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Towards the development of edible vaccines for human papillomavirus in bananas

Identifieur interne : 00BB28 ( Main/Exploration ); précédent : 00BB27; suivant : 00BB29

Towards the development of edible vaccines for human papillomavirus in bananas

Auteurs : J. Miller [Australie] ; D. Becker [Australie] ; B. Dugdale [Australie] ; R. Harding [Australie] ; J. Aaskov [Australie] ; I. Frazer [Australie] ; J. Dale [Australie]

Source :

RBID : Pascal:01-0384520

Descripteurs français

English descriptors

Abstract

The study of transgenic plants as vaccine production systems holds promise for the development of edible, oral vaccines for developing third world countries. We are developing bananas as a vaccine production system using microprojectile bombardment transformation and novel promoters. Further, we have engineered tobacco plants to express the coding region for the bovine papillomavirus (BPV) L1 protein (L1). The recombinant constructs contain the transgene under control of the cauliflower mosaic virus 35S promoter (CaMV35S) and the 5' untranslated region (UTR) of tobacco etch virus (TEV). Plants were transformed by Agrobacterium tumefaciens-mediated transformation of leaf discs and culture on selective media. Here we present analysis of plants transformed with BPV L1. Northern blot analysis indicated that BPV L1 mRNA of the appropriate molecular weight was produced in tissues of transformed plants, however recombinant protein was not detected in leaves or seeds of transgenic plants. In vitro translation of the BPV L1 coding region in wheat germ extracts was demonstrated, indicating that BPV Ll mRNA is translated in a plant system.


Affiliations:


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<div type="abstract" xml:lang="en">The study of transgenic plants as vaccine production systems holds promise for the development of edible, oral vaccines for developing third world countries. We are developing bananas as a vaccine production system using microprojectile bombardment transformation and novel promoters. Further, we have engineered tobacco plants to express the coding region for the bovine papillomavirus (BPV) L1 protein (L1). The recombinant constructs contain the transgene under control of the cauliflower mosaic virus 35S promoter (CaMV35S) and the 5' untranslated region (UTR) of tobacco etch virus (TEV). Plants were transformed by Agrobacterium tumefaciens-mediated transformation of leaf discs and culture on selective media. Here we present analysis of plants transformed with BPV L1. Northern blot analysis indicated that BPV L1 mRNA of the appropriate molecular weight was produced in tissues of transformed plants, however recombinant protein was not detected in leaves or seeds of transgenic plants. In vitro translation of the BPV L1 coding region in wheat germ extracts was demonstrated, indicating that BPV Ll mRNA is translated in a plant system.</div>
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