Drew W Lawrence, Miner Richard C, Marousek Gail I, Chou Sunwen
UCSF Mount Zion Medical Center, University of California, 1600 Divisadero Street, San Francisco, CA 94115, USA.
J Clin Virol. 2006 Oct;37(2):124-7. doi: 10.1016/j.jcv.2006.07.010. Epub 2006 Sep 8.
The cytomegalovirus (CMV) UL97 inhibitor drug maribavir (MBV) is undergoing clinical antiviral trials.
To assess the MBV sensitivity of CMV strains and isolates containing mutations that confer resistance to current antiviral drugs ganciclovir, cidofovir or foscarnet.
Resistant clinical isolates and laboratory strains containing UL97 and or UL54 DNA polymerase mutations were tested for sensitivity to all four drugs by standard plaque reduction assay and a reporter-based yield reduction assay. Sensitive control strains were also tested.
Eleven CMV strains or isolates resistant to GCV, four resistant to FOS and two resistant to CDV, were all sensitive to MBV. These viruses represent four UL97 mutations and three UL54 DNA polymerase mutations. The laboratory derived UL97 L397R mutant was highly MBV-resistant but remained sensitive to the other three drugs.
No cross-resistance has been detected between viruses resistant to MBV and those resistant to one or more of the current CMV antiviral drugs, consistent with differences in their mechanisms of action.
巨细胞病毒(CMV)UL97抑制剂药物马里巴韦(MBV)正在进行临床抗病毒试验。
评估含有对当前抗病毒药物更昔洛韦、西多福韦或膦甲酸钠耐药突变的CMV菌株和分离株对MBV的敏感性。
通过标准蚀斑减少试验和基于报告基因的产量减少试验,检测含有UL97和/或UL54 DNA聚合酶突变的耐药临床分离株和实验室菌株对这四种药物的敏感性。同时也检测了敏感对照菌株。
11株对更昔洛韦耐药的CMV菌株或分离株、4株对膦甲酸钠耐药的菌株和2株对西多福韦耐药的菌株,均对MBV敏感。这些病毒代表了4种UL97突变和3种UL54 DNA聚合酶突变。实验室衍生的UL97 L397R突变体对MBV高度耐药,但对其他三种药物仍敏感。
在对MBV耐药的病毒与对一种或多种当前CMV抗病毒药物耐药的病毒之间未检测到交叉耐药,这与其作用机制的差异一致。