Chlorogenic acid carbon dots inhibit NDV proliferation by suppressing virus-induced mitochondrial autophagy and MAVS degradation in host cells

自噬 病毒 新城疫 化学 线粒体 病毒复制 粒体自噬 降级(电信) 细胞生物学 病毒学 生物化学 活性氧 碳纤维 绿原酸 吸附 蛋白质降解 细胞凋亡 发病机制 生物物理学 碘尿苷 免疫系统 抗体 纳米颗粒 传染性 抗病毒药物 病菌 病毒病机
作者
Qian Yang,Luqing Zhang,Shuyao Yang,Hangyu Li,Yanwen Yang,Yi Liao,Yao Wang,Haibo Feng
出处
期刊:Materials today bio [Elsevier BV]
卷期号:35: 102459-102459 被引量:1
标识
DOI:10.1016/j.mtbio.2025.102459
摘要

Chlorogenic acid (CGA) is widely used to inhibit virus replication and transmission. However, it lacks targeting capabilities and sustained-release properties. In contrast, carbon quantum dots can not only inhibit virus replication directly but can also serve as drug carriers to enhance the targeting capacity and efficacy of antiviral drugs. In this study, CGA carbon dots (CGA-CDs) were prepared using a microwave-assisted synthesis method. The physicochemical characteristics and antiviral activities of CGA-CDs against Newcastle disease virus (NDV) were explored through a series of experiments. The average particle size of CGA-CDs was 5.675 ± 0.15 nm. The CGA-CDs were non-ordered carbon structures composed of C and O, with uniform size, good dispersion properties, and a surface rich in –COOH, –OH, and other hydrophilic groups. The optimal excitation wavelength of CGA-CDs was 390 nm, the emission wavelength was 450 nm, and the CGA-CDs thus emitted blue fluorescence. Notably, CGA-CDs produced significantly stronger antiviral effects than equivalent concentrations of CGA and could successfully inhibit virus adsorption and replication. Furthermore, CGA-CDs significantly inhibited virus-induced mitochondrial dysfunction, mitochondrial autophagy, and mitochondrial antiviral signaling protein (MAVS) degradation, providing superior antiviral efficacy. In vivo experiments further demonstrated the good biocompatibility of CGA-CDs. Moreover, in NDV-infected chickens, CGA-CDs significantly reduced the viral load in the spleen and proventriculus, alleviated pathological damage to major organs, enhanced antibody responses, and markedly lowered the mortality rate. In summary, CGA-CDs showed significant anti-NDV activity by inhibiting NDV adsorption and replication, likely through the inhibition of virus-induced mitophagy and MAVS degradation. These findings highlight the potential of CGA-CDs as potent antiviral agents.
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