Antibacterial and therapeutic effects of vancomycin-resistant Staphylococcus aureus bacteriocin (VRSAcin) in the treatment of VRSA skin infection in mice.

IF 3.5 3区 医学 Q3 IMMUNOLOGY
Microbial pathogenesis Pub Date : 2025-08-01 Epub Date: 2025-05-20 DOI:10.1016/j.micpath.2025.107729
Ahmed Qassim Al-Awadi, Mais Emad Ahmed, Mohammad Y Alfaifi, Ali A Shati, Serag Eldin I Elbehairi, Mohammed Aufy, Ahmed M Hussein
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引用次数: 0

Abstract

Vancomycin Staphylococcus aureus (VRSA) is a strain of S. aureus that is considered the main cause of bacterial skin and soft tissue infections. It has acquired resistance to vancomycin and represents a therapeutic challenge. The current study aimed to compare the possible therapeutic effects of VRSA bacteriocin (VRSAcin) on the treatment of skin infection in mice with those of an antibiotic (linezolid). The results showed that of the fifty swabs obtained from human skin wounds. One isolate was selected for VRSAcin extraction depending on its antibiotic resistance using an antibiotic susceptibility test.An agar well diffusion test was used to determine bacteriocin's antibacterial activity, as well as its a minimum inhibitory concentration, minimum bactericidal concentration, and antibiofilm efficiency against gram-positive and gram-negative bacteria that were resistant to many medicines. The freshly developed antibacterial substance VRSAcin shows promise. Bacteriocin from VRSA was extracted and studied the optimal conditions for the Production following Purification of bacteriocin by ammonium sulfate precipitation followed by cation-exchange chromatography. The molecular weight of bacteriocin about (29 kDa) were determined by Sodium Dodecyl Sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). The typical conditions for the production of VRSAcin include a pH of 7 and a temperature of 37 °C for 48 h. In mice, VRSA-contaminated wounds revealed severe tissue distraction and inflammation that extended to the hypodermis, while VRSA-treated skin showed mild changes and localized lesions to the epidermis and upper dermis. The skin of linezolid ointment-treated mice showed moderate to severe changes. In conclusion, VRSA strain infections in human burned skin were more common than expected. In vivo studies in mice indicated that wounded skin infected with VRSA can be treated with VRSAcin as an antibacterial agent that promotes healing processes with obvious superiority to linezolid ointment. As a result, the VRSA develops bacteriocins that are appropriate for regulating AMR, Gram-positive and Gram-negative bacteria, and may be useful in wound dressings.

耐万古霉素金黄色葡萄球菌细菌素(VRSAcin)对小鼠VRSA皮肤感染的抗菌和治疗作用。
万古霉素金黄色葡萄球菌(VRSA)是一种金黄色葡萄球菌,被认为是细菌性皮肤和软组织感染的主要原因。它已经获得了对万古霉素的耐药性,这是一个治疗挑战。本研究旨在比较VRSA细菌素(VRSAcin)与抗生素(利奈唑胺)治疗小鼠皮肤感染的可能治疗效果。结果表明,从人体皮肤伤口获得的50个拭子中,通过药敏试验选择一株分离菌进行VRSAcin的提取,并用琼脂孔扩散试验测定其抑菌活性、最低抑菌浓度、最低杀菌浓度以及对多种药物耐药的革兰氏阳性菌和革兰氏阴性菌的抗菌膜效率。新开发的抗菌物质VRSAcin显示出了希望。从VRSA中提取细菌素,并研究了硫酸铵沉淀-阳离子交换色谱法纯化细菌素的最佳工艺条件。采用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)测定了细菌素的分子量约为29 kDa。生产VRSAcin的典型条件包括pH为7,温度为37°C, 48小时。在小鼠中,vrsa污染的伤口显示出严重的组织分散和炎症,并延伸到真皮下,而vrsa处理的皮肤显示出轻微的变化和表皮和真皮上的局部病变。利奈唑胺软膏治疗小鼠的皮肤表现出中度至重度的变化。总之,人体烧伤皮肤中VRSA菌株感染比预期的更常见。小鼠体内研究表明,VRSA感染的损伤皮肤可以用VRSAcin作为抗菌药物治疗,促进愈合过程,与利奈唑胺软膏相比具有明显的优势。因此,VRSA开发出适合调节AMR、革兰氏阳性和革兰氏阴性细菌的细菌素,并可能用于伤口敷料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Microbial pathogenesis
Microbial pathogenesis 医学-免疫学
CiteScore
7.40
自引率
2.60%
发文量
472
审稿时长
56 days
期刊介绍: Microbial Pathogenesis publishes original contributions and reviews about the molecular and cellular mechanisms of infectious diseases. It covers microbiology, host-pathogen interaction and immunology related to infectious agents, including bacteria, fungi, viruses and protozoa. It also accepts papers in the field of clinical microbiology, with the exception of case reports. Research Areas Include: -Pathogenesis -Virulence factors -Host susceptibility or resistance -Immune mechanisms -Identification, cloning and sequencing of relevant genes -Genetic studies -Viruses, prokaryotic organisms and protozoa -Microbiota -Systems biology related to infectious diseases -Targets for vaccine design (pre-clinical studies)
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