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Interplay between intrinsic and acquired resistance to quinolones in Stenotrophomonas maltophilia
To analyse whether the mutation‐driven resistance‐acquisition potential of a given bacterium might be a function of its intrinsic resistome, quinolones were used as selective agents and Stenotrophomonas maltophilia was chosen as a bacterial model. S. maltophilia has two elements – SmQnr and SmeDEF –...
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Published in: | Environmental microbiology 2014-05, Vol.16 (5), p.1282-1296 |
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creator | García‐León, Guillermo Salgado, Fabiola Oliveros, Juan Carlos Sánchez, María Blanca Martínez, José Luis |
description | To analyse whether the mutation‐driven resistance‐acquisition potential of a given bacterium might be a function of its intrinsic resistome, quinolones were used as selective agents and Stenotrophomonas maltophilia was chosen as a bacterial model. S. maltophilia has two elements – SmQnr and SmeDEF – that are important in intrinsic resistance to quinolones. Using a battery of mutants in which either or both of these elements had been removed, the apparent mutation frequency for quinolone resistance and the phenotype of the selected mutants were found to be related to the intrinsic resistome and also depended on the concentration of the selector. Most mutants had phenotypes compatible with the overexpression of multidrug efflux pump(s); SmeDEF overexpression was the most common cause of quinolone resistance. Whole genome sequencing showed that mutations of the SmeRv regulator, which result in the overexpression of the efflux pump SmeVWX, are the cause of quinolone resistance in mutants not overexpressing SmeDEF. These results indicate that the development of mutation‐driven antibiotic resistance is highly dependent on the intrinsic resistome, which, at least for synthetic antibiotics such as quinolones, did not develop as a response to the presence of antibiotics in the natural ecosystems in which S. maltophilia evolved. |
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S. maltophilia has two elements – SmQnr and SmeDEF – that are important in intrinsic resistance to quinolones. Using a battery of mutants in which either or both of these elements had been removed, the apparent mutation frequency for quinolone resistance and the phenotype of the selected mutants were found to be related to the intrinsic resistome and also depended on the concentration of the selector. Most mutants had phenotypes compatible with the overexpression of multidrug efflux pump(s); SmeDEF overexpression was the most common cause of quinolone resistance. Whole genome sequencing showed that mutations of the SmeRv regulator, which result in the overexpression of the efflux pump SmeVWX, are the cause of quinolone resistance in mutants not overexpressing SmeDEF. These results indicate that the development of mutation‐driven antibiotic resistance is highly dependent on the intrinsic resistome, which, at least for synthetic antibiotics such as quinolones, did not develop as a response to the presence of antibiotics in the natural ecosystems in which S. maltophilia evolved.</description><identifier>ISSN: 1462-2912</identifier><identifier>EISSN: 1462-2920</identifier><identifier>DOI: 10.1111/1462-2920.12408</identifier><identifier>PMID: 24447641</identifier><language>eng</language><publisher>Oxford: Blackwell Science</publisher><subject>Animal, plant and microbial ecology ; Anti-Bacterial Agents - pharmacology ; antibiotic resistance ; Antibiotics ; bacteria ; Bacterial Proteins - metabolism ; Bacteriology ; batteries ; Biological and medical sciences ; Drug Resistance, Bacterial - genetics ; ecosystems ; Fundamental and applied biological sciences. Psychology ; gene overexpression ; General aspects ; genome ; Membrane Transport Proteins - metabolism ; Microbial ecology ; Microbiology ; Miscellaneous ; mutants ; Mutation ; phenotype ; quinolones ; Quinolones - pharmacology ; Stenotrophomonas maltophilia ; Stenotrophomonas maltophilia - drug effects ; Stenotrophomonas maltophilia - genetics ; Stenotrophomonas maltophilia - metabolism ; transporters</subject><ispartof>Environmental microbiology, 2014-05, Vol.16 (5), p.1282-1296</ispartof><rights>2014 Society for Applied Microbiology and John Wiley & Sons Ltd</rights><rights>2015 INIST-CNRS</rights><rights>2014 Society for Applied Microbiology and John Wiley & Sons Ltd.</rights><rights>Copyright © 2014 Society for Applied Microbiology and John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28428160$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24447641$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>García‐León, Guillermo</creatorcontrib><creatorcontrib>Salgado, Fabiola</creatorcontrib><creatorcontrib>Oliveros, Juan Carlos</creatorcontrib><creatorcontrib>Sánchez, María Blanca</creatorcontrib><creatorcontrib>Martínez, José Luis</creatorcontrib><title>Interplay between intrinsic and acquired resistance to quinolones in Stenotrophomonas maltophilia</title><title>Environmental microbiology</title><addtitle>Environ Microbiol</addtitle><description>To analyse whether the mutation‐driven resistance‐acquisition potential of a given bacterium might be a function of its intrinsic resistome, quinolones were used as selective agents and Stenotrophomonas maltophilia was chosen as a bacterial model. S. maltophilia has two elements – SmQnr and SmeDEF – that are important in intrinsic resistance to quinolones. Using a battery of mutants in which either or both of these elements had been removed, the apparent mutation frequency for quinolone resistance and the phenotype of the selected mutants were found to be related to the intrinsic resistome and also depended on the concentration of the selector. Most mutants had phenotypes compatible with the overexpression of multidrug efflux pump(s); SmeDEF overexpression was the most common cause of quinolone resistance. Whole genome sequencing showed that mutations of the SmeRv regulator, which result in the overexpression of the efflux pump SmeVWX, are the cause of quinolone resistance in mutants not overexpressing SmeDEF. These results indicate that the development of mutation‐driven antibiotic resistance is highly dependent on the intrinsic resistome, which, at least for synthetic antibiotics such as quinolones, did not develop as a response to the presence of antibiotics in the natural ecosystems in which S. maltophilia evolved.</description><subject>Animal, plant and microbial ecology</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>antibiotic resistance</subject><subject>Antibiotics</subject><subject>bacteria</subject><subject>Bacterial Proteins - metabolism</subject><subject>Bacteriology</subject><subject>batteries</subject><subject>Biological and medical sciences</subject><subject>Drug Resistance, Bacterial - genetics</subject><subject>ecosystems</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>gene overexpression</subject><subject>General aspects</subject><subject>genome</subject><subject>Membrane Transport Proteins - metabolism</subject><subject>Microbial ecology</subject><subject>Microbiology</subject><subject>Miscellaneous</subject><subject>mutants</subject><subject>Mutation</subject><subject>phenotype</subject><subject>quinolones</subject><subject>Quinolones - pharmacology</subject><subject>Stenotrophomonas maltophilia</subject><subject>Stenotrophomonas maltophilia - drug effects</subject><subject>Stenotrophomonas maltophilia - genetics</subject><subject>Stenotrophomonas maltophilia - metabolism</subject><subject>transporters</subject><issn>1462-2912</issn><issn>1462-2920</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNkk1v1DAQhiMEoqXlzA0iISQuoR7H8ccRVaWsWqjUpYKbNRs74JLYWztR2X-P010WiRO-eGb8zGhmXhfFCyDvIJ8TYJxWVNHsUkbko-JwH3m8t4EeFM9SuiUERC3I0-KAMsYEZ3BY4MKPNq573JQrO95b60vnx-h8cm2J3pTY3k0uWlNGm1wa0be2HEOZgz70wduU-XI5Wh_GGNY_whA8pnLAfsye6x0eF0867JN9vruPipsPZ19OP1aXV-eL0_eXVceAyApJZ1vVMGJXNWmMabLPaWOg5oQqQoEx0_LOKGkF1h1HIQxFw4VQABRIfVS83dZdx3A32TTqwaXW9j16G6akoamZZBIk-w8UJAepGprR1_-gt2GKPg8yU0JlRqhMvdxR02qwRq-jGzBu9J89Z-DNDsDUYt_FvEeX_nKSUQl8HqLZcveut5v9OxA9y61nQfUsrn6QW599WjwYOa_a5mWJ7K99HsafmmfNG_3187m--AZieaGUvs78qy3fYdD4PeZebpaUAMt_hFCRO_kNV-2zFg</recordid><startdate>201405</startdate><enddate>201405</enddate><creator>García‐León, Guillermo</creator><creator>Salgado, Fabiola</creator><creator>Oliveros, Juan Carlos</creator><creator>Sánchez, María Blanca</creator><creator>Martínez, José Luis</creator><general>Blackwell Science</general><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>Wiley Subscription Services, Inc</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QH</scope><scope>7QL</scope><scope>7ST</scope><scope>7T7</scope><scope>7TN</scope><scope>7U9</scope><scope>7UA</scope><scope>8FD</scope><scope>C1K</scope><scope>F1W</scope><scope>FR3</scope><scope>H94</scope><scope>H95</scope><scope>H97</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>SOI</scope><scope>7X8</scope></search><sort><creationdate>201405</creationdate><title>Interplay between intrinsic and acquired resistance to quinolones in Stenotrophomonas maltophilia</title><author>García‐León, Guillermo ; Salgado, Fabiola ; Oliveros, Juan Carlos ; Sánchez, María Blanca ; Martínez, José Luis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-f4108-a0fec9540eb305dd50fe625d13602902144dc6fd98e7a3f6a77d2ad6779112103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animal, plant and microbial ecology</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>antibiotic resistance</topic><topic>Antibiotics</topic><topic>bacteria</topic><topic>Bacterial Proteins - metabolism</topic><topic>Bacteriology</topic><topic>batteries</topic><topic>Biological and medical sciences</topic><topic>Drug Resistance, Bacterial - genetics</topic><topic>ecosystems</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>gene overexpression</topic><topic>General aspects</topic><topic>genome</topic><topic>Membrane Transport Proteins - metabolism</topic><topic>Microbial ecology</topic><topic>Microbiology</topic><topic>Miscellaneous</topic><topic>mutants</topic><topic>Mutation</topic><topic>phenotype</topic><topic>quinolones</topic><topic>Quinolones - pharmacology</topic><topic>Stenotrophomonas maltophilia</topic><topic>Stenotrophomonas maltophilia - drug effects</topic><topic>Stenotrophomonas maltophilia - genetics</topic><topic>Stenotrophomonas maltophilia - metabolism</topic><topic>transporters</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>García‐León, Guillermo</creatorcontrib><creatorcontrib>Salgado, Fabiola</creatorcontrib><creatorcontrib>Oliveros, Juan Carlos</creatorcontrib><creatorcontrib>Sánchez, María Blanca</creatorcontrib><creatorcontrib>Martínez, José Luis</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Aqualine</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Oceanic Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Water Resources Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Environmental microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>García‐León, Guillermo</au><au>Salgado, Fabiola</au><au>Oliveros, Juan Carlos</au><au>Sánchez, María Blanca</au><au>Martínez, José Luis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interplay between intrinsic and acquired resistance to quinolones in Stenotrophomonas maltophilia</atitle><jtitle>Environmental microbiology</jtitle><addtitle>Environ Microbiol</addtitle><date>2014-05</date><risdate>2014</risdate><volume>16</volume><issue>5</issue><spage>1282</spage><epage>1296</epage><pages>1282-1296</pages><issn>1462-2912</issn><eissn>1462-2920</eissn><abstract>To analyse whether the mutation‐driven resistance‐acquisition potential of a given bacterium might be a function of its intrinsic resistome, quinolones were used as selective agents and Stenotrophomonas maltophilia was chosen as a bacterial model. S. maltophilia has two elements – SmQnr and SmeDEF – that are important in intrinsic resistance to quinolones. Using a battery of mutants in which either or both of these elements had been removed, the apparent mutation frequency for quinolone resistance and the phenotype of the selected mutants were found to be related to the intrinsic resistome and also depended on the concentration of the selector. Most mutants had phenotypes compatible with the overexpression of multidrug efflux pump(s); SmeDEF overexpression was the most common cause of quinolone resistance. Whole genome sequencing showed that mutations of the SmeRv regulator, which result in the overexpression of the efflux pump SmeVWX, are the cause of quinolone resistance in mutants not overexpressing SmeDEF. These results indicate that the development of mutation‐driven antibiotic resistance is highly dependent on the intrinsic resistome, which, at least for synthetic antibiotics such as quinolones, did not develop as a response to the presence of antibiotics in the natural ecosystems in which S. maltophilia evolved.</abstract><cop>Oxford</cop><pub>Blackwell Science</pub><pmid>24447641</pmid><doi>10.1111/1462-2920.12408</doi><tpages>15</tpages></addata></record> |
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subjects | Animal, plant and microbial ecology Anti-Bacterial Agents - pharmacology antibiotic resistance Antibiotics bacteria Bacterial Proteins - metabolism Bacteriology batteries Biological and medical sciences Drug Resistance, Bacterial - genetics ecosystems Fundamental and applied biological sciences. Psychology gene overexpression General aspects genome Membrane Transport Proteins - metabolism Microbial ecology Microbiology Miscellaneous mutants Mutation phenotype quinolones Quinolones - pharmacology Stenotrophomonas maltophilia Stenotrophomonas maltophilia - drug effects Stenotrophomonas maltophilia - genetics Stenotrophomonas maltophilia - metabolism transporters |
title | Interplay between intrinsic and acquired resistance to quinolones in Stenotrophomonas maltophilia |
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