Colson Philippe, La Scola Bernard, Levasseur Anthony, Caetano-Anollés Gustavo, Raoult Didier
Unité de Recherche sur les Maladies Infectieuses et Tropicales Emergentes (URMITE), Aix-Marseille University, UM63, CNRS 7278, IRD 198, INSERM 1095, Institut Hospitalo-Universitaire (IHU) - Méditerranée Infection, AP-HM, 19-21 Boulevard Jean Moulin, 13385 Marseille, France.
Evolutionary Bioinformatics Laboratory, Department of Crop Sciences, University of Illinois, 332 National Soybean Research Center, 1101 West Peabody Drive, Urbana, Illinois 61801, USA.
Nat Rev Microbiol. 2017 Apr;15(4):243-254. doi: 10.1038/nrmicro.2016.197. Epub 2017 Feb 27.
The accidental discovery of the giant virus of amoeba - Acanthamoeba polyphaga mimivirus (APMV; more commonly known as mimivirus) - in 2003 changed the field of virology. Viruses were previously defined by their submicroscopic size, which probably prevented the search for giant viruses, which are visible by light microscopy. Extended studies of giant viruses of amoebae revealed that they have genetic, proteomic and structural complexities that were not thought to exist among viruses and that are comparable to those of bacteria, archaea and small eukaryotes. The giant virus particles contain mRNA and more than 100 proteins, they have gene repertoires that are broader than those of other viruses and, notably, some encode translation components. The infection cycles of giant viruses of amoebae involve virus entry by amoebal phagocytosis and replication in viral factories. In addition, mimiviruses are infected by virophages, defend against them through the mimivirus virophage resistance element (MIMIVIRE) system and have a unique mobilome. Overall, giant viruses of amoebae, including mimiviruses, marseilleviruses, pandoraviruses, pithoviruses, faustoviruses and molliviruses, challenge the definition and classification of viruses, and have increasingly been detected in humans.
2003年,变形虫巨型病毒——多噬棘阿米巴巨型病毒(APMV;通常称为米米病毒)的意外发现改变了病毒学领域。病毒以前是根据其亚微观大小来定义的,这可能阻碍了对巨型病毒的寻找,而巨型病毒在光学显微镜下是可见的。对变形虫巨型病毒的深入研究表明,它们具有遗传、蛋白质组和结构复杂性,这些复杂性在病毒中被认为不存在,并且与细菌、古细菌和小型真核生物的复杂性相当。巨型病毒颗粒含有信使核糖核酸(mRNA)和100多种蛋白质,它们的基因库比其他病毒的更广泛,值得注意的是,有些还编码翻译成分。变形虫巨型病毒的感染周期包括通过变形虫吞噬作用进入病毒以及在病毒工厂中进行复制。此外,米米病毒会被噬病毒体感染,通过米米病毒噬病毒体抗性元件(MIMIVIRE)系统抵御它们,并且拥有独特的可移动基因组。总体而言,包括米米病毒、马赛病毒、潘多拉病毒、髓病毒、法斯托病毒和莫利病毒在内的变形虫巨型病毒对病毒的定义和分类提出了挑战,并且在人类中越来越多地被检测到。