嗜粘杆菌衍生外膜囊泡作为治疗乳腺炎的新方法:来自体外和体内研究的见解

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Boqi Zhang, Nan Wang, Guitian He, Tong Chen, Jinxin Zong, Caomeihui Shen, Yueying Wang, Chuanghang Li, Xuanqi Yin, Yang Meng, Fuqiang Chang, Sihui Wang, Chunjin Li, Xu Zhou
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引用次数: 0

摘要

乳腺炎是影响乳制品行业的主要疾病。尽管抗生素是治疗乳腺炎最普遍的方法,但过度使用抗生素对公众健康构成重大风险。益生菌治疗已成为控制乳腺炎的一种有希望的替代方法,但缺乏对特定益生菌治疗乳腺炎的疗效和机制的全面研究。在这里,我们研究了嗜muciniphila (a.m uiniphila)及其衍生的外膜囊泡(AOMVs)作为乳腺炎治疗剂的潜力。通过对健康奶牛和乳腺炎奶牛牛奶中微生物群组成的分析,发现了微生物群落的显著差异。Spearman相关分析显示乳腺炎乳中Verrucomicrobia和Akkermansia的相对丰度与炎性细胞因子水平呈显著负相关。此外,我们评估了活的和巴氏灭菌的嗜粘杆菌在脂多糖(LPS)诱导的牛乳腺上皮细胞(MAC-T)炎症反应中的作用。与巴氏灭菌的嗜粘杆菌相比,活的嗜粘杆菌表现出更强的抗炎作用,特别是抑制TLR4和NF-κB信号通路。我们还证明嗜粘杆菌的这些作用可能是通过aomv介导的。随后,利用lps诱导的乳腺炎小鼠模型,在体内评估aomv的治疗潜力。结果表明,aomv靶向乳腺,减轻lps诱导的损伤,降低炎症细胞因子水平和信号通路激活。最后,我们对嗜粘杆菌对奶牛乳腺炎的治疗效果进行了初步研究。乳腺炎奶牛乳中添加嗜粘杆菌可显著降低乳腺炎奶牛乳中的体细胞计数。值得注意的是,5头奶牛中有4头SCC下降至2 × 105细胞/mL以下,加州乳腺炎试验结果为阴性。我们的研究结果为嗜粘液芽胞杆菌和aomv治疗乳腺炎的治疗潜力提供了令人信服的证据。这些结果不仅突出了嗜muciniphila作为一种潜在的益生菌的抗炎特性,为开发抗生素治疗的替代方案提供了新的策略,而且为探索外膜囊泡在宿主-微生物界面中的作用提供了理论基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Akkermansia muciniphila-Derived Outer Membrane Vesicles as a Novel Therapeutic Approach for Mastitis: Insights From In Vitro and Vivo Studies

Akkermansia muciniphila-Derived Outer Membrane Vesicles as a Novel Therapeutic Approach for Mastitis: Insights From In Vitro and Vivo Studies

Mastitis is a major disease affecting the dairy industry. Although antibiotics are the most prevalent treatment for mastitis, their overuse presents significant risks to public health. Probiotic therapy has emerged as a promising alternative for controlling mastitis, but there is a lack of comprehensive studies on the efficacy and mechanisms of specific probiotics in treating this condition. Here, we investigate the potential of Akkermansia muciniphila (A. muciniphila) and its derived outer membrane vesicles (AOMVs) as therapeutic agents for mastitis. Significant differences in microbial communities were identified through an analysis of the microbiota composition in milk from healthy and mastitis cows. Spearman's correlation analysis revealed a significant negative correlation between the relative abundances of Verrucomicrobia and Akkermansia and the levels of inflammatory cytokines in mastitis milk. Furthermore, we evaluated the roles of live and pasteurized A. muciniphila in lipopolysaccharide (LPS)-induced inflammatory responses in bovine mammary epithelial cells (MAC-T). Compared to pasteurized A. muciniphila, live A. muciniphila exhibited a stronger anti-inflammatory effect, notably inhibiting the TLR4 and NF-κB signaling pathways. We also demonstrated that these effects of A. muciniphila may be mediated through AOMVs. Subsequently, the therapeutic potential of AOMVs was evaluated in vivo using an LPS-induced mastitis mouse model. The results demonstrated that AOMVs targeted the mammary glands, alleviated LPS-induced damage, and reduced inflammatory cytokine levels and signaling pathway activation. Finally, we conducted a preliminary investigation to assess the therapeutic effects of A. muciniphila on mastitis in dairy cows. Administration of A. muciniphila significantly reduced somatic cell count (SCC) in the milk of cows with mastitis. Notably, four of the five treated cows showed a decrease in SCC to below 2 × 105 cells/mL, with negative results in the California Mastitis Test. Our findings provide compelling evidence for the therapeutic potential of A. muciniphila and AOMVs in the treatment of mastitis. These results not only highlight the anti-inflammatory properties of A. muciniphila as a potential probiotic, proposing novel strategies for developing alternatives to antibiotic therapies, but also provide a theoretical basis for exploring the role of outer membrane vesicles in the host-microbe interface.

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来源期刊
The FASEB Journal
The FASEB Journal 生物-生化与分子生物学
CiteScore
9.20
自引率
2.10%
发文量
6243
审稿时长
3 months
期刊介绍: The FASEB Journal publishes international, transdisciplinary research covering all fields of biology at every level of organization: atomic, molecular, cell, tissue, organ, organismic and population. While the journal strives to include research that cuts across the biological sciences, it also considers submissions that lie within one field, but may have implications for other fields as well. The journal seeks to publish basic and translational research, but also welcomes reports of pre-clinical and early clinical research. In addition to research, review, and hypothesis submissions, The FASEB Journal also seeks perspectives, commentaries, book reviews, and similar content related to the life sciences in its Up Front section.
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