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一种用于快速检测的高级一步法 RT-LAMP,结合高通量基于序列的系统发育基因组学揭示了不同的樱桃分离株。

An Advanced One-Step RT-LAMP for Rapid Detection of Combined with High-Throughput Sequence-Based Phylogenomics Reveal Divergent Flowering Cherry Isolates.

机构信息

Plant Sciences Unit, Flanders Research Institute for Agriculture, Fisheries and Food (ILVO), 9820 Merelbeke, Belgium.

Department of Integrated and Urban Phytopathology, Gembloux Agro-BioTech, University of Liège, 5030 Gembloux, Belgium.

出版信息

Plant Dis. 2022 Mar;106(3):835-845. doi: 10.1094/PDIS-03-21-0677-RE. Epub 2022 Mar 8.

Abstract

Little cherry virus 2 (LChV-2, genus ) is considered to be the main causal agent of the economically damaging little cherry disease, which can only be controlled by removal of infected trees. The widespread viral disease of sweet cherry ( L.) is affecting the survival of long-standing orchards in North America and Europe, hence the dire need for an early and accurate diagnosis to establish a sound disease control strategy. The endemic presence of LChV-2 is mainly confirmed using laborious time-consuming reverse-transcription (RT-PCR). A rapid reverse transcription loop-mediated isothermal amplification (RT-LAMP) assay targeting a conserved region of the coat protein was developed and compared with conventional RT-PCR for the specific detection of LChV-2. This affordable assay, combined with a simple RNA extraction, deploys desirable characteristics such as higher ability for faster (<15 min), more analytically sensitive (100-fold), and robust broad-range diagnosis of LChV-2 isolates from sweet cherry, ornamental flowering cherry displaying heterogenous viral etiology and, for the first time, newly identified potential insect vectors. Moreover, use of Sanger and total RNA high-throughput sequencing as complementary metaviromics approaches confirmed the LChV-2 RT-LAMP detection of divergent LChV-2 isolates in new hosts and the relationship of their whole-genome was exhaustively inferred using maximum-likelihood phylogenomics. This entails unprecedented critical understanding of a novel evolutionary clade further expanding LChV-2 viral diversity. In conclusion, this highly effective diagnostic platform facilitates strategical support for early in-field testing to reliably prevent dissemination of new LChV-2 outbreaks from propagative plant stocks or newly postulated insect vectors. Validated results and major advantages are herein thoroughly discussed, in light of the knowledge required to increase the potential accuracy of future diagnostics and the essential epidemiological considerations to proactively safeguard cherries and horticultural crop systems from little cherry disease.

摘要

李属坏死环斑病毒 2 型(LChV-2,属)被认为是造成樱桃毁灭性病害的主要病原,这种病害只能通过清除感病树木来控制。甜樱桃(L.)的这种广泛流行的病毒性病害正在影响北美和欧洲历史悠久的果园的生存,因此迫切需要进行早期、准确的诊断,以制定健全的疾病控制策略。李属坏死环斑病毒 2 型的地方性流行主要通过繁琐耗时的逆转录(RT-PCR)来确认。针对外壳蛋白保守区域,开发了一种快速逆转录环介导等温扩增(RT-LAMP)检测方法,并与传统 RT-PCR 进行了比较,用于特异性检测 LChV-2。这种经济实惠的检测方法结合简单的 RNA 提取,具有更高的能力,能够更快(<15 分钟)、更灵敏(100 倍)和稳健的广谱诊断甜樱桃、观赏开花樱桃中异质病毒病因的 LChV-2 分离物,以及首次鉴定的潜在昆虫媒介。此外,使用 Sanger 和总 RNA 高通量测序作为补充宏病毒组学方法,确认了 LChV-2 RT-LAMP 对新宿主中不同的 LChV-2 分离物的检测,并使用最大似然系统发生基因组学方法对其全基因组关系进行了详尽推断。这意味着对新型进化枝的认识达到了前所未有的关键程度,进一步扩大了李属坏死环斑病毒 2 型的病毒多样性。总之,这个高效的诊断平台为早期田间测试提供了战略支持,以可靠地防止新的李属坏死环斑病毒 2 型爆发从繁殖植物材料或新提出的昆虫媒介传播。本文深入讨论了验证结果和主要优势,考虑到提高未来诊断准确性所需的知识以及主动保护樱桃和园艺作物系统免受李属坏死环斑病毒病害的必要流行病学考虑因素。

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