Whole genome sequencing for tuberculosis disease species identification, lineage determination, and drug resistance detection in Kashgar prefecture, China

Author:

Liu Dongxin1,Badeerhan Gulina2,Emam Mawlanjan3,Jiang Mengnan1,Hong Geng1,Xie Mengjiao1,Liu Yang1,Wang Xijiang2,Wei Qiang1

Affiliation:

1. Chinese Center for Disease Control and Prevention

2. Xinjiang Uighur Autonomous Region Center for Disease Control and Prevention

3. Kashgar District Center for Disease Control and Prevention

Abstract

Abstract

Background We aimed to use whole genome sequencing (WGS) to determine species and lineage composition and drug resistant profile in a high tuberculosis (TB)-burden region of China. Methods We conducted WGS to 1791 acid-fast staining positive isolates and culture-positive isolates collected from Kashgar prefecture in 2020. Bioinformatic analysis was applied to confirm species, lineage and drug resistant mutations. The drug susceptibility testing were performed on confirmed Mycobacterium tuberculosis complex(MTBC) isolates. We determined the accuracy of WGS by comparing with phenotypes. Results 95.03% (1702/1791) were identified MTBC, 3.18% (57/1791) were nontuberculous mycobacteria (NTM), 0.61% (11/1791) and 0.89%(16/1791) were Nocardia and Gordonia respectively, 4 were identified as mixed infection. MTBC were composed of lineage 2 (45.83%, 780/1702), lineage 3 (462/1702, 27.14%), lineage 4 (455/1702, 26.73%), lineage 1(1/1702, 0.06%) and M.bovis (La1, 4/1702, 0.24%). Resistance to rifampicin, ethambutol, fluoroquinolones, aminoglycosides and ethionamide were accurately predicted with sensitivity of 96.43%, 83.33%,100%, 100% and 94.74% by WGS, and resistance to isoniazid with the sensitivity of 81.62% . Conclusions WGS can be an important approach in assessing TB control strategy and for determining therapeutic schemes in high TB-burden regions. The drug resistant TB of Kashgar prefecture is at low level and the application of WGS may prevent the increase of resistance rate.

Publisher

Springer Science and Business Media LLC

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