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Variant vicilins from a resistant Vigna unguiculata lineage (IT81D-1053)udaccumulate inside Callosobruchus maculatus larval midgut epithelium

机译:来自抗性Vigna unguiculata谱系的变异vicilins(IT81D-1053)积累在Callosobruchus maculatus幼虫中肠上皮内

摘要

It has been demonstrated that variant vicilins are the main resistance factor of cowpea seeds (Vigna unguiculata) against attack by the cowpea beetle Callosobruchus maculatus. There is evidence that the toxic properties of these storage proteins may be related to their interaction with glycoproteins and other microvillar membrane constituents along the digestive tract of the larvae. New findings have shown that following interaction with the microvilli, the vicilins are absorbed across the intestinal epithelium and thus reach the internal environment of the larvae. In the present paper we studied the insecticidal activity of the variant vicilins purified from a resistant cowpea variety (IT81D-1053). Bioassays showed that the seeds of this genotype affected larval growth, causing developmental retardation and 100% mortality. By feeding C. maculatus larvae on susceptible and IT81D-1053 derived vicilins (FITC labelled or unlabelled), followed by fluorescence and immunogold cytolocalization, we were able to demonstrate that both susceptible and variant forms are internalized in the midgut cells and migrate inside vesicular structures from the apex to the basal portion of the enterocytes. However, when larvae were fed with the labelled vicilins for 24 h and then returned to a control diet, the concentration of the variant form remained relatively high, suggesting that variant vicilins are not removed from the cells at the same rate as the non-variant vicilins. We suggest that the toxic effects of variant vicilins on midgut cells involve the binding of these proteins to the cell surface followed by internalization and interference with the normal physiology of the enterocytes, thereby affecting larval development in vivo.
机译:已经证明变种豌豆球蛋白是of豆种子(Vigna unguiculata)抵抗the豆甲虫Callosobruchus maculatus攻击的主要抗性因子。有证据表明,这些存储蛋白的毒性可能与它们与幼虫消化道上的糖蛋白和其他微绒膜成分相互作用。新发现表明,与微绒毛相互作用后,Vicilins跨肠上皮吸收,从而到达幼虫的内部环境。在本文中,我们研究了从抗性cow豆品种(IT81D-1053)纯化的变种丝胶蛋白的杀虫活性。生物测定法表明,该基因型的种子影响幼虫的生长,导致发育迟缓和100%的死亡率。通过在易感的和IT81D-1053衍生的胶束蛋白(FITC标记的或未标记的)上饲喂黄斑鱼幼虫,然后进行荧光和免疫金细胞定位,我们能够证明易感和变异形式均被中肠细胞内化并在囊泡结构内迁移从肠细胞的顶端到基部。然而,当幼虫饲喂标记的豌豆球蛋白24小时,然后返回对照饮食时,变体形式的浓度仍然相对较高,这表明变体豌豆球蛋白并未以与非变体相同的速率从细胞中去除。毒菌素。我们建议变种vicilins对中肠细胞的毒性作用涉及这些蛋白与细胞表面的结合,然后内化并干扰肠上皮细胞的正常生理,从而影响体内幼虫的发育。

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