Murine immune responses to a <it>Plasmodium vivax</it>-derived chimeric recombinant protein expressed in <it>Brassica napus</it>

<p>Abstract</p> <p>Background</p> <p>To develop a plant-based vaccine against <it>Plasmodium vivax</it>, two <it>P. vivax </it>candidate proteins were chosen. First, the merozoite surface protein-1 (MSP-1), a major asexual blood stage antigen tha...

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Main Authors: Chung Nam-Jun, Kim Tong-Soo, Jang Mi, Choi Yien, Won Chung Kyung, Mi Choi Kyung, Kim Hyung-Hwan, Lee Choonghee, Rhie Ho-Gun, Lee Ho-Sa, Sohn Youngjoo, Kim Hyuck, Lee Sung-Jae, Lee Hyeong-Woo
Format: Article
Language:English
Published: BMC 2011-04-01
Series:Malaria Journal
Online Access:http://www.malariajournal.com/content/10/1/106
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spelling doaj-740be3b3fc5a4467afb38b83dc2c76862020-11-24T23:27:18ZengBMCMalaria Journal1475-28752011-04-0110110610.1186/1475-2875-10-106Murine immune responses to a <it>Plasmodium vivax</it>-derived chimeric recombinant protein expressed in <it>Brassica napus</it>Chung Nam-JunKim Tong-SooJang MiChoi YienWon Chung KyungMi Choi KyungKim Hyung-HwanLee ChoongheeRhie Ho-GunLee Ho-SaSohn YoungjooKim HyuckLee Sung-JaeLee Hyeong-Woo<p>Abstract</p> <p>Background</p> <p>To develop a plant-based vaccine against <it>Plasmodium vivax</it>, two <it>P. vivax </it>candidate proteins were chosen. First, the merozoite surface protein-1 (MSP-1), a major asexual blood stage antigen that is currently considered a strong vaccine candidate. Second, the circumsporozoite protein (CSP), a component of sporozoites that contains a B-cell epitope.</p> <p>Methods</p> <p>A synthetic chimeric recombinant 516 bp gene encoding containing PvMSP-1, a Pro-Gly linker motif, and PvCSP was synthesized; the gene, named MLC, encoded a total of 172 amino acids. The recombinant gene was modified with regard to codon usage to optimize gene expression in <it>Brassica napus</it>. The Ti plasmid inducible gene transfer system was used for <it>MLC </it>chimeric recombinant gene expression in <it>B. napus</it>. Gene expression was confirmed by polymerase chain reaction (PCR), beta-glucuronidase reporter gene (GUS) assay, and Western blot.</p> <p>Results</p> <p>The MLC chimeric recombinant protein expressed in <it>B. napus </it>had a molecular weight of approximately 25 kDa. It exhibited a clinical sensitivity of 84.21% (n = 38) and a clinical specificity of 100% (n = 24) as assessed by enzyme-linked immunosorbent assay (ELISA). Oral immunization of BALB/c mice with MLC chimeric recombinant protein successfully induced antigen-specific IgG1 production. Additionally, the Th1-related cytokines IL-12 (p40), TNF, and IFN-γ were significantly increased in the spleens of the BALB/c mice.</p> <p>Conclusions</p> <p>The chimeric MLC recombinant protein produced in <it>B. napus </it>has potential as both as an antigen for diagnosis and as a valuable vaccine candidate for oral immunization against vivax malaria.</p> http://www.malariajournal.com/content/10/1/106
collection DOAJ
language English
format Article
sources DOAJ
author Chung Nam-Jun
Kim Tong-Soo
Jang Mi
Choi Yien
Won Chung Kyung
Mi Choi Kyung
Kim Hyung-Hwan
Lee Choonghee
Rhie Ho-Gun
Lee Ho-Sa
Sohn Youngjoo
Kim Hyuck
Lee Sung-Jae
Lee Hyeong-Woo
spellingShingle Chung Nam-Jun
Kim Tong-Soo
Jang Mi
Choi Yien
Won Chung Kyung
Mi Choi Kyung
Kim Hyung-Hwan
Lee Choonghee
Rhie Ho-Gun
Lee Ho-Sa
Sohn Youngjoo
Kim Hyuck
Lee Sung-Jae
Lee Hyeong-Woo
Murine immune responses to a <it>Plasmodium vivax</it>-derived chimeric recombinant protein expressed in <it>Brassica napus</it>
Malaria Journal
author_facet Chung Nam-Jun
Kim Tong-Soo
Jang Mi
Choi Yien
Won Chung Kyung
Mi Choi Kyung
Kim Hyung-Hwan
Lee Choonghee
Rhie Ho-Gun
Lee Ho-Sa
Sohn Youngjoo
Kim Hyuck
Lee Sung-Jae
Lee Hyeong-Woo
author_sort Chung Nam-Jun
title Murine immune responses to a <it>Plasmodium vivax</it>-derived chimeric recombinant protein expressed in <it>Brassica napus</it>
title_short Murine immune responses to a <it>Plasmodium vivax</it>-derived chimeric recombinant protein expressed in <it>Brassica napus</it>
title_full Murine immune responses to a <it>Plasmodium vivax</it>-derived chimeric recombinant protein expressed in <it>Brassica napus</it>
title_fullStr Murine immune responses to a <it>Plasmodium vivax</it>-derived chimeric recombinant protein expressed in <it>Brassica napus</it>
title_full_unstemmed Murine immune responses to a <it>Plasmodium vivax</it>-derived chimeric recombinant protein expressed in <it>Brassica napus</it>
title_sort murine immune responses to a <it>plasmodium vivax</it>-derived chimeric recombinant protein expressed in <it>brassica napus</it>
publisher BMC
series Malaria Journal
issn 1475-2875
publishDate 2011-04-01
description <p>Abstract</p> <p>Background</p> <p>To develop a plant-based vaccine against <it>Plasmodium vivax</it>, two <it>P. vivax </it>candidate proteins were chosen. First, the merozoite surface protein-1 (MSP-1), a major asexual blood stage antigen that is currently considered a strong vaccine candidate. Second, the circumsporozoite protein (CSP), a component of sporozoites that contains a B-cell epitope.</p> <p>Methods</p> <p>A synthetic chimeric recombinant 516 bp gene encoding containing PvMSP-1, a Pro-Gly linker motif, and PvCSP was synthesized; the gene, named MLC, encoded a total of 172 amino acids. The recombinant gene was modified with regard to codon usage to optimize gene expression in <it>Brassica napus</it>. The Ti plasmid inducible gene transfer system was used for <it>MLC </it>chimeric recombinant gene expression in <it>B. napus</it>. Gene expression was confirmed by polymerase chain reaction (PCR), beta-glucuronidase reporter gene (GUS) assay, and Western blot.</p> <p>Results</p> <p>The MLC chimeric recombinant protein expressed in <it>B. napus </it>had a molecular weight of approximately 25 kDa. It exhibited a clinical sensitivity of 84.21% (n = 38) and a clinical specificity of 100% (n = 24) as assessed by enzyme-linked immunosorbent assay (ELISA). Oral immunization of BALB/c mice with MLC chimeric recombinant protein successfully induced antigen-specific IgG1 production. Additionally, the Th1-related cytokines IL-12 (p40), TNF, and IFN-γ were significantly increased in the spleens of the BALB/c mice.</p> <p>Conclusions</p> <p>The chimeric MLC recombinant protein produced in <it>B. napus </it>has potential as both as an antigen for diagnosis and as a valuable vaccine candidate for oral immunization against vivax malaria.</p>
url http://www.malariajournal.com/content/10/1/106
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