Inhibition of Pseudomonas aeruginosa quorum sensing by chemical induction of the MexEF-oprN efflux pump
The cell-to-cell communication system quorum sensing (QS), used by various pathogenic bacteria to synchronize gene expression and increase host invasion potentials, is studied as a potential target for persistent infection control. To search for novel molecules targeting the QS system in the Gram-ne...
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Veröffentlicht in: | Antimicrobial agents and chemotherapy 2024-02, Vol.68 (2), p.e0138723-e0138723 |
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creator | Kristensen, Rasmus Andersen, Jens Bo Rybtke, Morten Jansen, Charlotte Uldahl Fritz, Blaine Gabriel Kiilerich, Rikke Overgaard Uhd, Jesper Bjarnsholt, Thomas Qvortrup, Katrine Tolker-Nielsen, Tim Givskov, Michael Jakobsen, Tim Holm |
description | The cell-to-cell communication system quorum sensing (QS), used by various pathogenic bacteria to synchronize gene expression and increase host invasion potentials, is studied as a potential target for persistent infection control. To search for novel molecules targeting the QS system in the Gram-negative opportunistic pathogen
, a chemical library consisting of 3,280 small compounds from LifeArc was screened. A series of 10 conjugated phenones that have not previously been reported to target bacteria were identified as inhibitors of QS in
. Two lead compounds (ethylthio enynone and propylthio enynone) were re-synthesized for verification of activity and further elucidation of the mode of action. The isomeric pure Z-ethylthio enynone was used for RNA sequencing, revealing a strong inhibitor of QS-regulated genes, and the QS-regulated virulence factors rhamnolipid and pyocyanin were significantly decreased by treatment with the compounds. A transposon mutagenesis screen performed in a newly constructed
monitor strain identified the target of Z-ethylthio enynone in
to be the MexEF-OprN efflux pump, which was further established using defined
knockout mutants. Our data indicate that the QS inhibitory capabilities of Z-ethylthio enynone were caused by the drainage of intracellular signal molecules as a response to chemical-induced stimulation of the MexEF-oprN efflux pump, thereby inhibiting the autogenerated positive feedback and its enhanced signal-molecule synthesis. |
doi_str_mv | 10.1128/aac.01387-23 |
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, a chemical library consisting of 3,280 small compounds from LifeArc was screened. A series of 10 conjugated phenones that have not previously been reported to target bacteria were identified as inhibitors of QS in
. Two lead compounds (ethylthio enynone and propylthio enynone) were re-synthesized for verification of activity and further elucidation of the mode of action. The isomeric pure Z-ethylthio enynone was used for RNA sequencing, revealing a strong inhibitor of QS-regulated genes, and the QS-regulated virulence factors rhamnolipid and pyocyanin were significantly decreased by treatment with the compounds. A transposon mutagenesis screen performed in a newly constructed
monitor strain identified the target of Z-ethylthio enynone in
to be the MexEF-OprN efflux pump, which was further established using defined
knockout mutants. Our data indicate that the QS inhibitory capabilities of Z-ethylthio enynone were caused by the drainage of intracellular signal molecules as a response to chemical-induced stimulation of the MexEF-oprN efflux pump, thereby inhibiting the autogenerated positive feedback and its enhanced signal-molecule synthesis.</description><identifier>ISSN: 0066-4804</identifier><identifier>EISSN: 1098-6596</identifier><identifier>DOI: 10.1128/aac.01387-23</identifier><identifier>PMID: 38189278</identifier><language>eng</language><publisher>United States: American Society for Microbiology</publisher><subject>Bacteriology ; Mechanisms of Action: Physiological Effects</subject><ispartof>Antimicrobial agents and chemotherapy, 2024-02, Vol.68 (2), p.e0138723-e0138723</ispartof><rights>Copyright © 2024 Kristensen et al.</rights><rights>Copyright © 2024 Kristensen et al. 2024 Kristensen et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a419t-747e89d6f1c475dd50060afc6b268e310554cabbaba1ec2c14ec19d2d42ce4b33</citedby><cites>FETCH-LOGICAL-a419t-747e89d6f1c475dd50060afc6b268e310554cabbaba1ec2c14ec19d2d42ce4b33</cites><orcidid>0000-0002-1671-2155 ; 0000-0002-9751-474X ; 0000-0002-8003-7414 ; 0000-0001-5004-8609</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/PMC10848761/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10848761/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38189278$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Carattoli, Alessandra</contributor><creatorcontrib>Kristensen, Rasmus</creatorcontrib><creatorcontrib>Andersen, Jens Bo</creatorcontrib><creatorcontrib>Rybtke, Morten</creatorcontrib><creatorcontrib>Jansen, Charlotte Uldahl</creatorcontrib><creatorcontrib>Fritz, Blaine Gabriel</creatorcontrib><creatorcontrib>Kiilerich, Rikke Overgaard</creatorcontrib><creatorcontrib>Uhd, Jesper</creatorcontrib><creatorcontrib>Bjarnsholt, Thomas</creatorcontrib><creatorcontrib>Qvortrup, Katrine</creatorcontrib><creatorcontrib>Tolker-Nielsen, Tim</creatorcontrib><creatorcontrib>Givskov, Michael</creatorcontrib><creatorcontrib>Jakobsen, Tim Holm</creatorcontrib><title>Inhibition of Pseudomonas aeruginosa quorum sensing by chemical induction of the MexEF-oprN efflux pump</title><title>Antimicrobial agents and chemotherapy</title><addtitle>Antimicrob Agents Chemother</addtitle><addtitle>Antimicrob Agents Chemother</addtitle><description>The cell-to-cell communication system quorum sensing (QS), used by various pathogenic bacteria to synchronize gene expression and increase host invasion potentials, is studied as a potential target for persistent infection control. To search for novel molecules targeting the QS system in the Gram-negative opportunistic pathogen
, a chemical library consisting of 3,280 small compounds from LifeArc was screened. A series of 10 conjugated phenones that have not previously been reported to target bacteria were identified as inhibitors of QS in
. Two lead compounds (ethylthio enynone and propylthio enynone) were re-synthesized for verification of activity and further elucidation of the mode of action. The isomeric pure Z-ethylthio enynone was used for RNA sequencing, revealing a strong inhibitor of QS-regulated genes, and the QS-regulated virulence factors rhamnolipid and pyocyanin were significantly decreased by treatment with the compounds. A transposon mutagenesis screen performed in a newly constructed
monitor strain identified the target of Z-ethylthio enynone in
to be the MexEF-OprN efflux pump, which was further established using defined
knockout mutants. Our data indicate that the QS inhibitory capabilities of Z-ethylthio enynone were caused by the drainage of intracellular signal molecules as a response to chemical-induced stimulation of the MexEF-oprN efflux pump, thereby inhibiting the autogenerated positive feedback and its enhanced signal-molecule synthesis.</description><subject>Bacteriology</subject><subject>Mechanisms of Action: Physiological Effects</subject><issn>0066-4804</issn><issn>1098-6596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp1kU1v1DAQhi0Eokvhxhn5CBIpHsdJnBOqqhYqlY8DnK2JM9l1ldipHaP235Nl2woOnEajeeedj4ex1yBOAKT-gGhPBJS6KWT5hG1AtLqoq7Z-yjZC1HWhtFBH7EVK12LNq1Y8Z0elBt3KRm_Y9tLvXOcWFzwPA_-eKPdhCh4TR4p563xIyG9yiHniiXxyfsu7O253NDmLI3e-z_ahfdkR_0K35xdFmONXTsMw5ls-52l-yZ4NOCZ6dR-P2c-L8x9nn4urb58uz06vClTQLkWjGtJtXw9gVVP1fbWuLHCwdSdrTSWIqlIWuw47BLLSgiILbS97JS2priyP2ceD75y7iXpLfok4mjm6CeOdCejMvxXvdmYbfhkQWummhtXh7b1DDDeZ0mImlyyNI3oKORnZAmglRLMf9v4gtTGkFGl4nAPC7OGYFY75A8fIvfzdQY5pkuY65OjXV_xP--bvOx6NH8iVvwE1KJp1</recordid><startdate>20240207</startdate><enddate>20240207</enddate><creator>Kristensen, Rasmus</creator><creator>Andersen, Jens Bo</creator><creator>Rybtke, Morten</creator><creator>Jansen, Charlotte Uldahl</creator><creator>Fritz, Blaine Gabriel</creator><creator>Kiilerich, Rikke Overgaard</creator><creator>Uhd, Jesper</creator><creator>Bjarnsholt, Thomas</creator><creator>Qvortrup, Katrine</creator><creator>Tolker-Nielsen, Tim</creator><creator>Givskov, Michael</creator><creator>Jakobsen, Tim Holm</creator><general>American Society for Microbiology</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-1671-2155</orcidid><orcidid>https://orcid.org/0000-0002-9751-474X</orcidid><orcidid>https://orcid.org/0000-0002-8003-7414</orcidid><orcidid>https://orcid.org/0000-0001-5004-8609</orcidid></search><sort><creationdate>20240207</creationdate><title>Inhibition of Pseudomonas aeruginosa quorum sensing by chemical induction of the MexEF-oprN efflux pump</title><author>Kristensen, Rasmus ; Andersen, Jens Bo ; Rybtke, Morten ; Jansen, Charlotte Uldahl ; Fritz, Blaine Gabriel ; Kiilerich, Rikke Overgaard ; Uhd, Jesper ; Bjarnsholt, Thomas ; Qvortrup, Katrine ; Tolker-Nielsen, Tim ; Givskov, Michael ; Jakobsen, Tim Holm</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a419t-747e89d6f1c475dd50060afc6b268e310554cabbaba1ec2c14ec19d2d42ce4b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Bacteriology</topic><topic>Mechanisms of Action: Physiological Effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kristensen, Rasmus</creatorcontrib><creatorcontrib>Andersen, Jens Bo</creatorcontrib><creatorcontrib>Rybtke, Morten</creatorcontrib><creatorcontrib>Jansen, Charlotte Uldahl</creatorcontrib><creatorcontrib>Fritz, Blaine Gabriel</creatorcontrib><creatorcontrib>Kiilerich, Rikke Overgaard</creatorcontrib><creatorcontrib>Uhd, Jesper</creatorcontrib><creatorcontrib>Bjarnsholt, Thomas</creatorcontrib><creatorcontrib>Qvortrup, Katrine</creatorcontrib><creatorcontrib>Tolker-Nielsen, Tim</creatorcontrib><creatorcontrib>Givskov, Michael</creatorcontrib><creatorcontrib>Jakobsen, Tim Holm</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Antimicrobial agents and chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kristensen, Rasmus</au><au>Andersen, Jens Bo</au><au>Rybtke, Morten</au><au>Jansen, Charlotte Uldahl</au><au>Fritz, Blaine Gabriel</au><au>Kiilerich, Rikke Overgaard</au><au>Uhd, Jesper</au><au>Bjarnsholt, Thomas</au><au>Qvortrup, Katrine</au><au>Tolker-Nielsen, Tim</au><au>Givskov, Michael</au><au>Jakobsen, Tim Holm</au><au>Carattoli, Alessandra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Inhibition of Pseudomonas aeruginosa quorum sensing by chemical induction of the MexEF-oprN efflux pump</atitle><jtitle>Antimicrobial agents and chemotherapy</jtitle><stitle>Antimicrob Agents Chemother</stitle><addtitle>Antimicrob Agents Chemother</addtitle><date>2024-02-07</date><risdate>2024</risdate><volume>68</volume><issue>2</issue><spage>e0138723</spage><epage>e0138723</epage><pages>e0138723-e0138723</pages><issn>0066-4804</issn><eissn>1098-6596</eissn><abstract>The cell-to-cell communication system quorum sensing (QS), used by various pathogenic bacteria to synchronize gene expression and increase host invasion potentials, is studied as a potential target for persistent infection control. To search for novel molecules targeting the QS system in the Gram-negative opportunistic pathogen
, a chemical library consisting of 3,280 small compounds from LifeArc was screened. A series of 10 conjugated phenones that have not previously been reported to target bacteria were identified as inhibitors of QS in
. Two lead compounds (ethylthio enynone and propylthio enynone) were re-synthesized for verification of activity and further elucidation of the mode of action. The isomeric pure Z-ethylthio enynone was used for RNA sequencing, revealing a strong inhibitor of QS-regulated genes, and the QS-regulated virulence factors rhamnolipid and pyocyanin were significantly decreased by treatment with the compounds. A transposon mutagenesis screen performed in a newly constructed
monitor strain identified the target of Z-ethylthio enynone in
to be the MexEF-OprN efflux pump, which was further established using defined
knockout mutants. Our data indicate that the QS inhibitory capabilities of Z-ethylthio enynone were caused by the drainage of intracellular signal molecules as a response to chemical-induced stimulation of the MexEF-oprN efflux pump, thereby inhibiting the autogenerated positive feedback and its enhanced signal-molecule synthesis.</abstract><cop>United States</cop><pub>American Society for Microbiology</pub><pmid>38189278</pmid><doi>10.1128/aac.01387-23</doi><tpages>25</tpages><orcidid>https://orcid.org/0000-0002-1671-2155</orcidid><orcidid>https://orcid.org/0000-0002-9751-474X</orcidid><orcidid>https://orcid.org/0000-0002-8003-7414</orcidid><orcidid>https://orcid.org/0000-0001-5004-8609</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bacteriology Mechanisms of Action: Physiological Effects |
title | Inhibition of Pseudomonas aeruginosa quorum sensing by chemical induction of the MexEF-oprN efflux pump |
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