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在缺乏I型干扰素的情况下,单纯疱疹病毒1型潜伏相关转录物增加γ34.5的表达并提高感染小鼠的死亡率。

In the Absence of Type-1 IFN, HSV-1 LAT Increases γ34.5 Expression and Enhances Mortality in Infected Mice.

作者信息

Oh Jay J, Jaggi Ujjaldeep, Arya Deepak, Wang Shaohui, Ghiasi Homayon

机构信息

Center for Neurobiology and Vaccine Development, Ophthalmology Research, Department of Surgery, Cedars-Sinai Burns & Allen Research Institute, CSMC-SSB3, 8700 Beverly Blvd., Los Angeles, CA 90048, USA.

出版信息

Viruses. 2025 Jul 29;17(8):1061. doi: 10.3390/v17081061.

Abstract

Type-I Interferon (IFN) is essential for antiviral immunity in both mice and humans; thus, we investigated whether LAT affects HSV-1 infectivity in the absence of IFN by infecting IFNαβR and wild-type control mice with HSV-1 McKrae (LAT-plus) and dLAT2903 (LAT-minus) viruses. IFNαβR mice survived ocular infection with the LAT-plus virus, while no infected mice survived infection with the LAT-minus virus. Increased death in infected mice correlated with a higher expression in the neurovirulence γ34.5 gene but not with gB expression. To determine the region of LAT that contributed to higher mortality, IFNαβR mice were infected with recombinant viruses expressing the first 1.5 kb or the first 811bp region of 1.5 kb LAT. Similar to LAT-plus infected mice, IFNαβR mice infected with LAT1.5kb were protected from death, while infection with the LAT811bp virus was similar to that of LAT-minus, suggesting that increased pathogenicity in the absence of LAT depends on the second half of 1.5 kb LAT. To confirm the in vivo upregulation of γ34.5 expression in the absence of LAT, rabbit skin and Neuro2A cells were infected with LAT-plus, LAT-minus, LAT1.5kb, or LAT811bp viruses. γ34.5 expression was significantly higher in LAT-minus- and LAT811bp-infected rabbit skin cells and Neuro2A cells than in LAT-plus- and LAT1.5kb-infected cells, suggesting that sequences after the 811bp of LAT contribute to γ34.5 upregulation. However, except for γ34.5 expression, ICP0, ICP4, and gB expression were not affected by the absence of LAT or truncated forms of LAT. To confirm that higher γ34.5 expression contributes to higher mortality in the absence of LAT, we infected IFNαβR mice with a recombinant virus lacking LAT and γ34.5 expression, and, in contrast to LAT-minus, all infected mice survived. Our results suggest that LAT controls γ34.5 expression and that higher γ34.5 expression and mortality in infected mice are associated with the second half of 1.5 kb LAT.

摘要

I型干扰素(IFN)对于小鼠和人类的抗病毒免疫至关重要;因此,我们通过用单纯疱疹病毒1型McKrae(LAT阳性)和dLAT2903(LAT阴性)病毒感染IFNαβR小鼠和野生型对照小鼠,研究了在没有IFN的情况下LAT是否会影响单纯疱疹病毒1型(HSV-1)的感染性。IFNαβR小鼠在眼部感染LAT阳性病毒后存活下来,而没有感染小鼠在感染LAT阴性病毒后存活。感染小鼠中死亡率增加与神经毒力γ34.5基因的较高表达相关,但与gB表达无关。为了确定LAT中导致较高死亡率的区域,用表达1.5 kb LAT的前1.5 kb或前811 bp区域的重组病毒感染IFNαβR小鼠。与感染LAT阳性的小鼠相似,感染LAT1.5kb的IFNαβR小鼠免受死亡,而感染LAT811bp病毒的情况与感染LAT阴性的情况相似,这表明在没有LAT的情况下致病性增加取决于1.5 kb LAT的后半部分。为了证实LAT缺失时γ34.5表达在体内的上调,用LAT阳性、LAT阴性、LAT1.5kb或LAT811bp病毒感染兔皮肤和Neuro2A细胞。在感染LAT阴性和LAT811bp的兔皮肤细胞和Neuro2A细胞中,γ34.5表达明显高于感染LAT阳性和LAT1.5kb的细胞,这表明LAT 811bp之后的序列有助于γ34.5上调。然而,除了γ34.5表达外,ICP0、ICP4和gB表达不受LAT缺失或LAT截短形式的影响。为了证实较高的γ34.5表达在LAT缺失时导致较高的死亡率,我们用一种缺乏LAT和γ34.5表达的重组病毒感染IFNαβR小鼠,与感染LAT阴性的情况相反,所有感染小鼠都存活了下来。我们的结果表明,LAT控制γ34.5表达,并且感染小鼠中较高的γ34.5表达和死亡率与1.5 kb LAT的后半部分相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65e8/12390724/83da140df78c/viruses-17-01061-g001a.jpg

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