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Densely adherent growth mode, rather than extracellular polymer substance matrix build-up ability, contributes to high resistance of Staphylococcus epidermidis biofilms to antibiotics
Objectives (i) To evaluate the role of the adherent growth mode and extracellular polymer substance build-up in biofilm resistance to antibiotics. (ii) To re-assess various mechanisms leading to biofilm resistance to antibiotics. Methods We compared the biofilm MICs, biofilm MBCs using the viable co...
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Published in: | Journal of antimicrobial chemotherapy 2010-07, Vol.65 (7), p.1405-1411 |
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description | Objectives (i) To evaluate the role of the adherent growth mode and extracellular polymer substance build-up in biofilm resistance to antibiotics. (ii) To re-assess various mechanisms leading to biofilm resistance to antibiotics. Methods We compared the biofilm MICs, biofilm MBCs using the viable count method, biofilm MBCs based on broth recovery methods and minimum biofilm eradication concentrations (MBECs) of antistaphylococcal antibiotics for multilayer biofilms formed by ‘biofilm-positive’ S. epidermidis strains and monolayer biofilms formed by their ‘biofilm-negative’ mutants/variants. Bacterial densities and the quantity of persister cells in both multilayer and monolayer biofilms were assessed to evaluate their roles in biofilm resistance. Results Monolayer and multilayer biofilms presented similar susceptibilities to multiple antibiotics, based on biofilm MIC, broth recovery-based biofilm MBC and MBEC results. Multilayer biofilms demonstrated higher viable count-based MBCs than monolayer biofilms. Both monolayer and multilayer biofilms had very high bacterial densities of ∼1011–12 cfu/mL. Persister cells were found in both monolayer and multilayer biofilms, but not in planktonic cultures at log phase. The presence of persister cells in monolayer and multilayer biofilms appeared to be strain and antibiotic dependent. Conclusions The adherent growth mode, rather than the ability to build up a typical multilayer biofilm structure, contributes to the high resistance of biofilms to antibiotics, and therefore might be the main virulence factor of coagulase-negative staphylococci (CoNS) with respect to antibiotic resistance. The presence of persister cells in CoNS biofilms plays an important role in antibiotic resistance. Growth at high bacterial densities is another significant factor in biofilm resistance. |
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(ii) To re-assess various mechanisms leading to biofilm resistance to antibiotics. Methods We compared the biofilm MICs, biofilm MBCs using the viable count method, biofilm MBCs based on broth recovery methods and minimum biofilm eradication concentrations (MBECs) of antistaphylococcal antibiotics for multilayer biofilms formed by ‘biofilm-positive’ S. epidermidis strains and monolayer biofilms formed by their ‘biofilm-negative’ mutants/variants. Bacterial densities and the quantity of persister cells in both multilayer and monolayer biofilms were assessed to evaluate their roles in biofilm resistance. Results Monolayer and multilayer biofilms presented similar susceptibilities to multiple antibiotics, based on biofilm MIC, broth recovery-based biofilm MBC and MBEC results. Multilayer biofilms demonstrated higher viable count-based MBCs than monolayer biofilms. Both monolayer and multilayer biofilms had very high bacterial densities of ∼1011–12 cfu/mL. Persister cells were found in both monolayer and multilayer biofilms, but not in planktonic cultures at log phase. The presence of persister cells in monolayer and multilayer biofilms appeared to be strain and antibiotic dependent. Conclusions The adherent growth mode, rather than the ability to build up a typical multilayer biofilm structure, contributes to the high resistance of biofilms to antibiotics, and therefore might be the main virulence factor of coagulase-negative staphylococci (CoNS) with respect to antibiotic resistance. The presence of persister cells in CoNS biofilms plays an important role in antibiotic resistance. Growth at high bacterial densities is another significant factor in biofilm resistance.</description><identifier>ISSN: 0305-7453</identifier><identifier>EISSN: 1460-2091</identifier><identifier>DOI: 10.1093/jac/dkq119</identifier><identifier>PMID: 20430788</identifier><identifier>CODEN: JACHDX</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Anti-Bacterial Agents - pharmacology ; antibiotic resistance ; Antibiotics ; Antibiotics. Antiinfectious agents. Antiparasitic agents ; Bacterial Adhesion ; Bacterial Proteins ; Bacteriology ; Biofilms ; Biofilms - drug effects ; Biofilms - growth & development ; Biological and medical sciences ; Biopolymers - metabolism ; Cell growth ; Chemotherapy ; coagulase-negative staphylococci ; Drug resistance ; Drug Resistance, Bacterial ; Humans ; Medical sciences ; Microbial Sensitivity Tests ; Microbial Viability - drug effects ; monolayer biofilms ; multilayer biofilms ; persister cells ; Pharmacology. Drug treatments ; Polymers ; Staphylococcus epidermidis ; Staphylococcus epidermidis - drug effects ; Staphylococcus epidermidis - physiology ; Staphylococcus infections ; Transcription Factors</subject><ispartof>Journal of antimicrobial chemotherapy, 2010-07, Vol.65 (7), p.1405-1411</ispartof><rights>2015 INIST-CNRS</rights><rights>Copyright Oxford Publishing Limited(England) Jul 2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c449t-41b79428c10a7699f7816b292801122411e0e7eaa6cbe9e5841b870ac7b4ae473</citedby><cites>FETCH-LOGICAL-c449t-41b79428c10a7699f7816b292801122411e0e7eaa6cbe9e5841b870ac7b4ae473</cites></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=22975394$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20430788$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Qu, Yue</creatorcontrib><creatorcontrib>Daley, Andrew J.</creatorcontrib><creatorcontrib>Istivan, Taghrid S.</creatorcontrib><creatorcontrib>Rouch, Duncan A.</creatorcontrib><creatorcontrib>Deighton, Margaret A.</creatorcontrib><title>Densely adherent growth mode, rather than extracellular polymer substance matrix build-up ability, contributes to high resistance of Staphylococcus epidermidis biofilms to antibiotics</title><title>Journal of antimicrobial chemotherapy</title><addtitle>J Antimicrob Chemother</addtitle><description>Objectives (i) To evaluate the role of the adherent growth mode and extracellular polymer substance build-up in biofilm resistance to antibiotics. (ii) To re-assess various mechanisms leading to biofilm resistance to antibiotics. Methods We compared the biofilm MICs, biofilm MBCs using the viable count method, biofilm MBCs based on broth recovery methods and minimum biofilm eradication concentrations (MBECs) of antistaphylococcal antibiotics for multilayer biofilms formed by ‘biofilm-positive’ S. epidermidis strains and monolayer biofilms formed by their ‘biofilm-negative’ mutants/variants. Bacterial densities and the quantity of persister cells in both multilayer and monolayer biofilms were assessed to evaluate their roles in biofilm resistance. Results Monolayer and multilayer biofilms presented similar susceptibilities to multiple antibiotics, based on biofilm MIC, broth recovery-based biofilm MBC and MBEC results. Multilayer biofilms demonstrated higher viable count-based MBCs than monolayer biofilms. Both monolayer and multilayer biofilms had very high bacterial densities of ∼1011–12 cfu/mL. Persister cells were found in both monolayer and multilayer biofilms, but not in planktonic cultures at log phase. The presence of persister cells in monolayer and multilayer biofilms appeared to be strain and antibiotic dependent. Conclusions The adherent growth mode, rather than the ability to build up a typical multilayer biofilm structure, contributes to the high resistance of biofilms to antibiotics, and therefore might be the main virulence factor of coagulase-negative staphylococci (CoNS) with respect to antibiotic resistance. The presence of persister cells in CoNS biofilms plays an important role in antibiotic resistance. Growth at high bacterial densities is another significant factor in biofilm resistance.</description><subject>Anti-Bacterial Agents - pharmacology</subject><subject>antibiotic resistance</subject><subject>Antibiotics</subject><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Bacterial Adhesion</subject><subject>Bacterial Proteins</subject><subject>Bacteriology</subject><subject>Biofilms</subject><subject>Biofilms - drug effects</subject><subject>Biofilms - growth & development</subject><subject>Biological and medical sciences</subject><subject>Biopolymers - metabolism</subject><subject>Cell growth</subject><subject>Chemotherapy</subject><subject>coagulase-negative staphylococci</subject><subject>Drug resistance</subject><subject>Drug Resistance, Bacterial</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Microbial Sensitivity Tests</subject><subject>Microbial Viability - drug effects</subject><subject>monolayer biofilms</subject><subject>multilayer biofilms</subject><subject>persister cells</subject><subject>Pharmacology. Drug treatments</subject><subject>Polymers</subject><subject>Staphylococcus epidermidis</subject><subject>Staphylococcus epidermidis - drug effects</subject><subject>Staphylococcus epidermidis - physiology</subject><subject>Staphylococcus infections</subject><subject>Transcription Factors</subject><issn>0305-7453</issn><issn>1460-2091</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqFkVGL1DAUhYso7rj64g-QIIggWzdp06Z5XFbdFQYUXUV8Cbfp7TazbdNNUpz5Zf49U2dcwRefws35zoV7TpI8ZfQ1ozI_3YA-bW5uGZP3khXjJU0zKtn9ZEVzWqSCF_lR8sj7DaW0LMrqYXKUUZ5TUVWr5OcbHD32OwJNhw7HQK6d_RE6MtgGT4iDEL9J6GAkuA0ONPb93IMjk-13Q5T8XPsAo0YyQHBmS-rZ9E06TwRq05uwOyHajlGp54CeBEs6c90Rh94cfLYlnwNM3a632mo9e4KTadANpjGe1Ma2ph9-O2EMJs7BaP84edBC7_HJ4T1Ovrx7e3V-ma4_XLw_P1unmnMZUs5qIXlWaUZBlFK2omJlncmsooxlGWcMKQoEKHWNEosqGipBQYuaA3KRHycv93snZ29n9EENxi8hwIh29iqmW3LOCv5_Ms-zklGx7Hz-D7mxsxvjGapYWil5VUXo1R7SznrvsFWTMwO4nWJULbWrWLva1x7hZ4eNcz1gc4f-6TkCLw4AeA1962Lyxv_lMimKXC5HpHsuloPbOx3cjSpFLgp1-e27-rouGP109VFd5L8AWGnJWA</recordid><startdate>20100701</startdate><enddate>20100701</enddate><creator>Qu, Yue</creator><creator>Daley, Andrew J.</creator><creator>Istivan, Taghrid S.</creator><creator>Rouch, Duncan A.</creator><creator>Deighton, Margaret A.</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><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>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7U7</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7X8</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope></search><sort><creationdate>20100701</creationdate><title>Densely adherent growth mode, rather than extracellular polymer substance matrix build-up ability, contributes to high resistance of Staphylococcus epidermidis biofilms to antibiotics</title><author>Qu, Yue ; Daley, Andrew J. ; Istivan, Taghrid S. ; Rouch, Duncan A. ; Deighton, Margaret A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c449t-41b79428c10a7699f7816b292801122411e0e7eaa6cbe9e5841b870ac7b4ae473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Anti-Bacterial Agents - pharmacology</topic><topic>antibiotic resistance</topic><topic>Antibiotics</topic><topic>Antibiotics. Antiinfectious agents. Antiparasitic agents</topic><topic>Bacterial Adhesion</topic><topic>Bacterial Proteins</topic><topic>Bacteriology</topic><topic>Biofilms</topic><topic>Biofilms - drug effects</topic><topic>Biofilms - growth & development</topic><topic>Biological and medical sciences</topic><topic>Biopolymers - metabolism</topic><topic>Cell growth</topic><topic>Chemotherapy</topic><topic>coagulase-negative staphylococci</topic><topic>Drug resistance</topic><topic>Drug Resistance, Bacterial</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Microbial Sensitivity Tests</topic><topic>Microbial Viability - drug effects</topic><topic>monolayer biofilms</topic><topic>multilayer biofilms</topic><topic>persister cells</topic><topic>Pharmacology. Drug treatments</topic><topic>Polymers</topic><topic>Staphylococcus epidermidis</topic><topic>Staphylococcus epidermidis - drug effects</topic><topic>Staphylococcus epidermidis - physiology</topic><topic>Staphylococcus infections</topic><topic>Transcription Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Qu, Yue</creatorcontrib><creatorcontrib>Daley, Andrew J.</creatorcontrib><creatorcontrib>Istivan, Taghrid S.</creatorcontrib><creatorcontrib>Rouch, Duncan A.</creatorcontrib><creatorcontrib>Deighton, Margaret A.</creatorcontrib><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>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><jtitle>Journal of antimicrobial chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Qu, Yue</au><au>Daley, Andrew J.</au><au>Istivan, Taghrid S.</au><au>Rouch, Duncan A.</au><au>Deighton, Margaret A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Densely adherent growth mode, rather than extracellular polymer substance matrix build-up ability, contributes to high resistance of Staphylococcus epidermidis biofilms to antibiotics</atitle><jtitle>Journal of antimicrobial chemotherapy</jtitle><addtitle>J Antimicrob Chemother</addtitle><date>2010-07-01</date><risdate>2010</risdate><volume>65</volume><issue>7</issue><spage>1405</spage><epage>1411</epage><pages>1405-1411</pages><issn>0305-7453</issn><eissn>1460-2091</eissn><coden>JACHDX</coden><abstract>Objectives (i) To evaluate the role of the adherent growth mode and extracellular polymer substance build-up in biofilm resistance to antibiotics. (ii) To re-assess various mechanisms leading to biofilm resistance to antibiotics. Methods We compared the biofilm MICs, biofilm MBCs using the viable count method, biofilm MBCs based on broth recovery methods and minimum biofilm eradication concentrations (MBECs) of antistaphylococcal antibiotics for multilayer biofilms formed by ‘biofilm-positive’ S. epidermidis strains and monolayer biofilms formed by their ‘biofilm-negative’ mutants/variants. Bacterial densities and the quantity of persister cells in both multilayer and monolayer biofilms were assessed to evaluate their roles in biofilm resistance. Results Monolayer and multilayer biofilms presented similar susceptibilities to multiple antibiotics, based on biofilm MIC, broth recovery-based biofilm MBC and MBEC results. Multilayer biofilms demonstrated higher viable count-based MBCs than monolayer biofilms. Both monolayer and multilayer biofilms had very high bacterial densities of ∼1011–12 cfu/mL. Persister cells were found in both monolayer and multilayer biofilms, but not in planktonic cultures at log phase. The presence of persister cells in monolayer and multilayer biofilms appeared to be strain and antibiotic dependent. Conclusions The adherent growth mode, rather than the ability to build up a typical multilayer biofilm structure, contributes to the high resistance of biofilms to antibiotics, and therefore might be the main virulence factor of coagulase-negative staphylococci (CoNS) with respect to antibiotic resistance. The presence of persister cells in CoNS biofilms plays an important role in antibiotic resistance. Growth at high bacterial densities is another significant factor in biofilm resistance.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>20430788</pmid><doi>10.1093/jac/dkq119</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anti-Bacterial Agents - pharmacology antibiotic resistance Antibiotics Antibiotics. Antiinfectious agents. Antiparasitic agents Bacterial Adhesion Bacterial Proteins Bacteriology Biofilms Biofilms - drug effects Biofilms - growth & development Biological and medical sciences Biopolymers - metabolism Cell growth Chemotherapy coagulase-negative staphylococci Drug resistance Drug Resistance, Bacterial Humans Medical sciences Microbial Sensitivity Tests Microbial Viability - drug effects monolayer biofilms multilayer biofilms persister cells Pharmacology. Drug treatments Polymers Staphylococcus epidermidis Staphylococcus epidermidis - drug effects Staphylococcus epidermidis - physiology Staphylococcus infections Transcription Factors |
title | Densely adherent growth mode, rather than extracellular polymer substance matrix build-up ability, contributes to high resistance of Staphylococcus epidermidis biofilms to antibiotics |
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