小鼠急性接触棒曲霉素导致肠道微生物群和代谢紊乱

IF 7.4 Q1 FOOD SCIENCE & TECHNOLOGY
Food frontiers Pub Date : 2024-04-11 DOI:10.1002/fft2.397
Ting Zhang, Zimeng Guo, Jiayin Che, Min Yan, Jingyimei Liang, Furong Wang, Jinhong Hu, Wei Song, Yahong Yuan, Tianli Yue
{"title":"小鼠急性接触棒曲霉素导致肠道微生物群和代谢紊乱","authors":"Ting Zhang,&nbsp;Zimeng Guo,&nbsp;Jiayin Che,&nbsp;Min Yan,&nbsp;Jingyimei Liang,&nbsp;Furong Wang,&nbsp;Jinhong Hu,&nbsp;Wei Song,&nbsp;Yahong Yuan,&nbsp;Tianli Yue","doi":"10.1002/fft2.397","DOIUrl":null,"url":null,"abstract":"<p>Patulin (PAT) is a common mycotoxin in moldy fruits that causes gastrointestinal injury if accidentally ingested. Some studies have reported the symptoms of intestinal injury caused by PAT. However, the effects of PAT on the gut microbiota and gut metabolism remain to be investigated, which is important for clarifying the toxicological mechanisms. Thus, C57/BL6J mice were gavaged once with 0, 1, 4, and 16 mg/kg body weight PAT, and the small intestinal and colonic contents were collected. The 16S rRNA sequencing and targeted and untargeted metabolomics were applied to assess the alterations in microbiota and metabolism, respectively. The results showed that <i>Mycoplasma</i>, <i>Dubosiella</i>, and <i>Enterorhabdus</i> were jointly affected by acute PAT exposure in the small intestinal and colonic contents. Some inflammation-related bacteria, such as <i>Mycoplasma</i> in the small intestine and <i>Mycoplasma</i>, <i>Alistipes</i>, <i>Eubacterium_coprostanoligenes_group</i>, and <i>Candidatus_saccharimona</i> in the colon, increased with increasing doses of PAT. In metabolic results, amino acids decreased and bile acids elevated in both intestinal contents; lipids increased in the small intestinal contents but decreased in the colonic contents. PAT mainly affected host amino acid and lipid metabolism; it also downregulated microbial tryptophan metabolism and short-chain fatty acid levels (mainly in the colon), which could be explained by the decrease of <i>Bacteroides</i> and <i>Lactobacillus</i>. These influences in microbial abundances and metabolic levels persisted after PAT and its products were cleared. These results fill a gap in the effects of PAT on the gut microbiota and provide a theoretical basis for elucidating the toxic mechanism of mycotoxins.</p>","PeriodicalId":73042,"journal":{"name":"Food frontiers","volume":null,"pages":null},"PeriodicalIF":7.4000,"publicationDate":"2024-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/fft2.397","citationCount":"0","resultStr":"{\"title\":\"Dysbiosis of intestinal microbiota and metabolism caused by acute patulin exposure in mice\",\"authors\":\"Ting Zhang,&nbsp;Zimeng Guo,&nbsp;Jiayin Che,&nbsp;Min Yan,&nbsp;Jingyimei Liang,&nbsp;Furong Wang,&nbsp;Jinhong Hu,&nbsp;Wei Song,&nbsp;Yahong Yuan,&nbsp;Tianli Yue\",\"doi\":\"10.1002/fft2.397\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Patulin (PAT) is a common mycotoxin in moldy fruits that causes gastrointestinal injury if accidentally ingested. Some studies have reported the symptoms of intestinal injury caused by PAT. However, the effects of PAT on the gut microbiota and gut metabolism remain to be investigated, which is important for clarifying the toxicological mechanisms. Thus, C57/BL6J mice were gavaged once with 0, 1, 4, and 16 mg/kg body weight PAT, and the small intestinal and colonic contents were collected. The 16S rRNA sequencing and targeted and untargeted metabolomics were applied to assess the alterations in microbiota and metabolism, respectively. The results showed that <i>Mycoplasma</i>, <i>Dubosiella</i>, and <i>Enterorhabdus</i> were jointly affected by acute PAT exposure in the small intestinal and colonic contents. Some inflammation-related bacteria, such as <i>Mycoplasma</i> in the small intestine and <i>Mycoplasma</i>, <i>Alistipes</i>, <i>Eubacterium_coprostanoligenes_group</i>, and <i>Candidatus_saccharimona</i> in the colon, increased with increasing doses of PAT. In metabolic results, amino acids decreased and bile acids elevated in both intestinal contents; lipids increased in the small intestinal contents but decreased in the colonic contents. PAT mainly affected host amino acid and lipid metabolism; it also downregulated microbial tryptophan metabolism and short-chain fatty acid levels (mainly in the colon), which could be explained by the decrease of <i>Bacteroides</i> and <i>Lactobacillus</i>. These influences in microbial abundances and metabolic levels persisted after PAT and its products were cleared. These results fill a gap in the effects of PAT on the gut microbiota and provide a theoretical basis for elucidating the toxic mechanism of mycotoxins.</p>\",\"PeriodicalId\":73042,\"journal\":{\"name\":\"Food frontiers\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":7.4000,\"publicationDate\":\"2024-04-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/fft2.397\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Food frontiers\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/fft2.397\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"FOOD SCIENCE & TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Food frontiers","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/fft2.397","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"FOOD SCIENCE & TECHNOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

棒曲霉素(PAT)是霉变水果中常见的一种霉菌毒素,一旦误食会造成肠胃损伤。一些研究报告了 PAT 引起的肠道损伤症状。然而,PAT 对肠道微生物群和肠道新陈代谢的影响仍有待研究,这对阐明其毒性机制非常重要。因此,给 C57/BL6J 小鼠灌胃一次 0、1、4 和 16 mg/kg 体重的 PAT,并收集小肠和结肠内容物。应用 16S rRNA 测序以及靶向和非靶向代谢组学分别评估了微生物群和代谢的改变。结果显示,小肠和结肠内容物中的支原体、Dubosiella和Enterorhabdus共同受到急性PAT暴露的影响。一些与炎症有关的细菌,如小肠中的支原体和结肠中的支原体、Alistipes、Eubacterium_coprostanoligenes_group 和 Candidatus_saccharimona,随着 PAT 剂量的增加而增加。在代谢结果中,两种肠内容物中的氨基酸都减少了,胆汁酸增加了;小肠内容物中的脂质增加了,但结肠内容物中的脂质减少了。PAT 主要影响宿主的氨基酸和脂质代谢;它还降低了微生物的色氨酸代谢和短链脂肪酸水平(主要在结肠中),这可以用乳酸杆菌和乳酸杆菌的减少来解释。这些对微生物丰度和代谢水平的影响在 PAT 及其产物被清除后依然存在。这些结果填补了 PAT 对肠道微生物群影响方面的空白,为阐明霉菌毒素的毒性机制提供了理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dysbiosis of intestinal microbiota and metabolism caused by acute patulin exposure in mice

Dysbiosis of intestinal microbiota and metabolism caused by acute patulin exposure in mice

Patulin (PAT) is a common mycotoxin in moldy fruits that causes gastrointestinal injury if accidentally ingested. Some studies have reported the symptoms of intestinal injury caused by PAT. However, the effects of PAT on the gut microbiota and gut metabolism remain to be investigated, which is important for clarifying the toxicological mechanisms. Thus, C57/BL6J mice were gavaged once with 0, 1, 4, and 16 mg/kg body weight PAT, and the small intestinal and colonic contents were collected. The 16S rRNA sequencing and targeted and untargeted metabolomics were applied to assess the alterations in microbiota and metabolism, respectively. The results showed that Mycoplasma, Dubosiella, and Enterorhabdus were jointly affected by acute PAT exposure in the small intestinal and colonic contents. Some inflammation-related bacteria, such as Mycoplasma in the small intestine and Mycoplasma, Alistipes, Eubacterium_coprostanoligenes_group, and Candidatus_saccharimona in the colon, increased with increasing doses of PAT. In metabolic results, amino acids decreased and bile acids elevated in both intestinal contents; lipids increased in the small intestinal contents but decreased in the colonic contents. PAT mainly affected host amino acid and lipid metabolism; it also downregulated microbial tryptophan metabolism and short-chain fatty acid levels (mainly in the colon), which could be explained by the decrease of Bacteroides and Lactobacillus. These influences in microbial abundances and metabolic levels persisted after PAT and its products were cleared. These results fill a gap in the effects of PAT on the gut microbiota and provide a theoretical basis for elucidating the toxic mechanism of mycotoxins.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
10.50
自引率
0.00%
发文量
0
审稿时长
10 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信