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核苷类似物2'-去甲-2'-脱氧鸟苷对人巨细胞病毒复制的影响。

Effects of the nucleoside analog 2'-nor-2'-deoxyguanosine on human cytomegalovirus replication.

作者信息

Tocci M J, Livelli T J, Perry H C, Crumpacker C S, Field A K

出版信息

Antimicrob Agents Chemother. 1984 Feb;25(2):247-52. doi: 10.1128/AAC.25.2.247.

DOI:10.1128/AAC.25.2.247
PMID:6324669
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC185483/
Abstract

The nucleoside analog 2'-nor-2'-deoxyguanosine (2'NDG) effectively inhibits the replication of several laboratory and clinical isolates of human cytomegalovirus. These isolates included viruses obtained from congenitally infected infants and patients suffering from acquired immune deficiency syndrome. The dose of 2'NDG that inhibited cytomegalovirus plaque formation ranged from 0.1 to 1.6 micrograms/ml. At 10 micrograms/ml, 2'NDG completely blocked the production of virus progeny but not the expression of immediate early and early virus gene functions. Cytomegalovirus DNA was not detectable in 2'NDG-treated virus-infected human embryo lung cells when assayed by CsCl density gradient centrifugation. In contrast, the guanosine analog acyclovir at 100 micrograms/ml did not inhibit the production of virus or the synthesis of cytomegalovirus DNA. In virus-infected cells, 2'NDG and acyclovir at 10 and 100 micrograms/ml, respectively, inhibited the incorporation of [3H]thymidine and 32Pi into cellular DNA by ca. 50%. Uninfected human embryo lung cells grown in these concentrations of acyclovir or 2'NDG exhibited a slightly transient lag phase but, overall, cell growth was not retarded, and there was no decrease in cell viability. The extended lag in cell division was not due to inactivation or breakdown of the antiviral compounds but may be due in part to a temporary decrease in cellular DNA synthesis.

摘要

核苷类似物2'-去甲-2'-脱氧鸟苷(2'NDG)能有效抑制几种人巨细胞病毒实验室分离株和临床分离株的复制。这些分离株包括从先天性感染婴儿和获得性免疫缺陷综合征患者身上获取的病毒。抑制巨细胞病毒空斑形成的2'NDG剂量范围为0.1至1.6微克/毫升。在10微克/毫升时,2'NDG完全阻断了病毒子代的产生,但不影响即刻早期和早期病毒基因功能的表达。当通过氯化铯密度梯度离心法检测时,在经2'NDG处理的病毒感染的人胚肺细胞中检测不到巨细胞病毒DNA。相比之下,100微克/毫升的鸟苷类似物阿昔洛韦并不抑制病毒的产生或巨细胞病毒DNA的合成。在病毒感染的细胞中,10微克/毫升的2'NDG和100微克/毫升的阿昔洛韦分别使[3H]胸腺嘧啶核苷和32Pi掺入细胞DNA的量约减少50%。在这些阿昔洛韦或2'NDG浓度下生长的未感染人胚肺细胞表现出轻微的短暂延迟期,但总体而言,细胞生长未受抑制,细胞活力也未降低。细胞分裂延迟延长并非由于抗病毒化合物的失活或分解,可能部分是由于细胞DNA合成暂时减少所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9e1/185483/83f97857a172/aac00191-0105-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9e1/185483/83f97857a172/aac00191-0105-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9e1/185483/83f97857a172/aac00191-0105-a.jpg

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本文引用的文献

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Stimulation of cellular DNA synthesis by human cytomegalovirus.人巨细胞病毒对细胞DNA合成的刺激作用。
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Inhibition of cellular alpha and virally induced deoxyribonucleic acid polymerases by the triphosphate of acyclovir.阿昔洛韦三磷酸盐对细胞α和病毒诱导的脱氧核糖核酸聚合酶的抑制作用。
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Effect of 9-(1,3-dihydroxy-2-propoxymethyl)guanine on human cytomegalovirus replication in vitro.9-(1,3-二羟基-2-丙氧甲基)鸟嘌呤对人巨细胞病毒体外复制的影响。
伐昔洛韦在成人实体器官移植受者中的应用:药代动力学和药效学特征及血药浓度测定的临床解读。
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Population pharmacokinetics of ganciclovir in newborns with congenital cytomegalovirus infections. NIAID Collaborative Antiviral Study Group.更昔洛韦在先天性巨细胞病毒感染新生儿中的群体药代动力学。美国国立过敏与传染病研究所协作抗病毒研究组。
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Inhibition by ganciclovir of cell growth and DNA synthesis of cells biochemically transformed with herpesvirus genetic information.更昔洛韦对被疱疹病毒遗传信息进行生化转化的细胞的细胞生长和DNA合成的抑制作用。
Antimicrob Agents Chemother. 1987 Jun;31(6):844-9. doi: 10.1128/AAC.31.6.844.
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Acyclic guanosine analogs as inhibitors of human cytomegalovirus.无环鸟苷类似物作为人巨细胞病毒的抑制剂
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Sequence and transcription analysis of the human cytomegalovirus DNA polymerase gene.人巨细胞病毒DNA聚合酶基因的序列与转录分析
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Activity of 9-(1,3-dihydroxy-2-propoxymethyl)guanine compared with that of acyclovir against human, monkey, and rodent cytomegaloviruses.9-(1,3-二羟基-2-丙氧基甲基)鸟嘌呤与阿昔洛韦对人、猴和啮齿动物巨细胞病毒的活性比较。
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5
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6
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Biochem Biophys Res Commun. 1982 Oct 29;108(4):1716-21. doi: 10.1016/s0006-291x(82)80109-5.
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Antimicrob Agents Chemother. 1982 Jul;22(1):55-61. doi: 10.1128/AAC.22.1.55.
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Proc Natl Acad Sci U S A. 1980 Apr;77(4):2270-3. doi: 10.1073/pnas.77.4.2270.
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J Virol. 1973 Jun;11(6):986-90. doi: 10.1128/JVI.11.6.986-990.1973.