甜菜卷曲顶端病毒对载体生物学的影响:首次对甜菜叶蝉进行转录组分析。

IF 3.6 4区 医学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Journal of General Virology Pub Date : 2024-07-01 DOI:10.1099/jgv.0.002012
Jinlong Han, Meihua Cui, Jordan Withycombe, Max Schmidtbauer, Judith Chiginsky, Oliver T Neher, Carl A Strausbaugh, Rajtilak Majumdar, Vamsi J Nalam, Punya Nachappa
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引用次数: 0

摘要

由甜菜卷缩顶端病毒(BCTV)引起的卷缩顶端病是影响美国西部甜菜的最严重的病毒病之一。该病毒仅由甜菜叶蝉(BLH,Circulifer tenellus)以循环和非繁殖的方式传播。尽管有关病毒与载体相互作用的知识越来越多,但由于有关病毒对载体影响的信息有限,以及缺乏有关 BLH 的基因组和转录组资源,我们对 BCTV 与 BLH 之间分子相互作用的了解受到了阻碍。本研究揭示了 BCTV 对 BLH 性能和转录组反应的重大影响。带病毒的BLH比不带病毒的BLH具有更高的繁殖力,这表现在与带病毒昆虫生殖细胞和胚胎的发育、存活率和繁殖力相关的差异表达转录本(DETs)的上调。相反,大多数与肌肉运动和运动活动有关的 DETs 在带毒昆虫中被下调,这意味着 BCTV 可能会改变昆虫的行为。此外,大量与先天免疫和解毒有关的 DETs 在带毒昆虫体内上调。病毒感染还诱导了初级代谢的显著改变,包括能量代谢(即葡萄糖苷酶)、脂质消化和运输、蛋白质降解以及其他细胞功能,特别是染色质重塑和DNA修复。这项研究首次对 BLH 进行了全面的转录组分析。本文的研究结果为了解病毒感染对 BLH 中各种生物过程的多方面影响提供了新的视角,为今后研究复杂的病毒-载体关系和卷曲病的潜在管理策略奠定了基础。
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Beet curly top virus affects vector biology: the first transcriptome analysis of the beet leafhopper.

Curly top disease, caused by beet curly top virus (BCTV), is among the most serious viral diseases affecting sugar beets in western USA. The virus is exclusively transmitted by the beet leafhopper (BLH, Circulifer tenellus) in a circulative and non-propagative manner. Despite the growing knowledge on virus-vector interactions, our understanding of the molecular interactions between BCTV and BLH is hampered by limited information regarding the virus impact on the vector and the lack of genomic and transcriptomic resources for BLH. This study unveils the significant impact of BCTV on both the performance and transcriptome response of BLHs. Viruliferous BLHs had higher fecundity than non-viruliferous counterparts, which was evident by upregulation of differentially expressed transcripts (DETs) associated with development, viability and fertility of germline and embryos in viruliferous insects. Conversely, most DETs associated with muscle movement and locomotor activities were downregulated in viruliferous insects, implying potential behavioural modifications by BCTV. Additionally, a great proportion of DETs related to innate immunity and detoxification were upregulated in viruliferous insects. Viral infection also induced notable alterations in primary metabolisms, including energy metabolism, namely glucosidases, lipid digestion and transport, and protein degradation, along with other cellular functions, particularly in chromatin remodelling and DNA repair. This study represents the first comprehensive transcriptome analysis for BLH. The presented findings provide new insights into the multifaceted effects of viral infection on various biological processes in BLH, offering a foundation for future investigations into the complex virus-vector relationship and potential management strategies for curly top disease.

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来源期刊
Journal of General Virology
Journal of General Virology 医学-病毒学
CiteScore
7.70
自引率
2.60%
发文量
91
审稿时长
3 months
期刊介绍: JOURNAL OF GENERAL VIROLOGY (JGV), a journal of the Society for General Microbiology (SGM), publishes high-calibre research papers with high production standards, giving the journal a worldwide reputation for excellence and attracting an eminent audience.
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