assessment of the human cytomegalovirus ul97 gene for identification of resistance to ganciclovir in iranian immunosuppressed patients

patients and methods in this study, 87 specimens from iranian patients were amplified using nested pcr amplification of the ul97 gene. sequence analyses of products were performed for identifying the mutated codons. results the present study show that the most frequent gcv-resistant mutations occurred in codons a594v (26.43%), h520q (18.39%), and m460v (13.79%), consequently occurring at a low frequency in the l595s (2.29%), e596g (1.14%), and del 594 (1.14%) codons, and with intermediate frequency in the c592g (10.34%), m460i (9.19%), and c603w (6.89%) codons. we describe for the first time a new gcv-resistance mutation, the deletion of codon 594, in the ul97 gene of iranian hcmv patients after gcv therapy, following renal transplantation. background human cytomegalovirus (hcmv) infections are a major cause of morbidity and mortality among immunocompromised patients. prolonged antiviral therapy is a cause of mutation and drug resistance in the hcmv genome. objectives the aim of this study was to identify resistance to ganciclovir (gcv) in iranian immunosuppressed patients at two different stages of the disease: early (before gcv is initiated) and late (after six months of gcv therapy). conclusions the findings of the present study can be utilized to detect gcv resistance patterns among iranian immunocompromised patients and to treat hcmv infections accordingly.