Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:BMC genomics 2016-02, Vol.17 (118), p.118-118, Article 118
Main Authors: 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
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-c628t-5f89038783fa1210a296686ac676155c1939f1c2096daf2c0d31d0c4b76549eb3
cites cdi_FETCH-LOGICAL-c628t-5f89038783fa1210a296686ac676155c1939f1c2096daf2c0d31d0c4b76549eb3
container_end_page 118
container_issue 118
container_start_page 118
container_title BMC genomics
container_volume 17
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
format article
fullrecord <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4756508</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A453871318</galeid><sourcerecordid>A453871318</sourcerecordid><originalsourceid>FETCH-LOGICAL-c628t-5f89038783fa1210a296686ac676155c1939f1c2096daf2c0d31d0c4b76549eb3</originalsourceid><addsrcrecordid>eNptkkFv1DAQhSMEoqXlB3BBkbjQQ4rHsccOB6RVVdpKi5AonC3HcXZdJfYSJ9v23-NoS-lWyAePxt88Pz1Nlr0Dcgog8VMEKpEVBLCgjMkCXmSHwAQUFJC9fFIfZG9ivCEEhKT8dXZAUUpGBT_MzIX1obfFrWts3oeonXGxz2_duHY-_3ZvQq3NaAc39bmuo7ExTvFzbrehm0YXvB7uc-2b3G6SQO9CF1bO6C53_aZLxYzE4-xVq7to3z7cR9mvr-c_zy6L5feLq7PFsjBI5VjwVlaklEKWrQYKRNMKUaI2KBA4N1CVVQuGkgob3VJDmhIaYlgtkLPK1uVR9mWnu5nq3jbG-nHQndoMrk82VdBO7b94t1arsFVMcOREJoGTncD62djlYqnmHkmBM07FFhL78eGzIfyebBxV71I8Xae9DVNUIBApsoqJhH54ht6EafApikSJUlQEBfyjVrqzyvk2JI9mFlULxlMuUMJs8fQ_VDpz-iZ427rU3xs42RtIzGjvxpWeYlRX1z_2WdixZggxDrZ9DAGImjdO7TYu5YBq3jg1237_NPTHib8rVv4BImPPog</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1773790671</pqid></control><display><type>article</type><title>Genome-wide mosaicism within Mycobacterium abscessus: evolutionary and epidemiological implications</title><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><source>PubMed Central (PMC)</source><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</creator><creatorcontrib>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</creatorcontrib><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><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 - genetics</topic><topic>Drug resistance</topic><topic>Evolution</topic><topic>Evolution, Molecular</topic><topic>Evolutionary genetics</topic><topic>Gene Flow</topic><topic>Gene Frequency</topic><topic>Gene Transfer, Horizontal</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genetic research</topic><topic>Genetics</topic><topic>Genome, Bacterial</topic><topic>Genomes</topic><topic>Genotype</topic><topic>HIV</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Identification and classification</topic><topic>Infections</topic><topic>Life Sciences</topic><topic>Lung diseases</topic><topic>Microbiological research</topic><topic>Models, Genetic</topic><topic>Mosaicism</topic><topic>Multilocus Sequence Typing</topic><topic>Mycobacteria</topic><topic>Mycobacterium</topic><topic>Mycobacterium - genetics</topic><topic>Phylogenetics</topic><topic>Phylogeny</topic><topic>Population</topic><topic>Sequence Analysis, DNA</topic><topic>Studies</topic><topic>Tuberculosis</topic><topic>Virulence (Microbiology)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Health Medical collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - 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>
fulltext fulltext
identifier ISSN: 1471-2164
ispartof BMC genomics, 2016-02, Vol.17 (118), p.118-118, Article 118
issn 1471-2164
1471-2164
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4756508
source Publicly Available Content Database (Proquest) (PQ_SDU_P3); PubMed Central (PMC)
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