Whole genome sequencing for the prediction of resistant tuberculosis strains from northern India

被引:0
作者
Saini, Aastha [1 ]
Dadwal, Rajneesh [1 ]
Yadav, Rakesh [1 ]
Kanaujia, Rimjhim [1 ]
Aggarwal, Ashutosh Nath [2 ]
Arora, Amit [1 ]
Sethi, Sunil [1 ,3 ]
机构
[1] PGIMER, Dept Med Microbiol, Chandigarh, India
[2] PGIMER, Dept Pulm Med, Chandigarh, India
[3] PGIMER, Dept Med Microbiol, Chandigarh 160012, India
关键词
Tuberculosis; Drug resistance; WGS; DRUG-RESISTANCE; LINEAGE; PERFORMANCE; MUTATIONS; 2ND-LINE;
D O I
10.1016/j.ijmmb.2024.100537
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Purpose: Tuberculosis is an important public health problem among infectious diseases. The problem becomes more concerning with the emergence of MDR-TB and pre-XDR-TB. Whole genome sequencing (WGS) detection of resistance has recently gained popularity as it has advantages over other commercial techniques. Methods: We performed in-house WGS followed by detailed analysis by an in-house pipeline to identify the resistance markers. This was accompanied by Phenotypic DST, and Sanger sequencing on all the 12 XDR, 06 preXDR, and 06 susceptible M. tb isolates. These results were collated with online M. tb WGS pipelines (TB profiler, PhyResSE, Mykrobe predictor) for comparative analysis. Results: Following our in-house analysis, we observed 64 non-synonymous SNPs, fifteen synonymous SNPs, and five INDELs in 25 drug resistance-associated genes/intergenic regions (IGRs) in M. tb isolates. Sensitivity for detecting XDR is 33%, 58%, 83%, and 83%, respectively, using Mykrobe predictor, PhyResSE, TB-profiler, and in-house pipeline for WGS analysis, respectively. TB-profiler detected a rare mutation H70R in the gyrA gene in one pre-XDR isolate. Lineage 2.2.1 East-Asian (Beijing sublineage type) predominated (60%) in WGS data analysis of the XDR isolates. Conclusions: Our findings suggest that in-house analysis of WGS data and TB-profiler sensitivity was better for the detection of second-line resistance as compared to other automated tested tools. Frequent upgradation of newer mutations associated with resistance needs to be updated, as it potentiates tailored treatment for patients.
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