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Single-cell RNA-seq landscape midbrain cell responses to red spotted grouper nervous necrosis virus infection

生物 石斑鱼 免疫系统 坏死 电池类型 肿瘤坏死因子α 小胶质细胞 细胞生物学 程序性细胞死亡 中脑 病毒 细胞 中枢神经系统 病毒学 免疫学 炎症 遗传学 神经科学 细胞凋亡 渔业
作者
Qing Wang,Cheng‐Yuan Peng,Min Yang,Fengqi Huang,Xuzhuo Duan,Shaowen Wang,Huitao Cheng,Huirong Yang,Huihong Zhao,Qiwei Qin
出处
期刊:PLOS Pathogens [Public Library of Science]
卷期号:17 (6): e1009665-e1009665 被引量:39
标识
DOI:10.1371/journal.ppat.1009665
摘要

Viral nervous necrosis (VNN) is an acute and serious fish disease caused by nervous necrosis virus (NNV) which has been reported massive mortality in more than fifty teleost species worldwide. VNN causes damage of necrosis and vacuolation to central nervous system (CNS) cells in fish. It is difficult to identify the specific type of cell targeted by NNV, and to decipher the host immune response because of the functional diversity and highly complex anatomical and cellular composition of the CNS. In this study, we found that the red spotted grouper NNV (RGNNV) mainly attacked the midbrain of orange-spotted grouper ( Epinephelus coioides ). We conducted single-cell RNA-seq analysis of the midbrain of healthy and RGNNV-infected fish and identified 35 transcriptionally distinct cell subtypes, including 28 neuronal and 7 non-neuronal cell types. An evaluation of the subpopulations of immune cells revealed that macrophages were enriched in RGNNV-infected fish, and the transcriptional profiles of macrophages indicated an acute cytokine and inflammatory response. Unsupervised pseudotime analysis of immune cells showed that microglia transformed into M1-type activated macrophages to produce cytokines to reduce the damage to nerve tissue caused by the virus. We also found that RGNNV targeted neuronal cell types was GLU1 and GLU3, and we found that the key genes and pathways by which causes cell cytoplasmic vacuoles and autophagy significant enrichment, this may be the major route viruses cause cell death. These data provided a comprehensive transcriptional perspective of the grouper midbrain and the basis for further research on how viruses infect the teleost CNS.

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