4.7 Article

Melatonin Maintains Homeostasis and Potentiates the Anti- inflammatory Response in Staphylococcus aureus-Induced Mastitis through microRNA-16b/YAP1

期刊

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
卷 70, 期 48, 页码 15255-15270

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jafc.2c05904

关键词

melatonin; S; aureus; mastitis; miR-16b; YAP1

资金

  1. National Natural Science Foundation of China [32272825]
  2. Jiangsu Agricultural Science and Technology Independent Innovation Fund [CX(21)3119]
  3. Basic Research Program of Jiangsu Province [BK20190881]
  4. Seed Industry Vitalization Program of Jiangsu Province [JBGS[2021]117]
  5. earmarked fund for Jiangsu Agricultural Industry Technology System [JATS[2022]486]
  6. Open Project Program of Joint International Research Laboratory of Agriculture and AgriProduct Safety
  7. Ministry of Education of China
  8. Yangzhou University [JILAR KF202013]
  9. Yangzhou University, China

向作者/读者索取更多资源

This study demonstrates the therapeutic effect of melatonin against Staphylococcus aureus by regulating the expression of miR-16b/YAP1, inhibiting inflammation. It provides a new strategy for the prevention of bovine mastitis.
Staphylococcus aureus is a highly infectious pathogen and is a considerable threat to food hygiene and safety. Although melatonin is thought to exert an ameliorative effect on bovine mastitis, the regulatory mechanisms are unclear. In this study, we first verified the therapeutic effect of melatonin against S. aureus in vitro and in vivo, a screening of differentially expressed miRNAs and mRNAs among the blank, and S. aureus and melatonin + S. aureus groups by high-throughput sequencing identified miR-16b and YAP1, which exhibited 1.95-fold upregulated and 1.05-fold downregulated expression, respectively. Moreover, epigenetic studies showed that S. aureus inhibited miR-16b expression by methylation (increased DNMT1 expression). Additionally, the DNMT1 expression level was significantly decreased by melatonin treatment, which might indicate that the inhibition of DNMT1 by melatonin reduces the effect of S. aureus on miR-16b. The flow cytometry, scanning and transmission electron microscopy, EdU assay, and cell morphology results indicated that miR-16b in bovine mammary epithelial cells (in vitro) and in mice (in vivo) can modulate the maintenance of homeostasis and potentiate the anti-inflammatory response. In addition, YAP1 was demonstrated to be the target gene of miR-16b through quantitative real-time polymerase chain reaction, western blot, RNA immunoprecipitation, and functional assays. This study indicates that melatonin inhibits S. aureus-induced inflammation via microRNA-16b/YAP1-mediated regulation, and these findings might provide a new strategy for the prevention of bovine mastitis, facilitating further studies good of zoonotic diseases caused by S. aureus infection.

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