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P33 蛋白是蚜虫(Kirkaldy)高效传播所必需的。

P33 Protein is Required for Efficient Transmission by the Aphid () (Kirkaldy).

机构信息

Plant Pathology Department, CREC-IFAS, University of Florida, 700 Experiment Station Road, Lake Alfred, FL 33850, USA.

出版信息

Viruses. 2020 Oct 6;12(10):1131. doi: 10.3390/v12101131.

Abstract

Plant viruses are threatening many valuable crops, and (CTV) is considered one of the most economically important plant viruses. CTV has destroyed millions of citrus trees in many regions of the world. Consequently, understanding of the transmission mechanism of CTV by its main vector, the brown citrus aphid, () (Kirkaldy) may lead to better control strategies for CTV. The objective of this study was to understand the CTV-vector relationship by exploring the influence of viral genetic diversity on virus transmission. We built several infectious clones with different 5'-proximal ends from different CTV strains and assessed their transmission by the brown citrus aphid. Replacement of the 5'- end of the T36 isolate with that of the T30 strain (poorly transmitted) did not increase the transmission rate of T36, whereas replacement with that of the T68-1 isolate (highly transmitted) increased the transmission rate of T36 from 1.5 to 23%. Finally, substitution of gene of the T36 strain with that of T68 increased the transmission rate from 1.5% to 17.8%. Although the underlying mechanisms that regulate the CTV transmission process by aphids have been explored in many ways, the roles of specific viral proteins are still not explicit. Our findings will improve our understanding of the transmission mechanisms of CTV by its aphid vector and may lead to the development of control strategies that interfere with its transmission by vector.

摘要

植物病毒正在威胁许多有价值的作物,而柑橘衰退病毒(CTV)被认为是最重要的植物病毒之一。CTV 已经摧毁了世界上许多地区数以百万计的柑橘树。因此,了解 CTV 主要载体——褐带柑橘蚜(() (Kirkaldy)的传播机制可能会导致更好的 CTV 控制策略。本研究的目的是通过探索病毒遗传多样性对病毒传播的影响来了解 CTV-载体关系。我们从不同的 CTV 株系构建了几个具有不同 5'端的传染性克隆,并评估了它们在褐带柑橘蚜中的传播情况。用 T30 株系(传播能力差)的 5'端替换 T36 分离株的 5'端并没有提高 T36 的传播率,而用 T68-1 分离株(高传播能力)的 5'端替换则将 T36 的传播率从 1.5%提高到 23%。最后,用 T68 的 基因替换 T36 株系的 基因将传播率从 1.5%提高到 17.8%。尽管已经通过多种方式探索了调节蚜虫传播 CTV 过程的潜在机制,但特定病毒蛋白的作用仍不明确。我们的发现将提高我们对 CTV 通过其蚜虫载体传播机制的理解,并可能导致开发出干扰其通过载体传播的控制策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f52/7600554/ce510c06200a/viruses-12-01131-g001.jpg

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