Linwen Cheng , Shiwen Zhang , Zhongyi Liu , Qiqi Jiang , Mingyou Li , Fei Ke , Lang Gui
{"title":"Transcriptome analysis of medaka spermatogonial stem cell line (SG3) infected with ranaviruses in vitro","authors":"Linwen Cheng , Shiwen Zhang , Zhongyi Liu , Qiqi Jiang , Mingyou Li , Fei Ke , Lang Gui","doi":"10.1016/j.fsi.2025.110453","DOIUrl":null,"url":null,"abstract":"<div><div>The medaka spermatogonial stem cell line (SG3) is a well-established cell line that can be induced to differentiate into sperm <em>in vitro</em>. <em>Ranavirus</em>, a genus of viruses widely distributed among fish, amphibians, and reptiles, poses a significant threat to these organisms. This study aimed to investigate the morphological changes and transcriptomic responses in SG3 following infection with three ranavirus strains: <em>Andrias davidianus</em> ranavirus (ADRV), <em>Rana grylio</em> virus (RGV), and <em>Siniperca chuatsi</em> ranavirus (SCRaV). Microscopic observations confirmed that SG3 cells were susceptible to all three ranaviruses, resulting in cellular swelling and membrane rupture, with infection confirmed through Real-time PCR. Transcriptomic profiling identified conserved responses: downregulation of early growth response protein (<em>Egr1</em>) and upregulation of myelocytomatosis oncogene (<em>MYC</em>). Ranavirus infection elevated alternative splicing events, with skipped exon events dominated and the maximal divergence observed at the 12 h post-infection. Key cellular metabolic pathways including glycolysis were disrupted, marked by coordinated upregulation of glycolytic enzymes and suppression of gluconeogenic enzymes. These results elucidate conserved molecular strategies underlying ranavirus-host interactions and metabolic mechanisms.</div></div>","PeriodicalId":12127,"journal":{"name":"Fish & shellfish immunology","volume":"165 ","pages":"Article 110453"},"PeriodicalIF":4.1000,"publicationDate":"2025-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fish & shellfish immunology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1050464825003420","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"FISHERIES","Score":null,"Total":0}
引用次数: 0
Abstract
The medaka spermatogonial stem cell line (SG3) is a well-established cell line that can be induced to differentiate into sperm in vitro. Ranavirus, a genus of viruses widely distributed among fish, amphibians, and reptiles, poses a significant threat to these organisms. This study aimed to investigate the morphological changes and transcriptomic responses in SG3 following infection with three ranavirus strains: Andrias davidianus ranavirus (ADRV), Rana grylio virus (RGV), and Siniperca chuatsi ranavirus (SCRaV). Microscopic observations confirmed that SG3 cells were susceptible to all three ranaviruses, resulting in cellular swelling and membrane rupture, with infection confirmed through Real-time PCR. Transcriptomic profiling identified conserved responses: downregulation of early growth response protein (Egr1) and upregulation of myelocytomatosis oncogene (MYC). Ranavirus infection elevated alternative splicing events, with skipped exon events dominated and the maximal divergence observed at the 12 h post-infection. Key cellular metabolic pathways including glycolysis were disrupted, marked by coordinated upregulation of glycolytic enzymes and suppression of gluconeogenic enzymes. These results elucidate conserved molecular strategies underlying ranavirus-host interactions and metabolic mechanisms.
期刊介绍:
Fish and Shellfish Immunology rapidly publishes high-quality, peer-refereed contributions in the expanding fields of fish and shellfish immunology. It presents studies on the basic mechanisms of both the specific and non-specific defense systems, the cells, tissues, and humoral factors involved, their dependence on environmental and intrinsic factors, response to pathogens, response to vaccination, and applied studies on the development of specific vaccines for use in the aquaculture industry.