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Main Authors: Wen, Xiaozhi, Guan, Lingfeng, Wang, Liqun, Zhang, Zihan, Wei, Xinyan, Qin, Qiwei, Wang, Shaowen
Format: Artículo científico
Language:en
Published: Fish & shellfish immunology 2025
Subjects:
Online Access:https://pubmed.ncbi.nlm.nih.gov/40472906/
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author Wen, Xiaozhi
Guan, Lingfeng
Wang, Liqun
Zhang, Zihan
Wei, Xinyan
Qin, Qiwei
Wang, Shaowen
author_facet Wen, Xiaozhi
Guan, Lingfeng
Wang, Liqun
Zhang, Zihan
Wei, Xinyan
Qin, Qiwei
Wang, Shaowen
Wen, Xiaozhi
Guan, Lingfeng
Wang, Liqun
Zhang, Zihan
Wei, Xinyan
Qin, Qiwei
Wang, Shaowen
collection PubMed - marine biology
contents The Ran GTPase inhibits SGIV and RGNNV infection by upregulating host immune response in grouper. Wen, Xiaozhi Guan, Lingfeng Wang, Liqun Zhang, Zihan Wei, Xinyan Qin, Qiwei Wang, Shaowen Animals Fish Diseases Bass DNA Virus Infections Fish Proteins Immunity, Innate Nodaviridae ran GTP-Binding Protein RNA Virus Infections Gene Expression Regulation Ranavirus Phylogeny Sequence Alignment Amino Acid Sequence Gene Expression Profiling Up-Regulation Ran is a small G-protein that acts as a "molecular switch" in nucleoplasmic transport regulating cellular activities. However, the functions of Ran in grouper and their effects on the viral infections are still unclear. In this study, we identified and characterized Ran in Epinephelus coioides (EcRan). EcRan encodes a 215 amino acid polypeptide containing key conserved domains including G1-G5 box and C terminal domains. EcRan was widely expressed in different tissues of healthy groupers, and showed obvious nucleus localization. Upon infection of Singapore grouper iridovirus (SGIV) or red spotted grouper nervous necrosis virus (RGNNV), EcRan transcript was significantly decreased. Moreover, overexpression of EcRan remarkably inhibited the replication of SGIV and RGNNV, whereas knockdown of EcRan notably promoted the replication of SGIV and RGNNV. In addition, overexpressed EcRan positively regulated the transcription of interferon (IFN)-related and inflammatory factors, including IFN regulatory factor 3 (IRF3), myxovirus resistance gene 1 (MXI), laboratory of genetics and physiology 2 (LGP2), tumor necrosis factor alpha (TNF-α), tumor necrosis factor receptor-associated factor 6 (TRAF6) and interleukin 8 (IL-8). The transcription of these immune genes was down regulated when EcRan transcription was inhibited by siRNA. Taken together, EcRan showed the antiviral effects against SGIV and RGNNV infections by positively regulating innate immune response.
format Artículo científico
id pubmed_40472906
institution PubMed
language en
publishDate 2025
publisher Fish & shellfish immunology
record_format pubmed
spellingShingle The Ran GTPase inhibits SGIV and RGNNV infection by upregulating host immune response in grouper.
Wen, Xiaozhi
Guan, Lingfeng
Wang, Liqun
Zhang, Zihan
Wei, Xinyan
Qin, Qiwei
Wang, Shaowen
Animals
Fish Diseases
Bass
DNA Virus Infections
Fish Proteins
Immunity, Innate
Nodaviridae
ran GTP-Binding Protein
RNA Virus Infections
Gene Expression Regulation
Ranavirus
Phylogeny
Sequence Alignment
Amino Acid Sequence
Gene Expression Profiling
Up-Regulation
The Ran GTPase inhibits SGIV and RGNNV infection by upregulating host immune response in grouper. Wen, Xiaozhi Guan, Lingfeng Wang, Liqun Zhang, Zihan Wei, Xinyan Qin, Qiwei Wang, Shaowen Animals Fish Diseases Bass DNA Virus Infections Fish Proteins Immunity, Innate Nodaviridae ran GTP-Binding Protein RNA Virus Infections Gene Expression Regulation Ranavirus Phylogeny Sequence Alignment Amino Acid Sequence Gene Expression Profiling Up-Regulation Ran is a small G-protein that acts as a "molecular switch" in nucleoplasmic transport regulating cellular activities. However, the functions of Ran in grouper and their effects on the viral infections are still unclear. In this study, we identified and characterized Ran in Epinephelus coioides (EcRan). EcRan encodes a 215 amino acid polypeptide containing key conserved domains including G1-G5 box and C terminal domains. EcRan was widely expressed in different tissues of healthy groupers, and showed obvious nucleus localization. Upon infection of Singapore grouper iridovirus (SGIV) or red spotted grouper nervous necrosis virus (RGNNV), EcRan transcript was significantly decreased. Moreover, overexpression of EcRan remarkably inhibited the replication of SGIV and RGNNV, whereas knockdown of EcRan notably promoted the replication of SGIV and RGNNV. In addition, overexpressed EcRan positively regulated the transcription of interferon (IFN)-related and inflammatory factors, including IFN regulatory factor 3 (IRF3), myxovirus resistance gene 1 (MXI), laboratory of genetics and physiology 2 (LGP2), tumor necrosis factor alpha (TNF-α), tumor necrosis factor receptor-associated factor 6 (TRAF6) and interleukin 8 (IL-8). The transcription of these immune genes was down regulated when EcRan transcription was inhibited by siRNA. Taken together, EcRan showed the antiviral effects against SGIV and RGNNV infections by positively regulating innate immune response.
title The Ran GTPase inhibits SGIV and RGNNV infection by upregulating host immune response in grouper.
topic Animals
Fish Diseases
Bass
DNA Virus Infections
Fish Proteins
Immunity, Innate
Nodaviridae
ran GTP-Binding Protein
RNA Virus Infections
Gene Expression Regulation
Ranavirus
Phylogeny
Sequence Alignment
Amino Acid Sequence
Gene Expression Profiling
Up-Regulation
url https://pubmed.ncbi.nlm.nih.gov/40472906/