Operationalising targeted next-generation sequencing for routine diagnosis of drug-resistant TB

被引:9
|
作者
Iyer, A. [1 ]
Ndlovu, Z. [2 ,3 ,6 ]
Sharma, J. [1 ]
Mansoor, H. [1 ]
Bharati, M. [1 ]
Kolan, S. [1 ]
Morales, M. [1 ]
Das, M. [1 ]
Issakidis, P. [2 ]
Ferlazzo, G. [2 ]
Hirani, N. [4 ]
Joshi, A. [4 ]
Tipre, P. [5 ]
Sutar, N. [5 ]
England, K.
机构
[1] Medecins Sans Frontieres MSF, Mumbai, India
[2] MSF, Southern African Med Unit, Cape Town, South Africa
[3] Stellenbosch Univ, Fac Med & Hlth Sci, Dept Global Hlth, Div Epidemiol & Biostat, Cape Town, South Africa
[4] Sir JJ Grp Hosp, Dept Mycobacteriol, Mumbai, India
[5] Natl TB Eliminat Programme, Mumbai, India
[6] Southern African Med Unit, Medecins Sans Frontieres MSF, Cape Town, South Africa
来源
PUBLIC HEALTH ACTION | 2023年 / 13卷 / 02期
关键词
tNGS; Deeplex-MycTB; resistotyping; MDR-TB;
D O I
10.5588/pha.22.0041
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
BACKGROUND: Phenotypic drug susceptibility testing (pDST) for Mycobacterium tuberculosis can take up to 8 weeks, while conventional molecular tests identify a limited set of resistance mutations. Targeted next-generation sequencing (tNGS) offers rapid results for predicting comprehensive drug resistance, and this study sought to explore its operational feasibility within a public health laboratory in Mumbai, India.METHODS: Pulmonary samples from consenting patients testing Xpert MTB-positive were tested for drug resistance by conventional methods and using tNGS. Laboratory operational and logistical implementation experiences from study team members are shared below.RESULTS: Of the total number of patients tested, 70% (113/161) had no history of previous TB or treatment; however, 88.2% (n = 142) had rifampicin-resistant/ multidrug-resistant TB (RR/MDR-TB). There was a high concordance between resistance predictions of tNGS and pDST for most drugs, with tNGS more accurately identifying resistance overall. tNGS was integrated and adapted into the laboratory workflow; however, batching samples caused significantly longer result turnaround time, fastest at 24 days. Manual DNA extraction caused inefficiencies; thus protocol optimisations were performed. Technical expertise was required for analysis of uncharacterised mutations and interpretation of report templates. tNGS cost per sample was US$230, while for pDST this was US$119. CONCLUSIONS: Implementation of tNGS is feasible in reference laboratories. It can rapidly identify drug resistance and should be considered as a potential alternative to pDST.
引用
收藏
页码:43 / 49
页数:7
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