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多拷贝α-淀粉酶基因对毁灭茎线虫寄生植物宿主至关重要。

Multi-copy alpha-amylase genes are crucial for Ditylenchus destructor to parasitize the plant host.

机构信息

State Key Laboratory of Agricultural Microbiology, College of Life Science and Technology, Huazhong Agricultural University, Wuhan, China.

出版信息

PLoS One. 2020 Oct 26;15(10):e0240805. doi: 10.1371/journal.pone.0240805. eCollection 2020.

Abstract

Ditylenchus destructor is a migratory plant-parasitic nematode that causes huge damage to global root and tuber production annually. The main plant hosts of D. destructor contain plenty of starch, which makes the parasitic environment of D. destructor to be different from those of most other plant-parasitic nematodes. It is speculated that D. destructor may harbor some unique pathogenesis-related genes to parasitize the starch-rich hosts. Herein, we focused on the multi-copy alpha-amylase genes in D. destructor, which encode a key starch-catalyzing enzyme. Our previously published D. destructor genome showed that it has three alpha-amylase encoding genes, Dd_02440, Dd_11154, and Dd_13225. Comparative analysis of alpha-amylases from different species demonstrated that the other plant-parasitic nematodes, even Ditylenchus dipsaci in the same genus, harbor only one or no alpha-amylase gene, and the three genes from D. destructor were closely clustered in the phylogenetic tree, indicating that there was a unique expansion of the alpha-amylase gene in D. destructor. The enzymatic activity of the three alpha-amylase proteins was verified by an enzyme assay. Quantitative real-time PCR assay showed that the expression of the three alpha-amylase genes in the post-hatching stage of D. destructor was found to be significantly higher than that in eggs. In the in situ hybridization assay, the expression of the genes was localized to the intestine, implying the association of these genes with nematode digestion. An infection assay in sweet potato demonstrated that RNA interference of any one alpha-amylase gene had no influence on the infectivity of D. destructor. Using the multi-target dsRNA cocktail method, it was found that silencing of two of the three genes inhibited nematode infection, and the infectivity of worms treated with three dsRNA simultaneously changed the most, which decreased by 76.6%. Thus, the multi-copy alpha-amylase genes in D. destructor are compensatory and crucial for nematodes to parasitize the plant host.

摘要

毁灭茎线虫是一种迁移性植物寄生线虫,每年都会对全球的根茎类作物生产造成巨大破坏。毁灭茎线虫的主要植物宿主含有大量淀粉,这使得其寄生环境与大多数其他植物寄生线虫不同。据推测,毁灭茎线虫可能拥有一些独特的与致病相关的基因,以寄生在富含淀粉的宿主上。在此,我们重点研究了毁灭茎线虫中的多拷贝α-淀粉酶基因,该基因编码一种关键的淀粉催化酶。我们之前发表的毁灭茎线虫基因组显示,它有三个α-淀粉酶编码基因,Dd_02440、Dd_11154 和 Dd_13225。对不同物种的α-淀粉酶进行比较分析表明,其他植物寄生线虫,甚至同属的 Ditylenchus dipsaci,只拥有一个或没有α-淀粉酶基因,而毁灭茎线虫的这三个基因在系统发育树中紧密聚类,表明α-淀粉酶基因在毁灭茎线虫中发生了独特的扩张。通过酶活性测定验证了这三个α-淀粉酶蛋白的酶活性。定量实时 PCR 分析显示,在毁灭茎线虫孵化后的阶段,这三个α-淀粉酶基因的表达显著高于卵期的表达。在原位杂交分析中,这些基因的表达定位于肠道,表明这些基因与线虫消化有关。在甘薯的侵染试验中,任何一个α-淀粉酶基因的 RNA 干扰都不会影响毁灭茎线虫的侵染性。利用多靶点 dsRNA 鸡尾酒方法,发现抑制三个基因中的两个会抑制线虫的侵染,而同时用三个 dsRNA 处理的线虫的侵染性变化最大,下降了 76.6%。因此,毁灭茎线虫中的多拷贝α-淀粉酶基因是互补的,对线虫寄生植物宿主至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/557c/7588122/2313a08331b0/pone.0240805.g001.jpg

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