Loading…
Antimicrobial Potential of Caffeic Acid against Staphylococcus aureus Clinical Strains
Phenolic compounds constitute one of the most promising and ubiquitous groups with many biological activities. Synergistic interactions between natural phenolic compounds and antibiotics could offer a desired alternative approach to the therapies against multidrug-resistant bacteria. The objective o...
Saved in:
Published in: | BioMed research international 2018-01, Vol.2018 (2018), p.1-9 |
---|---|
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-c461t-9cc34cf75b9e24b7e6aa577d8e18a1c3863dd1f00652a72fd68881386717215b3 |
---|---|
cites | cdi_FETCH-LOGICAL-c461t-9cc34cf75b9e24b7e6aa577d8e18a1c3863dd1f00652a72fd68881386717215b3 |
container_end_page | 9 |
container_issue | 2018 |
container_start_page | 1 |
container_title | BioMed research international |
container_volume | 2018 |
creator | Wąsik, Tomasz J. Korzeniowski, Konrad Idzik, Danuta Wojtyczka, Robert D. Miklasińska-Majdanik, Maria Kępa, Małgorzata Smoleń-Dzirba, Joanna |
description | Phenolic compounds constitute one of the most promising and ubiquitous groups with many biological activities. Synergistic interactions between natural phenolic compounds and antibiotics could offer a desired alternative approach to the therapies against multidrug-resistant bacteria. The objective of the presented study was to assess the antibacterial potential of caffeic acid (CA) alone and in antibiotic-phytochemical combination against Staphylococcus aureus reference and clinical strains isolated from infected wounds. The caffeic acid tested in the presented study showed diverse effects on S. aureus strains with the minimum inhibitory concentration (MIC) varied from 256 μg/mL to 1024 μg/mL. The supplementation of Mueller-Hinton agar (MHA) with 1/4 MIC of CA resulted in augmented antibacterial effect of erythromycin, clindamycin, and cefoxitin and to the lesser extent of vancomycin. The observed antimicrobial action of CA seemed to be rather strain than antibiotic dependent. Our data support the notion that CA alone exerts antibacterial activity against S. aureus clinical strains and has capacity to potentiate antimicrobial effect in combination with antibiotics. The synergy between CA and antibiotics demonstrates its potential as a novel antibacterial tool which could improve the treatment of intractable infections caused by multidrug-resistant strains. |
doi_str_mv | 10.1155/2018/7413504 |
format | article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6076962</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A621800669</galeid><sourcerecordid>A621800669</sourcerecordid><originalsourceid>FETCH-LOGICAL-c461t-9cc34cf75b9e24b7e6aa577d8e18a1c3863dd1f00652a72fd68881386717215b3</originalsourceid><addsrcrecordid>eNqNkd9rFDEQx4MotrR981kWfBH02kx-74twHP6CgoVWX8NsNrlL2ducm12l_71Z7ryqT-Zlhskn35nJl5AXQC8BpLxiFMyVFsAlFU_IKeMgFgoEPD3mnJ-Qi5zvaTkGFK3Vc3LCKVDJBJySb8t-jNvohtRE7KqbNPpSKFkK1QpD8NFVSxfbCtcY-zxWtyPuNg9dcsm5KVc4Db6EVRf76Mqz23GYuXPyLGCX_cUhnpGvH97frT4trr98_LxaXi-cUDAuaue4cEHLpvZMNNorRKl1azwYBMeN4m0LgVIlGWoWWmWMgVLWoBnIhp-Rd3vd3dRsfevK8AN2djfELQ4PNmG0f9_0cWPX6YdVVKtasSLw-iAwpO-Tz6Pdxux812Hv05Qto8awWgLUBX31D3qfpqEv6xVKG8Gl0vqRWmPnbexDKn3dLGqXioEpu6hZ6-2eKh-f8-DDcWSgdnbWzs7ag7MFf_nnmkf4t48FeLMHNrFv8Wf8TzlfGB_wkQZmhDH8F4Ajsy8</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2078435677</pqid></control><display><type>article</type><title>Antimicrobial Potential of Caffeic Acid against Staphylococcus aureus Clinical Strains</title><source>Wiley Online Library Open Access</source><source>Publicly Available Content Database</source><creator>Wąsik, Tomasz J. ; Korzeniowski, Konrad ; Idzik, Danuta ; Wojtyczka, Robert D. ; Miklasińska-Majdanik, Maria ; Kępa, Małgorzata ; Smoleń-Dzirba, Joanna</creator><contributor>Mahady, Gail B.</contributor><creatorcontrib>Wąsik, Tomasz J. ; Korzeniowski, Konrad ; Idzik, Danuta ; Wojtyczka, Robert D. ; Miklasińska-Majdanik, Maria ; Kępa, Małgorzata ; Smoleń-Dzirba, Joanna ; Mahady, Gail B.</creatorcontrib><description>Phenolic compounds constitute one of the most promising and ubiquitous groups with many biological activities. Synergistic interactions between natural phenolic compounds and antibiotics could offer a desired alternative approach to the therapies against multidrug-resistant bacteria. The objective of the presented study was to assess the antibacterial potential of caffeic acid (CA) alone and in antibiotic-phytochemical combination against Staphylococcus aureus reference and clinical strains isolated from infected wounds. The caffeic acid tested in the presented study showed diverse effects on S. aureus strains with the minimum inhibitory concentration (MIC) varied from 256 μg/mL to 1024 μg/mL. The supplementation of Mueller-Hinton agar (MHA) with 1/4 MIC of CA resulted in augmented antibacterial effect of erythromycin, clindamycin, and cefoxitin and to the lesser extent of vancomycin. The observed antimicrobial action of CA seemed to be rather strain than antibiotic dependent. Our data support the notion that CA alone exerts antibacterial activity against S. aureus clinical strains and has capacity to potentiate antimicrobial effect in combination with antibiotics. The synergy between CA and antibiotics demonstrates its potential as a novel antibacterial tool which could improve the treatment of intractable infections caused by multidrug-resistant strains.</description><identifier>ISSN: 2314-6133</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2018/7413504</identifier><identifier>PMID: 30105241</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Acids ; Anti-Bacterial Agents - pharmacology ; Anti-Infective Agents ; Antibacterial activity ; Antibiotics ; Antimicrobial agents ; Bacteria ; Bacterial infections ; Caffeic acid ; Caffeic Acids - pharmacology ; Cefoxitin ; Clindamycin ; Drug resistance ; Drug resistance in microorganisms ; Drug Synergism ; Erythromycin ; Flow cytometry ; Humans ; Methicillin ; Methicillin-Resistant Staphylococcus aureus ; Microbial Sensitivity Tests ; Minimum inhibitory concentration ; Molecular weight ; Multidrug resistance ; Pathogens ; Phenolic compounds ; Phenols ; Phytochemicals ; Skin ; Staphylococcus aureus ; Staphylococcus aureus - drug effects ; Staphylococcus aureus infections ; Staphylococcus infections ; Strains (organisms) ; Supplements ; Vancomycin</subject><ispartof>BioMed research international, 2018-01, Vol.2018 (2018), p.1-9</ispartof><rights>Copyright © 2018 Małgorzata Kępa et al.</rights><rights>COPYRIGHT 2018 John Wiley & Sons, Inc.</rights><rights>Copyright © 2018 Małgorzata Kępa et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2018 Małgorzata Kępa et al. 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c461t-9cc34cf75b9e24b7e6aa577d8e18a1c3863dd1f00652a72fd68881386717215b3</citedby><cites>FETCH-LOGICAL-c461t-9cc34cf75b9e24b7e6aa577d8e18a1c3863dd1f00652a72fd68881386717215b3</cites><orcidid>0000-0001-6525-9767 ; 0000-0002-0334-0938 ; 0000-0002-4013-6688</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2078435677/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2078435677?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,25731,27901,27902,36989,36990,44566,75096</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30105241$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Mahady, Gail B.</contributor><creatorcontrib>Wąsik, Tomasz J.</creatorcontrib><creatorcontrib>Korzeniowski, Konrad</creatorcontrib><creatorcontrib>Idzik, Danuta</creatorcontrib><creatorcontrib>Wojtyczka, Robert D.</creatorcontrib><creatorcontrib>Miklasińska-Majdanik, Maria</creatorcontrib><creatorcontrib>Kępa, Małgorzata</creatorcontrib><creatorcontrib>Smoleń-Dzirba, Joanna</creatorcontrib><title>Antimicrobial Potential of Caffeic Acid against Staphylococcus aureus Clinical Strains</title><title>BioMed research international</title><addtitle>Biomed Res Int</addtitle><description>Phenolic compounds constitute one of the most promising and ubiquitous groups with many biological activities. Synergistic interactions between natural phenolic compounds and antibiotics could offer a desired alternative approach to the therapies against multidrug-resistant bacteria. The objective of the presented study was to assess the antibacterial potential of caffeic acid (CA) alone and in antibiotic-phytochemical combination against Staphylococcus aureus reference and clinical strains isolated from infected wounds. The caffeic acid tested in the presented study showed diverse effects on S. aureus strains with the minimum inhibitory concentration (MIC) varied from 256 μg/mL to 1024 μg/mL. The supplementation of Mueller-Hinton agar (MHA) with 1/4 MIC of CA resulted in augmented antibacterial effect of erythromycin, clindamycin, and cefoxitin and to the lesser extent of vancomycin. The observed antimicrobial action of CA seemed to be rather strain than antibiotic dependent. Our data support the notion that CA alone exerts antibacterial activity against S. aureus clinical strains and has capacity to potentiate antimicrobial effect in combination with antibiotics. The synergy between CA and antibiotics demonstrates its potential as a novel antibacterial tool which could improve the treatment of intractable infections caused by multidrug-resistant strains.</description><subject>Acids</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Anti-Infective Agents</subject><subject>Antibacterial activity</subject><subject>Antibiotics</subject><subject>Antimicrobial agents</subject><subject>Bacteria</subject><subject>Bacterial infections</subject><subject>Caffeic acid</subject><subject>Caffeic Acids - pharmacology</subject><subject>Cefoxitin</subject><subject>Clindamycin</subject><subject>Drug resistance</subject><subject>Drug resistance in microorganisms</subject><subject>Drug Synergism</subject><subject>Erythromycin</subject><subject>Flow cytometry</subject><subject>Humans</subject><subject>Methicillin</subject><subject>Methicillin-Resistant Staphylococcus aureus</subject><subject>Microbial Sensitivity Tests</subject><subject>Minimum inhibitory concentration</subject><subject>Molecular weight</subject><subject>Multidrug resistance</subject><subject>Pathogens</subject><subject>Phenolic compounds</subject><subject>Phenols</subject><subject>Phytochemicals</subject><subject>Skin</subject><subject>Staphylococcus aureus</subject><subject>Staphylococcus aureus - drug effects</subject><subject>Staphylococcus aureus infections</subject><subject>Staphylococcus infections</subject><subject>Strains (organisms)</subject><subject>Supplements</subject><subject>Vancomycin</subject><issn>2314-6133</issn><issn>2314-6141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNqNkd9rFDEQx4MotrR981kWfBH02kx-74twHP6CgoVWX8NsNrlL2ducm12l_71Z7ryqT-Zlhskn35nJl5AXQC8BpLxiFMyVFsAlFU_IKeMgFgoEPD3mnJ-Qi5zvaTkGFK3Vc3LCKVDJBJySb8t-jNvohtRE7KqbNPpSKFkK1QpD8NFVSxfbCtcY-zxWtyPuNg9dcsm5KVc4Db6EVRf76Mqz23GYuXPyLGCX_cUhnpGvH97frT4trr98_LxaXi-cUDAuaue4cEHLpvZMNNorRKl1azwYBMeN4m0LgVIlGWoWWmWMgVLWoBnIhp-Rd3vd3dRsfevK8AN2djfELQ4PNmG0f9_0cWPX6YdVVKtasSLw-iAwpO-Tz6Pdxux812Hv05Qto8awWgLUBX31D3qfpqEv6xVKG8Gl0vqRWmPnbexDKn3dLGqXioEpu6hZ6-2eKh-f8-DDcWSgdnbWzs7ag7MFf_nnmkf4t48FeLMHNrFv8Wf8TzlfGB_wkQZmhDH8F4Ajsy8</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Wąsik, Tomasz J.</creator><creator>Korzeniowski, Konrad</creator><creator>Idzik, Danuta</creator><creator>Wojtyczka, Robert D.</creator><creator>Miklasińska-Majdanik, Maria</creator><creator>Kępa, Małgorzata</creator><creator>Smoleń-Dzirba, Joanna</creator><general>Hindawi Publishing Corporation</general><general>Hindawi</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</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>7QO</scope><scope>7T7</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6525-9767</orcidid><orcidid>https://orcid.org/0000-0002-0334-0938</orcidid><orcidid>https://orcid.org/0000-0002-4013-6688</orcidid></search><sort><creationdate>20180101</creationdate><title>Antimicrobial Potential of Caffeic Acid against Staphylococcus aureus Clinical Strains</title><author>Wąsik, Tomasz J. ; Korzeniowski, Konrad ; Idzik, Danuta ; Wojtyczka, Robert D. ; Miklasińska-Majdanik, Maria ; Kępa, Małgorzata ; Smoleń-Dzirba, Joanna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c461t-9cc34cf75b9e24b7e6aa577d8e18a1c3863dd1f00652a72fd68881386717215b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acids</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Anti-Infective Agents</topic><topic>Antibacterial activity</topic><topic>Antibiotics</topic><topic>Antimicrobial agents</topic><topic>Bacteria</topic><topic>Bacterial infections</topic><topic>Caffeic acid</topic><topic>Caffeic Acids - pharmacology</topic><topic>Cefoxitin</topic><topic>Clindamycin</topic><topic>Drug resistance</topic><topic>Drug resistance in microorganisms</topic><topic>Drug Synergism</topic><topic>Erythromycin</topic><topic>Flow cytometry</topic><topic>Humans</topic><topic>Methicillin</topic><topic>Methicillin-Resistant Staphylococcus aureus</topic><topic>Microbial Sensitivity Tests</topic><topic>Minimum inhibitory concentration</topic><topic>Molecular weight</topic><topic>Multidrug resistance</topic><topic>Pathogens</topic><topic>Phenolic compounds</topic><topic>Phenols</topic><topic>Phytochemicals</topic><topic>Skin</topic><topic>Staphylococcus aureus</topic><topic>Staphylococcus aureus - drug effects</topic><topic>Staphylococcus aureus infections</topic><topic>Staphylococcus infections</topic><topic>Strains (organisms)</topic><topic>Supplements</topic><topic>Vancomycin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wąsik, Tomasz J.</creatorcontrib><creatorcontrib>Korzeniowski, Konrad</creatorcontrib><creatorcontrib>Idzik, Danuta</creatorcontrib><creatorcontrib>Wojtyczka, Robert D.</creatorcontrib><creatorcontrib>Miklasińska-Majdanik, Maria</creatorcontrib><creatorcontrib>Kępa, Małgorzata</creatorcontrib><creatorcontrib>Smoleń-Dzirba, Joanna</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</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>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</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>Middle East & Africa Database</collection><collection>ProQuest Central Korea</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>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Applied & Life Sciences</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BioMed research international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wąsik, Tomasz J.</au><au>Korzeniowski, Konrad</au><au>Idzik, Danuta</au><au>Wojtyczka, Robert D.</au><au>Miklasińska-Majdanik, Maria</au><au>Kępa, Małgorzata</au><au>Smoleń-Dzirba, Joanna</au><au>Mahady, Gail B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antimicrobial Potential of Caffeic Acid against Staphylococcus aureus Clinical Strains</atitle><jtitle>BioMed research international</jtitle><addtitle>Biomed Res Int</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>2018</volume><issue>2018</issue><spage>1</spage><epage>9</epage><pages>1-9</pages><issn>2314-6133</issn><eissn>2314-6141</eissn><abstract>Phenolic compounds constitute one of the most promising and ubiquitous groups with many biological activities. Synergistic interactions between natural phenolic compounds and antibiotics could offer a desired alternative approach to the therapies against multidrug-resistant bacteria. The objective of the presented study was to assess the antibacterial potential of caffeic acid (CA) alone and in antibiotic-phytochemical combination against Staphylococcus aureus reference and clinical strains isolated from infected wounds. The caffeic acid tested in the presented study showed diverse effects on S. aureus strains with the minimum inhibitory concentration (MIC) varied from 256 μg/mL to 1024 μg/mL. The supplementation of Mueller-Hinton agar (MHA) with 1/4 MIC of CA resulted in augmented antibacterial effect of erythromycin, clindamycin, and cefoxitin and to the lesser extent of vancomycin. The observed antimicrobial action of CA seemed to be rather strain than antibiotic dependent. Our data support the notion that CA alone exerts antibacterial activity against S. aureus clinical strains and has capacity to potentiate antimicrobial effect in combination with antibiotics. The synergy between CA and antibiotics demonstrates its potential as a novel antibacterial tool which could improve the treatment of intractable infections caused by multidrug-resistant strains.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>30105241</pmid><doi>10.1155/2018/7413504</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-6525-9767</orcidid><orcidid>https://orcid.org/0000-0002-0334-0938</orcidid><orcidid>https://orcid.org/0000-0002-4013-6688</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2314-6133 |
ispartof | BioMed research international, 2018-01, Vol.2018 (2018), p.1-9 |
issn | 2314-6133 2314-6141 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6076962 |
source | Wiley Online Library Open Access; Publicly Available Content Database |
subjects | Acids Anti-Bacterial Agents - pharmacology Anti-Infective Agents Antibacterial activity Antibiotics Antimicrobial agents Bacteria Bacterial infections Caffeic acid Caffeic Acids - pharmacology Cefoxitin Clindamycin Drug resistance Drug resistance in microorganisms Drug Synergism Erythromycin Flow cytometry Humans Methicillin Methicillin-Resistant Staphylococcus aureus Microbial Sensitivity Tests Minimum inhibitory concentration Molecular weight Multidrug resistance Pathogens Phenolic compounds Phenols Phytochemicals Skin Staphylococcus aureus Staphylococcus aureus - drug effects Staphylococcus aureus infections Staphylococcus infections Strains (organisms) Supplements Vancomycin |
title | Antimicrobial Potential of Caffeic Acid against Staphylococcus aureus Clinical Strains |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-23T19%3A58%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Antimicrobial%20Potential%20of%20Caffeic%20Acid%20against%20Staphylococcus%20aureus%20Clinical%20Strains&rft.jtitle=BioMed%20research%20international&rft.au=W%C4%85sik,%20Tomasz%20J.&rft.date=2018-01-01&rft.volume=2018&rft.issue=2018&rft.spage=1&rft.epage=9&rft.pages=1-9&rft.issn=2314-6133&rft.eissn=2314-6141&rft_id=info:doi/10.1155/2018/7413504&rft_dat=%3Cgale_pubme%3EA621800669%3C/gale_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c461t-9cc34cf75b9e24b7e6aa577d8e18a1c3863dd1f00652a72fd68881386717215b3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2078435677&rft_id=info:pmid/30105241&rft_galeid=A621800669&rfr_iscdi=true |