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Genome-wide mosaicism within Mycobacterium abscessus: evolutionary and epidemiological implications
In mycobacteria, conjugation differs from the canonical Hfr model, but is still poorly understood. Here, we quantified this evolutionary processe in a natural mycobacterial population, taking advantage of a large clinical strain collection of the emerging pathogen Mycobacterium abscessus (MAB). Mult...
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Published in: | BMC genomics 2016-02, Vol.17 (118), p.118-118, Article 118 |
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creator | Sapriel, Guillaume Konjek, Julie Orgeur, Mickael Bouri, Laurent Frézal, Lise Roux, Anne-Laure Dumas, Emilie Brosch, Roland Bouchier, Christiane Brisse, Sylvain Vandenbogaert, Mathias Thiberge, Jean-Michel Caro, Valérie Ngeow, Yun Fong Tan, Joon Liang Herrmann, Jean-Louis Gaillard, Jean-Louis Heym, Beate Wirth, Thierry |
description | In mycobacteria, conjugation differs from the canonical Hfr model, but is still poorly understood. Here, we quantified this evolutionary processe in a natural mycobacterial population, taking advantage of a large clinical strain collection of the emerging pathogen Mycobacterium abscessus (MAB).
Multilocus sequence typing confirmed the existence of three M. abscessus subspecies, and unravelled extensive allelic exchange between them. Furthermore, an asymmetrical gene flow occurring between these main lineages was detected, resulting in highly admixed strains. Intriguingly, these mosaic strains were significantly associated with cystic fibrosis patients with lung infections or chronic colonization. Genome sequencing of those hybrid strains confirmed that half of their genomic content was remodelled in large genomic blocks, leading to original tri-modal 'patchwork' architecture. One of these hybrid strains acquired a locus conferring inducible macrolide resistance, and a large genomic insertion from a slowly growing pathogenic mycobacteria, suggesting an adaptive gene transfer. This atypical genomic architecture of the highly recombinogenic strains is consistent with the distributive conjugal transfer (DCT) observed in M. smegmatis. Intriguingly, no known DCT function was found in M. abscessus chromosome, however, a p-RAW-like genetic element was detected in one of the highly admixed strains.
Taken together, our results strongly suggest that MAB evolution is sporadically punctuated by dramatic genome wide remodelling events. These findings might have far reaching epidemiological consequences for emerging mycobacterial pathogens survey in the context of increasing numbers of rapidly growing mycobacteria and M. tuberculosis co-infections. |
doi_str_mv | 10.1186/s12864-016-2448-1 |
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Multilocus sequence typing confirmed the existence of three M. abscessus subspecies, and unravelled extensive allelic exchange between them. Furthermore, an asymmetrical gene flow occurring between these main lineages was detected, resulting in highly admixed strains. Intriguingly, these mosaic strains were significantly associated with cystic fibrosis patients with lung infections or chronic colonization. Genome sequencing of those hybrid strains confirmed that half of their genomic content was remodelled in large genomic blocks, leading to original tri-modal 'patchwork' architecture. One of these hybrid strains acquired a locus conferring inducible macrolide resistance, and a large genomic insertion from a slowly growing pathogenic mycobacteria, suggesting an adaptive gene transfer. This atypical genomic architecture of the highly recombinogenic strains is consistent with the distributive conjugal transfer (DCT) observed in M. smegmatis. Intriguingly, no known DCT function was found in M. abscessus chromosome, however, a p-RAW-like genetic element was detected in one of the highly admixed strains.
Taken together, our results strongly suggest that MAB evolution is sporadically punctuated by dramatic genome wide remodelling events. These findings might have far reaching epidemiological consequences for emerging mycobacterial pathogens survey in the context of increasing numbers of rapidly growing mycobacteria and M. tuberculosis co-infections.</description><identifier>ISSN: 1471-2164</identifier><identifier>EISSN: 1471-2164</identifier><identifier>DOI: 10.1186/s12864-016-2448-1</identifier><identifier>PMID: 26884275</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Antibiotics ; Bacterial Typing Techniques ; Chronic obstructive pulmonary disease ; Comparative Genomic Hybridization ; Conjugation, Genetic ; Cystic fibrosis ; Deoxyribonucleic acid ; DNA ; DNA, Bacterial - genetics ; Drug resistance ; Evolution ; Evolution, Molecular ; Evolutionary genetics ; Gene Flow ; Gene Frequency ; Gene Transfer, Horizontal ; Genes ; Genetic aspects ; Genetic research ; Genetics ; Genome, Bacterial ; Genomes ; Genotype ; HIV ; Human immunodeficiency virus ; Humans ; Identification and classification ; Infections ; Life Sciences ; Lung diseases ; Microbiological research ; Models, Genetic ; Mosaicism ; Multilocus Sequence Typing ; Mycobacteria ; Mycobacterium ; Mycobacterium - genetics ; Phylogenetics ; Phylogeny ; Population ; Sequence Analysis, DNA ; Studies ; Tuberculosis ; Virulence (Microbiology)</subject><ispartof>BMC genomics, 2016-02, Vol.17 (118), p.118-118, Article 118</ispartof><rights>COPYRIGHT 2016 BioMed Central Ltd.</rights><rights>Copyright BioMed Central 2016</rights><rights>Attribution</rights><rights>Sapriel et al. 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c628t-5f89038783fa1210a296686ac676155c1939f1c2096daf2c0d31d0c4b76549eb3</citedby><cites>FETCH-LOGICAL-c628t-5f89038783fa1210a296686ac676155c1939f1c2096daf2c0d31d0c4b76549eb3</cites><orcidid>0000-0002-6518-0423 ; 0000-0003-2587-3863 ; 0000-0002-7371-0172 ; 0000-0003-3549-1543 ; 0000-0003-2347-6418 ; 0000-0001-8477-5708 ; 0000-0002-2516-2108</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/PMC4756508/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1773790671?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25751,27922,27923,37010,37011,44588,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26884275$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.sorbonne-universite.fr/hal-01284527$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Sapriel, Guillaume</creatorcontrib><creatorcontrib>Konjek, Julie</creatorcontrib><creatorcontrib>Orgeur, Mickael</creatorcontrib><creatorcontrib>Bouri, Laurent</creatorcontrib><creatorcontrib>Frézal, Lise</creatorcontrib><creatorcontrib>Roux, Anne-Laure</creatorcontrib><creatorcontrib>Dumas, Emilie</creatorcontrib><creatorcontrib>Brosch, Roland</creatorcontrib><creatorcontrib>Bouchier, Christiane</creatorcontrib><creatorcontrib>Brisse, Sylvain</creatorcontrib><creatorcontrib>Vandenbogaert, Mathias</creatorcontrib><creatorcontrib>Thiberge, Jean-Michel</creatorcontrib><creatorcontrib>Caro, Valérie</creatorcontrib><creatorcontrib>Ngeow, Yun Fong</creatorcontrib><creatorcontrib>Tan, Joon Liang</creatorcontrib><creatorcontrib>Herrmann, Jean-Louis</creatorcontrib><creatorcontrib>Gaillard, Jean-Louis</creatorcontrib><creatorcontrib>Heym, Beate</creatorcontrib><creatorcontrib>Wirth, Thierry</creatorcontrib><title>Genome-wide mosaicism within Mycobacterium abscessus: evolutionary and epidemiological implications</title><title>BMC genomics</title><addtitle>BMC Genomics</addtitle><description>In mycobacteria, conjugation differs from the canonical Hfr model, but is still poorly understood. Here, we quantified this evolutionary processe in a natural mycobacterial population, taking advantage of a large clinical strain collection of the emerging pathogen Mycobacterium abscessus (MAB).
Multilocus sequence typing confirmed the existence of three M. abscessus subspecies, and unravelled extensive allelic exchange between them. Furthermore, an asymmetrical gene flow occurring between these main lineages was detected, resulting in highly admixed strains. Intriguingly, these mosaic strains were significantly associated with cystic fibrosis patients with lung infections or chronic colonization. Genome sequencing of those hybrid strains confirmed that half of their genomic content was remodelled in large genomic blocks, leading to original tri-modal 'patchwork' architecture. One of these hybrid strains acquired a locus conferring inducible macrolide resistance, and a large genomic insertion from a slowly growing pathogenic mycobacteria, suggesting an adaptive gene transfer. This atypical genomic architecture of the highly recombinogenic strains is consistent with the distributive conjugal transfer (DCT) observed in M. smegmatis. Intriguingly, no known DCT function was found in M. abscessus chromosome, however, a p-RAW-like genetic element was detected in one of the highly admixed strains.
Taken together, our results strongly suggest that MAB evolution is sporadically punctuated by dramatic genome wide remodelling events. These findings might have far reaching epidemiological consequences for emerging mycobacterial pathogens survey in the context of increasing numbers of rapidly growing mycobacteria and M. tuberculosis co-infections.</description><subject>Antibiotics</subject><subject>Bacterial Typing Techniques</subject><subject>Chronic obstructive pulmonary disease</subject><subject>Comparative Genomic Hybridization</subject><subject>Conjugation, Genetic</subject><subject>Cystic fibrosis</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA, Bacterial - genetics</subject><subject>Drug resistance</subject><subject>Evolution</subject><subject>Evolution, Molecular</subject><subject>Evolutionary genetics</subject><subject>Gene Flow</subject><subject>Gene Frequency</subject><subject>Gene Transfer, Horizontal</subject><subject>Genes</subject><subject>Genetic aspects</subject><subject>Genetic research</subject><subject>Genetics</subject><subject>Genome, Bacterial</subject><subject>Genomes</subject><subject>Genotype</subject><subject>HIV</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Identification and classification</subject><subject>Infections</subject><subject>Life Sciences</subject><subject>Lung diseases</subject><subject>Microbiological research</subject><subject>Models, Genetic</subject><subject>Mosaicism</subject><subject>Multilocus Sequence Typing</subject><subject>Mycobacteria</subject><subject>Mycobacterium</subject><subject>Mycobacterium - genetics</subject><subject>Phylogenetics</subject><subject>Phylogeny</subject><subject>Population</subject><subject>Sequence Analysis, DNA</subject><subject>Studies</subject><subject>Tuberculosis</subject><subject>Virulence (Microbiology)</subject><issn>1471-2164</issn><issn>1471-2164</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNptkkFv1DAQhSMEoqXlB3BBkbjQQ4rHsccOB6RVVdpKi5AonC3HcXZdJfYSJ9v23-NoS-lWyAePxt88Pz1Nlr0Dcgog8VMEKpEVBLCgjMkCXmSHwAQUFJC9fFIfZG9ivCEEhKT8dXZAUUpGBT_MzIX1obfFrWts3oeonXGxz2_duHY-_3ZvQq3NaAc39bmuo7ExTvFzbrehm0YXvB7uc-2b3G6SQO9CF1bO6C53_aZLxYzE4-xVq7to3z7cR9mvr-c_zy6L5feLq7PFsjBI5VjwVlaklEKWrQYKRNMKUaI2KBA4N1CVVQuGkgob3VJDmhIaYlgtkLPK1uVR9mWnu5nq3jbG-nHQndoMrk82VdBO7b94t1arsFVMcOREJoGTncD62djlYqnmHkmBM07FFhL78eGzIfyebBxV71I8Xae9DVNUIBApsoqJhH54ht6EafApikSJUlQEBfyjVrqzyvk2JI9mFlULxlMuUMJs8fQ_VDpz-iZ427rU3xs42RtIzGjvxpWeYlRX1z_2WdixZggxDrZ9DAGImjdO7TYu5YBq3jg1237_NPTHib8rVv4BImPPog</recordid><startdate>20160217</startdate><enddate>20160217</enddate><creator>Sapriel, Guillaume</creator><creator>Konjek, Julie</creator><creator>Orgeur, Mickael</creator><creator>Bouri, Laurent</creator><creator>Frézal, Lise</creator><creator>Roux, Anne-Laure</creator><creator>Dumas, Emilie</creator><creator>Brosch, Roland</creator><creator>Bouchier, Christiane</creator><creator>Brisse, Sylvain</creator><creator>Vandenbogaert, Mathias</creator><creator>Thiberge, Jean-Michel</creator><creator>Caro, Valérie</creator><creator>Ngeow, Yun Fong</creator><creator>Tan, Joon Liang</creator><creator>Herrmann, Jean-Louis</creator><creator>Gaillard, Jean-Louis</creator><creator>Heym, Beate</creator><creator>Wirth, Thierry</creator><general>BioMed Central Ltd</general><general>BioMed Central</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>ISR</scope><scope>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7SS</scope><scope>7TK</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-6518-0423</orcidid><orcidid>https://orcid.org/0000-0003-2587-3863</orcidid><orcidid>https://orcid.org/0000-0002-7371-0172</orcidid><orcidid>https://orcid.org/0000-0003-3549-1543</orcidid><orcidid>https://orcid.org/0000-0003-2347-6418</orcidid><orcidid>https://orcid.org/0000-0001-8477-5708</orcidid><orcidid>https://orcid.org/0000-0002-2516-2108</orcidid></search><sort><creationdate>20160217</creationdate><title>Genome-wide mosaicism within Mycobacterium abscessus: evolutionary and epidemiological implications</title><author>Sapriel, Guillaume ; Konjek, Julie ; Orgeur, Mickael ; Bouri, Laurent ; Frézal, Lise ; Roux, Anne-Laure ; Dumas, Emilie ; Brosch, Roland ; Bouchier, Christiane ; Brisse, Sylvain ; Vandenbogaert, Mathias ; Thiberge, Jean-Michel ; Caro, Valérie ; Ngeow, Yun Fong ; Tan, Joon Liang ; Herrmann, Jean-Louis ; Gaillard, Jean-Louis ; Heym, Beate ; Wirth, Thierry</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c628t-5f89038783fa1210a296686ac676155c1939f1c2096daf2c0d31d0c4b76549eb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Antibiotics</topic><topic>Bacterial Typing Techniques</topic><topic>Chronic obstructive pulmonary disease</topic><topic>Comparative Genomic Hybridization</topic><topic>Conjugation, Genetic</topic><topic>Cystic fibrosis</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA, Bacterial - 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Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BMC genomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sapriel, Guillaume</au><au>Konjek, Julie</au><au>Orgeur, Mickael</au><au>Bouri, Laurent</au><au>Frézal, Lise</au><au>Roux, Anne-Laure</au><au>Dumas, Emilie</au><au>Brosch, Roland</au><au>Bouchier, Christiane</au><au>Brisse, Sylvain</au><au>Vandenbogaert, Mathias</au><au>Thiberge, Jean-Michel</au><au>Caro, Valérie</au><au>Ngeow, Yun Fong</au><au>Tan, Joon Liang</au><au>Herrmann, Jean-Louis</au><au>Gaillard, Jean-Louis</au><au>Heym, Beate</au><au>Wirth, Thierry</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genome-wide mosaicism within Mycobacterium abscessus: evolutionary and epidemiological implications</atitle><jtitle>BMC genomics</jtitle><addtitle>BMC Genomics</addtitle><date>2016-02-17</date><risdate>2016</risdate><volume>17</volume><issue>118</issue><spage>118</spage><epage>118</epage><pages>118-118</pages><artnum>118</artnum><issn>1471-2164</issn><eissn>1471-2164</eissn><abstract>In mycobacteria, conjugation differs from the canonical Hfr model, but is still poorly understood. Here, we quantified this evolutionary processe in a natural mycobacterial population, taking advantage of a large clinical strain collection of the emerging pathogen Mycobacterium abscessus (MAB).
Multilocus sequence typing confirmed the existence of three M. abscessus subspecies, and unravelled extensive allelic exchange between them. Furthermore, an asymmetrical gene flow occurring between these main lineages was detected, resulting in highly admixed strains. Intriguingly, these mosaic strains were significantly associated with cystic fibrosis patients with lung infections or chronic colonization. Genome sequencing of those hybrid strains confirmed that half of their genomic content was remodelled in large genomic blocks, leading to original tri-modal 'patchwork' architecture. One of these hybrid strains acquired a locus conferring inducible macrolide resistance, and a large genomic insertion from a slowly growing pathogenic mycobacteria, suggesting an adaptive gene transfer. This atypical genomic architecture of the highly recombinogenic strains is consistent with the distributive conjugal transfer (DCT) observed in M. smegmatis. Intriguingly, no known DCT function was found in M. abscessus chromosome, however, a p-RAW-like genetic element was detected in one of the highly admixed strains.
Taken together, our results strongly suggest that MAB evolution is sporadically punctuated by dramatic genome wide remodelling events. These findings might have far reaching epidemiological consequences for emerging mycobacterial pathogens survey in the context of increasing numbers of rapidly growing mycobacteria and M. tuberculosis co-infections.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>26884275</pmid><doi>10.1186/s12864-016-2448-1</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-6518-0423</orcidid><orcidid>https://orcid.org/0000-0003-2587-3863</orcidid><orcidid>https://orcid.org/0000-0002-7371-0172</orcidid><orcidid>https://orcid.org/0000-0003-3549-1543</orcidid><orcidid>https://orcid.org/0000-0003-2347-6418</orcidid><orcidid>https://orcid.org/0000-0001-8477-5708</orcidid><orcidid>https://orcid.org/0000-0002-2516-2108</orcidid><oa>free_for_read</oa></addata></record> |
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recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4756508 |
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subjects | Antibiotics Bacterial Typing Techniques Chronic obstructive pulmonary disease Comparative Genomic Hybridization Conjugation, Genetic Cystic fibrosis Deoxyribonucleic acid DNA DNA, Bacterial - genetics Drug resistance Evolution Evolution, Molecular Evolutionary genetics Gene Flow Gene Frequency Gene Transfer, Horizontal Genes Genetic aspects Genetic research Genetics Genome, Bacterial Genomes Genotype HIV Human immunodeficiency virus Humans Identification and classification Infections Life Sciences Lung diseases Microbiological research Models, Genetic Mosaicism Multilocus Sequence Typing Mycobacteria Mycobacterium Mycobacterium - genetics Phylogenetics Phylogeny Population Sequence Analysis, DNA Studies Tuberculosis Virulence (Microbiology) |
title | Genome-wide mosaicism within Mycobacterium abscessus: evolutionary and epidemiological implications |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T12%3A31%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Genome-wide%20mosaicism%20within%20Mycobacterium%20abscessus:%20evolutionary%20and%20epidemiological%20implications&rft.jtitle=BMC%20genomics&rft.au=Sapriel,%20Guillaume&rft.date=2016-02-17&rft.volume=17&rft.issue=118&rft.spage=118&rft.epage=118&rft.pages=118-118&rft.artnum=118&rft.issn=1471-2164&rft.eissn=1471-2164&rft_id=info:doi/10.1186/s12864-016-2448-1&rft_dat=%3Cgale_pubme%3EA453871318%3C/gale_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c628t-5f89038783fa1210a296686ac676155c1939f1c2096daf2c0d31d0c4b76549eb3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1773790671&rft_id=info:pmid/26884275&rft_galeid=A453871318&rfr_iscdi=true |