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多瘤病毒的生物学、进化及医学重要性:最新进展

Biology, evolution, and medical importance of polyomaviruses: An update.

作者信息

Moens Ugo, Krumbholz Andi, Ehlers Bernhard, Zell Roland, Johne Reimar, Calvignac-Spencer Sébastien, Lauber Chris

机构信息

Department of Medical Biology, Faculty of Health Sciences, University of Tromsø, 9037 Tromsø, Norway.

Institute of Infection Medicine, University of Kiel and University Hospital Schleswig Holstein, Brunswiker Strasse 4, 24105 Kiel, Germany.

出版信息

Infect Genet Evol. 2017 Oct;54:18-38. doi: 10.1016/j.meegid.2017.06.011. Epub 2017 Jun 17.

Abstract

The family Polyomaviridae encompasses non-enveloped viruses with a circular dsDNA genome that is typically approximately 5000bp in length. Originally isolated from mammals, polyomavirus sequences have now been detected in invertebrates, fish, amphibians, reptiles and birds, although it remains to be determined whether all these animals are genuine hosts. The genomes of all polyomaviruses encode at least two regulatory proteins (large and small tumour antigen) and two structural proteins (capsid proteins VP1 and VP2) whose functions have been defined. The large and small tumour antigens have domains conserved among the polyomaviruses, which are responsible for specific interactions with cellular proteins and may result in alteration of the cell cycle. Additional open reading frames (ORFs) are present in the genomes of the different polyomavirus species. Some of these ORFs are transcribed and translated in viral proteins, but their functions remain poorly understood. Polyomaviruses have a restricted host specificity. This may indicate that co-divergence with their hosts, which has been demonstrated in a few cases, was an important factor during polyomavirus diversification. However, a strict co-divergence scenario fails to explain family-wide patterns of diversity, suggesting an important contribution of lineage duplication and, possibly to a lesser extent, recombination and cross-species transmission. Polyomaviruses are pathogens that can cause various malignant and non-malignant diseases in birds and mammals, including humans, but so far they have not been linked to disease in lower vertebrates. In immunosuppressed individuals, reactivation of polyomavirus BK or JC can cause serious disease of the urogenital tract and brain, respectively, while Merkel cell polyomavirus is most probably associated with the development of a highly aggressive neuroendocrine skin tumour in elderly or patients with pre-existing conditions. This review provides an update on the life cycle, prevalence, disease association, and evolution of the viruses belonging to this family.

摘要

多瘤病毒科包含无包膜病毒,其基因组为环状双链DNA,长度通常约为5000碱基对。多瘤病毒最初是从哺乳动物中分离出来的,现在在无脊椎动物、鱼类、两栖动物、爬行动物和鸟类中也检测到了多瘤病毒序列,不过这些动物是否都是真正的宿主仍有待确定。所有多瘤病毒的基因组都编码至少两种调节蛋白(大肿瘤抗原和小肿瘤抗原)和两种结构蛋白(衣壳蛋白VP1和VP2),其功能已得到明确。大肿瘤抗原和小肿瘤抗原具有在多瘤病毒中保守的结构域,这些结构域负责与细胞蛋白的特异性相互作用,并可能导致细胞周期的改变。不同多瘤病毒种类的基因组中还存在其他开放阅读框(ORF)。其中一些ORF转录并翻译为病毒蛋白,但其功能仍知之甚少。多瘤病毒具有有限的宿主特异性。这可能表明,在少数情况下已得到证实的与宿主的共同分化,是多瘤病毒多样化过程中的一个重要因素。然而,严格的共同分化情况无法解释全家族的多样性模式,这表明谱系重复以及可能在较小程度上的重组和跨物种传播起到了重要作用。多瘤病毒是病原体,可在鸟类和哺乳动物(包括人类)中引起各种恶性和非恶性疾病,但到目前为止,它们尚未与低等脊椎动物的疾病相关联。在免疫抑制个体中,多瘤病毒BK或JC的重新激活可分别导致泌尿生殖道和脑部的严重疾病,而默克尔细胞多瘤病毒很可能与老年人或已有疾病患者中高度侵袭性神经内分泌皮肤肿瘤的发生有关。本综述提供了关于该病毒科病毒的生命周期、流行情况、疾病关联和进化的最新信息。

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