# Waste to Worth: A diagnostic accuracy of Xpert MTB/XDR on contaminated liquid cultures to salvage the detection of drug-resistant tuberculosis

**Authors:** Yonas Ghebrekristos, Erick Auma, Zama Mahlobo, Rouxjeane Venter, Natalie Beylis, Jay Achar, Brigitta Derendinger, Sarishna Singh, Megan Burger, Christoffel Opperman, Robin Warren, Grant Theron

PMC · DOI: 10.21203/rs.3.rs-6409041/v1 · Research Square · 2025-04-12

## TL;DR

This study shows that Xpert MTB/XDR can accurately detect drug-resistant tuberculosis from contaminated cultures, improving diagnostic accuracy and reducing delays.

## Contribution

The study introduces a novel use of Xpert MTB/XDR on contaminated cultures to salvage drug resistance testing for TB.

## Key findings

- Xpert MTB/XDR showed 100% sensitivity and high specificity for detecting drug resistance in contaminated cultures.
- Using Xpert MTB/XDR on contaminated cultures could reduce the time to drug susceptibility test results by up to 22 days.
- The method salvaged TB detection in 89% of contaminated cultures in Cohort A and 57% in Cohort B.

## Abstract

Mycobacterium Growth Indicator Tube (MGIT) 960 culture is critical for tuberculosis (TB) drug susceptibility testing (DST) but vulnerable to contamination. We evaluated the accuracy of Xpert MTB/XDR, a molecular DST for isoniazid, fluoroquinolone, amikacin, and ethionamide, on to-be-discarded contaminated growth.

Xpert MTB/XDR was applied to acid-fast bacilli-negative contaminated cultures from sputum from people with rifampicin-resistant TB when Xpert MTB/XDR on sputum was unsuccessful (not resistant or susceptible for all drugs) 1) at diagnosis (Cohort A) or 2) during treatment monitoring (Cohort B). Future DSTs within three months served as a reference standard. We determined potential care cascade improvements.

In Cohort A, 10% (66/650) of people were culture-contaminated. 89% (59/66) were contaminated growth Xpert MTB/XDR TB-positive. Sensitivity and specificity for isoniazid, fluoroquinolone, amikacin, and ethionamide resistance were 100% [95% confidence interval (CI) 85, 100] and 100% (79, 100), 100% (59, 100) and 100% (89, 100), 100% (16, 100) and 100% (91, 100), and 100% (72, 100) and 96% (78, 100), respectively. In Cohort B, 22% (28/129) of people with a contaminated culture were Xpert MTB/XDR TB-positive. Of these, 57% (16/28), 7% (2/28), and 43% (12/28) were isoniazid-, fluoroquinolone-, and ethionamide-resistant (in 2, 1, and 4 people respectively, this would be the first resistant result). In both cohorts, time-to-DST could improve a median (IQR) of 22 (12–42) days.

Xpert MTB/XDR on contaminated MGIT960 cultures had high sensitivity and specificity for DST. This approach could mitigate culture contamination’s negative effects and improve gaps in the drug-resistant TB diagnostic cascade.

## Linked entities

- **Chemicals:** isoniazid (PubChem CID 3767), amikacin (PubChem CID 37768), ethionamide (PubChem CID 2761171), rifampicin (PubChem CID 135398735)
- **Diseases:** tuberculosis (MONDO:0018076), drug-resistant tuberculosis (MONDO:0041806)
- **Species:** Mycobacterium (taxon 1763)

## Full-text entities

- **Diseases:** XDR (MESH:D054908), TB (MESH:D014376), drug-resistant tuberculosis (MESH:D018088)
- **Species:** Mycobacterium (genus) [taxon 1763]
- **Cell lines:** MGIT — Canis lupus familiaris (Dog), Spontaneously immortalized cell line (CVCL_6453)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12036451/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12036451/full.md

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Source: https://tomesphere.com/paper/PMC12036451