Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2010 May;48(5):1536-41.
doi: 10.1128/JCM.01758-09. Epub 2010 Mar 3.

Clinical evaluation of TRCRapid M.TB for detection of Mycobacterium tuberculosis complex in respiratory and nonrespiratory specimens

Affiliations
Comparative Study

Clinical evaluation of TRCRapid M.TB for detection of Mycobacterium tuberculosis complex in respiratory and nonrespiratory specimens

Haruka Tanaka et al. J Clin Microbiol. 2010 May.

Abstract

The rapid and accurate diagnosis of tuberculosis is crucial to providing optimal treatment and reducing the spread of infection. We evaluated respiratory and nonrespiratory clinical specimens using a new automated Mycobacterium tuberculosis complex (MTBC) rRNA detection kit (TRCRapid M.TB; Tosoh Bioscience, Tokyo, Japan), which is based on the transcription-reverse transcription concerted reaction (TRC). TRC enables the rapid and completely homogeneous real-time monitoring of isothermal RNA sequence amplification without any postamplification procedures. The results were compared with those obtained by M. tuberculosis culture. A total of 1,155 respiratory specimens and 420 nonrespiratory specimens collected from 1,282 patients were investigated. Of the 45 specimens culture positive for MTBC, 42 were TRC positive, and of the 1,530 specimens culture negative for MTBC, 1,523 were TRC negative. Compared to the results of culture, the overall sensitivity and specificity of TRC were 96.6% and 99.9%, respectively, for respiratory specimens and 87.5% and 98.5%, respectively, for nonrespiratory specimens. The sensitivities of TRC were 100% for smear-positive respiratory and nonrespiratory specimens, 88.9% for smear-negative respiratory specimens, and 80% for smear-negative nonrespiratory specimens. No significant differences in test performance between respiratory and nonrespiratory specimens were observed. The TRC method proved to be clinically useful for the rapid identification of MTBC in respiratory and nonrespiratory specimens and in both smear-positive and smear-negative samples.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Bergmann, J. S., W. E. Keating, and G. L. Woods. 2000. Clinical evaluation of the BDProbeTec ET system for rapid detection of Mycobacterium tuberculosis. J. Clin. Microbiol. 38:863-865. - PMC - PubMed
    1. Bogard, M., J. Vincelette, R. Antinozzi, R. Alonso, T. Fenner, J. Schirm, D. Aubert, C. Gaudreau, E. Sala, M. J. Ruiz-Serrano, H. Petersen, L. A. Oostendorp, and H. Burkardt. 2001. Multicenter study of a commercial, automated polymerase chain reaction system for the rapid detection of Mycobacterium tuberculosis in respiratory specimens in routine clinical practice. Eur. J. Clin. Microbiol. Infect. Dis. 20:724-731. - PubMed
    1. DiDomenico, N., H. Link, R. Knobel, T. Caratsch, W. Weschler, Z. G. Loewy, and M. Rosenstraus. 1996. COBAS AMPLICOR: fully automated RNA and DNA amplification and detection system for routine diagnostic PCR. Clin. Chem. 42:1915-1923. - PubMed
    1. Eing, B. R., A. Becker, A. Sohns, and R. Ringelmann. 1998. Comparison of Roche Cobas Amplicor Mycobacterium tuberculosis assay with in-house PCR and culture for detection of M. tuberculosis. J. Clin. Microbiol. 36:2023-2029. - PMC - PubMed
    1. Fairfax, M. R. 1996. Evaluation of the Gen-Probe amplified Mycobacterium tuberculosis direct detection test. Am. J. Clin. Pathol. 106:594-599. - PubMed

MeSH terms