Jiahui Zou , Jinli Guo , Shan Tian , Shaoyu Tu , Tong Chen , Meijun Jiang , Huimin Sun , Meilin Jin , Huanchun Chen , Hongbo Zhou
{"title":"Pre-mRNA切割复合体II蛋白Pcf11通过与病毒NP相互作用并促进聚合酶活性促进猪流感病毒复制","authors":"Jiahui Zou , Jinli Guo , Shan Tian , Shaoyu Tu , Tong Chen , Meijun Jiang , Huimin Sun , Meilin Jin , Huanchun Chen , Hongbo Zhou","doi":"10.1016/j.micres.2025.128183","DOIUrl":null,"url":null,"abstract":"<div><div>Swine influenza virus (SIV) poses a significant threat to the pig industry and public health safety due to rapid viral evolution and potential interspecies transmission. Identifying the key host factors that involved in viral replication can not only provide new insights into the regulatory mechanism of viral replication, but also provide theoretical support for the development of new antiviral therapeutics. Here, the Pre-mRNA cleavage complex II protein Pcf11 (PCF11) was revealed to promote the proliferation of SIV and other influenza viruses. Mechanically, PCF11 promoted the synthesis of viral mRNA and the assembly of vRNP, thus facilitating the transcription and replication of viral genome. Furthermore, PCF11 can interact with viral NP proteins to promote the polymerase activity of SIV. Additionally, PCF11 was revealed to negatively regulate the IFN-β signaling pathway, facilitating the replication of RNA viruses. In conclusion, this study emphasizes that PCF11 promotes SIV proliferation by regulating viral genome replication, transcription, and innate immune responses, thus providing a potential target for developing antiviral therapeutics.</div></div>","PeriodicalId":18564,"journal":{"name":"Microbiological research","volume":"297 ","pages":"Article 128183"},"PeriodicalIF":6.9000,"publicationDate":"2025-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Pre-mRNA cleavage complex II protein Pcf11 facilitates swine influenza virus replication by interacting with viral NP and promoting polymerase activity\",\"authors\":\"Jiahui Zou , Jinli Guo , Shan Tian , Shaoyu Tu , Tong Chen , Meijun Jiang , Huimin Sun , Meilin Jin , Huanchun Chen , Hongbo Zhou\",\"doi\":\"10.1016/j.micres.2025.128183\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Swine influenza virus (SIV) poses a significant threat to the pig industry and public health safety due to rapid viral evolution and potential interspecies transmission. Identifying the key host factors that involved in viral replication can not only provide new insights into the regulatory mechanism of viral replication, but also provide theoretical support for the development of new antiviral therapeutics. Here, the Pre-mRNA cleavage complex II protein Pcf11 (PCF11) was revealed to promote the proliferation of SIV and other influenza viruses. Mechanically, PCF11 promoted the synthesis of viral mRNA and the assembly of vRNP, thus facilitating the transcription and replication of viral genome. Furthermore, PCF11 can interact with viral NP proteins to promote the polymerase activity of SIV. Additionally, PCF11 was revealed to negatively regulate the IFN-β signaling pathway, facilitating the replication of RNA viruses. In conclusion, this study emphasizes that PCF11 promotes SIV proliferation by regulating viral genome replication, transcription, and innate immune responses, thus providing a potential target for developing antiviral therapeutics.</div></div>\",\"PeriodicalId\":18564,\"journal\":{\"name\":\"Microbiological research\",\"volume\":\"297 \",\"pages\":\"Article 128183\"},\"PeriodicalIF\":6.9000,\"publicationDate\":\"2025-04-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Microbiological research\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0944501325001399\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbiological research","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0944501325001399","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Pre-mRNA cleavage complex II protein Pcf11 facilitates swine influenza virus replication by interacting with viral NP and promoting polymerase activity
Swine influenza virus (SIV) poses a significant threat to the pig industry and public health safety due to rapid viral evolution and potential interspecies transmission. Identifying the key host factors that involved in viral replication can not only provide new insights into the regulatory mechanism of viral replication, but also provide theoretical support for the development of new antiviral therapeutics. Here, the Pre-mRNA cleavage complex II protein Pcf11 (PCF11) was revealed to promote the proliferation of SIV and other influenza viruses. Mechanically, PCF11 promoted the synthesis of viral mRNA and the assembly of vRNP, thus facilitating the transcription and replication of viral genome. Furthermore, PCF11 can interact with viral NP proteins to promote the polymerase activity of SIV. Additionally, PCF11 was revealed to negatively regulate the IFN-β signaling pathway, facilitating the replication of RNA viruses. In conclusion, this study emphasizes that PCF11 promotes SIV proliferation by regulating viral genome replication, transcription, and innate immune responses, thus providing a potential target for developing antiviral therapeutics.
期刊介绍:
Microbiological Research is devoted to publishing reports on prokaryotic and eukaryotic microorganisms such as yeasts, fungi, bacteria, archaea, and protozoa. Research on interactions between pathogenic microorganisms and their environment or hosts are also covered.