• 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

将卡里霉素重新用作抗人类冠状病毒的抗病毒药物,包括当前大流行的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)。

Repurposing carrimycin as an antiviral agent against human coronaviruses, including the currently pandemic SARS-CoV-2.

作者信息

Yan Haiyan, Sun Jing, Wang Kun, Wang Huiqiang, Wu Shuo, Bao Linlin, He Weiqing, Wang Dong, Zhu Airu, Zhang Tian, Gao Rongmei, Dong Biao, Li Jianrui, Yang Lu, Zhong Ming, Lv Qi, Qin Feifei, Zhuang Zhen, Huang Xiaofang, Yang Xinyi, Li Yuhuan, Che Yongsheng, Jiang Jiandong

机构信息

CAMS Key Laboratory of Antiviral Drug Research, Beijing Key Laboratory of Antimicrobial Agents, NHC Key Laboratory of Biotechnology of Antibiotics, Institute of Medicinal Biotechnology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100050, China.

State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, the First Affiliated Hospital of Guangzhou Medical University, Guangzhou 510182, China.

出版信息

Acta Pharm Sin B. 2021 Sep;11(9):2850-2858. doi: 10.1016/j.apsb.2021.02.024. Epub 2021 Mar 11.

DOI:10.1016/j.apsb.2021.02.024
PMID:33723501
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7946546/
Abstract

COVID-19 pandemic caused by SARS-CoV-2 infection severely threatens global health and economic development. No effective antiviral drug is currently available to treat COVID-19 and any other human coronavirus infections. We report herein that a macrolide antibiotic, carrimycin, potently inhibited the cytopathic effects (CPE) and reduced the levels of viral protein and RNA in multiple cell types infected by human coronavirus 229E, OC43, and SARS-CoV-2. Time-of-addition and pseudotype virus infection studies indicated that carrimycin inhibited one or multiple post-entry replication events of human coronavirus infection. In support of this notion, metabolic labelling studies showed that carrimycin significantly inhibited the synthesis of viral RNA. Our studies thus strongly suggest that carrimycin is an antiviral agent against a broad-spectrum of human coronaviruses and its therapeutic efficacy to COVID-19 is currently under clinical investigation.

摘要

由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染引起的2019冠状病毒病(COVID-19)大流行严重威胁全球健康和经济发展。目前尚无有效的抗病毒药物可用于治疗COVID-19及任何其他人类冠状病毒感染。我们在此报告,一种大环内酯类抗生素卡里霉素能有效抑制细胞病变效应(CPE),并降低在被人类冠状病毒229E、OC43和SARS-CoV-2感染的多种细胞类型中病毒蛋白和RNA的水平。加药时间和假型病毒感染研究表明,卡里霉素抑制人类冠状病毒感染的一个或多个进入后复制事件。支持这一观点的是,代谢标记研究表明卡里霉素显著抑制病毒RNA的合成。因此,我们的研究强烈表明,卡里霉素是一种针对广谱人类冠状病毒的抗病毒药物,其对COVID-19的治疗效果目前正在临床研究中。

相似文献

1
Repurposing carrimycin as an antiviral agent against human coronaviruses, including the currently pandemic SARS-CoV-2.将卡里霉素重新用作抗人类冠状病毒的抗病毒药物,包括当前大流行的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)。
Acta Pharm Sin B. 2021 Sep;11(9):2850-2858. doi: 10.1016/j.apsb.2021.02.024. Epub 2021 Mar 11.
2
Cytopathic Effect Assay and Plaque Assay to Evaluate Activity of Antiviral Compounds Against Human Coronaviruses 229E, OC43, and NL63.细胞病变效应测定和噬斑测定以评估抗病毒化合物对人冠状病毒229E、OC43和NL63的活性
Bio Protoc. 2022 Feb 5;12(3):e4314. doi: 10.21769/BioProtoc.4314.
3
Repurposing old drugs as antiviral agents for coronaviruses.将老药重新用作冠状病毒的抗病毒药物。
Biomed J. 2020 Aug;43(4):368-374. doi: 10.1016/j.bj.2020.05.003. Epub 2020 May 23.
4
Carrimycin inhibits coronavirus replication by decreasing the efficiency of programmed -1 ribosomal frameshifting through directly binding to the RNA pseudoknot of viral frameshift-stimulatory element.卡里霉素通过直接结合病毒移码刺激元件的RNA假结,降低程序性-1核糖体移码效率,从而抑制冠状病毒复制。
Acta Pharm Sin B. 2024 Jun;14(6):2567-2580. doi: 10.1016/j.apsb.2024.02.023. Epub 2024 Mar 3.
5
LY6E Restricts Entry of Human Coronaviruses, Including Currently Pandemic SARS-CoV-2.LY6E限制包括当前大流行的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)在内的人类冠状病毒的进入。
J Virol. 2020 Aug 31;94(18). doi: 10.1128/JVI.00562-20.
6
Human Milk Antibodies Against S1 and S2 Subunits from SARS-CoV-2, HCoV-OC43, and HCoV-229E in Mothers with A Confirmed COVID-19 PCR, Viral SYMPTOMS, and Unexposed Mothers.母亲在确诊 COVID-19 PCR、出现病毒症状且未暴露于病毒的情况下,母乳中针对 SARS-CoV-2、HCoV-OC43 和 HCoV-229E 的 S1 和 S2 亚单位的人乳抗体。
Int J Mol Sci. 2021 Feb 9;22(4):1749. doi: 10.3390/ijms22041749.
7
Inhibition of SARS-CoV-2 by Highly Potent Broad-Spectrum Anti-Coronaviral Tylophorine-Based Derivatives.高效广谱抗冠状病毒的娃儿藤碱衍生物对严重急性呼吸综合征冠状病毒2的抑制作用
Front Pharmacol. 2020 Dec 14;11:606097. doi: 10.3389/fphar.2020.606097. eCollection 2020.
8
Neutralizing and binding activities against SARS-CoV-1/2, MERS-CoV, and human coronaviruses 229E and OC43 by normal human intravenous immunoglobulin derived from healthy donors in Japan.来源于日本健康供体的正常人静脉注射免疫球蛋白对 SARS-CoV-1/2、MERS-CoV 以及人类冠状病毒 229E 和 OC43 的中和及结合活性。
Transfusion. 2021 Feb;61(2):356-360. doi: 10.1111/trf.16161. Epub 2020 Oct 26.
9
A bivalent protein targeting glycans and HR1 domain in spike protein potently inhibited infection of SARS-CoV-2 and other human coronaviruses.一种靶向聚糖和刺突蛋白中HR1结构域的二价蛋白有效抑制了SARS-CoV-2和其他人类冠状病毒的感染。
Cell Biosci. 2021 Jul 8;11(1):128. doi: 10.1186/s13578-021-00638-w.
10
Assessment of Antiviral Coatings for High-Touch Surfaces by Using Human Coronaviruses HCoV-229E and SARS-CoV-2.采用人冠状病毒 HCoV-229E 和 SARS-CoV-2 评估高接触表面的抗病毒涂层。
Appl Environ Microbiol. 2021 Sep 10;87(19):e0109821. doi: 10.1128/AEM.01098-21.

引用本文的文献

1
Disruption of Spike Priming in Virus Entry: Tetrandrine as a Pan-Coronavirus Inhibitor.病毒进入过程中刺突蛋白引发的破坏:粉防己碱作为一种泛冠状病毒抑制剂
MedComm (2020). 2025 Aug 31;6(9):e70353. doi: 10.1002/mco2.70353. eCollection 2025 Sep.
2
Efficacy of carrimycin against complex and .卡里霉素对复合物及……的疗效
Microbiol Spectr. 2025 Sep 2;13(9):e0242224. doi: 10.1128/spectrum.02422-24. Epub 2025 Aug 8.
3
Enhancement of carrimycin production in Streptomyces spiramyceticus 54-IA by the reporter-guided selection method with traditional mutagenesis.

本文引用的文献

1
SARS-CoV-2-related pneumonia cases in pneumonia picture in Russia in March-May 2020: Secondary bacterial pneumonia and viral co-infections.2020 年 3 月至 5 月俄罗斯肺炎图像中的 SARS-CoV-2 相关肺炎病例:继发性细菌性肺炎和病毒合并感染。
J Glob Health. 2020 Dec;10(2):020504. doi: 10.7189/jogh.10.020504.
2
Secondary Bacterial Infections in Patients With Viral Pneumonia.病毒性肺炎患者的继发性细菌感染
Front Med (Lausanne). 2020 Aug 5;7:420. doi: 10.3389/fmed.2020.00420. eCollection 2020.
3
Molecular pathogenesis of secondary bacterial infection associated to viral infections including SARS-CoV-2.
通过传统诱变的报告基因引导筛选方法提高螺旋链霉菌54-IA中卡里霉素的产量。
BMC Microbiol. 2025 Aug 6;25(1):484. doi: 10.1186/s12866-025-04120-2.
4
Diammonium Glycyrrhizinate Exerts Broad-Spectrum Antiviral Activity Against Human Coronaviruses by Interrupting Spike-Mediated Cellular Entry.甘草酸二铵通过阻断刺突介导的细胞进入对人类冠状病毒发挥广谱抗病毒活性。
Int J Mol Sci. 2025 Jun 30;26(13):6334. doi: 10.3390/ijms26136334.
5
Carrimycin exhibited broad spectrum inhibitory activities against coronaviruses replication through down-regulating host factor TMEM41B.卡里霉素通过下调宿主因子TMEM41B对冠状病毒复制表现出广谱抑制活性。
Acta Pharmacol Sin. 2025 May 15. doi: 10.1038/s41401-025-01577-9.
6
Isovalerylspiramycin I alleviates liver injury and liver fibrosis by targeting the nucleotide-binding protein 2 (NUBP2)-vascular non-inflammatory molecule-1 (VNN1) pathway.异戊酰螺旋霉素I通过靶向核苷酸结合蛋白2(NUBP2)-血管非炎症分子1(VNN1)途径减轻肝损伤和肝纤维化。
J Pharm Anal. 2025 Mar;15(3):101048. doi: 10.1016/j.jpha.2024.101048. Epub 2024 Jul 18.
7
Precision spatiotemporal analysis of large-scale compound-protein interactions through molecular dynamics simulation.通过分子动力学模拟对大规模复合蛋白相互作用进行精确的时空分析。
PNAS Nexus. 2025 Mar 22;4(3):pgaf094. doi: 10.1093/pnasnexus/pgaf094. eCollection 2025 Mar.
8
Mycophenolate mofetil exerts broad-spectrum antiviral activity against coronaviruses including SARS-CoV-2.霉酚酸酯对包括SARS-CoV-2在内的冠状病毒具有广谱抗病毒活性。
Virol J. 2025 Mar 4;22(1):56. doi: 10.1186/s12985-025-02673-2.
9
Carrimycin, as One of the Drugs in Combination Therapy, for the Treatment of Carbapenem-Resistant Infection.卡里霉素作为联合治疗药物之一,用于治疗耐碳青霉烯类感染。
Infect Drug Resist. 2024 Aug 19;17:3617-3621. doi: 10.2147/IDR.S468413. eCollection 2024.
10
Carrimycin inhibits coronavirus replication by decreasing the efficiency of programmed -1 ribosomal frameshifting through directly binding to the RNA pseudoknot of viral frameshift-stimulatory element.卡里霉素通过直接结合病毒移码刺激元件的RNA假结,降低程序性-1核糖体移码效率,从而抑制冠状病毒复制。
Acta Pharm Sin B. 2024 Jun;14(6):2567-2580. doi: 10.1016/j.apsb.2024.02.023. Epub 2024 Mar 3.
与病毒感染(包括 SARS-CoV-2)相关的继发性细菌感染的分子发病机制。
J Infect Public Health. 2020 Oct;13(10):1397-1404. doi: 10.1016/j.jiph.2020.07.003. Epub 2020 Jul 14.
4
The molecular virology of coronaviruses.冠状病毒的分子病毒学。
J Biol Chem. 2020 Sep 11;295(37):12910-12934. doi: 10.1074/jbc.REV120.013930. Epub 2020 Jul 13.
5
LY6E Restricts Entry of Human Coronaviruses, Including Currently Pandemic SARS-CoV-2.LY6E限制包括当前大流行的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)在内的人类冠状病毒的进入。
J Virol. 2020 Aug 31;94(18). doi: 10.1128/JVI.00562-20.
6
The potential of drug repositioning as a short-term strategy for the control and treatment of COVID-19 (SARS-CoV-2): a systematic review.药物重定位作为控制和治疗 COVID-19(SARS-CoV-2)的短期策略的潜力:系统评价。
Arch Virol. 2020 Aug;165(8):1729-1737. doi: 10.1007/s00705-020-04693-5. Epub 2020 Jun 8.
7
Remdesivir for the Treatment of Covid-19 - Final Report.瑞德西韦治疗 COVID-19 的疗效 - 最终报告。
N Engl J Med. 2020 Nov 5;383(19):1813-1826. doi: 10.1056/NEJMoa2007764. Epub 2020 Oct 8.
8
Structure of the RNA-dependent RNA polymerase from COVID-19 virus.COVID-19 病毒的依赖 RNA 的 RNA 聚合酶的结构。
Science. 2020 May 15;368(6492):779-782. doi: 10.1126/science.abb7498. Epub 2020 Apr 10.
9
Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China.中国武汉地区 2019 年新型冠状病毒感染患者的临床特征。
Lancet. 2020 Feb 15;395(10223):497-506. doi: 10.1016/S0140-6736(20)30183-5. Epub 2020 Jan 24.
10
A Novel Coronavirus from Patients with Pneumonia in China, 2019.2019 年中国肺炎患者中的一种新型冠状病毒。
N Engl J Med. 2020 Feb 20;382(8):727-733. doi: 10.1056/NEJMoa2001017. Epub 2020 Jan 24.