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与ICP34.5基因共线的单纯疱疹病毒1型LAT基因区域不参与自发再激活。

The region of the herpes simplex virus type 1 LAT gene that is colinear with the ICP34.5 gene is not involved in spontaneous reactivation.

作者信息

Perng G C, Chokephaibulkit K, Thompson R L, Sawtell N M, Slanina S M, Ghiasi H, Nesburn A B, Wechsler S L

机构信息

Ophthalmology Research Laboratories, Cedars-Sinai Medical Center Research Institute, Los Angeles, California 90048, USA.

出版信息

J Virol. 1996 Jan;70(1):282-91. doi: 10.1128/JVI.70.1.282-291.1996.

Abstract

The goal of this report was to determine if the region of the LAT gene that is colinear with ICP34.5 (kb 6.2 to 7.1 of LAT) is involved in spontaneous reactivation of herpes simplex virus type 1. We inserted one copy of the ICP34.5 gene into the unique long region of a herpes simplex virus type 1 (strain McKrae) mutant lacking both copies of ICP34.5 (one in each viral long repeat) and the corresponding 917-nucleotide colinear portion of LAT (kb 6.2 to 7.1). Rabbits were ocularly infected with this mutant, and spontaneous reactivation relative to that for the wild-type virus and the original mutant was measured. As we previously reported, the original ICP34.5-deleted virus (d34.5) was significantly impaired for spontaneous reactivation and virulence (G. C. Perng, R. L. Thompson, N. M. Sawtell, W. E. Taylor, S. M. Slanina, H. Ghiasi, R. Kaiwar, A. B. Nesburn, and S. L. Wechsler, J. Virol. 69:3033-3041, 1995). In contrast, we report here that restoration of one copy of ICP34.5 at a distant location completely restored the wild-type level of in vivo spontaneous reactivation, despite retention of the deletion in LAT (spontaneous reactivation rate = 0.3 to 1.4% for the ICP34.5 deletion mutant, 7.7 to 19.6% for the wild type, and 9 to 16.1% for virus with one copy of ICP34.5). Thus, the 917-nucleotide region of LAT from kb 6.2 to 7.1 was not involved in the LAT function required for wild-type spontaneous reactivation. We also found that restoration of a single ICP34.5 gene in a novel location did not restore wild-type virulence (rabbit death rate = 0% [0 of 15] for the original ICP34.5 deletion mutant, 8% [2 of 24] for the single-copy IPC34.5 virus, and 52% [14 of 27] for wild-type virus; P < 0.001 for one versus two copies of ICP34.5). It is likely that either two gene doses of ICP34.5 or its location in the long repeat is essential for full functionality of ICP34.5's virulence function. Furthermore, the ability of the single-copy ICP34.5 virus to reactivate at wild-type levels despite being significantly less virulent than wild-type virus separates the spontaneous reactivation phenotype from the virulence phenotype.

摘要

本报告的目的是确定LAT基因中与ICP34.5共线的区域(LAT的6.2至7.1 kb)是否参与单纯疱疹病毒1型的自发再激活。我们将一份ICP34.5基因插入到一株单纯疱疹病毒1型(McKrae株)突变体的独特长区域,该突变体缺失了两份ICP34.5(分别位于每个病毒长重复序列中)以及LAT相应的917个核苷酸的共线部分(6.2至7.1 kb)。用该突变体对兔子进行眼内感染,并测量相对于野生型病毒和原始突变体的自发再激活情况。正如我们之前所报道的,原始的缺失ICP34.5的病毒(d34.5)在自发再激活和毒力方面显著受损(G.C.Perng、R.L.Thompson、N.M.Sawtell、W.E.Taylor、S.M.Slanina、H.Ghiasi、R.Kaiwar、A.B.Nesburn和S.L.Wechsler,《病毒学杂志》69:3033 - 3041,1995年)。相比之下,我们在此报告,尽管LAT中仍保留缺失部分,但在一个较远位置恢复一份ICP34.5基因可完全恢复体内自发再激活的野生型水平(ICP34.5缺失突变体的自发再激活率为0.3%至1.4%,野生型为7.7%至19.6%,带有一份ICP34.5基因的病毒为9%至16.1%)。因此,LAT从6.2至7.1 kb的917个核苷酸区域不参与野生型自发再激活所需的LAT功能。我们还发现,在一个新位置恢复单个ICP34.5基因并不能恢复野生型毒力(原始ICP34.5缺失突变体的兔子死亡率为0%[15只中0只死亡],单拷贝ICP34.5病毒为8%[24只中2只死亡],野生型病毒为52%[27只中14只死亡];一份与两份ICP34.5基因相比,P<0.001)。很可能两份剂量的ICP34.5基因或其在长重复序列中的位置对于ICP34.5毒力功能的完全发挥至关重要。此外,单拷贝ICP34.5病毒尽管毒力明显低于野生型病毒,但仍能以野生型水平进行再激活,这将自发再激活表型与毒力表型区分开来。

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