Sources of Multidrug Resistance in Patients With Previous Isoniazid-Resistant Tuberculosis Identified Using Whole Genome Sequencing: A Longitudinal Cohort Study. (13th March 2020)

• Record Type: Journal Article
• Authors: Srinivasan, Vijay; Ha, Vu T N; Vinh, Dao N; Thai, Phan V K; Ha, Dang T M; Lan, Nguyen H; Hai, Hoang T; Walker, Timothy M; Thu, Do D A; Dunstan, Sarah J; Thwaites, Guy E; Ashton, Philip M; Caws, Maxine; Thuong, Nguyen T T
• Is Part Of: Clinical infectious diseases. Volume 71:Number 10(2020)
• Page Start: e532
• Page End: e539
• Publication Date: 2020-03-13
• Subjects: tuberculosis -- multidrug resistance -- isoniazid resistance -- whole genome sequencing -- rifampicin resistance; Communicable diseases -- Periodicals; 616.905
• DOI: 10.1093/cid/ciaa254
• Languages: English
• ISSNs: 1058-4838

Abstract

Abstract: Background: Meta-analysis of patients with isoniazid-resistant tuberculosis (TB) given standard first-line anti-TB treatment indicated an increased risk of multidrug-resistant TB (MDR-TB) emerging (8%), compared to drug-sensitive TB (0.3%). Here we use whole genome sequencing (WGS) to investigate whether treatment of patients with preexisting isoniazid-resistant disease with first-line anti-TB therapy risks selecting for rifampicin resistance, and hence MDR-TB. Methods: Patients with isoniazid-resistant pulmonary TB were recruited and followed up for 24 months. Drug susceptibility testing was performed by microscopic observation drug susceptibility assay, mycobacterial growth indicator tube, and by WGS on isolates at first presentation and in the case of re-presentation. Where MDR-TB was diagnosed, WGS was used to determine the genomic relatedness between initial and subsequent isolates. De novo emergence of MDR-TB was assumed where the genomic distance was 5 or fewer single-nucleotide polymorphisms (SNPs), whereas reinfection with a different MDR-TB strain was assumed where the distance was 10 or more SNPs. Results: Two hundred thirty-nine patients with isoniazid-resistant pulmonary TB were recruited. Fourteen (14/239 [5.9%]) patients were diagnosed with a second episode of TB that was multidrug resistant. Six (6/239 [2.5%]) were identified as having evolved MDR-TB de novo and 6 as having been reinfected with a different strain. In 2 cases, the genomic distance was between 5 and 10 SNPs and therefore indeterminate. Conclusions: In isoniazid-resistant TB, de novo emergence and reinfection of MDR-TB strains equally contributed to MDR development. Early diagnosis and optimal treatment of isoniazid-resistant TB are urgently needed to avert the de novo emergence of MDR-TB during treatment. Abstract : We investigated the sources of multidrug-resistant (MDR) tuberculosis (TB) in patients with isoniazid-resistant TB treated with first-line anti-TB therapy and show that reinfection with a new MDR-TB strain was just as common as the emergence of rifampicin resistance among these patients.