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在患有进行性多灶性白质脑炎和脑膜脑炎的 SIV 感染猕猴中,神经元经常被 SV40 病毒感染。

Frequent infection of neurons by SV40 virus in SIV-infected macaque monkeys with progressive multifocal leukoencephalopathy and meningoencephalitis.

机构信息

Department of Comparative Pathology, New England Primate Research Center, Harvard Medical School, Southborough, Massachusetts.

Division of NeuroVirology, Department of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts.

出版信息

Am J Pathol. 2013 Dec;183(6):1910-1917. doi: 10.1016/j.ajpath.2013.08.007. Epub 2013 Oct 1.

Abstract

Simian virus 40 (SV40), family Polyomaviridae, in immunocompromised macaques can cause fatal demyelinating central nervous system disease analogous to progressive multifocal leukoencephalopathy caused by John Cunningham (JC) virus in immunocompromised humans. Recently, we have demonstrated that JC virus can infect cerebellar granule cell neurons and cortical pyramidal neurons in immunosuppressed people. To examine whether SV40 neuronal infection occurs spontaneously in immunosuppressed macaques, we analyzed archival brain specimens from 20 simian immunodeficiency virus-infected rhesus with AIDS and 1 cynomolgus post-transplant selected with SV40 brain infection from archival records from 1991 to 2012. In addition to white matter SV40 distribution in classic demyelinating progressive multifocal leukoencephalopathy, some of the 21 monkeys exhibited meningeal, subpial neocortical, and periventricular virus. This distribution pattern corresponded to broader viral tropism with neuronal infection in 14 (66.7%) of 21 cases. In all 14 cases, identified neurons were positive for early SV40 transcript large T antigen, but only 4 of the 14 cases exhibited late viral transcript viral protein 1-positive neurons. SV40-infected neurons were detected in frontal, parietal, occipital, and temporal cortices, hippocampus, thalamus, and brain stem. These observations confirm that spontaneous SV40 neuronal infection occurs in immunosuppressed macaques, which parallels JC virus-neuronal infection in immunosuppressed patients. Neuronal infection may be an important aspect of both SV40 and JC virus neuropathogenesis in their respective hosts.

摘要

猿猴病毒 40(SV40),多瘤病毒科,在免疫功能低下的猕猴中可引起致命的脱髓鞘中枢神经系统疾病,类似于免疫功能低下的人类中由约翰·坎宁安(JC)病毒引起的进行性多灶性白质脑炎。最近,我们已经证明 JC 病毒可以感染免疫抑制人群中的小脑颗粒神经元和皮质锥体细胞。为了研究 SV40 神经元感染是否会在免疫抑制的猕猴中自发发生,我们分析了 20 只感染猿猴免疫缺陷病毒(SIV)的恒河猴的存档脑组织样本,这些猴子患有艾滋病,以及 1 只从 1991 年至 2012 年的存档记录中选择的患有 SV40 脑感染的食蟹猴。除了经典脱髓鞘进行性多灶性白质脑炎中的白质 SV40 分布外,21 只猴子中的一些还表现出脑膜、皮层下和脑室周围的病毒。这种分布模式与更广泛的病毒嗜性相对应,在 21 例中的 14 例(66.7%)中观察到神经元感染。在所有 14 例中,鉴定出的神经元均为早期 SV40 转录物大 T 抗原阳性,但只有 14 例中的 4 例表现出晚期病毒转录物病毒蛋白 1 阳性神经元。SV40 感染的神经元在额、顶、枕和颞叶皮质、海马体、丘脑和脑干中被检测到。这些观察结果证实,SV40 神经元感染会在免疫抑制的猕猴中自发发生,这与免疫抑制患者中的 JC 病毒-神经元感染相平行。神经元感染可能是 SV40 和 JC 病毒在各自宿主中的神经发病机制的一个重要方面。

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