Human Cytomegalovirus-IE1 induces neonate liver injury in transgenic mouse.

IF 3.3 3区 医学 Q3 IMMUNOLOGY
Microbial pathogenesis Pub Date : 2025-08-01 Epub Date: 2025-05-24 DOI:10.1016/j.micpath.2025.107750
Guanghui Song, Shuo Han, Xianjuan Zhang
{"title":"Human Cytomegalovirus-IE1 induces neonate liver injury in transgenic mouse.","authors":"Guanghui Song, Shuo Han, Xianjuan Zhang","doi":"10.1016/j.micpath.2025.107750","DOIUrl":null,"url":null,"abstract":"<p><p>Congenital human cytomegalovirus (HCMV) is a significant contributor to liver damage in infants and children. HCMV-encoded IE1 protein plays an important role in viral replication and disease progression. To investigate the effects IE1 on neonate liver, the transgenic mouse model (IE1 mice) and transcriptome sequencing were performed. The results showed that compared to wild-type mice, IE1 can cause liver injury by affecting drug metabolism, fatty acid metabolism, steroid hormone biosynthesis, and retinol metabolism. Furthermore, cytochrome P450 (CYP) enzymes family play a crucial role in liver metabolism disorder of IE1 mice. Combined with the results of the PPI analysis and qRT-PCR validation, Cyp4f39, Cyp3a44, and Cyp3a11 may be the key genes of IE1 causing liver injury. Overall, our study highlights the potential harmful effects of the HCMV IE1 protein on the neonatal liver, offering new insights into the mechanisms underlying liver injury associated with congenital HCMV infection.</p>","PeriodicalId":18599,"journal":{"name":"Microbial pathogenesis","volume":" ","pages":"107750"},"PeriodicalIF":3.3000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microbial pathogenesis","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.micpath.2025.107750","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/5/24 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Congenital human cytomegalovirus (HCMV) is a significant contributor to liver damage in infants and children. HCMV-encoded IE1 protein plays an important role in viral replication and disease progression. To investigate the effects IE1 on neonate liver, the transgenic mouse model (IE1 mice) and transcriptome sequencing were performed. The results showed that compared to wild-type mice, IE1 can cause liver injury by affecting drug metabolism, fatty acid metabolism, steroid hormone biosynthesis, and retinol metabolism. Furthermore, cytochrome P450 (CYP) enzymes family play a crucial role in liver metabolism disorder of IE1 mice. Combined with the results of the PPI analysis and qRT-PCR validation, Cyp4f39, Cyp3a44, and Cyp3a11 may be the key genes of IE1 causing liver injury. Overall, our study highlights the potential harmful effects of the HCMV IE1 protein on the neonatal liver, offering new insights into the mechanisms underlying liver injury associated with congenital HCMV infection.

人巨细胞病毒ie1诱导转基因小鼠新生儿肝损伤
先天性人类巨细胞病毒(HCMV)是婴儿和儿童肝损伤的重要因素。hcmv编码的IE1蛋白在病毒复制和疾病进展中起重要作用。为了研究IE1对新生儿肝脏的影响,我们建立了IE1转基因小鼠模型,并进行了转录组测序。结果表明,与野生型小鼠相比,IE1可通过影响药物代谢、脂肪酸代谢、类固醇激素生物合成和视黄醇代谢等途径引起肝损伤。此外,细胞色素P450 (CYP)酶家族在IE1小鼠肝脏代谢紊乱中起重要作用。结合PPI分析和qRT-PCR验证结果,Cyp4f39、Cyp3a44、Cyp3a11可能是IE1引起肝损伤的关键基因。总的来说,我们的研究强调了HCMV IE1蛋白对新生儿肝脏的潜在有害影响,为先天性HCMV感染相关的肝损伤机制提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Microbial pathogenesis
Microbial pathogenesis 医学-免疫学
CiteScore
7.40
自引率
2.60%
发文量
472
审稿时长
56 days
期刊介绍: Microbial Pathogenesis publishes original contributions and reviews about the molecular and cellular mechanisms of infectious diseases. It covers microbiology, host-pathogen interaction and immunology related to infectious agents, including bacteria, fungi, viruses and protozoa. It also accepts papers in the field of clinical microbiology, with the exception of case reports. Research Areas Include: -Pathogenesis -Virulence factors -Host susceptibility or resistance -Immune mechanisms -Identification, cloning and sequencing of relevant genes -Genetic studies -Viruses, prokaryotic organisms and protozoa -Microbiota -Systems biology related to infectious diseases -Targets for vaccine design (pre-clinical studies)
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信