Genomic diversity in autopsy samples reveals within-host dissemination of HIV-associated Mycobacterium tuberculosis

Genomic analysis of Mycobacterium tuberculosis in postmortem biopsies provides a window into intrahost diversification of a disseminated pathogen. Mycobacterium tuberculosis remains a leading cause of death worldwide, especially among individuals infected with HIV 1 . Whereas phylogenetic analysis h...

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Published inNature medicine Vol. 22; no. 12; pp. 1470 - 1474
Main Authors Lieberman, Tami D, Wilson, Douglas, Misra, Reshma, Xiong, Lealia L, Moodley, Prashini, Cohen, Ted, Kishony, Roy
Format Journal Article
LanguageEnglish
Published New York Nature Publishing Group US 01.12.2016
Nature Publishing Group
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Abstract Genomic analysis of Mycobacterium tuberculosis in postmortem biopsies provides a window into intrahost diversification of a disseminated pathogen. Mycobacterium tuberculosis remains a leading cause of death worldwide, especially among individuals infected with HIV 1 . Whereas phylogenetic analysis has revealed M. tuberculosis spread throughout history 2 , 3 , 4 , 5 and in local outbreaks 6 , 7 , 8 , much less is understood about its dissemination within the body. Here we report genomic analysis of 2,693 samples collected post mortem from lung and extrapulmonary biopsies of 44 subjects in KwaZulu-Natal, South Africa, who received minimal antitubercular treatment and most of whom were HIV seropositive. We found that purifying selection occurred within individual patients, without the need for patient-to-patient transmission. Despite negative selection, mycobacteria diversified within individuals to form sublineages that co-existed for years. These sublineages, as well as distinct strains from mixed infections, were differentially distributed throughout the lung, suggesting temporary barriers to pathogen migration. As a consequence, samples taken from the upper airway often captured only a fraction of the population diversity, challenging current methods of outbreak tracing and resistance diagnostics. Phylogenetic analysis indicated that dissemination from the lungs to extrapulmonary sites was as frequent as between lung sites, supporting the idea of similar migration routes within and between organs, at least in subjects with HIV. Genomic diversity therefore provides a record of pathogen diversification and repeated dissemination across the body.
AbstractList Genomic analysis of Mycobacterium tuberculosis in postmortem biopsies provides a window into intrahost diversification of a disseminated pathogen. Mycobacterium tuberculosis remains a leading cause of death worldwide, especially among individuals infected with HIV 1 . Whereas phylogenetic analysis has revealed M. tuberculosis spread throughout history 2 , 3 , 4 , 5 and in local outbreaks 6 , 7 , 8 , much less is understood about its dissemination within the body. Here we report genomic analysis of 2,693 samples collected post mortem from lung and extrapulmonary biopsies of 44 subjects in KwaZulu-Natal, South Africa, who received minimal antitubercular treatment and most of whom were HIV seropositive. We found that purifying selection occurred within individual patients, without the need for patient-to-patient transmission. Despite negative selection, mycobacteria diversified within individuals to form sublineages that co-existed for years. These sublineages, as well as distinct strains from mixed infections, were differentially distributed throughout the lung, suggesting temporary barriers to pathogen migration. As a consequence, samples taken from the upper airway often captured only a fraction of the population diversity, challenging current methods of outbreak tracing and resistance diagnostics. Phylogenetic analysis indicated that dissemination from the lungs to extrapulmonary sites was as frequent as between lung sites, supporting the idea of similar migration routes within and between organs, at least in subjects with HIV. Genomic diversity therefore provides a record of pathogen diversification and repeated dissemination across the body.
Mycobacterium tuberculosis remains a leading cause of death worldwide, especially among individuals infected with HIV1. Whereas phylogenetic analysis has revealed M. tuberculosis spread throughout history25 and in local outbreaks68, much less is understood about its dissemination within the body. Here we report genomic analysis of 2,693 samples collected post mortem from lung and extrapulmonary biopsies of 44 subjects in KwaZulu-Natal, South Africa, who received minimal antitubercular treatment and most of whom were HIV seropositive. We found that purifying selection occurred within individual patients, without the need for patient-to-patient transmission. Despite negative selection, mycobacteria diversified within individuals to form sublineages that co-existed for years. These sublineages,as well as distinct strains from mixed infections, were differentially distributed throughout the lung, suggesting temporary barriers to pathogen migration. As a consequence, samples taken from the upper airway often captured onlya fraction of the population diversity, challenging current methods of outbreak tracing and resistance diagnostics. Phylogenetic analysis indicated that dissemination from the lungs to extrapulmonary sites was as frequent as between lung sites, supporting the idea of similar migration routes within and between organs, at least in subjects with HIV. Genomic diversity therefore provides a record of pathogen diversification and repeated dissemination across the body.
Mycobacterium tuberculosis remains a leading cause of death worldwide, especially among individuals infected with HIV. Whereas phylogenetic analysis has revealed M. tuberculosis spread throughout history and in local outbreaks, much less is understood about its dissemination within the body. Here we report genomic analysis of 2,693 samples collected post mortem from lung and extrapulmonary biopsies of 44 subjects in KwaZulu-Natal, South Africa, who received minimal antitubercular treatment and most of whom were HIV seropositive. We found that purifying selection occurred within individual patients, without the need for patient-to-patient transmission. Despite negative selection, mycobacteria diversified within individuals to form sublineages that co-existed for years. These sublineages, as well as distinct strains from mixed infections, were differentially distributed throughout the lung, suggesting temporary barriers to pathogen migration. As a consequence, samples taken from the upper airway often captured only a fraction of the population diversity, challenging current methods of outbreak tracing and resistance diagnostics. Phylogenetic analysis indicated that dissemination from the lungs to extrapulmonary sites was as frequent as between lung sites, supporting the idea of similar migration routes within and between organs, at least in subjects with HIV. Genomic diversity therefore provides a record of pathogen diversification and repeated dissemination across the body.
Audience Academic
Author Xiong, Lealia L
Moodley, Prashini
Misra, Reshma
Wilson, Douglas
Kishony, Roy
Lieberman, Tami D
Cohen, Ted
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  organization: Department of Systems Biology, Harvard Medical School, Center for Microbiome Informatics and Therapeutics, Massachusetts Institute of Technology
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  organization: Department of Internal Medicine, Edendale Hospital, University of KwaZulu-Natal
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  orcidid: 0000-0002-5512-9456
  surname: Misra
  fullname: Misra, Reshma
  organization: Department of Infection Prevention and Control, Nelson R Mandela School of Medicine, University of KwaZulu-Natal
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  givenname: Lealia L
  orcidid: 0000-0001-7636-5936
  surname: Xiong
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  surname: Cohen
  fullname: Cohen, Ted
  email: theodore.cohen@yale.edu
  organization: Department of Epidemiology of Microbial Diseases, Yale School of Public Health, Division of Global Health Equity, Brigham and Women's Hospital, Department of Epidemiology, Harvard School of Public Health
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  givenname: Roy
  surname: Kishony
  fullname: Kishony, Roy
  email: rkishony@technion.ac.il
  organization: Department of Systems Biology, Harvard Medical School, Faculty of Biology, Technion–Israel Institute of Technology, Faculty of Computer Science, Technion–Israel Institute of Technology
BackLink https://www.ncbi.nlm.nih.gov/pubmed/27798613$$D View this record in MEDLINE/PubMed
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– reference: JorthPRegional isolation drives bacterial diversification within cystic fibrosis lungsCell Host Microbe20151830731910.1016/j.chom.2015.07.0061:CAS:528:DC%2BC2MXhtlOmtbrK262994324589543
– reference: SsengoobaWde JongBCJolobaMLCobelensFGMeehanCJWhole-genome sequencing reveals mycobacterial microevolution among concurrent isolates from sputum and blood in HIV-infected TB patientsBMC Infect. Dis.20161637110.1186/s12879-016-1737-21:CAS:528:DC%2BC2sXhslartLrM274950024974755
– reference: BosKIPre-Columbian mycobacterial genomes reveal seals as a source of New World human tuberculosisNature201451449449710.1038/nature135911:CAS:528:DC%2BC2cXhvVSmtbnP251411814550673
– reference: MiddlebrookGDubosRJPierceCVirulence and morphological characteristics of mammalian tubercle bacilliJ. Exp. Med.19478617518410.1084/jem.86.2.1751:STN:280:DC%2BC3critVeksg%3D%3D198716652135722
– reference: FischerAVázquez-GarcíaIIllingworthCJRMustonenVHigh-definition reconstruction of clonal composition in cancerCell Rep.20147174017521:CAS:528:DC%2BC2cXpslCgurs%3D248820044062932
– reference: World Health Organization. Global tuberculosis report 2015 1–204 (World Health Organization, Geneva, Switzerland, 2015).
– reference: MankiewiczELiivakMPhage types of Mycobacterium tuberculosis in cultures isolated from Eskimo patientsAm. Rev. Respir. Dis.19751113073121:STN:280:DyaE2M7is1CitQ%3D%3D804287
– reference: CohenTMixed-strain Mycobacterium tuberculosis infections and the implications for tuberculosis treatment and controlClin. Microbiol. Rev.20122570871910.1128/CMR.00021-121:CAS:528:DC%2BC38XhvVWjsbrO230343273485752
– reference: LinPLSterilization of granulomas is common in active and latent tuberculosis despite within-host variability in bacterial killingNat. Med.201420757910.1038/nm.34121:CAS:528:DC%2BC3sXhvFensLrN24336248
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– reference: LiebermanTDGenetic variation of a bacterial pathogen within individuals with cystic fibrosis provides a record of selective pressuresNat. Genet.201446828710.1038/ng.28481:CAS:528:DC%2BC3sXhvV2htr7M24316980
– reference: HatherellH-AInterpreting whole-genome sequencing for investigating tuberculosis transmission: a systematic reviewBMC Med.2016142110.1186/s12916-016-0566-x1:CAS:528:DC%2BC2sXisVGquro%3D270054334804562
– reference: JiaoWVembuSDeshwarAGSteinLMorrisQInferring clonal evolution of tumors from single-nucleotide somatic mutationsBMC Bioinformatics2014153510.1186/1471-2105-15-351:CAS:528:DC%2BC2MXjsFaqur0%3D244843233922638
– reference: CasaliNMicroevolution of extensively drug-resistant tuberculosis in RussiaGenome Res.20122273574510.1101/gr.128678.1111:CAS:528:DC%2BC38Xlt1egtro%3D222945183317155
– reference: TiemersmaEWvan der WerfMJBorgdorffMWWilliamsBGNagelkerkeNJDNatural history of tuberculosis: duration and fatality of untreated pulmonary tuberculosis in HIV-negative patients: a systematic reviewPLoS One20116e1760110.1371/journal.pone.00176011:CAS:528:DC%2BC3MXkvVers7Y%3D214837323070694
– reference: Pérez-LagoLWhole-genome sequencing analysis of intrapatient microevolution in Mycobacterium tuberculosis: potential impact on the inference of tuberculosis transmissionJ. Infect. Dis.20142099810810.1093/infdis/jit43923945373
– reference: CohenKAEvolution of extensively drug-resistant tuberculosis over four decades: whole-genome sequencing and dating analysis of Mycobacterium tuberculosis isolates from KwaZulu-NatalPLoS Med.201512e100188010.1371/journal.pmed.10018801:CAS:528:DC%2BC1cXltlCnsrY%3D264187374587932
– reference: BaymMInexpensive multiplexed library preparation for megabase-sized genomesPLoS One201510e0128036260007374441430
– reference: LeeRSPopulation genomics of Mycobacterium tuberculosis in the InuitProc. Natl. Acad. Sci. USA2015112136091361410.1073/pnas.15070711121:CAS:528:DC%2BC2MXhs1yksbbE264834624640744
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– reference: ZetolaNMClinical outcomes among persons with pulmonary tuberculosis caused by Mycobacterium tuberculosis isolates with phenotypic heterogeneity in results of drug-susceptibility testsJ. Infect. Dis.20142091754176310.1093/infdis/jiu0401:CAS:528:DC%2BC2cXnvVSnurk%3D244435464017367
– reference: Guerra-AssunçãoJALarge-scale whole-genome sequencing of M. tuberculosis provides insights into transmission in a high-prevalence areaeLife20154e0516610.7554/eLife.051661:CAS:528:DC%2BC28XpsFyqt7g%3D4384740
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– reference: LiuQWithin-patient microevolution of Mycobacterium tuberculosis correlates with heterogeneous responses to treatmentSci. Rep.201551750710.1038/srep175071:CAS:528:DC%2BC2MXhvFGntbvE266204464664930
– reference: PatersonGKCapturing the cloud of diversity reveals complexity and heterogeneity of MRSA carriage, infection and transmissionNat. Commun.20156656010.1038/ncomms75601:CAS:528:DC%2BC2MXosFeltbk%3D25814293
– reference: ColijnCCohenTGaneshAMurrayMSpontaneous emergence of multiple drug resistance in tuberculosis before and during therapyPLoS One20116e1832710.1371/journal.pone.00183271:CAS:528:DC%2BC3MXkslyisr0%3D214791713068161
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Snippet Genomic analysis of Mycobacterium tuberculosis in postmortem biopsies provides a window into intrahost diversification of a disseminated pathogen....
Mycobacterium tuberculosis remains a leading cause of death worldwide, especially among individuals infected with HIV. Whereas phylogenetic analysis has...
Mycobacterium tuberculosis remains a leading cause of death worldwide, especially among individuals infected with HIV1. Whereas phylogenetic analysis has...
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pubmed
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springer
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StartPage 1470
SubjectTerms 631/181/2474
631/326/107
631/326/325/2482
692/308/174
692/699/255/1856
Adult
Aged
Autopsies
Autopsy
Bacteria
Bacteriological Techniques
Biodiversity
Biomedicine
Cancer Research
Coinfection - microbiology
DNA, Bacterial - genetics
Female
Genetic aspects
Genetic diversity
Genetic Variation
Genomics
HIV
HIV Infections - complications
Human immunodeficiency virus
Humans
Infectious Diseases
Lentivirus
letter
Liver - microbiology
Lung - microbiology
Lymph Nodes - microbiology
Male
Metabolic Diseases
Middle Aged
Molecular Medicine
Mycobacterium tuberculosis
Mycobacterium tuberculosis - genetics
Neurosciences
Outbreaks
Pathogens
Phylogeny
Polymorphism, Single Nucleotide
Retroviridae
South Africa
Spleen - microbiology
Tuberculosis
Tuberculosis - complications
Tuberculosis - microbiology
Tuberculosis, Hepatic - complications
Tuberculosis, Hepatic - microbiology
Tuberculosis, Lymph Node - complications
Tuberculosis, Lymph Node - microbiology
Tuberculosis, Pulmonary - complications
Tuberculosis, Pulmonary - microbiology
Tuberculosis, Splenic - complications
Tuberculosis, Splenic - microbiology
Title Genomic diversity in autopsy samples reveals within-host dissemination of HIV-associated Mycobacterium tuberculosis
URI https://link.springer.com/article/10.1038/nm.4205
https://www.ncbi.nlm.nih.gov/pubmed/27798613
https://www.proquest.com/docview/1846364131
https://www.proquest.com/docview/1835003426
https://www.proquest.com/docview/1855078724
Volume 22
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