在烟草中由定义明确的序列变异引发的长期感染期间宿主内柑橘赤霉病病毒的种群数量

Viruses Pub Date : 2024-08-30 DOI:10.3390/v16091385
Tathiana Ferreira Sa Antunes, José C. Huguet-Tapia, Santiago F. Elena, Svetlana Y. Folimonova
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摘要

由于病毒 RNA 依赖性 RNA 聚合酶容易出错,RNA 病毒的复制导致病毒基因组的多样性,其中包含点突变、缺失、插入和基因组重排。柑橘三裂叶病毒(CTV)是柑橘类重要经济病害的病原体,具有内在的遗传稳定性。虽然该病毒似乎有某种机制限制单核苷酸变体的积累,但据报道,CTV 的某些变体在病毒感染过程中会产生有缺陷的病毒基因组(DVGs)。变体 T36(CTV-T36)在植物感染过程中产生的宿主内多样性仍不清楚。为了解决这个问题,我们分析了用 CTV-T36 的感染性 cDNA 克隆接种的烟草植物最初感染叶片和系统叶片中积累的 RNA 种类,这证明感染是由已知的、定义明确的病毒序列变体引发的。在感染过程中,CTV-T36 限制了单核苷酸突变体的积累。因此,在所有样本中都发现了四种类型的 DVG:缺失、插入、拷贝和快回,其中缺失和插入是最常见的类型。整个基因组中 DVG 重组和短直接序列重复的热点表明,序列互补性可能会介导 DVG 的形成。总之,我们的研究说明了在 CTV-T36 感染过程中形成了多种 DVG。据我们所知,这是第一项分析草本宿主中明确定义的 CTV 序列变体的遗传变异和重组的研究。
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Intra-Host Citrus Tristeza Virus Populations during Prolonged Infection Initiated by a Well-Defined Sequence Variant in Nicotiana benthamiana
Due to the error-prone nature of viral RNA-dependent RNA polymerases, the replication of RNA viruses results in a diversity of viral genomes harboring point mutations, deletions, insertions, and genome rearrangements. Citrus tristeza virus (CTV), a causal agent of diseases of economically important citrus species, shows intrinsic genetic stability. While the virus appears to have some mechanism that limits the accumulation of single-nucleotide variants, the production of defective viral genomes (DVGs) during virus infection has been reported for certain variants of CTV. The intra-host diversity generated during plant infection with variant T36 (CTV-T36) remains unclear. To address this, we analyzed the RNA species accumulated in the initially infected and systemic leaves of Nicotiana benthamiana plants inoculated with an infectious cDNA clone of CTV-T36, which warranted that infection was initiated by a known, well-defined sequence variant of the virus. CTV-T36 limited the accumulation of single-nucleotide mutants during infection. With that, four types of DVGs—deletions, insertions, and copy- and snap-backs—were found in all the samples, with deletions and insertions being the most common types. Hot-spots across the genome for DVG recombination and short direct sequence repeats suggest that sequence complementarity could mediate DVG formation. In conclusion, our study illustrates the formation of diverse DVGs during CTV-T36 infection. To the best of our knowledge, this is the first study that has analyzed the genetic variability and recombination of a well-defined sequence variant of CTV in an herbaceous host.
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