番茄黑环病毒缺陷病毒基因组在宿主间传播过程中的种群动态。

IF 4 2区 医学 Q2 VIROLOGY Journal of Virology Pub Date : 2024-11-19 Epub Date: 2024-10-31 DOI:10.1128/jvi.01244-24
Daria Budzyńska, Julia Minicka, María J Olmo-Uceda, Santiago F Elena, Beata Hasiów-Jaroszewska
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引用次数: 0

摘要

缺陷病毒基因组(DVGs)是在病毒基因组容易出错的复制过程中出现的,包含缺失、插入、基因组重排和高突变。这些大效应突变导致 DVGs 在没有辅助野生型病毒的情况下无法完成感染循环。研究表明,当病毒在同一宿主体内以高感染倍率连续传代时,体外 DVGs 通常会在病毒群中积累。为了研究宿主间传播对体内 DVG 形成和种群动态的影响,我们用番茄黑环病毒(TBRV)进行了进化实验。TBRV依次通过四种不同宿主的组合:藜、烟草、莴苣和菠菜。每隔五次传代就更换宿主。根据 20 次传代后病毒 RNA 测序获得的 RNA-Seq 数据,分析了 DVGs 的多样性和种群动态。我们的研究结果表明,当病毒在不同宿主物种中传代时,有可能产生 TBRV DVGs。不同宿主植物组合中的 DVG 丰度水平各不相同,这微弱地表明宿主物种的过去序列可能在 DVG 的产生中起了作用。TBRV 进化种群中最丰富的 DVG 来自 RNA1。缺失是最常见的一类 DVG,其次是插入。缺失DVG亚群在物种组成上表现出极大的多样性,缺失物种的丰富程度与其丰富程度相关。以小缺失为特征的较长 DVGs 占主导地位,而短于 1,000 个核苷酸的 DVGs 不足 2%:在感染人类、动物和植物的不同病毒物种中,已在体内和体外发现了缺陷病毒基因组(DVGs)。番茄黑环病毒(TBRV)等病毒在宿主体内传递过程中形成缺陷病毒基因组的能力已得到证实。在我们的研究中,我们分析了 TBRV 通过四种不同宿主组合后获得的 RNA-Seq 数据。我们的研究结果表明,不同宿主植物组合的 DVG 丰度水平各不相同。缺失是最常见的一类 DVG,以长的物种为主。此外,还发现了 TBRV 基因组中的保守连接位点,这导致在独立进化的病毒系中产生相同的缺失。总之,我们的研究结果为了解植物病毒 DVGs 的起源和结构提供了重要依据。这些结果将有助于理解病毒进化和宿主与病毒之间的相互作用。
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Population dynamics of defective viral genomes of tomato black ring virus during host-to-host transmission.

Defective viral genomes (DVGs) emerge during error-prone replication of viral genomes and contain deletions, insertions, genomic rearrangements, and hypermutations. These large-effect mutations result in the inability of DVGs to complete an infectious cycle in the absence of a helper wild-type virus. It has been shown that in vitro DVGs usually accumulate in viral populations when a virus is serially passaged in the same host at a high multiplicity of infection. To investigate the impact of host-to-host transmission on DVG formation and population dynamics in vivo, we conducted evolution experiments with tomato black ring virus (TBRV). TBRV was sequentially passaged through a combination of four distinct host species: quinoa, tobacco, lettuce, and spinach. The host was changed every fifth passage. The diversity and population dynamics of DVGs were analyzed based on the RNA-Seq data obtained through sequencing of viral RNA after 20 passages. Our findings indicate the possibility of TBRV DVGs generation when the virus was passaged through different host species. The level of DVG abundance varied across host plant combinations, with a weak indication that the host species past sequence may play a role in DVGs generation. Most abundant DVGs in the TBRV evolved populations were derived from RNA1. Deletions were the most prevalent class of DVGs, followed by insertions. The deletion DVG subpopulation exhibited substantial diversity in species composition and the richness of the deletions species was correlated with their abundance. Longer DVGs characterized by small deletions were predominant, whereas those shorter than 1,000 nucleotides constituted less than 2%.

Importance: Defective viral genomes (DVGs) have been identified in vivo and in vitro for different virus species infecting humans, animals, and plants. The ability to form DVGs during the passaging of virus in one host has been demonstrated, i.e., for tomato black ring virus (TBRV). In our research, RNA-Seq data obtained after TBRV passaging through a combination of four distinct host species were analyzed. Our results indicate that the level of DVG abundance varied across host plant combinations. Deletions were the most prevalent class of DVGs, with the domination of longer species. Additionally, the conserved junction sites in the TBRV genome were identified, resulting in the generation of identical deletions in independently evolved viral lineages. In summary, our findings provide significant insights into the origin and structure of DVGs of plant viruses. The obtained results will help in understanding viral evolution and host-virus interactions.

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来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
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