Yuxuan Wang , Bin Liu , Jiaqi Liang , Weilong Yang , Hailong Wang , Kun Ouyang , Junyi Luo , Jiajie Sun , Qianyun Xi , Yongliang Zhang , Meng Li , Ting Chen
{"title":"CircLSM14A通过miR-27b-5p/HMGB1轴调控PEDV复制。","authors":"Yuxuan Wang , Bin Liu , Jiaqi Liang , Weilong Yang , Hailong Wang , Kun Ouyang , Junyi Luo , Jiajie Sun , Qianyun Xi , Yongliang Zhang , Meng Li , Ting Chen","doi":"10.1016/j.vetmic.2025.110762","DOIUrl":null,"url":null,"abstract":"<div><div>Circular RNAs (circRNAs) play crucial roles in various physiological and pathological processes, including the complex interactions between viruses and hosts. However, the regulatory mechanism by which porcine milk exosome-derived circRNAs affect porcine epidemic diarrhea virus (PEDV) replication remains poorly understood. Building on our previous sequencing analysis of non-coding RNAs in porcine milk exosomes, we identified circRNA molecules that may regulate PEDV replication in the intestines of piglets and validated these findings at both the cellular and piglet intestinal organoid levels. The results demonstrated that circLSM14A was present in porcine milk exosomes, acted as an endogenous miR-27b-5p sponge, and sequestered and inhibited miR-27b-5p activity. This inhibition increased the expression of high mobility group protein 1 (HMGB1), which subsequently promoted the expression of downstream signaling molecules, including TLR4, NF-κB1, NF-κB2, Rel, and Beclin1, and ultimately enhanced PEDV replication at cellular and intestinal organoid levels. This study identifies circLSM14A as one of the regulators involved in PEDV replication in porcine milk exosomes. These findings advance our understanding of the biological functions of circLSM14A and clarify the role of non-coding RNAs carried by milk exosomes in regulating PEDV replication. This research provides new insights and approaches for the prevention and control of PEDV.</div></div>","PeriodicalId":23551,"journal":{"name":"Veterinary microbiology","volume":"311 ","pages":"Article 110762"},"PeriodicalIF":2.7000,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"CircLSM14A regulates PEDV replication via the miR-27b-5p/HMGB1 axis\",\"authors\":\"Yuxuan Wang , Bin Liu , Jiaqi Liang , Weilong Yang , Hailong Wang , Kun Ouyang , Junyi Luo , Jiajie Sun , Qianyun Xi , Yongliang Zhang , Meng Li , Ting Chen\",\"doi\":\"10.1016/j.vetmic.2025.110762\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Circular RNAs (circRNAs) play crucial roles in various physiological and pathological processes, including the complex interactions between viruses and hosts. However, the regulatory mechanism by which porcine milk exosome-derived circRNAs affect porcine epidemic diarrhea virus (PEDV) replication remains poorly understood. Building on our previous sequencing analysis of non-coding RNAs in porcine milk exosomes, we identified circRNA molecules that may regulate PEDV replication in the intestines of piglets and validated these findings at both the cellular and piglet intestinal organoid levels. The results demonstrated that circLSM14A was present in porcine milk exosomes, acted as an endogenous miR-27b-5p sponge, and sequestered and inhibited miR-27b-5p activity. This inhibition increased the expression of high mobility group protein 1 (HMGB1), which subsequently promoted the expression of downstream signaling molecules, including TLR4, NF-κB1, NF-κB2, Rel, and Beclin1, and ultimately enhanced PEDV replication at cellular and intestinal organoid levels. This study identifies circLSM14A as one of the regulators involved in PEDV replication in porcine milk exosomes. These findings advance our understanding of the biological functions of circLSM14A and clarify the role of non-coding RNAs carried by milk exosomes in regulating PEDV replication. This research provides new insights and approaches for the prevention and control of PEDV.</div></div>\",\"PeriodicalId\":23551,\"journal\":{\"name\":\"Veterinary microbiology\",\"volume\":\"311 \",\"pages\":\"Article 110762\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-10-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Veterinary microbiology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0378113525003980\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Veterinary microbiology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0378113525003980","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
CircLSM14A regulates PEDV replication via the miR-27b-5p/HMGB1 axis
Circular RNAs (circRNAs) play crucial roles in various physiological and pathological processes, including the complex interactions between viruses and hosts. However, the regulatory mechanism by which porcine milk exosome-derived circRNAs affect porcine epidemic diarrhea virus (PEDV) replication remains poorly understood. Building on our previous sequencing analysis of non-coding RNAs in porcine milk exosomes, we identified circRNA molecules that may regulate PEDV replication in the intestines of piglets and validated these findings at both the cellular and piglet intestinal organoid levels. The results demonstrated that circLSM14A was present in porcine milk exosomes, acted as an endogenous miR-27b-5p sponge, and sequestered and inhibited miR-27b-5p activity. This inhibition increased the expression of high mobility group protein 1 (HMGB1), which subsequently promoted the expression of downstream signaling molecules, including TLR4, NF-κB1, NF-κB2, Rel, and Beclin1, and ultimately enhanced PEDV replication at cellular and intestinal organoid levels. This study identifies circLSM14A as one of the regulators involved in PEDV replication in porcine milk exosomes. These findings advance our understanding of the biological functions of circLSM14A and clarify the role of non-coding RNAs carried by milk exosomes in regulating PEDV replication. This research provides new insights and approaches for the prevention and control of PEDV.
期刊介绍:
Veterinary Microbiology is concerned with microbial (bacterial, fungal, viral) diseases of domesticated vertebrate animals (livestock, companion animals, fur-bearing animals, game, poultry, fish) that supply food, other useful products or companionship. In addition, Microbial diseases of wild animals living in captivity, or as members of the feral fauna will also be considered if the infections are of interest because of their interrelation with humans (zoonoses) and/or domestic animals. Studies of antimicrobial resistance are also included, provided that the results represent a substantial advance in knowledge. Authors are strongly encouraged to read - prior to submission - the Editorials (''Scope or cope'' and ''Scope or cope II'') published previously in the journal. The Editors reserve the right to suggest submission to another journal for those papers which they feel would be more appropriate for consideration by that journal.
Original research papers of high quality and novelty on aspects of control, host response, molecular biology, pathogenesis, prevention, and treatment of microbial diseases of animals are published. Papers dealing primarily with immunology, epidemiology, molecular biology and antiviral or microbial agents will only be considered if they demonstrate a clear impact on a disease. Papers focusing solely on diagnostic techniques (such as another PCR protocol or ELISA) will not be published - focus should be on a microorganism and not on a particular technique. Papers only reporting microbial sequences, transcriptomics data, or proteomics data will not be considered unless the results represent a substantial advance in knowledge.
Drug trial papers will be considered if they have general application or significance. Papers on the identification of microorganisms will also be considered, but detailed taxonomic studies do not fall within the scope of the journal. Case reports will not be published, unless they have general application or contain novel aspects. Papers of geographically limited interest, which repeat what had been established elsewhere will not be considered. The readership of the journal is global.