Loading…
Extracellular protease in Actinomycetes culture supernatants inhibits and detaches Staphylococcus aureus biofilm formation
Bacterial biofilms are associated with chronic infections due to their resistance to antimicrobial agents. Staphylococcus aureus is a versatile human pathogen and can form biofilms on human tissues and diverse medical devices. To identify novel biofilm inhibitors of S. aureus, the supernatants from...
Saved in:
Published in: | Biotechnology letters 2012-04, Vol.34 (4), p.655-661 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c470t-69125656cf1d8b1240c9e33d04834ad74bda386442ba1404fda5054c167906e73 |
---|---|
cites | cdi_FETCH-LOGICAL-c470t-69125656cf1d8b1240c9e33d04834ad74bda386442ba1404fda5054c167906e73 |
container_end_page | 661 |
container_issue | 4 |
container_start_page | 655 |
container_title | Biotechnology letters |
container_volume | 34 |
creator | Park, Joo-Hyeon Lee, Jin-Hyung Kim, Chang-Jin Lee, Jae-Chan Cho, Moo Hwan Lee, Jintae |
description | Bacterial biofilms are associated with chronic infections due to their resistance to antimicrobial agents. Staphylococcus aureus is a versatile human pathogen and can form biofilms on human tissues and diverse medical devices. To identify novel biofilm inhibitors of S. aureus, the supernatants from a library of 458 Actinomycetes strains were screened. The culture supernatants (1% v/v) of more than 10 Actinomycetes strains inhibited S. aureus biofilm formation by more than 80% without affecting the growth. The culture supernatants of these biofilm-reducing Actinomycetes strains contained a protease (equivalent to 0.1 μg proteinase K ml−1), which both inhibited S. aureus biofilm formation and detached pre-existing S. aureus biofilms. This study suggests that protease treatment could be a feasible tool to reduce and eradicate S. aureus biofilms. |
doi_str_mv | 10.1007/s10529-011-0825-z |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_968174153</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1685806261</sourcerecordid><originalsourceid>FETCH-LOGICAL-c470t-69125656cf1d8b1240c9e33d04834ad74bda386442ba1404fda5054c167906e73</originalsourceid><addsrcrecordid>eNqF0k1v1DAQBuAIgehS-AFcIEJCcAnM-DM5VlVbkCpxKD1HE8dhXSXxYjtSd3893u4CEodysiU_M5b9TlG8RviEAPpzRJCsqQCxgprJavekWKHUvFJaq6fFClBgJUXDTooXMd4BQKNBPy9OGEMFnOOq2F3cp0DGjuMyUig3wSdL0ZZuLs9McrOftsYmG0uzjGkJtozLxoaZEs0pZrV2ncsbmvuyt4nMOtObRJv1dvTGG7Pks1yWl875wY1TOfgwUXJ-flk8G2iM9tVxPS1uLy--n3-prr9dfT0_u66M0JAq1SCTSiozYF93yASYxnLeg6i5oF6LrideKyFYRyhADD1JkMKg0g0oq_lp8eHQNz_u52JjaicX9y-m2folto2qUQuU_P-S6ZrzGjDLj49KVLWsQTG1p-_-oXd-yT84PvQDDc3DzXhAJvgYgx3aTXAThW2L0O6zbg9Ztznrdp91u8s1b46Nl26y_Z-K3-Fm8P4IKBoah0CzcfGvy7-KNZfZvT24gXxLP0I2tzcsD08eGKEA1KOC5VlT_Bcv0MSi</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>927070953</pqid></control><display><type>article</type><title>Extracellular protease in Actinomycetes culture supernatants inhibits and detaches Staphylococcus aureus biofilm formation</title><source>Springer Nature</source><creator>Park, Joo-Hyeon ; Lee, Jin-Hyung ; Kim, Chang-Jin ; Lee, Jae-Chan ; Cho, Moo Hwan ; Lee, Jintae</creator><creatorcontrib>Park, Joo-Hyeon ; Lee, Jin-Hyung ; Kim, Chang-Jin ; Lee, Jae-Chan ; Cho, Moo Hwan ; Lee, Jintae</creatorcontrib><description>Bacterial biofilms are associated with chronic infections due to their resistance to antimicrobial agents. Staphylococcus aureus is a versatile human pathogen and can form biofilms on human tissues and diverse medical devices. To identify novel biofilm inhibitors of S. aureus, the supernatants from a library of 458 Actinomycetes strains were screened. The culture supernatants (1% v/v) of more than 10 Actinomycetes strains inhibited S. aureus biofilm formation by more than 80% without affecting the growth. The culture supernatants of these biofilm-reducing Actinomycetes strains contained a protease (equivalent to 0.1 μg proteinase K ml−1), which both inhibited S. aureus biofilm formation and detached pre-existing S. aureus biofilms. This study suggests that protease treatment could be a feasible tool to reduce and eradicate S. aureus biofilms.</description><identifier>ISSN: 0141-5492</identifier><identifier>EISSN: 1573-6776</identifier><identifier>DOI: 10.1007/s10529-011-0825-z</identifier><identifier>PMID: 22160331</identifier><identifier>CODEN: BILED3</identifier><language>eng</language><publisher>Heidelberg: Springer-Verlag</publisher><subject>Actinobacteria - enzymology ; Actinomycetales ; Actinomycetes ; Anti-Bacterial Agents - metabolism ; antibiotic resistance ; Antimicrobial agents ; Bacteria ; Bacterial Adhesion - drug effects ; Bioengineering ; biofilm ; Biofilms ; Biofilms - drug effects ; Biofilms - growth & development ; Biological and medical sciences ; Biotechnology ; Cellular biology ; Culture ; Fundamental and applied biological sciences. Psychology ; Humans ; Inhibitors ; Medical equipment ; pathogens ; Peptide Hydrolases - metabolism ; Protease ; Proteases ; proteinases ; Staphylococcus aureus ; Staphylococcus aureus - drug effects ; Staphylococcus aureus - physiology ; Staphylococcus infections ; Strain</subject><ispartof>Biotechnology letters, 2012-04, Vol.34 (4), p.655-661</ispartof><rights>2015 INIST-CNRS</rights><rights>Springer Science+Business Media B.V. 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-69125656cf1d8b1240c9e33d04834ad74bda386442ba1404fda5054c167906e73</citedby><cites>FETCH-LOGICAL-c470t-69125656cf1d8b1240c9e33d04834ad74bda386442ba1404fda5054c167906e73</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=25651835$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22160331$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Joo-Hyeon</creatorcontrib><creatorcontrib>Lee, Jin-Hyung</creatorcontrib><creatorcontrib>Kim, Chang-Jin</creatorcontrib><creatorcontrib>Lee, Jae-Chan</creatorcontrib><creatorcontrib>Cho, Moo Hwan</creatorcontrib><creatorcontrib>Lee, Jintae</creatorcontrib><title>Extracellular protease in Actinomycetes culture supernatants inhibits and detaches Staphylococcus aureus biofilm formation</title><title>Biotechnology letters</title><addtitle>Biotechnol Lett</addtitle><description>Bacterial biofilms are associated with chronic infections due to their resistance to antimicrobial agents. Staphylococcus aureus is a versatile human pathogen and can form biofilms on human tissues and diverse medical devices. To identify novel biofilm inhibitors of S. aureus, the supernatants from a library of 458 Actinomycetes strains were screened. The culture supernatants (1% v/v) of more than 10 Actinomycetes strains inhibited S. aureus biofilm formation by more than 80% without affecting the growth. The culture supernatants of these biofilm-reducing Actinomycetes strains contained a protease (equivalent to 0.1 μg proteinase K ml−1), which both inhibited S. aureus biofilm formation and detached pre-existing S. aureus biofilms. This study suggests that protease treatment could be a feasible tool to reduce and eradicate S. aureus biofilms.</description><subject>Actinobacteria - enzymology</subject><subject>Actinomycetales</subject><subject>Actinomycetes</subject><subject>Anti-Bacterial Agents - metabolism</subject><subject>antibiotic resistance</subject><subject>Antimicrobial agents</subject><subject>Bacteria</subject><subject>Bacterial Adhesion - drug effects</subject><subject>Bioengineering</subject><subject>biofilm</subject><subject>Biofilms</subject><subject>Biofilms - drug effects</subject><subject>Biofilms - growth & development</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cellular biology</subject><subject>Culture</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Inhibitors</subject><subject>Medical equipment</subject><subject>pathogens</subject><subject>Peptide Hydrolases - metabolism</subject><subject>Protease</subject><subject>Proteases</subject><subject>proteinases</subject><subject>Staphylococcus aureus</subject><subject>Staphylococcus aureus - drug effects</subject><subject>Staphylococcus aureus - physiology</subject><subject>Staphylococcus infections</subject><subject>Strain</subject><issn>0141-5492</issn><issn>1573-6776</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqF0k1v1DAQBuAIgehS-AFcIEJCcAnM-DM5VlVbkCpxKD1HE8dhXSXxYjtSd3893u4CEodysiU_M5b9TlG8RviEAPpzRJCsqQCxgprJavekWKHUvFJaq6fFClBgJUXDTooXMd4BQKNBPy9OGEMFnOOq2F3cp0DGjuMyUig3wSdL0ZZuLs9McrOftsYmG0uzjGkJtozLxoaZEs0pZrV2ncsbmvuyt4nMOtObRJv1dvTGG7Pks1yWl875wY1TOfgwUXJ-flk8G2iM9tVxPS1uLy--n3-prr9dfT0_u66M0JAq1SCTSiozYF93yASYxnLeg6i5oF6LrideKyFYRyhADD1JkMKg0g0oq_lp8eHQNz_u52JjaicX9y-m2folto2qUQuU_P-S6ZrzGjDLj49KVLWsQTG1p-_-oXd-yT84PvQDDc3DzXhAJvgYgx3aTXAThW2L0O6zbg9Ztznrdp91u8s1b46Nl26y_Z-K3-Fm8P4IKBoah0CzcfGvy7-KNZfZvT24gXxLP0I2tzcsD08eGKEA1KOC5VlT_Bcv0MSi</recordid><startdate>20120401</startdate><enddate>20120401</enddate><creator>Park, Joo-Hyeon</creator><creator>Lee, Jin-Hyung</creator><creator>Kim, Chang-Jin</creator><creator>Lee, Jae-Chan</creator><creator>Cho, Moo Hwan</creator><creator>Lee, Jintae</creator><general>Springer-Verlag</general><general>Springer</general><general>Springer Nature B.V</general><scope>FBQ</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>3V.</scope><scope>7QL</scope><scope>7QR</scope><scope>7T7</scope><scope>7TB</scope><scope>7U5</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>L6V</scope><scope>L7M</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>Q9U</scope><scope>7X8</scope><scope>7QO</scope></search><sort><creationdate>20120401</creationdate><title>Extracellular protease in Actinomycetes culture supernatants inhibits and detaches Staphylococcus aureus biofilm formation</title><author>Park, Joo-Hyeon ; Lee, Jin-Hyung ; Kim, Chang-Jin ; Lee, Jae-Chan ; Cho, Moo Hwan ; Lee, Jintae</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-69125656cf1d8b1240c9e33d04834ad74bda386442ba1404fda5054c167906e73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Actinobacteria - enzymology</topic><topic>Actinomycetales</topic><topic>Actinomycetes</topic><topic>Anti-Bacterial Agents - metabolism</topic><topic>antibiotic resistance</topic><topic>Antimicrobial agents</topic><topic>Bacteria</topic><topic>Bacterial Adhesion - drug effects</topic><topic>Bioengineering</topic><topic>biofilm</topic><topic>Biofilms</topic><topic>Biofilms - drug effects</topic><topic>Biofilms - growth & development</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Cellular biology</topic><topic>Culture</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Inhibitors</topic><topic>Medical equipment</topic><topic>pathogens</topic><topic>Peptide Hydrolases - metabolism</topic><topic>Protease</topic><topic>Proteases</topic><topic>proteinases</topic><topic>Staphylococcus aureus</topic><topic>Staphylococcus aureus - drug effects</topic><topic>Staphylococcus aureus - physiology</topic><topic>Staphylococcus infections</topic><topic>Strain</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Joo-Hyeon</creatorcontrib><creatorcontrib>Lee, Jin-Hyung</creatorcontrib><creatorcontrib>Kim, Chang-Jin</creatorcontrib><creatorcontrib>Lee, Jae-Chan</creatorcontrib><creatorcontrib>Cho, Moo Hwan</creatorcontrib><creatorcontrib>Lee, Jintae</creatorcontrib><collection>AGRIS</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>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Chemoreception Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Engineering Collection</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Science Journals</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Engineering Collection</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><jtitle>Biotechnology letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Joo-Hyeon</au><au>Lee, Jin-Hyung</au><au>Kim, Chang-Jin</au><au>Lee, Jae-Chan</au><au>Cho, Moo Hwan</au><au>Lee, Jintae</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Extracellular protease in Actinomycetes culture supernatants inhibits and detaches Staphylococcus aureus biofilm formation</atitle><jtitle>Biotechnology letters</jtitle><addtitle>Biotechnol Lett</addtitle><date>2012-04-01</date><risdate>2012</risdate><volume>34</volume><issue>4</issue><spage>655</spage><epage>661</epage><pages>655-661</pages><issn>0141-5492</issn><eissn>1573-6776</eissn><coden>BILED3</coden><abstract>Bacterial biofilms are associated with chronic infections due to their resistance to antimicrobial agents. Staphylococcus aureus is a versatile human pathogen and can form biofilms on human tissues and diverse medical devices. To identify novel biofilm inhibitors of S. aureus, the supernatants from a library of 458 Actinomycetes strains were screened. The culture supernatants (1% v/v) of more than 10 Actinomycetes strains inhibited S. aureus biofilm formation by more than 80% without affecting the growth. The culture supernatants of these biofilm-reducing Actinomycetes strains contained a protease (equivalent to 0.1 μg proteinase K ml−1), which both inhibited S. aureus biofilm formation and detached pre-existing S. aureus biofilms. This study suggests that protease treatment could be a feasible tool to reduce and eradicate S. aureus biofilms.</abstract><cop>Heidelberg</cop><pub>Springer-Verlag</pub><pmid>22160331</pmid><doi>10.1007/s10529-011-0825-z</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0141-5492 |
ispartof | Biotechnology letters, 2012-04, Vol.34 (4), p.655-661 |
issn | 0141-5492 1573-6776 |
language | eng |
recordid | cdi_proquest_miscellaneous_968174153 |
source | Springer Nature |
subjects | Actinobacteria - enzymology Actinomycetales Actinomycetes Anti-Bacterial Agents - metabolism antibiotic resistance Antimicrobial agents Bacteria Bacterial Adhesion - drug effects Bioengineering biofilm Biofilms Biofilms - drug effects Biofilms - growth & development Biological and medical sciences Biotechnology Cellular biology Culture Fundamental and applied biological sciences. Psychology Humans Inhibitors Medical equipment pathogens Peptide Hydrolases - metabolism Protease Proteases proteinases Staphylococcus aureus Staphylococcus aureus - drug effects Staphylococcus aureus - physiology Staphylococcus infections Strain |
title | Extracellular protease in Actinomycetes culture supernatants inhibits and detaches Staphylococcus aureus biofilm formation |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T15%3A14%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Extracellular%20protease%20in%20Actinomycetes%20culture%20supernatants%20inhibits%20and%20detaches%20Staphylococcus%20aureus%20biofilm%20formation&rft.jtitle=Biotechnology%20letters&rft.au=Park,%20Joo-Hyeon&rft.date=2012-04-01&rft.volume=34&rft.issue=4&rft.spage=655&rft.epage=661&rft.pages=655-661&rft.issn=0141-5492&rft.eissn=1573-6776&rft.coden=BILED3&rft_id=info:doi/10.1007/s10529-011-0825-z&rft_dat=%3Cproquest_cross%3E1685806261%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c470t-69125656cf1d8b1240c9e33d04834ad74bda386442ba1404fda5054c167906e73%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=927070953&rft_id=info:pmid/22160331&rfr_iscdi=true |