Shi Zhihai, Wang Wenjia, Shokrollahi Borhan, Wang Wenqi, Abdel-Shafy Hamdy, Deng Tingxian
Institute of Animal Husbandry and Veterinary Medicine, Henan Academy of Agricultural Sciences, Zhengzhou 450002, China.
Guangxi Provincial Key Laboratory of Buffalo Genetics, Breeding and Reproduction Technology, Buffalo Research Institute, Chinese Academy of Agricultural Sciences, Nanning 530001, China.
J Agric Food Chem. 2025 Apr 16;73(15):8784-8797. doi: 10.1021/acs.jafc.4c10550. Epub 2025 Apr 1.
Mastitis is a prevalent inflammatory disease in dairy herds and presents substantial economic and welfare challenges. Although antibiotics are the most widely used and effective treatment for mastitis, research into alternative antibiotics with plant-derived compounds has gained increasing attention due to the high side effects of antibiotics. Quercetin is known to play a crucial role in regulating inflammation, yet its role in preventing and treating mastitis requires further investigation. To fill this gap, we construct a bovine mastitis model using () as the pathogen and bovine mammary epithelial cells (BMECs) as the cell model. Based on this, our study further investigated the therapeutic potential of quercetin by using assays and murine models. Our results demonstrated that quercetin inhibited the inflammatory response and reduced morphological damage in -induced BMECs by disrupting cell adhesion. Direct RNA sequencing revealed that multiple genes enriched in the TNF/IL-17 pathway were pivotal in the ability of quercetin to mitigate inflammation, which was influenced by N6-methyladenosine (m6A) methylation. Quercetin effectively modulated CCL5 expression, a key chemokine in inflammatory responses in -induced BMECs, through m6A methylation mediated by YTHDF2, revealing a novel epigenetic mechanism in mastitis. RNA-seq analysis showed that quercetin significantly altered genes related to inflammation, extracellular matrix regulation, and matrix metalloproteinase activity, including MMP3, MMP1, MMP1A, and IGFBP3, indicating its impact on tissue remodeling and inflammation. Additionally, quercetin disrupted adhesion to BMECs, inhibited biofilm formation, and reduced the severity of infection. The assay supported the notion that quercetin regulates CCL5 activity to alleviate the inflammatory response in an m6A-YTHDF2-dependent manner. This study demonstrated the dual role of quercetin in inflammation suppression and epigenetic modulation via m6A, positioning quercetin as a promising therapeutic for bovine mastitis and suggesting new treatment strategies targeting CCL5- and m6A-related pathways.
乳腺炎是奶牛群中一种普遍的炎症性疾病,带来了重大的经济和福利挑战。尽管抗生素是治疗乳腺炎最广泛使用且有效的方法,但由于抗生素的高副作用,对植物源化合物替代抗生素的研究越来越受到关注。已知槲皮素在调节炎症中起关键作用,但其在预防和治疗乳腺炎中的作用仍需进一步研究。为填补这一空白,我们以()作为病原体,构建了牛乳腺炎模型,并以牛乳腺上皮细胞(BMECs)作为细胞模型。在此基础上,我们的研究通过使用()实验和小鼠模型进一步研究了槲皮素的治疗潜力。我们的结果表明,槲皮素通过破坏细胞黏附来抑制炎症反应,并减少()诱导的BMECs中的形态损伤。直接RNA测序显示,富集于TNF/IL-17途径的多个基因在槲皮素减轻炎症的能力中起关键作用,这受到N6-甲基腺苷(m6A)甲基化的影响。槲皮素通过YTHDF2介导的m6A甲基化有效地调节了CCL5的表达,CCL5是()诱导的BMECs炎症反应中的关键趋化因子,揭示了乳腺炎中的一种新的表观遗传机制。RNA-seq分析表明,槲皮素显著改变了与炎症、细胞外基质调节和基质金属蛋白酶活性相关的基因,包括MMP3、MMP1、MMP1A和IGFBP3,表明其对组织重塑和炎症的影响。此外,槲皮素破坏了()与BMECs的黏附,抑制了生物膜形成,并降低了感染的严重程度。()实验支持了槲皮素以m6A-YTHDF2依赖性方式调节CCL5活性以减轻炎症反应的观点。这项研究证明了槲皮素在通过m6A抑制炎症和表观遗传调节中的双重作用,将槲皮素定位为牛乳腺炎的一种有前景的治疗方法,并提出了针对CCL5和m6A相关途径的新治疗策略。