Rapid, antibiotic incubation-free determination of tuberculosis drug resistance using machine learning and Raman spectroscopy

Author:

Ogunlade Babatunde1,Tadesse Loza F.2345ORCID,Li Hongquan6,Vu Nhat7ORCID,Banaei Niaz8,Barczak Amy K.4910ORCID,Saleh Amr A. E.111ORCID,Prakash Manu2ORCID,Dionne Jennifer A.112

Affiliation:

1. Department of Materials Science and Engineering, Stanford University, Stanford, CA 94305

2. Department of Bioengineering, Stanford University School of Medicine and School of Engineering, Stanford, CA 94305

3. Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02142

4. The Ragon Institute of Mass General, Massachusetts Institute of Technology, and Harvard, Cambridge, MA 02139

5. Jameel Clinic for AI & Healthcare, Massachusetts Institute of Technology, Cambridge, MA 02139

6. Department of Electrical Engineering, Stanford University, Stanford, CA 94305

7. Pumpkinseed Technologies, Inc., Palo Alto, CA 94306

8. Department of Pathology, Stanford University School of Medicine, Stanford, CA 94305

9. Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA 02114

10. Department of Medicine, Harvard Medical School, Boston, MA 02115

11. Department of Engineering Mathematics and Physics, Cairo University, Faculty of Engineering, Giza 12613, Egypt

12. Department of Radiology, Molecular Imaging Program at Stanford, Stanford University School of Medicine, Stanford, CA 94035

Abstract

Tuberculosis (TB) is the world’s deadliest infectious disease, with over 1.5 million deaths and 10 million new cases reported anually. The causative organism Mycobacterium tuberculosis (Mtb) can take nearly 40 d to culture, a required step to determine the pathogen’s antibiotic susceptibility. Both rapid identification and rapid antibiotic susceptibility testing of Mtb are essential for effective patient treatment and combating antimicrobial resistance. Here, we demonstrate a rapid, culture-free, and antibiotic incubation-free drug susceptibility test for TB using Raman spectroscopy and machine learning. We collect few-to-single-cell Raman spectra from over 25,000 cells of the Mtb complex strain Bacillus Calmette-Guérin (BCG) resistant to one of the four mainstay anti-TB drugs, isoniazid, rifampicin, moxifloxacin, and amikacin, as well as a pan-susceptible wildtype strain. By training a neural network on this data, we classify the antibiotic resistance profile of each strain, both on dried samples and on patient sputum samples. On dried samples, we achieve >98% resistant versus susceptible classification accuracy across all five BCG strains. In patient sputum samples, we achieve ~79% average classification accuracy. We develop a feature recognition algorithm in order to verify that our machine learning model is using biologically relevant spectral features to assess the resistance profiles of our mycobacterial strains. Finally, we demonstrate how this approach can be deployed in resource-limited settings by developing a low-cost, portable Raman microscope that costs <$5,000. We show how this instrument and our machine learning model enable combined microscopy and spectroscopy for accurate few-to-single-cell drug susceptibility testing of BCG.

Funder

National Science Foundation

NIH

Bill and Melinda Gates Foundation

Publisher

Proceedings of the National Academy of Sciences

Reference42 articles.

1. “Global tuberculosis report 2022” (WHO Tech. Rep. 2023).

2. “WHO consolidated guidelines on tuberculosis: module 3: diagnosis: rapid diagnostics for tuberculosis detection 2021 update” (WHO Tech. Rep. 2021).

3. Advances in tuberculosis diagnostics: the Xpert MTB/RIF assay and future prospects for a point-of-care test

4. RNA signatures allow rapid identification of pathogens and antibiotic susceptibilities

5. World Health Organisation High priority target product profiles for new tuberculosis diagnostics: Report of a consensus meeting (World Health Organisation Geneva 2014).

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