Response of the hepatic transcriptome to aflatoxin B1 in ducklings

Toxicon. 2016 Mar 1:111:69-76. doi: 10.1016/j.toxicon.2015.12.022. Epub 2016 Jan 4.

Abstract

This study was conducted to determine the effects of aflatoxin B1 (AFB1) on the hepatic transcriptome in ducklings through RNA-sequencing (RNA-Seq). Twenty four, 1-day-old ducklings were divided into 4 treatment groups. Each group received an oral dose of AFB1 at 0, 10, 20, 40 μg/kg BW per day for 2 weeks. Administration of 20 and 40 μg/kg BW of AFB1 significantly decreased body weight, feed intake, serum total protein and albumin, while increasing serum aspartate aminotransferase and alanine aminotransferase activities, and hepatic histopathological lesions. Furthermore, RNA was extracted from the liver of ducklings administrated 0 and 40 μg/kg BW of AFB1. Two RNA-Seq libraries were created from pooled samples and produced over 149 M reads, totaling 14.9 Gb of sequence. Approximately 96,953 predicted transcripts were assembled, 749 of which had significant differential expressions (≥ 2-fold) between the control and AFB1 treatment. GO and KEGG pathway analysis results showed that many genes involved in phase I metabolism, phase II detoxification, oxidation-reduction process, carcinogenesis, apoptosis and cell cycle, and fatty acid metabolism were affected by AFB1 exposure. Conclusion, this study determined the hepatic transcriptome responded to AFB1 exposure, and provide candidate genes can be targeted to prevent and/or reduce aflatoxicosis in ducklings.

Keywords: Aflatoxin B(1); Duckling; Gene expression; Liver; RNA-Seq.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aflatoxin B1 / administration & dosage
  • Aflatoxin B1 / toxicity*
  • Animals
  • Chemical and Drug Induced Liver Injury / metabolism
  • Chemical and Drug Induced Liver Injury / veterinary*
  • Dose-Response Relationship, Drug
  • Ducks* / blood
  • Gene Expression Regulation / drug effects*
  • Liver / drug effects*
  • Liver / metabolism
  • Male
  • Transcriptome / drug effects*

Substances

  • Aflatoxin B1