Loading…
Antimicrobial Activity of Corynebacterium amycolatum ICIS 53 and Corynebacterium amycolatum ICIS 82 Against Urogenital Isolates of Multidrug-Resistant Staphylococcus aureus
Intermicrobial interactions play a key role in the regulation of microbial populations and the colonization of various ecological niches. In the present study, we assessed the effect of cell-free supernatants (CFSs) from the vaginal isolates Corynebacterium amycolatum ICIS 53 and Corynebacterium amy...
Saved in:
Published in: | Current microbiology 2024-12, Vol.81 (12), p.426-426, Article 426 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c289t-9cdd8c2ea62c14947f7bff0ef2754d10dc1ca432d76189c99ce4dc7f06b84c3e3 |
container_end_page | 426 |
container_issue | 12 |
container_start_page | 426 |
container_title | Current microbiology |
container_volume | 81 |
creator | Gladysheva, Irina V. Stroganova, Elena A. Chertkov, Konstantin L. Cherkasov, Sergey V. |
description | Intermicrobial interactions play a key role in the regulation of microbial populations and the colonization of various ecological niches. In the present study, we assessed the effect of cell-free supernatants (CFSs) from the vaginal isolates
Corynebacterium amycolatum
ICIS 53 and
Corynebacterium amycolatum
ICIS 82 on urogenital test strain biofilm formation of
Staphylococcus aureus
. Our studies showed that the CFSs of both
C. amycolatum
strains significantly reduced biofilm formation and disrupted preformed
S. aureus
biofilms. Pretreatment with
C. amycolatum
ICIS 53 or
C. amycolatum
ICIS 82 CFSs decreased the cell surface hydrophobicity and exopolysaccharide production of all the test
S. aureus
isolates. The scanning electron microscopy (SEM) results showed that the CFSs of corynebacteria caused the
S. aureus
biofilms to be small clusters scattered across the surface, there were no fibres or adhesions between cells, and the cell membrane was not damaged. Treatment of preformed biofilms with CFSs from both
C. amycolatum
strains resulted in a flat, scattered, and unstructured architecture. The
S. aureus
cell membrane was damaged. GC‒MS analysis of the CFS of
C. amycolatum
ICIS 53 revealed the presence of 22 chemical compounds, including long-chain fatty alcohols, esters, fatty acids and heterocyclic pyrrolizines and pyrazoles, that, according to the literature, exhibit a wide range of biological activities. The results of the present work provide insight for the study of
Corynebacterium
microorganisms as a source of multifunctional bioactive compounds, which may find promising applications in the medical, biotechnological and pharmaceutical industries. |
doi_str_mv | 10.1007/s00284-024-03936-x |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3153821282</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3153821282</sourcerecordid><originalsourceid>FETCH-LOGICAL-c289t-9cdd8c2ea62c14947f7bff0ef2754d10dc1ca432d76189c99ce4dc7f06b84c3e3</originalsourceid><addsrcrecordid>eNqNkcuKFDEYRoM4OO3oC7iQgBs3pblVVbJsGi8NI8Jc1iGVpNoMVUmbyzD1Tj6k6elRwYXOIiSQ838fyQHgFUbvMEL9-4QQ4axBpC4qaNfcPQErzChpkBD4KVghymjDuxafgucp3SCEiUD4GTilgjHOkFiBH2uf3ex0DINTE1zr7G5dXmAY4SbExdtB6WyjKzNU86LDpHI9bjfbS9hSqLz5L8YJXO-U8ynD6xh21rtci7bpwNh0KPpSpuxMLLvmwiaXsvIZXma1_7ZMQQetS4KqRFvSC3AyqinZlw_7Gbj--OFq87k5__ppu1mfN5pwkRuhjeGaWNURjZlg_dgP44jsSPqWGYyMxlrVbzJ9h7nQQmjLjO5H1A2caWrpGXh7zN3H8L3YlOXskrbTpLwNJUmKW8oJJpw8AiWoFbRtu4q--Qu9CSX6-pB7Cou-pbRS5EhVJSlFO8p9dLOKi8RIHrTLo3ZZtct77fKuDr1-iC7DbM3vkV-eK0CPQKpXfmfjn-5_xP4ExTS7qg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3120197533</pqid></control><display><type>article</type><title>Antimicrobial Activity of Corynebacterium amycolatum ICIS 53 and Corynebacterium amycolatum ICIS 82 Against Urogenital Isolates of Multidrug-Resistant Staphylococcus aureus</title><source>Springer Nature</source><creator>Gladysheva, Irina V. ; Stroganova, Elena A. ; Chertkov, Konstantin L. ; Cherkasov, Sergey V.</creator><creatorcontrib>Gladysheva, Irina V. ; Stroganova, Elena A. ; Chertkov, Konstantin L. ; Cherkasov, Sergey V.</creatorcontrib><description>Intermicrobial interactions play a key role in the regulation of microbial populations and the colonization of various ecological niches. In the present study, we assessed the effect of cell-free supernatants (CFSs) from the vaginal isolates
Corynebacterium amycolatum
ICIS 53 and
Corynebacterium amycolatum
ICIS 82 on urogenital test strain biofilm formation of
Staphylococcus aureus
. Our studies showed that the CFSs of both
C. amycolatum
strains significantly reduced biofilm formation and disrupted preformed
S. aureus
biofilms. Pretreatment with
C. amycolatum
ICIS 53 or
C. amycolatum
ICIS 82 CFSs decreased the cell surface hydrophobicity and exopolysaccharide production of all the test
S. aureus
isolates. The scanning electron microscopy (SEM) results showed that the CFSs of corynebacteria caused the
S. aureus
biofilms to be small clusters scattered across the surface, there were no fibres or adhesions between cells, and the cell membrane was not damaged. Treatment of preformed biofilms with CFSs from both
C. amycolatum
strains resulted in a flat, scattered, and unstructured architecture. The
S. aureus
cell membrane was damaged. GC‒MS analysis of the CFS of
C. amycolatum
ICIS 53 revealed the presence of 22 chemical compounds, including long-chain fatty alcohols, esters, fatty acids and heterocyclic pyrrolizines and pyrazoles, that, according to the literature, exhibit a wide range of biological activities. The results of the present work provide insight for the study of
Corynebacterium
microorganisms as a source of multifunctional bioactive compounds, which may find promising applications in the medical, biotechnological and pharmaceutical industries.</description><identifier>ISSN: 0343-8651</identifier><identifier>ISSN: 1432-0991</identifier><identifier>EISSN: 1432-0991</identifier><identifier>DOI: 10.1007/s00284-024-03936-x</identifier><identifier>PMID: 39448409</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Alcohols ; Anti-Bacterial Agents - pharmacology ; Antimicrobial activity ; antimicrobial properties ; Bioactive compounds ; biofilm ; Biofilms ; Biofilms - drug effects ; Biofilms - growth & development ; Biological effects ; Biomedical and Life Sciences ; Biotechnology ; Cell membranes ; Cell surface ; Chemical compounds ; Corynebacterium ; Corynebacterium - drug effects ; Corynebacterium - isolation & purification ; Corynebacterium - physiology ; Corynebacterium amycolatum ; Drug resistance ; Drug Resistance, Multiple, Bacterial ; Ecological niches ; electron microscopy ; Esters ; Exopolysaccharides ; Female ; Fibers ; Humans ; Hydrophobicity ; Life Sciences ; Methicillin-Resistant Staphylococcus aureus - drug effects ; Microbial Sensitivity Tests ; Microbiology ; Microorganisms ; Multidrug resistance ; multiple drug resistance ; Pharmaceutical industry ; Population studies ; Pyrazoles ; Scanning electron microscopy ; Staphylococcal Infections - microbiology ; Staphylococcus aureus ; Staphylococcus aureus - drug effects ; Staphylococcus aureus - physiology ; Strains (organisms) ; Vagina - microbiology</subject><ispartof>Current microbiology, 2024-12, Vol.81 (12), p.426-426, Article 426</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c289t-9cdd8c2ea62c14947f7bff0ef2754d10dc1ca432d76189c99ce4dc7f06b84c3e3</cites><orcidid>0000-0001-6231-7028 ; 0000-0003-1974-6008 ; 0000-0002-0707-2977 ; 0000-0002-6583-516X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27900,27901</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39448409$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gladysheva, Irina V.</creatorcontrib><creatorcontrib>Stroganova, Elena A.</creatorcontrib><creatorcontrib>Chertkov, Konstantin L.</creatorcontrib><creatorcontrib>Cherkasov, Sergey V.</creatorcontrib><title>Antimicrobial Activity of Corynebacterium amycolatum ICIS 53 and Corynebacterium amycolatum ICIS 82 Against Urogenital Isolates of Multidrug-Resistant Staphylococcus aureus</title><title>Current microbiology</title><addtitle>Curr Microbiol</addtitle><addtitle>Curr Microbiol</addtitle><description>Intermicrobial interactions play a key role in the regulation of microbial populations and the colonization of various ecological niches. In the present study, we assessed the effect of cell-free supernatants (CFSs) from the vaginal isolates
Corynebacterium amycolatum
ICIS 53 and
Corynebacterium amycolatum
ICIS 82 on urogenital test strain biofilm formation of
Staphylococcus aureus
. Our studies showed that the CFSs of both
C. amycolatum
strains significantly reduced biofilm formation and disrupted preformed
S. aureus
biofilms. Pretreatment with
C. amycolatum
ICIS 53 or
C. amycolatum
ICIS 82 CFSs decreased the cell surface hydrophobicity and exopolysaccharide production of all the test
S. aureus
isolates. The scanning electron microscopy (SEM) results showed that the CFSs of corynebacteria caused the
S. aureus
biofilms to be small clusters scattered across the surface, there were no fibres or adhesions between cells, and the cell membrane was not damaged. Treatment of preformed biofilms with CFSs from both
C. amycolatum
strains resulted in a flat, scattered, and unstructured architecture. The
S. aureus
cell membrane was damaged. GC‒MS analysis of the CFS of
C. amycolatum
ICIS 53 revealed the presence of 22 chemical compounds, including long-chain fatty alcohols, esters, fatty acids and heterocyclic pyrrolizines and pyrazoles, that, according to the literature, exhibit a wide range of biological activities. The results of the present work provide insight for the study of
Corynebacterium
microorganisms as a source of multifunctional bioactive compounds, which may find promising applications in the medical, biotechnological and pharmaceutical industries.</description><subject>Alcohols</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Antimicrobial activity</subject><subject>antimicrobial properties</subject><subject>Bioactive compounds</subject><subject>biofilm</subject><subject>Biofilms</subject><subject>Biofilms - drug effects</subject><subject>Biofilms - growth & development</subject><subject>Biological effects</subject><subject>Biomedical and Life Sciences</subject><subject>Biotechnology</subject><subject>Cell membranes</subject><subject>Cell surface</subject><subject>Chemical compounds</subject><subject>Corynebacterium</subject><subject>Corynebacterium - drug effects</subject><subject>Corynebacterium - isolation & purification</subject><subject>Corynebacterium - physiology</subject><subject>Corynebacterium amycolatum</subject><subject>Drug resistance</subject><subject>Drug Resistance, Multiple, Bacterial</subject><subject>Ecological niches</subject><subject>electron microscopy</subject><subject>Esters</subject><subject>Exopolysaccharides</subject><subject>Female</subject><subject>Fibers</subject><subject>Humans</subject><subject>Hydrophobicity</subject><subject>Life Sciences</subject><subject>Methicillin-Resistant Staphylococcus aureus - drug effects</subject><subject>Microbial Sensitivity Tests</subject><subject>Microbiology</subject><subject>Microorganisms</subject><subject>Multidrug resistance</subject><subject>multiple drug resistance</subject><subject>Pharmaceutical industry</subject><subject>Population studies</subject><subject>Pyrazoles</subject><subject>Scanning electron microscopy</subject><subject>Staphylococcal Infections - microbiology</subject><subject>Staphylococcus aureus</subject><subject>Staphylococcus aureus - drug effects</subject><subject>Staphylococcus aureus - physiology</subject><subject>Strains (organisms)</subject><subject>Vagina - microbiology</subject><issn>0343-8651</issn><issn>1432-0991</issn><issn>1432-0991</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqNkcuKFDEYRoM4OO3oC7iQgBs3pblVVbJsGi8NI8Jc1iGVpNoMVUmbyzD1Tj6k6elRwYXOIiSQ838fyQHgFUbvMEL9-4QQ4axBpC4qaNfcPQErzChpkBD4KVghymjDuxafgucp3SCEiUD4GTilgjHOkFiBH2uf3ex0DINTE1zr7G5dXmAY4SbExdtB6WyjKzNU86LDpHI9bjfbS9hSqLz5L8YJXO-U8ynD6xh21rtci7bpwNh0KPpSpuxMLLvmwiaXsvIZXma1_7ZMQQetS4KqRFvSC3AyqinZlw_7Gbj--OFq87k5__ppu1mfN5pwkRuhjeGaWNURjZlg_dgP44jsSPqWGYyMxlrVbzJ9h7nQQmjLjO5H1A2caWrpGXh7zN3H8L3YlOXskrbTpLwNJUmKW8oJJpw8AiWoFbRtu4q--Qu9CSX6-pB7Cou-pbRS5EhVJSlFO8p9dLOKi8RIHrTLo3ZZtct77fKuDr1-iC7DbM3vkV-eK0CPQKpXfmfjn-5_xP4ExTS7qg</recordid><startdate>20241201</startdate><enddate>20241201</enddate><creator>Gladysheva, Irina V.</creator><creator>Stroganova, Elena A.</creator><creator>Chertkov, Konstantin L.</creator><creator>Cherkasov, Sergey V.</creator><general>Springer US</general><general>Springer Nature B.V</general><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>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0001-6231-7028</orcidid><orcidid>https://orcid.org/0000-0003-1974-6008</orcidid><orcidid>https://orcid.org/0000-0002-0707-2977</orcidid><orcidid>https://orcid.org/0000-0002-6583-516X</orcidid></search><sort><creationdate>20241201</creationdate><title>Antimicrobial Activity of Corynebacterium amycolatum ICIS 53 and Corynebacterium amycolatum ICIS 82 Against Urogenital Isolates of Multidrug-Resistant Staphylococcus aureus</title><author>Gladysheva, Irina V. ; Stroganova, Elena A. ; Chertkov, Konstantin L. ; Cherkasov, Sergey V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c289t-9cdd8c2ea62c14947f7bff0ef2754d10dc1ca432d76189c99ce4dc7f06b84c3e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Alcohols</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Antimicrobial activity</topic><topic>antimicrobial properties</topic><topic>Bioactive compounds</topic><topic>biofilm</topic><topic>Biofilms</topic><topic>Biofilms - drug effects</topic><topic>Biofilms - growth & development</topic><topic>Biological effects</topic><topic>Biomedical and Life Sciences</topic><topic>Biotechnology</topic><topic>Cell membranes</topic><topic>Cell surface</topic><topic>Chemical compounds</topic><topic>Corynebacterium</topic><topic>Corynebacterium - drug effects</topic><topic>Corynebacterium - isolation & purification</topic><topic>Corynebacterium - physiology</topic><topic>Corynebacterium amycolatum</topic><topic>Drug resistance</topic><topic>Drug Resistance, Multiple, Bacterial</topic><topic>Ecological niches</topic><topic>electron microscopy</topic><topic>Esters</topic><topic>Exopolysaccharides</topic><topic>Female</topic><topic>Fibers</topic><topic>Humans</topic><topic>Hydrophobicity</topic><topic>Life Sciences</topic><topic>Methicillin-Resistant Staphylococcus aureus - drug effects</topic><topic>Microbial Sensitivity Tests</topic><topic>Microbiology</topic><topic>Microorganisms</topic><topic>Multidrug resistance</topic><topic>multiple drug resistance</topic><topic>Pharmaceutical industry</topic><topic>Population studies</topic><topic>Pyrazoles</topic><topic>Scanning electron microscopy</topic><topic>Staphylococcal Infections - microbiology</topic><topic>Staphylococcus aureus</topic><topic>Staphylococcus aureus - drug effects</topic><topic>Staphylococcus aureus - physiology</topic><topic>Strains (organisms)</topic><topic>Vagina - microbiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gladysheva, Irina V.</creatorcontrib><creatorcontrib>Stroganova, Elena A.</creatorcontrib><creatorcontrib>Chertkov, Konstantin L.</creatorcontrib><creatorcontrib>Cherkasov, Sergey V.</creatorcontrib><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>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids 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>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Current microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gladysheva, Irina V.</au><au>Stroganova, Elena A.</au><au>Chertkov, Konstantin L.</au><au>Cherkasov, Sergey V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antimicrobial Activity of Corynebacterium amycolatum ICIS 53 and Corynebacterium amycolatum ICIS 82 Against Urogenital Isolates of Multidrug-Resistant Staphylococcus aureus</atitle><jtitle>Current microbiology</jtitle><stitle>Curr Microbiol</stitle><addtitle>Curr Microbiol</addtitle><date>2024-12-01</date><risdate>2024</risdate><volume>81</volume><issue>12</issue><spage>426</spage><epage>426</epage><pages>426-426</pages><artnum>426</artnum><issn>0343-8651</issn><issn>1432-0991</issn><eissn>1432-0991</eissn><abstract>Intermicrobial interactions play a key role in the regulation of microbial populations and the colonization of various ecological niches. In the present study, we assessed the effect of cell-free supernatants (CFSs) from the vaginal isolates
Corynebacterium amycolatum
ICIS 53 and
Corynebacterium amycolatum
ICIS 82 on urogenital test strain biofilm formation of
Staphylococcus aureus
. Our studies showed that the CFSs of both
C. amycolatum
strains significantly reduced biofilm formation and disrupted preformed
S. aureus
biofilms. Pretreatment with
C. amycolatum
ICIS 53 or
C. amycolatum
ICIS 82 CFSs decreased the cell surface hydrophobicity and exopolysaccharide production of all the test
S. aureus
isolates. The scanning electron microscopy (SEM) results showed that the CFSs of corynebacteria caused the
S. aureus
biofilms to be small clusters scattered across the surface, there were no fibres or adhesions between cells, and the cell membrane was not damaged. Treatment of preformed biofilms with CFSs from both
C. amycolatum
strains resulted in a flat, scattered, and unstructured architecture. The
S. aureus
cell membrane was damaged. GC‒MS analysis of the CFS of
C. amycolatum
ICIS 53 revealed the presence of 22 chemical compounds, including long-chain fatty alcohols, esters, fatty acids and heterocyclic pyrrolizines and pyrazoles, that, according to the literature, exhibit a wide range of biological activities. The results of the present work provide insight for the study of
Corynebacterium
microorganisms as a source of multifunctional bioactive compounds, which may find promising applications in the medical, biotechnological and pharmaceutical industries.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>39448409</pmid><doi>10.1007/s00284-024-03936-x</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0001-6231-7028</orcidid><orcidid>https://orcid.org/0000-0003-1974-6008</orcidid><orcidid>https://orcid.org/0000-0002-0707-2977</orcidid><orcidid>https://orcid.org/0000-0002-6583-516X</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0343-8651 |
ispartof | Current microbiology, 2024-12, Vol.81 (12), p.426-426, Article 426 |
issn | 0343-8651 1432-0991 1432-0991 |
language | eng |
recordid | cdi_proquest_miscellaneous_3153821282 |
source | Springer Nature |
subjects | Alcohols Anti-Bacterial Agents - pharmacology Antimicrobial activity antimicrobial properties Bioactive compounds biofilm Biofilms Biofilms - drug effects Biofilms - growth & development Biological effects Biomedical and Life Sciences Biotechnology Cell membranes Cell surface Chemical compounds Corynebacterium Corynebacterium - drug effects Corynebacterium - isolation & purification Corynebacterium - physiology Corynebacterium amycolatum Drug resistance Drug Resistance, Multiple, Bacterial Ecological niches electron microscopy Esters Exopolysaccharides Female Fibers Humans Hydrophobicity Life Sciences Methicillin-Resistant Staphylococcus aureus - drug effects Microbial Sensitivity Tests Microbiology Microorganisms Multidrug resistance multiple drug resistance Pharmaceutical industry Population studies Pyrazoles Scanning electron microscopy Staphylococcal Infections - microbiology Staphylococcus aureus Staphylococcus aureus - drug effects Staphylococcus aureus - physiology Strains (organisms) Vagina - microbiology |
title | Antimicrobial Activity of Corynebacterium amycolatum ICIS 53 and Corynebacterium amycolatum ICIS 82 Against Urogenital Isolates of Multidrug-Resistant Staphylococcus aureus |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-24T21%3A05%3A06IST&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=Antimicrobial%20Activity%20of%20Corynebacterium%20amycolatum%20ICIS%2053%20and%20Corynebacterium%20amycolatum%20ICIS%2082%20Against%20Urogenital%20Isolates%20of%20Multidrug-Resistant%20Staphylococcus%20aureus&rft.jtitle=Current%20microbiology&rft.au=Gladysheva,%20Irina%20V.&rft.date=2024-12-01&rft.volume=81&rft.issue=12&rft.spage=426&rft.epage=426&rft.pages=426-426&rft.artnum=426&rft.issn=0343-8651&rft.eissn=1432-0991&rft_id=info:doi/10.1007/s00284-024-03936-x&rft_dat=%3Cproquest_cross%3E3153821282%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c289t-9cdd8c2ea62c14947f7bff0ef2754d10dc1ca432d76189c99ce4dc7f06b84c3e3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3120197533&rft_id=info:pmid/39448409&rfr_iscdi=true |