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需要加速有氧糖酵解和磷酸戊糖途径的代谢物水平,以提高传染性脾肾坏死病毒在中国鲈鱼脑细胞中的复制效率。

Accelerated Metabolite Levels of Aerobic Glycolysis and the Pentose Phosphate Pathway Are Required for Efficient Replication of Infectious Spleen and Kidney Necrosis Virus in Chinese Perch Brain Cells.

机构信息

Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Key Laboratory of fishery Drug Development, Ministry of Agriculture and Rural Affairs, Key Laboratory of Aquatic Animal Immune Technology, Guangdong Provinces, Guangzhou 510380, China.

College of Fisheries and Life Science, Shanghai Ocean University, Shanghai 201306, China.

出版信息

Biomolecules. 2019 Sep 2;9(9):440. doi: 10.3390/biom9090440.

DOI:10.3390/biom9090440
PMID:31480692
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6770389/
Abstract

Glucose is a main carbon and energy source for virus proliferation and is usually involved in the glycolysis, pentose phosphate pathway (PPP), and tricarboxylic acid cycle (TCA cycle) pathways. In this study, we investigated the roles of glucose-related metabolic pathways during the replication of infectious spleen and kidney necrosis virus (ISKNV), which has caused serious economic losses in the cultured Chinese perch () industry. We found that ISKNV infection enhanced the metabolic pathways of the PPP and the TCA cycle at the early stage of the ISKNV infection cycle and enhanced the glycolysis pathway at the late stage of the ISKNV infection cycle though the comprehensive analysis of transcriptomics, proteomics, and metabolomics. The advanced results proved that ISKNV replication induced upregulation of aerobic glycolysis at the late stage of ISKNV infection cycle and aerobic glycolysis were required for ISKNV multiplication. In addition, the PPP, providing nucleotide biosynthesis, was also required for ISKNV multiplication. However, the TCA cycle involving glucose was not important and necessary for ISKNV multiplication. The results reported here provide new insights into viral pathogenesis mechanism of metabolic shift, as well as antiviral treatment strategies.

摘要

葡萄糖是病毒增殖的主要碳源和能量来源,通常参与糖酵解、磷酸戊糖途径(PPP)和三羧酸循环(TCA 循环)途径。在这项研究中,我们研究了葡萄糖相关代谢途径在传染性脾坏死病毒(ISKNV)复制过程中的作用,ISKNV 感染已导致养殖鲈鱼()产业遭受严重的经济损失。我们发现,通过转录组学、蛋白质组学和代谢组学的综合分析,ISKNV 感染在感染周期的早期增强了 PPP 和 TCA 循环的代谢途径,在感染周期的晚期增强了糖酵解途径。先进的结果证明,ISKNV 复制在 ISKNV 感染周期的晚期诱导有氧糖酵解的上调,有氧糖酵解是 ISKNV 增殖所必需的。此外,提供核苷酸生物合成的 PPP 也需要用于 ISKNV 增殖。然而,涉及葡萄糖的 TCA 循环对于 ISKNV 的增殖并不重要和必要。这里报道的结果为代谢重编程的病毒发病机制以及抗病毒治疗策略提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b31/6770389/b4b0ef9610aa/biomolecules-09-00440-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b31/6770389/4dd00fe6f9a1/biomolecules-09-00440-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b31/6770389/85e1946e515a/biomolecules-09-00440-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b31/6770389/75284b450436/biomolecules-09-00440-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b31/6770389/6e2b46a99fd6/biomolecules-09-00440-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b31/6770389/209ef9da21e9/biomolecules-09-00440-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b31/6770389/b4b0ef9610aa/biomolecules-09-00440-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b31/6770389/4dd00fe6f9a1/biomolecules-09-00440-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b31/6770389/85e1946e515a/biomolecules-09-00440-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b31/6770389/75284b450436/biomolecules-09-00440-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b31/6770389/6e2b46a99fd6/biomolecules-09-00440-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b31/6770389/209ef9da21e9/biomolecules-09-00440-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b31/6770389/b4b0ef9610aa/biomolecules-09-00440-g006.jpg

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