4.7 Article

Combined Analysis of DNA Methylome and Transcriptome Reveal Novel Candidate Genes Related to PorcineEscherichia coliF4ab/ac-Induced Diarrhea

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcimb.2020.00250

Keywords

DNA methylome; transcriptome; enterotoxigenicEscherichia coli; diarrhea; pig

Funding

  1. National Natural Science Foundation of China [31702093, 31572361]
  2. China Postdoctoral Science Foundation [2019M652449]
  3. National Major Special Project of China for the Cultivation of New Varieties of Transgenic Organisms [2014ZX0800945B]
  4. Shandong Double Tops Program [SYL2017YSTD12]

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EnterotoxigenicEscherichia coli(ETEC) that express F4 (K88) fimbriae are the principal microorganisms responsible for bacterial diarrhea in neonatal and pre-weaning piglets. To better understand the molecular effects of ETEC F4ab/ac infection, we performed a genome-wide comparison of the changes in DNA methylation and gene expression in ETEC F4ab/ac infected porcine intestinal epithelial cells. We characterized the pattern of changes in methylation and found 3297 and 1593 differentially methylated regions in cells infected with F4ab and F4ac, respectively. Moreover, 606 and 780 differentially expressed genes (DEGs) in ETEC F4ab and F4ac infected cells were detected and these genes were highly enriched in immune/defense response related pathways. Integrative analysis identified 27 and 10 genes showing inverse correlations between promoter methylation and expression with ETEC F4ab/ac infection. Altered DNA methylation and expression of various genes suggested their roles and potential functional interactions upon ETEC F4ab/ac infection. Further functional analyses revealed that three DEGs (S100A9, SGO1, andESPL1) in F4ab infected cells and three DEGs (MAP3K21, PAK6, andMPZL1) in F4ac infected cells are likely involved in the host cells response to ETEC infection. Our data provides further insight into the epigenetic and transcriptomic alterations of ETEC F4ab/ac infected porcine intestinal epithelial cells, and may advance the identification of biomarkers and drug targets for predicting susceptibility to and controlling ETEC F4ab/ac induced diarrhea.

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