Abstract Title:

Expression of cholera toxin B subunit in transgenic tomato plants.

Abstract Source:

Transgenic Res. 2002 Oct;11(5):447-54. PMID: 12437076

Abstract Author(s):

Dewal Jani, Laxman Singh Meena, Quazi Mohammad Rizwan-ul-Haq, Yogendra Singh, Arun K Sharma, Akhilesh K Tyagi

Article Affiliation:

Department of Plant Molecular Biology, University of Delhi, New Delhi, India.

Abstract:

Cholera toxin, secreted by Vibrio cholerae, consists of A and B subunits. The latter binds to G(M1)-ganglioside receptors as a pentamer (approximately 55 kDa). Tomato plants were transformed with the gene encoding cholera toxin B subunit (ctxB) along with an endoplasmic reticulum retention signal (SEKDEL) under the control of the CaMV 35S promoter via Agrobacterium-mediated transformation. PCR and Southern analysis confirmed the presence of the ctxB gene in transformed tomato plants. Northern analysis showed the presence of the ctxB-specific transcript. Immunoblot assays of the plant-derived protein extract showed the presence of cholera toxin subunit B (CTB) with mobility similar to purified CTB from V. cholerae. Both tomato leaves and fruits expressed CTB at levels up to 0.02 and 0.04% of total soluble protein, respectively. The G(M1)-ELISA showed that the plant-derived CTB bound specifically to G(M1)-ganglioside receptor, suggesting that it retained its native pentameric form. This study forms a basis for exploring the utility of CTB to develop tomato-based edible vaccines against cholera.

Study Type : In Vitro Study
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