Iron chelator, exopolysaccharide and protease production in Staphylococcus epidermidis: a comparative study of the effects of specific growth rate in biofilm and planktonic culture
1 Department of Pharmacy, University of Manchester, Oxford Road, Manchester M13 9PL, UK 2 Pharmaceutical Sciences Institute, Department of Pharmaceutical and Biological Sciences, University of Aston, Birmingham B4 7ET, UK ABSTRACT Summary: The growth rate of Staphylococcus epidermidis was controlled...
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Veröffentlicht in: | Microbiology (Society for General Microbiology) 1994-01, Vol.140 (1), p.153-157 |
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creator | Evans, Elwyn Brown, Michael R. W Gilbert, Peter |
description | 1 Department of Pharmacy, University of Manchester, Oxford Road, Manchester M13 9PL, UK
2 Pharmaceutical Sciences Institute, Department of Pharmaceutical and Biological Sciences, University of Aston, Birmingham B4 7ET, UK
ABSTRACT
Summary: The growth rate of Staphylococcus epidermidis was controlled for populations growing as a biofilm and perfused with supplemented, simple-salts medium. Production of iron chelators, extracellular protease and exopolysaccharide (EPS) by these populations was assessed as a function of specific growth rate and compared to that by planktonic populations grown in the same medium within a chemostat. Perfused biofilms increased their iron chelator and protease production with increasing growth rate. Chemostat populations decreased their production of iron chelators with increasing growth rate, whilst showing much enhanced production of proteases at intermediate growth rates (µ 0·15-0·25 h –1 ). Production of iron chelator and protease was generally 2-50 times higher by biofilms than by planktonic populations. EPS production was low and relatively unaffected by growth rate for the chemostat cultures (about 0·2 µg per unit cell mass) but high for the attached biofilms, particularly at slow growth rates (about 4 µg per unit cell mass). EPS production within the biofilms decreased markedly with increasing growth rate. At growth rates of 0·35 h –1 and above, the levels of EPS for biofilms and planktonic populations were equivalent. The results of this study clearly indicate that growth as a biofilm markedly influences extracellular virulence factor production by S. epidermidis .
Author for correspondence: Peter Gilbert. Tel: +44 61 275 2361. Fax: +44 61 275 2396.
Keywords: Staphylococcus epidermidis , bofilms, exopolysaccharide, growth rate, virulence factors
Present address: Institute of Ophthalmology, Moorfields Eye Hospital, London, UK. |
doi_str_mv | 10.1099/13500872-140-1-153 |
format | Article |
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2 Pharmaceutical Sciences Institute, Department of Pharmaceutical and Biological Sciences, University of Aston, Birmingham B4 7ET, UK
ABSTRACT
Summary: The growth rate of Staphylococcus epidermidis was controlled for populations growing as a biofilm and perfused with supplemented, simple-salts medium. Production of iron chelators, extracellular protease and exopolysaccharide (EPS) by these populations was assessed as a function of specific growth rate and compared to that by planktonic populations grown in the same medium within a chemostat. Perfused biofilms increased their iron chelator and protease production with increasing growth rate. Chemostat populations decreased their production of iron chelators with increasing growth rate, whilst showing much enhanced production of proteases at intermediate growth rates (µ 0·15-0·25 h –1 ). Production of iron chelator and protease was generally 2-50 times higher by biofilms than by planktonic populations. EPS production was low and relatively unaffected by growth rate for the chemostat cultures (about 0·2 µg per unit cell mass) but high for the attached biofilms, particularly at slow growth rates (about 4 µg per unit cell mass). EPS production within the biofilms decreased markedly with increasing growth rate. At growth rates of 0·35 h –1 and above, the levels of EPS for biofilms and planktonic populations were equivalent. The results of this study clearly indicate that growth as a biofilm markedly influences extracellular virulence factor production by S. epidermidis .
Author for correspondence: Peter Gilbert. Tel: +44 61 275 2361. Fax: +44 61 275 2396.
Keywords: Staphylococcus epidermidis , bofilms, exopolysaccharide, growth rate, virulence factors
Present address: Institute of Ophthalmology, Moorfields Eye Hospital, London, UK.</description><identifier>ISSN: 1350-0872</identifier><identifier>EISSN: 1465-2080</identifier><identifier>DOI: 10.1099/13500872-140-1-153</identifier><identifier>PMID: 8162184</identifier><language>eng</language><publisher>Reading: Soc General Microbiol</publisher><subject>Animals ; Bacterial Adhesion - physiology ; Bacteriological Techniques ; Bacteriology ; Biological and medical sciences ; Culture Media ; Endopeptidases - biosynthesis ; Fundamental and applied biological sciences. Psychology ; Humans ; Kinetics ; Microbiology ; Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains ; Polysaccharides, Bacterial - biosynthesis ; Siderophores - biosynthesis ; Staphylococcus epidermidis - growth & development ; Staphylococcus epidermidis - metabolism ; Staphylococcus epidermidis - pathogenicity ; Virulence - physiology</subject><ispartof>Microbiology (Society for General Microbiology), 1994-01, Vol.140 (1), p.153-157</ispartof><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-31b100c6fea54c5508451f6c894204cdcfff318d0749f11790c6015b2f7ffa883</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4032978$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8162184$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Evans, Elwyn</creatorcontrib><creatorcontrib>Brown, Michael R. W</creatorcontrib><creatorcontrib>Gilbert, Peter</creatorcontrib><title>Iron chelator, exopolysaccharide and protease production in Staphylococcus epidermidis: a comparative study of the effects of specific growth rate in biofilm and planktonic culture</title><title>Microbiology (Society for General Microbiology)</title><addtitle>Microbiology</addtitle><description>1 Department of Pharmacy, University of Manchester, Oxford Road, Manchester M13 9PL, UK
2 Pharmaceutical Sciences Institute, Department of Pharmaceutical and Biological Sciences, University of Aston, Birmingham B4 7ET, UK
ABSTRACT
Summary: The growth rate of Staphylococcus epidermidis was controlled for populations growing as a biofilm and perfused with supplemented, simple-salts medium. Production of iron chelators, extracellular protease and exopolysaccharide (EPS) by these populations was assessed as a function of specific growth rate and compared to that by planktonic populations grown in the same medium within a chemostat. Perfused biofilms increased their iron chelator and protease production with increasing growth rate. Chemostat populations decreased their production of iron chelators with increasing growth rate, whilst showing much enhanced production of proteases at intermediate growth rates (µ 0·15-0·25 h –1 ). Production of iron chelator and protease was generally 2-50 times higher by biofilms than by planktonic populations. EPS production was low and relatively unaffected by growth rate for the chemostat cultures (about 0·2 µg per unit cell mass) but high for the attached biofilms, particularly at slow growth rates (about 4 µg per unit cell mass). EPS production within the biofilms decreased markedly with increasing growth rate. At growth rates of 0·35 h –1 and above, the levels of EPS for biofilms and planktonic populations were equivalent. The results of this study clearly indicate that growth as a biofilm markedly influences extracellular virulence factor production by S. epidermidis .
Author for correspondence: Peter Gilbert. Tel: +44 61 275 2361. Fax: +44 61 275 2396.
Keywords: Staphylococcus epidermidis , bofilms, exopolysaccharide, growth rate, virulence factors
Present address: Institute of Ophthalmology, Moorfields Eye Hospital, London, UK.</description><subject>Animals</subject><subject>Bacterial Adhesion - physiology</subject><subject>Bacteriological Techniques</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Culture Media</subject><subject>Endopeptidases - biosynthesis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Kinetics</subject><subject>Microbiology</subject><subject>Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains</subject><subject>Polysaccharides, Bacterial - biosynthesis</subject><subject>Siderophores - biosynthesis</subject><subject>Staphylococcus epidermidis - growth & development</subject><subject>Staphylococcus epidermidis - metabolism</subject><subject>Staphylococcus epidermidis - pathogenicity</subject><subject>Virulence - physiology</subject><issn>1350-0872</issn><issn>1465-2080</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkc1u1TAQhSMEKm3hBZCQvECIBYGZxPljhyoKlSqxANaW72R8Y0jiYDuU-148II7upaw81vlm5tgny54hvEHourdYVgBtU-QoIcccq_JBdo6yrvICWniY6gTkG_E4uwjhO0ASAc-ysxbrAlt5nv258W4WNPCoo_OvBf92ixsPQRMN2tuehZ57sXgXWQfein6laFOPncWXqJfhMDpyRGsQvCTeT7a34Z3Qgty0aK-j_cUixLU_CGdEHFiwMUwxbNewMFljSey9u4uDSDhvk3fWGTtOx-Wjnn9ENyeK1jGunp9kj4weAz89nZfZt-sPX68-5befP95cvb_NSTYQ8xJ3CEC1YV1JqipoZYWmpraTBUjqyRhTYttDIzuD2HSJBax2hWmM0W1bXmYvj3PTs3-uHKKabCAekyF2a1BNLWXXFU0CiyNI3oXg2ajF20n7g0JQW1TqX1QqRaVQpahS0_PT9HU3cX_fcsom6S9Oug6kR-P1TDbcYxLKoms2k6-O2GD3w531rPY8TzY5SZ-YDNP_jX8BlC-t1w</recordid><startdate>19940101</startdate><enddate>19940101</enddate><creator>Evans, Elwyn</creator><creator>Brown, Michael R. 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W ; Gilbert, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-31b100c6fea54c5508451f6c894204cdcfff318d0749f11790c6015b2f7ffa883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animals</topic><topic>Bacterial Adhesion - physiology</topic><topic>Bacteriological Techniques</topic><topic>Bacteriology</topic><topic>Biological and medical sciences</topic><topic>Culture Media</topic><topic>Endopeptidases - biosynthesis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Kinetics</topic><topic>Microbiology</topic><topic>Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains</topic><topic>Polysaccharides, Bacterial - biosynthesis</topic><topic>Siderophores - biosynthesis</topic><topic>Staphylococcus epidermidis - growth & development</topic><topic>Staphylococcus epidermidis - metabolism</topic><topic>Staphylococcus epidermidis - pathogenicity</topic><topic>Virulence - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Evans, Elwyn</creatorcontrib><creatorcontrib>Brown, Michael R. W</creatorcontrib><creatorcontrib>Gilbert, Peter</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>Microbiology (Society for General Microbiology)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Evans, Elwyn</au><au>Brown, Michael R. W</au><au>Gilbert, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Iron chelator, exopolysaccharide and protease production in Staphylococcus epidermidis: a comparative study of the effects of specific growth rate in biofilm and planktonic culture</atitle><jtitle>Microbiology (Society for General Microbiology)</jtitle><addtitle>Microbiology</addtitle><date>1994-01-01</date><risdate>1994</risdate><volume>140</volume><issue>1</issue><spage>153</spage><epage>157</epage><pages>153-157</pages><issn>1350-0872</issn><eissn>1465-2080</eissn><abstract>1 Department of Pharmacy, University of Manchester, Oxford Road, Manchester M13 9PL, UK
2 Pharmaceutical Sciences Institute, Department of Pharmaceutical and Biological Sciences, University of Aston, Birmingham B4 7ET, UK
ABSTRACT
Summary: The growth rate of Staphylococcus epidermidis was controlled for populations growing as a biofilm and perfused with supplemented, simple-salts medium. Production of iron chelators, extracellular protease and exopolysaccharide (EPS) by these populations was assessed as a function of specific growth rate and compared to that by planktonic populations grown in the same medium within a chemostat. Perfused biofilms increased their iron chelator and protease production with increasing growth rate. Chemostat populations decreased their production of iron chelators with increasing growth rate, whilst showing much enhanced production of proteases at intermediate growth rates (µ 0·15-0·25 h –1 ). Production of iron chelator and protease was generally 2-50 times higher by biofilms than by planktonic populations. EPS production was low and relatively unaffected by growth rate for the chemostat cultures (about 0·2 µg per unit cell mass) but high for the attached biofilms, particularly at slow growth rates (about 4 µg per unit cell mass). EPS production within the biofilms decreased markedly with increasing growth rate. At growth rates of 0·35 h –1 and above, the levels of EPS for biofilms and planktonic populations were equivalent. The results of this study clearly indicate that growth as a biofilm markedly influences extracellular virulence factor production by S. epidermidis .
Author for correspondence: Peter Gilbert. Tel: +44 61 275 2361. Fax: +44 61 275 2396.
Keywords: Staphylococcus epidermidis , bofilms, exopolysaccharide, growth rate, virulence factors
Present address: Institute of Ophthalmology, Moorfields Eye Hospital, London, UK.</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>8162184</pmid><doi>10.1099/13500872-140-1-153</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Bacterial Adhesion - physiology Bacteriological Techniques Bacteriology Biological and medical sciences Culture Media Endopeptidases - biosynthesis Fundamental and applied biological sciences. Psychology Humans Kinetics Microbiology Pathogenicity, virulence, toxins, bacteriocins, pyrogens, host-bacteria relations, miscellaneous strains Polysaccharides, Bacterial - biosynthesis Siderophores - biosynthesis Staphylococcus epidermidis - growth & development Staphylococcus epidermidis - metabolism Staphylococcus epidermidis - pathogenicity Virulence - physiology |
title | Iron chelator, exopolysaccharide and protease production in Staphylococcus epidermidis: a comparative study of the effects of specific growth rate in biofilm and planktonic culture |
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