论文标题
牧场的摄入量可以防止肠鹅肠道碱性磷酸酶促进肠道菌群促进的商业饮食诱导的脂多糖的产生
Pasture Intake Protects Against Commercial Diet-induced Lipopolysaccharide Production Facilitated by Gut Microbiota through Activating Intestinal Alkaline Phosphatase Enzyme in Meat Geese
论文作者
论文摘要
内部进食系统(IHF,低饮食纤维来源)可能会通过增加的内毒素血症(脂多糖)而导致肉类鹅的盲肠微生物群组成和炎症反应改变,而肠道碱性磷酸酶(ALP)产生降低。尚未在肉鹅中研究人造牧场放牧系统(AGF,高饮食纤维来源)对调节肠道菌群结构和肠道屏障功能的影响。通过减少LPS诱导的活性氧(ROS)的产生,肠道ALP功能调节肠道微生物稳态和屏障功能似乎可以抑制促炎性细胞因子。我们研究的目的是研究该酶在减弱ROS的产生中是否可以发挥关键作用,然后ROS促进NF- \ k {appa} B途径诱导的肉鹅的全身性炎症。首先,我们通过肉鹅中的16个SRNA测序评估了IHF和AGF对肠道微生物组成的影响。在肠道菌群分析中,与IHF肉鹅相比,补充牧场的肉鹅表现出微生物丰富性和多样性的显着降低,表现出AGF系统的抗菌,抗氧化和抗炎能力。通过血清和盲肠组织的蛋白质表达以及盲肠组织的定量PCR分析。我们证实了代表LPS去磷酸化介导的TLR4/MYD88诱导的AGF肉鹅的ROS还原机制的肠道ALP诱导的NRF2信号通路的显着增加。此外,对肠道菌群的前44个宿主标记的相关性分析表明,通过减少ROS介导的NF- \ k {appA} B途径诱导的肠道渗透性,全身性炎症和衰老表型,人为的牧场摄入诱导的肠道屏障功能。
In-house feeding system (IHF, a low dietary fiber source) may cause altered cecal microbiota composition and inflammatory responses in meat geese via increased endotoxemia (lipopolysaccharides) with reduced intestinal alkaline phosphatase (ALP) production. The effects of artificial pasture grazing system (AGF, a high dietary fiber source) on modulating gut microbiota architecture and gut barrier functions have not been investigated in meat geese. The intestinal ALP functions to regulate gut microbial homeostasis and barrier function appears to inhibit pro-inflammatory cytokines by reducing LPS-induced reactive oxygen species (ROS) production. The purpose of our study was to investigate whether this enzyme could play a critical role in attenuating ROS generation and then ROS facilitated NF-\k{appa}B pathway-induced systemic inflammation in meat geese. First, we assessed the impacts of IHF and AGF on gut microbial composition via 16 sRNA sequencing in meat geese. In the gut microbiota analysis, meat geese supplemented with pasture demonstrated a significant reduction in microbial richness and diversity compared to IHF meat geese demonstrating antimicrobial, antioxidation, and anti-inflammatory ability of AGF system. Second host markers analysis through protein expression of serum and cecal tissues and quantitative PCR of cecal tissues were evaluated. We confirmed a significant increase in intestinal ALP-induced Nrf2 signaling pathway representing LPS dephosphorylation mediated TLR4/MyD88 induced ROS reduction mechanisms in AGF meat geese. Further, the correlation analysis of top 44 host markers with gut microbiota shows that artificial pasture intake induced gut barrier functions via reducing ROS-mediated NF-\k{appa}B pathway-induced gut permeability, systemic inflammation, and aging phenotypes.