Lineage-specific expansions of polinton-like viruses in photosynthetic cryptophytes.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Paul-Adrian Bulzu, Helena Henriques Vieira, Rohit Ghai
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引用次数: 0

Abstract

Background: Polinton-like viruses (PLVs) are diverse eukaryotic DNA viral elements (14-40 kb) that often undergo significant expansion within protist genomes through repeated insertion events. Emerging evidence indicates they function as antiviral defense systems in protists, reducing the progeny yield of their infecting giant viruses (phylum Nucleocytoviricota) and influencing the population dynamics and evolution of both viruses and their hosts. While many PLVs have been identified within the genomes of sequenced protists, most were recovered from metagenomic data. Even with the large number of PLVs identified from metagenomic data, their host-virus linkages remain unknown owing to the scarcity of ecologically relevant protist genomes. Additionally, the extent of PLV diversification within abundant freshwater taxa remains undetermined. In order to tackle these questions, high-quality genomes of abundant and representative taxa that bridge genomic and metagenomic PLVs are necessary. In this regard, cryptophytes, which are among the most widely distributed, abundant organisms in freshwaters and have remained largely out of bounds of genomic and metagenomic approaches, are ideal candidates for investigating the diversification of such viral elements both in cellular and environmental context.

Results: We leveraged long-read sequencing to recover large (200-600 Mb), high-quality, and highly repetitive (> 60%) genomes of representative freshwater and marine photosynthetic cryptophytes. We uncovered over a thousand complete PLVs within these genomes, revealing vast lineage-specific expansions, particularly in the common freshwater cryptophyte Rhodomonas lacustris. By combining deep sequence homology annotation with biological network analyses, we discern well-defined PLV groups defined by characteristic gene-sharing patterns and the use of distinct strategies for replication and integration within host genomes. Finally, the PLVs recovered from these cryptophyte genomes also allow us to assign host-virus linkages in environmental sequencing data.

Conclusions: Our findings provide a primer for understanding the evolutionary history, gene content, modes of replication and infection strategies of cryptophyte PLVs, with special emphasis on their expansion as endogenous viral elements (EVEs) in freshwater bloom-forming R. lacustris. Video Abstract.

光合隐生植物中花粉样病毒的谱系特异性扩增。
背景:波林顿样病毒(Polinton-like virus, PLVs)是多种真核生物DNA病毒元件(14-40 kb),通常通过重复插入事件在原生生物基因组中进行显著扩增。新出现的证据表明,它们在原生生物中起抗病毒防御系统的作用,降低其感染的巨型病毒(核细胞病毒门)的后代产量,并影响病毒及其宿主的种群动态和进化。虽然许多plv已经在测序的原生生物的基因组中被鉴定出来,但大多数是从宏基因组数据中恢复的。即使从宏基因组数据中鉴定出大量plv,由于缺乏生态相关的原生生物基因组,它们与宿主-病毒的联系仍然未知。此外,在丰富的淡水类群中,PLV的多样化程度仍不确定。为了解决这些问题,需要大量的、有代表性的类群的高质量基因组,作为基因组和宏基因组plv的桥梁。在这方面,作为淡水中分布最广泛、数量最多的生物之一,隐生植物在很大程度上超出了基因组学和宏基因组学方法的范围,是研究这些病毒成分在细胞和环境背景下多样化的理想候选者。结果:我们利用长读测序恢复了代表性淡水和海洋光合隐生植物的大(200- 600mb)、高质量和高重复(bbb60 %)基因组。我们在这些基因组中发现了超过1000个完整的plv,揭示了巨大的谱系特异性扩展,特别是在常见的淡水隐生植物湖红单胞菌中。通过将深度序列同源性注释与生物网络分析相结合,我们识别出定义良好的PLV群体,这些群体由特征基因共享模式定义,并使用不同的策略在宿主基因组中进行复制和整合。最后,从这些隐生植物基因组中恢复的plv也允许我们在环境测序数据中分配宿主-病毒联系。结论:我们的研究结果为了解隐生plv的进化历史、基因含量、复制模式和感染策略提供了基础,特别强调了它们作为内源性病毒元件(EVEs)在淡水湖泊水华形成中的扩展。视频摘要。
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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