小麦胚芽日粮对四川白鹅肠道抗氧化能力、免疫功能和肠道微生物群的影响

IF 4 2区 生物学 Q2 MICROBIOLOGY Frontiers in Microbiology Pub Date : 2024-09-11 DOI:10.3389/fmicb.2024.1435454
Xin Wang, Dongmei Jiang, Xiaoguang An, Shuo Li, Yuxin Qi, Yujie Yang, Zelong Wang, Qian Sun, Weikang Ling, Chengweng Ji, Yuxuan Qi, Hengyong Xu, Chunchun Han, Hua Zhao, Bo Kang
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We assessed various aspects of geese intestinal health, including barrier function, digestibility, antioxidant capacity, immunity, microbiota, and metabolism.ResultsThe study revealed a significant increase in villus height (VH), villus height-to-crypt depth (VH/CD) ratio, amylase, and lipase activities in the duodenum and ileum, increased putrescine levels in the duodenum and jejunum, as well as spermidine levels in the jejunum (<jats:italic>P</jats:italic> &amp;lt; 0.05). LWG increased the total antioxidant capacity (T-AOC) in the duodenum, while decreasing levels of intestinal malondialdehyde (MDA), serum lipopolysaccharide (LPS), interleukin-6 (IL-6), and diamine oxidase (DAO) activity (<jats:italic>P</jats:italic> &amp;lt; 0.05). Furthermore, LWG increased the relative abundance of <jats:italic>Oscillospiraceae_unclassified</jats:italic>, <jats:italic>Ligilactobacillus</jats:italic>, and <jats:italic>Roseburia</jats:italic>, as well as increased levels of acetic acid, butyric acid, and valeric acid, while decreasing the relative abundance of <jats:italic>Subdoligranulum</jats:italic>, <jats:italic>Flavonifractor</jats:italic>, and <jats:italic>Klebsiella</jats:italic>. Additionally, we observed 17 up-regulated genes and 25 down-regulated genes in the jejunum, which are associated with the cell cycle and immunity. These genes play roles in pathways such as the p53 signaling pathway, cell cycle regulation, and pathways associated with immune modulation. On the other hand, HWG increased intestinal VH and spermidine levels, as well as amylase and lipase activities in the duodenum (<jats:italic>P</jats:italic> &amp;lt; 0.05). It also elevated ileal T-AOC and sIgA levels (<jats:italic>P</jats:italic> &amp;lt; 0.05), while reducing intestinal MDA content, serum LPS levels, DAO activity, and propionic acid in cecum contents (<jats:italic>P</jats:italic> &amp;lt; 0.05). Moreover, HWG increased the relative abundance of <jats:italic>Ligilactobacillus</jats:italic>, <jats:italic>Oscillospiraceae_unclassified</jats:italic>, and <jats:italic>Roseburia</jats:italic> (<jats:italic>P</jats:italic> &amp;lt; 0.05).ConclusionOverall, wheat germ diets, particularly the LWG diet demonstrated the ability to enhance antioxidant capacity, digestibility, immunity, and barrier properties of the intestinal tract, while modulating the gut microbiota and metabolism. Therefore, wheat germ diets hold promise in improving intestinal health by preserving barrier function and regulating flora structure.","PeriodicalId":12466,"journal":{"name":"Frontiers in Microbiology","volume":null,"pages":null},"PeriodicalIF":4.0000,"publicationDate":"2024-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effects of wheat germ diet on intestinal antioxidant capacity, immunological function and gut microbiota of Sichuan white geese\",\"authors\":\"Xin Wang, Dongmei Jiang, Xiaoguang An, Shuo Li, Yuxin Qi, Yujie Yang, Zelong Wang, Qian Sun, Weikang Ling, Chengweng Ji, Yuxuan Qi, Hengyong Xu, Chunchun Han, Hua Zhao, Bo Kang\",\"doi\":\"10.3389/fmicb.2024.1435454\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"BackgroundWheat germ is known for its antioxidant, anti-inflammatory, and disease resistance properties in animals. 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LWG increased the total antioxidant capacity (T-AOC) in the duodenum, while decreasing levels of intestinal malondialdehyde (MDA), serum lipopolysaccharide (LPS), interleukin-6 (IL-6), and diamine oxidase (DAO) activity (<jats:italic>P</jats:italic> &amp;lt; 0.05). Furthermore, LWG increased the relative abundance of <jats:italic>Oscillospiraceae_unclassified</jats:italic>, <jats:italic>Ligilactobacillus</jats:italic>, and <jats:italic>Roseburia</jats:italic>, as well as increased levels of acetic acid, butyric acid, and valeric acid, while decreasing the relative abundance of <jats:italic>Subdoligranulum</jats:italic>, <jats:italic>Flavonifractor</jats:italic>, and <jats:italic>Klebsiella</jats:italic>. Additionally, we observed 17 up-regulated genes and 25 down-regulated genes in the jejunum, which are associated with the cell cycle and immunity. 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引用次数: 0

摘要

背景小麦胚芽在动物体内具有抗氧化、抗炎和抗病的作用,但其对四川白鹅肠道的影响尚不清楚。本研究将 30 只 250 日龄的鹅分为三个等量组,即对照组、LWG 组(21.8% 小麦胚芽)和 HWG 组(43.6% 小麦胚芽),实验持续 12 周。研究结果表明,绒毛高度(VH)、绒毛高度与绒毛深度比(VH/CD)、十二指肠和回肠中淀粉酶和脂肪酶活性显著增加,十二指肠和空肠中腐乳蛋白含量增加,空肠中精胺含量增加(P&;lt;0.05)。LWG提高了十二指肠的总抗氧化能力(T-AOC),同时降低了肠道丙二醛(MDA)、血清脂多糖(LPS)、白细胞介素-6(IL-6)和二胺氧化酶(DAO)活性的水平(P &;lt;0.05)。此外,LWG 增加了 Oscillospiraceae_unclassified、Ligilactobacillus 和 Roseburia 的相对丰度,并提高了乙酸、丁酸和戊酸的水平,同时降低了 Subdoligranulum、Flavonifractor 和 Klebsiella 的相对丰度。此外,我们还观察到空肠中有 17 个基因上调,25 个基因下调,这些基因与细胞周期和免疫有关。这些基因在 p53 信号通路、细胞周期调控和免疫调节相关通路中发挥作用。另一方面,HWG 增加了肠道 VH 和亚精胺的水平,以及十二指肠中淀粉酶和脂肪酶的活性(P&P;lt; 0.05)。它还提高了回肠 T-AOC 和 sIgA 水平(P&;lt; 0.05),同时降低了肠道 MDA 含量、血清 LPS 水平、DAO 活性和盲肠内容物中的丙酸含量(P&;lt; 0.05)。总之,小麦胚芽日粮,尤其是 LWG 日粮能够提高抗氧化能力、消化率、免疫力和肠道屏障性能,同时调节肠道微生物群和新陈代谢。因此,小麦胚芽膳食有望通过保护屏障功能和调节菌群结构来改善肠道健康。
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Effects of wheat germ diet on intestinal antioxidant capacity, immunological function and gut microbiota of Sichuan white geese
BackgroundWheat germ is known for its antioxidant, anti-inflammatory, and disease resistance properties in animals. However, its effect on the gut of Sichuan white geese remains unclear.MethodIn this study, thirty 250-day-old geese were divided into three equal groups, the control group, LWG group (21.8% wheat germ) and HWG group (43.6% wheat germ), the experiment lasted 12 weeks. We assessed various aspects of geese intestinal health, including barrier function, digestibility, antioxidant capacity, immunity, microbiota, and metabolism.ResultsThe study revealed a significant increase in villus height (VH), villus height-to-crypt depth (VH/CD) ratio, amylase, and lipase activities in the duodenum and ileum, increased putrescine levels in the duodenum and jejunum, as well as spermidine levels in the jejunum (P &lt; 0.05). LWG increased the total antioxidant capacity (T-AOC) in the duodenum, while decreasing levels of intestinal malondialdehyde (MDA), serum lipopolysaccharide (LPS), interleukin-6 (IL-6), and diamine oxidase (DAO) activity (P &lt; 0.05). Furthermore, LWG increased the relative abundance of Oscillospiraceae_unclassified, Ligilactobacillus, and Roseburia, as well as increased levels of acetic acid, butyric acid, and valeric acid, while decreasing the relative abundance of Subdoligranulum, Flavonifractor, and Klebsiella. Additionally, we observed 17 up-regulated genes and 25 down-regulated genes in the jejunum, which are associated with the cell cycle and immunity. These genes play roles in pathways such as the p53 signaling pathway, cell cycle regulation, and pathways associated with immune modulation. On the other hand, HWG increased intestinal VH and spermidine levels, as well as amylase and lipase activities in the duodenum (P &lt; 0.05). It also elevated ileal T-AOC and sIgA levels (P &lt; 0.05), while reducing intestinal MDA content, serum LPS levels, DAO activity, and propionic acid in cecum contents (P &lt; 0.05). Moreover, HWG increased the relative abundance of Ligilactobacillus, Oscillospiraceae_unclassified, and Roseburia (P &lt; 0.05).ConclusionOverall, wheat germ diets, particularly the LWG diet demonstrated the ability to enhance antioxidant capacity, digestibility, immunity, and barrier properties of the intestinal tract, while modulating the gut microbiota and metabolism. Therefore, wheat germ diets hold promise in improving intestinal health by preserving barrier function and regulating flora structure.
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来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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