• 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

携带 和 基因突变的多重耐药重组人巨细胞病毒的药物敏感性和复制能力。

Drug Susceptibility and Replicative Capacity of Multidrug-Resistant Recombinant Human Cytomegalovirus Harboring Mutations in and Genes.

机构信息

Research Center in Infectious Diseases, CHU of Quebec and Laval University, Quebec City, Quebec, Canada.

Research Center in Infectious Diseases, CHU of Quebec and Laval University, Quebec City, Quebec, Canada

出版信息

Antimicrob Agents Chemother. 2017 Oct 24;61(11). doi: 10.1128/AAC.01044-17. Print 2017 Nov.

DOI:10.1128/AAC.01044-17
PMID:28807919
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5655094/
Abstract

Letermovir is an investigational antiviral agent with a novel mechanism of action involving the viral terminase (pUL56). We evaluated the impact of the V236M mutation in the gene alone and in combination with the E756K mutation in the gene on drug susceptibility and viral replicative capacity of recombinant human cytomegalovirus. The double mutant exhibited at least borderline resistance to all antivirals tested (ganciclovir, foscarnet, cidofovir, brincidofovir, and letermovir) and replicated less efficiently than the wild-type virus .

摘要

洛韦莫韦是一种具有新型作用机制的抗病毒药物,该机制涉及病毒末端酶(pUL56)。我们评估了 基因中的 V236M 突变单独存在和与 基因中的 E756K 突变共同存在对重组人巨细胞病毒药物敏感性和病毒复制能力的影响。双突变体对所有测试的抗病毒药物(更昔洛韦、膦甲酸钠、西多福韦、布西福韦和洛韦莫韦)至少表现出边缘耐药性,并且复制效率低于野生型病毒。

相似文献

1
Drug Susceptibility and Replicative Capacity of Multidrug-Resistant Recombinant Human Cytomegalovirus Harboring Mutations in and Genes.携带 和 基因突变的多重耐药重组人巨细胞病毒的药物敏感性和复制能力。
Antimicrob Agents Chemother. 2017 Oct 24;61(11). doi: 10.1128/AAC.01044-17. Print 2017 Nov.
2
New Locus of Drug Resistance in the Human Cytomegalovirus UL56 Gene Revealed by Exposure to Letermovir and Ganciclovir.人巨细胞病毒 UL56 基因中雷帕霉素和更昔洛韦耐药新位点的揭示。
Antimicrob Agents Chemother. 2018 Aug 27;62(9). doi: 10.1128/AAC.00922-18. Print 2018 Sep.
3
Generation and characterization of a GCV resistant HCMV UL97-mutation and a drug sensitive UL54-mutation.生成并鉴定具有 GCV 抗性的 HCMV UL97 突变株和具有药物敏感性的 UL54 突变株。
Antiviral Res. 2013 Dec;100(3):575-7. doi: 10.1016/j.antiviral.2013.09.026. Epub 2013 Oct 10.
4
Identification of newly detected, drug-related HCMV UL97- and UL54-mutations using a modified plaque reduction assay.采用改良的蚀斑减少试验鉴定新发现的与药物相关的 HCMV UL97 和 UL54 突变。
J Clin Virol. 2015 Aug;69:150-5. doi: 10.1016/j.jcv.2015.06.090. Epub 2015 Jun 19.
5
A novel mutation in the UL54 gene of human cytomegalovirus isolates that confers resistance to foscarnet.人巨细胞病毒分离株UL54基因中的一种新型突变,该突变赋予对膦甲酸钠的抗性。
Antivir Ther. 2006;11(4):537-40.
6
Variations in the cytomegalovirus DNA polymerase and phosphotransferase genes in relation to foscarnet and ganciclovir sensitivity.巨细胞病毒DNA聚合酶和磷酸转移酶基因变异与膦甲酸钠和更昔洛韦敏感性的关系。
J Clin Virol. 2001 Dec;23(1-2):1-15. doi: 10.1016/s1386-6532(01)00160-3.
7
Phenotypic diversity of cytomegalovirus DNA polymerase gene variants observed after antiviral therapy.抗病毒治疗后观察到的巨细胞病毒 DNA 聚合酶基因突变体的表型多样性。
J Clin Virol. 2011 Apr;50(4):287-91. doi: 10.1016/j.jcv.2011.01.004. Epub 2011 Feb 3.
8
Novel Cytomegalovirus UL54 DNA Polymerase Gene Mutations Selected In Vitro That Confer Brincidofovir Resistance.体外筛选出的赋予更昔洛韦抗性的新型巨细胞病毒UL54 DNA聚合酶基因突变
Antimicrob Agents Chemother. 2016 May 23;60(6):3845-8. doi: 10.1128/AAC.00214-16. Print 2016 Jun.
9
Fast breakthrough of resistant cytomegalovirus during secondary letermovir prophylaxis in a hematopoietic stem cell transplant recipient.造血干细胞移植受者在二次莱曲莫韦预防治疗期间出现耐药巨细胞病毒的快速突破。
BMC Infect Dis. 2019 May 8;19(1):388. doi: 10.1186/s12879-019-4016-1.
10
Comparison of Cytomegalovirus Terminase Gene Mutations Selected after Exposure to Three Distinct Inhibitor Compounds.比较接触三种不同抑制剂化合物后选择的巨细胞病毒终止酶基因突变。
Antimicrob Agents Chemother. 2017 Oct 24;61(11). doi: 10.1128/AAC.01325-17. Print 2017 Nov.

引用本文的文献

1
Cost Effectiveness of Letermovir for Cytomegalovirus Prophylaxis Compared with Pre-Emptive Therapy in Allogeneic Hematopoietic Stem Cell Transplant Recipients in the United States.在美国异基因造血干细胞移植受者中,与抢先治疗相比,来特莫韦预防巨细胞病毒感染的成本效益分析
Pharmacoecon Open. 2023 May;7(3):393-404. doi: 10.1007/s41669-023-00398-y. Epub 2023 Feb 25.
2
Assessment of UL56 Mutations before Letermovir Therapy in Refractory Cytomegalovirus Transplant Recipients.难治性巨细胞病毒移植受者在使用来特莫韦治疗前的 UL56 突变评估。
Microbiol Spectr. 2022 Apr 27;10(2):e0019122. doi: 10.1128/spectrum.00191-22. Epub 2022 Mar 28.
3
Cytomegalovirus Viral Load in Transplanted Patients Using the NeuMoDx™ (Qiagen) Automated System: A 1-Month Experience Feedback.使用 NeuMoDx™(Qiagen)自动化系统检测移植患者巨细胞病毒载量:1 个月经验反馈。
Viruses. 2021 Aug 16;13(8):1619. doi: 10.3390/v13081619.
4
Letermovir Resistance in Hematopoietic Stem Cell Transplant Recipients: The Risks Associated with Cytomegalovirus Prophylaxis.造血干细胞移植受者中莱特莫韦的耐药性:与巨细胞病毒预防相关的风险
J Infect Dis. 2020 Mar 16;221(7):1036-1038. doi: 10.1093/infdis/jiz578.
5
Letermovir Resistance Analysis in a Clinical Trial of Cytomegalovirus Prophylaxis for Hematopoietic Stem Cell Transplant Recipients.造血干细胞移植受者巨细胞病毒预防的临床试验中的来特莫韦耐药分析。
J Infect Dis. 2020 Mar 16;221(7):1117-1126. doi: 10.1093/infdis/jiz577.
6
Antiviral prophylaxis for cytomegalovirus infection in allogeneic hematopoietic cell transplantation.异基因造血细胞移植中巨细胞病毒感染的抗病毒预防。
Blood Adv. 2018 Aug 28;2(16):2159-2175. doi: 10.1182/bloodadvances.2018016493.
7
The human cytomegalovirus terminase complex as an antiviral target: a close-up view.人类巨细胞病毒终止酶复合物作为抗病毒靶点:特写。
FEMS Microbiol Rev. 2018 Mar 1;42(2):137-145. doi: 10.1093/femsre/fuy004.

本文引用的文献

1
Cytomegalovirus disease in hematopoietic stem cell transplant patients: current and future therapeutic options.造血干细胞移植患者的巨细胞病毒病:当前及未来的治疗选择
Curr Opin Infect Dis. 2017 Aug;30(4):372-376. doi: 10.1097/QCO.0000000000000375.
2
Rapid In Vitro Evolution of Human Cytomegalovirus UL56 Mutations That Confer Letermovir Resistance.导致来特莫韦耐药的人巨细胞病毒UL56突变的快速体外进化
Antimicrob Agents Chemother. 2015 Oct;59(10):6588-93. doi: 10.1128/AAC.01623-15. Epub 2015 Aug 10.
3
Characterization of Cytomegalovirus Breakthrough Events in a Phase 2 Prophylaxis Trial of Letermovir (AIC246, MK 8228).在来特莫韦(AIC246,MK 8228)2期预防试验中巨细胞病毒突破事件的特征分析
J Infect Dis. 2016 Jan 1;213(1):23-30. doi: 10.1093/infdis/jiv352. Epub 2015 Jun 25.
4
Phenotypic characterization of two naturally occurring human Cytomegalovirus sequence polymorphisms located in a distinct region of ORF UL56 known to be involved in in vitro resistance to letermovir.对位于开放阅读框UL56一个独特区域的两种自然发生的人巨细胞病毒序列多态性进行表型特征分析,该区域已知与体外对来特莫韦的耐药性有关。
Antiviral Res. 2015 Apr;116:48-50. doi: 10.1016/j.antiviral.2015.01.006. Epub 2015 Jan 28.
5
Characterization of multiple cytomegalovirus drug resistance mutations detected in a hematopoietic stem cell transplant recipient by recombinant phenotyping.通过重组表型分析鉴定造血干细胞移植受者中多种巨细胞病毒药物耐药突变。
J Clin Microbiol. 2014 Nov;52(11):4043-6. doi: 10.1128/JCM.02205-14. Epub 2014 Aug 20.
6
Geno- and phenotypic characterization of human cytomegalovirus mutants selected in vitro after letermovir (AIC246) exposure.体外筛选使用乐韦替尼(AIC246)后选择的人巨细胞病毒突变体的基因和表型特征。
Antimicrob Agents Chemother. 2014;58(1):610-3. doi: 10.1128/AAC.01794-13. Epub 2013 Nov 4.
7
Novel method based on "en passant" mutagenesis coupled with a gaussia luciferase reporter assay for studying the combined effects of human cytomegalovirus mutations.基于“顺式”突变与海肾荧光素酶报告基因检测联合研究人巨细胞病毒突变的协同作用的新方法。
J Clin Microbiol. 2013 Oct;51(10):3216-24. doi: 10.1128/JCM.01275-13. Epub 2013 Jul 17.
8
CMV: Prevention, Diagnosis and Therapy.巨细胞病毒:预防、诊断与治疗。
Am J Transplant. 2013 Feb;13 Suppl 3:24-40; quiz 40. doi: 10.1111/ajt.12006.
9
Synthesis and early development of hexadecyloxypropylcidofovir: an oral antipoxvirus nucleoside phosphonate.十六烷氧基丙基西多福韦的合成与早期开发:一种口服抗痘病毒核苷膦酸酯。
Viruses. 2010 Oct;2(10):2213-2225. doi: 10.3390/v2102213. Epub 2010 Sep 30.
10
The novel anticytomegalovirus compound AIC246 (Letermovir) inhibits human cytomegalovirus replication through a specific antiviral mechanism that involves the viral terminase.新型抗巨细胞病毒化合物 AIC246(来特莫韦)通过一种特定的抗病毒机制抑制人类巨细胞病毒复制,该机制涉及病毒末端酶。
J Virol. 2011 Oct;85(20):10884-93. doi: 10.1128/JVI.05265-11. Epub 2011 Jul 13.