六神丸通过NLRP3炎性体和TLR2-NF-κB/p38 MAPK信号通路减轻金黄色葡萄球菌的毒性和炎症反应。

IF 4.8 2区 医学 Q2 IMMUNOLOGY
Yudi Song, Qinhai Ma, Jincan Luo, Zifeng Yang, Jiqiang Li, Jin Zhao
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引用次数: 0

摘要

传染病一直是全球健康的主要威胁,其中细菌感染尤为突出。金黄色葡萄球菌(S. aureus)感染导致的死亡人数最多。抑制金黄色葡萄球菌诱导的毒力因子和过度炎症已成为一种潜在的抗生素替代/协同疗法,同时不会造成更大的生存压力,以防止未来出现 "超级细菌"。六神丸是一种传统中药,可用于多种细菌感染性疾病。在这项工作中,我们研究了六神丸的治疗效果,并探索了六神丸在体内和体外针对金黄色葡萄球菌的潜在机制。通过最小抑菌浓度(MIC)检测、溶血检测、侵袭检测、钉螺黄素检测和耐药性进化检测,结果表明,LSW可减轻金黄色葡萄球菌的毒力,但不抑制金黄色葡萄球菌的活性,且短期使用LSW不会使细菌产生耐药性。生物膜抑制实验表明,LSW能抑制金黄色葡萄球菌生物膜的形成,并能破坏成熟的生物膜。使用RT-qPCR、ELISA和Western blot分析的体外实验表明,LSW可抑制HK-S. aureus和S. aureus通过NLRP3炎性体和TLR2-NF-κB/p38 MAPK通路引发的炎症反应。此外,LSW还能减轻金黄色葡萄球菌引起的肺损伤。综上所述,LSW是一种很有前景的抗菌、抗病毒和抗炎药物,可为LSW在临床上治疗金黄色葡萄球菌感染相关疾病的传统应用提供药理学依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Liushen Wan alleviates the virulence and inflammation of Staphylococcus aureus via NLRP3 inflammasome and TLR2-NF-κB/p38 MAPK signaling pathways.

Infectious diseases have been a major threat to health worldwide, with bacterial infections being particularly prominent. Staphylococcus aureus (S. aureus) infections are associated with the most deaths. Inhibition of virulence factor and excessive inflammation induced by S. aureus has become a potential antibiotic alternative/synergistic therapy without causing greater survival pressure to prevent the emergence of "superbugs" in the future. Liushen Wan (LSW), a traditional Chinese medicine, used for multiple bacterial infectious diseases. In this work, we researched its therapeutic effect and explored the potential mechanism of LSW aiming at S. aureus in vivo and in vitro. Minimal inhibitory concentration (MIC) assay, hemolysis assay, invasion assay, staphyloxanthin assay and evolution of resistance assay were performed to show that LSW alleviated the virulence of S. aureus without suppressing S. aureus activity, and short-term use of LSW did not make bacteria resistant to it. Biofilm inhibition assay demonstrated that LSW inhibited the formation of biofilm and destroyed mature biofilm of S. aureus. In vitro experiments using RT-qPCR, ELISA and western blot analysis indicated LSW inhibited the inflammatory reaction triggered by HK-S. aureus and S. aureus through NLRP3 inflammasome and TLR2-NF-κB/p38 MAPK pathway. Moreover, LSW alleviated lung damage induced by S. aureus. Taken together, LSW is a promising antibacterial, anti-virulence and anti-inflammatory drug, which could provide the pharmacological basis on the traditional application of LSW for diseases associated with S. aureus infection in clinical.

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来源期刊
CiteScore
8.40
自引率
3.60%
发文量
935
审稿时长
53 days
期刊介绍: International Immunopharmacology is the primary vehicle for the publication of original research papers pertinent to the overlapping areas of immunology, pharmacology, cytokine biology, immunotherapy, immunopathology and immunotoxicology. Review articles that encompass these subjects are also welcome. The subject material appropriate for submission includes: • Clinical studies employing immunotherapy of any type including the use of: bacterial and chemical agents; thymic hormones, interferon, lymphokines, etc., in transplantation and diseases such as cancer, immunodeficiency, chronic infection and allergic, inflammatory or autoimmune disorders. • Studies on the mechanisms of action of these agents for specific parameters of immune competence as well as the overall clinical state. • Pre-clinical animal studies and in vitro studies on mechanisms of action with immunopotentiators, immunomodulators, immunoadjuvants and other pharmacological agents active on cells participating in immune or allergic responses. • Pharmacological compounds, microbial products and toxicological agents that affect the lymphoid system, and their mechanisms of action. • Agents that activate genes or modify transcription and translation within the immune response. • Substances activated, generated, or released through immunologic or related pathways that are pharmacologically active. • Production, function and regulation of cytokines and their receptors. • Classical pharmacological studies on the effects of chemokines and bioactive factors released during immunological reactions.
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