Emergence of antiviral resistance during oral valganciclovir treatment of an infant with congenital cytomegalovirus (CMV) infection

被引:18
作者
Choi, Yeon [1 ]
Sharon, B. [1 ]
Balfour, H. H., Jr. [2 ]
Belani, K. [3 ,4 ]
Pozos, T. C. [3 ,4 ]
Schleiss, M. R. [1 ]
机构
[1] Univ Minnesota, Sch Med, Ctr Infect Dis & Microbiol Translat Res, Div Pediat Infect Dis & Immunol, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Med, Div Lab Med & Pathol, Minneapolis, MN 55455 USA
[3] Childrens Hosp, Minneapolis, MN 55404 USA
[4] Clin Minnesota, Minneapolis, MN 55404 USA
关键词
Congenital cytomegalovirus infection; Antiviral therapy; Ganciclovir resistance; UL97; mutation; ORGAN TRANSPLANT RECIPIENTS; GANCICLOVIR RESISTANCE; DRUG-RESISTANCE; DISEASE; MUTATIONS; STRATEGIES; MANAGEMENT; THERAPY; STRAINS; IMMUNODEFICIENCY;
D O I
10.1016/j.jcv.2013.04.004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Congenital infection with human cytomegalovirus (CMV) is a major cause of morbidity, including sensorineural hearing loss (SNHL), in newborns. Antiviral therapy with ganciclovir (GCV) and its oral prodrug, valganciclovir (VAL-GCV) are increasingly being administered to infected infants, toward the goal of improving neurodevelopmental and auditory outcomes. In this case report, we describe a symptomatic congenitally infected infant treated with VAL-GCV in whom GCV resistance was suspected, based on a 50-fold increase in viral load after 6 weeks of oral therapy. Analyses of CMV sequences from both blood and urine demonstrated populations of viruses with M460V and L595F mutations in the UL97 phosphotransferase gene. In contrast, analysis of viral DNA retrieved from the newborn dried blood spot demonstrated wild-type UL97 sequences. DNAemia resolved after the discontinuation of VAL-GCV. Long-term VAL-GCV therapy in congenitally infected infants can select for resistant viral variants, and anticipatory virological monitoring may be warranted. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:356 / 360
页数:5
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