Targeted-antibacterial-plasmids (TAPs) combining conjugation and CRISPR/Cas systems achieve strain-specific antibacterial activity
Abstract The global emergence of drug-resistant bacteria leads to the loss of efficacy of our antibiotics arsenal and severely limits the success of currently available treatments. Here, we developed an innovative strategy based on targeted-antibacterial-plasmids (TAPs) that use bacterial conjugatio...
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Veröffentlicht in: | Nucleic acids research 2021-04, Vol.49 (6), p.3584-3598 |
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creator | Reuter, Audrey Hilpert, Cécile Dedieu-Berne, Annick Lematre, Sophie Gueguen, Erwan Launay, Guillaume Bigot, Sarah Lesterlin, Christian |
description | Abstract
The global emergence of drug-resistant bacteria leads to the loss of efficacy of our antibiotics arsenal and severely limits the success of currently available treatments. Here, we developed an innovative strategy based on targeted-antibacterial-plasmids (TAPs) that use bacterial conjugation to deliver CRISPR/Cas systems exerting a strain-specific antibacterial activity. TAPs are highly versatile as they can be directed against any specific genomic or plasmid DNA using the custom algorithm (CSTB) that identifies appropriate targeting spacer sequences. We demonstrate the ability of TAPs to induce strain-selective killing by introducing lethal double strand breaks (DSBs) into the targeted genomes. TAPs directed against a plasmid-born carbapenem resistance gene efficiently resensitise the strain to the drug. This work represents an essential step toward the development of an alternative to antibiotic treatments, which could be used for in situ microbiota modification to eradicate targeted resistant and/or pathogenic bacteria without affecting other non-targeted bacterial species. |
doi_str_mv | 10.1093/nar/gkab126 |
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The global emergence of drug-resistant bacteria leads to the loss of efficacy of our antibiotics arsenal and severely limits the success of currently available treatments. Here, we developed an innovative strategy based on targeted-antibacterial-plasmids (TAPs) that use bacterial conjugation to deliver CRISPR/Cas systems exerting a strain-specific antibacterial activity. TAPs are highly versatile as they can be directed against any specific genomic or plasmid DNA using the custom algorithm (CSTB) that identifies appropriate targeting spacer sequences. We demonstrate the ability of TAPs to induce strain-selective killing by introducing lethal double strand breaks (DSBs) into the targeted genomes. TAPs directed against a plasmid-born carbapenem resistance gene efficiently resensitise the strain to the drug. This work represents an essential step toward the development of an alternative to antibiotic treatments, which could be used for in situ microbiota modification to eradicate targeted resistant and/or pathogenic bacteria without affecting other non-targeted bacterial species.</description><identifier>ISSN: 0305-1048</identifier><identifier>EISSN: 1362-4962</identifier><identifier>DOI: 10.1093/nar/gkab126</identifier><identifier>PMID: 33660775</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Bacteriology ; Carbapenem-Resistant Enterobacteriaceae ; Carbapenem-Resistant Enterobacteriaceae - genetics ; Conjugation, Genetic ; CRISPR-Cas Systems ; Enterobacteriaceae ; Enterobacteriaceae - genetics ; Escherichia coli ; Escherichia coli - genetics ; Life Sciences ; Microbiology and Parasitology ; Pharmaceutical sciences ; Pharmacology ; Plasmids ; Plasmids - genetics ; RNA ; RNA - chemistry ; Software ; Species Specificity ; Synthetic Biology and Bioengineering</subject><ispartof>Nucleic acids research, 2021-04, Vol.49 (6), p.3584-3598</ispartof><rights>The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research. 2021</rights><rights>The Author(s) 2021. Published by Oxford University Press on behalf of Nucleic Acids Research.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c446t-882f5a8bcf53e9acfe76b2ec5790e5adc3d5350e0f62a54e4b629feafe10a1c53</citedby><cites>FETCH-LOGICAL-c446t-882f5a8bcf53e9acfe76b2ec5790e5adc3d5350e0f62a54e4b629feafe10a1c53</cites><orcidid>0000-0002-9108-0848 ; 0000-0002-9340-6303 ; 0000-0001-8784-1491</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/PMC8034655/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8034655/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,861,882,1599,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33660775$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03384939$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Reuter, Audrey</creatorcontrib><creatorcontrib>Hilpert, Cécile</creatorcontrib><creatorcontrib>Dedieu-Berne, Annick</creatorcontrib><creatorcontrib>Lematre, Sophie</creatorcontrib><creatorcontrib>Gueguen, Erwan</creatorcontrib><creatorcontrib>Launay, Guillaume</creatorcontrib><creatorcontrib>Bigot, Sarah</creatorcontrib><creatorcontrib>Lesterlin, Christian</creatorcontrib><title>Targeted-antibacterial-plasmids (TAPs) combining conjugation and CRISPR/Cas systems achieve strain-specific antibacterial activity</title><title>Nucleic acids research</title><addtitle>Nucleic Acids Res</addtitle><description>Abstract
The global emergence of drug-resistant bacteria leads to the loss of efficacy of our antibiotics arsenal and severely limits the success of currently available treatments. Here, we developed an innovative strategy based on targeted-antibacterial-plasmids (TAPs) that use bacterial conjugation to deliver CRISPR/Cas systems exerting a strain-specific antibacterial activity. TAPs are highly versatile as they can be directed against any specific genomic or plasmid DNA using the custom algorithm (CSTB) that identifies appropriate targeting spacer sequences. We demonstrate the ability of TAPs to induce strain-selective killing by introducing lethal double strand breaks (DSBs) into the targeted genomes. TAPs directed against a plasmid-born carbapenem resistance gene efficiently resensitise the strain to the drug. This work represents an essential step toward the development of an alternative to antibiotic treatments, which could be used for in situ microbiota modification to eradicate targeted resistant and/or pathogenic bacteria without affecting other non-targeted bacterial species.</description><subject>Bacteriology</subject><subject>Carbapenem-Resistant Enterobacteriaceae</subject><subject>Carbapenem-Resistant Enterobacteriaceae - genetics</subject><subject>Conjugation, Genetic</subject><subject>CRISPR-Cas Systems</subject><subject>Enterobacteriaceae</subject><subject>Enterobacteriaceae - genetics</subject><subject>Escherichia coli</subject><subject>Escherichia coli - genetics</subject><subject>Life Sciences</subject><subject>Microbiology and Parasitology</subject><subject>Pharmaceutical sciences</subject><subject>Pharmacology</subject><subject>Plasmids</subject><subject>Plasmids - genetics</subject><subject>RNA</subject><subject>RNA - chemistry</subject><subject>Software</subject><subject>Species Specificity</subject><subject>Synthetic Biology and Bioengineering</subject><issn>0305-1048</issn><issn>1362-4962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><sourceid>EIF</sourceid><recordid>eNp9kc9r2zAUx8VYWbNup92HT6NleJGsH7YvgxDWtRBY6bKzeJafHXW27FpyINf95XVIWtoedpLQ--jz3uNLyCdGvzGa87mDYV7_hYIl6g2ZMa6SWOQqeUtmlFMZMyqyU_Le-ztKmWBSvCOnnCtF01TOyL81DDUGLGNwwRZgAg4WmrhvwLe29NH5enHjLyLTtYV11tXTzd2NNQTbuQhcGS1vr3_f3M6X4CO_8wFbH4HZWNxi5MMA1sW-R2Mra6IXLSYq2K0Nuw_kpILG48fjeUb-XP5YL6_i1a-f18vFKjZCqBBnWVJJyApTSY45mApTVSRoZJpTlFAaXkouKdJKJSAFikIleYVQIaPAjORn5PvB249Fi6VBN43X6H6wLQw73YHVLyvObnTdbXVGuVByL7g4CDavvl0tVnr_RjnPRM7zLZvY82Ozobsf0QfdWm-wacBhN3qdiDxllCZij349oGbovB-wenIzqvcJ6ylhfUx4oj8_3-KJfYx0Ar4cgG7s_2t6AJius1Y</recordid><startdate>20210406</startdate><enddate>20210406</enddate><creator>Reuter, Audrey</creator><creator>Hilpert, Cécile</creator><creator>Dedieu-Berne, Annick</creator><creator>Lematre, Sophie</creator><creator>Gueguen, Erwan</creator><creator>Launay, Guillaume</creator><creator>Bigot, Sarah</creator><creator>Lesterlin, Christian</creator><general>Oxford University Press</general><scope>TOX</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>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9108-0848</orcidid><orcidid>https://orcid.org/0000-0002-9340-6303</orcidid><orcidid>https://orcid.org/0000-0001-8784-1491</orcidid></search><sort><creationdate>20210406</creationdate><title>Targeted-antibacterial-plasmids (TAPs) combining conjugation and CRISPR/Cas systems achieve strain-specific antibacterial activity</title><author>Reuter, Audrey ; Hilpert, Cécile ; Dedieu-Berne, Annick ; Lematre, Sophie ; Gueguen, Erwan ; Launay, Guillaume ; Bigot, Sarah ; Lesterlin, Christian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c446t-882f5a8bcf53e9acfe76b2ec5790e5adc3d5350e0f62a54e4b629feafe10a1c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Bacteriology</topic><topic>Carbapenem-Resistant Enterobacteriaceae</topic><topic>Carbapenem-Resistant Enterobacteriaceae - genetics</topic><topic>Conjugation, Genetic</topic><topic>CRISPR-Cas Systems</topic><topic>Enterobacteriaceae</topic><topic>Enterobacteriaceae - genetics</topic><topic>Escherichia coli</topic><topic>Escherichia coli - genetics</topic><topic>Life Sciences</topic><topic>Microbiology and Parasitology</topic><topic>Pharmaceutical sciences</topic><topic>Pharmacology</topic><topic>Plasmids</topic><topic>Plasmids - genetics</topic><topic>RNA</topic><topic>RNA - chemistry</topic><topic>Software</topic><topic>Species Specificity</topic><topic>Synthetic Biology and Bioengineering</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reuter, Audrey</creatorcontrib><creatorcontrib>Hilpert, Cécile</creatorcontrib><creatorcontrib>Dedieu-Berne, Annick</creatorcontrib><creatorcontrib>Lematre, Sophie</creatorcontrib><creatorcontrib>Gueguen, Erwan</creatorcontrib><creatorcontrib>Launay, Guillaume</creatorcontrib><creatorcontrib>Bigot, Sarah</creatorcontrib><creatorcontrib>Lesterlin, Christian</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</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>Nucleic acids research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reuter, Audrey</au><au>Hilpert, Cécile</au><au>Dedieu-Berne, Annick</au><au>Lematre, Sophie</au><au>Gueguen, Erwan</au><au>Launay, Guillaume</au><au>Bigot, Sarah</au><au>Lesterlin, Christian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeted-antibacterial-plasmids (TAPs) combining conjugation and CRISPR/Cas systems achieve strain-specific antibacterial activity</atitle><jtitle>Nucleic acids research</jtitle><addtitle>Nucleic Acids Res</addtitle><date>2021-04-06</date><risdate>2021</risdate><volume>49</volume><issue>6</issue><spage>3584</spage><epage>3598</epage><pages>3584-3598</pages><issn>0305-1048</issn><eissn>1362-4962</eissn><abstract>Abstract
The global emergence of drug-resistant bacteria leads to the loss of efficacy of our antibiotics arsenal and severely limits the success of currently available treatments. Here, we developed an innovative strategy based on targeted-antibacterial-plasmids (TAPs) that use bacterial conjugation to deliver CRISPR/Cas systems exerting a strain-specific antibacterial activity. TAPs are highly versatile as they can be directed against any specific genomic or plasmid DNA using the custom algorithm (CSTB) that identifies appropriate targeting spacer sequences. We demonstrate the ability of TAPs to induce strain-selective killing by introducing lethal double strand breaks (DSBs) into the targeted genomes. TAPs directed against a plasmid-born carbapenem resistance gene efficiently resensitise the strain to the drug. This work represents an essential step toward the development of an alternative to antibiotic treatments, which could be used for in situ microbiota modification to eradicate targeted resistant and/or pathogenic bacteria without affecting other non-targeted bacterial species.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>33660775</pmid><doi>10.1093/nar/gkab126</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-9108-0848</orcidid><orcidid>https://orcid.org/0000-0002-9340-6303</orcidid><orcidid>https://orcid.org/0000-0001-8784-1491</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bacteriology Carbapenem-Resistant Enterobacteriaceae Carbapenem-Resistant Enterobacteriaceae - genetics Conjugation, Genetic CRISPR-Cas Systems Enterobacteriaceae Enterobacteriaceae - genetics Escherichia coli Escherichia coli - genetics Life Sciences Microbiology and Parasitology Pharmaceutical sciences Pharmacology Plasmids Plasmids - genetics RNA RNA - chemistry Software Species Specificity Synthetic Biology and Bioengineering |
title | Targeted-antibacterial-plasmids (TAPs) combining conjugation and CRISPR/Cas systems achieve strain-specific antibacterial activity |
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