Analytical and Clinical Evaluation of the Epistem Genedrive Assay for Detection of Mycobacterium tuberculosis

Author:

Shenai Shubhada1,Armstrong Derek T.2,Valli Eloise3,Dolinger David L.3,Nakiyingi Lydia4,Dietze Reynaldo5,Dalcolmo Margareth Pretti6,Nicol Mark P.7,Zemanay Widaad7,Manabe Yuka24,Hadad David Jamil5,Marques-Rodrigues Patricia5,Palaci Moises5,Peres Renata L.5,Gaeddert Mary8,Armakovitch Sandra8,Nonyane Bareng A. S.9,Denkinger Claudia M.3,Banada Padmapriya1,Joloba Moses L.10,Ellner Jerrold8,Boehme Catharina3,Alland David1,Dorman Susan E.2

Affiliation:

1. Division of Infectious Diseases, Center for Emerging Pathogens, Rutgers—New Jersey Medical School, Rutgers Biomedical & Health Sciences, Newark, New Jersey, USA

2. Johns Hopkins University School of Medicine, Baltimore, Maryland, USA

3. Foundation for Innovative New Diagnostics, Geneva, Switzerland

4. Infectious Disease Institute and Makerere University, Kampala, Uganda

5. Universidade Federal do Espirito Santo, Vitoria, Brazil

6. Centro de Referência Helio Fraga, FIOCRUZ, Rio de Janeiro, Brazil

7. University of Cape Town and National Health Laboratory Service, Cape Town, South Africa

8. Boston Medical Center, Boston, Massachusetts, USA

9. Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA

10. Makerere University Mycobacteriology Laboratory, Kampala, Uganda

Abstract

ABSTRACT The Epistem Genedrive assay rapidly detects the Mycobacterium tuberculosis complex from sputum and is currently available for clinical use. However, the analytical and clinical performance of this test has not been fully evaluated. The analytical limit of detection (LOD) of the Genedrive PCR amplification was tested with genomic DNA; the performance of the complete (sample processing plus amplification) system was tested by spiking M. tuberculosis mc 2 6030 cells into distilled water and M. tuberculosis -negative sputum. Specificity was tested using common respiratory pathogens and nontuberculosis mycobacteria. A clinical evaluation enrolled adults with suspected pulmonary tuberculosis, obtained three sputum samples from each participant, and compared the accuracy of the Genedrive to that of the Xpert MTB/RIF assay using M. tuberculosis cultures as the reference standard. The Genedrive assay had an LOD of 1 pg/μl (100 genomic DNA copies/reaction). The LODs of the system were 2.5 × 10 4 CFU/ml and 2.5 × 10 5 CFU/ml for cells spiked into water and sputum, respectively. False-positive rpoB probe signals were observed in 3/32 (9.4%) of the negative controls and also in few samples containing Mycobacterium abscessus , Mycobacterium gordonae , or Mycobacterium thermoresistibile . In the clinical study, among 336 analyzed participants, the overall sensitivities for the tuberculosis case detection of Genedrive, Xpert, and smear microscopy were 45.4% (95% confidence interval [CI], 35.2% to 55.8%), 91.8% (95% CI, 84.4% to 96.4%), and 77.3% (95% CI, 67.7% to 85.2%), respectively. The sensitivities of Genedrive and Xpert for the detection of smear-microscopy-negative tuberculosis were 0% (95% CI, 0% to 15.4%) and 68.2% (95% CI, 45.1% to 86.1%), respectively. The Genedrive assay did not meet performance standards recommended by the World Health Organization for a smear microscopy replacement tuberculosis test. Epistem is working on modifications to improve the assay.

Funder

The National Institutes of Health

The Foundation for Innovative New Diagnostics

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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