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Fate of Transgenic DNA from Orally Administered Bt MON810 Maize and Effects on Immune Response and Growth in Pigs

We assessed the effect of short-term feeding of genetically modified (GM: Bt MON810) maize on immune responses and growth in weanling pigs and determined the fate of the transgenic DNA and protein in-vivo. Pigs were fed a diet containing 38.9% GM or non-GM isogenic parent line maize for 31 days. We...

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Autores principales: Walsh, Maria C., Buzoianu, Stefan G., Gardiner, Gillian E., Rea, Mary C., Gelencsér, Eva, Jánosi, Anna, Epstein, Michelle M., Ross, R. Paul, Lawlor, Peadar G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223173/
https://www.ncbi.nlm.nih.gov/pubmed/22132091
http://dx.doi.org/10.1371/journal.pone.0027177
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author Walsh, Maria C.
Buzoianu, Stefan G.
Gardiner, Gillian E.
Rea, Mary C.
Gelencsér, Eva
Jánosi, Anna
Epstein, Michelle M.
Ross, R. Paul
Lawlor, Peadar G.
author_facet Walsh, Maria C.
Buzoianu, Stefan G.
Gardiner, Gillian E.
Rea, Mary C.
Gelencsér, Eva
Jánosi, Anna
Epstein, Michelle M.
Ross, R. Paul
Lawlor, Peadar G.
author_sort Walsh, Maria C.
collection PubMed
description We assessed the effect of short-term feeding of genetically modified (GM: Bt MON810) maize on immune responses and growth in weanling pigs and determined the fate of the transgenic DNA and protein in-vivo. Pigs were fed a diet containing 38.9% GM or non-GM isogenic parent line maize for 31 days. We observed that IL-12 and IFNγ production from mitogenic stimulated peripheral blood mononuclear cells decreased (P<0.10) following 31 days of GM maize exposure. While Cry1Ab-specific IgG and IgA were not detected in the plasma of GM maize-fed pigs, the detection of the cry1Ab gene and protein was limited to the gastrointestinal digesta and was not found in the kidneys, liver, spleen, muscle, heart or blood. Feeding GM maize to weanling pigs had no effect on growth performance or body weight. IL-6 and IL-4 production from isolated splenocytes were increased (P<0.05) in response to feeding GM maize while the proportion of CD4(+) T cells in the spleen decreased. In the ileum, the proportion of B cells and macrophages decreased while the proportion of CD4(+) T cells increased in GM maize-fed pigs. IL-8 and IL-4 production from isolated intraepithelial and lamina propria lymphocytes were also increased (P<0.05) in response to feeding GM maize. In conclusion, there was no evidence of cry1Ab gene or protein translocation to the organs and blood of weaning pigs. The growth of pigs was not affected by feeding GM maize. Alterations in immune responses were detected; however, their biologic relevance is questionable.
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spelling pubmed-32231732011-11-30 Fate of Transgenic DNA from Orally Administered Bt MON810 Maize and Effects on Immune Response and Growth in Pigs Walsh, Maria C. Buzoianu, Stefan G. Gardiner, Gillian E. Rea, Mary C. Gelencsér, Eva Jánosi, Anna Epstein, Michelle M. Ross, R. Paul Lawlor, Peadar G. PLoS One Research Article We assessed the effect of short-term feeding of genetically modified (GM: Bt MON810) maize on immune responses and growth in weanling pigs and determined the fate of the transgenic DNA and protein in-vivo. Pigs were fed a diet containing 38.9% GM or non-GM isogenic parent line maize for 31 days. We observed that IL-12 and IFNγ production from mitogenic stimulated peripheral blood mononuclear cells decreased (P<0.10) following 31 days of GM maize exposure. While Cry1Ab-specific IgG and IgA were not detected in the plasma of GM maize-fed pigs, the detection of the cry1Ab gene and protein was limited to the gastrointestinal digesta and was not found in the kidneys, liver, spleen, muscle, heart or blood. Feeding GM maize to weanling pigs had no effect on growth performance or body weight. IL-6 and IL-4 production from isolated splenocytes were increased (P<0.05) in response to feeding GM maize while the proportion of CD4(+) T cells in the spleen decreased. In the ileum, the proportion of B cells and macrophages decreased while the proportion of CD4(+) T cells increased in GM maize-fed pigs. IL-8 and IL-4 production from isolated intraepithelial and lamina propria lymphocytes were also increased (P<0.05) in response to feeding GM maize. In conclusion, there was no evidence of cry1Ab gene or protein translocation to the organs and blood of weaning pigs. The growth of pigs was not affected by feeding GM maize. Alterations in immune responses were detected; however, their biologic relevance is questionable. Public Library of Science 2011-11-23 /pmc/articles/PMC3223173/ /pubmed/22132091 http://dx.doi.org/10.1371/journal.pone.0027177 Text en Walsh et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Walsh, Maria C.
Buzoianu, Stefan G.
Gardiner, Gillian E.
Rea, Mary C.
Gelencsér, Eva
Jánosi, Anna
Epstein, Michelle M.
Ross, R. Paul
Lawlor, Peadar G.
Fate of Transgenic DNA from Orally Administered Bt MON810 Maize and Effects on Immune Response and Growth in Pigs
title Fate of Transgenic DNA from Orally Administered Bt MON810 Maize and Effects on Immune Response and Growth in Pigs
title_full Fate of Transgenic DNA from Orally Administered Bt MON810 Maize and Effects on Immune Response and Growth in Pigs
title_fullStr Fate of Transgenic DNA from Orally Administered Bt MON810 Maize and Effects on Immune Response and Growth in Pigs
title_full_unstemmed Fate of Transgenic DNA from Orally Administered Bt MON810 Maize and Effects on Immune Response and Growth in Pigs
title_short Fate of Transgenic DNA from Orally Administered Bt MON810 Maize and Effects on Immune Response and Growth in Pigs
title_sort fate of transgenic dna from orally administered bt mon810 maize and effects on immune response and growth in pigs
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3223173/
https://www.ncbi.nlm.nih.gov/pubmed/22132091
http://dx.doi.org/10.1371/journal.pone.0027177
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