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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
Main Authors: 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
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container_issue 52
container_start_page e2412154
container_title Advanced materials (Weinheim)
container_volume 36
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.
doi_str_mv 10.1002/adma.202412154
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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. 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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. 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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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