Loading…

Restricted Structural Gene Polymorphism in the Mycobacterium tuberculosis Complex Indicates Evolutionarily Recent Global Dissemination

One-third of humans are infected with Mycobacterium tuberculosis, the causative agent of tuberculosis. Sequence analysis of two megabases in 26 structural genes or loci in strains recovered globally discovered a striking reduction of silent nucleotide substitutions compared with other human bacteria...

Full description

Saved in:
Bibliographic Details
Published in:Proceedings of the National Academy of Sciences - PNAS 1997-09, Vol.94 (18), p.9869-9874
Main Authors: Sreevatsan, Srinand, Pan, Xi, Stockbauer, Kathryn E., Connell, Nancy D., Kreiswirth, Barry N., Whittam, Thomas S., Musser, James M.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c518t-d189c7c7fc4193b2d3f8ab99ed8c6bdb0b36fb12e02ec6c8d7f675bf152f8b173
cites cdi_FETCH-LOGICAL-c518t-d189c7c7fc4193b2d3f8ab99ed8c6bdb0b36fb12e02ec6c8d7f675bf152f8b173
container_end_page 9874
container_issue 18
container_start_page 9869
container_title Proceedings of the National Academy of Sciences - PNAS
container_volume 94
creator Sreevatsan, Srinand
Pan, Xi
Stockbauer, Kathryn E.
Connell, Nancy D.
Kreiswirth, Barry N.
Whittam, Thomas S.
Musser, James M.
description One-third of humans are infected with Mycobacterium tuberculosis, the causative agent of tuberculosis. Sequence analysis of two megabases in 26 structural genes or loci in strains recovered globally discovered a striking reduction of silent nucleotide substitutions compared with other human bacterial pathogens. The lack of neutral mutations in structural genes indicates that M. tuberculosis is evolutionarily young and has recently spread globally. Species diversity is largely caused by rapidly evolving insertion sequences, which means that mobile element movement is a fundamental process generating genomic variation in this pathogen. Three genetic groups of M. tuberculosis were identified based on two polymorphisms that occur at high frequency in the genes encoding catalase-peroxidase and the A subunit of gyrase. Group 1 organisms are evolutionarily old and allied with M. bovis, the cause of bovine tuberculosis. A subset of several distinct insertion sequence IS6110 subtypes of this genetic group have IS6110 integrated at the identical chromosomal insertion site, located between dnaA and dnaN in the region containing the origin of replication. Remarkably, study of ≈ 6,000 isolates from patients in Houston and the New York City area discovered that 47 of 48 relatively large case clusters were caused by genotypic group 1 and 2 but not group 3 organisms. The observation that the newly emergent group 3 organisms are associated with sporadic rather than clustered cases suggests that the pathogen is evolving toward a state of reduced transmissability or virulence.
doi_str_mv 10.1073/pnas.94.18.9869
format article
fullrecord <record><control><sourceid>jstor_pnas_</sourceid><recordid>TN_cdi_pnas_primary_94_18_9869</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>43119</jstor_id><sourcerecordid>43119</sourcerecordid><originalsourceid>FETCH-LOGICAL-c518t-d189c7c7fc4193b2d3f8ab99ed8c6bdb0b36fb12e02ec6c8d7f675bf152f8b173</originalsourceid><addsrcrecordid>eNqFkktvEzEUhUcIVEJhjYQEsljAKqmvZzJjS2xQWkKlIlCBtWV7PMSRZzz1o2r-QH83HiWKCgtY3cX5ztF9FcVLwAvATXk2DiIsWLUAumC0Zo-KGWAG87pi-HExw5g0c1qR6mnxLIQtxpgtKT4pThhplgTorLi_1iF6o6Ju0ffok4rJC4vWetDom7O73vlxY0KPzIDiRqMvO-WkyLg3qUcxSe1Vsi6YgFauH62-Q5dDa5SIOqCLW2dTNG4Q3tgdutZKDxGtbU6w6NyEoHsziAl4XjzphA36xaGeFj8_XfxYfZ5ffV1frj5ezdUSaJy3QJlqVNOpClgpSVt2VEjGdEtVLVuJZVl3EojGRKta0bbp6mYpO1iSjkpoytPiwz53TLLX7dRPHpeP3vTC77gThv-pDGbDf7lbTkpCq2x_d7B7d5Py5nhvgtLWikG7FHjDSFU2GP8XhBowroBm8O1f4NYlP-QdcIKhBFLClHa2h5R3IXjdHRsGzKc34NMbcFZxoHx6g-x4_XDOI3-4e9bfHPTJeFQfBrz_J8C7ZG3UdzGTr_bkNkTnj2hVQj7Rb3Bz1Mo</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>201312310</pqid></control><display><type>article</type><title>Restricted Structural Gene Polymorphism in the Mycobacterium tuberculosis Complex Indicates Evolutionarily Recent Global Dissemination</title><source>Open Access: PubMed Central</source><source>JSTOR</source><creator>Sreevatsan, Srinand ; Pan, Xi ; Stockbauer, Kathryn E. ; Connell, Nancy D. ; Kreiswirth, Barry N. ; Whittam, Thomas S. ; Musser, James M.</creator><creatorcontrib>Sreevatsan, Srinand ; Pan, Xi ; Stockbauer, Kathryn E. ; Connell, Nancy D. ; Kreiswirth, Barry N. ; Whittam, Thomas S. ; Musser, James M.</creatorcontrib><description>One-third of humans are infected with Mycobacterium tuberculosis, the causative agent of tuberculosis. Sequence analysis of two megabases in 26 structural genes or loci in strains recovered globally discovered a striking reduction of silent nucleotide substitutions compared with other human bacterial pathogens. The lack of neutral mutations in structural genes indicates that M. tuberculosis is evolutionarily young and has recently spread globally. Species diversity is largely caused by rapidly evolving insertion sequences, which means that mobile element movement is a fundamental process generating genomic variation in this pathogen. Three genetic groups of M. tuberculosis were identified based on two polymorphisms that occur at high frequency in the genes encoding catalase-peroxidase and the A subunit of gyrase. Group 1 organisms are evolutionarily old and allied with M. bovis, the cause of bovine tuberculosis. A subset of several distinct insertion sequence IS6110 subtypes of this genetic group have IS6110 integrated at the identical chromosomal insertion site, located between dnaA and dnaN in the region containing the origin of replication. Remarkably, study of ≈ 6,000 isolates from patients in Houston and the New York City area discovered that 47 of 48 relatively large case clusters were caused by genotypic group 1 and 2 but not group 3 organisms. The observation that the newly emergent group 3 organisms are associated with sporadic rather than clustered cases suggests that the pathogen is evolving toward a state of reduced transmissability or virulence.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.94.18.9869</identifier><identifier>PMID: 9275218</identifier><language>eng</language><publisher>United States: National Academy of Sciences of the United States of America</publisher><subject>Alleles ; Animals ; Bacteria ; Biological Evolution ; Biological Sciences ; Cattle ; Codons ; Evolution ; Genes, Bacterial ; Genetic variation ; Genetics ; Genomics ; Humans ; Mycobacterium tuberculosis ; Mycobacterium tuberculosis - genetics ; Nucleotides ; Pathogens ; Polymorphism, Genetic ; Transposons ; Tuberculosis</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1997-09, Vol.94 (18), p.9869-9874</ispartof><rights>Copyright 1993-1997 National Academy of Sciences</rights><rights>Copyright National Academy of Sciences Sep 2, 1997</rights><rights>Copyright © 1997, The National Academy of Sciences of the USA 1997</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c518t-d189c7c7fc4193b2d3f8ab99ed8c6bdb0b36fb12e02ec6c8d7f675bf152f8b173</citedby><cites>FETCH-LOGICAL-c518t-d189c7c7fc4193b2d3f8ab99ed8c6bdb0b36fb12e02ec6c8d7f675bf152f8b173</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/94/18.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/43119$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/43119$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,53769,53771,58216,58449</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9275218$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sreevatsan, Srinand</creatorcontrib><creatorcontrib>Pan, Xi</creatorcontrib><creatorcontrib>Stockbauer, Kathryn E.</creatorcontrib><creatorcontrib>Connell, Nancy D.</creatorcontrib><creatorcontrib>Kreiswirth, Barry N.</creatorcontrib><creatorcontrib>Whittam, Thomas S.</creatorcontrib><creatorcontrib>Musser, James M.</creatorcontrib><title>Restricted Structural Gene Polymorphism in the Mycobacterium tuberculosis Complex Indicates Evolutionarily Recent Global Dissemination</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>One-third of humans are infected with Mycobacterium tuberculosis, the causative agent of tuberculosis. Sequence analysis of two megabases in 26 structural genes or loci in strains recovered globally discovered a striking reduction of silent nucleotide substitutions compared with other human bacterial pathogens. The lack of neutral mutations in structural genes indicates that M. tuberculosis is evolutionarily young and has recently spread globally. Species diversity is largely caused by rapidly evolving insertion sequences, which means that mobile element movement is a fundamental process generating genomic variation in this pathogen. Three genetic groups of M. tuberculosis were identified based on two polymorphisms that occur at high frequency in the genes encoding catalase-peroxidase and the A subunit of gyrase. Group 1 organisms are evolutionarily old and allied with M. bovis, the cause of bovine tuberculosis. A subset of several distinct insertion sequence IS6110 subtypes of this genetic group have IS6110 integrated at the identical chromosomal insertion site, located between dnaA and dnaN in the region containing the origin of replication. Remarkably, study of ≈ 6,000 isolates from patients in Houston and the New York City area discovered that 47 of 48 relatively large case clusters were caused by genotypic group 1 and 2 but not group 3 organisms. The observation that the newly emergent group 3 organisms are associated with sporadic rather than clustered cases suggests that the pathogen is evolving toward a state of reduced transmissability or virulence.</description><subject>Alleles</subject><subject>Animals</subject><subject>Bacteria</subject><subject>Biological Evolution</subject><subject>Biological Sciences</subject><subject>Cattle</subject><subject>Codons</subject><subject>Evolution</subject><subject>Genes, Bacterial</subject><subject>Genetic variation</subject><subject>Genetics</subject><subject>Genomics</subject><subject>Humans</subject><subject>Mycobacterium tuberculosis</subject><subject>Mycobacterium tuberculosis - genetics</subject><subject>Nucleotides</subject><subject>Pathogens</subject><subject>Polymorphism, Genetic</subject><subject>Transposons</subject><subject>Tuberculosis</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNqFkktvEzEUhUcIVEJhjYQEsljAKqmvZzJjS2xQWkKlIlCBtWV7PMSRZzz1o2r-QH83HiWKCgtY3cX5ztF9FcVLwAvATXk2DiIsWLUAumC0Zo-KGWAG87pi-HExw5g0c1qR6mnxLIQtxpgtKT4pThhplgTorLi_1iF6o6Ju0ffok4rJC4vWetDom7O73vlxY0KPzIDiRqMvO-WkyLg3qUcxSe1Vsi6YgFauH62-Q5dDa5SIOqCLW2dTNG4Q3tgdutZKDxGtbU6w6NyEoHsziAl4XjzphA36xaGeFj8_XfxYfZ5ffV1frj5ezdUSaJy3QJlqVNOpClgpSVt2VEjGdEtVLVuJZVl3EojGRKta0bbp6mYpO1iSjkpoytPiwz53TLLX7dRPHpeP3vTC77gThv-pDGbDf7lbTkpCq2x_d7B7d5Py5nhvgtLWikG7FHjDSFU2GP8XhBowroBm8O1f4NYlP-QdcIKhBFLClHa2h5R3IXjdHRsGzKc34NMbcFZxoHx6g-x4_XDOI3-4e9bfHPTJeFQfBrz_J8C7ZG3UdzGTr_bkNkTnj2hVQj7Rb3Bz1Mo</recordid><startdate>19970902</startdate><enddate>19970902</enddate><creator>Sreevatsan, Srinand</creator><creator>Pan, Xi</creator><creator>Stockbauer, Kathryn E.</creator><creator>Connell, Nancy D.</creator><creator>Kreiswirth, Barry N.</creator><creator>Whittam, Thomas S.</creator><creator>Musser, James M.</creator><general>National Academy of Sciences of the United States of America</general><general>National Acad Sciences</general><general>National Academy of Sciences</general><general>The National Academy of Sciences of the USA</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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19970902</creationdate><title>Restricted Structural Gene Polymorphism in the Mycobacterium tuberculosis Complex Indicates Evolutionarily Recent Global Dissemination</title><author>Sreevatsan, Srinand ; Pan, Xi ; Stockbauer, Kathryn E. ; Connell, Nancy D. ; Kreiswirth, Barry N. ; Whittam, Thomas S. ; Musser, James M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c518t-d189c7c7fc4193b2d3f8ab99ed8c6bdb0b36fb12e02ec6c8d7f675bf152f8b173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Alleles</topic><topic>Animals</topic><topic>Bacteria</topic><topic>Biological Evolution</topic><topic>Biological Sciences</topic><topic>Cattle</topic><topic>Codons</topic><topic>Evolution</topic><topic>Genes, Bacterial</topic><topic>Genetic variation</topic><topic>Genetics</topic><topic>Genomics</topic><topic>Humans</topic><topic>Mycobacterium tuberculosis</topic><topic>Mycobacterium tuberculosis - genetics</topic><topic>Nucleotides</topic><topic>Pathogens</topic><topic>Polymorphism, Genetic</topic><topic>Transposons</topic><topic>Tuberculosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sreevatsan, Srinand</creatorcontrib><creatorcontrib>Pan, Xi</creatorcontrib><creatorcontrib>Stockbauer, Kathryn E.</creatorcontrib><creatorcontrib>Connell, Nancy D.</creatorcontrib><creatorcontrib>Kreiswirth, Barry N.</creatorcontrib><creatorcontrib>Whittam, Thomas S.</creatorcontrib><creatorcontrib>Musser, James M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sreevatsan, Srinand</au><au>Pan, Xi</au><au>Stockbauer, Kathryn E.</au><au>Connell, Nancy D.</au><au>Kreiswirth, Barry N.</au><au>Whittam, Thomas S.</au><au>Musser, James M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Restricted Structural Gene Polymorphism in the Mycobacterium tuberculosis Complex Indicates Evolutionarily Recent Global Dissemination</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>1997-09-02</date><risdate>1997</risdate><volume>94</volume><issue>18</issue><spage>9869</spage><epage>9874</epage><pages>9869-9874</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>One-third of humans are infected with Mycobacterium tuberculosis, the causative agent of tuberculosis. Sequence analysis of two megabases in 26 structural genes or loci in strains recovered globally discovered a striking reduction of silent nucleotide substitutions compared with other human bacterial pathogens. The lack of neutral mutations in structural genes indicates that M. tuberculosis is evolutionarily young and has recently spread globally. Species diversity is largely caused by rapidly evolving insertion sequences, which means that mobile element movement is a fundamental process generating genomic variation in this pathogen. Three genetic groups of M. tuberculosis were identified based on two polymorphisms that occur at high frequency in the genes encoding catalase-peroxidase and the A subunit of gyrase. Group 1 organisms are evolutionarily old and allied with M. bovis, the cause of bovine tuberculosis. A subset of several distinct insertion sequence IS6110 subtypes of this genetic group have IS6110 integrated at the identical chromosomal insertion site, located between dnaA and dnaN in the region containing the origin of replication. Remarkably, study of ≈ 6,000 isolates from patients in Houston and the New York City area discovered that 47 of 48 relatively large case clusters were caused by genotypic group 1 and 2 but not group 3 organisms. The observation that the newly emergent group 3 organisms are associated with sporadic rather than clustered cases suggests that the pathogen is evolving toward a state of reduced transmissability or virulence.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>9275218</pmid><doi>10.1073/pnas.94.18.9869</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0027-8424
ispartof Proceedings of the National Academy of Sciences - PNAS, 1997-09, Vol.94 (18), p.9869-9874
issn 0027-8424
1091-6490
language eng
recordid cdi_pnas_primary_94_18_9869
source Open Access: PubMed Central; JSTOR
subjects Alleles
Animals
Bacteria
Biological Evolution
Biological Sciences
Cattle
Codons
Evolution
Genes, Bacterial
Genetic variation
Genetics
Genomics
Humans
Mycobacterium tuberculosis
Mycobacterium tuberculosis - genetics
Nucleotides
Pathogens
Polymorphism, Genetic
Transposons
Tuberculosis
title Restricted Structural Gene Polymorphism in the Mycobacterium tuberculosis Complex Indicates Evolutionarily Recent Global Dissemination
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-23T13%3A07%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_pnas_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Restricted%20Structural%20Gene%20Polymorphism%20in%20the%20Mycobacterium%20tuberculosis%20Complex%20Indicates%20Evolutionarily%20Recent%20Global%20Dissemination&rft.jtitle=Proceedings%20of%20the%20National%20Academy%20of%20Sciences%20-%20PNAS&rft.au=Sreevatsan,%20Srinand&rft.date=1997-09-02&rft.volume=94&rft.issue=18&rft.spage=9869&rft.epage=9874&rft.pages=9869-9874&rft.issn=0027-8424&rft.eissn=1091-6490&rft_id=info:doi/10.1073/pnas.94.18.9869&rft_dat=%3Cjstor_pnas_%3E43119%3C/jstor_pnas_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c518t-d189c7c7fc4193b2d3f8ab99ed8c6bdb0b36fb12e02ec6c8d7f675bf152f8b173%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=201312310&rft_id=info:pmid/9275218&rft_jstor_id=43119&rfr_iscdi=true