Spermidine Associated with Gut Microbiota Protects Against MRSA Bloodstream Infection by Promoting Macrophage M2 Polarization.

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL ACS Infectious Diseases Pub Date : 2024-11-08 Epub Date: 2024-10-09 DOI:10.1021/acsinfecdis.3c00669
Qingqing Li, Ping Tian, Mingjuan Guo, Xiaoqiang Liu, Tingting Su, Mingyang Tang, Bao Meng, Liang Yu, Yi Yang, Yanyan Liu, Yasheng Li, Jiabin Li
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Abstract

Methicillin-resistant Staphylococcus aureus (MRSA) is a major human pathogen that causes various diseases. Extensive researches highlight the significant role of gut microbiota and its metabolites, particularly spermidine, in infectious diseases. However, the immunomodulatory mechanisms of spermidine in MRSA-induced bloodstream infection remain unclear. Here, we confirmed the protective effects of spermidine in bloodstream infection in mice. Spermidine reduced the bacterial load and expression of inflammatory factors by shifting the macrophage phenotype to an anti-inflammatory phenotype, ultimately prolonging the survival of the infected mice. The protective effect against MRSA infection may rely on the elevated expression of protein tyrosine phosphatase nonreceptor 2 (PTPN2). Collectively, these findings confirm the immunoprotective effects of spermidine via binding to PTPN2 in MRSA bloodstream infection, providing new ideas for the treatment of related infectious diseases.

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与肠道微生物群相关的精胺可通过促进巨噬细胞 M2 极化防止 MRSA 血流感染。
耐甲氧西林金黄色葡萄球菌(MRSA)是导致各种疾病的主要人类病原体。大量研究表明,肠道微生物群及其代谢产物,尤其是亚精胺,在感染性疾病中发挥着重要作用。然而,精胺在 MRSA 引起的血流感染中的免疫调节机制仍不清楚。在这里,我们证实了精胺对小鼠血流感染的保护作用。精胺通过将巨噬细胞表型转变为抗炎表型,减少了细菌负荷和炎症因子的表达,最终延长了感染小鼠的存活时间。对 MRSA 感染的保护作用可能依赖于蛋白酪氨酸磷酸酶非受体 2(PTPN2)表达的升高。总之,这些发现证实了亚精胺通过与 PTPN2 结合对 MRSA 血流感染具有免疫保护作用,为相关传染病的治疗提供了新思路。
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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
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.
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