Ying Zhou, Ying Wang, Xiangyu Meng, Ming Xiong, Xianxian Dong, Hui Peng, Fangyi Chen, Ke-Jian Wang
{"title":"新鉴定的Scylla paramamosain抗菌肽Scymicrosin7-26在体外和体内对耐甲氧西林金黄色葡萄球菌具有有效的抗菌活性。","authors":"Ying Zhou, Ying Wang, Xiangyu Meng, Ming Xiong, Xianxian Dong, Hui Peng, Fangyi Chen, Ke-Jian Wang","doi":"10.1021/acsinfecdis.5c00034","DOIUrl":null,"url":null,"abstract":"<p><p>Methicillin-resistant <i>Staphylococcus aureus</i> (MRSA) is a predominant pathogen causing skin and soft tissue infections, which significantly hinders the wound healing process and contributes to high mortality rates. The rise of multidrug-resistant bacteria, coupled with the limited availability of new antibiotics, underscores the pressing need for the development of innovative antimicrobial substances. Antimicrobial peptides (AMPs), with their multitargeted and rapid antimicrobial activity, are promising candidates to address this crisis. In this study, we identified a novel AMP, Scymicrosin<sub>7-26</sub>, derived from <i>Scylla paramamosain</i>, which demonstrated potent antimicrobial activity against a variety of MDR strains, particularly MRSA. Confocal microscopy and transmission electron microscopy observations showed that Scymicrosin<sub>7-26</sub> bound to MRSA, and had a disruptive effect on cell walls and cell membranes, rapidly penetrating and killing MRSA. Notably, Scymicrosin<sub>7-26</sub> exhibited good stability under various ionic conditions, thermal stresses and certain serum concentration, had no obvious toxic effects on HaCaT cells, and its ability to penetrate HaCaT cells indicated its potential for intracellular targeted therapy. <i>In vitro</i>, Scymicrosin<sub>7-26</sub> significantly reduced the number of MRSA in HaCaT cells and inhibited intracellular MRSA proliferation. After verifying the low toxicity of Scymicrosin<sub>7-26</sub> <i>in vivo</i> in the Marine model organism─marine medaka (<i>Oryzias melastigma</i>), a wound model of MRSA-infected mice was made, and topical administration of Scymicrosin<sub>7-26</sub> in hypromellose gels could significantly reduce bacterial burden and promote wound closure. Histological analysis confirmed that Scymicrosin<sub>7-26</sub> alleviated tissue damage and was comparable to the effect of vancomycin treatment. Collectively, Scymicrosin<sub>7-26</sub> is promising for the treatment of MRSA wound infections and could be a valuable addition to the arsenal against antibiotic-resistant bacteria.</p>","PeriodicalId":17,"journal":{"name":"ACS Infectious Diseases","volume":"11 5","pages":"1216-1232"},"PeriodicalIF":3.8000,"publicationDate":"2025-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Newly Identified Antimicrobial Peptide Scymicrosin<sub>7-26</sub> from <i>Scylla paramamosain</i> Showing Potent Antimicrobial Activity Against Methicillin-Resistant <i>Staphylococcus aureus</i> <i>In Vitro</i> and <i>In Vivo</i>.\",\"authors\":\"Ying Zhou, Ying Wang, Xiangyu Meng, Ming Xiong, Xianxian Dong, Hui Peng, Fangyi Chen, Ke-Jian Wang\",\"doi\":\"10.1021/acsinfecdis.5c00034\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Methicillin-resistant <i>Staphylococcus aureus</i> (MRSA) is a predominant pathogen causing skin and soft tissue infections, which significantly hinders the wound healing process and contributes to high mortality rates. The rise of multidrug-resistant bacteria, coupled with the limited availability of new antibiotics, underscores the pressing need for the development of innovative antimicrobial substances. Antimicrobial peptides (AMPs), with their multitargeted and rapid antimicrobial activity, are promising candidates to address this crisis. In this study, we identified a novel AMP, Scymicrosin<sub>7-26</sub>, derived from <i>Scylla paramamosain</i>, which demonstrated potent antimicrobial activity against a variety of MDR strains, particularly MRSA. Confocal microscopy and transmission electron microscopy observations showed that Scymicrosin<sub>7-26</sub> bound to MRSA, and had a disruptive effect on cell walls and cell membranes, rapidly penetrating and killing MRSA. Notably, Scymicrosin<sub>7-26</sub> exhibited good stability under various ionic conditions, thermal stresses and certain serum concentration, had no obvious toxic effects on HaCaT cells, and its ability to penetrate HaCaT cells indicated its potential for intracellular targeted therapy. <i>In vitro</i>, Scymicrosin<sub>7-26</sub> significantly reduced the number of MRSA in HaCaT cells and inhibited intracellular MRSA proliferation. After verifying the low toxicity of Scymicrosin<sub>7-26</sub> <i>in vivo</i> in the Marine model organism─marine medaka (<i>Oryzias melastigma</i>), a wound model of MRSA-infected mice was made, and topical administration of Scymicrosin<sub>7-26</sub> in hypromellose gels could significantly reduce bacterial burden and promote wound closure. Histological analysis confirmed that Scymicrosin<sub>7-26</sub> alleviated tissue damage and was comparable to the effect of vancomycin treatment. Collectively, Scymicrosin<sub>7-26</sub> is promising for the treatment of MRSA wound infections and could be a valuable addition to the arsenal against antibiotic-resistant bacteria.</p>\",\"PeriodicalId\":17,\"journal\":{\"name\":\"ACS Infectious Diseases\",\"volume\":\"11 5\",\"pages\":\"1216-1232\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-05-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Infectious Diseases\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1021/acsinfecdis.5c00034\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/4/22 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Infectious Diseases","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1021/acsinfecdis.5c00034","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/4/22 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Newly Identified Antimicrobial Peptide Scymicrosin7-26 from Scylla paramamosain Showing Potent Antimicrobial Activity Against Methicillin-Resistant Staphylococcus aureusIn Vitro and In Vivo.
Methicillin-resistant Staphylococcus aureus (MRSA) is a predominant pathogen causing skin and soft tissue infections, which significantly hinders the wound healing process and contributes to high mortality rates. The rise of multidrug-resistant bacteria, coupled with the limited availability of new antibiotics, underscores the pressing need for the development of innovative antimicrobial substances. Antimicrobial peptides (AMPs), with their multitargeted and rapid antimicrobial activity, are promising candidates to address this crisis. In this study, we identified a novel AMP, Scymicrosin7-26, derived from Scylla paramamosain, which demonstrated potent antimicrobial activity against a variety of MDR strains, particularly MRSA. Confocal microscopy and transmission electron microscopy observations showed that Scymicrosin7-26 bound to MRSA, and had a disruptive effect on cell walls and cell membranes, rapidly penetrating and killing MRSA. Notably, Scymicrosin7-26 exhibited good stability under various ionic conditions, thermal stresses and certain serum concentration, had no obvious toxic effects on HaCaT cells, and its ability to penetrate HaCaT cells indicated its potential for intracellular targeted therapy. In vitro, Scymicrosin7-26 significantly reduced the number of MRSA in HaCaT cells and inhibited intracellular MRSA proliferation. After verifying the low toxicity of Scymicrosin7-26in vivo in the Marine model organism─marine medaka (Oryzias melastigma), a wound model of MRSA-infected mice was made, and topical administration of Scymicrosin7-26 in hypromellose gels could significantly reduce bacterial burden and promote wound closure. Histological analysis confirmed that Scymicrosin7-26 alleviated tissue damage and was comparable to the effect of vancomycin treatment. Collectively, Scymicrosin7-26 is promising for the treatment of MRSA wound infections and could be a valuable addition to the arsenal against antibiotic-resistant bacteria.
期刊介绍:
ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to:
* Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials.
* Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets.
* Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance.
* Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents.
* Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota.
* Small molecule vaccine adjuvants for infectious disease.
* Viral and bacterial biochemistry and molecular biology.