{"title":"一种新的高通量厌氧培养方法通过肠道菌群调节来评估食物健康效应","authors":"Xin-Yue Liu, Ling-Qin Zhu, Qun-Ying Jin, Hua-Zheng Peng, Tang-Jun Zhu","doi":"10.1002/fsn3.70978","DOIUrl":null,"url":null,"abstract":"<p>As health demands grow, nutritional evaluation now extends beyond nutrient supply, and health-effect–based methods are gradually gaining traction. However, assessing food impacts on gut microbiota remains complex and costly. This study developed a cost-effective in vitro method for evaluating food effects on individual gut microbiota, integrating 96-well microplates, multilayer liquid sealing, and high-throughput multiomics (16S rRNA sequencing + untargeted metabolomics) to enable large-scale anaerobic culture and dynamic growth monitoring under aerobic conditions. Using this method, the fermented products of <i>Pichia fermentans</i> were shown to significantly boost <i>Bifidobacterium</i> abundance (4.6-fold to 5.6-fold vs. control) by Day 4, though microbial diversity decreased. Testing raw (RA) versus cooked (CO) pecan kernels, RA significantly promoted health-associated genera: <i>Blautia</i>, which showed progressive enrichment (rising 17-fold from Day 2 to Day 4 in RA) and reached 193.8 times the control level (5.1%, <i>p</i> = 0.0127), with potential anti-inflammatory implications; <i>Fusicatenibacter</i>, surging to 1274.3 times the control (3.3%, <i>p</i> = 0.001) and 5.6 times higher than CO (<i>p</i> = 0.0332), suggesting potential cognitive benefits; and <i>Bacteroides</i>, whose reduction was significantly attenuated in RA compared to control (<i>p</i> = 0.0002), potentially supporting bile acid metabolism relevant to ulcerative colitis management. In contrast, CO favored opportunistic pathogens: <i>Raoultella</i> was exclusively elevated in CO relative to both control and RA (<i>p</i> < 0.05); <i>Klebsiella</i> abundance was notably higher in CO than in RA (<i>p</i> < 0.05), though increased in both groups versus control. Untargeted metabolomics indicated RA upregulated C5-branched dibasic acid metabolism and secondary bile acid biosynthesis, accumulating metabolites (e.g., CLA, 7-KDA) associated with these pathways. This method aids in optimizing food processing and guiding precision nutrition strategies.</p>","PeriodicalId":12418,"journal":{"name":"Food Science & Nutrition","volume":"13 9","pages":""},"PeriodicalIF":3.8000,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/fsn3.70978","citationCount":"0","resultStr":"{\"title\":\"A Novel High-Throughput Anaerobic Culture Method to Evaluate Food Health Effects via Gut Microbiota Modulation\",\"authors\":\"Xin-Yue Liu, Ling-Qin Zhu, Qun-Ying Jin, Hua-Zheng Peng, Tang-Jun Zhu\",\"doi\":\"10.1002/fsn3.70978\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>As health demands grow, nutritional evaluation now extends beyond nutrient supply, and health-effect–based methods are gradually gaining traction. However, assessing food impacts on gut microbiota remains complex and costly. This study developed a cost-effective in vitro method for evaluating food effects on individual gut microbiota, integrating 96-well microplates, multilayer liquid sealing, and high-throughput multiomics (16S rRNA sequencing + untargeted metabolomics) to enable large-scale anaerobic culture and dynamic growth monitoring under aerobic conditions. Using this method, the fermented products of <i>Pichia fermentans</i> were shown to significantly boost <i>Bifidobacterium</i> abundance (4.6-fold to 5.6-fold vs. control) by Day 4, though microbial diversity decreased. Testing raw (RA) versus cooked (CO) pecan kernels, RA significantly promoted health-associated genera: <i>Blautia</i>, which showed progressive enrichment (rising 17-fold from Day 2 to Day 4 in RA) and reached 193.8 times the control level (5.1%, <i>p</i> = 0.0127), with potential anti-inflammatory implications; <i>Fusicatenibacter</i>, surging to 1274.3 times the control (3.3%, <i>p</i> = 0.001) and 5.6 times higher than CO (<i>p</i> = 0.0332), suggesting potential cognitive benefits; and <i>Bacteroides</i>, whose reduction was significantly attenuated in RA compared to control (<i>p</i> = 0.0002), potentially supporting bile acid metabolism relevant to ulcerative colitis management. In contrast, CO favored opportunistic pathogens: <i>Raoultella</i> was exclusively elevated in CO relative to both control and RA (<i>p</i> < 0.05); <i>Klebsiella</i> abundance was notably higher in CO than in RA (<i>p</i> < 0.05), though increased in both groups versus control. Untargeted metabolomics indicated RA upregulated C5-branched dibasic acid metabolism and secondary bile acid biosynthesis, accumulating metabolites (e.g., CLA, 7-KDA) associated with these pathways. This method aids in optimizing food processing and guiding precision nutrition strategies.</p>\",\"PeriodicalId\":12418,\"journal\":{\"name\":\"Food Science & Nutrition\",\"volume\":\"13 9\",\"pages\":\"\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-09-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/fsn3.70978\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Food Science & Nutrition\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/fsn3.70978\",\"RegionNum\":2,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"FOOD SCIENCE & TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Food Science & Nutrition","FirstCategoryId":"97","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/fsn3.70978","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"FOOD SCIENCE & TECHNOLOGY","Score":null,"Total":0}
A Novel High-Throughput Anaerobic Culture Method to Evaluate Food Health Effects via Gut Microbiota Modulation
As health demands grow, nutritional evaluation now extends beyond nutrient supply, and health-effect–based methods are gradually gaining traction. However, assessing food impacts on gut microbiota remains complex and costly. This study developed a cost-effective in vitro method for evaluating food effects on individual gut microbiota, integrating 96-well microplates, multilayer liquid sealing, and high-throughput multiomics (16S rRNA sequencing + untargeted metabolomics) to enable large-scale anaerobic culture and dynamic growth monitoring under aerobic conditions. Using this method, the fermented products of Pichia fermentans were shown to significantly boost Bifidobacterium abundance (4.6-fold to 5.6-fold vs. control) by Day 4, though microbial diversity decreased. Testing raw (RA) versus cooked (CO) pecan kernels, RA significantly promoted health-associated genera: Blautia, which showed progressive enrichment (rising 17-fold from Day 2 to Day 4 in RA) and reached 193.8 times the control level (5.1%, p = 0.0127), with potential anti-inflammatory implications; Fusicatenibacter, surging to 1274.3 times the control (3.3%, p = 0.001) and 5.6 times higher than CO (p = 0.0332), suggesting potential cognitive benefits; and Bacteroides, whose reduction was significantly attenuated in RA compared to control (p = 0.0002), potentially supporting bile acid metabolism relevant to ulcerative colitis management. In contrast, CO favored opportunistic pathogens: Raoultella was exclusively elevated in CO relative to both control and RA (p < 0.05); Klebsiella abundance was notably higher in CO than in RA (p < 0.05), though increased in both groups versus control. Untargeted metabolomics indicated RA upregulated C5-branched dibasic acid metabolism and secondary bile acid biosynthesis, accumulating metabolites (e.g., CLA, 7-KDA) associated with these pathways. This method aids in optimizing food processing and guiding precision nutrition strategies.
期刊介绍:
Food Science & Nutrition is the peer-reviewed journal for rapid dissemination of research in all areas of food science and nutrition. The Journal will consider submissions of quality papers describing the results of fundamental and applied research related to all aspects of human food and nutrition, as well as interdisciplinary research that spans these two fields.