Dissection of mammary cell landscape in ruminal dysbiosis-induced mastitis by single-cell RNA sequencing.

IF 11.4 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Caijun Zhao, Zhuohan Li, Miao Liu, Lijuan Bao, Chongshan Yuan, Yihong Zhao, Keyi Wu, Min Qiu, Yuhong He, Naisheng Zhang, Xiaoyu Hu, Yun Zhang, Fanglei Han, Yunhe Fu
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Abstract

Growing evidence has underscored the contribution of gastrointestinal dysbiosis to the onset of mastitis, however, the local cellular changes responsible for the pathological processes of ruminal dysbiosis-induced mastitis (RDIM) are still unclear. Here, we profiled mammary single-cell transcriptomes in goats with RDIM, complemented by ruminal metagenomic and untargeted metabolomic analyses of rumen fluid and serum. Our results indicated that compromised lactation and barrier integrity in LumSec were linked to RDIM. Increased inflammatory macrophages and DCs, γδT and CD4+ TH cell populations, along with reduced Tex/Treg and B cells were implicated in RDIM. Fibroblasts exhibited increased gene expression related to the extracellular matrix, while lymphatic endothelial cells and Vas-venous structures displayed elevated inflammatory gene expression. Tight junction integrity and apelin signaling pathways were compromised in Vas-capillary during RDIM. Notably, metagenomic analysis indicated that RDIM correlated with reduced ruminal microbial diversity and shifts in microbial community composition. Key metabolic pathways including microbial tryptophan metabolism, secondary bile acid biosynthesis, and vitamin metabolism were significantly diminished during RDIM. Furthermore, tryptophan-induced AHR signaling and secondary bile acid receptor GPBAR1, primarily expressed in vascular endothelial cells and macrophages, respectively, which were reduced during RDIM. Collectively, our study provides a comprehensive atlas of mammary cell landscapes in RDIM, which may enhance the understanding of mastitis pathogenesis.

单细胞RNA测序分析瘤胃生态失调性乳腺炎乳腺细胞景观。
越来越多的证据强调了胃肠道生态失调对乳腺炎发病的贡献,然而,负责瘤胃生态失调诱导乳腺炎(RDIM)病理过程的局部细胞变化仍不清楚。在这里,我们分析了RDIM山羊的乳腺单细胞转录组,并辅以瘤胃宏基因组学和瘤胃液和血清的非靶向代谢组学分析。我们的研究结果表明,LumSec的泌乳和屏障完整性受损与RDIM有关。炎症性巨噬细胞和dc、γδT和CD4+ TH细胞群的增加以及Tex/Treg和B细胞的减少与RDIM有关。成纤维细胞显示与细胞外基质相关的基因表达增加,而淋巴内皮细胞和血管-静脉结构显示炎症基因表达升高。在RDIM期间,vas -毛细血管的紧密连接完整性和apelin信号通路受到破坏。宏基因组分析显示,RDIM与瘤胃微生物多样性降低和微生物群落组成变化相关。关键的代谢途径包括微生物色氨酸代谢、次生胆汁酸生物合成和维生素代谢在RDIM期间显著减少。此外,色氨酸诱导的AHR信号和次级胆汁酸受体GPBAR1,主要分别在血管内皮细胞和巨噬细胞中表达,在RDIM期间减少。总的来说,我们的研究提供了RDIM中乳腺细胞景观的全面图谱,这可能会增强对乳腺炎发病机制的理解。
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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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