Devi-Rao G B, Aguilar J S, Rice M K, Garza H H, Bloom D C, Hill J M, Wagner E K
Department of Molecular Biology and Biochemistry, University of California-Irvine 92697-3900, USA.
J Virol. 1997 Sep;71(9):7039-47. doi: 10.1128/JVI.71.9.7039-7047.1997.
PCR analysis of herpes simplex virus (HSV) genome replication and productive-cycle transcription was used to examine the role of the cornea in the latency-associated transcript (LAT)-mediated reactivation of HSV type 1 (HSV-1) in the rabbit eye model. The reduced relative reactivation frequency of 17 delta Pst (a LAT- virus) compared to those of wild-type and LAT+ rescuants correlated with reduced levels of viral DNA and transcription in the cornea following epinephrine induction. The timing of virus appearance in the cornea was most consistent with tissue peripheral to the cornea itself mediating a LAT-sensitive step in the reactivation process. Specific results include the following. (i) While viral DNA was found in the corneas of rabbits latently infected with either the LAT+ or LAT- virus prior to and during the first 16 to 24 h following induction, more was found in animals infected with the LAT+ virus. (ii) A significant increase in levels of viral DNA occurred 20 to 168 h following induction. (iii) The average relative amount of viral DNA was lower at all time points following reactivation of animals infected with the LAT- virus. (iv) Expression of productive-cycle transcripts could be detected in corneas of some rabbits latently infected with either the LAT+ or LAT- virus, and the amount recovered and the timing of appearance differed during the reactivation of rabbits latently infected with the LAT+ or LAT- virus. (v) Despite the reduced recoveries of LAT- virus DNA and productive-cycle transcripts in reactivating corneas in vivo compared to those of their LAT+ counterparts, such differences were not detected in cultured keratinocytes or in experiments in which relatively high titers of virus were superinfected into the eyes of latently infected rabbits. (vi) A number of LAT(+)-virus-infected rabbits expressed LAT in corneas isolated from uninduced rabbits. When seen, its amount was significantly higher than that of a productive-cycle (VP5) transcript.
利用聚合酶链反应(PCR)分析单纯疱疹病毒(HSV)基因组复制和生产周期转录,以研究在兔眼模型中角膜在1型单纯疱疹病毒(HSV-1)潜伏相关转录本(LAT)介导的再激活过程中的作用。与野生型和LAT+拯救病毒相比,17 delta Pst(一种LAT缺陷病毒)的相对再激活频率降低,这与肾上腺素诱导后角膜中病毒DNA水平和转录水平降低相关。病毒在角膜中出现的时间与角膜本身周围组织介导再激活过程中LAT敏感步骤最为一致。具体结果如下。(i)在诱导前及诱导后的最初16至24小时内,在潜伏感染LAT+或LAT-病毒的兔角膜中均发现了病毒DNA,但在感染LAT+病毒的动物中发现的更多。(ii)诱导后20至168小时,病毒DNA水平显著增加。(iii)感染LAT-病毒的动物再激活后,在所有时间点病毒DNA的平均相对量均较低。(iv)在一些潜伏感染LAT+或LAT-病毒的兔角膜中可检测到生产周期转录本的表达,在潜伏感染LAT+或LAT-病毒的兔再激活过程中,回收的量和出现的时间有所不同。(v)尽管与LAT+病毒相比,LAT-病毒DNA和生产周期转录本在体内再激活角膜中的回收率降低,但在培养的角质形成细胞中或在将相对高滴度病毒超感染到潜伏感染兔眼中的实验中未检测到此类差异。(vi)一些感染LAT(+)病毒的兔在未诱导兔分离的角膜中表达LAT。当检测到时,其含量显著高于生产周期(VP5)转录本。