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RNA-seq analysis of different inflammatory reactions induced by lipopolysaccharide and lipoteichoic acid in bovine mammary epithelial cells

机译:脂多糖和脂乳腺上皮细胞脂多糖和脂脂酸诱导的不同炎症反应的RNA-SEQ分析

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摘要

Lipopolysaccharide (LPS) and lipoteichoic acid (LTA) are key virulence factors of Escherichia coli and Staphylococcus aureus respectively, and both of them could cause inflammatory reaction in bovine mammary glands. In this study, we used bovine mammary epithelial cells (BMECs) as pattern recognition receptors and stimulated them with LPS or LTA to investigate the global transcriptional response variations of BMECs to these two different virulent factors through RNA-Seq analysis. We found 100 differentially expressed genes (DEGs) with 95 up-regulated and 5 down-regulated genes in LPS-treated group, whereas 24 DEGs with 12 up-regulated and 12 down-regulated genes in LTA-treated group compared to control. Although the number and expression changes of DEGs are significantly different between LPS vs Control and LTA vs Control, KEGG pathway enrichment analysis showed the majorities of DEGs in each pair were enriched on cytokine-cytokine receptor interaction, NF-kappa B signaling pathway, and NOD-like receptor signaling pathway, especially cytokines and chemokines. These results provided a comprehensive analysis of gene expression profiles elicited by LPS and LTA in BMECs, contributing to the understanding of early "pathogen-host" interactions during intramammary infections.
机译:脂多糖(LPS)和脂素酸(LTA)分别是大肠杆菌和金黄色葡萄球菌的关键毒力因子,它们两者都可能引起牛乳腺的炎症反应。在这项研究中,我们使用牛乳腺上皮细胞(BMEC)作为模式识别受体,并用LPS或LTA刺激它们通过RNA-SEQ分析研究BMEC对这两种不同毒力因子的全局转录响应变化。我们发现100个差异表达的基因(DEGS),其中LPS处理基团中有95个上调和5个下调基因,而在LTA治疗组中具有12个上调和12个下调基因的24℃与对照组合。虽然DEG的数量和表达变化在LPS VS控制和LTA对照之间显着差异,但KEGG途径富集分析显示每对的多数次数富集在细胞因子 - 细胞因子受体相互作用,NF-Kappa信号通路和点头上富集 - 状受体信号传导途径,尤其是细胞因子和趋化因子。这些结果提供了对BMEC中LPS和LTA引发的基因表达谱的综合分析,有助于了解脑内感染期间的早期“病原体 - 宿主”相互作用。

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