Journal
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE
Volume 68, Issue 2, Pages 123-131Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.diagmicrobio.2010.06.006
Keywords
Molecular diagnostic techniques; Mycobacterium; Atypical mycobacteria; Tuberculosis
Categories
Funding
- Fondo de Investigaciones Sanitarias [IF01-3624, IF08-36173]
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We evaluated the ability of a novel DNA strip assay (Speed-oligo (R) Mycobacteria) to differentiate mycobacterial species. It is based on polymerase chain reaction targeting 16S rRNA and 16S-23S rRNA regions and double-reverse hybridization on a dipstick using probes bound to colloidal gold and to the membrane. We blindly tested its capacity to identify 182 acid-fast bacilli grown on fresh liquid (BacT/ Alert, MGIT) and solid (Lowenstein-Jensen) cultures (from Spanish mycobacteriology laboratories), previously identified by means of Genotype (R) Mycob.CM/AS or Gen-Probe (R) AccuprobeMTC, and 11 collection strains of mycobacteria-related organisms. Discrepancies were resolved by 16S rRNA sequencing. Results were interpreted by identification of 7 specific bands for the following: Mycobacterium sp., M. fortuitum, Mycobacterium avium intracellulare complex, Mycobacterium tuberculosis complex, Mycobacterium kansasii, M. gordonae, and M. abscessus-chelonae complex. No cross-reactivity was observed with any mycobacteria-related organism. Concordant results were obtained for 177/182 bacilli (97.2%). There was only 1 major discrepancy, misidentification of Mycobacterium marinum as M. kansasii, verified by sequencing. (C) 2010 Elsevier Inc. All rights reserved.
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