Hongye Cui , Haiyue Chen , Yuhui Wang , Yaoda Wang , Tianmei Hu , Liwen Xu , Baozhou Wu , Shuguang Hao , Xiong Hu , Jiping Zhang , Yu Liu , Weiwei Zeng
{"title":"Identification of a novel birnavirus strain in diseased Siniperca chuatsi and transcriptome profiling of virus-infected MFSB cells","authors":"Hongye Cui , Haiyue Chen , Yuhui Wang , Yaoda Wang , Tianmei Hu , Liwen Xu , Baozhou Wu , Shuguang Hao , Xiong Hu , Jiping Zhang , Yu Liu , Weiwei Zeng","doi":"10.1016/j.aquaculture.2025.742618","DOIUrl":null,"url":null,"abstract":"<div><div>In August 2023, an outbreak of disease occurred in a pond containing <em>Siniperca chuatsi</em> fingerlings at a farm in Foshan, Guangdong province, resulting in a mortality rate exceeding 90 %. In this study, a novel birnavirus strain was isolated and identified from the diseased <em>Siniperca chuatsi</em> using cell culture, electron microscopy (EM), immunofluorescence assay (IFA), whole genome sequencing, and genetic evolutionary analysis. The virus was provisionally named <em>Siniperca chuatsi</em> Birnavirus FS202308 (SCBV-FS202308). Additionally, we analyzed the transcriptomic expression of SCBV-202308-infected mandarin fish spinal bulb (MFSB) cells. Results showed the MFSB cells inoculated with tissue homogenate exhibited typical cytopathic effects (CPE) post-infection. EM revealed a large number of icosahedral virion particles with a diameter approximately 60 nm were observed in the cells. Whole genome sequencing and phylogenetic analyses confirmed that the virus is a member of the family <em>Birnavirus</em>, specifically classified within the genus <em>Blosnavirus</em>. IFA utilizing antibodies against VP2 of SCBV and against IPNV revealed strong green fluorescent signals in the infected cells. Additionally, the challenge test demonstrated that all virus-inoculated <em>S. chuatsi</em> were successfully reinfected with SCBV-FS202308, resulting in a final mortality rate of approximately 20 %. Moreover, transcriptome analysis identified 2882 up-regulated and 3101 down-regulated genes in SCBV-FS202308-infected cells compared to the uninfected MFSB cells. Additionally, 522 genes were differentially enriched in pathways associated with immune signaling, such as the MAPK signaling, PI3K-Akt signaling, and Rap1 signaling pathways. This suggests that the virus elicits a robust immune response upon infecting host cells. This study represents the first report on the isolation, identification, and characterization of birnavirus from <em>Siniperca chuatsi.</em></div></div>","PeriodicalId":8375,"journal":{"name":"Aquaculture","volume":"606 ","pages":"Article 742618"},"PeriodicalIF":3.9000,"publicationDate":"2025-04-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Aquaculture","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0044848625005046","RegionNum":1,"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
In August 2023, an outbreak of disease occurred in a pond containing Siniperca chuatsi fingerlings at a farm in Foshan, Guangdong province, resulting in a mortality rate exceeding 90 %. In this study, a novel birnavirus strain was isolated and identified from the diseased Siniperca chuatsi using cell culture, electron microscopy (EM), immunofluorescence assay (IFA), whole genome sequencing, and genetic evolutionary analysis. The virus was provisionally named Siniperca chuatsi Birnavirus FS202308 (SCBV-FS202308). Additionally, we analyzed the transcriptomic expression of SCBV-202308-infected mandarin fish spinal bulb (MFSB) cells. Results showed the MFSB cells inoculated with tissue homogenate exhibited typical cytopathic effects (CPE) post-infection. EM revealed a large number of icosahedral virion particles with a diameter approximately 60 nm were observed in the cells. Whole genome sequencing and phylogenetic analyses confirmed that the virus is a member of the family Birnavirus, specifically classified within the genus Blosnavirus. IFA utilizing antibodies against VP2 of SCBV and against IPNV revealed strong green fluorescent signals in the infected cells. Additionally, the challenge test demonstrated that all virus-inoculated S. chuatsi were successfully reinfected with SCBV-FS202308, resulting in a final mortality rate of approximately 20 %. Moreover, transcriptome analysis identified 2882 up-regulated and 3101 down-regulated genes in SCBV-FS202308-infected cells compared to the uninfected MFSB cells. Additionally, 522 genes were differentially enriched in pathways associated with immune signaling, such as the MAPK signaling, PI3K-Akt signaling, and Rap1 signaling pathways. This suggests that the virus elicits a robust immune response upon infecting host cells. This study represents the first report on the isolation, identification, and characterization of birnavirus from Siniperca chuatsi.
期刊介绍:
Aquaculture is an international journal for the exploration, improvement and management of all freshwater and marine food resources. It publishes novel and innovative research of world-wide interest on farming of aquatic organisms, which includes finfish, mollusks, crustaceans and aquatic plants for human consumption. Research on ornamentals is not a focus of the Journal. Aquaculture only publishes papers with a clear relevance to improving aquaculture practices or a potential application.