Sources of Multidrug Resistance in Patients With Previous Isoniazid-Resistant Tuberculosis Identified Using Whole Genome Sequencing: A Longitudinal Cohort Study

Abstract Background Meta-analysis of patients with isoniazid-resistant tuberculosis (TB) given standard first-line anti-TB treatment indicated an increased risk of multidrug-resistant TB (MDR-TB) emerging (8%), compared to drug-sensitive TB (0.3%). Here we use whole genome sequencing (WGS) to invest...

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Veröffentlicht in:Clinical infectious diseases 2020-12, Vol.71 (10), p.e532-e539
Hauptverfasser: Srinivasan, Vijay, Ha, Vu T N, Vinh, Dao N, Thai, Phan V K, Ha, Dang T M, Lan, Nguyen H, Hai, Hoang T, Walker, Timothy M, Thu, Do D A, Dunstan, Sarah J, Thwaites, Guy E, Ashton, Philip M, Caws, Maxine, Thuong, Nguyen T T
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container_end_page e539
container_issue 10
container_start_page e532
container_title Clinical infectious diseases
container_volume 71
creator Srinivasan, Vijay
Ha, Vu T N
Vinh, Dao N
Thai, Phan V K
Ha, Dang T M
Lan, Nguyen H
Hai, Hoang T
Walker, Timothy M
Thu, Do D A
Dunstan, Sarah J
Thwaites, Guy E
Ashton, Philip M
Caws, Maxine
Thuong, Nguyen T T
description Abstract Background Meta-analysis of patients with isoniazid-resistant tuberculosis (TB) given standard first-line anti-TB treatment indicated an increased risk of multidrug-resistant TB (MDR-TB) emerging (8%), compared to drug-sensitive TB (0.3%). Here we use whole genome sequencing (WGS) to investigate whether treatment of patients with preexisting isoniazid-resistant disease with first-line anti-TB therapy risks selecting for rifampicin resistance, and hence MDR-TB. Methods Patients with isoniazid-resistant pulmonary TB were recruited and followed up for 24 months. Drug susceptibility testing was performed by microscopic observation drug susceptibility assay, mycobacterial growth indicator tube, and by WGS on isolates at first presentation and in the case of re-presentation. Where MDR-TB was diagnosed, WGS was used to determine the genomic relatedness between initial and subsequent isolates. De novo emergence of MDR-TB was assumed where the genomic distance was 5 or fewer single-nucleotide polymorphisms (SNPs), whereas reinfection with a different MDR-TB strain was assumed where the distance was 10 or more SNPs. Results Two hundred thirty-nine patients with isoniazid-resistant pulmonary TB were recruited. Fourteen (14/239 [5.9%]) patients were diagnosed with a second episode of TB that was multidrug resistant. Six (6/239 [2.5%]) were identified as having evolved MDR-TB de novo and 6 as having been reinfected with a different strain. In 2 cases, the genomic distance was between 5 and 10 SNPs and therefore indeterminate. Conclusions In isoniazid-resistant TB, de novo emergence and reinfection of MDR-TB strains equally contributed to MDR development. Early diagnosis and optimal treatment of isoniazid-resistant TB are urgently needed to avert the de novo emergence of MDR-TB during treatment. We investigated the sources of multidrug-resistant (MDR) tuberculosis (TB) in patients with isoniazid-resistant TB treated with first-line anti-TB therapy and show that reinfection with a new MDR-TB strain was just as common as the emergence of rifampicin resistance among these patients.
doi_str_mv 10.1093/cid/ciaa254
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Here we use whole genome sequencing (WGS) to investigate whether treatment of patients with preexisting isoniazid-resistant disease with first-line anti-TB therapy risks selecting for rifampicin resistance, and hence MDR-TB. Methods Patients with isoniazid-resistant pulmonary TB were recruited and followed up for 24 months. Drug susceptibility testing was performed by microscopic observation drug susceptibility assay, mycobacterial growth indicator tube, and by WGS on isolates at first presentation and in the case of re-presentation. Where MDR-TB was diagnosed, WGS was used to determine the genomic relatedness between initial and subsequent isolates. De novo emergence of MDR-TB was assumed where the genomic distance was 5 or fewer single-nucleotide polymorphisms (SNPs), whereas reinfection with a different MDR-TB strain was assumed where the distance was 10 or more SNPs. Results Two hundred thirty-nine patients with isoniazid-resistant pulmonary TB were recruited. Fourteen (14/239 [5.9%]) patients were diagnosed with a second episode of TB that was multidrug resistant. Six (6/239 [2.5%]) were identified as having evolved MDR-TB de novo and 6 as having been reinfected with a different strain. In 2 cases, the genomic distance was between 5 and 10 SNPs and therefore indeterminate. Conclusions In isoniazid-resistant TB, de novo emergence and reinfection of MDR-TB strains equally contributed to MDR development. Early diagnosis and optimal treatment of isoniazid-resistant TB are urgently needed to avert the de novo emergence of MDR-TB during treatment. We investigated the sources of multidrug-resistant (MDR) tuberculosis (TB) in patients with isoniazid-resistant TB treated with first-line anti-TB therapy and show that reinfection with a new MDR-TB strain was just as common as the emergence of rifampicin resistance among these patients.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1093/cid/ciaa254</identifier><identifier>PMID: 32166306</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Antitubercular Agents - pharmacology ; Antitubercular Agents - therapeutic use ; Humans ; Isoniazid - pharmacology ; Longitudinal Studies ; Microbial Sensitivity Tests ; Mycobacterium tuberculosis - genetics ; Online Only ; Tuberculosis, Multidrug-Resistant - drug therapy ; Tuberculosis, Multidrug-Resistant - epidemiology ; Whole Genome Sequencing</subject><ispartof>Clinical infectious diseases, 2020-12, Vol.71 (10), p.e532-e539</ispartof><rights>The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America. 2020</rights><rights>The Author(s) 2020. Published by Oxford University Press for the Infectious Diseases Society of America.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-fbdafd0757998d9d5b9a65fc5ad1db7787fed3c5d5a08a110b065f666b6fb6523</citedby><cites>FETCH-LOGICAL-c412t-fbdafd0757998d9d5b9a65fc5ad1db7787fed3c5d5a08a110b065f666b6fb6523</cites><orcidid>0000-0003-3434-5608</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,1578,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32166306$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Srinivasan, Vijay</creatorcontrib><creatorcontrib>Ha, Vu T N</creatorcontrib><creatorcontrib>Vinh, Dao N</creatorcontrib><creatorcontrib>Thai, Phan V K</creatorcontrib><creatorcontrib>Ha, Dang T M</creatorcontrib><creatorcontrib>Lan, Nguyen H</creatorcontrib><creatorcontrib>Hai, Hoang T</creatorcontrib><creatorcontrib>Walker, Timothy M</creatorcontrib><creatorcontrib>Thu, Do D A</creatorcontrib><creatorcontrib>Dunstan, Sarah J</creatorcontrib><creatorcontrib>Thwaites, Guy E</creatorcontrib><creatorcontrib>Ashton, Philip M</creatorcontrib><creatorcontrib>Caws, Maxine</creatorcontrib><creatorcontrib>Thuong, Nguyen T T</creatorcontrib><title>Sources of Multidrug Resistance in Patients With Previous Isoniazid-Resistant Tuberculosis Identified Using Whole Genome Sequencing: A Longitudinal Cohort Study</title><title>Clinical infectious diseases</title><addtitle>Clin Infect Dis</addtitle><description>Abstract Background Meta-analysis of patients with isoniazid-resistant tuberculosis (TB) given standard first-line anti-TB treatment indicated an increased risk of multidrug-resistant TB (MDR-TB) emerging (8%), compared to drug-sensitive TB (0.3%). Here we use whole genome sequencing (WGS) to investigate whether treatment of patients with preexisting isoniazid-resistant disease with first-line anti-TB therapy risks selecting for rifampicin resistance, and hence MDR-TB. Methods Patients with isoniazid-resistant pulmonary TB were recruited and followed up for 24 months. Drug susceptibility testing was performed by microscopic observation drug susceptibility assay, mycobacterial growth indicator tube, and by WGS on isolates at first presentation and in the case of re-presentation. Where MDR-TB was diagnosed, WGS was used to determine the genomic relatedness between initial and subsequent isolates. De novo emergence of MDR-TB was assumed where the genomic distance was 5 or fewer single-nucleotide polymorphisms (SNPs), whereas reinfection with a different MDR-TB strain was assumed where the distance was 10 or more SNPs. Results Two hundred thirty-nine patients with isoniazid-resistant pulmonary TB were recruited. Fourteen (14/239 [5.9%]) patients were diagnosed with a second episode of TB that was multidrug resistant. Six (6/239 [2.5%]) were identified as having evolved MDR-TB de novo and 6 as having been reinfected with a different strain. In 2 cases, the genomic distance was between 5 and 10 SNPs and therefore indeterminate. Conclusions In isoniazid-resistant TB, de novo emergence and reinfection of MDR-TB strains equally contributed to MDR development. Early diagnosis and optimal treatment of isoniazid-resistant TB are urgently needed to avert the de novo emergence of MDR-TB during treatment. We investigated the sources of multidrug-resistant (MDR) tuberculosis (TB) in patients with isoniazid-resistant TB treated with first-line anti-TB therapy and show that reinfection with a new MDR-TB strain was just as common as the emergence of rifampicin resistance among these patients.</description><subject>Antitubercular Agents - pharmacology</subject><subject>Antitubercular Agents - therapeutic use</subject><subject>Humans</subject><subject>Isoniazid - pharmacology</subject><subject>Longitudinal Studies</subject><subject>Microbial Sensitivity Tests</subject><subject>Mycobacterium tuberculosis - genetics</subject><subject>Online Only</subject><subject>Tuberculosis, Multidrug-Resistant - drug therapy</subject><subject>Tuberculosis, Multidrug-Resistant - epidemiology</subject><subject>Whole Genome Sequencing</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><sourceid>EIF</sourceid><recordid>eNp9kU1rVDEUhoNYbK2u3EtWIsityc1Ncq8LoQzaDoxYnJYuQ24-ZiJ3kjEfhfpr_KlmmGmpGxfhJOc8ec9JXgDeYHSG0UA-KqfrkrKl3TNwginhDaMDfl73iPZN15P-GLxM6SdCGPeIvgDHpMWMEcROwJ9lKFGZBIOF38qUnY5lBX-Y5FKWXhnoPLyS2RmfE7x1eQ2vorlzoSQ4T8E7-dvp5gHP8LqMJqoyhZqAc11vOeuMhjfJ-RW8XYfJwAvjw8bApflVjFc1_wmew0XwK5eLdl5OcBbWIWa4rOf7V-DIyimZ14d4Cm6-frmeXTaL7xfz2fmiUR1uc2NHLa1GnPJh6PWg6ThIRq2iUmM9ct5zazRRVFOJeokxGlEtM8ZGZkdGW3IKPu91t2XcGK3q6FFOYhvdRsZ7EaQT_1a8W4tVuBOcd93Q7wTeHwRiqC9LWWxcUmaapDf1u0RLOCeEk2GHftijKoaUorGPbTASO09F9VQcPK3026eTPbIPJlbg3R4IZftfpb_U-bCq</recordid><startdate>20201217</startdate><enddate>20201217</enddate><creator>Srinivasan, Vijay</creator><creator>Ha, Vu T N</creator><creator>Vinh, Dao N</creator><creator>Thai, Phan V K</creator><creator>Ha, Dang T M</creator><creator>Lan, Nguyen H</creator><creator>Hai, Hoang T</creator><creator>Walker, Timothy M</creator><creator>Thu, Do D A</creator><creator>Dunstan, Sarah J</creator><creator>Thwaites, Guy E</creator><creator>Ashton, Philip M</creator><creator>Caws, Maxine</creator><creator>Thuong, Nguyen T T</creator><general>Oxford University Press</general><scope>TOX</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-3434-5608</orcidid></search><sort><creationdate>20201217</creationdate><title>Sources of Multidrug Resistance in Patients With Previous Isoniazid-Resistant Tuberculosis Identified Using Whole Genome Sequencing: A Longitudinal Cohort Study</title><author>Srinivasan, Vijay ; 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Here we use whole genome sequencing (WGS) to investigate whether treatment of patients with preexisting isoniazid-resistant disease with first-line anti-TB therapy risks selecting for rifampicin resistance, and hence MDR-TB. Methods Patients with isoniazid-resistant pulmonary TB were recruited and followed up for 24 months. Drug susceptibility testing was performed by microscopic observation drug susceptibility assay, mycobacterial growth indicator tube, and by WGS on isolates at first presentation and in the case of re-presentation. Where MDR-TB was diagnosed, WGS was used to determine the genomic relatedness between initial and subsequent isolates. De novo emergence of MDR-TB was assumed where the genomic distance was 5 or fewer single-nucleotide polymorphisms (SNPs), whereas reinfection with a different MDR-TB strain was assumed where the distance was 10 or more SNPs. Results Two hundred thirty-nine patients with isoniazid-resistant pulmonary TB were recruited. Fourteen (14/239 [5.9%]) patients were diagnosed with a second episode of TB that was multidrug resistant. Six (6/239 [2.5%]) were identified as having evolved MDR-TB de novo and 6 as having been reinfected with a different strain. In 2 cases, the genomic distance was between 5 and 10 SNPs and therefore indeterminate. Conclusions In isoniazid-resistant TB, de novo emergence and reinfection of MDR-TB strains equally contributed to MDR development. Early diagnosis and optimal treatment of isoniazid-resistant TB are urgently needed to avert the de novo emergence of MDR-TB during treatment. We investigated the sources of multidrug-resistant (MDR) tuberculosis (TB) in patients with isoniazid-resistant TB treated with first-line anti-TB therapy and show that reinfection with a new MDR-TB strain was just as common as the emergence of rifampicin resistance among these patients.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>32166306</pmid><doi>10.1093/cid/ciaa254</doi><orcidid>https://orcid.org/0000-0003-3434-5608</orcidid><oa>free_for_read</oa></addata></record>
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subjects Antitubercular Agents - pharmacology
Antitubercular Agents - therapeutic use
Humans
Isoniazid - pharmacology
Longitudinal Studies
Microbial Sensitivity Tests
Mycobacterium tuberculosis - genetics
Online Only
Tuberculosis, Multidrug-Resistant - drug therapy
Tuberculosis, Multidrug-Resistant - epidemiology
Whole Genome Sequencing
title Sources of Multidrug Resistance in Patients With Previous Isoniazid-Resistant Tuberculosis Identified Using Whole Genome Sequencing: A Longitudinal Cohort Study
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