Bacterial cellulose with CHAPK-mediated specific antimicrobial activity against Staphylococcus aureus

Wound healing represents a complex biological process often hampered by bacterial infections, in particular those caused by Staphylococcus aureus , which is already multiresistant to many antibiotics. In this sense, enzybiotics have additional advantages over conventional antibiotics, since they pro...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cellulose (London) 2024-09, Vol.31 (14), p.8711-8725
Hauptverfasser: Blanco, Francisco G., Campano, Cristina, Rivero-Buceta, Virginia, Hernández-Arriaga, Ana M., Prieto, M. Auxiliadora
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 8725
container_issue 14
container_start_page 8711
container_title Cellulose (London)
container_volume 31
creator Blanco, Francisco G.
Campano, Cristina
Rivero-Buceta, Virginia
Hernández-Arriaga, Ana M.
Prieto, M. Auxiliadora
description Wound healing represents a complex biological process often hampered by bacterial infections, in particular those caused by Staphylococcus aureus , which is already multiresistant to many antibiotics. In this sense, enzybiotics have additional advantages over conventional antibiotics, since they provide pathogen specificity and do not contribute to antibiotic resistance. However, their soluble administration at the wound site would result in enzyme leakage. On the other hand, bacterial cellulose (BC) pellicles present a very promising dressing and scaffold, given its high purity, water retention capacity, and barrier effect in the wound against possible contaminants. In this study, we present a novel approach that incorporates the enzybiotic CHAP K into BC to develop functionalized membranes that exhibit targeted and controlled antimicrobial activity against S. aureus . The kinetic tests revealed a continuous loading of the enzybiotic into BC until it reaches a maximum and a two-stage release process, characterized by an initial fast release followed by a sustained release. Attenuated total Reflection Fourier Transform Infrared Spectroscopy (ATR-FTIR), Scanning Electron Microscopy (SEM), and Confocal Laser Scanning Microscopy (CLSM) confirmed the incorporation and the preferential surface localization of CHAP K within the BC membranes. Finally, the BC/CHAP K materials demonstrated the sustained reduction of up to 4 logarithmic units in the viability of S. aureus . Overall, the biomaterials developed here exhibit promising antimicrobial efficacy against S. aureus , offering a potential strategy for wound management and skin infection control while maintaining unharmed the commensal skin microbiota, which impairment could compromise the integrity of the skin barrier function.
doi_str_mv 10.1007/s10570-024-06123-0
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_3112659729</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3112659729</sourcerecordid><originalsourceid>FETCH-LOGICAL-c244t-9b704a2ddb58d97c28e12a29e55ca3e29f5f191cb09c8a7d99cdce3a5a260b683</originalsourceid><addsrcrecordid>eNp9kMFKxDAQhoMouK6-gKeA5-okbdrmuC7qioKCCt5Cmk53s3TbmqTKvr1ZV_DmaQ7zf_8wHyHnDC4ZQHHlGYgCEuBZAjnjaQIHZMJEwZOy5O-HZAIyl3GdymNy4v0aAGTB2YTgtTYBndUtNdi2Y9t7pF82rOh8MXt-SDZYWx2wpn5AYxtrqO6C3Vjj-moHRdp-2rCleqlt5wN9CXpYbdve9MaMnurR4ehPyVGjW49nv3NK3m5vXueL5PHp7n4-e0wMz7KQyKqATPO6rkRZy8LwEhnXXKIQRqfIZSMaJpmpQJpSF7WUpjaYaqF5DlVeplNyse8dXP8xog9q3Y-uiydVyhjPRXxaxhTfp-IT3jts1ODsRrutYqB2OtVep4o61Y9OBRFK95CP4W6J7q_6H-obqqF6AQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3112659729</pqid></control><display><type>article</type><title>Bacterial cellulose with CHAPK-mediated specific antimicrobial activity against Staphylococcus aureus</title><source>SpringerNature Journals</source><creator>Blanco, Francisco G. ; Campano, Cristina ; Rivero-Buceta, Virginia ; Hernández-Arriaga, Ana M. ; Prieto, M. Auxiliadora</creator><creatorcontrib>Blanco, Francisco G. ; Campano, Cristina ; Rivero-Buceta, Virginia ; Hernández-Arriaga, Ana M. ; Prieto, M. Auxiliadora</creatorcontrib><description>Wound healing represents a complex biological process often hampered by bacterial infections, in particular those caused by Staphylococcus aureus , which is already multiresistant to many antibiotics. In this sense, enzybiotics have additional advantages over conventional antibiotics, since they provide pathogen specificity and do not contribute to antibiotic resistance. However, their soluble administration at the wound site would result in enzyme leakage. On the other hand, bacterial cellulose (BC) pellicles present a very promising dressing and scaffold, given its high purity, water retention capacity, and barrier effect in the wound against possible contaminants. In this study, we present a novel approach that incorporates the enzybiotic CHAP K into BC to develop functionalized membranes that exhibit targeted and controlled antimicrobial activity against S. aureus . The kinetic tests revealed a continuous loading of the enzybiotic into BC until it reaches a maximum and a two-stage release process, characterized by an initial fast release followed by a sustained release. Attenuated total Reflection Fourier Transform Infrared Spectroscopy (ATR-FTIR), Scanning Electron Microscopy (SEM), and Confocal Laser Scanning Microscopy (CLSM) confirmed the incorporation and the preferential surface localization of CHAP K within the BC membranes. Finally, the BC/CHAP K materials demonstrated the sustained reduction of up to 4 logarithmic units in the viability of S. aureus . Overall, the biomaterials developed here exhibit promising antimicrobial efficacy against S. aureus , offering a potential strategy for wound management and skin infection control while maintaining unharmed the commensal skin microbiota, which impairment could compromise the integrity of the skin barrier function.</description><identifier>ISSN: 0969-0239</identifier><identifier>EISSN: 1572-882X</identifier><identifier>DOI: 10.1007/s10570-024-06123-0</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Antibiotics ; Antimicrobial agents ; Biological activity ; Biomedical materials ; Bioorganic Chemistry ; Cellulose ; Ceramics ; Chemistry ; Chemistry and Materials Science ; Composites ; Contaminants ; Fourier transforms ; Glass ; Infrared reflection ; Membranes ; Microscopy ; Natural Materials ; Organic Chemistry ; Original Research ; Physical Chemistry ; Polymer Sciences ; Scanning microscopy ; Sustainable Development ; Sustained release ; Wound healing</subject><ispartof>Cellulose (London), 2024-09, Vol.31 (14), p.8711-8725</ispartof><rights>The Author(s) 2024</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c244t-9b704a2ddb58d97c28e12a29e55ca3e29f5f191cb09c8a7d99cdce3a5a260b683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10570-024-06123-0$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10570-024-06123-0$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,27924,27925,41488,42557,51319</link.rule.ids></links><search><creatorcontrib>Blanco, Francisco G.</creatorcontrib><creatorcontrib>Campano, Cristina</creatorcontrib><creatorcontrib>Rivero-Buceta, Virginia</creatorcontrib><creatorcontrib>Hernández-Arriaga, Ana M.</creatorcontrib><creatorcontrib>Prieto, M. Auxiliadora</creatorcontrib><title>Bacterial cellulose with CHAPK-mediated specific antimicrobial activity against Staphylococcus aureus</title><title>Cellulose (London)</title><addtitle>Cellulose</addtitle><description>Wound healing represents a complex biological process often hampered by bacterial infections, in particular those caused by Staphylococcus aureus , which is already multiresistant to many antibiotics. In this sense, enzybiotics have additional advantages over conventional antibiotics, since they provide pathogen specificity and do not contribute to antibiotic resistance. However, their soluble administration at the wound site would result in enzyme leakage. On the other hand, bacterial cellulose (BC) pellicles present a very promising dressing and scaffold, given its high purity, water retention capacity, and barrier effect in the wound against possible contaminants. In this study, we present a novel approach that incorporates the enzybiotic CHAP K into BC to develop functionalized membranes that exhibit targeted and controlled antimicrobial activity against S. aureus . The kinetic tests revealed a continuous loading of the enzybiotic into BC until it reaches a maximum and a two-stage release process, characterized by an initial fast release followed by a sustained release. Attenuated total Reflection Fourier Transform Infrared Spectroscopy (ATR-FTIR), Scanning Electron Microscopy (SEM), and Confocal Laser Scanning Microscopy (CLSM) confirmed the incorporation and the preferential surface localization of CHAP K within the BC membranes. Finally, the BC/CHAP K materials demonstrated the sustained reduction of up to 4 logarithmic units in the viability of S. aureus . Overall, the biomaterials developed here exhibit promising antimicrobial efficacy against S. aureus , offering a potential strategy for wound management and skin infection control while maintaining unharmed the commensal skin microbiota, which impairment could compromise the integrity of the skin barrier function.</description><subject>Antibiotics</subject><subject>Antimicrobial agents</subject><subject>Biological activity</subject><subject>Biomedical materials</subject><subject>Bioorganic Chemistry</subject><subject>Cellulose</subject><subject>Ceramics</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Composites</subject><subject>Contaminants</subject><subject>Fourier transforms</subject><subject>Glass</subject><subject>Infrared reflection</subject><subject>Membranes</subject><subject>Microscopy</subject><subject>Natural Materials</subject><subject>Organic Chemistry</subject><subject>Original Research</subject><subject>Physical Chemistry</subject><subject>Polymer Sciences</subject><subject>Scanning microscopy</subject><subject>Sustainable Development</subject><subject>Sustained release</subject><subject>Wound healing</subject><issn>0969-0239</issn><issn>1572-882X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><recordid>eNp9kMFKxDAQhoMouK6-gKeA5-okbdrmuC7qioKCCt5Cmk53s3TbmqTKvr1ZV_DmaQ7zf_8wHyHnDC4ZQHHlGYgCEuBZAjnjaQIHZMJEwZOy5O-HZAIyl3GdymNy4v0aAGTB2YTgtTYBndUtNdi2Y9t7pF82rOh8MXt-SDZYWx2wpn5AYxtrqO6C3Vjj-moHRdp-2rCleqlt5wN9CXpYbdve9MaMnurR4ehPyVGjW49nv3NK3m5vXueL5PHp7n4-e0wMz7KQyKqATPO6rkRZy8LwEhnXXKIQRqfIZSMaJpmpQJpSF7WUpjaYaqF5DlVeplNyse8dXP8xog9q3Y-uiydVyhjPRXxaxhTfp-IT3jts1ODsRrutYqB2OtVep4o61Y9OBRFK95CP4W6J7q_6H-obqqF6AQ</recordid><startdate>20240901</startdate><enddate>20240901</enddate><creator>Blanco, Francisco G.</creator><creator>Campano, Cristina</creator><creator>Rivero-Buceta, Virginia</creator><creator>Hernández-Arriaga, Ana M.</creator><creator>Prieto, M. Auxiliadora</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20240901</creationdate><title>Bacterial cellulose with CHAPK-mediated specific antimicrobial activity against Staphylococcus aureus</title><author>Blanco, Francisco G. ; Campano, Cristina ; Rivero-Buceta, Virginia ; Hernández-Arriaga, Ana M. ; Prieto, M. Auxiliadora</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c244t-9b704a2ddb58d97c28e12a29e55ca3e29f5f191cb09c8a7d99cdce3a5a260b683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Antibiotics</topic><topic>Antimicrobial agents</topic><topic>Biological activity</topic><topic>Biomedical materials</topic><topic>Bioorganic Chemistry</topic><topic>Cellulose</topic><topic>Ceramics</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Composites</topic><topic>Contaminants</topic><topic>Fourier transforms</topic><topic>Glass</topic><topic>Infrared reflection</topic><topic>Membranes</topic><topic>Microscopy</topic><topic>Natural Materials</topic><topic>Organic Chemistry</topic><topic>Original Research</topic><topic>Physical Chemistry</topic><topic>Polymer Sciences</topic><topic>Scanning microscopy</topic><topic>Sustainable Development</topic><topic>Sustained release</topic><topic>Wound healing</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Blanco, Francisco G.</creatorcontrib><creatorcontrib>Campano, Cristina</creatorcontrib><creatorcontrib>Rivero-Buceta, Virginia</creatorcontrib><creatorcontrib>Hernández-Arriaga, Ana M.</creatorcontrib><creatorcontrib>Prieto, M. Auxiliadora</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>CrossRef</collection><jtitle>Cellulose (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Blanco, Francisco G.</au><au>Campano, Cristina</au><au>Rivero-Buceta, Virginia</au><au>Hernández-Arriaga, Ana M.</au><au>Prieto, M. Auxiliadora</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bacterial cellulose with CHAPK-mediated specific antimicrobial activity against Staphylococcus aureus</atitle><jtitle>Cellulose (London)</jtitle><stitle>Cellulose</stitle><date>2024-09-01</date><risdate>2024</risdate><volume>31</volume><issue>14</issue><spage>8711</spage><epage>8725</epage><pages>8711-8725</pages><issn>0969-0239</issn><eissn>1572-882X</eissn><abstract>Wound healing represents a complex biological process often hampered by bacterial infections, in particular those caused by Staphylococcus aureus , which is already multiresistant to many antibiotics. In this sense, enzybiotics have additional advantages over conventional antibiotics, since they provide pathogen specificity and do not contribute to antibiotic resistance. However, their soluble administration at the wound site would result in enzyme leakage. On the other hand, bacterial cellulose (BC) pellicles present a very promising dressing and scaffold, given its high purity, water retention capacity, and barrier effect in the wound against possible contaminants. In this study, we present a novel approach that incorporates the enzybiotic CHAP K into BC to develop functionalized membranes that exhibit targeted and controlled antimicrobial activity against S. aureus . The kinetic tests revealed a continuous loading of the enzybiotic into BC until it reaches a maximum and a two-stage release process, characterized by an initial fast release followed by a sustained release. Attenuated total Reflection Fourier Transform Infrared Spectroscopy (ATR-FTIR), Scanning Electron Microscopy (SEM), and Confocal Laser Scanning Microscopy (CLSM) confirmed the incorporation and the preferential surface localization of CHAP K within the BC membranes. Finally, the BC/CHAP K materials demonstrated the sustained reduction of up to 4 logarithmic units in the viability of S. aureus . Overall, the biomaterials developed here exhibit promising antimicrobial efficacy against S. aureus , offering a potential strategy for wound management and skin infection control while maintaining unharmed the commensal skin microbiota, which impairment could compromise the integrity of the skin barrier function.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s10570-024-06123-0</doi><tpages>15</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0969-0239
ispartof Cellulose (London), 2024-09, Vol.31 (14), p.8711-8725
issn 0969-0239
1572-882X
language eng
recordid cdi_proquest_journals_3112659729
source SpringerNature Journals
subjects Antibiotics
Antimicrobial agents
Biological activity
Biomedical materials
Bioorganic Chemistry
Cellulose
Ceramics
Chemistry
Chemistry and Materials Science
Composites
Contaminants
Fourier transforms
Glass
Infrared reflection
Membranes
Microscopy
Natural Materials
Organic Chemistry
Original Research
Physical Chemistry
Polymer Sciences
Scanning microscopy
Sustainable Development
Sustained release
Wound healing
title Bacterial cellulose with CHAPK-mediated specific antimicrobial activity against Staphylococcus aureus
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T05%3A27%3A15IST&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=Bacterial%20cellulose%20with%20CHAPK-mediated%20specific%20antimicrobial%20activity%20against%20Staphylococcus%20aureus&rft.jtitle=Cellulose%20(London)&rft.au=Blanco,%20Francisco%20G.&rft.date=2024-09-01&rft.volume=31&rft.issue=14&rft.spage=8711&rft.epage=8725&rft.pages=8711-8725&rft.issn=0969-0239&rft.eissn=1572-882X&rft_id=info:doi/10.1007/s10570-024-06123-0&rft_dat=%3Cproquest_cross%3E3112659729%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3112659729&rft_id=info:pmid/&rfr_iscdi=true