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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。

A novel mutation in the UL54 gene of human cytomegalovirus isolates that confers resistance to foscarnet.

作者信息

Ducancelle Alexandra, Champier Gaël, Alain Sophie, Petit Françoise, Le Pors Marie-José Sanson, Mazeron Marie-Christine

机构信息

Service de Bactériologie-Virologie, Hôpital Lariboisière, Assistance Publique-Hôpitaux de Paris, Paris, France.

出版信息

Antivir Ther. 2006;11(4):537-40.

Abstract

Foscarnet is currently licensed for the treatment of human cytomegalovirus (HCMV) infection. Mutations proven to confer resistance to foscarnet have mostly been mapped to regions II, III and VI of the HCMV UL54-encoded DNA polymerase. We previously showed that sequential foscarnet-resistant HCMV isolates recovered from a patient with lymphoma had change N495K in region delta-C of the DNA polymerase. To evaluate the impact of change N495K on HCMV sensitivity to foscarnet, a recombinant HCMV strain carrying the mutation was produced by homologous recombination. The recombinant virus showed a 3.4-fold increase in foscarnet resistance, and remained sensitive to ganciclovir and cidofovir. In addition, the recombinant strain showed a reduction of infectious virus yield compared with its parent strain. Change N495K should be added to the list of mutations conferring resistance to foscarnet and be taken into account in the genotypic diagnosis of antiviral resistance.

摘要

膦甲酸钠目前已获许可用于治疗人类巨细胞病毒(HCMV)感染。已证实赋予对膦甲酸钠耐药性的突变大多定位在HCMV UL54编码的DNA聚合酶的II、III和VI区域。我们之前表明,从一名淋巴瘤患者中分离出的对膦甲酸钠耐药的HCMV连续分离株在DNA聚合酶的δ-C区域有N495K变化。为了评估N495K变化对HCMV对膦甲酸钠敏感性的影响,通过同源重组产生了携带该突变的重组HCMV毒株。重组病毒对膦甲酸钠的耐药性增加了3.4倍,并且对更昔洛韦和西多福韦仍敏感。此外,与亲本毒株相比,重组毒株的感染性病毒产量有所降低。N495K变化应添加到赋予对膦甲酸钠耐药性的突变列表中,并在抗病毒耐药性的基因诊断中予以考虑。

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