Jian Ji, Yongli Ye, Jiadi Sun, Lina Sheng, Jinyou Li, Jin Yang, Bing Wu, Yuting Wang, Xingxing Gao, Liang Luo, Jianfeng Ping, Yinzhi Zhang, Xiulan Sun
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This findings revealed that F. graminearum spore exposure not only impaired pulmonary clearance mechanisms but also significantly upregulated the expression of proinflammatory cytokines, including interleukin-6 (IL-6), interleukin-1β (IL-1β), and tumor necrosis factor-α (TNF-α). Moreover, spore invasion led to an increase in Staphylococcus abundance and activation of both triglyceride and galactose metabolic pathways. Antibiotic treatment disrupted the gut and respiratory microbiota, facilitating F. graminearum lung colonization, which is evidenced by elevated inflammatory markers in alveolar fluid and dysregulated lung metabolism. It is demonstrated that the gut microbiota influences susceptibility to fungal pneumonia by acting as an intermediary in the gut-lung axis through the bloodstream, thereby modulating lung metabolism and inflammatory responses. 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引用次数: 0
摘要
真菌性肺炎是一种危害大、发病率高的严重疾病,在诊断和治疗方面都面临着重大挑战。肠道和呼吸道微生物群在保护肺部健康免受真菌肺炎方面发挥着关键作用。本研究通过肺部途径感染禾本科镰刀菌(Fusarium graminearum, F. graminearum)建立真菌性肺炎,探讨肠道菌群状态对BALB/c小鼠真菌性肺炎易感性的影响。研究结果表明,暴露于禾状芽孢杆菌孢子不仅损害肺清除机制,而且显著上调促炎细胞因子的表达,包括白细胞介素-6 (IL-6)、白细胞介素-1β (IL-1β)和肿瘤坏死因子-α (TNF-α)。此外,孢子入侵导致葡萄球菌丰度增加,并激活甘油三酯和半乳糖代谢途径。抗生素治疗破坏了肠道和呼吸道微生物群,促进了谷粒F. graminearum肺定植,肺泡液中炎症标志物升高和肺代谢失调证明了这一点。研究表明,肠道微生物群通过血液在肠-肺轴中充当中介,从而调节肺代谢和炎症反应,从而影响真菌肺炎的易感性。这些发现为新的治疗策略开辟了道路,例如肠道微生物群调节,用于预防和治疗真菌性肺炎。
Homeostasis of Gut Microbiota Protects against Susceptibility to Fungal Pneumonia.
Fungal pneumonia is a serious disease with great harm and high prevalence, presenting significant challenges in diagnosis and treatment. The gut and respiratory microbiota play a critical role in protecting lung health against fungal pneumonia. Here, it is established fungal pneumonia by infection via the sinopulmonary route with Fusarium graminearum (F. graminearum) to investigate the influence of gut microbiota state on susceptibility to fungal pneumonia in BALB/c mice. This findings revealed that F. graminearum spore exposure not only impaired pulmonary clearance mechanisms but also significantly upregulated the expression of proinflammatory cytokines, including interleukin-6 (IL-6), interleukin-1β (IL-1β), and tumor necrosis factor-α (TNF-α). Moreover, spore invasion led to an increase in Staphylococcus abundance and activation of both triglyceride and galactose metabolic pathways. Antibiotic treatment disrupted the gut and respiratory microbiota, facilitating F. graminearum lung colonization, which is evidenced by elevated inflammatory markers in alveolar fluid and dysregulated lung metabolism. It is demonstrated that the gut microbiota influences susceptibility to fungal pneumonia by acting as an intermediary in the gut-lung axis through the bloodstream, thereby modulating lung metabolism and inflammatory responses. These findings open avenues for novel therapeutic strategies, such as gut microbiota modulation, for the prevention and treatment of fungal pneumonia.
期刊介绍:
Advanced Science is a prestigious open access journal that focuses on interdisciplinary research in materials science, physics, chemistry, medical and life sciences, and engineering. The journal aims to promote cutting-edge research by employing a rigorous and impartial review process. It is committed to presenting research articles with the highest quality production standards, ensuring maximum accessibility of top scientific findings. With its vibrant and innovative publication platform, Advanced Science seeks to revolutionize the dissemination and organization of scientific knowledge.