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Clinical utility of target-based next-generation sequencing for drug-resistant TB

BACKGROUND: In high TB burden countries, access to drug susceptibility testing is a major bottleneck. Targeted next-generation sequencing (tNGS) is a promising technology for rapid resistance detection. This study assessed the role of tNGS for the diagnosis of drug-resistant TB (DR-TB). METHODS: A t...

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Autores principales: Mansoor, H., Hirani, N., Chavan, V., Das, M., Sharma, J., Bharati, M., Oswal, V., Iyer, A., Morales, M., Joshi, A., Ferlazzo, G., Isaakidis, P., Ndlovu, Z., England, K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union Against Tuberculosis and Lung Disease 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9879084/
https://www.ncbi.nlm.nih.gov/pubmed/36853141
http://dx.doi.org/10.5588/ijtld.22.0138
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author Mansoor, H.
Hirani, N.
Chavan, V.
Das, M.
Sharma, J.
Bharati, M.
Oswal, V.
Iyer, A.
Morales, M.
Joshi, A.
Ferlazzo, G.
Isaakidis, P.
Ndlovu, Z.
England, K.
author_facet Mansoor, H.
Hirani, N.
Chavan, V.
Das, M.
Sharma, J.
Bharati, M.
Oswal, V.
Iyer, A.
Morales, M.
Joshi, A.
Ferlazzo, G.
Isaakidis, P.
Ndlovu, Z.
England, K.
author_sort Mansoor, H.
collection PubMed
description BACKGROUND: In high TB burden countries, access to drug susceptibility testing is a major bottleneck. Targeted next-generation sequencing (tNGS) is a promising technology for rapid resistance detection. This study assessed the role of tNGS for the diagnosis of drug-resistant TB (DR-TB). METHODS: A total of 161 samples from bacteriologically confirmed TB cases were subjected to tNGS using the Deeplex(®) Myc-TB kit and sequenced using the MiSeq platform. These samples were also processed for conventional phenotypic DST (pDST) using 13 drugs on Mycobacteria Growth Indicator Tube and line-probe assays (MTBDRplus and MTBDRsl). RESULTS: There were 146 DR-TB and 15 drug-susceptible TB (DS-TB) samples. About 70% of patients with DR-TB had no previous TB treatment history. Overall, 88.2% had rifampicin-resistant/multidrug-resistant TB (RR/MDR-TB), 58.5% pre-extensively drug-resistant TB (pre-XDR-TB) and 9.2% had XDR-TB as defined by the WHO (2020). Around 8% (n = 13) of samples were non-culturable; however, identified 8 were resistant to first and second-line drugs using tNGS. Resistance frequency was similar across methods, with discordance in drugs less reliable using pDST or with limited mutational representation within databases. Sensitivities were aligned with literature reports for most drugs. We observed 10% heteroresistance, while 75% of strains were of Lineages 2 and 3. CONCLUSIONS: Programme data supported tNGS in the diagnosis of DR-TB for early treatment using individualised regimens.
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spelling pubmed-98790842023-01-29 Clinical utility of target-based next-generation sequencing for drug-resistant TB Mansoor, H. Hirani, N. Chavan, V. Das, M. Sharma, J. Bharati, M. Oswal, V. Iyer, A. Morales, M. Joshi, A. Ferlazzo, G. Isaakidis, P. Ndlovu, Z. England, K. Int J Tuberc Lung Dis Original Articles BACKGROUND: In high TB burden countries, access to drug susceptibility testing is a major bottleneck. Targeted next-generation sequencing (tNGS) is a promising technology for rapid resistance detection. This study assessed the role of tNGS for the diagnosis of drug-resistant TB (DR-TB). METHODS: A total of 161 samples from bacteriologically confirmed TB cases were subjected to tNGS using the Deeplex(®) Myc-TB kit and sequenced using the MiSeq platform. These samples were also processed for conventional phenotypic DST (pDST) using 13 drugs on Mycobacteria Growth Indicator Tube and line-probe assays (MTBDRplus and MTBDRsl). RESULTS: There were 146 DR-TB and 15 drug-susceptible TB (DS-TB) samples. About 70% of patients with DR-TB had no previous TB treatment history. Overall, 88.2% had rifampicin-resistant/multidrug-resistant TB (RR/MDR-TB), 58.5% pre-extensively drug-resistant TB (pre-XDR-TB) and 9.2% had XDR-TB as defined by the WHO (2020). Around 8% (n = 13) of samples were non-culturable; however, identified 8 were resistant to first and second-line drugs using tNGS. Resistance frequency was similar across methods, with discordance in drugs less reliable using pDST or with limited mutational representation within databases. Sensitivities were aligned with literature reports for most drugs. We observed 10% heteroresistance, while 75% of strains were of Lineages 2 and 3. CONCLUSIONS: Programme data supported tNGS in the diagnosis of DR-TB for early treatment using individualised regimens. International Union Against Tuberculosis and Lung Disease 2023-01 2023-01-01 /pmc/articles/PMC9879084/ /pubmed/36853141 http://dx.doi.org/10.5588/ijtld.22.0138 Text en © 2023 The Union https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
spellingShingle Original Articles
Mansoor, H.
Hirani, N.
Chavan, V.
Das, M.
Sharma, J.
Bharati, M.
Oswal, V.
Iyer, A.
Morales, M.
Joshi, A.
Ferlazzo, G.
Isaakidis, P.
Ndlovu, Z.
England, K.
Clinical utility of target-based next-generation sequencing for drug-resistant TB
title Clinical utility of target-based next-generation sequencing for drug-resistant TB
title_full Clinical utility of target-based next-generation sequencing for drug-resistant TB
title_fullStr Clinical utility of target-based next-generation sequencing for drug-resistant TB
title_full_unstemmed Clinical utility of target-based next-generation sequencing for drug-resistant TB
title_short Clinical utility of target-based next-generation sequencing for drug-resistant TB
title_sort clinical utility of target-based next-generation sequencing for drug-resistant tb
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9879084/
https://www.ncbi.nlm.nih.gov/pubmed/36853141
http://dx.doi.org/10.5588/ijtld.22.0138
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