• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

依托红霉素酯通过直接灭活病毒颗粒强效抑制 HCoV-OC43。

Erythromycin Estolate Is a Potent Inhibitor Against HCoV-OC43 by Directly Inactivating the Virus Particle.

机构信息

Shanghai Public Health Clinical Center, Fudan University, Shanghai, China.

Department of Laboratory Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.

出版信息

Front Cell Infect Microbiol. 2022 Jul 7;12:905248. doi: 10.3389/fcimb.2022.905248. eCollection 2022.

DOI:10.3389/fcimb.2022.905248
PMID:35873167
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9301004/
Abstract

In addition to antibacterial effects, macrolide antibiotics exhibit other extensive pharmacological effects, such as anti-inflammatory and antiviral activities. Erythromycin estolate, one of the macrolide antibiotics, was previously investigated to effectively inhibit infections of various flaviviruses including Zika virus, dengue virus, and yellow fever virus, but its antiviral effect against human coronavirus remains unknown. Thus, the current study was designed to evaluate the antiviral efficacy of erythromycin estolate against human coronavirus strain OC43 (HCoV-OC43) and to illustrate the underlying mechanisms. Erythromycin estolate effectively inhibited HCoV-OC43 infection in different cell types and significantly reduced virus titers at safe concentration without cell cytotoxicity. Furthermore, erythromycin estolate was identified to inhibit HCoV-OC43 infection at the early stage and to irreversibly inactivate virus by disrupting the integrity of the viral membrane whose lipid component might be the target of action. Together, it was demonstrated that erythromycin estolate could be a potential therapeutic drug for HCoV-OC43 infection.

摘要

除了抗菌作用外,大环内酯类抗生素还具有其他广泛的药理作用,如抗炎和抗病毒作用。红霉素依托酯是大环内酯类抗生素之一,先前的研究表明它能有效抑制多种黄病毒的感染,包括寨卡病毒、登革热病毒和黄热病病毒,但它对人类冠状病毒的抗病毒作用尚不清楚。因此,本研究旨在评估红霉素依托酯对人冠状病毒 OC43 株(HCoV-OC43)的抗病毒疗效,并阐明其潜在机制。红霉素依托酯能有效抑制不同细胞类型中的 HCoV-OC43 感染,并在无细胞毒性的安全浓度下显著降低病毒滴度。此外,红霉素依托酯被鉴定能在早期抑制 HCoV-OC43 感染,并通过破坏病毒膜的完整性不可逆地灭活病毒,其脂质成分可能是作用靶点。总之,研究表明红霉素依托酯可能是治疗 HCoV-OC43 感染的潜在药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd7d/9301004/27e888cd19bd/fcimb-12-905248-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd7d/9301004/ac1ffc0b27f7/fcimb-12-905248-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd7d/9301004/6f551b609f1d/fcimb-12-905248-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd7d/9301004/c65e041cc9cc/fcimb-12-905248-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd7d/9301004/fd1cb24b46b0/fcimb-12-905248-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd7d/9301004/27e888cd19bd/fcimb-12-905248-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd7d/9301004/ac1ffc0b27f7/fcimb-12-905248-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd7d/9301004/6f551b609f1d/fcimb-12-905248-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd7d/9301004/c65e041cc9cc/fcimb-12-905248-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd7d/9301004/fd1cb24b46b0/fcimb-12-905248-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd7d/9301004/27e888cd19bd/fcimb-12-905248-g005.jpg

相似文献

1
Erythromycin Estolate Is a Potent Inhibitor Against HCoV-OC43 by Directly Inactivating the Virus Particle.依托红霉素酯通过直接灭活病毒颗粒强效抑制 HCoV-OC43。
Front Cell Infect Microbiol. 2022 Jul 7;12:905248. doi: 10.3389/fcimb.2022.905248. eCollection 2022.
2
Erythromycin Estolate Inhibits Zika Virus Infection by Blocking Viral Entry as a Viral Inactivator.红霉素依托酯通过作为病毒失活剂阻断病毒进入来抑制寨卡病毒感染。
Viruses. 2019 Nov 15;11(11):1064. doi: 10.3390/v11111064.
3
Overlapping and distinct molecular determinants dictating the antiviral activities of TRIM56 against flaviviruses and coronavirus.决定TRIM56对黄病毒和冠状病毒抗病毒活性的重叠且独特的分子决定因素。
J Virol. 2014 Dec;88(23):13821-35. doi: 10.1128/JVI.02505-14. Epub 2014 Sep 24.
4
Natural Bis-Benzylisoquinoline Alkaloids-Tetrandrine, Fangchinoline, and Cepharanthine, Inhibit Human Coronavirus OC43 Infection of MRC-5 Human Lung Cells.天然双苄基异喹啉生物碱——粉防己碱、蝙蝠葛碱和山乌龟碱抑制人冠状病毒 OC43 感染 MRC-5 人肺细胞。
Biomolecules. 2019 Nov 4;9(11):696. doi: 10.3390/biom9110696.
5
Auraptene Has Antiviral Activity against Human Coronavirus OC43 in MRC-5 Cells.白皮杉醇对 MRC-5 细胞中的人冠状病毒 OC43 具有抗病毒活性。
Nutrients. 2023 Jun 29;15(13):2960. doi: 10.3390/nu15132960.
6
The ns12.9 Accessory Protein of Human Coronavirus OC43 Is a Viroporin Involved in Virion Morphogenesis and Pathogenesis.人冠状病毒OC43的ns12.9辅助蛋白是一种参与病毒体形态发生和发病机制的病毒孔蛋白。
J Virol. 2015 Nov;89(22):11383-95. doi: 10.1128/JVI.01986-15. Epub 2015 Sep 2.
7
Novel treatment with neuroprotective and antiviral properties against a neuroinvasive human respiratory virus.新型治疗方法具有神经保护和抗病毒特性,可对抗神经侵袭性人呼吸道病毒。
J Virol. 2014 Feb;88(3):1548-63. doi: 10.1128/JVI.02972-13. Epub 2013 Nov 13.
8
Axonal Transport Enables Neuron-to-Neuron Propagation of Human Coronavirus OC43.轴突运输使人类冠状病毒 OC43 能够在神经元之间传播。
J Virol. 2018 Aug 16;92(17). doi: 10.1128/JVI.00404-18. Print 2018 Sep 1.
9
Antiviral activity of chloroquine against human coronavirus OC43 infection in newborn mice.氯喹对新生小鼠人冠状病毒OC43感染的抗病毒活性
Antimicrob Agents Chemother. 2009 Aug;53(8):3416-21. doi: 10.1128/AAC.01509-08. Epub 2009 Jun 8.
10
A nano-luciferase expressing human coronavirus OC43 for countermeasure development.一种表达纳米荧光素酶的人冠状病毒 OC43,用于开发对策。
Virus Res. 2024 Jan 2;339:199286. doi: 10.1016/j.virusres.2023.199286. Epub 2023 Dec 5.

引用本文的文献

1
A Comparison of Conserved Features in the Human Coronavirus Family Shows That Studies of Viruses Less Pathogenic than SARS-CoV-2, Such as HCoV-OC43, Are Good Model Systems for Elucidating Basic Mechanisms of Infection and Replication in Standard Laboratories.人类冠状病毒家族保守特征的比较表明,对致病性低于SARS-CoV-2的病毒(如HCoV-OC43)的研究是在标准实验室中阐明感染和复制基本机制的良好模型系统。
Viruses. 2025 Feb 13;17(2):256. doi: 10.3390/v17020256.
2
Repositioning of Antibiotics in the Treatment of Viral Infections.抗生素在病毒感染治疗中的再定位。
Curr Microbiol. 2024 Oct 26;81(12):427. doi: 10.1007/s00284-024-03948-7.
3

本文引用的文献

1
Molnupiravir for Oral Treatment of Covid-19 in Nonhospitalized Patients.莫努匹韦片用于非住院 COVID-19 患者的口服治疗。
N Engl J Med. 2022 Feb 10;386(6):509-520. doi: 10.1056/NEJMoa2116044. Epub 2021 Dec 16.
2
Covid-19: FDA expert panel recommends authorising molnupiravir but also voices concerns.新冠疫情:美国食品药品监督管理局专家小组建议批准莫努匹拉韦,但也表达了担忧。
BMJ. 2021 Dec 2;375:n2984. doi: 10.1136/bmj.n2984.
3
The Molecular Tweezer CLR01 Inhibits Antibody-Resistant Cell-to-Cell Spread of Human Cytomegalovirus.分子钳 CLR01 抑制人巨细胞病毒耐药细胞间传播。
Zafirlukast, as a viral inactivator, potently inhibits infection of several flaviviruses, including Zika virus, dengue virus, and yellow fever virus.
扎夫鲁司特作为一种病毒灭活剂,能强烈抑制几种黄病毒的感染,包括寨卡病毒、登革热病毒和黄热病病毒。
Antimicrob Agents Chemother. 2024 Jul 9;68(7):e0016824. doi: 10.1128/aac.00168-24. Epub 2024 May 29.
4
The nucleoside analog 4'-fluorouridine suppresses the replication of multiple enteroviruses by targeting 3D polymerase.核苷类似物4'-氟尿苷通过靶向3D聚合酶抑制多种肠道病毒的复制。
Antimicrob Agents Chemother. 2024 Jun 5;68(6):e0005424. doi: 10.1128/aac.00054-24. Epub 2024 Apr 30.
5
iNGNN-DTI: prediction of drug-target interaction with interpretable nested graph neural network and pretrained molecule models.INGNN-DTI:利用可解释嵌套图神经网络和预训练分子模型预测药物-靶标相互作用。
Bioinformatics. 2024 Mar 4;40(3). doi: 10.1093/bioinformatics/btae135.
6
A cysteine protease inhibitor GC376 displays potent antiviral activity against coxsackievirus infection.一种半胱氨酸蛋白酶抑制剂GC376对柯萨奇病毒感染显示出强大的抗病毒活性。
Curr Res Microb Sci. 2023 Sep 16;5:100203. doi: 10.1016/j.crmicr.2023.100203. eCollection 2023.
7
Acriflavine and proflavine hemisulfate as potential antivirals by targeting M.吖啶黄素和普罗黄素半硫酸盐通过靶向 M. 作为潜在的抗病毒药物。
Bioorg Chem. 2022 Dec;129:106185. doi: 10.1016/j.bioorg.2022.106185. Epub 2022 Oct 7.
Viruses. 2021 Aug 25;13(9):1685. doi: 10.3390/v13091685.
4
Macrolides May Prevent Severe Acute Respiratory Syndrome Coronavirus 2 Entry into Cells: A Quantitative Structure Activity Relationship Study and Experimental Validation.大环内酯类药物可能通过预防严重急性呼吸综合征冠状病毒 2 进入细胞来发挥作用:定量构效关系研究和实验验证。
J Chem Inf Model. 2021 Apr 26;61(4):2016-2025. doi: 10.1021/acs.jcim.0c01394. Epub 2021 Mar 18.
5
Inhibitors of endosomal acidification suppress SARS-CoV-2 replication and relieve viral pneumonia in hACE2 transgenic mice.内体酸化抑制剂抑制 SARS-CoV-2 复制并缓解 hACE2 转基因小鼠的病毒性肺炎。
Virol J. 2021 Feb 27;18(1):46. doi: 10.1186/s12985-021-01515-1.
6
Drug repurposing approach to combating coronavirus: Potential drugs and drug targets.药物重定位方法对抗冠状病毒:潜在药物和药物靶点。
Med Res Rev. 2021 May;41(3):1375-1426. doi: 10.1002/med.21763. Epub 2020 Dec 5.
7
Current status of antivirals and druggable targets of SARS CoV-2 and other human pathogenic coronaviruses.SARS-CoV-2 及其他人类致病冠状病毒的抗病毒药物和可用药靶的现状。
Drug Resist Updat. 2020 Dec;53:100721. doi: 10.1016/j.drup.2020.100721. Epub 2020 Aug 26.
8
Azithromycin in viral infections.阿奇霉素治疗病毒感染。
Rev Med Virol. 2021 Mar;31(2):e2163. doi: 10.1002/rmv.2163. Epub 2020 Sep 23.
9
Synergistic antiviral effect of hydroxychloroquine and azithromycin in combination against SARS-CoV-2: What molecular dynamics studies of virus-host interactions reveal.羟氯喹和阿奇霉素联合对抗 SARS-CoV-2 的协同抗病毒作用:病毒-宿主相互作用的分子动力学研究揭示了什么。
Int J Antimicrob Agents. 2020 Aug;56(2):106020. doi: 10.1016/j.ijantimicag.2020.106020. Epub 2020 May 13.
10
Azithromycin in the treatment of COVID-19: a review.阿奇霉素治疗 COVID-19:综述。
Expert Rev Anti Infect Ther. 2021 Feb;19(2):147-163. doi: 10.1080/14787210.2020.1813024. Epub 2020 Oct 6.