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耐更昔洛韦的巨细胞病毒临床分离株:对更昔洛韦的耐药模式。

Ganciclovir-resistant cytomegalovirus clinical isolates: mode of resistance to ganciclovir.

作者信息

Stanat S C, Reardon J E, Erice A, Jordan M C, Drew W L, Biron K K

机构信息

Wellcome Research Laboratories, Research Triangle Park, North Carolina 27709.

出版信息

Antimicrob Agents Chemother. 1991 Nov;35(11):2191-7. doi: 10.1128/AAC.35.11.2191.

Abstract

Cytomegalovirus strains with reduced in vitro susceptibilities to ganciclovir have been recovered from patients who failed long-term ganciclovir therapy. The ganciclovir-resistant clinical isolates in this study were unable to induce ganciclovir phosphorylation in virus-infected cells. The viral DNA polymerase function appeared unaltered in one genetically pure ganciclovir-resistant strain, compared with that of its wild-type ganciclovir-sensitive counterpart. All nine of the ganciclovir-resistant strains were susceptible to foscarnet. Moreover, these strains were sensitive to inhibition both by vidarabine and 1-(2'-deoxy-2'-fluoro-beta-D-arabinofuranosyl)-5-iodocytosine (FIAC), antiviral agents that are activated by cellular enzymes, and by (S)-1(3-hydroxy-2-phosphonylmethoxypropyl)cytosine (HPMPC), which is a monophosphate nucleoside analog. The in vitro resistance to ganciclovir of the ganciclovir-resistant clinical isolates studied was attributed to the inability of the cells infected with these isolates to phosphorylate ganciclovir; the virally encoded DNA polymerase did not appear to play a role in this ganciclovir resistance.

摘要

从长期使用更昔洛韦治疗失败的患者中分离出了对更昔洛韦体外敏感性降低的巨细胞病毒株。本研究中对更昔洛韦耐药的临床分离株在病毒感染的细胞中无法诱导更昔洛韦磷酸化。与野生型对更昔洛韦敏感的对应株相比,在一株基因纯合的对更昔洛韦耐药的毒株中,病毒DNA聚合酶功能似乎未改变。所有9株对更昔洛韦耐药的毒株对膦甲酸钠敏感。此外,这些毒株对阿糖腺苷以及1-(2'-脱氧-2'-氟-β-D-阿拉伯呋喃糖基)-5-碘胞嘧啶(FIAC,一种由细胞酶激活的抗病毒药物)和(S)-1(3-羟基-2-膦酰甲氧基丙基)胞嘧啶(HPMPC,一种单磷酸核苷类似物)的抑制作用均敏感。所研究的对更昔洛韦耐药的临床分离株对更昔洛韦的体外耐药性归因于感染这些分离株的细胞无法使更昔洛韦磷酸化;病毒编码的DNA聚合酶似乎在这种更昔洛韦耐药性中不起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0d8/245358/7b590ca97e34/aac00055-0057-a.jpg

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