Martin Melanie, Gilbert Christian, Covington Emma, Boivin Guy
Research Center in Infectious Diseases, Centre Hospitalier Universitaire de Quebec and Laval University, Quebec City, Canada.
J Infect Dis. 2006 Sep 1;194(5):579-83. doi: 10.1086/505882. Epub 2006 Jul 24.
A method based on manipulation of the human cytomegalovirus genome in a bacterial artificial chromosome was developed to determine the role played by 6 UL97 mutations of unknown significance. These mutations were found in blood samples from solid-organ transplant recipients in a trial comparing valganciclovir and oral ganciclovir prophylaxis. Recombinant viruses containing UL97 mutations P405L, A427V, M550I, A582V, Y617H, and A674T were generated in a bacterial system. Viral stocks were subsequently reconstituted in human fibroblasts, and ganciclovir susceptibilities were tested using a plaque-reduction assay. All recombinant viruses containing these unknown mutations were found to be susceptible to ganciclovir.
开发了一种基于在细菌人工染色体中操纵人巨细胞病毒基因组的方法,以确定6个意义不明的UL97突变所起的作用。这些突变是在一项比较缬更昔洛韦和口服更昔洛韦预防的试验中,在实体器官移植受者的血样中发现的。在细菌系统中产生了含有UL97突变P405L、A427V、M550I、A582V、Y617H和A674T的重组病毒。随后在人成纤维细胞中重建病毒储备,并使用蚀斑减少试验测试更昔洛韦敏感性。发现所有含有这些不明突变的重组病毒对更昔洛韦敏感。