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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
Main Authors: Qu, Yue, Daley, Andrew J., Istivan, Taghrid S., Rouch, Duncan A., Deighton, Margaret A.
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container_title Journal of antimicrobial chemotherapy
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creator Qu, Yue
Daley, Andrew J.
Istivan, Taghrid S.
Rouch, Duncan A.
Deighton, Margaret A.
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.
doi_str_mv 10.1093/jac/dkq119
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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 &amp; 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. 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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><subject>Anti-Bacterial Agents - pharmacology</subject><subject>antibiotic resistance</subject><subject>Antibiotics</subject><subject>Antibiotics. Antiinfectious agents. 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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.</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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source Oxford Journals Online
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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