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Wiley InterScience

Plant Biotechnology Journal

Plant Biotechnology Journal

Volume 6 Issue 2, Pages 135 - 145

Published Online: 3 Sep 2007

Journal compilation © 2010 Blackwell Publishing Ltd


Plant Biotechnology Journal is published by Wiley-Blackwell in association with the Society for Experimental Biology (SEB) and the Association of Applied Biologists (AAB).
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Alleviating peanut allergy using genetic engineering: the silencing of the immunodominant allergen Ara h 2 leads to its significant reduction and a decrease in peanut allergenicity
Hortense W. Dodo 1,*, Koffi N. Konan 1 , Fur C. Chen 3 , Marceline Egnin 4 and Olga M. Viquez 2
  1 Department of Food and Animal Sciences, Food Biotechnology Laboratory, Alabama A&M University, Normal, AL 35762, USA
  2 Department of Pathology, Vanderbilt University, Nashville, TN 37232, USA
  3 Institute of Agricultural and Environmental Research, Tennessee State University, Nashville, TN 37209-1561, USA
  4 Center for Plant Biotechnology Research, College of Agricultural, Environmental, and Natural Sciences, Tuskegee University, Tuskegee, AL 36088, USA
  * Correspondence (fax: 256-372-5432, e-mail: hortense.dodo@email.aamu.edu; hortense.dodo@aamu.edu)
Copyright © 2007 The Authors
Journal compilation © 2007 Blackwell Publishing Ltd
KEYWORDS
peanut allergy • allergen Ara h 2 • gene silencing • hypoallergenic peanut • transgenic peanut

ABSTRACT

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 T0 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.


Received 19 November 2006; revised 18 July 2007; accepted 24 July 2007.

DIGITAL OBJECT IDENTIFIER (DOI)
10.1111/j.1467-7652.2007.00292.x About DOI

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