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Expression and functional validation of heat-labile enterotoxin B (LTB) and cholera toxin B (CTB) subunits in transgenic rice (Oryza sativa)

We expressed the heat-labile enterotoxin B (LTB) subunit from enterotoxigenic Escherichia coli and the cholera toxin B (CTB) subunit from Vibrio cholerae under the control of the rice (Oryza sativa) globulin (Glb) promoter. Binding of recombinant LTB and CTB proteins was confirmed based on G(M1)-gan...

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Autores principales: Soh, Ho Seob, Chung, Ha Young, Lee, Hyun Ho, Ajjappala, Hemavathi, Jang, Kyoungok, Park, Jong-Hwa, Sim, Joon-Soo, Lee, Gee Young, Lee, Hyun Ju, Han, Young Hee, Lim, Jae Wook, Choi, Inchan, Chung, In Sik, Hahn, Bum-Soo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380882/
https://www.ncbi.nlm.nih.gov/pubmed/25853032
http://dx.doi.org/10.1186/s40064-015-0847-4
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author Soh, Ho Seob
Chung, Ha Young
Lee, Hyun Ho
Ajjappala, Hemavathi
Jang, Kyoungok
Park, Jong-Hwa
Sim, Joon-Soo
Lee, Gee Young
Lee, Hyun Ju
Han, Young Hee
Lim, Jae Wook
Choi, Inchan
Chung, In Sik
Hahn, Bum-Soo
author_facet Soh, Ho Seob
Chung, Ha Young
Lee, Hyun Ho
Ajjappala, Hemavathi
Jang, Kyoungok
Park, Jong-Hwa
Sim, Joon-Soo
Lee, Gee Young
Lee, Hyun Ju
Han, Young Hee
Lim, Jae Wook
Choi, Inchan
Chung, In Sik
Hahn, Bum-Soo
author_sort Soh, Ho Seob
collection PubMed
description We expressed the heat-labile enterotoxin B (LTB) subunit from enterotoxigenic Escherichia coli and the cholera toxin B (CTB) subunit from Vibrio cholerae under the control of the rice (Oryza sativa) globulin (Glb) promoter. Binding of recombinant LTB and CTB proteins was confirmed based on G(M1)-ganglioside binding enzyme-linked immunosorbent assays (G(M1)-ELISA). Real-time PCR of three generations (T(3), T(4), and T(5)) in homozygous lines (LCI-11) showed single copies of LTB, CTB, bar and Tnos. LTB and CTB proteins in rice transgenic lines were detected by Western blot analysis. Immunogenicity trials of rice-derived CTB and LTB antigens were evaluated through oral and intraperitoneal administration in mice, respectively. The results revealed that LTB- and CTB-specific IgG levels were enhanced in the sera of intraperitoneally immunized mice. Similarly, the toxin-neutralizing activity of CTB and LTB in serum of orally immunized mice was associated with elevated levels of both IgG and IgA. The results of the present study suggest that the combined expression of CTB and LTB proteins can be utilized to produce vaccines against enterotoxigenic strains of Escherichia coli and Vibrio cholera, for the prevention of diarrhea.
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spelling pubmed-43808822015-04-07 Expression and functional validation of heat-labile enterotoxin B (LTB) and cholera toxin B (CTB) subunits in transgenic rice (Oryza sativa) Soh, Ho Seob Chung, Ha Young Lee, Hyun Ho Ajjappala, Hemavathi Jang, Kyoungok Park, Jong-Hwa Sim, Joon-Soo Lee, Gee Young Lee, Hyun Ju Han, Young Hee Lim, Jae Wook Choi, Inchan Chung, In Sik Hahn, Bum-Soo Springerplus Research We expressed the heat-labile enterotoxin B (LTB) subunit from enterotoxigenic Escherichia coli and the cholera toxin B (CTB) subunit from Vibrio cholerae under the control of the rice (Oryza sativa) globulin (Glb) promoter. Binding of recombinant LTB and CTB proteins was confirmed based on G(M1)-ganglioside binding enzyme-linked immunosorbent assays (G(M1)-ELISA). Real-time PCR of three generations (T(3), T(4), and T(5)) in homozygous lines (LCI-11) showed single copies of LTB, CTB, bar and Tnos. LTB and CTB proteins in rice transgenic lines were detected by Western blot analysis. Immunogenicity trials of rice-derived CTB and LTB antigens were evaluated through oral and intraperitoneal administration in mice, respectively. The results revealed that LTB- and CTB-specific IgG levels were enhanced in the sera of intraperitoneally immunized mice. Similarly, the toxin-neutralizing activity of CTB and LTB in serum of orally immunized mice was associated with elevated levels of both IgG and IgA. The results of the present study suggest that the combined expression of CTB and LTB proteins can be utilized to produce vaccines against enterotoxigenic strains of Escherichia coli and Vibrio cholera, for the prevention of diarrhea. Springer International Publishing 2015-03-28 /pmc/articles/PMC4380882/ /pubmed/25853032 http://dx.doi.org/10.1186/s40064-015-0847-4 Text en © Soh et al.; licensee Springer. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research
Soh, Ho Seob
Chung, Ha Young
Lee, Hyun Ho
Ajjappala, Hemavathi
Jang, Kyoungok
Park, Jong-Hwa
Sim, Joon-Soo
Lee, Gee Young
Lee, Hyun Ju
Han, Young Hee
Lim, Jae Wook
Choi, Inchan
Chung, In Sik
Hahn, Bum-Soo
Expression and functional validation of heat-labile enterotoxin B (LTB) and cholera toxin B (CTB) subunits in transgenic rice (Oryza sativa)
title Expression and functional validation of heat-labile enterotoxin B (LTB) and cholera toxin B (CTB) subunits in transgenic rice (Oryza sativa)
title_full Expression and functional validation of heat-labile enterotoxin B (LTB) and cholera toxin B (CTB) subunits in transgenic rice (Oryza sativa)
title_fullStr Expression and functional validation of heat-labile enterotoxin B (LTB) and cholera toxin B (CTB) subunits in transgenic rice (Oryza sativa)
title_full_unstemmed Expression and functional validation of heat-labile enterotoxin B (LTB) and cholera toxin B (CTB) subunits in transgenic rice (Oryza sativa)
title_short Expression and functional validation of heat-labile enterotoxin B (LTB) and cholera toxin B (CTB) subunits in transgenic rice (Oryza sativa)
title_sort expression and functional validation of heat-labile enterotoxin b (ltb) and cholera toxin b (ctb) subunits in transgenic rice (oryza sativa)
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4380882/
https://www.ncbi.nlm.nih.gov/pubmed/25853032
http://dx.doi.org/10.1186/s40064-015-0847-4
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