Diagnostic accuracy of the FluoroType MTB and MTBDR VER 2.0 assays for the centralized high-throughput detection of Mycobacterium tuberculosis complex DNA and isoniazid and rifampicin resistance
dc.contributor.author | Dippenaar, Anzaan | en_ZA |
dc.contributor.author | Derendinger, Brigitta | en_ZA |
dc.contributor.author | Dolby, Tania | en_ZA |
dc.contributor.author | Beylis, Natalie | en_ZA |
dc.contributor.author | Van Helden, Paul D. | en_ZA |
dc.contributor.author | Theron, Grant | en_ZA |
dc.contributor.author | Warren, Robin M. | en_ZA |
dc.contributor.author | De Vos, Margaretha | en_ZA |
dc.date.accessioned | 2023-05-10T07:30:32Z | |
dc.date.available | 2023-05-10T07:30:32Z | |
dc.date.issued | 2021-09 | |
dc.description | CITATION: Dippenaar, A. et al 2021. Diagnostic accuracy of the FluoroType MTB and MTBDR VER 2.0 assays for the centralized high-throughput detection of Mycobacterium tuberculosis complex DNA and isoniazid and rifampicin resistance. Clinical Microbiology and Infection 27(2021):4 pages. doi.10.1016/j.cmi.2021.04.022 | en_ZA |
dc.description | The original publication is available at: sciencedirect.com | en_ZA |
dc.description.abstract | Objectives To evaluate the accuracy of two new molecular diagnostic tests for the detection of drug-resistant tuberculosis, the FluoroType MTB and MTBDR VER 2.0 assays, in combination with manual and automated DNA extraction methods. Methods Sputa from 360 Xpert Ultra Mycobacterium tuberculosis complex (MTBC)-positive patients and 250 Xpert Ultra MTBC-negative patients were tested. GenoType MTBDRplus served as reference for MTBC and drug resistance detection. Sanger sequencing was used to resolve discrepancies. Results FluoroType MTB VER 2.0 showed similar MTBC sensitivity compared with FluoroType MTBDR VER 2.0 (manual DNA extraction: 91.6% (294/321) versus 89.8% (291/324); p 0.4); automated DNA extraction: 92.1% (305/331) versus 87.7% (291/332); p 0.05)). FluoroType MTBDR VER2.0 showed comparable diagnostic accuracy to FluoroType MTBDR VER1.0 as previously reported for the detection of MTBC and rifampicin and isoniazid resistance. Conclusions The FluoroType MTB and MTBDR VER 2.0 assays together with an automated DNA extraction and PCR set-up platform may improve laboratory operational efficiency for the diagnosis of MTBC and resistance to rifampicin and isoniazid and show promise for the implementation in a centralized molecular drug susceptibility testing model. | en_ZA |
dc.description.version | Publisher’s version | en_ZA |
dc.format.extent | 4 pages | en_ZA |
dc.identifier.issn | 1198-743X (online) | en_ZA |
dc.identifier.other | doi.10.1016/j.cmi.2021.04.022 | en_ZA |
dc.identifier.uri | http://hdl.handle.net/10019.1/126883 | |
dc.language.iso | en_ZA | en_ZA |
dc.publisher | Elsevier Ltd | en_ZA |
dc.rights.holder | Authors retain copyright | en_ZA |
dc.subject | Antitubercular agents | en_ZA |
dc.subject | Mycobacterium tuberculosis | en_ZA |
dc.subject | Multidrug-resistant tuberculosis | en_ZA |
dc.subject | Molecular diagnosis | en_ZA |
dc.subject | Rifampicin | en_ZA |
dc.subject | Tuberculosis | en_ZA |
dc.title | Diagnostic accuracy of the FluoroType MTB and MTBDR VER 2.0 assays for the centralized high-throughput detection of Mycobacterium tuberculosis complex DNA and isoniazid and rifampicin resistance | en_ZA |
dc.type | Article | en_ZA |