Effects of Ecklonia cava subspp. kurome and stolonifera ethanolic/aqueous extracts on caecal microbiota in mice fed a high-sucrose and low-dietary fibre diet
{"title":"Effects of Ecklonia cava subspp. kurome and stolonifera ethanolic/aqueous extracts on caecal microbiota in mice fed a high-sucrose and low-dietary fibre diet","authors":"Sae Fujita, Kazuya Koga, Ayaka Nakamura, Hajime Takahashi, Yumeng Xia, Takashi Kuda","doi":"10.1007/s10811-024-03278-y","DOIUrl":null,"url":null,"abstract":"<p>The traditional and local edible brown algae <i>Ecklonia cava</i> subspp. <i>kurome</i> (EK) and <i>stolonifera</i> (ES) are rich in minerals, phlorotannins (brown algal polyphenols), and water-soluble dietary fibres (alginate, laminaran, and fucoidans). These dried powders increase not only alginate- and laminaran-degrading <i>Bacteroides acidifaciens-</i> and <i>B. intestinalis-</i>like bacteria but also <i>Faecalibaculum</i>. To elucidate the effect of EK and ES ingredients, other than dietary fibres, on gut microbiota, 100 mL of ethanolic/aqueous extract solutions (EK-S, ES-S; final solvent was distilled water) were prepared from 100 g of dried samples. EK-S and ES-S contained total phenolic contents of 160 and 120 μmol phloroglucinol equivalent mL<sup>-1</sup>, respectively. A diet containing 5% (v/w) EK-S or ES-S was fed to ICR mice for 14 days. Amplicon sequencing of the 16S rDNA (V4) gene revealed that EK-S and ES-S increased <i>Faecalibaculum</i> abundance 2-fold and more, and this was the predominant genus (37–38%) in mice. However, the abundances of <i>B. acidifaciens-</i> and <i>B. intestinalis-</i>like bacteria did not increase. <i>Akkermansia muciniphila</i>-like bacteria were higher in EK-S-fed mice. <i>Faecalibaculum</i> and <i>Akkermansia</i> are regarded as desirable gut commensals correlated with anti-inflammatory and immunomodulatory effects on the host’s health. These results suggest that phlorotannins have beneficial functional effects on indigenous gut bacteria responsible for host health.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s10811-024-03278-y","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
Abstract
The traditional and local edible brown algae Ecklonia cava subspp. kurome (EK) and stolonifera (ES) are rich in minerals, phlorotannins (brown algal polyphenols), and water-soluble dietary fibres (alginate, laminaran, and fucoidans). These dried powders increase not only alginate- and laminaran-degrading Bacteroides acidifaciens- and B. intestinalis-like bacteria but also Faecalibaculum. To elucidate the effect of EK and ES ingredients, other than dietary fibres, on gut microbiota, 100 mL of ethanolic/aqueous extract solutions (EK-S, ES-S; final solvent was distilled water) were prepared from 100 g of dried samples. EK-S and ES-S contained total phenolic contents of 160 and 120 μmol phloroglucinol equivalent mL-1, respectively. A diet containing 5% (v/w) EK-S or ES-S was fed to ICR mice for 14 days. Amplicon sequencing of the 16S rDNA (V4) gene revealed that EK-S and ES-S increased Faecalibaculum abundance 2-fold and more, and this was the predominant genus (37–38%) in mice. However, the abundances of B. acidifaciens- and B. intestinalis-like bacteria did not increase. Akkermansia muciniphila-like bacteria were higher in EK-S-fed mice. Faecalibaculum and Akkermansia are regarded as desirable gut commensals correlated with anti-inflammatory and immunomodulatory effects on the host’s health. These results suggest that phlorotannins have beneficial functional effects on indigenous gut bacteria responsible for host health.