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胆固醇生物合成调节 CSFV 复制。

Cholesterol Biosynthesis Modulates CSFV Replication.

机构信息

College of Animal Sciences, Jilin University, Changchun 130062, China.

Chongqing Research Institute, Jilin University, Chongqing 401120, China.

出版信息

Viruses. 2022 Jun 30;14(7):1450. doi: 10.3390/v14071450.

Abstract

Classical swine fever (CSF) caused by the classical swine fever virus (CSFV) has resulted in severe losses to the pig industry worldwide. It has been proposed that lipid synthesis is essential for viral replication, and lipids are involved in viral protein maturation and envelope production. However, the specific crosstalk between CSFV and host cell lipid metabolism is still unknown. In this study, we found that CSFV infection increased intracellular cholesterol levels in PK-15 cells. Further analysis demonstrated that CSFV infection upregulated PCSK9 expression to block the uptake of exogenous cholesterol by LDLR and enhanced the cholesterol biosynthesis pathway, which disrupted the type I IFN response in PK-15 cells. Our findings provide new insight into the mechanisms underpinning the pathogenesis of CSFV and hint at methods for controlling the disease.

摘要

经典猪瘟(CSF)由经典猪瘟病毒(CSFV)引起,给全球养猪业造成了严重损失。据报道,脂质合成对病毒复制至关重要,脂质参与病毒蛋白成熟和包膜生成。然而,CSFV 与宿主细胞脂质代谢之间的确切相互作用仍不清楚。在本研究中,我们发现 CSFV 感染可增加 PK-15 细胞内胆固醇水平。进一步分析表明,CSFV 感染上调 PCSK9 的表达,阻断 LDLR 摄取外源性胆固醇,并增强胆固醇生物合成途径,从而破坏 PK-15 细胞中的 I 型 IFN 反应。我们的研究结果为 CSFV 发病机制提供了新的见解,并提示了控制该病的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/deeb/9316236/7d57ebc16be4/viruses-14-01450-g001.jpg

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