Insights into the antimicrobial properties of a cationic steroid and antibiofilm performance in PDMS-based coatings to potentially treat urinary infections
Currently, multidrug-resistant (MDR) infections are one of the most important threats, driving the search for new antimicrobial compounds. Cationic peptide antibiotics (CPAs) and ceragenins (CSAs) contain in their structures cationic groups and adopt a facially amphiphilic conformation, conferring t...
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creator | Neves, Ana Rita Freitas-Silva, Joana Durães, Fernando Silva, Elisabete R Rodrigues, Inês C Mergulhão, Filipe Gomes, Marisa Teixeira-Santos, Rita Bernardes André, Maria Silva, Renata Remião, Fernando Pinto, Eugénia da Costa, Paulo Martins Sousa, Emília Correia da Silva, Marta |
description | Currently, multidrug-resistant (MDR) infections are one of the most important threats, driving the search for new antimicrobial compounds. Cationic peptide antibiotics (CPAs) and ceragenins (CSAs) contain in their structures cationic groups and adopt a facially amphiphilic conformation, conferring the ability to permeate the membranes of bacteria and fungi. Keeping these features in mind, an amine steroid,
DOCA-NH
2
, was found to be active against reference strains and MDR isolates of Gram-positive
Enterococcus faecalis
and
Staphylococcus aureus
and Gram-negative
Escherichia coli
and
Pseudomonas aeruginosa
. The compound was active against all the tested microorganisms, having bactericidal and fungicidal activity, displaying minimal inhibitory concentrations (MICs) between 16 and 128 μg mL
−1
. No synergy with clinically relevant antibacterial drugs was found. However, the compound was able to completely inhibit the biofilm formation of bacteria exposed to the MIC of the compound. For
E. coli
and
E. faecalis
, inhibition of biofilm formation occurred at half the MIC. Besides,
DOCA-NH
2
inhibited the dimorphic transition of
Candida albicans
at concentrations 4 times lower than the MIC, and can reduce the microorganism virulence and biofilm formation was significantly reduced at both MIC and half the MIC. Polydimethylsiloxane-based coatings containing
DOCA-NH
2
(0.5, 1.0, and 1.5 wt%) were prepared and tested against the
E. coli
biofilm formation under hydrodynamic conditions similar to those prevailing in ureteral stents. A biofilm reduction of approximately 80% was achieved when compared to the control.
Currently, multidrug-resistant (MDR) infections are one of the most important threats, driving the search for new antimicrobial compounds. |
doi_str_mv | 10.1039/d3tb01185b |
format | Article |
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DOCA-NH
2
, was found to be active against reference strains and MDR isolates of Gram-positive
Enterococcus faecalis
and
Staphylococcus aureus
and Gram-negative
Escherichia coli
and
Pseudomonas aeruginosa
. The compound was active against all the tested microorganisms, having bactericidal and fungicidal activity, displaying minimal inhibitory concentrations (MICs) between 16 and 128 μg mL
−1
. No synergy with clinically relevant antibacterial drugs was found. However, the compound was able to completely inhibit the biofilm formation of bacteria exposed to the MIC of the compound. For
E. coli
and
E. faecalis
, inhibition of biofilm formation occurred at half the MIC. Besides,
DOCA-NH
2
inhibited the dimorphic transition of
Candida albicans
at concentrations 4 times lower than the MIC, and can reduce the microorganism virulence and biofilm formation was significantly reduced at both MIC and half the MIC. Polydimethylsiloxane-based coatings containing
DOCA-NH
2
(0.5, 1.0, and 1.5 wt%) were prepared and tested against the
E. coli
biofilm formation under hydrodynamic conditions similar to those prevailing in ureteral stents. A biofilm reduction of approximately 80% was achieved when compared to the control.
Currently, multidrug-resistant (MDR) infections are one of the most important threats, driving the search for new antimicrobial compounds.</description><identifier>ISSN: 2050-750X</identifier><identifier>EISSN: 2050-7518</identifier><identifier>DOI: 10.1039/d3tb01185b</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Antibiotics ; Antiinfectives and antibacterials ; Bacteria ; Biofilms ; Cations ; Coatings ; Conformation ; E coli ; Fungicidal activity ; Fungicides ; Implants ; Microorganisms ; Minimum inhibitory concentration ; Multidrug resistance ; Peptide antibiotics ; Polydimethylsiloxane ; Steroids ; Ureteral stents ; Virulence</subject><ispartof>Journal of materials chemistry. B, Materials for biology and medicine, 2023-09, Vol.11 (36), p.8697-8716</ispartof><rights>Copyright Royal Society of Chemistry 2023</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2321-60fc303f2e35840ebfc178fb0342d8b78719f2e0c3a5e0a0e9ef732b2150795e3</citedby><cites>FETCH-LOGICAL-c2321-60fc303f2e35840ebfc178fb0342d8b78719f2e0c3a5e0a0e9ef732b2150795e3</cites><orcidid>0000-0002-5570-7244 ; 0000-0002-5397-4672</orcidid></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></links><search><creatorcontrib>Neves, Ana Rita</creatorcontrib><creatorcontrib>Freitas-Silva, Joana</creatorcontrib><creatorcontrib>Durães, Fernando</creatorcontrib><creatorcontrib>Silva, Elisabete R</creatorcontrib><creatorcontrib>Rodrigues, Inês C</creatorcontrib><creatorcontrib>Mergulhão, Filipe</creatorcontrib><creatorcontrib>Gomes, Marisa</creatorcontrib><creatorcontrib>Teixeira-Santos, Rita</creatorcontrib><creatorcontrib>Bernardes André, Maria</creatorcontrib><creatorcontrib>Silva, Renata</creatorcontrib><creatorcontrib>Remião, Fernando</creatorcontrib><creatorcontrib>Pinto, Eugénia</creatorcontrib><creatorcontrib>da Costa, Paulo Martins</creatorcontrib><creatorcontrib>Sousa, Emília</creatorcontrib><creatorcontrib>Correia da Silva, Marta</creatorcontrib><title>Insights into the antimicrobial properties of a cationic steroid and antibiofilm performance in PDMS-based coatings to potentially treat urinary infections</title><title>Journal of materials chemistry. B, Materials for biology and medicine</title><description>Currently, multidrug-resistant (MDR) infections are one of the most important threats, driving the search for new antimicrobial compounds. Cationic peptide antibiotics (CPAs) and ceragenins (CSAs) contain in their structures cationic groups and adopt a facially amphiphilic conformation, conferring the ability to permeate the membranes of bacteria and fungi. Keeping these features in mind, an amine steroid,
DOCA-NH
2
, was found to be active against reference strains and MDR isolates of Gram-positive
Enterococcus faecalis
and
Staphylococcus aureus
and Gram-negative
Escherichia coli
and
Pseudomonas aeruginosa
. The compound was active against all the tested microorganisms, having bactericidal and fungicidal activity, displaying minimal inhibitory concentrations (MICs) between 16 and 128 μg mL
−1
. No synergy with clinically relevant antibacterial drugs was found. However, the compound was able to completely inhibit the biofilm formation of bacteria exposed to the MIC of the compound. For
E. coli
and
E. faecalis
, inhibition of biofilm formation occurred at half the MIC. Besides,
DOCA-NH
2
inhibited the dimorphic transition of
Candida albicans
at concentrations 4 times lower than the MIC, and can reduce the microorganism virulence and biofilm formation was significantly reduced at both MIC and half the MIC. Polydimethylsiloxane-based coatings containing
DOCA-NH
2
(0.5, 1.0, and 1.5 wt%) were prepared and tested against the
E. coli
biofilm formation under hydrodynamic conditions similar to those prevailing in ureteral stents. A biofilm reduction of approximately 80% was achieved when compared to the control.
Currently, multidrug-resistant (MDR) infections are one of the most important threats, driving the search for new antimicrobial compounds.</description><subject>Antibiotics</subject><subject>Antiinfectives and antibacterials</subject><subject>Bacteria</subject><subject>Biofilms</subject><subject>Cations</subject><subject>Coatings</subject><subject>Conformation</subject><subject>E coli</subject><subject>Fungicidal activity</subject><subject>Fungicides</subject><subject>Implants</subject><subject>Microorganisms</subject><subject>Minimum inhibitory concentration</subject><subject>Multidrug resistance</subject><subject>Peptide antibiotics</subject><subject>Polydimethylsiloxane</subject><subject>Steroids</subject><subject>Ureteral stents</subject><subject>Virulence</subject><issn>2050-750X</issn><issn>2050-7518</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpFkU1LAzEQhhdRsGgv3oWAN2F1kuxH9ui3hYqCCt6WJDvRlN1NTdJDf4t_1tSK5jKBPO-8k3ey7IjCGQXenHc8KqBUlGonmzAoIa9LKnb_7vC2n01DWEA6glaCF5PsazYG-_4RA7FjdCR-IJFjtIPV3ikre7L0bok-WgzEGSKJltG60WoSInpnu4R3PxJlnbH9QBJtnB_kqDH1JE_XD8-5kgE7ol3Sju-BJKOli5hEsu_XJHqUkay8HaVfJ41BvfEIh9mekX3A6W89yF5vb16u7vP5493s6mKea8YZzSswmgM3DHkpCkBlNK2FUcAL1glVi5o26RE0lyWCBGzQ1JwpRkuomxL5QXay7Zv--rnCENuFW_kxWbZMVBUvoKiaRJ1uqZRMCB5Nu_R2SBO3FNpN_u01f7n8yf8ywcdb2Af9x_3vh38D-AWE7g</recordid><startdate>20230920</startdate><enddate>20230920</enddate><creator>Neves, Ana Rita</creator><creator>Freitas-Silva, Joana</creator><creator>Durães, Fernando</creator><creator>Silva, Elisabete R</creator><creator>Rodrigues, Inês C</creator><creator>Mergulhão, Filipe</creator><creator>Gomes, Marisa</creator><creator>Teixeira-Santos, Rita</creator><creator>Bernardes André, Maria</creator><creator>Silva, Renata</creator><creator>Remião, Fernando</creator><creator>Pinto, Eugénia</creator><creator>da Costa, Paulo Martins</creator><creator>Sousa, Emília</creator><creator>Correia da Silva, Marta</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><orcidid>https://orcid.org/0000-0002-5570-7244</orcidid><orcidid>https://orcid.org/0000-0002-5397-4672</orcidid></search><sort><creationdate>20230920</creationdate><title>Insights into the antimicrobial properties of a cationic steroid and antibiofilm performance in PDMS-based coatings to potentially treat urinary infections</title><author>Neves, Ana Rita ; Freitas-Silva, Joana ; Durães, Fernando ; Silva, Elisabete R ; Rodrigues, Inês C ; Mergulhão, Filipe ; Gomes, Marisa ; Teixeira-Santos, Rita ; Bernardes André, Maria ; Silva, Renata ; Remião, Fernando ; Pinto, Eugénia ; da Costa, Paulo Martins ; Sousa, Emília ; Correia da Silva, Marta</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2321-60fc303f2e35840ebfc178fb0342d8b78719f2e0c3a5e0a0e9ef732b2150795e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Antibiotics</topic><topic>Antiinfectives and antibacterials</topic><topic>Bacteria</topic><topic>Biofilms</topic><topic>Cations</topic><topic>Coatings</topic><topic>Conformation</topic><topic>E coli</topic><topic>Fungicidal activity</topic><topic>Fungicides</topic><topic>Implants</topic><topic>Microorganisms</topic><topic>Minimum inhibitory concentration</topic><topic>Multidrug resistance</topic><topic>Peptide antibiotics</topic><topic>Polydimethylsiloxane</topic><topic>Steroids</topic><topic>Ureteral stents</topic><topic>Virulence</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Neves, Ana Rita</creatorcontrib><creatorcontrib>Freitas-Silva, Joana</creatorcontrib><creatorcontrib>Durães, Fernando</creatorcontrib><creatorcontrib>Silva, Elisabete R</creatorcontrib><creatorcontrib>Rodrigues, Inês C</creatorcontrib><creatorcontrib>Mergulhão, Filipe</creatorcontrib><creatorcontrib>Gomes, Marisa</creatorcontrib><creatorcontrib>Teixeira-Santos, Rita</creatorcontrib><creatorcontrib>Bernardes André, Maria</creatorcontrib><creatorcontrib>Silva, Renata</creatorcontrib><creatorcontrib>Remião, Fernando</creatorcontrib><creatorcontrib>Pinto, Eugénia</creatorcontrib><creatorcontrib>da Costa, Paulo Martins</creatorcontrib><creatorcontrib>Sousa, Emília</creatorcontrib><creatorcontrib>Correia da Silva, Marta</creatorcontrib><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of materials chemistry. B, Materials for biology and medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Neves, Ana Rita</au><au>Freitas-Silva, Joana</au><au>Durães, Fernando</au><au>Silva, Elisabete R</au><au>Rodrigues, Inês C</au><au>Mergulhão, Filipe</au><au>Gomes, Marisa</au><au>Teixeira-Santos, Rita</au><au>Bernardes André, Maria</au><au>Silva, Renata</au><au>Remião, Fernando</au><au>Pinto, Eugénia</au><au>da Costa, Paulo Martins</au><au>Sousa, Emília</au><au>Correia da Silva, Marta</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insights into the antimicrobial properties of a cationic steroid and antibiofilm performance in PDMS-based coatings to potentially treat urinary infections</atitle><jtitle>Journal of materials chemistry. B, Materials for biology and medicine</jtitle><date>2023-09-20</date><risdate>2023</risdate><volume>11</volume><issue>36</issue><spage>8697</spage><epage>8716</epage><pages>8697-8716</pages><issn>2050-750X</issn><eissn>2050-7518</eissn><abstract>Currently, multidrug-resistant (MDR) infections are one of the most important threats, driving the search for new antimicrobial compounds. Cationic peptide antibiotics (CPAs) and ceragenins (CSAs) contain in their structures cationic groups and adopt a facially amphiphilic conformation, conferring the ability to permeate the membranes of bacteria and fungi. Keeping these features in mind, an amine steroid,
DOCA-NH
2
, was found to be active against reference strains and MDR isolates of Gram-positive
Enterococcus faecalis
and
Staphylococcus aureus
and Gram-negative
Escherichia coli
and
Pseudomonas aeruginosa
. The compound was active against all the tested microorganisms, having bactericidal and fungicidal activity, displaying minimal inhibitory concentrations (MICs) between 16 and 128 μg mL
−1
. No synergy with clinically relevant antibacterial drugs was found. However, the compound was able to completely inhibit the biofilm formation of bacteria exposed to the MIC of the compound. For
E. coli
and
E. faecalis
, inhibition of biofilm formation occurred at half the MIC. Besides,
DOCA-NH
2
inhibited the dimorphic transition of
Candida albicans
at concentrations 4 times lower than the MIC, and can reduce the microorganism virulence and biofilm formation was significantly reduced at both MIC and half the MIC. Polydimethylsiloxane-based coatings containing
DOCA-NH
2
(0.5, 1.0, and 1.5 wt%) were prepared and tested against the
E. coli
biofilm formation under hydrodynamic conditions similar to those prevailing in ureteral stents. A biofilm reduction of approximately 80% was achieved when compared to the control.
Currently, multidrug-resistant (MDR) infections are one of the most important threats, driving the search for new antimicrobial compounds.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d3tb01185b</doi><tpages>2</tpages><orcidid>https://orcid.org/0000-0002-5570-7244</orcidid><orcidid>https://orcid.org/0000-0002-5397-4672</orcidid></addata></record> |
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language | eng |
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source | Royal Society Of Chemistry Journals 2008- |
subjects | Antibiotics Antiinfectives and antibacterials Bacteria Biofilms Cations Coatings Conformation E coli Fungicidal activity Fungicides Implants Microorganisms Minimum inhibitory concentration Multidrug resistance Peptide antibiotics Polydimethylsiloxane Steroids Ureteral stents Virulence |
title | Insights into the antimicrobial properties of a cationic steroid and antibiofilm performance in PDMS-based coatings to potentially treat urinary infections |
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