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Response of the Hepatic Transcriptome to Aflatoxin B(1) in Domestic Turkey (Meleagris gallopavo)
Dietary exposure to aflatoxin B(1) (AFB(1)) is detrimental to avian health and leads to major economic losses for the poultry industry. AFB(1) is especially hepatotoxic in domestic turkeys (Meleagris gallopavo), since these birds are unable to detoxify AFB(1) by glutathione-conjugation. The impacts...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076218/ https://www.ncbi.nlm.nih.gov/pubmed/24979717 http://dx.doi.org/10.1371/journal.pone.0100930 |
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author | Monson, Melissa S. Settlage, Robert E. McMahon, Kevin W. Mendoza, Kristelle M. Rawal, Sumit El-Nezami, Hani S. Coulombe, Roger A. Reed, Kent M. |
author_facet | Monson, Melissa S. Settlage, Robert E. McMahon, Kevin W. Mendoza, Kristelle M. Rawal, Sumit El-Nezami, Hani S. Coulombe, Roger A. Reed, Kent M. |
author_sort | Monson, Melissa S. |
collection | PubMed |
description | Dietary exposure to aflatoxin B(1) (AFB(1)) is detrimental to avian health and leads to major economic losses for the poultry industry. AFB(1) is especially hepatotoxic in domestic turkeys (Meleagris gallopavo), since these birds are unable to detoxify AFB(1) by glutathione-conjugation. The impacts of AFB(1) on the turkey hepatic transcriptome and the potential protection from pretreatment with a Lactobacillus-based probiotic mixture were investigated through RNA-sequencing. Animals were divided into four treatment groups and RNA was subsequently recovered from liver samples. Four pooled RNA-seq libraries were sequenced to produce over 322 M reads totaling 13.8 Gb of sequence. Approximately 170,000 predicted transcripts were de novo assembled, of which 803 had significant differential expression in at least one pair-wise comparison between treatment groups. Functional analysis linked many of the transcripts significantly affected by AFB(1) exposure to cancer, apoptosis, the cell cycle or lipid regulation. Most notable were transcripts from the genes encoding E3 ubiquitin-protein ligase Mdm2, osteopontin, S-adenosylmethionine synthase isoform type-2, and lipoprotein lipase. Expression was modulated by the probiotics, but treatment did not completely mitigate the effects of AFB(1). Genes identified through transcriptome analysis provide candidates for further study of AFB(1) toxicity and targets for efforts to improve the health of domestic turkeys exposed to AFB(1). |
format | Online Article Text |
id | pubmed-4076218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-40762182014-07-02 Response of the Hepatic Transcriptome to Aflatoxin B(1) in Domestic Turkey (Meleagris gallopavo) Monson, Melissa S. Settlage, Robert E. McMahon, Kevin W. Mendoza, Kristelle M. Rawal, Sumit El-Nezami, Hani S. Coulombe, Roger A. Reed, Kent M. PLoS One Research Article Dietary exposure to aflatoxin B(1) (AFB(1)) is detrimental to avian health and leads to major economic losses for the poultry industry. AFB(1) is especially hepatotoxic in domestic turkeys (Meleagris gallopavo), since these birds are unable to detoxify AFB(1) by glutathione-conjugation. The impacts of AFB(1) on the turkey hepatic transcriptome and the potential protection from pretreatment with a Lactobacillus-based probiotic mixture were investigated through RNA-sequencing. Animals were divided into four treatment groups and RNA was subsequently recovered from liver samples. Four pooled RNA-seq libraries were sequenced to produce over 322 M reads totaling 13.8 Gb of sequence. Approximately 170,000 predicted transcripts were de novo assembled, of which 803 had significant differential expression in at least one pair-wise comparison between treatment groups. Functional analysis linked many of the transcripts significantly affected by AFB(1) exposure to cancer, apoptosis, the cell cycle or lipid regulation. Most notable were transcripts from the genes encoding E3 ubiquitin-protein ligase Mdm2, osteopontin, S-adenosylmethionine synthase isoform type-2, and lipoprotein lipase. Expression was modulated by the probiotics, but treatment did not completely mitigate the effects of AFB(1). Genes identified through transcriptome analysis provide candidates for further study of AFB(1) toxicity and targets for efforts to improve the health of domestic turkeys exposed to AFB(1). Public Library of Science 2014-06-30 /pmc/articles/PMC4076218/ /pubmed/24979717 http://dx.doi.org/10.1371/journal.pone.0100930 Text en © 2014 Monson 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 Monson, Melissa S. Settlage, Robert E. McMahon, Kevin W. Mendoza, Kristelle M. Rawal, Sumit El-Nezami, Hani S. Coulombe, Roger A. Reed, Kent M. Response of the Hepatic Transcriptome to Aflatoxin B(1) in Domestic Turkey (Meleagris gallopavo) |
title | Response of the Hepatic Transcriptome to Aflatoxin B(1) in Domestic Turkey (Meleagris gallopavo) |
title_full | Response of the Hepatic Transcriptome to Aflatoxin B(1) in Domestic Turkey (Meleagris gallopavo) |
title_fullStr | Response of the Hepatic Transcriptome to Aflatoxin B(1) in Domestic Turkey (Meleagris gallopavo) |
title_full_unstemmed | Response of the Hepatic Transcriptome to Aflatoxin B(1) in Domestic Turkey (Meleagris gallopavo) |
title_short | Response of the Hepatic Transcriptome to Aflatoxin B(1) in Domestic Turkey (Meleagris gallopavo) |
title_sort | response of the hepatic transcriptome to aflatoxin b(1) in domestic turkey (meleagris gallopavo) |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076218/ https://www.ncbi.nlm.nih.gov/pubmed/24979717 http://dx.doi.org/10.1371/journal.pone.0100930 |
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