Deciphering the antiviral mechanisms of Fangqin Qinggan decoction against influenza A virus: a multi-omics and machine learning approach

汤剂 传统医学 中医药 计算生物学 医学 甲型流感病毒 人工智能 抗病毒治疗 机制(生物学) 2019年冠状病毒病(COVID-19) 深度学习 呼吸系统 鼻病毒 严重急性呼吸综合征冠状病毒2型(SARS-CoV-2) 2019-20冠状病毒爆发 生物信息学 基础(证据) 冠状病毒 梅德林 免疫学 多发性硬化 药理学
作者
Hang Lei,Hao Zhang,Yixi Xu,Lianjiang Hu,Bin Zhang,Hao Zhou,Ping Wang,Simin Chen,Shijun Xu
出处
期刊:Chinese Medicine [BioMed Central]
卷期号:20 (1): 158-158 被引量:2
标识
DOI:10.1186/s13020-025-01211-0
摘要

BACKGROUND: Influenza A virus (IAV) infection poses a significant global health burden, contributing to high morbidity and mortality in both humans and animals through rapid viral transmission and dysregulated inflammatory responses. Fangqin Qinggan Decoction (FQ-01), a traditional Chinese medicine (TCM) formula, has demonstrated clinical efficacy in treating viral upper respiratory infections, however, its underlying therapeutic mechanisms remain poorly understood. METHODS: The therapeutic efficacy and mechanisms of FQ-01 against IAV infection were comprehensively investigated using a multidisciplinary approach, including in vivo murine models, histopathological (H&E staining), RT-qPCR, immunohistochemistry (IHC), network pharmacology, weighted gene co-expression network analysis (WGCNA), machine learning (LASSO), transcriptomics, metabolomics, molecular docking and molecular dynamics (MD) simulation. RESULTS: FQ-01 significantly improved survival rates, reduced clinical mortality, and mitigated pulmonary inflammation in an IAV-infected mice while suppressing viral replication. Integrated bioinformatics and LASSO regression analyses identified 20 genes associated with FQ-01's antiviral effects, with Myd88 and Ccl5 emerging as key targets. Transcriptomic profiling of murine lung tissues further validated these genes as critical mediators of FQ-01's therapeutic action. Spearman correlation analysis revealed strong associations between Myd88/Ccl5 expression and serum/lung metabolites, particularly 3-indolyl sulfate and inosine. Subsequent in vivo RT-qPCR and IHC validation, molecular docking, and MD simulations confirmed that FQ-01 exerts its anti-IAV effects by inhibiting Myd88 and Ccl5 expression. CONCLUSIONS: Our findings elucidate the molecular mechanisms underlying FQ-01's therapeutic potential against IAV infection, highlighting Myd88 and Ccl5 as promising targets for antiviral and anti-inflammatory interventions. This study provides a foundation for further exploration of TCM-based strategies in combating influenza and related respiratory infections.
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