Simeng Qin , Yifeng Zhu , Gang Tian , Martin Blomberg Jensen , Keying Zhang , Xuemei Ding , Shiping Bai , Jianping Wang , Yue Xuan , Qiufeng Zeng
{"title":"饲粮抗性淀粉通过恢复肉鸭肠道微生物稳态和维持肠道屏障功能来预防抗生素后肠道损伤","authors":"Simeng Qin , Yifeng Zhu , Gang Tian , Martin Blomberg Jensen , Keying Zhang , Xuemei Ding , Shiping Bai , Jianping Wang , Yue Xuan , Qiufeng Zeng","doi":"10.1016/j.psj.2025.105213","DOIUrl":null,"url":null,"abstract":"<div><div>Resistant starch (<strong>RS</strong>) is recognized as a nutritional strategy that supports gut and overall host health by modulating gut microbiota. To directly assess the effects of RS on gut microbiota and its role in improving intestinal barrier function in meat ducks, this study first established an antibiotic-induced microbial dysbiosis model, which was characterized by reduced gut microbial diversity, intestinal dysfunction, and an inflammatory outburst following antibiotic exposure. Whereafter, in addition to the control group, ducks treated with antibiotics for 7 consecutive days were further allocated to two groups and fed the basal diet and RS diet that derived from 12 % raw potato starch until 21 d. The results demonstrated that dietary RS supplementation reversed the antibiotic-induced reduction in microbial diversity and restored the Firmicutes-to-Bacteroidetes ratio. Additionally, RS inclusion enriched beneficial bacterial genera, including <em>Coprobacter, Odoribacter</em>, and <em>Faecalibacterium</em> (LDA score > 3). Post-antibiotic intervention led to a reduction in villus density and muscular thickness, accompanied by a significant downregulation (<em>P</em> < 0.05) of <em>zonula occludens-1</em> and <em>mucin-2</em> expression, along with increased serum pro-inflammatory cytokine levels (<em>P</em> < 0.05). Notably, dietary RS supplementation significantly enhanced (<em>P</em> < 0.05) the expression of <em>glucagon-like peptide receptor</em> and the anti-apoptotic factor <em>Bcl-2</em>, while suppressing caspase transcription. This resulted in increased villus height and muscular thickness in the ileum (<em>P</em> < 0.05). Furthermore, RS intervention remarkably reduced (<em>P</em> < 0.05) pro-inflammatory cytokine levels, particularly interleukin-1β and tumor necrosis factor-α, in both the ileum and serum. These effects were likely linked to alterations in cecal microbiota, including increased abundances of <em>Barnesiella, Ruminiclostridium 9, Megamonas, Faecalitalea, Adlercreutzia, Coprobacter</em> and <em>Collinsella</em>. In conclusion, dietary RS supplementation mitigated antibiotic-induced cecal microbial dysbiosis and restored intestinal structure by promoting enterocyte proliferation and reducing apoptosis. Consequently, RS supplementation helped alleviate systemic inflammation in meat ducks following antibiotic treatment.</div></div>","PeriodicalId":20459,"journal":{"name":"Poultry Science","volume":"104 7","pages":"Article 105213"},"PeriodicalIF":3.8000,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dietary resistant starch protects against post-antibiotic intestinal damage by restoring microbial homeostasis and preserving intestinal barrier function in meat duck\",\"authors\":\"Simeng Qin , Yifeng Zhu , Gang Tian , Martin Blomberg Jensen , Keying Zhang , Xuemei Ding , Shiping Bai , Jianping Wang , Yue Xuan , Qiufeng Zeng\",\"doi\":\"10.1016/j.psj.2025.105213\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Resistant starch (<strong>RS</strong>) is recognized as a nutritional strategy that supports gut and overall host health by modulating gut microbiota. To directly assess the effects of RS on gut microbiota and its role in improving intestinal barrier function in meat ducks, this study first established an antibiotic-induced microbial dysbiosis model, which was characterized by reduced gut microbial diversity, intestinal dysfunction, and an inflammatory outburst following antibiotic exposure. Whereafter, in addition to the control group, ducks treated with antibiotics for 7 consecutive days were further allocated to two groups and fed the basal diet and RS diet that derived from 12 % raw potato starch until 21 d. The results demonstrated that dietary RS supplementation reversed the antibiotic-induced reduction in microbial diversity and restored the Firmicutes-to-Bacteroidetes ratio. Additionally, RS inclusion enriched beneficial bacterial genera, including <em>Coprobacter, Odoribacter</em>, and <em>Faecalibacterium</em> (LDA score > 3). Post-antibiotic intervention led to a reduction in villus density and muscular thickness, accompanied by a significant downregulation (<em>P</em> < 0.05) of <em>zonula occludens-1</em> and <em>mucin-2</em> expression, along with increased serum pro-inflammatory cytokine levels (<em>P</em> < 0.05). Notably, dietary RS supplementation significantly enhanced (<em>P</em> < 0.05) the expression of <em>glucagon-like peptide receptor</em> and the anti-apoptotic factor <em>Bcl-2</em>, while suppressing caspase transcription. This resulted in increased villus height and muscular thickness in the ileum (<em>P</em> < 0.05). Furthermore, RS intervention remarkably reduced (<em>P</em> < 0.05) pro-inflammatory cytokine levels, particularly interleukin-1β and tumor necrosis factor-α, in both the ileum and serum. These effects were likely linked to alterations in cecal microbiota, including increased abundances of <em>Barnesiella, Ruminiclostridium 9, Megamonas, Faecalitalea, Adlercreutzia, Coprobacter</em> and <em>Collinsella</em>. In conclusion, dietary RS supplementation mitigated antibiotic-induced cecal microbial dysbiosis and restored intestinal structure by promoting enterocyte proliferation and reducing apoptosis. Consequently, RS supplementation helped alleviate systemic inflammation in meat ducks following antibiotic treatment.</div></div>\",\"PeriodicalId\":20459,\"journal\":{\"name\":\"Poultry Science\",\"volume\":\"104 7\",\"pages\":\"Article 105213\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-04-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Poultry Science\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0032579125004559\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"AGRICULTURE, DAIRY & ANIMAL SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Poultry Science","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0032579125004559","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"AGRICULTURE, DAIRY & ANIMAL SCIENCE","Score":null,"Total":0}
Dietary resistant starch protects against post-antibiotic intestinal damage by restoring microbial homeostasis and preserving intestinal barrier function in meat duck
Resistant starch (RS) is recognized as a nutritional strategy that supports gut and overall host health by modulating gut microbiota. To directly assess the effects of RS on gut microbiota and its role in improving intestinal barrier function in meat ducks, this study first established an antibiotic-induced microbial dysbiosis model, which was characterized by reduced gut microbial diversity, intestinal dysfunction, and an inflammatory outburst following antibiotic exposure. Whereafter, in addition to the control group, ducks treated with antibiotics for 7 consecutive days were further allocated to two groups and fed the basal diet and RS diet that derived from 12 % raw potato starch until 21 d. The results demonstrated that dietary RS supplementation reversed the antibiotic-induced reduction in microbial diversity and restored the Firmicutes-to-Bacteroidetes ratio. Additionally, RS inclusion enriched beneficial bacterial genera, including Coprobacter, Odoribacter, and Faecalibacterium (LDA score > 3). Post-antibiotic intervention led to a reduction in villus density and muscular thickness, accompanied by a significant downregulation (P < 0.05) of zonula occludens-1 and mucin-2 expression, along with increased serum pro-inflammatory cytokine levels (P < 0.05). Notably, dietary RS supplementation significantly enhanced (P < 0.05) the expression of glucagon-like peptide receptor and the anti-apoptotic factor Bcl-2, while suppressing caspase transcription. This resulted in increased villus height and muscular thickness in the ileum (P < 0.05). Furthermore, RS intervention remarkably reduced (P < 0.05) pro-inflammatory cytokine levels, particularly interleukin-1β and tumor necrosis factor-α, in both the ileum and serum. These effects were likely linked to alterations in cecal microbiota, including increased abundances of Barnesiella, Ruminiclostridium 9, Megamonas, Faecalitalea, Adlercreutzia, Coprobacter and Collinsella. In conclusion, dietary RS supplementation mitigated antibiotic-induced cecal microbial dysbiosis and restored intestinal structure by promoting enterocyte proliferation and reducing apoptosis. Consequently, RS supplementation helped alleviate systemic inflammation in meat ducks following antibiotic treatment.
期刊介绍:
First self-published in 1921, Poultry Science is an internationally renowned monthly journal, known as the authoritative source for a broad range of poultry information and high-caliber research. The journal plays a pivotal role in the dissemination of preeminent poultry-related knowledge across all disciplines. As of January 2020, Poultry Science will become an Open Access journal with no subscription charges, meaning authors who publish here can make their research immediately, permanently, and freely accessible worldwide while retaining copyright to their work. Papers submitted for publication after October 1, 2019 will be published as Open Access papers.
An international journal, Poultry Science publishes original papers, research notes, symposium papers, and reviews of basic science as applied to poultry. This authoritative source of poultry information is consistently ranked by ISI Impact Factor as one of the top 10 agriculture, dairy and animal science journals to deliver high-caliber research. Currently it is the highest-ranked (by Impact Factor and Eigenfactor) journal dedicated to publishing poultry research. Subject areas include breeding, genetics, education, production, management, environment, health, behavior, welfare, immunology, molecular biology, metabolism, nutrition, physiology, reproduction, processing, and products.