转基因无核和野生型油菜对蚜虫的防御反应

IF 1.2 3区 农林科学 Q3 ENTOMOLOGY Arthropod-Plant Interactions Pub Date : 2024-12-04 DOI:10.1007/s11829-024-10108-y
Mubasher Ahmad Malik, Jorge Poveda, Zeshan Hassan
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引用次数: 0

摘要

内源性蛋白质复合物黑芥子酶和硫代葡萄糖苷形成十字花科植物对害虫的防御系统。转基因消融黑松香细胞产生的无核甘蓝型油菜种子用于研究植物与蚜虫的相互作用。本研究通过非选择实验,研究了brvicoryne brassicae(专一型)和Lipaphis erysimi(通才型)蚜虫在MINELESS转基因幼苗和野生型栽培品种Westar上的表现和繁殖力。取食偏好表明,芸苔芽孢杆菌偏爱野生型幼苗,而erysimi偏爱MINELESS幼苗。通才蚜虫和专才蚜虫的后代对野生型和无性蚜虫幼苗的建立和影响不同。野生型和无菌性幼苗的硫代葡萄糖苷水解产物均高于无菌性油菜。此外,除3,4 -上皮丁烷腈外,异硫氰酸烯丙基在L. erysimi的影响下呈下降趋势。L. erysimi侵染诱导硫代葡萄糖苷的减少,而B. brassicae侵染则产生相反的效果。综上所述,暗香细胞影响了蚜虫对甘蓝型油菜的偏好。
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Defense responses of transgenic MINELESS and wild-type oilseed rape (Brassica napus L.) against aphids

The endogenous protein complex myrosinase and glucosinolates form a defense system in cruciferous plants against insect pests. Transgenic ablation of myrosin cells produced MINELESS seeds of Brassica napus used to investigate plant–aphid interactions. In the present study, we conducted a non-choice experiment to test the performance and fecundity of the aphids Brevicoryne brassicae (specialist) and Lipaphis erysimi (generalist) on MINELESS transgenic seedlings and the wild-type cultivar Westar. Feeding preference showed that B. brassicae preferred wild-type seedlings and L. erysimi preferred MINELESS. Progeny of generalist and specialist aphids establish and affect wild-type and MINELESS seedlings differently. Glucosinolate hydrolysis products were higher under the influence of B. brassicae in both wild-type and MINELESS seedlings. In addition, allyl isothiocyanate decreased under the influence of L. erysimi, except 3,4 -epithiobutane nitrile. Infestation by L. erysimi induced the reduction of glucosinolates, whereas B. brassicae had an opposite effect. In conclusion, the present study showed that myrosin cells affected the preference of aphid species for Brassica napus plants.

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来源期刊
Arthropod-Plant Interactions
Arthropod-Plant Interactions 生物-昆虫学
CiteScore
3.00
自引率
6.20%
发文量
58
审稿时长
6 months
期刊介绍: Arthropod-Plant Interactions is dedicated to publishing high quality original papers and reviews with a broad fundamental or applied focus on ecological, biological, and evolutionary aspects of the interactions between insects and other arthropods with plants. Coverage extends to all aspects of such interactions including chemical, biochemical, genetic, and molecular analysis, as well reporting on multitrophic studies, ecophysiology, and mutualism. Arthropod-Plant Interactions encourages the submission of forum papers that challenge prevailing hypotheses. The journal encourages a diversity of opinion by presenting both invited and unsolicited review papers.
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