Rapid Drug Susceptibility Testing of Drug-Resistant Mycobacterium tuberculosis Isolates Directly from Clinical Samples by Use of Amplicon Sequencing: a Proof-of-Concept Study

Author:

Colman Rebecca E.1ORCID,Anderson Julia1,Lemmer Darrin1,Lehmkuhl Erik1,Georghiou Sophia B.2,Heaton Hannah1,Wiggins Kristin1,Gillece John D.1,Schupp James M.1,Catanzaro Donald G.3,Crudu Valeriu4,Cohen Ted5,Rodwell Timothy C.2,Engelthaler David M.1

Affiliation:

1. Pathogen Genomics, Translational Genomics Research Institute, Flagstaff, Arizona, USA

2. Division of Pulmonary, Critical Care, and Sleep Medicine, University of San Diego, San Diego, California, USA

3. College of Education and Health Professions, University of Arkansas, Fayetteville, Arkansas, USA

4. Phthisiopneumology Institute (PPI), Chisinau, Republic of Moldova

5. Yale School of Public Health, New Haven, Connecticut, USA

Abstract

ABSTRACT Increasingly complex drug-resistant tuberculosis (DR-TB) is a major global health concern and one of the primary reasons why TB is now the leading infectious cause of death worldwide. Rapid characterization of a DR-TB patient's complete drug resistance profile would facilitate individualized treatment in place of empirical treatment, improve treatment outcomes, prevent amplification of resistance, and reduce the transmission of DR-TB. The use of targeted next-generation sequencing (NGS) to obtain drug resistance profiles directly from patient sputum samples has the potential to enable comprehensive evidence-based treatment plans to be implemented quickly, rather than in weeks to months, which is currently needed for phenotypic drug susceptibility testing (DST) results. In this pilot study, we evaluated the performance of amplicon sequencing of Mycobacterium tuberculosis DNA from patient sputum samples using a tabletop NGS technology and automated data analysis to provide a rapid DST solution (the Next Gen-RDST assay). One hundred sixty-six out of 176 (94.3%) sputum samples from the Republic of Moldova yielded complete Next Gen-RDST assay profiles for 7 drugs of interest. We found a high level of concordance of our Next Gen-RDST assay results with phenotypic DST (97.0%) and pyrosequencing (97.8%) results from the same clinical samples. Our Next Gen-RDST assay was also able to estimate the proportion of resistant-to-wild-type alleles down to mixtures of ≤1%, which demonstrates the ability to detect very low levels of resistant variants not detected by pyrosequencing and possibly below the threshold for phenotypic growth methods. The assay as described here could be used as a clinical or surveillance tool.

Funder

HHS | NIH | National Institute of Allergy and Infectious Diseases

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference48 articles.

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2. WHO. 2013. Global tuberculosis report 2013. Report WHO/HTM/TB/2013.11. World Health Organization, Geneva, Switzerland. http://apps.who.int/iris/bitstream/10665/91355/1/9789241564656_eng.pdf.

3. National Committee for Clinical Laboratory Standards. 2003. Susceptibility testing of mycobacteria, nocardiae, and other aerobic actinomycetes: approved standard, vol 23. M24-A. National Committee for Clinical Laboratory Standards, Villanova, PA.

4. WHO. 2008. Policy guidance on drug-susceptibility testing (DST) of second-line antituberculosis drugs. Report WHO/HTM/TB/2008.392. World Health Organization, Geneva, Switzerland. http://apps.who.int/iris/bitstream/10665/70500/1/WHO_HTM_TB_2008.392_eng.pdf.

5. Drug susceptibility testing of Mycobacterium tuberculosis against second-line drugs using the Bactec MGIT 960 system;Rodrigues C;Int J Tuberc Lung Dis,2008

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