Department of Virology and Bacteriology, Institute of Plant Protection-National Research Institute, Poznan, Poland.
Instituto de Biología Integrativa de Sistemas (I2SysBio), CSIC-Universitat de València, Valencia, Spain.
J Virol. 2024 Nov 19;98(11):e0124424. doi: 10.1128/jvi.01244-24. Epub 2024 Oct 31.
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 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 , 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%.
Defective viral genomes (DVGs) have been identified and 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.
缺陷病毒基因组 (DVGs) 是在病毒基因组易错复制过程中产生的,包含缺失、插入、基因组重排和超突变。这些大效应突变导致 DVG 在没有辅助野生型病毒的情况下无法完成感染周期。已经表明,当病毒在同一宿主中以高感染复数连续传代时,DVGs 通常在病毒群体中积累。为了研究宿主间传播对 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 先后通过四个不同宿主物种(藜麦、烟草、生菜和菠菜)的组合进行传代。每传代五次就更换一次宿主。根据通过 20 次传代后对病毒 RNA 进行测序获得的 RNA-Seq 数据,分析了 DVG 的多样性和种群动态。我们的研究结果表明,当病毒通过不同的宿主物种传代时,有可能产生 TBRV 的 DVG。不同宿主植物组合中 DVG 的丰度水平不同,有微弱的迹象表明,宿主物种的过去序列可能在 DVG 的产生中起作用。在 TBRV 进化种群中最丰富的 DVG 来源于 RNA1。缺失是最常见的 DVG 类型,其次是插入。缺失 DVG 亚群在物种组成上表现出很大的多样性,缺失物种的丰富度与它们的丰度相关。具有小缺失的较长 DVG 占主导地位,而长度小于 1000 个核苷酸的 DVG 不到 2%。
已鉴定出缺陷病毒基因组 (DVGs) 并用于感染人类、动物和植物的不同病毒物种。已经证明,在一个宿主中病毒传代过程中能够形成 DVG,即番茄黑环病毒 (TBRV)。在我们的研究中,分析了 TBRV 通过四个不同宿主物种的组合传代后获得的 RNA-Seq 数据。我们的研究结果表明,在不同的宿主植物组合中,DVG 的丰度水平不同。缺失是最常见的 DVG 类型,较长的缺失占主导地位。此外,还鉴定了 TBRV 基因组中的保守连接位点,导致在独立进化的病毒谱系中产生相同的缺失。总之,我们的研究结果为植物病毒 DVG 的起源和结构提供了重要的见解。所获得的结果将有助于理解病毒进化和宿主-病毒相互作用。