Faizi Khan R, Mori S, Eizuru Y, Kumura Ishii K, Minamishima Y
Department of Microbiology, Miyazaki Medical College, Kiyotake, Japan.
Antiviral Res. 1998 Dec;40(1-2):95-103. doi: 10.1016/s0166-3542(98)00051-5.
We isolated a ganciclovir (GCV)-resistant human cytomegalovirus (HCMV) from a laboratory strain, AD169, and analysed the mutant. Attempts were also made to identify directly the mutated gene. The 50% inhibitory concentration (IC50) of GCV for the mutant strain was five times higher than that of the wild-type strain. The mutant strain showed similar sensitivity to phosphonoacetic acid and cidofovir as the wild-type strain. These data suggest mutation in the UL97 gene encoding for the phosphotransferase that phosphorylates GCV. Molecular analysis of the mutant strain revealed that a single base substitution of adenine by cytosine occurred at the 1796 nucleotide position of the UL97 gene region, resulting in the substitution of lysine by threonine at codon 599 in the UL97 gene product. Marker transfer experiment confirmed that this mutation conferred HCMV resistance to GCV. The mutation at codon 599 was easily identified by means of RsaI digestion of the selected PCR product.
我们从实验室菌株AD169中分离出一株耐更昔洛韦(GCV)的人巨细胞病毒(HCMV),并对该突变体进行了分析。我们还尝试直接鉴定突变基因。GCV对突变株的50%抑制浓度(IC50)比野生型菌株高五倍。突变株对膦甲酸和西多福韦的敏感性与野生型菌株相似。这些数据表明,编码磷酸化GCV的磷酸转移酶的UL97基因发生了突变。对突变株的分子分析显示,在UL97基因区域的第1796个核苷酸位置发生了腺嘌呤被胞嘧啶的单碱基替换,导致UL97基因产物中第599位密码子的赖氨酸被苏氨酸取代。标记转移实验证实,这种突变赋予了HCMV对GCV的抗性。通过对选定的PCR产物进行RsaI酶切,可以很容易地鉴定出第599位密码子的突变。