N6-Methyladenosine Modification Profile in Bovine Mammary Epithelial Cells Treated with Heat-Inactivated Staphylococcus aureus

Oxid Med Cell Longev. 2022 Feb 23:2022:1704172. doi: 10.1155/2022/1704172. eCollection 2022.

Abstract

The symptoms of mastitis caused by Staphylococcus aureus (S. aureus) in dairy cows are not obvious and difficult to identify, resulting in major economic losses. N6-Methyladenosine (m6A) modification has been reported to be closely associated with the occurrence of many diseases. However, only a few reports have described the role of m6A modification in S. aureus-induced mastitis. In this study, after 24 h of treatment with inactivated S. aureus, MAC-T cells (an immortalized bovine mammary epithelial cell line) showed increased expression levels of the inflammatory factors IL-1β, IL-6, TNF-α, and reactive oxygen species. We found that the mRNA levels of METLL3, METLL14, WTAP, and ALKBH5 were also upregulated. Methylated RNA immunoprecipitation sequencing analysis revealed that 133 genes were m6A hypermethylated, and 711 genes were m6A hypomethylated. Biological functional analysis revealed that the differential m6A methylated genes were mainly related to oxidative stress, lipid metabolism, inflammatory response, and so on. In the present study, we also identified 62 genes with significant changes in m6A modification and mRNA expression levels. These findings elucidated the m6A modification spectrum induced by S. aureus in MAC-T cells and provide the basis for subsequent m6A research on mastitis.

MeSH terms

  • Adenosine / analogs & derivatives
  • Animals
  • Cattle
  • Cell Line, Transformed
  • Cytokines / metabolism
  • Epithelial Cells / metabolism*
  • Epithelial Cells / microbiology*
  • Female
  • Hot Temperature*
  • Mammary Glands, Animal / cytology*
  • Mastitis / genetics
  • Mastitis / metabolism*
  • Mastitis / microbiology
  • Methylation
  • Microbial Viability*
  • RNA / metabolism
  • RNA Processing, Post-Transcriptional / genetics
  • RNA, Messenger / metabolism
  • Reactive Oxygen Species / metabolism
  • Signal Transduction / genetics*
  • Staphylococcal Infections / genetics
  • Staphylococcal Infections / metabolism*
  • Staphylococcal Infections / microbiology
  • Staphylococcus aureus*
  • Up-Regulation / genetics

Substances

  • Cytokines
  • RNA, Messenger
  • Reactive Oxygen Species
  • RNA
  • N-methyladenosine
  • Adenosine