Anamica Bedi de Silva, Shawn W Polson, Christopher R Schvarcz, Grieg F Steward, Kyle F Edwards
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Three of the viruses form a clade that is adjacent to previously sequenced <i>Micromonas</i> viruses, while the fourth virus is relatively divergent from previously sequenced prasinoviruses. We identified 61 putative genes not previously found in prasinovirus isolates, including a phosphate transporter and a potential apoptosis inhibitor novel to marine viruses. Forty-eight genes in the new viruses are also found in host genome(s) and may have been acquired through horizontal gene transfer. By analyzing the coding sequences of all published prasinoviruses, we found that ~25% of prasinovirus gene content is significantly correlated with host genus identity (i.e., <i>Micromonas</i>, <i>Ostreococcus</i>, or <i>Bathycoccus</i>), and the functions of these genes suggest that much of the viral life cycle is differentially adapted to the three host genera. 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引用次数: 0
摘要
感染浮游植物的病毒是海洋生态系统不可分割的一部分,但绝大多数病毒多样性仍未得到培育。在这里,我们引入了感染广泛存在的海洋微真核生物小单胞菌(Micromonas commoda)的四个近乎完整的病毒基因组组装,使报道的小单胞菌dsDNA病毒基因组数量增加了一倍。所有的宿主和病毒分离物都是从北太平洋的热带水域获得的,这是第一次发现感染绿藻类的病毒。新分离株的基因组长度在205 ~ 212 kb之间,系统发育分析表明这4株都属于Prasinovirus属。其中三种病毒形成一个分支,与先前测序的小单胞菌病毒相邻,而第四种病毒与先前测序的prasinovirus相对不同。我们鉴定了61个先前未在prasinovirus分离物中发现的假定基因,包括一个磷酸盐转运蛋白和一个海洋病毒新发现的潜在细胞凋亡抑制剂。新病毒中的48个基因也在宿主基因组中发现,可能是通过水平基因转移获得的。通过分析所有已发表的prasinovirus的编码序列,我们发现~25%的prasinovirus基因含量与宿主属(即Micromonas, Ostreococcus, or Bathycoccus)的身份显著相关,这些基因的功能表明病毒生命周期的大部分是不同地适应三种宿主属的。从全球调查数据中绘制的宏基因组图谱显示,其中一种新分离株McV-SA1在多个海洋盆地中相对常见。这里分析的基因组代表了第一批来自热带北太平洋的病毒,这些病毒感染了丰富的浮游植物目。比较来自同一地点的分离株表明,共同发生并可能竞争宿主的病毒之间具有高度的基因组多样性。比较所有已发表的prasinovirus基因组,突出了可能与适应不同宿主属相关的基因功能。宏基因组数据表明,这些病毒是全球分布的,其中一种新分离株可能是最丰富的海洋病毒之一。
Genomic diversity and global distribution of four new prasinoviruses from the tropical north Pacific.
Viruses that infect phytoplankton are an integral part of marine ecosystems, but the vast majority of viral diversity remains uncultivated. Here, we introduce four near-complete genomic assemblies of viruses that infect the widespread marine picoeukaryote Micromonas commoda, doubling the number of reported genomes of Micromonas dsDNA viruses. All host and virus isolates were obtained from tropical waters of the North Pacific, a first for viruses infecting green algae in the order Mamiellales. Genome length of the new isolates ranges from 205 to 212 kb, and phylogenetic analysis shows that all four are members of the genus Prasinovirus. Three of the viruses form a clade that is adjacent to previously sequenced Micromonas viruses, while the fourth virus is relatively divergent from previously sequenced prasinoviruses. We identified 61 putative genes not previously found in prasinovirus isolates, including a phosphate transporter and a potential apoptosis inhibitor novel to marine viruses. Forty-eight genes in the new viruses are also found in host genome(s) and may have been acquired through horizontal gene transfer. By analyzing the coding sequences of all published prasinoviruses, we found that ~25% of prasinovirus gene content is significantly correlated with host genus identity (i.e., Micromonas, Ostreococcus, or Bathycoccus), and the functions of these genes suggest that much of the viral life cycle is differentially adapted to the three host genera. Mapping of metagenomic reads from global survey data indicates that one of the new isolates, McV-SA1, is relatively common in multiple ocean basins.IMPORTANCEThe genomes analyzed here represent the first viruses from the tropical North Pacific that infect the abundant phytoplankton order Mamiellales. Comparing isolates from the same location demonstrates high genomic diversity among viruses that co-occur and presumably compete for hosts. Comparing all published prasinovirus genomes highlights gene functions that are likely associated with adaptation to different host genera. Metagenomic data indicate these viruses are globally distributed, and one of the novel isolates may be among the most abundant marine viruses.
期刊介绍:
Microbiology Spectrum publishes commissioned review articles on topics in microbiology representing ten content areas: Archaea; Food Microbiology; Bacterial Genetics, Cell Biology, and Physiology; Clinical Microbiology; Environmental Microbiology and Ecology; Eukaryotic Microbes; Genomics, Computational, and Synthetic Microbiology; Immunology; Pathogenesis; and Virology. Reviews are interrelated, with each review linking to other related content. A large board of Microbiology Spectrum editors aids in the development of topics for potential reviews and in the identification of an editor, or editors, who shepherd each collection.