Mozar Michael, Claverie Jean-Michel
Structural and Genomic Information Laboratory, UMR 7256 (IMM FR 3479) CNRS Aix-Marseille Université, 163 Avenue de Luminy, Case 934, 13288 Marseille cedex 9, France.
Structural and Genomic Information Laboratory, UMR 7256 (IMM FR 3479) CNRS Aix-Marseille Université, 163 Avenue de Luminy, Case 934, 13288 Marseille cedex 9, France; Assistance Publique des Hopitaux de Marseille. La Timone, 13005 Marseille, France.
Virology. 2014 Oct;466-467:112-22. doi: 10.1016/j.virol.2014.05.013. Epub 2014 Jun 5.
Since the pioneering Global Ocean Sampling project, large-scale sequencing of environmental DNA has become a common approach to assess the biodiversity of diverse environments, with an emphasis on microbial populations: unicellular eukaryotes ("protists"), bacteria, archaea, and their innumerous associated viruses and phages. However, the global analysis of the viral diversity ("the virome") from sequence data is fundamentally hampered by the lack of a universal gene that would allow their unambiguous identification and reliable separation from cellular microorganisms. The problem has been made even more difficult with the discovery of micron-sized giant viruses for which the usual fractionation protocol on a "sterilizing" filter is no longer an option. In the present proof-of-principle work we used actual metagenomic data to show that glutamine-hydrolysing asparagine synthase is a reliable sequence probe to discover new members of the Mimiviridae family, hint at the existence of a new family of large DNA viruses, and point out misidentified database entries.
自开创性的全球海洋采样项目以来,对环境DNA进行大规模测序已成为评估各种环境生物多样性的常用方法,重点是微生物种群:单细胞真核生物(“原生生物”)、细菌、古菌及其无数相关病毒和噬菌体。然而,从序列数据对病毒多样性(“病毒组”)进行全球分析,从根本上受到缺乏通用基因的阻碍,该基因可用于明确识别病毒并将其与细胞微生物可靠分离。随着微米级巨型病毒的发现,这个问题变得更加棘手,因为对于这些病毒,通常在“除菌”滤膜上进行的分级分离方案不再可行。在本原理验证工作中,我们使用实际宏基因组数据表明,谷氨酰胺水解天冬酰胺合成酶是一种可靠的序列探针,可用于发现 Mimiviridae 科的新成员,暗示存在一个新的大型DNA病毒科,并指出数据库中错误识别的条目。