Mineralo-organic particles inhibit influenza A virus infection by targeting viral hemagglutinin activity.

Nanomedicine (London, England) Pub Date : 2024-01-01 Epub Date: 2024-09-25 DOI:10.1080/17435889.2024.2403326
Huan-Jung Chiang, Hsin-Hsin Peng, Kuo-Feng Weng, Kuei-Ching Hsiung, Chieh-Yu Liang, Shun-Li Kuo, David M Ojcius, John Ding-E Young, Shin-Ru Shih
{"title":"Mineralo-organic particles inhibit influenza A virus infection by targeting viral hemagglutinin activity.","authors":"Huan-Jung Chiang, Hsin-Hsin Peng, Kuo-Feng Weng, Kuei-Ching Hsiung, Chieh-Yu Liang, Shun-Li Kuo, David M Ojcius, John Ding-E Young, Shin-Ru Shih","doi":"10.1080/17435889.2024.2403326","DOIUrl":null,"url":null,"abstract":"<p><p><b>Aim:</b> Mineralo-organic particles, naturally present in human body fluids, participate in ectopic calcification and inflammatory diseases. These particles coexist with influenza A virus (IAV) in the same microenvironment during viral infection. Our objective was to investigate the functional consequences of the potential interactions between these particles and the virions.<b>Materials & methods:</b> We used <i>in vitro</i> models, including electron microscopy, fluorescence microscopy, hemagglutination assay and viral infection assays to examine the interactions.<b>Results:</b> Mineralo-organic particles bind to IAV virions through interactions involving particle-bound fetuin-A and mineral content, effectively engaging viral hemagglutinin. These interactions result in hindered viral infection.<b>Conclusion:</b> These findings uncover the novel interactions between mineralo-organic particles and IAV, highlighting the impact of virus microenvironment complexity.</p>","PeriodicalId":74240,"journal":{"name":"Nanomedicine (London, England)","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11492690/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nanomedicine (London, England)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/17435889.2024.2403326","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/9/25 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Aim: Mineralo-organic particles, naturally present in human body fluids, participate in ectopic calcification and inflammatory diseases. These particles coexist with influenza A virus (IAV) in the same microenvironment during viral infection. Our objective was to investigate the functional consequences of the potential interactions between these particles and the virions.Materials & methods: We used in vitro models, including electron microscopy, fluorescence microscopy, hemagglutination assay and viral infection assays to examine the interactions.Results: Mineralo-organic particles bind to IAV virions through interactions involving particle-bound fetuin-A and mineral content, effectively engaging viral hemagglutinin. These interactions result in hindered viral infection.Conclusion: These findings uncover the novel interactions between mineralo-organic particles and IAV, highlighting the impact of virus microenvironment complexity.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
矿物有机微粒通过靶向病毒血凝素活性抑制甲型流感病毒感染。
目的:天然存在于人体体液中的矿物有机微粒参与了异位钙化和炎症性疾病。在病毒感染期间,这些颗粒与甲型流感病毒(IAV)共存于同一微环境中。我们的目的是研究这些颗粒与病毒之间潜在相互作用的功能性后果:我们使用了体外模型,包括电子显微镜、荧光显微镜、血凝试验和病毒感染试验来研究这些相互作用:结果:矿物-有机颗粒通过与颗粒结合的胎盘素-A和矿物成分的相互作用与 IAV 病毒结合,有效地与病毒血凝素结合。这些相互作用导致病毒感染受阻:这些发现揭示了矿物有机微粒与 IAV 之间的新型相互作用,凸显了病毒微环境复杂性的影响。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Applying the lessons learned from the COVID-19 pandemic to the next generation of nanocarrier-based vaccines. The potential of ceramic nanomaterials in preventive dentistry. Pluronic F127/lecithin PLGA nanoparticles as carriers of monocyte-targeted jakinibs: a potential therapeutic platform. Hispolon-loaded lipid nanocapsules for the management of hepatocellular carcinoma: comparative study with solid lipid nanoparticles and suspension. Nanoformulations of amphotericin B to resolve challenges in antifungal therapy.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1