Isolation of Genetically Tractable Most-Wanted Bacteria by Metaparental Mating
Metagenomics has rapidly advanced our inventory and appreciation of the genetic potential inherent to the gut microbiome. However it is widely accepted that two key constraints to further genetic dissection of the gut microbiota and host-microbe interactions have been our inability to recover new is...
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description | Metagenomics has rapidly advanced our inventory and appreciation of the genetic potential inherent to the gut microbiome. However it is widely accepted that two key constraints to further genetic dissection of the gut microbiota and host-microbe interactions have been our inability to recover new isolates from the human gut and the paucity of genetically tractable gut microbes. To address this challenge we developed a modular RP4 mobilisable recombinant vector system and an approach termed metaparental mating to support the rapid and directed isolation of genetically tractable fastidious gut bacteria. Using this approach we isolated transconjugants affiliated with
Clostridium
cluster IV (
Faecalibacterium
and
Oscillibacter
spp.),
Clostridium
cluster XI (
Anaerococcus
) and
Clostridium
XIVa (
Blautia
spp.) and group 2 ruminococci amongst others and demonstrated that the recombinant vectors were stably maintained in their recipient hosts. By a similar approach we constructed fluorescently labelled bacterial transconjugants affiliated with
Clostridium
cluster IV (including
Flavonifractor
and
Pseudoflavonifractor
spp.),
Clostridium
XIVa (
Blautia
spp.) and
Clostridium
cluster XVIII (
Clostridium ramosum
) that expressed a flavin mononucleotide-based reporter gene (
evoglow-C-Bs2
). Our approach will advance the integration of bacterial genetics with metagenomics and realize new directions to support a more mechanistic dissection of host-microbe associations relevant to human health and disease. |
doi_str_mv | 10.1038/srep13282 |
format | Article |
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Clostridium
cluster IV (
Faecalibacterium
and
Oscillibacter
spp.),
Clostridium
cluster XI (
Anaerococcus
) and
Clostridium
XIVa (
Blautia
spp.) and group 2 ruminococci amongst others and demonstrated that the recombinant vectors were stably maintained in their recipient hosts. By a similar approach we constructed fluorescently labelled bacterial transconjugants affiliated with
Clostridium
cluster IV (including
Flavonifractor
and
Pseudoflavonifractor
spp.),
Clostridium
XIVa (
Blautia
spp.) and
Clostridium
cluster XVIII (
Clostridium ramosum
) that expressed a flavin mononucleotide-based reporter gene (
evoglow-C-Bs2
). Our approach will advance the integration of bacterial genetics with metagenomics and realize new directions to support a more mechanistic dissection of host-microbe associations relevant to human health and disease.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep13282</identifier><identifier>PMID: 26293474</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/326/2565/855 ; 631/326/41/2482 ; Aerobiosis ; Anaerobiosis ; Antibiotics ; Bacteria ; Biodiversity ; Clostridium - genetics ; Clostridium - isolation & purification ; Conjugation, Genetic ; Dissection ; E coli ; Flavin mononucleotide ; Fluorescent Dyes - metabolism ; Genetic Vectors - metabolism ; Genetics ; Humanities and Social Sciences ; Integration ; Intestinal microflora ; Metagenomics - methods ; Microbiota ; Microscopy, Fluorescence ; multidisciplinary ; Phylogeny ; Polymerase Chain Reaction ; Reporter gene ; Science ; Vectors</subject><ispartof>Scientific reports, 2015-08, Vol.5 (1), p.13282-13282, Article 13282</ispartof><rights>The Author(s) 2015</rights><rights>Copyright Nature Publishing Group Aug 2015</rights><rights>Copyright © 2015, Macmillan Publishers Limited 2015 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-c17467eeecb7960129eb71de6fa3a089a617b5d16b75a1fe1ad599c84e136ac3</citedby><cites>FETCH-LOGICAL-c438t-c17467eeecb7960129eb71de6fa3a089a617b5d16b75a1fe1ad599c84e136ac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642544/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642544/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,27901,27902,41096,42165,51551,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26293474$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cuív, Páraic Ó</creatorcontrib><creatorcontrib>Smith, Wendy J.</creatorcontrib><creatorcontrib>Pottenger, Sian</creatorcontrib><creatorcontrib>Burman, Sriti</creatorcontrib><creatorcontrib>Shanahan, Erin R.</creatorcontrib><creatorcontrib>Morrison, Mark</creatorcontrib><title>Isolation of Genetically Tractable Most-Wanted Bacteria by Metaparental Mating</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Metagenomics has rapidly advanced our inventory and appreciation of the genetic potential inherent to the gut microbiome. However it is widely accepted that two key constraints to further genetic dissection of the gut microbiota and host-microbe interactions have been our inability to recover new isolates from the human gut and the paucity of genetically tractable gut microbes. To address this challenge we developed a modular RP4 mobilisable recombinant vector system and an approach termed metaparental mating to support the rapid and directed isolation of genetically tractable fastidious gut bacteria. Using this approach we isolated transconjugants affiliated with
Clostridium
cluster IV (
Faecalibacterium
and
Oscillibacter
spp.),
Clostridium
cluster XI (
Anaerococcus
) and
Clostridium
XIVa (
Blautia
spp.) and group 2 ruminococci amongst others and demonstrated that the recombinant vectors were stably maintained in their recipient hosts. By a similar approach we constructed fluorescently labelled bacterial transconjugants affiliated with
Clostridium
cluster IV (including
Flavonifractor
and
Pseudoflavonifractor
spp.),
Clostridium
XIVa (
Blautia
spp.) and
Clostridium
cluster XVIII (
Clostridium ramosum
) that expressed a flavin mononucleotide-based reporter gene (
evoglow-C-Bs2
). Our approach will advance the integration of bacterial genetics with metagenomics and realize new directions to support a more mechanistic dissection of host-microbe associations relevant to human health and disease.</description><subject>631/326/2565/855</subject><subject>631/326/41/2482</subject><subject>Aerobiosis</subject><subject>Anaerobiosis</subject><subject>Antibiotics</subject><subject>Bacteria</subject><subject>Biodiversity</subject><subject>Clostridium - genetics</subject><subject>Clostridium - isolation & purification</subject><subject>Conjugation, Genetic</subject><subject>Dissection</subject><subject>E coli</subject><subject>Flavin mononucleotide</subject><subject>Fluorescent Dyes - metabolism</subject><subject>Genetic Vectors - metabolism</subject><subject>Genetics</subject><subject>Humanities and Social Sciences</subject><subject>Integration</subject><subject>Intestinal microflora</subject><subject>Metagenomics - methods</subject><subject>Microbiota</subject><subject>Microscopy, Fluorescence</subject><subject>multidisciplinary</subject><subject>Phylogeny</subject><subject>Polymerase Chain Reaction</subject><subject>Reporter gene</subject><subject>Science</subject><subject>Vectors</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNplkUFrHCEYhiU0NCHJoX8gDPTSFKZRx9HxUkhDmwSy6WWhR_nG-WY7wdWNuoX997FssmxaL4rfw-MrLyEfGP3CaNNdpogr1vCOH5BjTkVb84bzd3vnI3KW0iMtq-VaMP2eHHHJdSOUOCYPdyk4yFPwVRirG_SYJwvObap5BJuhd1jNQsr1L_AZh-pbucQ4QdVvqhlmWEFEn8FVsyLxi1NyOIJLePayn5D5j-_z69v6_ufN3fXVfW1F0-XaMiWkQkTbKy0p4xp7xQaUIzRAOw2Sqb4dmOxVC2xEBkOrte0EskaCbU7I1612te6XONgSIYIzqzgtIW5MgMm8nfjpt1mEP0ZIwVshiuDTiyCGpzWmbJZTsugceAzrZJiiklOleVfQj_-gj2EdffmdYZ3Wirecs0JdbCkbQyqVjLswjJq_PZldT4U930-_I19bKcDnLZDKyC8w7j35n-0ZZRSczw</recordid><startdate>20150821</startdate><enddate>20150821</enddate><creator>Cuív, Páraic Ó</creator><creator>Smith, Wendy J.</creator><creator>Pottenger, Sian</creator><creator>Burman, Sriti</creator><creator>Shanahan, Erin R.</creator><creator>Morrison, Mark</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</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>CCPQU</scope><scope>DWQXO</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>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20150821</creationdate><title>Isolation of Genetically Tractable Most-Wanted Bacteria by Metaparental Mating</title><author>Cuív, Páraic Ó ; Smith, Wendy J. ; Pottenger, Sian ; Burman, Sriti ; Shanahan, Erin R. ; Morrison, Mark</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-c17467eeecb7960129eb71de6fa3a089a617b5d16b75a1fe1ad599c84e136ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>631/326/2565/855</topic><topic>631/326/41/2482</topic><topic>Aerobiosis</topic><topic>Anaerobiosis</topic><topic>Antibiotics</topic><topic>Bacteria</topic><topic>Biodiversity</topic><topic>Clostridium - genetics</topic><topic>Clostridium - isolation & purification</topic><topic>Conjugation, Genetic</topic><topic>Dissection</topic><topic>E coli</topic><topic>Flavin mononucleotide</topic><topic>Fluorescent Dyes - metabolism</topic><topic>Genetic Vectors - metabolism</topic><topic>Genetics</topic><topic>Humanities and Social Sciences</topic><topic>Integration</topic><topic>Intestinal microflora</topic><topic>Metagenomics - methods</topic><topic>Microbiota</topic><topic>Microscopy, Fluorescence</topic><topic>multidisciplinary</topic><topic>Phylogeny</topic><topic>Polymerase Chain Reaction</topic><topic>Reporter gene</topic><topic>Science</topic><topic>Vectors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cuív, Páraic Ó</creatorcontrib><creatorcontrib>Smith, Wendy J.</creatorcontrib><creatorcontrib>Pottenger, Sian</creatorcontrib><creatorcontrib>Burman, Sriti</creatorcontrib><creatorcontrib>Shanahan, Erin R.</creatorcontrib><creatorcontrib>Morrison, Mark</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</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 Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</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 Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cuív, Páraic Ó</au><au>Smith, Wendy J.</au><au>Pottenger, Sian</au><au>Burman, Sriti</au><au>Shanahan, Erin R.</au><au>Morrison, Mark</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Isolation of Genetically Tractable Most-Wanted Bacteria by Metaparental Mating</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2015-08-21</date><risdate>2015</risdate><volume>5</volume><issue>1</issue><spage>13282</spage><epage>13282</epage><pages>13282-13282</pages><artnum>13282</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Metagenomics has rapidly advanced our inventory and appreciation of the genetic potential inherent to the gut microbiome. However it is widely accepted that two key constraints to further genetic dissection of the gut microbiota and host-microbe interactions have been our inability to recover new isolates from the human gut and the paucity of genetically tractable gut microbes. To address this challenge we developed a modular RP4 mobilisable recombinant vector system and an approach termed metaparental mating to support the rapid and directed isolation of genetically tractable fastidious gut bacteria. Using this approach we isolated transconjugants affiliated with
Clostridium
cluster IV (
Faecalibacterium
and
Oscillibacter
spp.),
Clostridium
cluster XI (
Anaerococcus
) and
Clostridium
XIVa (
Blautia
spp.) and group 2 ruminococci amongst others and demonstrated that the recombinant vectors were stably maintained in their recipient hosts. By a similar approach we constructed fluorescently labelled bacterial transconjugants affiliated with
Clostridium
cluster IV (including
Flavonifractor
and
Pseudoflavonifractor
spp.),
Clostridium
XIVa (
Blautia
spp.) and
Clostridium
cluster XVIII (
Clostridium ramosum
) that expressed a flavin mononucleotide-based reporter gene (
evoglow-C-Bs2
). Our approach will advance the integration of bacterial genetics with metagenomics and realize new directions to support a more mechanistic dissection of host-microbe associations relevant to human health and disease.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>26293474</pmid><doi>10.1038/srep13282</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Nature Free; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry; Springer Nature OA Free Journals |
subjects | 631/326/2565/855 631/326/41/2482 Aerobiosis Anaerobiosis Antibiotics Bacteria Biodiversity Clostridium - genetics Clostridium - isolation & purification Conjugation, Genetic Dissection E coli Flavin mononucleotide Fluorescent Dyes - metabolism Genetic Vectors - metabolism Genetics Humanities and Social Sciences Integration Intestinal microflora Metagenomics - methods Microbiota Microscopy, Fluorescence multidisciplinary Phylogeny Polymerase Chain Reaction Reporter gene Science Vectors |
title | Isolation of Genetically Tractable Most-Wanted Bacteria by Metaparental Mating |
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