Dodo Hortense W, Konan Koffi N, Chen Fur C, Egnin Marceline, Viquez Olga M
Department of Food and Animal Sciences, Food Biotechnology Laboratory, Alabama A&M University, Normal, AL 35762, USA.
Plant Biotechnol J. 2008 Feb;6(2):135-45. doi: 10.1111/j.1467-7652.2007.00292.x. Epub 2007 Sep 3.
Peanut allergy is one of the most life-threatening food allergies and one of the serious challenges facing the peanut and food industries. Current proposed solutions focus primarily on ways to alter the immune system of patients allergic to peanut. However, with the advent of genetic engineering novel strategies can be proposed to solve the problem of peanut allergy from the source. The objectives of this study were to eliminate the immunodominant Ara h 2 protein from transgenic peanut using RNA interference (RNAi), and to evaluate the allergenicity of resulting transgenic peanut seeds. A 265-bp-long PCR product was generated from the coding region of Ara h 2 genomic DNA, and cloned as inverted repeats in pHANNIBAL, an RNAi-inducing plant transformation vector. The Ara h 2-specific RNAi transformation cassette was subcloned into a binary pART27 vector to construct plasmid pDK28. Transgenic peanuts were produced by infecting peanut hypocotyl explants with Agrobacterium tumefaciens EHA 105 harbouring the pDK28 construct. A total of 59 kanamycin-resistant peanut plants were regenerated with phenotype and growth rates comparable to wild type. PCR and Southern analyses revealed that 44% of plants stably integrated the transgene. Sandwich ELISA performed using Ara h 2-mAbs revealed a significant (P < 0.05) reduction in Ara h 2 content in several transgenic seeds. Western immunobloting performed with Ara h 2-mAb corroborated the results obtained with ELISA and showed absence of the Ara h 2 protein from crude extracts of several transgenic seeds of the T(0) plants. The allergenicity of transgenic peanut seeds expressed as IgE binding capacity was evaluated by ELISA using sera of patients allergic to peanut. The data showed a significant decrease in the IgE binding capacity of selected transgenic seeds compared to wild type, hence, demonstrating the feasibility of alleviating peanut allergy using the RNAi technology.
花生过敏是最危及生命的食物过敏之一,也是花生和食品行业面临的严峻挑战之一。目前提出的解决方案主要集中在改变对花生过敏患者的免疫系统的方法上。然而,随着基因工程的出现,可以提出新的策略从源头上解决花生过敏问题。本研究的目的是利用RNA干扰(RNAi)从转基因花生中消除免疫显性Ara h 2蛋白,并评估所得转基因花生种子的致敏性。从Ara h 2基因组DNA的编码区产生了一个265 bp长的PCR产物,并作为反向重复序列克隆到RNAi诱导植物转化载体pHANNIBAL中。将Ara h 2特异性RNAi转化盒亚克隆到二元pART27载体中构建质粒pDK28。通过用携带pDK28构建体的根癌农杆菌EHA 105感染花生下胚轴外植体来生产转基因花生。共再生了59株抗卡那霉素的花生植株,其表型和生长速率与野生型相当。PCR和Southern分析表明,44%的植株稳定整合了转基因。使用Ara h 2单克隆抗体进行的夹心ELISA显示,几种转基因种子中Ara h 2含量显著降低(P < 0.05)。用Ara h 2单克隆抗体进行的Western免疫印迹证实了ELISA获得的结果,并显示T(0)代植株的几种转基因种子的粗提物中不存在Ara h 2蛋白。用对花生过敏患者的血清通过ELISA评估以IgE结合能力表示的转基因花生种子的致敏性。数据显示,与野生型相比,所选转基因种子的IgE结合能力显著降低,因此证明了使用RNAi技术减轻花生过敏的可行性。