miRNA-seq analysis of liver tissue from largemouth bass (Micropterus salmoides) in response to oxytetracycline and enzyme-treated soy protein

Comp Biochem Physiol Part D Genomics Proteomics. 2024 Mar:49:101202. doi: 10.1016/j.cbd.2024.101202. Epub 2024 Feb 1.

Abstract

The specific miRNA regulation triggered by enzyme-treated soybean protein in response to well-known stressors, such as the prophylactic use of the antimicrobial oxytetracycline, remains unknown. Hence, this study aimed to evaluate the regulatory changes of hepatic miRNAs induced by oxytetracycline and enzyme-treated soybean protein in largemouth bass dietary formulations. The experiment was designed with three groups: the normal control (NC), the oxytetracycline exposure treatment group (OTC), and the pre-treatment with enzyme-treated soybean protein before oxytetracycline exposure group (ETSP). miRNA sequencing was employed to characterize the differences between these groups. In conclusion, the NC group exhibited up-regulation of 13 host miRNAs and down-regulation of 1 miRNA compared to the OTC group, whereas the ETSP group showed an increasing trend of 36 host miRNAs and a decreasing trend of 13 host miRNAs compared to the OTC group. Nine miRNAs were identified as prudential targets for enzyme-treated soy protein, protecting the largemouth bass liver from oxytetracycline. Furthermore, gene ontology analysis revealed nine key miRNAs that mediate signaling pathways with significant differences. The cellular lipid metabolic process was identified as the most important biological process, and the propanoate metabolism pathway was highlighted as significant. These results will facilitate further exploration of the mechanism by which enzyme-treated soy protein alleviates the effects of oxytetracycline on largemouth bass in water environments.

Keywords: Enzyme-treated soy protein; Largemouth bass; Lipid metabolic; Oxytetracycline; miRNA-Seq.

MeSH terms

  • Animals
  • Bass* / genetics
  • Liver / metabolism
  • MicroRNAs* / genetics
  • Oxytetracycline* / metabolism
  • Oxytetracycline* / pharmacology
  • Soybean Proteins / metabolism
  • Soybean Proteins / pharmacology

Substances

  • Soybean Proteins
  • Oxytetracycline
  • MicroRNAs