmicrobio.2024.116526
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
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
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