Guanli Dai , Yanlong Zhou , Daming Song , Yiping Cai , Lijiao Yan , Dan Li , Haixue Zheng
{"title":"抗炎剂35通过抑制p65的核易位来减少ASFV复制","authors":"Guanli Dai , Yanlong Zhou , Daming Song , Yiping Cai , Lijiao Yan , Dan Li , Haixue Zheng","doi":"10.1016/j.virol.2025.110664","DOIUrl":null,"url":null,"abstract":"<div><div>African swine fever (ASF), caused by the African swine fever virus (ASFV), is a highly contagious infectious disease. To date, no safe and effective vaccine or therapeutic drug is available for ASFV. In this study, we identified Anti-inflammatory agent 35 (A35) as a negative regulator of ASFV replication. Real-time quantitative PCR, hemadsorption assay, and Western blotting analyses revealed that A35 inhibits ASFV genome replication and structural protein expression in <em>vitro</em>. Further studies demonstrated that A35 suppresses TNF-α or ASFV-triggered NF-κB signaling pathway. Reporter assays showed that A35 inhibited p65-triggered NF-κB signaling pathway. Mechanistic studies have found that A35 can inhibit the nuclear translocation of p65. Additionally, overexpression of p65 enhanced ASFV replication, whereas knockdown of p65 had opposite effects. This study reveals, for the first time, that A35 exerts its anti-ASFV effects by targeting NF-κB signal transduction, providing a theoretical basis and candidate compound for the development of novel anti-ASFV agents based on the structural optimization of natural products.</div></div>","PeriodicalId":23666,"journal":{"name":"Virology","volume":"611 ","pages":"Article 110664"},"PeriodicalIF":2.4000,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Anti-inflammatory agent 35 reduces ASFV replication by suppressing the nuclear translocation of p65\",\"authors\":\"Guanli Dai , Yanlong Zhou , Daming Song , Yiping Cai , Lijiao Yan , Dan Li , Haixue Zheng\",\"doi\":\"10.1016/j.virol.2025.110664\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>African swine fever (ASF), caused by the African swine fever virus (ASFV), is a highly contagious infectious disease. To date, no safe and effective vaccine or therapeutic drug is available for ASFV. In this study, we identified Anti-inflammatory agent 35 (A35) as a negative regulator of ASFV replication. Real-time quantitative PCR, hemadsorption assay, and Western blotting analyses revealed that A35 inhibits ASFV genome replication and structural protein expression in <em>vitro</em>. Further studies demonstrated that A35 suppresses TNF-α or ASFV-triggered NF-κB signaling pathway. Reporter assays showed that A35 inhibited p65-triggered NF-κB signaling pathway. Mechanistic studies have found that A35 can inhibit the nuclear translocation of p65. Additionally, overexpression of p65 enhanced ASFV replication, whereas knockdown of p65 had opposite effects. This study reveals, for the first time, that A35 exerts its anti-ASFV effects by targeting NF-κB signal transduction, providing a theoretical basis and candidate compound for the development of novel anti-ASFV agents based on the structural optimization of natural products.</div></div>\",\"PeriodicalId\":23666,\"journal\":{\"name\":\"Virology\",\"volume\":\"611 \",\"pages\":\"Article 110664\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2025-08-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Virology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0042682225002776\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"VIROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Virology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0042682225002776","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"VIROLOGY","Score":null,"Total":0}
Anti-inflammatory agent 35 reduces ASFV replication by suppressing the nuclear translocation of p65
African swine fever (ASF), caused by the African swine fever virus (ASFV), is a highly contagious infectious disease. To date, no safe and effective vaccine or therapeutic drug is available for ASFV. In this study, we identified Anti-inflammatory agent 35 (A35) as a negative regulator of ASFV replication. Real-time quantitative PCR, hemadsorption assay, and Western blotting analyses revealed that A35 inhibits ASFV genome replication and structural protein expression in vitro. Further studies demonstrated that A35 suppresses TNF-α or ASFV-triggered NF-κB signaling pathway. Reporter assays showed that A35 inhibited p65-triggered NF-κB signaling pathway. Mechanistic studies have found that A35 can inhibit the nuclear translocation of p65. Additionally, overexpression of p65 enhanced ASFV replication, whereas knockdown of p65 had opposite effects. This study reveals, for the first time, that A35 exerts its anti-ASFV effects by targeting NF-κB signal transduction, providing a theoretical basis and candidate compound for the development of novel anti-ASFV agents based on the structural optimization of natural products.
期刊介绍:
Launched in 1955, Virology is a broad and inclusive journal that welcomes submissions on all aspects of virology including plant, animal, microbial and human viruses. The journal publishes basic research as well as pre-clinical and clinical studies of vaccines, anti-viral drugs and their development, anti-viral therapies, and computational studies of virus infections. Any submission that is of broad interest to the community of virologists/vaccinologists and reporting scientifically accurate and valuable research will be considered for publication, including negative findings and multidisciplinary work.Virology is open to reviews, research manuscripts, short communication, registered reports as well as follow-up manuscripts.