Increasing numbers of plant-made vaccines and pharmaceuticals are entering the late stage of product development and commercialization. Despite the theoretical benefits of such production, expression of parasite antigens in plants, particularly those from Plasmodium, the causative parasites for malaria, have achieved only limited success. We have previously shown that stable transformation of tobacco plants with a plant-codon optimized form of the Plasmodium yoelii merozoite surface protein 4 ⁄ 5 (PyMSP4 ⁄ 5) gene resulted in PyMSP4 ⁄ 5 expression of up to 0.25% of total soluble protein. In this report, we describe the rapid expression of PyMSP4 ⁄5 in Nicotiana benthamiana leaves using the deconstructed tobacco mosaic virus-based magnICON expression system. PyMSP4 ⁄ 5 yields of up to 10% TSP or 1–2 mg⁄g of fresh weight were consistently achieved. Characterization of the recombinant plantmade PyMSP4 ⁄ 5 indicates that it is structurally similar to PyMSP4 ⁄ 5 expressed by Escherichia coli. It is notable that the plant-made PyMSP4 ⁄ 5 protein retained its immunogenicity following long-term storage at ambient temperature within freezedried leaves. With assistance from a mucosal adjuvant the PyMSP4 ⁄ 5-containing leaves induced PyMSP4 ⁄ 5-specific antibodies when delivered orally to naı¨ve mice or mice primed by a DNA vaccine. This study provides evidence that immunogenic Plasmodium antigens can be produced in large quantities in plants using the magnICON viral vector system. Introduction Malaria is a major world health problem caused by species of Plasmodium, a protozoan parasite. Development of vaccines targeting various stages of the parasite life cycle, in combination with currently available control measures, appears to be necessary for the eventual elimination of this disease. Owing to the relative poverty and lack of infrastructure in many malaria-endemic areas, a successful immunization strategy will have more probability of success if it
Production and characterization of an orally immunogenic Plasmodium antigen in plants using a virus-based expression system RID F-7326-2010 / Webster, De; Wang, L; Mulcair, M; Ma, C; Santi, L; Mason, Hs; Wesselingh, Sl; Coppel, Rl. - In: PLANT BIOTECHNOLOGY JOURNAL. - ISSN 1467-7644. - 7:9(2009), pp. 846-855. [10.1111/j.1467-7652.2009.00447.x]
Production and characterization of an orally immunogenic Plasmodium antigen in plants using a virus-based expression system RID F-7326-2010
Santi L;
2009
Abstract
Increasing numbers of plant-made vaccines and pharmaceuticals are entering the late stage of product development and commercialization. Despite the theoretical benefits of such production, expression of parasite antigens in plants, particularly those from Plasmodium, the causative parasites for malaria, have achieved only limited success. We have previously shown that stable transformation of tobacco plants with a plant-codon optimized form of the Plasmodium yoelii merozoite surface protein 4 ⁄ 5 (PyMSP4 ⁄ 5) gene resulted in PyMSP4 ⁄ 5 expression of up to 0.25% of total soluble protein. In this report, we describe the rapid expression of PyMSP4 ⁄5 in Nicotiana benthamiana leaves using the deconstructed tobacco mosaic virus-based magnICON expression system. PyMSP4 ⁄ 5 yields of up to 10% TSP or 1–2 mg⁄g of fresh weight were consistently achieved. Characterization of the recombinant plantmade PyMSP4 ⁄ 5 indicates that it is structurally similar to PyMSP4 ⁄ 5 expressed by Escherichia coli. It is notable that the plant-made PyMSP4 ⁄ 5 protein retained its immunogenicity following long-term storage at ambient temperature within freezedried leaves. With assistance from a mucosal adjuvant the PyMSP4 ⁄ 5-containing leaves induced PyMSP4 ⁄ 5-specific antibodies when delivered orally to naı¨ve mice or mice primed by a DNA vaccine. This study provides evidence that immunogenic Plasmodium antigens can be produced in large quantities in plants using the magnICON viral vector system. Introduction Malaria is a major world health problem caused by species of Plasmodium, a protozoan parasite. Development of vaccines targeting various stages of the parasite life cycle, in combination with currently available control measures, appears to be necessary for the eventual elimination of this disease. Owing to the relative poverty and lack of infrastructure in many malaria-endemic areas, a successful immunization strategy will have more probability of success if itI documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


