Enterogenic Stenotrophomonas maltophilia migrates to the mammary gland to induce mastitis by activating the calcium-ROS-AMPK-mTOR-autophagy pathway

IF 7 1区 农林科学 Q1 Agricultural and Biological Sciences
Zhaoqi He, Caijun Zhao, Yuhong He, Zhuoyu Liu, Guyue Fan, Kun Zhu, Yiqi Wang, Naisheng Zhang, Yunhe Fu, Xiaoyu Hu
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Abstract

Mastitis is an inflammatory disease of the mammary gland that has serious economic impacts on the dairy industry and endangers food safety. Our previous study found that the body has a gut/rumen-mammary gland axis and that disturbance of the gut/rumen microbiota could result in ‘gastroenterogenic mastitis’. However, the mechanism has not been fully clarified. Recently, we found that long-term feeding of a high-concentrate diet induced mastitis in dairy cows, and the abundance of Stenotrophomonas maltophilia (S. maltophilia) was significantly increased in both the rumen and milk microbiota. Accordingly, we hypothesized that ‘gastroenterogenic mastitis’ can be induced by the migration of endogenous gut bacteria to the mammary gland. Therefore, this study investigated the mechanism by which enterogenic S. maltophilia induces mastitis. First, S. maltophilia was labelled with superfolder GFP and administered to mice via gavage. The results showed that treatment with S. maltophilia promoted the occurrence of mastitis and increased the permeability of the blood-milk barrier, leading to intestinal inflammation and intestinal leakage. Furthermore, tracking of ingested S. maltophilia revealed that S. maltophilia could migrate from the gut to the mammary gland and induce mastitis. Subsequently, mammary gland transcriptome analysis showed that the calcium and AMPK signalling pathways were significantly upregulated in mice treated with S. maltophilia. Then, using mouse mammary epithelial cells (MMECs), we verified that S. maltophilia induces mastitis through activation of the calcium-ROS-AMPK-mTOR-autophagy pathway. In conclusion, the results showed that enterogenic S. maltophilia could migrate from the gut to the mammary gland via the gut-mammary axis and activate the calcium-ROS-AMPK-mTOR-autophagy pathway to induce mastitis. Targeting the gut-mammary gland axis may also be an effective method to treat mastitis.
肠源性嗜麦芽血单胞菌通过激活钙-ROS-AMPK-mTOR-自噬途径迁移到乳腺诱发乳腺炎
乳腺炎是一种乳腺炎症性疾病,对乳制品行业造成严重的经济影响,并危及食品安全。我们之前的研究发现,人体有一个肠道/乳腺-乳腺轴,肠道/乳腺微生物群紊乱可能导致 "胃肠源性乳腺炎"。然而,其机制尚未完全阐明。最近,我们发现长期饲喂高浓缩饲料会诱发奶牛乳腺炎,而且瘤胃和牛奶微生物群中的嗜麦芽霉单胞菌(S. maltophilia)数量显著增加。因此,我们推测 "肠胃源性乳腺炎 "可能是由内源性肠道细菌迁移到乳腺而诱发的。因此,本研究调查了肠源性嗜麦芽酵母菌诱发乳腺炎的机制。首先,嗜麦芽糖酵母菌被标记为超级夹子 GFP,并通过灌胃给小鼠喂食。结果表明,嗜麦芽酵母菌能促进乳腺炎的发生,并增加血乳屏障的通透性,导致肠道炎症和肠道渗漏。此外,对摄入的嗜麦芽糖酵母菌进行追踪发现,嗜麦芽糖酵母菌可从肠道迁移到乳腺并诱发乳腺炎。随后,乳腺转录组分析表明,嗜麦芽糖酵母菌治疗小鼠的钙和 AMPK 信号通路显著上调。然后,我们利用小鼠乳腺上皮细胞(MMECs)验证了嗜麦芽糖酵母菌是通过激活钙-ROS-AMPK-mTOR-自噬途径诱导乳腺炎的。总之,研究结果表明,肠源性嗜麦芽糖酵母菌可通过肠道-乳腺轴从肠道迁移到乳腺,并激活钙-ROS-AMPK-mTOR-自噬途径诱发乳腺炎。针对肠道-乳腺轴也可能是治疗乳腺炎的有效方法。
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来源期刊
Journal of Animal Science and Biotechnology
Journal of Animal Science and Biotechnology AGRICULTURE, DAIRY & ANIMAL SCIENCE-
CiteScore
9.90
自引率
2.90%
发文量
822
审稿时长
17 weeks
期刊介绍: Journal of Animal Science and Biotechnology is an open access, peer-reviewed journal that encompasses all aspects of animal science and biotechnology. That includes domestic animal production, animal genetics and breeding, animal reproduction and physiology, animal nutrition and biochemistry, feed processing technology and bioevaluation, animal biotechnology, and meat science.
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