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关于在人类细胞中观察到的异常类米米病毒结构的问题。

Questions on unusual Mimivirus-like structures observed in human cells.

作者信息

Lusi Elena Angela, Maloney Dan, Caicci Federico, Guarascio Paolo

机构信息

St Vincent Health Care Group, University College of Dublin, Dublin 4, Ireland.

Bioinformatics Solutions Inc., Waterloo, ON, N2L 6J2, Canada.

出版信息

F1000Res. 2017 Mar 14;6:262. doi: 10.12688/f1000research.11007.1. eCollection 2017.

DOI:10.12688/f1000research.11007.1
PMID:28663783
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5473404/
Abstract

Mimiviruses or giant viruses that infect amoebas have the ability to retain the Gram stain, which is usually used to colour bacteria. There is some evidence suggesting that Mimiviruses can also infect human cells. Guided by these premises, we performed a routine Gram stain on a variety of human specimens to see if we could detect the same Gram positive blue granules that identify Mimiviruses in the amoebas.  We analysed 24 different human specimens (liver, brain, kidney, lymph node and ovary) using Gram stain histochemistry, electron microscopy immunogold, high resolution mass spectrometry and protein identification.  We detected in the human cells Gram positive granules that were distinct from bacteria. The fine blue granules displayed the same pattern of the Gram positive granules that diagnose Mimiviruses in the cytoplasm of the amoebas. Electron microscopy confirmed the presence of human Mimiviruses-like structures and mass spectrometry identified histone H4 peptides, which had the same footprints as giant viruses. However, some differences were noted: the Mimivirus-like structures identified in the human cells were ubiquitous and manifested a distinct mammalian retroviral antigenicity.  Our main hypotheses are that the structures could be either giant viruses having a retroviral antigenicity or ancestral cellular components having a viral origin. However, other possible alternatives have been proposed to explain the nature and function of the newly identified structures.

摘要

感染变形虫的拟菌病毒或巨型病毒能够保留革兰氏染色,而革兰氏染色通常用于给细菌染色。有一些证据表明拟菌病毒也能感染人类细胞。基于这些前提,我们对各种人类标本进行了常规革兰氏染色,以查看是否能检测到与在变形虫中识别拟菌病毒相同的革兰氏阳性蓝色颗粒。我们使用革兰氏染色组织化学、电子显微镜免疫金法、高分辨率质谱法和蛋白质鉴定法分析了24种不同的人类标本(肝脏、大脑、肾脏、淋巴结和卵巢)。我们在人类细胞中检测到了与细菌不同的革兰氏阳性颗粒。这些细小的蓝色颗粒呈现出与在变形虫细胞质中诊断拟菌病毒的革兰氏阳性颗粒相同的模式。电子显微镜证实了人类中存在类似拟菌病毒的结构,质谱法鉴定出了组蛋白H4肽,其特征与巨型病毒相同。然而,也注意到了一些差异:在人类细胞中鉴定出的类似拟菌病毒的结构普遍存在,并表现出独特的哺乳动物逆转录病毒抗原性。我们的主要假设是,这些结构可能要么是具有逆转录病毒抗原性的巨型病毒,要么是具有病毒起源的原始细胞成分。然而,也有人提出了其他可能的解释来阐述新鉴定结构的性质和功能。

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本文引用的文献

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Marseillevirus in lymphoma: a giant in the lymph node.马塞利亚病毒与淋巴瘤:淋巴结中的巨无霸
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The role of giant viruses of amoebas in humans.变形虫巨型病毒在人类中的作用。
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Evolution of viruses and cells: do we need a fourth domain of life to explain the origin of eukaryotes?病毒与细胞的演化:我们是否需要生命的第四个域来解释真核生物的起源?
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Histone chaperones link histone nuclear import and chromatin assembly.组蛋白伴侣将组蛋白核输入与染色质组装联系起来。
Biochim Biophys Acta. 2013 Mar-Apr;1819(3-4):277-89.
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All roads lead to chromatin: multiple pathways for histone deposition.条条大路通染色质:组蛋白沉积的多种途径。
Biochim Biophys Acta. 2013 Mar-Apr;1819(3-4):238-46.
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Giant viruses of amoebae as potential human pathogens.原生动物巨型病毒可能成为人类病原体。
Intervirology. 2013;56(6):376-85. doi: 10.1159/000354558. Epub 2013 Oct 17.
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Orphan viruses, orphan diseases: still the raw material for virus discovery.孤儿病毒、罕见病:依然是病毒发现的素材
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