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The MTB/MDR ELITe MGB ® Kit: Performance Assessment for Pulmonary, Extra-Pulmonary, and Resistant Tuberculosis Diagnosis, and Integration in the Laboratory Workflow of a French Center.
- Source :
-
Pathogens (Basel, Switzerland) [Pathogens] 2021 Feb 06; Vol. 10 (2). Date of Electronic Publication: 2021 Feb 06. - Publication Year :
- 2021
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Abstract
- A rapid and reliable diagnostic for tuberculosis, including the detection of both rifampicin (RIF) and isoniazid (INH) resistance, is essential for appropriate patient care. Nucleic acid amplification tests are a fast alternative to methods based on Mycobacterium tuberculosis complex (MTB) cultures. Thus, the performance of the MDR/MTB ELITe MGB <superscript>®</superscript> Kit on the ELITe InGenius <superscript>®</superscript> platform was retrospectively evaluated for MTB detection on pulmonary and extra-pulmonary samples and for RIF/INH resistance detection on MTB strains. The sensitivity and specificity of the kit for MTB detection compared to the MTB culture were 80.0% and 100.0%, respectively. For the antimicrobial susceptibility prediction, the agreement with phenotypic antimicrobial susceptibility testing (AST) was 92.0%. For RIF, the sensitivity was 100.0% and the specificity was 95.5%. For INH, the sensitivity and specificity were 75.0% and 100.0%, respectively. A single RIF false-positive result was obtained for a strain with a low level of RIF resistance that was not detected by phenotypic AST, but carrying a rpoB L452P mutation. INH false-negative results (3) were due to mutations on the katG gene that were not probed by the test. Overall, the MTB/MDR ELITe MGB <superscript>®</superscript> Kit presents a strong performance for MTB detection and for the detection of both RIF and INH resistance, with an easy integration in laboratory workflow thanks to its fully automatized system.
Details
- Language :
- English
- ISSN :
- 2076-0817
- Volume :
- 10
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Pathogens (Basel, Switzerland)
- Publication Type :
- Academic Journal
- Accession number :
- 33561935
- Full Text :
- https://doi.org/10.3390/pathogens10020176