| Literature DB >> 26119174 |
Ning Tang1, Andrea Frank2, Vihanga Pahalawatta3, John Lampinen4, Anke Coblenz-Korte5, Chad Dunn6, Cheng Li7, Gavin Cloherty8, Klara Abravaya9, Gregor Leckie10.
Abstract
Nucleic acid amplification test (NAAT)-based assays provide fast and sensitive results compared to conventional TB tests. The performance of the new Abbott Molecular MTB assay for the qualitative detection of MTB complex using the automated m2000™ system or manual sample preparation is summarized in this paper. The assay detects eight MTB complex subspecies. The observed limit of detection (LOD) when used to test an MTB H37Rv panel was 2.45 colony forming units (cfu)/mL, while the claimed assay LOD with this MTB strain is 17 cfu/mL. No cross reactivity, or carryover were observed in the study. The clinical sensitivity of the assay was 93% overall; 99% in smear positive, culture positive specimens, and 81% in smear negative, culture positive samples. The clinical specificity was 97%. The inhibition rate in the study was 0.34%. The data suggest that Abbott RealTime MTB is a reliable, robust and sensitive assay for the molecular detection of MTB.Entities:
Keywords: Co-infection; Inactivation; Mycobacterium; Reproducibility; Respiratory; Sensitivity; Specificity
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Year: 2015 PMID: 26119174 DOI: 10.1016/j.tube.2015.05.010
Source DB: PubMed Journal: Tuberculosis (Edinb) ISSN: 1472-9792 Impact factor: 3.131