用于耐药结核病常规诊断的靶向新一代测序的运作。

IF 1.3 Q4 RESPIRATORY SYSTEM
A Iyer, Z Ndlovu, J Sharma, H Mansoor, M Bharati, S Kolan, M Morales, M Das, P Issakidis, G Ferlazzo, N Hirani, A Joshi, P Tipre, N Sutar, K England
{"title":"用于耐药结核病常规诊断的靶向新一代测序的运作。","authors":"A Iyer,&nbsp;Z Ndlovu,&nbsp;J Sharma,&nbsp;H Mansoor,&nbsp;M Bharati,&nbsp;S Kolan,&nbsp;M Morales,&nbsp;M Das,&nbsp;P Issakidis,&nbsp;G Ferlazzo,&nbsp;N Hirani,&nbsp;A Joshi,&nbsp;P Tipre,&nbsp;N Sutar,&nbsp;K England","doi":"10.5588/pha.22.0041","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Phenotypic drug susceptibility testing (pDST) for <i>Mycobacterium tuberculosis</i> 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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>Of the total number of patients tested, 70% (113/161) had no history of previous TB or treatment; however, 88.2% (<i>n</i> = 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.</p><p><strong>Conclusions: </strong>Implementation of tNGS is feasible in reference laboratories. It can rapidly identify drug resistance and should be considered as a potential alternative to pDST.</p>","PeriodicalId":46239,"journal":{"name":"Public Health Action","volume":"13 2","pages":"43-49"},"PeriodicalIF":1.3000,"publicationDate":"2023-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290261/pdf/","citationCount":"0","resultStr":"{\"title\":\"Operationalising targeted next-generation sequencing for routine diagnosis of drug-resistant TB.\",\"authors\":\"A Iyer,&nbsp;Z Ndlovu,&nbsp;J Sharma,&nbsp;H Mansoor,&nbsp;M Bharati,&nbsp;S Kolan,&nbsp;M Morales,&nbsp;M Das,&nbsp;P Issakidis,&nbsp;G Ferlazzo,&nbsp;N Hirani,&nbsp;A Joshi,&nbsp;P Tipre,&nbsp;N Sutar,&nbsp;K England\",\"doi\":\"10.5588/pha.22.0041\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Phenotypic drug susceptibility testing (pDST) for <i>Mycobacterium tuberculosis</i> 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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>Of the total number of patients tested, 70% (113/161) had no history of previous TB or treatment; however, 88.2% (<i>n</i> = 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.</p><p><strong>Conclusions: </strong>Implementation of tNGS is feasible in reference laboratories. It can rapidly identify drug resistance and should be considered as a potential alternative to pDST.</p>\",\"PeriodicalId\":46239,\"journal\":{\"name\":\"Public Health Action\",\"volume\":\"13 2\",\"pages\":\"43-49\"},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2023-06-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10290261/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Public Health Action\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5588/pha.22.0041\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"RESPIRATORY SYSTEM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Public Health Action","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5588/pha.22.0041","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"RESPIRATORY SYSTEM","Score":null,"Total":0}
引用次数: 0

摘要

背景:结核分枝杆菌的表型药敏试验(pDST)可能需要长达8周的时间,而传统的分子试验鉴定出一组有限的耐药突变。靶向下一代测序(tNGS)为预测全面耐药性提供了快速结果,本研究试图在印度孟买的一个公共卫生实验室探索其操作可行性。方法:采用常规方法和tNGS对Xpert mtb阳性患者肺标本进行耐药检测。下面分享了研究小组成员的实验室操作和后勤实施经验。结果:在接受检测的患者总数中,70%(113/161)没有结核病史或治疗史;然而,88.2% (n = 142)患有利福平耐药/耐多药结核病(RR/MDR-TB)。对于大多数药物,tNGS和pDST的耐药预测之间存在高度一致性,tNGS总体上更准确地识别耐药。将tNGS整合并适应到实验室工作流程中;然而,批量样品导致结果周转时间明显延长,最快为24天。人工DNA提取效率低下;因此,执行了协议优化。分析无特征的突变和解释报告模板需要技术专门知识。每个样品的tNGS成本为230美元,而pDST的成本为119美元。结论:在参比实验室实施tNGS是可行的。它可以快速识别耐药性,应被视为pDST的潜在替代品。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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

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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Public Health Action
Public Health Action RESPIRATORY SYSTEM-
自引率
0.00%
发文量
29
期刊介绍: Launched on 1 May 2011, Public Health Action (PHA) is an official publication of the International Union Against Tuberculosis and Lung Disease (The Union). It is an open access, online journal available world-wide to physicians, health workers, researchers, professors, students and decision-makers, including public health centres, medical, university and pharmaceutical libraries, hospitals, clinics, foundations and institutions. PHA is a peer-reviewed scholarly journal that actively encourages, communicates and reports new knowledge, dialogue and controversy in health systems and services for people in vulnerable and resource-limited communities — all topics that reflect the mission of The Union, Health solutions for the poor.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信