# Diagnostic performance of the FluoroType MTBDR assay for rifampicin and isoniazid resistance in routine laboratory setting

**Authors:** Ivy Rukasha, Kabelo G. Kaapu, Molebogeng R. Lekalakala-Mokaba

PMC · DOI: 10.4102/phcfm.v18i1.5034 · African Journal of Primary Health Care & Family Medicine · 2026-01-08

## TL;DR

This study evaluates a new test for detecting drug-resistant tuberculosis in a real-world lab setting, showing it performs well compared to existing methods.

## Contribution

The study validates FluoroType MTBDR as a fast and reliable diagnostic tool for drug-resistant TB in routine laboratory settings.

## Key findings

- FluoroType MTBDR demonstrated 100% specificity and 96% sensitivity for detecting rifampicin resistance.
- It showed 91% sensitivity and 99% specificity for isoniazid resistance, comparable to established methods.

## Abstract

Drug-resistant tuberculosis (DR-TB) continues to be a major public health threat, especially in high-burden settings like South Africa. Rapid and accurate diagnosis of resistance to rifampicin (RIF) and isoniazid (INH) is essential to ensure that patients receive the right treatment as early as possible. Current diagnostic tools, though effective, have limitations. This study addresses the urgent need for faster, reliable alternatives to improve DR-TB detection.

The aim of this study is to assess the performance of the FluoroType MTBDR assay in detecting resistance to RIF and INH in a real-world diagnostic setting.

The study was carried out at the National Health Laboratory Services (NHLS) Polokwane Laboratory, a routine laboratory in Limpopo province, South Africa.

We tested 152 Mycobacterium tuberculosis (MTB) isolates collected from the 2023 laboratory repository using the FluoroType MTBDR version 2 assay. These results were compared with those from two established methods: GenoType MTBDRplus and Xpert MTB/RIF Ultra. Whole genome sequencing (WGS) was used to resolve any discrepancies, serving as the reference standard. Diagnostic accuracy was evaluated using sensitivity, specificity and predictive values.

Of the 152 isolates, 65% were drug-resistant. FluoroType MTBDR showed excellent performance – 100% specificity and 96% sensitivity for RIF resistance and 91% sensitivity and 99% specificity for INH resistance – competing with the GenoType MTBDRplus.

FluoroType MTBDR offers a reliable, rapid alternative for detecting DR-TB, with the potential to improve timely diagnosis and treatment.

This study highlights the FluoroType MTBDR assay as a valuable diagnostic tool for routine use, contributing to improved TB control strategies, especially in resource-limited, high-burden settings, consistent with the journal’s scope.

## Linked entities

- **Diseases:** tuberculosis (MONDO:0018076), drug-resistant tuberculosis (MONDO:0041806)
- **Species:** Mycobacterium tuberculosis (taxon 1773)

## Full-text entities

- **Genes:** LPA (lipoprotein(a)) [NCBI Gene 4018] {aka AK38, APOA, LP}, INHA (inhibin subunit alpha) [NCBI Gene 3623], RHOF (ras homolog family member F, filopodia associated) [NCBI Gene 54509] {aka ARHF, RIF}, atpE [NCBI Gene 886937], Rv1979c (permease) [NCBI Gene 885819], pepQ (cytoplasmic peptidase PepQ) [NCBI Gene 888409], MMUT (methylmalonyl-CoA mutase) [NCBI Gene 4594] {aka MCM, MUT}, Rv0678 (hypothetical protein) [NCBI Gene 888235]
- **Diseases:** TB (MESH:D014390), TB (MESH:D014376), drug (MESH:D000081015), human immunodeficiency viruses (HIV)-infected (MESH:D007239), RIF resistance (MESH:D060467), DR-TB (MESH:D018088)
- **Chemicals:** MGIT medium (-), INH (MESH:D007538), RIF (MESH:D012293)
- **Species:** Mycobacterium tuberculosis complex (species group) [taxon 77643], Homo sapiens (human, species) [taxon 9606], Mycobacterium tuberculosis (species) [taxon 1773]
- **Mutations:** Asp435Val, Ser450Leu, G 741Arg, c.-777C > T, 657_Asn660del, 18_27delACCCATTACA

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12869507/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12869507/full.md

## References

13 references — full list in the complete paper: https://tomesphere.com/paper/PMC12869507/full.md

---
Source: https://tomesphere.com/paper/PMC12869507