Department of Veterinary and Biomedical Sciences, Nebraska Center for Virology, University of Nebraska, Lincoln, Nebraska 68503, USA.
J Neurovirol. 2009 Sep;15(5-6):439-48. doi: 10.3109/13550280903296353.
Expression of the first 1.5 kb of the latency-associated transcript (LAT) that is encoded by herpes simplex virus type 1 (HSV-1) is sufficient for wild-type (wt) levels of reactivation from latency in small animal models. Peptide-specific immunoglobulin G (IgG) was generated against open reading frames (ORFs) that are located within the first 1.5 kb of LAT coding sequences. Cells stably transfected with LAT or trigeminal ganglionic neurons of mice infected with a LAT expressing virus appeared to express the L2 or L8 ORF. Only L2 ORF expression was readily detected in trigeminal ganglionic neurons of latently infected mice.
单纯疱疹病毒 1 型(HSV-1)的潜伏相关转录物(LAT)的前 1.5kb 表达足以在小动物模型中从潜伏状态引发野生型(wt)水平的再激活。针对位于 LAT 编码序列前 1.5kb 内的开放阅读框(ORF)生成了肽特异性免疫球蛋白 G(IgG)。稳定转染 LAT 的细胞或感染表达 LAT 的病毒的三叉神经节神经元似乎表达 L2 或 L8 ORF。只有在潜伏感染的小鼠的三叉神经节神经元中才能轻易检测到 L2 ORF 的表达。