Loading…
Escherichia coli EC93 deploys two plasmid-encoded class I contact-dependent growth inhibition systems for antagonistic bacterial interactions
The phenomenon of contact-dependent growth inhibition (CDI) and the genes required for CDI ( ) were identified and isolated in 2005 from an isolate (EC93) from rats. Although the locus has been the focus of extensive research during the past 15 years, little is known about the EC93 isolate from whic...
Saved in:
Published in: | Microbial genomics 2021-03, Vol.7 (3) |
---|---|
Main Authors: | , , , , , , , , , |
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-c462t-a1623f0c826676ad0aa98cfbfe360c9c0ec0db0911f2ecdc75d73ffd22103d9e3 |
---|---|
cites | cdi_FETCH-LOGICAL-c462t-a1623f0c826676ad0aa98cfbfe360c9c0ec0db0911f2ecdc75d73ffd22103d9e3 |
container_end_page | |
container_issue | 3 |
container_start_page | |
container_title | Microbial genomics |
container_volume | 7 |
creator | Wäneskog, Marcus Halvorsen, Tiffany Filek, Klara Xu, Feifei Hammarlöf, Disa L Hayes, Christopher S Braaten, Bruce A Low, David A Poole, Stephen J Koskiniemi, Sanna |
description | The phenomenon of contact-dependent growth inhibition (CDI) and the genes required for CDI (
) were identified and isolated in 2005 from an
isolate (EC93) from rats. Although the
locus has been the focus of extensive research during the past 15 years, little is known about the EC93 isolate from which it originates. Here we sequenced the EC93 genome and find two complete and functional
loci (including the previously identified
locus), both carried on a large 127 kb plasmid. These
systems are differentially expressed in laboratory media, enabling EC93 to outcompete
cells lacking cognate
immunity genes. The two CDI systems deliver distinct effector peptides that each dissipate the membrane potential of target cells, although the two toxins display different toxic potencies. Despite the differential expression and toxic potencies of these CDI systems, both yielded similar competitive advantages against
cells lacking immunity. This can be explained by the fact that the less expressed
system (
) delivers a more potent toxin than the highly expressed
system. Moreover, our results indicate that unlike most sequenced CDI
bacterial isolates, the two
loci of
EC93 are located on a plasmid and are expressed in laboratory media. |
doi_str_mv | 10.1099/mgen.0.000534 |
format | article |
fullrecord | <record><control><sourceid>pubmed_swepu</sourceid><recordid>TN_cdi_swepub_primary_oai_DiVA_org_uu_442303</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>33646095</sourcerecordid><originalsourceid>FETCH-LOGICAL-c462t-a1623f0c826676ad0aa98cfbfe360c9c0ec0db0911f2ecdc75d73ffd22103d9e3</originalsourceid><addsrcrecordid>eNqF0c1u3CAQB3BUNWqiJMdeKx6g3gxgY3OpFG23SaRIvbS9IsyHTWvDyrBd7UPknUu0aZqcemJG_IaR-CP0nsCKgBBX82DDClYA0LD6DTqj0LRV0zXd2xf1KbpM6WcxpOm4aJt36JQxXnMQzRl62CQ92sXr0Sus4-TxZi0YNnY7xUPCeR_xdlJp9qayQUdjDdalT_iu6JCVzlWxNhgbMh6WuM8j9mH0vc8-BpwOKds5YRcXrAofYvApe437MlnWqqnoUpSu8HSBTpyakr18Os_R9y-bb-vb6v7rzd36-r7SNae5UoRT5kB3lPOWKwNKiU673lnGQQsNVoPpQRDiqNVGt41pmXOGUgLMCMvO0cfju2lvt7tebhc_q-Ugo_Lys_9xLeMyyN1O1jVlwAqv_s9_5VFSwZq2Lf7T0Rc8W6PL3yxqejX2-ib4UQ7xt-yIAA71v4V6iSkt1j3PEpCPycvH5CXIY_LFf3i58Fn_zZn9AdYJsA8</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Escherichia coli EC93 deploys two plasmid-encoded class I contact-dependent growth inhibition systems for antagonistic bacterial interactions</title><source>PubMed Central</source><creator>Wäneskog, Marcus ; Halvorsen, Tiffany ; Filek, Klara ; Xu, Feifei ; Hammarlöf, Disa L ; Hayes, Christopher S ; Braaten, Bruce A ; Low, David A ; Poole, Stephen J ; Koskiniemi, Sanna</creator><creatorcontrib>Wäneskog, Marcus ; Halvorsen, Tiffany ; Filek, Klara ; Xu, Feifei ; Hammarlöf, Disa L ; Hayes, Christopher S ; Braaten, Bruce A ; Low, David A ; Poole, Stephen J ; Koskiniemi, Sanna</creatorcontrib><description>The phenomenon of contact-dependent growth inhibition (CDI) and the genes required for CDI (
) were identified and isolated in 2005 from an
isolate (EC93) from rats. Although the
locus has been the focus of extensive research during the past 15 years, little is known about the EC93 isolate from which it originates. Here we sequenced the EC93 genome and find two complete and functional
loci (including the previously identified
locus), both carried on a large 127 kb plasmid. These
systems are differentially expressed in laboratory media, enabling EC93 to outcompete
cells lacking cognate
immunity genes. The two CDI systems deliver distinct effector peptides that each dissipate the membrane potential of target cells, although the two toxins display different toxic potencies. Despite the differential expression and toxic potencies of these CDI systems, both yielded similar competitive advantages against
cells lacking immunity. This can be explained by the fact that the less expressed
system (
) delivers a more potent toxin than the highly expressed
system. Moreover, our results indicate that unlike most sequenced CDI
bacterial isolates, the two
loci of
EC93 are located on a plasmid and are expressed in laboratory media.</description><identifier>ISSN: 2057-5858</identifier><identifier>EISSN: 2057-5858</identifier><identifier>DOI: 10.1099/mgen.0.000534</identifier><identifier>PMID: 33646095</identifier><language>eng</language><publisher>England: Microbiology Society</publisher><subject>competition ; contact-dependent growth inhibition ; Escherichia coli ; Escherichia coli - genetics ; Escherichia coli - growth & development ; Escherichia coli - metabolism ; Escherichia coli Proteins - genetics ; Escherichia coli Proteins - metabolism ; genome ; Genome, Bacterial ; Membrane Proteins - genetics ; Membrane Proteins - metabolism ; Microbial Interactions ; Plasmids - genetics ; Plasmids - metabolism ; regulation ; toxic potency ; toxin</subject><ispartof>Microbial genomics, 2021-03, Vol.7 (3)</ispartof><rights>2021 The Authors 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c462t-a1623f0c826676ad0aa98cfbfe360c9c0ec0db0911f2ecdc75d73ffd22103d9e3</citedby><cites>FETCH-LOGICAL-c462t-a1623f0c826676ad0aa98cfbfe360c9c0ec0db0911f2ecdc75d73ffd22103d9e3</cites><orcidid>0000-0003-1946-1520 ; 0000-0002-3275-0936 ; 0000-0003-2480-5631 ; 0000-0001-9845-7313 ; 0000-0002-2216-6445 ; 0000-0003-2518-4494 ; 0000-0002-8077-7615 ; 0000-0002-5504-0590</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/PMC8190604/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8190604/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33646095$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-293577$$DView record from Swedish Publication Index$$Hfree_for_read</backlink><backlink>$$Uhttps://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-442303$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Wäneskog, Marcus</creatorcontrib><creatorcontrib>Halvorsen, Tiffany</creatorcontrib><creatorcontrib>Filek, Klara</creatorcontrib><creatorcontrib>Xu, Feifei</creatorcontrib><creatorcontrib>Hammarlöf, Disa L</creatorcontrib><creatorcontrib>Hayes, Christopher S</creatorcontrib><creatorcontrib>Braaten, Bruce A</creatorcontrib><creatorcontrib>Low, David A</creatorcontrib><creatorcontrib>Poole, Stephen J</creatorcontrib><creatorcontrib>Koskiniemi, Sanna</creatorcontrib><title>Escherichia coli EC93 deploys two plasmid-encoded class I contact-dependent growth inhibition systems for antagonistic bacterial interactions</title><title>Microbial genomics</title><addtitle>Microb Genom</addtitle><description>The phenomenon of contact-dependent growth inhibition (CDI) and the genes required for CDI (
) were identified and isolated in 2005 from an
isolate (EC93) from rats. Although the
locus has been the focus of extensive research during the past 15 years, little is known about the EC93 isolate from which it originates. Here we sequenced the EC93 genome and find two complete and functional
loci (including the previously identified
locus), both carried on a large 127 kb plasmid. These
systems are differentially expressed in laboratory media, enabling EC93 to outcompete
cells lacking cognate
immunity genes. The two CDI systems deliver distinct effector peptides that each dissipate the membrane potential of target cells, although the two toxins display different toxic potencies. Despite the differential expression and toxic potencies of these CDI systems, both yielded similar competitive advantages against
cells lacking immunity. This can be explained by the fact that the less expressed
system (
) delivers a more potent toxin than the highly expressed
system. Moreover, our results indicate that unlike most sequenced CDI
bacterial isolates, the two
loci of
EC93 are located on a plasmid and are expressed in laboratory media.</description><subject>competition</subject><subject>contact-dependent growth inhibition</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - growth & development</subject><subject>Escherichia coli - metabolism</subject><subject>Escherichia coli Proteins - genetics</subject><subject>Escherichia coli Proteins - metabolism</subject><subject>genome</subject><subject>Genome, Bacterial</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - metabolism</subject><subject>Microbial Interactions</subject><subject>Plasmids - genetics</subject><subject>Plasmids - metabolism</subject><subject>regulation</subject><subject>toxic potency</subject><subject>toxin</subject><issn>2057-5858</issn><issn>2057-5858</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqF0c1u3CAQB3BUNWqiJMdeKx6g3gxgY3OpFG23SaRIvbS9IsyHTWvDyrBd7UPknUu0aZqcemJG_IaR-CP0nsCKgBBX82DDClYA0LD6DTqj0LRV0zXd2xf1KbpM6WcxpOm4aJt36JQxXnMQzRl62CQ92sXr0Sus4-TxZi0YNnY7xUPCeR_xdlJp9qayQUdjDdalT_iu6JCVzlWxNhgbMh6WuM8j9mH0vc8-BpwOKds5YRcXrAofYvApe437MlnWqqnoUpSu8HSBTpyakr18Os_R9y-bb-vb6v7rzd36-r7SNae5UoRT5kB3lPOWKwNKiU673lnGQQsNVoPpQRDiqNVGt41pmXOGUgLMCMvO0cfju2lvt7tebhc_q-Ugo_Lys_9xLeMyyN1O1jVlwAqv_s9_5VFSwZq2Lf7T0Rc8W6PL3yxqejX2-ib4UQ7xt-yIAA71v4V6iSkt1j3PEpCPycvH5CXIY_LFf3i58Fn_zZn9AdYJsA8</recordid><startdate>20210301</startdate><enddate>20210301</enddate><creator>Wäneskog, Marcus</creator><creator>Halvorsen, Tiffany</creator><creator>Filek, Klara</creator><creator>Xu, Feifei</creator><creator>Hammarlöf, Disa L</creator><creator>Hayes, Christopher S</creator><creator>Braaten, Bruce A</creator><creator>Low, David A</creator><creator>Poole, Stephen J</creator><creator>Koskiniemi, Sanna</creator><general>Microbiology Society</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>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8V</scope><scope>ACNBI</scope><scope>D8T</scope><scope>DF2</scope><scope>ZZAVC</scope><orcidid>https://orcid.org/0000-0003-1946-1520</orcidid><orcidid>https://orcid.org/0000-0002-3275-0936</orcidid><orcidid>https://orcid.org/0000-0003-2480-5631</orcidid><orcidid>https://orcid.org/0000-0001-9845-7313</orcidid><orcidid>https://orcid.org/0000-0002-2216-6445</orcidid><orcidid>https://orcid.org/0000-0003-2518-4494</orcidid><orcidid>https://orcid.org/0000-0002-8077-7615</orcidid><orcidid>https://orcid.org/0000-0002-5504-0590</orcidid></search><sort><creationdate>20210301</creationdate><title>Escherichia coli EC93 deploys two plasmid-encoded class I contact-dependent growth inhibition systems for antagonistic bacterial interactions</title><author>Wäneskog, Marcus ; Halvorsen, Tiffany ; Filek, Klara ; Xu, Feifei ; Hammarlöf, Disa L ; Hayes, Christopher S ; Braaten, Bruce A ; Low, David A ; Poole, Stephen J ; Koskiniemi, Sanna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c462t-a1623f0c826676ad0aa98cfbfe360c9c0ec0db0911f2ecdc75d73ffd22103d9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>competition</topic><topic>contact-dependent growth inhibition</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Escherichia coli - growth & development</topic><topic>Escherichia coli - metabolism</topic><topic>Escherichia coli Proteins - genetics</topic><topic>Escherichia coli Proteins - metabolism</topic><topic>genome</topic><topic>Genome, Bacterial</topic><topic>Membrane Proteins - genetics</topic><topic>Membrane Proteins - metabolism</topic><topic>Microbial Interactions</topic><topic>Plasmids - genetics</topic><topic>Plasmids - metabolism</topic><topic>regulation</topic><topic>toxic potency</topic><topic>toxin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wäneskog, Marcus</creatorcontrib><creatorcontrib>Halvorsen, Tiffany</creatorcontrib><creatorcontrib>Filek, Klara</creatorcontrib><creatorcontrib>Xu, Feifei</creatorcontrib><creatorcontrib>Hammarlöf, Disa L</creatorcontrib><creatorcontrib>Hayes, Christopher S</creatorcontrib><creatorcontrib>Braaten, Bruce A</creatorcontrib><creatorcontrib>Low, David A</creatorcontrib><creatorcontrib>Poole, Stephen J</creatorcontrib><creatorcontrib>Koskiniemi, Sanna</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Kungliga Tekniska Högskolan</collection><collection>SWEPUB Uppsala universitet full text</collection><collection>SWEPUB Freely available online</collection><collection>SWEPUB Uppsala universitet</collection><collection>SwePub Articles full text</collection><jtitle>Microbial genomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wäneskog, Marcus</au><au>Halvorsen, Tiffany</au><au>Filek, Klara</au><au>Xu, Feifei</au><au>Hammarlöf, Disa L</au><au>Hayes, Christopher S</au><au>Braaten, Bruce A</au><au>Low, David A</au><au>Poole, Stephen J</au><au>Koskiniemi, Sanna</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Escherichia coli EC93 deploys two plasmid-encoded class I contact-dependent growth inhibition systems for antagonistic bacterial interactions</atitle><jtitle>Microbial genomics</jtitle><addtitle>Microb Genom</addtitle><date>2021-03-01</date><risdate>2021</risdate><volume>7</volume><issue>3</issue><issn>2057-5858</issn><eissn>2057-5858</eissn><abstract>The phenomenon of contact-dependent growth inhibition (CDI) and the genes required for CDI (
) were identified and isolated in 2005 from an
isolate (EC93) from rats. Although the
locus has been the focus of extensive research during the past 15 years, little is known about the EC93 isolate from which it originates. Here we sequenced the EC93 genome and find two complete and functional
loci (including the previously identified
locus), both carried on a large 127 kb plasmid. These
systems are differentially expressed in laboratory media, enabling EC93 to outcompete
cells lacking cognate
immunity genes. The two CDI systems deliver distinct effector peptides that each dissipate the membrane potential of target cells, although the two toxins display different toxic potencies. Despite the differential expression and toxic potencies of these CDI systems, both yielded similar competitive advantages against
cells lacking immunity. This can be explained by the fact that the less expressed
system (
) delivers a more potent toxin than the highly expressed
system. Moreover, our results indicate that unlike most sequenced CDI
bacterial isolates, the two
loci of
EC93 are located on a plasmid and are expressed in laboratory media.</abstract><cop>England</cop><pub>Microbiology Society</pub><pmid>33646095</pmid><doi>10.1099/mgen.0.000534</doi><orcidid>https://orcid.org/0000-0003-1946-1520</orcidid><orcidid>https://orcid.org/0000-0002-3275-0936</orcidid><orcidid>https://orcid.org/0000-0003-2480-5631</orcidid><orcidid>https://orcid.org/0000-0001-9845-7313</orcidid><orcidid>https://orcid.org/0000-0002-2216-6445</orcidid><orcidid>https://orcid.org/0000-0003-2518-4494</orcidid><orcidid>https://orcid.org/0000-0002-8077-7615</orcidid><orcidid>https://orcid.org/0000-0002-5504-0590</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2057-5858 |
ispartof | Microbial genomics, 2021-03, Vol.7 (3) |
issn | 2057-5858 2057-5858 |
language | eng |
recordid | cdi_swepub_primary_oai_DiVA_org_uu_442303 |
source | PubMed Central |
subjects | competition contact-dependent growth inhibition Escherichia coli Escherichia coli - genetics Escherichia coli - growth & development Escherichia coli - metabolism Escherichia coli Proteins - genetics Escherichia coli Proteins - metabolism genome Genome, Bacterial Membrane Proteins - genetics Membrane Proteins - metabolism Microbial Interactions Plasmids - genetics Plasmids - metabolism regulation toxic potency toxin |
title | Escherichia coli EC93 deploys two plasmid-encoded class I contact-dependent growth inhibition systems for antagonistic bacterial interactions |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-03-08T20%3A19%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_swepu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Escherichia%20coli%20EC93%20deploys%20two%20plasmid-encoded%20class%20I%20contact-dependent%20growth%20inhibition%20systems%20for%20antagonistic%20bacterial%20interactions&rft.jtitle=Microbial%20genomics&rft.au=W%C3%A4neskog,%20Marcus&rft.date=2021-03-01&rft.volume=7&rft.issue=3&rft.issn=2057-5858&rft.eissn=2057-5858&rft_id=info:doi/10.1099/mgen.0.000534&rft_dat=%3Cpubmed_swepu%3E33646095%3C/pubmed_swepu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c462t-a1623f0c826676ad0aa98cfbfe360c9c0ec0db0911f2ecdc75d73ffd22103d9e3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/33646095&rfr_iscdi=true |