Direct and Simultaneous Identification of Mycobacterium tuberculosis complex (MTBC) and Mycobacterium tuberculosis (MTB) by Rapid Multiplex nested PCR-ICT assay
Journal
Journal of Microbiological Methods
Journal Volume
66
Journal Issue
3
Pages
440-448
Date Issued
2006
Author(s)
Soo P.-C.
Horng Y.-T.
Shen B.-J.
Tu H.-H.
Wei J.-R.
Hsieh S.-C.
Huang C.-C.
Abstract
The Mycobacterium tuberculosis (MTB) shows different virulence and host infection range from other members of the M. tuberculosis complex (MTBC). Differential identification of MTB from MTBC is thus important in certain occasions. The currently commercially available molecular assays which use either IS6110 or 16S rDNA fragment as identification targets are mainly designed for identifying MTBC but not for MTB. Comparative genomic DNA analysis has provided valuable information on regions of difference (RD) present in MTB but not in other members of the MTBC. RD9 region is further suggested to be a potential target for differential identification of MTB from MTBC. In this study, using IS6110 and Rv3618 (belong to RD9) as the specific identification targets for MTBC and MTB, respectively, we developed and tested a multiplex nested PCR-ICT (immuno-chromatography test) assay for simultaneously and directly detecting not only MTBC but also MTB from 1500 clinical sputum specimens. The results were compared with traditional culture and biochemical identification results together with patients' clinical assessments. This assay showed a 95.5% sensitivity, 97.9% specificity, 2.1% false positive rate and 4.5% false negative rate towards detection of MTBC, and a 93.0% sensitivity, 99.8% specificity, 0.2% false positive rate and 7.0% false negative rate for detection of MTB. This detection system shows great potential in clinical application. ? 2006 Elsevier B.V. All rights reserved.
SDGs
Other Subjects
bacterial DNA; DNA fragment; genomic DNA; analytical error; article; bacterium culture; bacterium identification; chromatography; clinical assessment; controlled study; diagnostic value; DNA determination; Mycobacterium tuberculosis; nonhuman; priority journal; sensitivity and sensibility; sputum analysis; Chromatography; DNA Transposable Elements; DNA, Bacterial; False Negative Reactions; False Positive Reactions; Humans; Mycobacterium tuberculosis; Polymerase Chain Reaction; Reference Values; Sensitivity and Specificity; Tuberculosis; Mycobacterium tuberculosis; Mycobacterium tuberculosis complex
Type
journal article