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 in | Nature medicine Vol. 22; no. 12; pp. 1470 - 1474 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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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 |
Author_xml | – sequence: 1 givenname: Tami D surname: Lieberman fullname: Lieberman, Tami D organization: Department of Systems Biology, Harvard Medical School, Center for Microbiome Informatics and Therapeutics, Massachusetts Institute of Technology – sequence: 2 givenname: Douglas surname: Wilson fullname: Wilson, Douglas organization: Department of Internal Medicine, Edendale Hospital, University of KwaZulu-Natal – sequence: 3 givenname: Reshma 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 – sequence: 4 givenname: Lealia L orcidid: 0000-0001-7636-5936 surname: Xiong fullname: Xiong, Lealia L organization: Department of Systems Biology, Harvard Medical School – sequence: 5 givenname: Prashini surname: Moodley fullname: Moodley, Prashini organization: Department of Infection Prevention and Control, Nelson R Mandela School of Medicine, University of KwaZulu-Natal – sequence: 6 givenname: Ted 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 – sequence: 7 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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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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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 |
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