Antibacterial effect of bacteriocin XJS01 and its application as antibiofilm agents to treat multidrug-resistant Staphylococcus aureus infection

التفاصيل البيبلوغرافية
العنوان: Antibacterial effect of bacteriocin XJS01 and its application as antibiofilm agents to treat multidrug-resistant Staphylococcus aureus infection
المؤلفون: Yan-Mei Zhang, Yi-Zhou Xiang, Lian-Bing Lin, Lin-Yu Yang, Xian-Yu Deng, Qi-Lin Zhang, Gang Wu, Xiao-Jie Yang
المصدر: International Journal of Biological Macromolecules. 196:13-22
بيانات النشر: Elsevier BV, 2022.
سنة النشر: 2022
مصطلحات موضوعية: Staphylococcus aureus, medicine.drug_class, Antibiotics, Mupirocin, Microbial Sensitivity Tests, medicine.disease_cause, Hemolysis, Biochemistry, Microbiology, Mice, chemistry.chemical_compound, Bacteriocins, Bacteriocin, Structural Biology, Drug Resistance, Multiple, Bacterial, medicine, Animals, Humans, Cytotoxicity, Molecular Biology, Wound Healing, biology, Chemistry, Macrophages, Biofilm, General Medicine, Hydrogen-Ion Concentration, Staphylococcal Infections, biology.organism_classification, Anti-Bacterial Agents, Multiple drug resistance, Disease Models, Animal, Biofilms, Cytokines, Bacteria
الوصف: Multidrug-resistant (MDR) Staphylococcus aureus biofilms have emerged as a serious threat to human health. Recently, the development of antibiotic replacement therapy has gained much attention due to the potential application of bacteriocin. The present study sought to evaluate the antibacterial effect of bacteriocin XJS01 against MDR S. aureus, a previously reported bacteriocin against S. aureus strain 2612:1606BL1486 (S. aureus_26, an MDR strain demonstrated here), and its potential application as an antibiofilm agent. The minimum bactericide concentration of XJS01 against MDR S. aureus_26 was 33.18 μg/mL. XJS01 exhibited excellent storage stability and resistance against acid and reduced the density of established MDR S. aureus_26 biofilm. The hemolytic and HEK293T cytotoxicity activities of XJS01 and the histological analyses in mice confirmed its safety. Moreover, XJS01 effectively disrupted the MDR S. aureus_26 biofilm established on the skin wound surface and reduced the biofilm-isolated bacteria, thereby decreasing the release of pro-inflammatory cytokines and the proliferation of alternatively activated macrophages. Compared to mupirocin, XJS01 exhibited an excellent therapeutic effect on mice skin wounds, confirming it to be a potential alternative to antibiotics.
تدمد: 0141-8130
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4efac4f283f7696755ca0f3a769fa1e1
https://doi.org/10.1016/j.ijbiomac.2021.11.136
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....4efac4f283f7696755ca0f3a769fa1e1
قاعدة البيانات: OpenAIRE