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在蛋内注射木寡糖和甘露寡糖对肉鸡肠道健康的影响。

Impact of in ovo administration of xylo- and mannooligosaccharides on broiler chicken gut health.

作者信息

Bełdowska Aleksandra, Siwek Maria, Biesek Jakub, Barszcz Marcin, Tuśnio Anna, Gawin Kamil, Dunisławska Aleksandra

机构信息

Department of Animal Biotechnology and Genetics, Faculty of Animal Breeding and Biology, Bydgoszcz University of Science and Technology, Mazowiecka 28, 85-084 Bydgoszcz, Poland.

Department of Animal Biotechnology and Genetics, Faculty of Animal Breeding and Biology, Bydgoszcz University of Science and Technology, Mazowiecka 28, 85-084 Bydgoszcz, Poland.

出版信息

Poult Sci. 2024 Dec;103(12):104261. doi: 10.1016/j.psj.2024.104261. Epub 2024 Aug 24.

DOI:10.1016/j.psj.2024.104261
PMID:39265513
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11416585/
Abstract

The intestinal mucosa creates a connection between the gut microbiota and the host. This study aimed to modify the gut microbiota of broiler chickens by in ovo stimulation with xylo-oligosaccharide (XOS) and manno-oligosaccharide (MOS) prebiotics and to determine the changes occurring in specific gut segments. Three hundred incubated eggs of Ross 308 broiler chickens on the 12th d of incubation were injected with: saline (control), xylotriose (XOS3), xylotetrose (XOS4), mannotriose (MOS3) or mannotetrose (MOS4). Tissue and digesta samples were collected post-mortem from 8 randomly selected individuals from each group, on d 42 after hatching. Gene expression analysis in the cecum and ileum was performed by RT-qPCR for a panel of genes: innate immune response genes (IL-2, IL-4, IL-6, IL-8, IL-10, IL-12, IL-17, IL-1β, IFNγ, IFNβ), nutrient sensing and nutrient transport genes (FFAR2, FFAR4, GLUT1, GLUT2, GLUT5), host defence peptides (AvBD1, CATHL2), and barrier function genes (MUC6, CLDN1, TJAP). The relative abundance of bacteria was determined by qPCR for individual bacteria (Akkermansia muciniphilla, Bifidobacterium spp., Clostridium difficile, Escherichia coli, Faecalibacterium prausnitzii, and Lactobacillus spp.). Stimulation with prebiotics caused changes in the abundance of bacteria especially Lactobacillus spp. and Bifidobacterium spp. in the cecum. The abundance of both genera increased in each study group compared to the control group. The highest abundance of Bifidobacterium spp. in the ileum was found in the MOS3 group compared to the control group. There were changes in the XOS4 and MOS3 groups in the expression of: FFAR4, GLUT1, AvBD1, CATHL2, IL-2, IL-12, and IL-17 in the caecum. In conclusion, in ovo administration of prebiotics increased intestinal colonization by bacteria. The prebiotics influenced gene expression levels via changes in the gut microbiota.

摘要

肠道黏膜在肠道微生物群与宿主之间建立了联系。本研究旨在通过在孵化期对罗斯308肉鸡进行卵内木寡糖(XOS)和甘露寡糖(MOS)益生元刺激来改变其肠道微生物群,并确定特定肠道段发生的变化。在孵化第12天,对300枚罗斯308肉鸡种蛋注射:生理盐水(对照组)、木三糖(XOS3)、木四糖(XOS4)、甘露三糖(MOS3)或甘露四糖(MOS4)。孵化后第42天,从每组随机选取8只个体处死后采集组织和消化物样本。通过RT-qPCR对盲肠和回肠中的一组基因进行基因表达分析:先天性免疫反应基因(IL-2、IL-4、IL-6、IL-8、IL-10、IL-12、IL-17、IL-1β、IFNγ、IFNβ)、营养感知和营养转运基因(FFAR2、FFAR4、GLUT1、GLUT2、GLUT5)、宿主防御肽(AvBD1、CATHL2)以及屏障功能基因(MUC6、CLDN1、TJAP)。通过qPCR测定个体细菌(嗜黏蛋白阿克曼氏菌、双歧杆菌属、艰难梭菌、大肠杆菌、普拉梭菌和乳酸杆菌属)的相对丰度。益生元刺激导致细菌丰度发生变化,尤其是盲肠中的乳酸杆菌属和双歧杆菌属。与对照组相比,每个研究组中这两个属的丰度均增加。与对照组相比,MOS3组回肠中双歧杆菌属的丰度最高。XOS4组和MOS3组盲肠中FFAR4、GLUT1、AvBD1、CATHL2、IL-2、IL-12和IL-17的表达发生了变化。总之,卵内施用益生元增加了细菌在肠道的定植。益生元通过改变肠道微生物群影响基因表达水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/11416585/f659a5b20844/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/11416585/131da11a6868/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/11416585/d30d5975f675/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/11416585/821a39676c9f/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/11416585/3145e778ddb8/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/11416585/f659a5b20844/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/11416585/131da11a6868/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/11416585/d30d5975f675/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/11416585/821a39676c9f/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/11416585/3145e778ddb8/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee91/11416585/f659a5b20844/gr5.jpg

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