TY - JOUR
T1 - Targeted next generation sequencing directly from sputum for comprehensive genetic information on drug resistant Mycobacterium tuberculosis
AU - Kambli, Priti
AU - Ajbani, Kanchan
AU - Kazi, Mubin
AU - Sadani, Meeta
AU - Naik, Swapna
AU - Shetty, Anjali
AU - Tornheim, Jeffrey A.
AU - Singh, Harpreet
AU - Rodrigues, Camilla
N1 - Funding Information:
This work was fully supported by the Indian Council of Medical Research (ICMR), New Delhi [grant numbers: ISRM/Ad-hoc/28/2019-20 ID No.2019-2528]. JAT was supported by NIH/ NIAID ( K23AI135102 ).
Funding Information:
This work was fully supported by the Indian Council of Medical Research (ICMR), New Delhi [grant numbers: ISRM/Ad-hoc/28/2019-20 ID No.2019-2528]. JAT was supported by NIH/NIAID (K23AI135102).
Funding Information:
The study was performed at the mycobacteriology laboratory of the P. D. Hinduja National Hospital and Medical Research Centre (PDHNH), a tertiary care hospital in Mumbai, India, where 51% of patients requesting DST are found to have at least MDR-TB [ 8 ]. The study was funded by Indian Council of Medical Research (ICMR) [ISRM/Ad-hoc/28/2019-20 ID No.2019-2528] and approved by Independent Ethics Committee (IEC) of P.D. Hinduja National Hospital [1288-19-CR] for the period of August 2019-August 2020. Sputum specimens that were smear-positive for acid-fast bacilli (AFB) and Xpert MTB/RIF positive for MTB were included in this study ( Fig. 1 ).
Publisher Copyright:
© 2021
PY - 2021/3
Y1 - 2021/3
N2 - Background: Timely drug resistance detection is essential to global tuberculosis management. Unfortunately, rapid molecular tests assess resistance to only a few drugs, with culture required for comprehensive susceptibility test results. Methods: We evaluated targeted next generation sequencing (tNGS) for tuberculosis on 40 uncultured sputum samples. Resistance profiles from tNGS were compared with profiles from Xpert MTB/RIF, line probe assay (LPA), pyrosequencing (PSQ), and phenotypic testing. Concordance, sensitivity, specificity, and overall test agreement were compared across assays. Results: tNGS provided results for 39 of 40 samples (97.5%) with faster turnaround than phenotypic testing (median 3 vs. 21 days, p = 0.0068). Most samples were isoniazid and rifampin resistant (N = 31, 79.5%), 21 (53.8%) were fluoroquinolone resistant, and 3 (7.7%) were also resistant to Kanamycin. Half were of the Beijing lineage (N = 20, 51.3%). tNGS from uncultured sputum identified all resistance to isoniazid, rifampin, fluoroquinolones, and second-line injectable drugs that was identified by other methods. Agreement between tNGS and existing assays was excellent for isoniazid, rifampin, and SLDs, very good for levofloxacin, and good for moxifloxacin. Conclusion: tNGS can rapidly identify tuberculosis, lineage, and drug resistance with faster turnaround than phenotypic testing. tNGS is a potential alternative to phenotypic testing in high-burden settings.
AB - Background: Timely drug resistance detection is essential to global tuberculosis management. Unfortunately, rapid molecular tests assess resistance to only a few drugs, with culture required for comprehensive susceptibility test results. Methods: We evaluated targeted next generation sequencing (tNGS) for tuberculosis on 40 uncultured sputum samples. Resistance profiles from tNGS were compared with profiles from Xpert MTB/RIF, line probe assay (LPA), pyrosequencing (PSQ), and phenotypic testing. Concordance, sensitivity, specificity, and overall test agreement were compared across assays. Results: tNGS provided results for 39 of 40 samples (97.5%) with faster turnaround than phenotypic testing (median 3 vs. 21 days, p = 0.0068). Most samples were isoniazid and rifampin resistant (N = 31, 79.5%), 21 (53.8%) were fluoroquinolone resistant, and 3 (7.7%) were also resistant to Kanamycin. Half were of the Beijing lineage (N = 20, 51.3%). tNGS from uncultured sputum identified all resistance to isoniazid, rifampin, fluoroquinolones, and second-line injectable drugs that was identified by other methods. Agreement between tNGS and existing assays was excellent for isoniazid, rifampin, and SLDs, very good for levofloxacin, and good for moxifloxacin. Conclusion: tNGS can rapidly identify tuberculosis, lineage, and drug resistance with faster turnaround than phenotypic testing. tNGS is a potential alternative to phenotypic testing in high-burden settings.
KW - Drug resistant tuberculosis
KW - Mutations
KW - Sequencing
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U2 - 10.1016/j.tube.2021.102051
DO - 10.1016/j.tube.2021.102051
M3 - Article
C2 - 33450448
AN - SCOPUS:85099186243
SN - 1472-9792
VL - 127
JO - Tuberculosis
JF - Tuberculosis
M1 - 102051
ER -