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Comparative transcriptome analysis of rainbow trout gonadal cells (RTG-2) infected with U and J genogroup infectious hematopoietic necrosis virus.
Zhao, Jing-Zhuang; Xu, Li-Ming; Ren, Guang-Ming; Shao, Yi-Zhi; Liu, Qi; Teng, Chun-Bo; Lu, Tong-Yan.
Afiliación
  • Zhao JZ; Cell Biology Laboratory, College of Life Science, Northeast Forestry University, Harbin, China.
  • Xu LM; Heilongjiang River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Harbin, China.
  • Ren GM; Key Laboratory of Aquatic Animal Diseases and Immune Technology of Heilongjiang Province, Harbin, China.
  • Shao YZ; Heilongjiang River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Harbin, China.
  • Liu Q; Heilongjiang River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Harbin, China.
  • Teng CB; Heilongjiang River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Harbin, China.
  • Lu TY; Heilongjiang River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Harbin, China.
Front Microbiol ; 13: 1109606, 2022.
Article en En | MEDLINE | ID: mdl-36733771
Infectious hematopoietic necrosis virus (IHNV) is the causative pathogen of infectious hematopoietic necrosis, outbreaks of which are responsible for significant losses in rainbow trout aquaculture. Strains of IHNV isolated worldwide have been classified into five major genogroups, J, E, L, M, and U. To date, comparative transcriptomic analysis has only been conducted individually for the J and M genogroups. In this study, we compared the transcriptome profiles in U genogroup and J genogroup IHNV-infected RTG-2 cells with mock-infected RTG-2 cells. The RNA-seq results revealed 17,064 new genes, of which 7,390 genes were functionally annotated. Differentially expressed gene (DEG) analysis between U and J IHNV-infected cells revealed 2,238 DEGs, including 1,011 downregulated genes and 1,227 upregulated genes. Among the 2,238 DEGs, 345 new genes were discovered. The DEGs related to immune responses, cellular signal transduction, and viral diseases were further analyzed. RT-qPCR validation confirmed that the changes in expression of the immune response-related genes trpm2, sting, itgb7, ripk2, and irf1, cellular signal transduction-related genes irl, cacnb2, bmp2l, gadd45α, and plk2, and viral disease-related genes mlf1, mtor, armc5, pik3r1, and c-myc were consistent with the results of transcriptome analysis. Taken together, our findings provide a comprehensive transcriptional analysis of the differential virulence of the U and J genogroups of IHNV, and shed new light on the pathogenic mechanisms of IHNV strains.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Front Microbiol Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Front Microbiol Año: 2022 Tipo del documento: Article País de afiliación: China