Coevolutionary and Phylogenetic Analysis of Mimiviral Replication Machinery Suggest the Cellular Origin of Mimiviruses. (11th February 2021)

• Record Type: Journal Article
• Authors: Patil, Supriya; Kondabagil, Kiran
• Editors: Hepp, Crystal
• Is Part Of: Molecular biology and evolution. Volume 38:Number 5(2021)
• Page Start: 2014
• Page End: 2029
• Publication Date: 2021-02-11
• Subjects: DNA replication -- Mimivirus -- giant viruses -- evolution -- phylogenetic -- correlation analysis -- MDS -- coevolution -- HGT -- evolutionary selection -- purifying selection -- phylogenetic trees -- NCLDVs -- HGT -- LUCA -- LUCELLA; Molecular biology -- Periodicals; Molecular evolution -- Periodicals; Evolution, Molecular -- Periodicals; Molecular Biology -- Periodicals; 572.8
• DOI: 10.1093/molbev/msab003
• Languages: English
• ISSNs: 0737-4038

Abstract

Abstract: Mimivirus is one of the most complex and largest viruses known. The origin and evolution of Mimivirus and other giant viruses have been a subject of intense study in the last two decades. The two prevailing hypotheses on the origin of Mimivirus and other viruses are the reduction hypothesis, which posits that viruses emerged from modern unicellular organisms; whereas the virus-first hypothesis proposes viruses as relics of precellular forms of life. In this study, to gain insights into the origin of Mimivirus, we have carried out extensive phylogenetic, correlation, and multidimensional scaling analyses of the putative proteins involved in the replication of its 1.2-Mb large genome. Correlation analysis and multidimensional scaling methods were validated using bacteriophage, bacteria, archaea, and eukaryotic replication proteins before applying to Mimivirus. We show that a large fraction of mimiviral replication proteins, including polymerase B, clamp, and clamp loaders are of eukaryotic origin and are coevolving. Although phylogenetic analysis places some components along the lineages of phage and bacteria, we show that all the replication-related genes have been homogenized and are under purifying selection. Collectively our analysis supports the idea that Mimivirus originated from a complex cellular ancestor. We hypothesize that Mimivirus has largely retained complex replication machinery reminiscent of its progenitor while losing most of the other genes related to processes such as metabolism and translation.