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非致病性草鱼呼肠孤病毒感染导致草鱼细胞系发生凋亡和自噬。

Non-pathogenic grass carp reovirus infection leads to both apoptosis and autophagy in a grass carp cell line.

机构信息

National Demonstration Center for Experimental Fisheries Science Education, Shanghai Ocean University, Shanghai, 201306, China; Yangtze River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Wuhan, 430223, China.

Yangtze River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Wuhan, 430223, China.

出版信息

Fish Shellfish Immunol. 2022 Aug;127:681-689. doi: 10.1016/j.fsi.2022.06.022. Epub 2022 Jun 21.

DOI:10.1016/j.fsi.2022.06.022
PMID:35738488
Abstract

A novel GCRV strain isolated from healthy grass carp was named as grass carp reovirus - HH196 (GCRV-HH196), and its infection mechanism remains unclear. In this study, the grass carp ovary cell line (GCO cells) was used to investigate the cell death involved in GCRV-HH196 infection. The results showed that DNA damage, cells volume reduction and cytoplasm shrinkage happened during GCRV-HH196 infection. The mRNA expression levels of pro-apoptotic genes were up-regulated during infection. Two initiators of apoptosis, caspase 8 and caspase 9, and the executioner of apoptosis, caspase 3, were all significantly activated in GCRV-HH196-infected cells. Flow cytometry analysis showed that the number of apoptotic cells in infected cells was significantly higher than that in control cells as the infection progress. Meanwhile, autophagy was also involved in the regulation of GCRV - HH196 infection. We observed that LC3 puncta existed in cytoplasm in GCRV-HH196-infected cells. Furthermore, the protein level of LC3-Ⅱ and Beclin-1 increased, while that of p-Akt decreased in GCRV-HH196-infected cells. These results demonstrated that GCRV-HH196 may regulate apoptosis and autophagy for the virus proliferation and spread, which set a foundation for further research on the interaction between GCRV-HH196 and host.

摘要

一株从健康草鱼中分离得到的新型草鱼呼肠孤病毒(GCRV)被命名为草鱼呼肠孤病毒 HH196(GCRV-HH196),但其感染机制尚不清楚。本研究采用草鱼卵巢细胞系(GCO 细胞)研究了 GCRV-HH196 感染过程中涉及的细胞死亡。结果表明,在 GCRV-HH196 感染过程中发生 DNA 损伤、细胞体积缩小和细胞质收缩。感染过程中促凋亡基因的 mRNA 表达水平上调。两种凋亡起始酶 caspase 8 和 caspase 9 以及凋亡执行酶 caspase 3 在 GCRV-HH196 感染细胞中均被显著激活。流式细胞术分析显示,随着感染的进展,感染细胞中凋亡细胞的数量明显高于对照细胞。同时,自噬也参与了 GCRV-HH196 感染的调控。我们观察到 GCRV-HH196 感染细胞的细胞质中存在 LC3 斑点。此外,GCRV-HH196 感染细胞中 LC3-Ⅱ和 Beclin-1 的蛋白水平增加,而 p-Akt 的蛋白水平降低。这些结果表明,GCRV-HH196 可能通过调节细胞凋亡和自噬来促进病毒的增殖和扩散,为进一步研究 GCRV-HH196 与宿主之间的相互作用奠定了基础。

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