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二甲双胍对牛病毒性腹泻病毒感染影响的转录组学分析

Transcriptomic Analysis of Metformin's Effect on Bovine Viral Diarrhea Virus Infection.

作者信息

Li Zeyu, He Yuanxiu, Chen Junzhen, Ran Duoliang, Yue Jianbo, Fu Qiang, Shi Huijun

机构信息

College of Veterinary Medicine, Xinjiang Agricultural University, Urumqi 830052, China.

Xinjiajng Key Laboratory of New Drug Study and Creation for Herbivorous Animals, Urumqi 830052, China.

出版信息

Vet Sci. 2024 Aug 15;11(8):376. doi: 10.3390/vetsci11080376.

Abstract

(1) Background: Bovine viral diarrhea virus (BVDV) causes calf diarrhea, bovine respiratory syndrome, and cow abortion, resulting in substantial economic losses in the cattle industry. Owing to its persistent infection mechanism, BVDV is a major challenge in the treatment of cattle. (2) Methods: To determine how metformin (Met) inhibits the interaction between BVDV and host cells, we treated BVDV-infected cells with Met. We then performed an RNA sequencing (RNA-seq) analysis of Met-treated cells infected with BVDV to identify differentially expressed genes (DEGs). Consequently, the RNA-seq results were validated through real-time quantitative PCR (qPCR). (3) Results: Our analysis revealed 3169 DEGs in the Met-treated cells (Met group) vs. the negative controls (NC group) and 2510 DEGs in the BVDV-infected cells after pretreatment with Met (MetBVDV group) vs. the BVDV-infected cells (BVDV group). The DEGs were involved in MDBK interactions during BVDV infection, as indicated by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses. The potential interactions of the DEGs were confirmed via a protein-protein interaction (PPI) network. Met treatment induced autophagy signaling activity and the expression of the autophagy-related genes ATG2A, ATG4B, ATG10, and ATG12 in BVDV-infected Met-pretreated cells. (4) Conclusions: We found that the host transcriptomic profile was affected by BVDV infection and Met pretreatment. These findings offer valuable new insights and provide support for future studies on the inhibition of BVDV replication by Met.

摘要

(1) 背景:牛病毒性腹泻病毒(BVDV)可引发犊牛腹泻、牛呼吸道综合征以及母牛流产,给养牛业造成巨大经济损失。由于其持续感染机制,BVDV成为牛治疗中的一项重大挑战。(2) 方法:为确定二甲双胍(Met)如何抑制BVDV与宿主细胞之间的相互作用,我们用Met处理感染BVDV的细胞。随后,我们对经Met处理的感染BVDV的细胞进行RNA测序(RNA-seq)分析,以鉴定差异表达基因(DEG)。因此,通过实时定量PCR(qPCR)对RNA-seq结果进行了验证。(3) 结果:我们的分析显示,与阴性对照(NC组)相比,Met处理的细胞(Met组)中有3169个DEG;与感染BVDV的细胞(BVDV组)相比,用Met预处理后感染BVDV的细胞(MetBVDV组)中有2510个DEG。基因本体论(GO)和京都基因与基因组百科全书(KEGG)通路分析表明,这些DEG参与了BVDV感染期间的MDBK相互作用。通过蛋白质-蛋白质相互作用(PPI)网络证实了DEG的潜在相互作用。Met处理诱导了感染BVDV的Met预处理细胞中的自噬信号活性以及自噬相关基因ATG2A、ATG4B、ATG10和ATG12的表达。(4) 结论:我们发现宿主转录组图谱受到BVDV感染和Met预处理的影响。这些发现提供了有价值的新见解,并为未来关于Met抑制BVDV复制的研究提供了支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae79/11358930/1df1b00fe766/vetsci-11-00376-g001a.jpg

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