Genomic epidemiology of tuberculosis in eastern Malaysia: insights for strengthening public health responses
Tuberculosis is a leading public health priority in eastern Malaysia. Knowledge of the genomic epidemiology of tuberculosis can help tailor public health interventions. Our aims were to determine tuberculosis genomic epidemiology and characterize resistance mutations in the ethnically diverse city o...
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| Veröffentlicht in: | Microbial genomics 2021-05, Vol.7 (5) |
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| description | Tuberculosis is a leading public health priority in eastern Malaysia. Knowledge of the genomic epidemiology of tuberculosis can help tailor public health interventions. Our aims were to determine tuberculosis genomic epidemiology and characterize resistance mutations in the ethnically diverse city of Kota Kinabalu, Sabah, located at the nexus of Malaysia, Indonesia, Philippines and Brunei. We used an archive of prospectively collected
samples paired with epidemiological data. We collected sputum and demographic data from consecutive consenting outpatients with pulmonary tuberculosis at the largest tuberculosis clinic from 2012 to 2014, and selected samples from tuberculosis inpatients from the tertiary referral centre during 2012-2014 and 2016-2017. Two hundred and eight
.
sequences were available for analysis, representing 8 % of cases notified during the study periods. Whole-genome phylogenetic analysis demonstrated that most strains were lineage 1 (195/208, 93.8 %), with the remainder being lineages 2 (8/208, 3.8 %) or 4 (5/208, 2.4 %). Lineages or sub-lineages were not associated with patient ethnicity. The lineage 1 strains were diverse, with sub-lineage 1.2.1 being dominant (192, 98 %). Lineage 1.2.1.3 isolates were geographically most widely distributed. The greatest diversity occurred in a border town sub-district. The time to the most recent common ancestor for the three major lineage 1.2.1 clades was estimated to be the year 1966 (95 % HPD 1948-1976). An association was found between failure of culture conversion by week 8 of treatment and infection with lineage 2 (4/6, 67 %) compared with lineage 1 strains (4/83, 5 %) ( |
| doi_str_mv | 10.1099/mgen.0.000573 |
| format | Article |
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samples paired with epidemiological data. We collected sputum and demographic data from consecutive consenting outpatients with pulmonary tuberculosis at the largest tuberculosis clinic from 2012 to 2014, and selected samples from tuberculosis inpatients from the tertiary referral centre during 2012-2014 and 2016-2017. Two hundred and eight
.
sequences were available for analysis, representing 8 % of cases notified during the study periods. Whole-genome phylogenetic analysis demonstrated that most strains were lineage 1 (195/208, 93.8 %), with the remainder being lineages 2 (8/208, 3.8 %) or 4 (5/208, 2.4 %). Lineages or sub-lineages were not associated with patient ethnicity. The lineage 1 strains were diverse, with sub-lineage 1.2.1 being dominant (192, 98 %). Lineage 1.2.1.3 isolates were geographically most widely distributed. The greatest diversity occurred in a border town sub-district. The time to the most recent common ancestor for the three major lineage 1.2.1 clades was estimated to be the year 1966 (95 % HPD 1948-1976). An association was found between failure of culture conversion by week 8 of treatment and infection with lineage 2 (4/6, 67 %) compared with lineage 1 strains (4/83, 5 %) (
<0.001), supporting evidence of greater virulence of lineage 2 strains. Eleven potential transmission clusters (SNP difference ≤12) were identified; at least five included people living in different sub-districts. Some linked cases spanned the whole 4-year study period. One cluster involved a multidrug-resistant tuberculosis strain matching a drug-susceptible strain from 3 years earlier. Drug resistance mutations were uncommon, but revealed one phenotype-genotype mismatch in a genotypically multidrug-resistant isolate, and rare nonsense mutations within the
gene in two isolates. Consistent with the regionally mobile population,
strains in Kota Kinabalu were diverse, although several lineage 1 strains dominated and were locally well established. Transmission clusters - uncommonly identified, likely attributable to incomplete sampling - showed clustering occurring across the community, not confined to households or sub-districts. The findings indicate that public health priorities should include active case finding and early institution of tuberculosis management in mobile populations, while there is a need to upscale effective contact investigation beyond households to include other contacts within social networks.</description><identifier>ISSN: 2057-5858</identifier><identifier>EISSN: 2057-5858</identifier><identifier>DOI: 10.1099/mgen.0.000573</identifier><identifier>PMID: 33945455</identifier><language>eng</language><publisher>England: Microbiology Society</publisher><subject>Adolescent ; Adult ; Cluster Analysis ; Female ; Genome, Bacterial ; Genomics ; Genotype ; Humans ; Malaysia - epidemiology ; Male ; Molecular Epidemiology ; Mutation ; Mycobacterium tuberculosis - classification ; Mycobacterium tuberculosis - genetics ; Phylogeny ; Public Health ; Sputum ; Tuberculosis - epidemiology ; Tuberculosis - transmission ; Tuberculosis, Multidrug-Resistant - epidemiology ; Tuberculosis, Pulmonary - epidemiology ; Whole Genome Sequencing ; Young Adult</subject><ispartof>Microbial genomics, 2021-05, Vol.7 (5)</ispartof><rights>2021 The Authors 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-3a32851a7408fbbe06d3b5a9b55da4832f340fb446a3c4db761e9a0edfa944053</citedby><cites>FETCH-LOGICAL-c387t-3a32851a7408fbbe06d3b5a9b55da4832f340fb446a3c4db761e9a0edfa944053</cites><orcidid>0000-0001-7993-820X ; 0000-0002-2253-5749 ; 0000-0002-4300-455X ; 0000-0002-0197-7820 ; 0000-0002-8123-476X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8209721/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8209721/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,862,883,27907,27908,53774,53776</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33945455$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bainomugisa, Arnold</creatorcontrib><creatorcontrib>Meumann, Ella M</creatorcontrib><creatorcontrib>Rajahram, Giri Shan</creatorcontrib><creatorcontrib>Ong, Rick Twee-Hee</creatorcontrib><creatorcontrib>Coin, Lachlan</creatorcontrib><creatorcontrib>Paul, Dawn Carmel</creatorcontrib><creatorcontrib>William, Timothy</creatorcontrib><creatorcontrib>Coulter, Christopher</creatorcontrib><creatorcontrib>Ralph, Anna P</creatorcontrib><title>Genomic epidemiology of tuberculosis in eastern Malaysia: insights for strengthening public health responses</title><title>Microbial genomics</title><addtitle>Microb Genom</addtitle><description>Tuberculosis is a leading public health priority in eastern Malaysia. Knowledge of the genomic epidemiology of tuberculosis can help tailor public health interventions. Our aims were to determine tuberculosis genomic epidemiology and characterize resistance mutations in the ethnically diverse city of Kota Kinabalu, Sabah, located at the nexus of Malaysia, Indonesia, Philippines and Brunei. We used an archive of prospectively collected
samples paired with epidemiological data. We collected sputum and demographic data from consecutive consenting outpatients with pulmonary tuberculosis at the largest tuberculosis clinic from 2012 to 2014, and selected samples from tuberculosis inpatients from the tertiary referral centre during 2012-2014 and 2016-2017. Two hundred and eight
.
sequences were available for analysis, representing 8 % of cases notified during the study periods. Whole-genome phylogenetic analysis demonstrated that most strains were lineage 1 (195/208, 93.8 %), with the remainder being lineages 2 (8/208, 3.8 %) or 4 (5/208, 2.4 %). Lineages or sub-lineages were not associated with patient ethnicity. The lineage 1 strains were diverse, with sub-lineage 1.2.1 being dominant (192, 98 %). Lineage 1.2.1.3 isolates were geographically most widely distributed. The greatest diversity occurred in a border town sub-district. The time to the most recent common ancestor for the three major lineage 1.2.1 clades was estimated to be the year 1966 (95 % HPD 1948-1976). An association was found between failure of culture conversion by week 8 of treatment and infection with lineage 2 (4/6, 67 %) compared with lineage 1 strains (4/83, 5 %) (
<0.001), supporting evidence of greater virulence of lineage 2 strains. Eleven potential transmission clusters (SNP difference ≤12) were identified; at least five included people living in different sub-districts. Some linked cases spanned the whole 4-year study period. One cluster involved a multidrug-resistant tuberculosis strain matching a drug-susceptible strain from 3 years earlier. Drug resistance mutations were uncommon, but revealed one phenotype-genotype mismatch in a genotypically multidrug-resistant isolate, and rare nonsense mutations within the
gene in two isolates. Consistent with the regionally mobile population,
strains in Kota Kinabalu were diverse, although several lineage 1 strains dominated and were locally well established. Transmission clusters - uncommonly identified, likely attributable to incomplete sampling - showed clustering occurring across the community, not confined to households or sub-districts. The findings indicate that public health priorities should include active case finding and early institution of tuberculosis management in mobile populations, while there is a need to upscale effective contact investigation beyond households to include other contacts within social networks.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Cluster Analysis</subject><subject>Female</subject><subject>Genome, Bacterial</subject><subject>Genomics</subject><subject>Genotype</subject><subject>Humans</subject><subject>Malaysia - epidemiology</subject><subject>Male</subject><subject>Molecular Epidemiology</subject><subject>Mutation</subject><subject>Mycobacterium tuberculosis - classification</subject><subject>Mycobacterium tuberculosis - genetics</subject><subject>Phylogeny</subject><subject>Public Health</subject><subject>Sputum</subject><subject>Tuberculosis - epidemiology</subject><subject>Tuberculosis - transmission</subject><subject>Tuberculosis, Multidrug-Resistant - epidemiology</subject><subject>Tuberculosis, Pulmonary - epidemiology</subject><subject>Whole Genome Sequencing</subject><subject>Young Adult</subject><issn>2057-5858</issn><issn>2057-5858</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkcGL1TAQxoMo7rLu0avk6KXPtEnaxIMgi67Cihc9h2k7bSNp8sykwvvv7fLWZT19w8yPbz74GHtdi0MtrH23zhgP4iCE0J18xi6bXStttHn-ZL5g10S_dqbWprWdfskupLRKK60vWbjFmFY_cDz6EVefQppPPE28bD3mYQuJPHEfOQIVzJF_gwAn8vB-X5Kfl0J8SplTyRjnsmD0cebHrQ-754IQysIz0jFFQnrFXkwQCK8f9Ir9_Pzpx82X6u777debj3fVIE1XKgmyMbqGTgkz9T2KdpS9BttrPYIyspmkElOvVAtyUGPftTVaEDhOYJUSWl6xD2ffPceK44CxZAjumP0K-eQSePf_JfrFzemPM42wXVPvBm8fDHL6vSEVt3oaMASImDZyjW4aaVuj7Y5WZ3TIiSjj9PimFu6-JHdfkhPuXNLOv3ma7ZH-V4n8CwOykX4</recordid><startdate>20210501</startdate><enddate>20210501</enddate><creator>Bainomugisa, Arnold</creator><creator>Meumann, Ella M</creator><creator>Rajahram, Giri Shan</creator><creator>Ong, Rick Twee-Hee</creator><creator>Coin, Lachlan</creator><creator>Paul, Dawn Carmel</creator><creator>William, Timothy</creator><creator>Coulter, Christopher</creator><creator>Ralph, Anna P</creator><general>Microbiology Society</general><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/0000-0001-7993-820X</orcidid><orcidid>https://orcid.org/0000-0002-2253-5749</orcidid><orcidid>https://orcid.org/0000-0002-4300-455X</orcidid><orcidid>https://orcid.org/0000-0002-0197-7820</orcidid><orcidid>https://orcid.org/0000-0002-8123-476X</orcidid></search><sort><creationdate>20210501</creationdate><title>Genomic epidemiology of tuberculosis in eastern Malaysia: insights for strengthening public health responses</title><author>Bainomugisa, Arnold ; 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Knowledge of the genomic epidemiology of tuberculosis can help tailor public health interventions. Our aims were to determine tuberculosis genomic epidemiology and characterize resistance mutations in the ethnically diverse city of Kota Kinabalu, Sabah, located at the nexus of Malaysia, Indonesia, Philippines and Brunei. We used an archive of prospectively collected
samples paired with epidemiological data. We collected sputum and demographic data from consecutive consenting outpatients with pulmonary tuberculosis at the largest tuberculosis clinic from 2012 to 2014, and selected samples from tuberculosis inpatients from the tertiary referral centre during 2012-2014 and 2016-2017. Two hundred and eight
.
sequences were available for analysis, representing 8 % of cases notified during the study periods. Whole-genome phylogenetic analysis demonstrated that most strains were lineage 1 (195/208, 93.8 %), with the remainder being lineages 2 (8/208, 3.8 %) or 4 (5/208, 2.4 %). Lineages or sub-lineages were not associated with patient ethnicity. The lineage 1 strains were diverse, with sub-lineage 1.2.1 being dominant (192, 98 %). Lineage 1.2.1.3 isolates were geographically most widely distributed. The greatest diversity occurred in a border town sub-district. The time to the most recent common ancestor for the three major lineage 1.2.1 clades was estimated to be the year 1966 (95 % HPD 1948-1976). An association was found between failure of culture conversion by week 8 of treatment and infection with lineage 2 (4/6, 67 %) compared with lineage 1 strains (4/83, 5 %) (
<0.001), supporting evidence of greater virulence of lineage 2 strains. Eleven potential transmission clusters (SNP difference ≤12) were identified; at least five included people living in different sub-districts. Some linked cases spanned the whole 4-year study period. One cluster involved a multidrug-resistant tuberculosis strain matching a drug-susceptible strain from 3 years earlier. Drug resistance mutations were uncommon, but revealed one phenotype-genotype mismatch in a genotypically multidrug-resistant isolate, and rare nonsense mutations within the
gene in two isolates. Consistent with the regionally mobile population,
strains in Kota Kinabalu were diverse, although several lineage 1 strains dominated and were locally well established. Transmission clusters - uncommonly identified, likely attributable to incomplete sampling - showed clustering occurring across the community, not confined to households or sub-districts. The findings indicate that public health priorities should include active case finding and early institution of tuberculosis management in mobile populations, while there is a need to upscale effective contact investigation beyond households to include other contacts within social networks.</abstract><cop>England</cop><pub>Microbiology Society</pub><pmid>33945455</pmid><doi>10.1099/mgen.0.000573</doi><orcidid>https://orcid.org/0000-0001-7993-820X</orcidid><orcidid>https://orcid.org/0000-0002-2253-5749</orcidid><orcidid>https://orcid.org/0000-0002-4300-455X</orcidid><orcidid>https://orcid.org/0000-0002-0197-7820</orcidid><orcidid>https://orcid.org/0000-0002-8123-476X</orcidid><oa>free_for_read</oa></addata></record> |
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| subjects | Adolescent Adult Cluster Analysis Female Genome, Bacterial Genomics Genotype Humans Malaysia - epidemiology Male Molecular Epidemiology Mutation Mycobacterium tuberculosis - classification Mycobacterium tuberculosis - genetics Phylogeny Public Health Sputum Tuberculosis - epidemiology Tuberculosis - transmission Tuberculosis, Multidrug-Resistant - epidemiology Tuberculosis, Pulmonary - epidemiology Whole Genome Sequencing Young Adult |
| title | Genomic epidemiology of tuberculosis in eastern Malaysia: insights for strengthening public health responses |
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