Whole Genome Sequencing Assessing Impact of Diabetes Mellitus on Tuberculosis Mutations and Type of Recurrence in India

Author:

Mave Vidya123ORCID,Chen Liang4,Ranganathan Uma Devi5,Kadam Dileep6,Vishwanathan Vijay7,Lokhande Rahul6,S Siva Kumar5,Kagal Anju6,Pradhan Neeta N13,Shivakumar Shri Vijay Bala Yogendra3,Paradkar Mandar S13,Deshmukh Sona13,Tornheim Jeffrey A2,Kornfeld Hardy8,Farhat Maha9,Gupta Amita2,Padmapriyadarsini Chandrasekaran5,Gupte Nikhil123,Golub Jonathan E2,Mathema Barun10,Kreiswirth Barry N4

Affiliation:

1. Byramjee-Jeejeebhoy Medical College–Johns Hopkins University Clinical Research Site , Pune , India

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

3. Johns Hopkins India , Pune , India

4. Hackensack Meridian Health, Center for Discovery and Innovation , Nutley, New Jersey , USA

5. ICMR-National Institute for Research in Tuberculosis , Chennai , India

6. Byramjee-Jeejeebhoy Government Medical College , Pune , India

7. Professor M. Vishwanathan Diabetes Research Center , Chennai , India

8. University of Massachusetts , Boston, Massachusetts , USA

9. Harvard Medical School , Boston, Massachusetts , USA

10. Columbia University , New York, New York , USA

Abstract

Abstract Background Evidence describing the impact of diabetes mellitus (DM) on the recurrence and mutation rate of Mycobacterium tuberculosis (Mtb) is limited. Methods This study was nested in 3 cohort studies of tuberculosis (TB) patients with and without DM in India. Paired Mtb isolates recovered at baseline and treatment failure/recurrence underwent whole genome sequencing. We compared acquisition of single-nucleotide polymorphisms (SNPs), TB drug resistance mutations, and type of recurrence (endogenous reactivation [<8 SNPs] or exogenous reinfection [≥8 SNPs]) by DM status. Results Of 1633 enrolled in the 3 parent cohorts, 236 (14.5%) had microbiologically confirmed TB treatment failure/recurrence; 76 Mtb isolate pairs were available for sequencing (22 in TB-DM and 54 in TB-only). The SNP acquisition rate was overall was 0.43 (95% confidence interval [CI], .25–.64) per 1 person-year (PY); 0.77 (95% CI, .40–1.35) per 1 PY, and 0.44 (95% CI, .19–.86) per 1 PY at treatment failure and recurrence, respectively. Significant difference in SNP rates by DM status was seen at recurrence (0.21 [95% CI, .04–.61]) per 1 PY for TB-only vs 1.28 (95% CI, .41–2.98) per 1 PY for TB-DM; P = .02). No significant difference in SNP rates by DM status was observed at treatment failure. Acquired TB drug resistance was seen in 4 of 18 (22%) in TB-DM vs 4 of 45 (9%) in TB-only (P = .21). Thirteen (17%) participants had exogenous reinfection; the reinfection rate at recurrence was 25% (3/12) for TB-DM vs 17% (4/24) in TB-only (P = .66). Conclusions Considerable intrahost Mtb mutation rates were present at recurrence among patients with DM in India. One-fourth of patients with DM had exogenous reinfection at recurrence.

Funder

US Civilian Research and Development Foundation

National Institutes of Health

National Institute of Allergy and Infectious Diseases

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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