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LysSYL‐Loaded pH‐Switchable Self‐Assembling Peptide Hydrogels Promote Methicillin‐Resistant Staphylococcus Aureus Elimination and Wound Healing
Staphylococcus aureus (S. aureus), especially methicillin‐resistant S. aureus (MRSA), causes wound infections, whose treatment remains a clinical challenge. Bacterium‐infected wounds often create acidic niches with a pH 4.5–6.5. Endolysin LysSYL, which is derived from phage SYL, shows promise as an...
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Published in: | Advanced materials (Weinheim) 2024-12, Vol.36 (52), p.e2412154-n/a |
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creator | Liu, He Wei, Xuemei Peng, Huagang Yang, Yi Hu, Zhen Rao, Yifan Wang, Zhefen Dou, Jianxiong Huang, Xiaonan Hu, Qiwen Tan, Li Wang, Yuting Chen, Juan Liu, Lu Yang, Yuhua Wu, Jianghong Hu, Xiaomei Lu, Shuguang Shang, Weilong Rao, Xiancai |
description | Staphylococcus aureus (S. aureus), especially methicillin‐resistant S. aureus (MRSA), causes wound infections, whose treatment remains a clinical challenge. Bacterium‐infected wounds often create acidic niches with a pH 4.5–6.5. Endolysin LysSYL, which is derived from phage SYL, shows promise as an antistaphylococcal agent. However, endolysins generally exhibit instability and possess low bioavailability in acidic microenvironments. Here, an array of self‐assembling peptides is designed, and peptide L5 is screened out based on its gel formation property and bioavailability. L5 exerted a pH‐switchable antimicrobial effect (pH 5.5) and formed biocompatible hydrogels at neutral pH (pH 7.4). The LysSYL‐loaded L5 can assemble L5@LysSYL hydrogels, increase thermal stability, and exhibit the slow‐release effect of LysSYL. Effective elimination of S. aureus is achieved by L5@LysSYL through bacterial membrane disruption and cell separation inhibition. Moreover, L5@LysSYL hydrogels exhibit great potential in promoting wound healing in a mouse wound model infected by MRSA. Furthermore, L5@LysSYL hydrogels are safe and can decrease the cytokine levels and increase the number of key factors for vessel formation, which contribute to wound healing. Overall, the self‐assembling L5@LysSYL can effectively clean MRSA and promote wound healing, which suggests its potential as a pH‐sensitive wound dressing for the management of wound infections.
The LysSYL‐loaded L5 can assemble pH‐sensitive L5@LysSYL hydrogels at neutral pH and exhibit the slow‐release effect of LysSYL at acidic pH. L5@LysSYL hydrogels effectively eliminate MRSA through multiple synergistic modes, including bacterial membrane disruption, cross‐wall disturbing, and cell separation inhibition. Moreover, L5@LysSYL hydrogels promote wound healing and show promise as a wound dressing for the management of wound infections. |
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The LysSYL‐loaded L5 can assemble pH‐sensitive L5@LysSYL hydrogels at neutral pH and exhibit the slow‐release effect of LysSYL at acidic pH. L5@LysSYL hydrogels effectively eliminate MRSA through multiple synergistic modes, including bacterial membrane disruption, cross‐wall disturbing, and cell separation inhibition. Moreover, L5@LysSYL hydrogels promote wound healing and show promise as a wound dressing for the management of wound infections.</description><identifier>ISSN: 0935-9648</identifier><identifier>ISSN: 1521-4095</identifier><identifier>EISSN: 1521-4095</identifier><identifier>DOI: 10.1002/adma.202412154</identifier><identifier>PMID: 39548922</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Animals ; Anti-Bacterial Agents - chemistry ; Anti-Bacterial Agents - pharmacology ; Bacteria ; Bioavailability ; Biocompatibility ; endolysins ; Endopeptidases - chemistry ; Endopeptidases - pharmacology ; Humans ; Hydrogels ; Hydrogels - chemistry ; Hydrogels - pharmacology ; Hydrogen-Ion Concentration ; Methicillin-Resistant Staphylococcus aureus - drug effects ; Mice ; peptide hydrogels ; Peptides ; Peptides - chemistry ; Peptides - pharmacology ; pH‐sensitive ; Self-assembly ; self‐organizing ; Staphylococcal Infections - drug therapy ; Staphylococcus aureus (S. aureus) ; Staphylococcus infections ; Thermal stability ; Wound healing ; Wound Healing - drug effects ; Wound Infection - drug therapy ; Wound Infection - microbiology ; wound infections</subject><ispartof>Advanced materials (Weinheim), 2024-12, Vol.36 (52), p.e2412154-n/a</ispartof><rights>2024 The Author(s). Advanced Materials published by Wiley‐VCH GmbH</rights><rights>2024 The Author(s). Advanced Materials published by Wiley‐VCH GmbH.</rights><rights>2024. This article is published under http://creativecommons.org/licenses/by-nc/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-c3144-a10202bc799153d56de63702286d5fcd245c55f62b9e1c7008d3c944c6825d153</cites><orcidid>0000-0002-9905-760X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39548922$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, He</creatorcontrib><creatorcontrib>Wei, Xuemei</creatorcontrib><creatorcontrib>Peng, Huagang</creatorcontrib><creatorcontrib>Yang, Yi</creatorcontrib><creatorcontrib>Hu, Zhen</creatorcontrib><creatorcontrib>Rao, Yifan</creatorcontrib><creatorcontrib>Wang, Zhefen</creatorcontrib><creatorcontrib>Dou, Jianxiong</creatorcontrib><creatorcontrib>Huang, Xiaonan</creatorcontrib><creatorcontrib>Hu, Qiwen</creatorcontrib><creatorcontrib>Tan, Li</creatorcontrib><creatorcontrib>Wang, Yuting</creatorcontrib><creatorcontrib>Chen, Juan</creatorcontrib><creatorcontrib>Liu, Lu</creatorcontrib><creatorcontrib>Yang, Yuhua</creatorcontrib><creatorcontrib>Wu, Jianghong</creatorcontrib><creatorcontrib>Hu, Xiaomei</creatorcontrib><creatorcontrib>Lu, Shuguang</creatorcontrib><creatorcontrib>Shang, Weilong</creatorcontrib><creatorcontrib>Rao, Xiancai</creatorcontrib><title>LysSYL‐Loaded pH‐Switchable Self‐Assembling Peptide Hydrogels Promote Methicillin‐Resistant Staphylococcus Aureus Elimination and Wound Healing</title><title>Advanced materials (Weinheim)</title><addtitle>Adv Mater</addtitle><description>Staphylococcus aureus (S. aureus), especially methicillin‐resistant S. aureus (MRSA), causes wound infections, whose treatment remains a clinical challenge. Bacterium‐infected wounds often create acidic niches with a pH 4.5–6.5. Endolysin LysSYL, which is derived from phage SYL, shows promise as an antistaphylococcal agent. However, endolysins generally exhibit instability and possess low bioavailability in acidic microenvironments. Here, an array of self‐assembling peptides is designed, and peptide L5 is screened out based on its gel formation property and bioavailability. L5 exerted a pH‐switchable antimicrobial effect (pH 5.5) and formed biocompatible hydrogels at neutral pH (pH 7.4). The LysSYL‐loaded L5 can assemble L5@LysSYL hydrogels, increase thermal stability, and exhibit the slow‐release effect of LysSYL. Effective elimination of S. aureus is achieved by L5@LysSYL through bacterial membrane disruption and cell separation inhibition. Moreover, L5@LysSYL hydrogels exhibit great potential in promoting wound healing in a mouse wound model infected by MRSA. Furthermore, L5@LysSYL hydrogels are safe and can decrease the cytokine levels and increase the number of key factors for vessel formation, which contribute to wound healing. Overall, the self‐assembling L5@LysSYL can effectively clean MRSA and promote wound healing, which suggests its potential as a pH‐sensitive wound dressing for the management of wound infections.
The LysSYL‐loaded L5 can assemble pH‐sensitive L5@LysSYL hydrogels at neutral pH and exhibit the slow‐release effect of LysSYL at acidic pH. L5@LysSYL hydrogels effectively eliminate MRSA through multiple synergistic modes, including bacterial membrane disruption, cross‐wall disturbing, and cell separation inhibition. Moreover, L5@LysSYL hydrogels promote wound healing and show promise as a wound dressing for the management of wound infections.</description><subject>Animals</subject><subject>Anti-Bacterial Agents - chemistry</subject><subject>Anti-Bacterial Agents - pharmacology</subject><subject>Bacteria</subject><subject>Bioavailability</subject><subject>Biocompatibility</subject><subject>endolysins</subject><subject>Endopeptidases - chemistry</subject><subject>Endopeptidases - pharmacology</subject><subject>Humans</subject><subject>Hydrogels</subject><subject>Hydrogels - chemistry</subject><subject>Hydrogels - pharmacology</subject><subject>Hydrogen-Ion Concentration</subject><subject>Methicillin-Resistant Staphylococcus aureus - drug effects</subject><subject>Mice</subject><subject>peptide hydrogels</subject><subject>Peptides</subject><subject>Peptides - chemistry</subject><subject>Peptides - pharmacology</subject><subject>pH‐sensitive</subject><subject>Self-assembly</subject><subject>self‐organizing</subject><subject>Staphylococcal Infections - drug therapy</subject><subject>Staphylococcus aureus (S. aureus)</subject><subject>Staphylococcus infections</subject><subject>Thermal stability</subject><subject>Wound healing</subject><subject>Wound Healing - drug effects</subject><subject>Wound Infection - drug therapy</subject><subject>Wound Infection - microbiology</subject><subject>wound infections</subject><issn>0935-9648</issn><issn>1521-4095</issn><issn>1521-4095</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNqFkc1u1DAUhSMEotPCliWKxIZNBtuxPfEKRaVlkFJRMSDEynLsmxlXThzihCo7HoEd78eT4NGU4WfDxteyv3Pso5MkTzBaYoTIC2VatSSIUEwwo_eSBWYEZxQJdj9ZIJGzTHBanCSnIdwghARH_GFykgtGC0HIIvlezWHzqfrx9VvllQGT9uu439zaUe9U7SDdgGviSRkCtLWz3Ta9hn60BtL1bAa_BRfS68G3foT0Csad1dZFLEreQbBhVN2YbkbV72bntdd6Cmk5DRDHhbOt7dRofZeqzqQf_RTXNaj9K4-SB41yAR7fzbPkw-XF-_N1Vr19_ea8rDKdY0ozhVEMX-uVEJjlhnEDPF8hQgpuWKMNoUwz1nBSC8B6hVBhci0o1bwgzETJWfLy4NtPdQtGQzcOysl-sK0aZumVlX_fdHYnt_6LxJgXOMciOjy_cxj85wnCKFsbNDinOvBTkDkmgmCBEI_os3_QGz8NXcwXKSo4w3S1N1weKD34EAZojr_BSO5Ll_vS5bH0KHj6Z4Yj_qvlCIgDcGsdzP-xk-Wrq_K3-U_F2r8g</recordid><startdate>202412</startdate><enddate>202412</enddate><creator>Liu, He</creator><creator>Wei, Xuemei</creator><creator>Peng, Huagang</creator><creator>Yang, Yi</creator><creator>Hu, Zhen</creator><creator>Rao, Yifan</creator><creator>Wang, Zhefen</creator><creator>Dou, Jianxiong</creator><creator>Huang, Xiaonan</creator><creator>Hu, Qiwen</creator><creator>Tan, Li</creator><creator>Wang, Yuting</creator><creator>Chen, Juan</creator><creator>Liu, Lu</creator><creator>Yang, Yuhua</creator><creator>Wu, Jianghong</creator><creator>Hu, Xiaomei</creator><creator>Lu, Shuguang</creator><creator>Shang, Weilong</creator><creator>Rao, Xiancai</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</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>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-9905-760X</orcidid></search><sort><creationdate>202412</creationdate><title>LysSYL‐Loaded pH‐Switchable Self‐Assembling Peptide Hydrogels Promote Methicillin‐Resistant Staphylococcus Aureus Elimination and Wound Healing</title><author>Liu, He ; Wei, Xuemei ; Peng, Huagang ; Yang, Yi ; Hu, Zhen ; Rao, Yifan ; Wang, Zhefen ; Dou, Jianxiong ; Huang, Xiaonan ; Hu, Qiwen ; Tan, Li ; Wang, Yuting ; Chen, Juan ; Liu, Lu ; Yang, Yuhua ; Wu, Jianghong ; Hu, Xiaomei ; Lu, Shuguang ; Shang, Weilong ; Rao, Xiancai</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3144-a10202bc799153d56de63702286d5fcd245c55f62b9e1c7008d3c944c6825d153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Anti-Bacterial Agents - chemistry</topic><topic>Anti-Bacterial Agents - pharmacology</topic><topic>Bacteria</topic><topic>Bioavailability</topic><topic>Biocompatibility</topic><topic>endolysins</topic><topic>Endopeptidases - chemistry</topic><topic>Endopeptidases - pharmacology</topic><topic>Humans</topic><topic>Hydrogels</topic><topic>Hydrogels - chemistry</topic><topic>Hydrogels - pharmacology</topic><topic>Hydrogen-Ion Concentration</topic><topic>Methicillin-Resistant Staphylococcus aureus - drug effects</topic><topic>Mice</topic><topic>peptide hydrogels</topic><topic>Peptides</topic><topic>Peptides - chemistry</topic><topic>Peptides - pharmacology</topic><topic>pH‐sensitive</topic><topic>Self-assembly</topic><topic>self‐organizing</topic><topic>Staphylococcal Infections - drug therapy</topic><topic>Staphylococcus aureus (S. aureus)</topic><topic>Staphylococcus infections</topic><topic>Thermal stability</topic><topic>Wound healing</topic><topic>Wound Healing - drug effects</topic><topic>Wound Infection - drug therapy</topic><topic>Wound Infection - microbiology</topic><topic>wound infections</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, He</creatorcontrib><creatorcontrib>Wei, Xuemei</creatorcontrib><creatorcontrib>Peng, Huagang</creatorcontrib><creatorcontrib>Yang, Yi</creatorcontrib><creatorcontrib>Hu, Zhen</creatorcontrib><creatorcontrib>Rao, Yifan</creatorcontrib><creatorcontrib>Wang, Zhefen</creatorcontrib><creatorcontrib>Dou, Jianxiong</creatorcontrib><creatorcontrib>Huang, Xiaonan</creatorcontrib><creatorcontrib>Hu, Qiwen</creatorcontrib><creatorcontrib>Tan, Li</creatorcontrib><creatorcontrib>Wang, Yuting</creatorcontrib><creatorcontrib>Chen, Juan</creatorcontrib><creatorcontrib>Liu, Lu</creatorcontrib><creatorcontrib>Yang, Yuhua</creatorcontrib><creatorcontrib>Wu, Jianghong</creatorcontrib><creatorcontrib>Hu, Xiaomei</creatorcontrib><creatorcontrib>Lu, Shuguang</creatorcontrib><creatorcontrib>Shang, Weilong</creatorcontrib><creatorcontrib>Rao, Xiancai</creatorcontrib><collection>Wiley Online Library 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>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Advanced materials (Weinheim)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, He</au><au>Wei, Xuemei</au><au>Peng, Huagang</au><au>Yang, Yi</au><au>Hu, Zhen</au><au>Rao, Yifan</au><au>Wang, Zhefen</au><au>Dou, Jianxiong</au><au>Huang, Xiaonan</au><au>Hu, Qiwen</au><au>Tan, Li</au><au>Wang, Yuting</au><au>Chen, Juan</au><au>Liu, Lu</au><au>Yang, Yuhua</au><au>Wu, Jianghong</au><au>Hu, Xiaomei</au><au>Lu, Shuguang</au><au>Shang, Weilong</au><au>Rao, Xiancai</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>LysSYL‐Loaded pH‐Switchable Self‐Assembling Peptide Hydrogels Promote Methicillin‐Resistant Staphylococcus Aureus Elimination and Wound Healing</atitle><jtitle>Advanced materials (Weinheim)</jtitle><addtitle>Adv Mater</addtitle><date>2024-12</date><risdate>2024</risdate><volume>36</volume><issue>52</issue><spage>e2412154</spage><epage>n/a</epage><pages>e2412154-n/a</pages><issn>0935-9648</issn><issn>1521-4095</issn><eissn>1521-4095</eissn><abstract>Staphylococcus aureus (S. aureus), especially methicillin‐resistant S. aureus (MRSA), causes wound infections, whose treatment remains a clinical challenge. Bacterium‐infected wounds often create acidic niches with a pH 4.5–6.5. Endolysin LysSYL, which is derived from phage SYL, shows promise as an antistaphylococcal agent. However, endolysins generally exhibit instability and possess low bioavailability in acidic microenvironments. Here, an array of self‐assembling peptides is designed, and peptide L5 is screened out based on its gel formation property and bioavailability. L5 exerted a pH‐switchable antimicrobial effect (pH 5.5) and formed biocompatible hydrogels at neutral pH (pH 7.4). The LysSYL‐loaded L5 can assemble L5@LysSYL hydrogels, increase thermal stability, and exhibit the slow‐release effect of LysSYL. Effective elimination of S. aureus is achieved by L5@LysSYL through bacterial membrane disruption and cell separation inhibition. Moreover, L5@LysSYL hydrogels exhibit great potential in promoting wound healing in a mouse wound model infected by MRSA. Furthermore, L5@LysSYL hydrogels are safe and can decrease the cytokine levels and increase the number of key factors for vessel formation, which contribute to wound healing. Overall, the self‐assembling L5@LysSYL can effectively clean MRSA and promote wound healing, which suggests its potential as a pH‐sensitive wound dressing for the management of wound infections.
The LysSYL‐loaded L5 can assemble pH‐sensitive L5@LysSYL hydrogels at neutral pH and exhibit the slow‐release effect of LysSYL at acidic pH. L5@LysSYL hydrogels effectively eliminate MRSA through multiple synergistic modes, including bacterial membrane disruption, cross‐wall disturbing, and cell separation inhibition. Moreover, L5@LysSYL hydrogels promote wound healing and show promise as a wound dressing for the management of wound infections.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>39548922</pmid><doi>10.1002/adma.202412154</doi><tpages>19</tpages><orcidid>https://orcid.org/0000-0002-9905-760X</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Anti-Bacterial Agents - chemistry Anti-Bacterial Agents - pharmacology Bacteria Bioavailability Biocompatibility endolysins Endopeptidases - chemistry Endopeptidases - pharmacology Humans Hydrogels Hydrogels - chemistry Hydrogels - pharmacology Hydrogen-Ion Concentration Methicillin-Resistant Staphylococcus aureus - drug effects Mice peptide hydrogels Peptides Peptides - chemistry Peptides - pharmacology pH‐sensitive Self-assembly self‐organizing Staphylococcal Infections - drug therapy Staphylococcus aureus (S. aureus) Staphylococcus infections Thermal stability Wound healing Wound Healing - drug effects Wound Infection - drug therapy Wound Infection - microbiology wound infections |
title | LysSYL‐Loaded pH‐Switchable Self‐Assembling Peptide Hydrogels Promote Methicillin‐Resistant Staphylococcus Aureus Elimination and Wound Healing |
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