Azithromycin Inhibits the Replication of Zika Virus

Eve Bosseboeuf, M. Aubry, T. Nhan, J. Pina, J. Rolain, D. Raoult, D. Musso
{"title":"Azithromycin Inhibits the Replication of Zika Virus","authors":"Eve Bosseboeuf, M. Aubry, T. Nhan, J. Pina, J. Rolain, D. Raoult, D. Musso","doi":"10.4172/1948-5964.1000173","DOIUrl":null,"url":null,"abstract":"Background: The emergence of Zika virus (ZIKV) is associated to dramatic complications in fetuses and neonates. As there is no vaccine and no drug to prevent and treat ZIKV infections, there is an urgent need to have active drugs against ZIKV that can be used during pregnancy. Large screening strategies suggested that azithromycin (AZ) has an in vitro activity against ZIKV, we provide additional data supporting this hypothesis. Methods: We tested the efficacy of AZ on ZIKV-infected Vero cells at a concentration that can be reached in vivo in amniotic fluid. We conducted two experiments with addition to infected cells of a single dose or multi doses of 50 mg/L of AZ, and analyzed ZIKV replication by immunofluorescence assay (IFA) and by measuring viral RNA loads at different times up to 96 h post-infection (hpi). Results: Addition of a single dose of 50 mg/L of AZ prevented replication of ZIKV during 48 hpi; after 48 hpi, ZIKV replication was detected by IFA but viral RNA loads remained lower than in untreated infected cells. ZIKV replication was inhibited by addition of multi doses of 50 mg/L of AZ. Conclusions: Our data confirm the in vitro activity of AZ against ZIKV. Since there will be no active specific drugs and vaccine available soon against ZIKV, AZ might be the first compound that could prevent and treat ZIKV infections, with the advantages of being an approved and safe drug usable during pregnancy.","PeriodicalId":15020,"journal":{"name":"Journal of Antivirals & Antiretrovirals","volume":"44 1","pages":"6-11"},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"114","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Antivirals & Antiretrovirals","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4172/1948-5964.1000173","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 114

Abstract

Background: The emergence of Zika virus (ZIKV) is associated to dramatic complications in fetuses and neonates. As there is no vaccine and no drug to prevent and treat ZIKV infections, there is an urgent need to have active drugs against ZIKV that can be used during pregnancy. Large screening strategies suggested that azithromycin (AZ) has an in vitro activity against ZIKV, we provide additional data supporting this hypothesis. Methods: We tested the efficacy of AZ on ZIKV-infected Vero cells at a concentration that can be reached in vivo in amniotic fluid. We conducted two experiments with addition to infected cells of a single dose or multi doses of 50 mg/L of AZ, and analyzed ZIKV replication by immunofluorescence assay (IFA) and by measuring viral RNA loads at different times up to 96 h post-infection (hpi). Results: Addition of a single dose of 50 mg/L of AZ prevented replication of ZIKV during 48 hpi; after 48 hpi, ZIKV replication was detected by IFA but viral RNA loads remained lower than in untreated infected cells. ZIKV replication was inhibited by addition of multi doses of 50 mg/L of AZ. Conclusions: Our data confirm the in vitro activity of AZ against ZIKV. Since there will be no active specific drugs and vaccine available soon against ZIKV, AZ might be the first compound that could prevent and treat ZIKV infections, with the advantages of being an approved and safe drug usable during pregnancy.
阿奇霉素抑制寨卡病毒的复制
背景:寨卡病毒(ZIKV)的出现与胎儿和新生儿的严重并发症有关。由于没有预防和治疗寨卡病毒感染的疫苗和药物,因此迫切需要在怀孕期间使用针对寨卡病毒的有效药物。大型筛选策略提示阿奇霉素(AZ)具有抗寨卡病毒的体外活性,我们提供了支持这一假设的额外数据。方法:在羊水中检测AZ对zikv感染的Vero细胞在体内达到的浓度的效果。在感染细胞中分别添加单剂量或多剂量50mg /L的AZ进行实验,并通过免疫荧光法(IFA)和感染后96 h (hpi)不同时间的病毒RNA载量测定来分析ZIKV复制。结果:在48hpi期间,单次添加50mg /L的AZ可阻止ZIKV的复制;48hpi后,IFA检测到ZIKV复制,但病毒RNA载量仍低于未处理的感染细胞。多剂量50mg /L的AZ可以抑制ZIKV的复制。结论:我们的数据证实了AZ对ZIKV的体外活性。由于目前还没有针对寨卡病毒的活性特异性药物和疫苗,阿斯利康可能是第一种可以预防和治疗寨卡病毒感染的化合物,其优点是它是一种经批准的安全药物,可在怀孕期间使用。
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
自引率
0.00%
发文量
0
×
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:481959085
Book学术官方微信