Boivin Guy, Goyette Nathalie, Gilbert Christian, Covington Emma
Research Center in Infectious Diseases, Centre Hospitalier Universitaire de Quebec and Laval University, Quebec City, Canada.
J Med Virol. 2005 Nov;77(3):425-9. doi: 10.1002/jmv.20471.
We previously reported the absence of CMV UL97 (kinase) gene resistance mutations up to 12 months post-transplant following 100 days of valganciclovir prophylaxis, and a low incidence of resistance mutations following 100 days of oral ganciclovir prophylaxis in a prospective multicenter study in solid organ transplant recipients excluding lung transplants. Herein, we report UL54 (DNA polymerase) gene sequencing results for all patients with previous UL97 PCR-positive samples (n = 99) in our study. One UL54 resistance mutation (L545S known to confer ganciclovir and cidofovir resistance) was detected in a routine day-100 sample from an asymptomatic patient who received oral ganciclovir. Notably, this CMV UL54 mutation occurred in the absence of a UL97 mutation. Additionally, new UL54 variants were observed. Thus, emergence of CMV UL54 mutations in the absence of UL97 mutations is a rare but possible event that is not necessarily associated with detrimental clinical outcome in solid organ transplant recipients.
我们先前报道,在实体器官移植受者(不包括肺移植受者)的一项前瞻性多中心研究中,在接受100天缬更昔洛韦预防治疗后,移植后长达12个月未检测到巨细胞病毒(CMV)UL97(激酶)基因耐药突变,而在接受100天口服更昔洛韦预防治疗后,耐药突变发生率较低。在此,我们报告了我们研究中所有先前UL97 PCR检测呈阳性样本患者(n = 99)的UL54(DNA聚合酶)基因测序结果。在一名接受口服更昔洛韦治疗的无症状患者的第100天常规样本中检测到一个UL54耐药突变(L545S,已知可导致对更昔洛韦和西多福韦耐药)。值得注意的是,该CMV UL54突变发生时不存在UL97突变。此外,还观察到了新的UL54变异体。因此,在不存在UL97突变的情况下出现CMV UL54突变是一种罕见但可能发生的事件,在实体器官移植受者中不一定与有害的临床结局相关。