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1型单纯疱疹病毒对9-β-D-阿拉伯呋喃糖基腺嘌呤的表面耐药株研究

Study on the apparent resistant strains of herpes simplex virus type 1 against 9-beta-D-arabinofuranosyladenine.

作者信息

Yoshida T, Suzutani T, Azuma M

机构信息

Department of Microbiology, Asahikawa Medical College, Japan.

出版信息

Tohoku J Exp Med. 1988 Nov;156(3):279-90. doi: 10.1620/tjem.156.279.

DOI:10.1620/tjem.156.279
PMID:2855280
Abstract

The appearance of drug resistant strains of herpes simplex virus type 1 (HSV-1) against 9-beta-D-arabinofuranosyladenine (araA), in comparison with 5-iodo-2'-deoxyuridine (IUdR) and 9-(2-hydroxyethoxymethyl)guanine (acycloguanosine, ACG), has been investigated in green monkey kidney cell cultures (Vero) and human embryo lung cell cultures (HEL). Growth curves of HSV-1 in Vero cells and HEL cells in the presence or absence of 20 micrograms/ml of araA showed that not only the viruses produced by these cells in the presence of araA but also the viruses produced in the absence of araA were resistant to the same concentration of araA. However, both viruses were unable to grow in the presence of a combination of 20 micrograms/ml of araA and 3 micrograms/ml of erythro-9-(2-hydroxy-3-nonyl)adenine (EHNA) which is an inhibitor of adenosine deaminase. On the other hand, the viruses produced only in the presence of IUdR or ACG were resistant to each drug. All virus clones obtained from five serial clonings in the presence of araA alone or araA and EHNA in combination were not resistant to araA. These results show that the strain of HSV-1 resistant to araA is an apparently resistant strain, and a truly resistant strain to araA may not be established as easily as the truly resistant strains to IUdR and ACG.

摘要

在绿猴肾细胞培养物(Vero)和人胚肺细胞培养物(HEL)中,研究了1型单纯疱疹病毒(HSV-1)对9-β-D-阿拉伯呋喃糖基腺嘌呤(araA)的耐药菌株的出现情况,并与5-碘-2'-脱氧尿苷(IUdR)和9-(2-羟基乙氧基甲基)鸟嘌呤(阿昔洛韦,ACG)进行了比较。在存在或不存在20微克/毫升araA的情况下,HSV-1在Vero细胞和HEL细胞中的生长曲线表明,不仅这些细胞在araA存在下产生的病毒,而且在araA不存在下产生的病毒对相同浓度的araA均具有抗性。然而,当存在20微克/毫升araA和3微克/毫升的红细胞-9-(2-羟基-3-壬基)腺嘌呤(EHNA,一种腺苷脱氨酶抑制剂)的组合时,两种病毒均无法生长。另一方面,仅在IUdR或ACG存在下产生的病毒对每种药物具有抗性。从仅存在araA或araA与EHNA组合的情况下进行的五次连续克隆中获得的所有病毒克隆均对araA不耐药。这些结果表明,对araA耐药的HSV-1菌株是一种明显耐药的菌株,与对IUdR和ACG真正耐药的菌株相比,对araA真正耐药的菌株可能不容易建立。

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1
Study on the apparent resistant strains of herpes simplex virus type 1 against 9-beta-D-arabinofuranosyladenine.1型单纯疱疹病毒对9-β-D-阿拉伯呋喃糖基腺嘌呤的表面耐药株研究
Tohoku J Exp Med. 1988 Nov;156(3):279-90. doi: 10.1620/tjem.156.279.
2
In vitro and in vivo resistance of herpes simplex virus to 9-(2-hydroxyethoxymethyl)guanine (acycloguanosine).单纯疱疹病毒对9-(2-羟乙氧甲基)鸟嘌呤(阿昔洛韦)的体外和体内抗性
Antimicrob Agents Chemother. 1980 Feb;17(2):144-50. doi: 10.1128/AAC.17.2.144.
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[Research of suppression of the herpes simplex virus reproduction with drug resistance by combination phosphite of acycloguanosine with some antiherpetic drugs].[阿昔洛韦亚磷酸酯与某些抗疱疹药物联合对耐药单纯疱疹病毒复制的抑制作用研究]
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The antiviral activity of 9-beta-D-arabinofuranosyladenine is enhanced by the 2',3'-dideoxyriboside, the 2',3'-didehydro-2',3'-dideoxyriboside and the 3'-azido-2',3'-dideoxyriboside of 2,6-diaminopurine.2,6-二氨基嘌呤的2',3'-二脱氧核糖核苷、2',3'-二脱氢-2',3'-二脱氧核糖核苷和3'-叠氮基-2',3'-二脱氧核糖核苷可增强9-β-D-阿拉伯呋喃糖基腺嘌呤的抗病毒活性。
Biochem Biophys Res Commun. 1989 Feb 28;159(1):61-7. doi: 10.1016/0006-291x(89)92404-2.
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Mutations in the herpes simplex virus DNA polymerase gene can confer resistance to 9-beta-D-arabinofuranosyladenine.单纯疱疹病毒DNA聚合酶基因的突变可赋予对9-β-D-阿拉伯呋喃糖基腺嘌呤的抗性。
J Virol. 1982 Mar;41(3):909-18. doi: 10.1128/JVI.41.3.909-918.1982.
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Combination chemotherapy: interaction of 5-methoxymethyldeoxyuridine with trifluorothymidine, phosphonoformate and acycloguanosine against herpes simplex viruses.联合化疗:5-甲氧基甲基脱氧尿苷与三氟胸苷、膦甲酸和阿昔洛韦对单纯疱疹病毒的相互作用
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Combination chemotherapy: interaction of 5-methoxymethyldeoxyuridine with adenine arabinoside, 5-ethyldeoxyuridine, 5-iododeoxyuridine, and phosphonoacetic acid against herpes simplex virus types 1 and 2.联合化疗:5-甲氧基甲基脱氧尿苷与阿糖腺苷、5-乙基脱氧尿苷、5-碘脱氧尿苷及膦甲酸对1型和2型单纯疱疹病毒的相互作用
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Erythro-9-(2-hydroxy-3-nonyl)adenine as a specific inhibitor of herpes simplex virus replication in the presence and absence of adenosine analogues.在有和没有腺苷类似物存在的情况下,9-(2-羟基-3-壬基)腺嘌呤作为单纯疱疹病毒复制的特异性抑制剂。
Proc Natl Acad Sci U S A. 1978 Oct;75(10):4684-8. doi: 10.1073/pnas.75.10.4684.
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Comparative activity of various compounds against clinical strains of herpes simplex virus.多种化合物对单纯疱疹病毒临床菌株的比较活性
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[The suppression of a herpes simplex virus reproduction with drug resistance by combination 15lys-bis-nt and phosphate of acycloguanosine with some antiherpetic drugs].[15赖氨酸-双核苷酸与阿昔洛韦磷酸盐及某些抗疱疹药物联合对耐药单纯疱疹病毒复制的抑制作用]
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J Clin Microbiol. 1998 Nov;36(11):3198-204. doi: 10.1128/JCM.36.11.3198-3204.1998.
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