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巨细胞病毒DNA聚合酶序列V区的缺失突变赋予多药耐药性。

A deletion mutation in region V of the cytomegalovirus DNA polymerase sequence confers multidrug resistance.

作者信息

Chou S, Miner R C, Drew W L

机构信息

VA Medical Center P3ID, Portland, OR 97201, USA.

出版信息

J Infect Dis. 2000 Dec;182(6):1765-8. doi: 10.1086/317618. Epub 2000 Oct 17.

Abstract

A patient with AIDS and cytomegalovirus (CMV) retinitis received ganciclovir and foscarnet for 20 and 5 months, respectively, with evidence of periodic disease progression. After this therapy, a CMV isolate from the patient was resistant to ganciclovir, foscarnet, and cidofovir. Sequence analysis showed a known ganciclovir resistance mutation in the viral UL97 phosphotransferase (L595F) and a new mutation in conserved region V of the DNA polymerase gene (pol) sequence (codons 981-982 deleted). The pol mutation was transferred to a laboratory CMV strain (Towne) by homologous recombination and selection with either ganciclovir or foscarnet. Recombinant viruses containing this deletion showed a 6-8-fold increased ganciclovir resistance and a 3-5-fold increased resistance to both foscarnet and cidofovir, compared with the wild-type CMV. A single mutation in region V of CMV pol can, therefore, confer multiple drug resistance in a clinical isolate.

摘要

一名患有艾滋病和巨细胞病毒(CMV)视网膜炎的患者分别接受了更昔洛韦和膦甲酸治疗20个月和5个月,但有疾病周期性进展的证据。经过这种治疗后,从该患者分离出的CMV毒株对更昔洛韦、膦甲酸和西多福韦耐药。序列分析显示,病毒UL97磷酸转移酶存在已知的更昔洛韦耐药突变(L595F),并且DNA聚合酶基因(pol)序列的保守区域V出现新突变(密码子981 - 982缺失)。通过同源重组并用更昔洛韦或膦甲酸进行选择,将pol突变转移到实验室CMV毒株(Towne株)。与野生型CMV相比,含有该缺失的重组病毒对更昔洛韦的耐药性增加了6 - 8倍,对膦甲酸和西多福韦的耐药性增加了3 - 5倍。因此,CMV pol区域V中的单个突变可使临床分离株产生多重耐药性。

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