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Exopolysaccharides Produced by Intestinal Bifidobacterium Strains Act as Fermentable Substrates for Human Intestinal Bacteria
Eleven exopolysaccharides (EPS) isolated from different human intestinal Bifidobacterium strains were tested in fecal slurry batch cultures and compared with glucose and the prebiotic inulin for their abilities to act as fermentable substrates for intestinal bacteria. During incubation, the increase...
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Published in: | Applied and Environmental Microbiology 2008-08, Vol.74 (15), p.4737-4745 |
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description | Eleven exopolysaccharides (EPS) isolated from different human intestinal Bifidobacterium strains were tested in fecal slurry batch cultures and compared with glucose and the prebiotic inulin for their abilities to act as fermentable substrates for intestinal bacteria. During incubation, the increases in levels of short-chain fatty acids (SCFA) were considerably more pronounced in cultures with EPS, glucose, and inulin than in controls without carbohydrates added, indicating that the substrates assayed were fermented by intestinal bacteria. Shifts in molar proportions of SCFA during incubation with EPS and inulin caused a decrease in the acetic acid-to-propionic acid ratio, a possible indicator of the hypolipidemic effect of prebiotics, with the lowest values for this parameter being obtained for EPS from the species Bifidobacterium longum and from Bifidobacterium pseudocatenulatum strain C52. This behavior was contrary to that found with glucose, a carbohydrate not considered to be a prebiotic and for which a clear increase of this ratio was obtained during incubation. Quantitative real-time PCR showed that EPS exerted a moderate bifidogenic effect, which was comparable to that of inulin for some polymers but which was lower than that found for glucose. PCR-denaturing gradient gel electrophoresis of 16S rRNA gene fragments using universal primers was employed to analyze microbial groups other than bifidobacteria. Changes in banding patterns during incubation with EPS indicated microbial rearrangements of Bacteroides and Escherichia coli relatives. Moreover, the use of EPS from B. pseudocatenulatum in fecal cultures from some individuals accounted for the prevalence of Desulfovibrio and Faecalibacterium prausnitzii, whereas incubation with EPS from B. longum supported populations close to Anaerostipes, Prevotella, and/or OSCILLOSPIRA: Thus, EPS synthesized by intestinal bifidobacteria could act as fermentable substrates for microorganisms in the human gut environment, modifying interactions among intestinal populations. |
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During incubation, the increases in levels of short-chain fatty acids (SCFA) were considerably more pronounced in cultures with EPS, glucose, and inulin than in controls without carbohydrates added, indicating that the substrates assayed were fermented by intestinal bacteria. Shifts in molar proportions of SCFA during incubation with EPS and inulin caused a decrease in the acetic acid-to-propionic acid ratio, a possible indicator of the hypolipidemic effect of prebiotics, with the lowest values for this parameter being obtained for EPS from the species Bifidobacterium longum and from Bifidobacterium pseudocatenulatum strain C52. This behavior was contrary to that found with glucose, a carbohydrate not considered to be a prebiotic and for which a clear increase of this ratio was obtained during incubation. Quantitative real-time PCR showed that EPS exerted a moderate bifidogenic effect, which was comparable to that of inulin for some polymers but which was lower than that found for glucose. PCR-denaturing gradient gel electrophoresis of 16S rRNA gene fragments using universal primers was employed to analyze microbial groups other than bifidobacteria. Changes in banding patterns during incubation with EPS indicated microbial rearrangements of Bacteroides and Escherichia coli relatives. Moreover, the use of EPS from B. pseudocatenulatum in fecal cultures from some individuals accounted for the prevalence of Desulfovibrio and Faecalibacterium prausnitzii, whereas incubation with EPS from B. longum supported populations close to Anaerostipes, Prevotella, and/or OSCILLOSPIRA: Thus, EPS synthesized by intestinal bifidobacteria could act as fermentable substrates for microorganisms in the human gut environment, modifying interactions among intestinal populations.</description><identifier>ISSN: 0099-2240</identifier><identifier>EISSN: 1098-5336</identifier><identifier>EISSN: 1098-6596</identifier><identifier>DOI: 10.1128/AEM.00325-08</identifier><identifier>PMID: 18539803</identifier><identifier>CODEN: AEMIDF</identifier><language>eng</language><publisher>Washington, DC: American Society for Microbiology</publisher><subject>Bacteria ; Bacteroides ; Batch culture ; Bifidobacterium - genetics ; Bifidobacterium - isolation & purification ; Bifidobacterium - metabolism ; Biological and medical sciences ; Digestive system ; DNA, Bacterial - genetics ; Fatty acids ; Feces ; Fermentation ; Fundamental and applied biological sciences. Psychology ; Glucose ; Humans ; Intestines - microbiology ; Meeting Presentations ; Microbiology ; Polymerase Chain Reaction ; Polysaccharides, Bacterial - biosynthesis ; Polysaccharides, Bacterial - metabolism ; RNA, Bacterial - genetics ; RNA, Ribosomal, 16S - genetics ; Substrate Specificity</subject><ispartof>Applied and Environmental Microbiology, 2008-08, Vol.74 (15), p.4737-4745</ispartof><rights>2008 INIST-CNRS</rights><rights>Copyright American Society for Microbiology Aug 2008</rights><rights>Copyright © 2008, American Society for Microbiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c521t-cce117c9c8c36832ef4ad2cc80217ab7e8ee3a7b2d48d5d4b154ccc8139b61f83</citedby><cites>FETCH-LOGICAL-c521t-cce117c9c8c36832ef4ad2cc80217ab7e8ee3a7b2d48d5d4b154ccc8139b61f83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2519331/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2519331/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,309,310,314,727,780,784,789,790,885,3188,3189,23930,23931,25140,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20558763$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18539803$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Salazar, Nuria</creatorcontrib><creatorcontrib>Gueimonde, Miguel</creatorcontrib><creatorcontrib>Hernández-Barranco, Ana María</creatorcontrib><creatorcontrib>Ruas-Madiedo, Patricia</creatorcontrib><creatorcontrib>de los Reyes-Gavilán, Clara G</creatorcontrib><title>Exopolysaccharides Produced by Intestinal Bifidobacterium Strains Act as Fermentable Substrates for Human Intestinal Bacteria</title><title>Applied and Environmental Microbiology</title><addtitle>Appl Environ Microbiol</addtitle><description>Eleven exopolysaccharides (EPS) isolated from different human intestinal Bifidobacterium strains were tested in fecal slurry batch cultures and compared with glucose and the prebiotic inulin for their abilities to act as fermentable substrates for intestinal bacteria. During incubation, the increases in levels of short-chain fatty acids (SCFA) were considerably more pronounced in cultures with EPS, glucose, and inulin than in controls without carbohydrates added, indicating that the substrates assayed were fermented by intestinal bacteria. Shifts in molar proportions of SCFA during incubation with EPS and inulin caused a decrease in the acetic acid-to-propionic acid ratio, a possible indicator of the hypolipidemic effect of prebiotics, with the lowest values for this parameter being obtained for EPS from the species Bifidobacterium longum and from Bifidobacterium pseudocatenulatum strain C52. This behavior was contrary to that found with glucose, a carbohydrate not considered to be a prebiotic and for which a clear increase of this ratio was obtained during incubation. Quantitative real-time PCR showed that EPS exerted a moderate bifidogenic effect, which was comparable to that of inulin for some polymers but which was lower than that found for glucose. PCR-denaturing gradient gel electrophoresis of 16S rRNA gene fragments using universal primers was employed to analyze microbial groups other than bifidobacteria. Changes in banding patterns during incubation with EPS indicated microbial rearrangements of Bacteroides and Escherichia coli relatives. 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Psychology</subject><subject>Glucose</subject><subject>Humans</subject><subject>Intestines - microbiology</subject><subject>Meeting Presentations</subject><subject>Microbiology</subject><subject>Polymerase Chain Reaction</subject><subject>Polysaccharides, Bacterial - biosynthesis</subject><subject>Polysaccharides, Bacterial - metabolism</subject><subject>RNA, Bacterial - genetics</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>Substrate Specificity</subject><issn>0099-2240</issn><issn>1098-5336</issn><issn>1098-6596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFksFv0zAUxiMEYt3gxhkspHEi49mOE_uCVKaOTRoCqexsvThO6ymJi50APfC_49JqY1w4-fB-_r7v-XOWvaBwRimT7-aLT2cAnIkc5KNsRkHJXHBePs5mAErljBVwlB3HeAsABZTyaXZEpeBKAp9lvxY__cZ324jGrDG4xkbyJfhmMrYh9ZZcDaONoxuwIx9c6xpfoxltcFNPlmNAN0QyNyPBSC5s6O0wYt1ZspzqmKbpKml9IJdTj8MDqb0IPsuetNhF-_xwnmQ3F4uv55f59eePV-fz69wIRsfcGEtpZZSRhpeSM9sW2DBjJDBaYV1ZaS3HqmZNIRvRFDUVhUljylVd0lbyk-z9Xncz1b1tTMoZsNOb4HoMW-3R6YeTwa31yn_XTFDFOU0Cbw4CwX-b0hq6d9HYrsPB-inqUvGyBFX-F2RUQKmESuDrf8BbP4X0OIkBoaoK6M727R4ywccYbHsXmYLeta9T-_pP-xp2a778e817-FB3Ak4PAEaDXRtwMC7ecclYyKrk9-HWbrX-4YLVGHuNttdVoanQRcWrBL3aQy16jauQhG6WDChP344qlTx_A7ZMzsM</recordid><startdate>20080801</startdate><enddate>20080801</enddate><creator>Salazar, Nuria</creator><creator>Gueimonde, Miguel</creator><creator>Hernández-Barranco, Ana María</creator><creator>Ruas-Madiedo, Patricia</creator><creator>de los Reyes-Gavilán, Clara G</creator><general>American Society for Microbiology</general><general>American Society for Microbiology (ASM)</general><scope>FBQ</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20080801</creationdate><title>Exopolysaccharides Produced by Intestinal Bifidobacterium Strains Act as Fermentable Substrates for Human Intestinal Bacteria</title><author>Salazar, Nuria ; Gueimonde, Miguel ; Hernández-Barranco, Ana María ; Ruas-Madiedo, Patricia ; de los Reyes-Gavilán, Clara G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c521t-cce117c9c8c36832ef4ad2cc80217ab7e8ee3a7b2d48d5d4b154ccc8139b61f83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Bacteria</topic><topic>Bacteroides</topic><topic>Batch culture</topic><topic>Bifidobacterium - genetics</topic><topic>Bifidobacterium - isolation & purification</topic><topic>Bifidobacterium - metabolism</topic><topic>Biological and medical sciences</topic><topic>Digestive system</topic><topic>DNA, Bacterial - genetics</topic><topic>Fatty acids</topic><topic>Feces</topic><topic>Fermentation</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Glucose</topic><topic>Humans</topic><topic>Intestines - microbiology</topic><topic>Meeting Presentations</topic><topic>Microbiology</topic><topic>Polymerase Chain Reaction</topic><topic>Polysaccharides, Bacterial - biosynthesis</topic><topic>Polysaccharides, Bacterial - metabolism</topic><topic>RNA, Bacterial - genetics</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>Substrate Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Salazar, Nuria</creatorcontrib><creatorcontrib>Gueimonde, Miguel</creatorcontrib><creatorcontrib>Hernández-Barranco, Ana María</creatorcontrib><creatorcontrib>Ruas-Madiedo, Patricia</creatorcontrib><creatorcontrib>de los Reyes-Gavilán, Clara G</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Applied and Environmental Microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Salazar, Nuria</au><au>Gueimonde, Miguel</au><au>Hernández-Barranco, Ana María</au><au>Ruas-Madiedo, Patricia</au><au>de los Reyes-Gavilán, Clara G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Exopolysaccharides Produced by Intestinal Bifidobacterium Strains Act as Fermentable Substrates for Human Intestinal Bacteria</atitle><jtitle>Applied and Environmental Microbiology</jtitle><addtitle>Appl Environ Microbiol</addtitle><date>2008-08-01</date><risdate>2008</risdate><volume>74</volume><issue>15</issue><spage>4737</spage><epage>4745</epage><pages>4737-4745</pages><issn>0099-2240</issn><eissn>1098-5336</eissn><eissn>1098-6596</eissn><coden>AEMIDF</coden><abstract>Eleven exopolysaccharides (EPS) isolated from different human intestinal Bifidobacterium strains were tested in fecal slurry batch cultures and compared with glucose and the prebiotic inulin for their abilities to act as fermentable substrates for intestinal bacteria. During incubation, the increases in levels of short-chain fatty acids (SCFA) were considerably more pronounced in cultures with EPS, glucose, and inulin than in controls without carbohydrates added, indicating that the substrates assayed were fermented by intestinal bacteria. Shifts in molar proportions of SCFA during incubation with EPS and inulin caused a decrease in the acetic acid-to-propionic acid ratio, a possible indicator of the hypolipidemic effect of prebiotics, with the lowest values for this parameter being obtained for EPS from the species Bifidobacterium longum and from Bifidobacterium pseudocatenulatum strain C52. This behavior was contrary to that found with glucose, a carbohydrate not considered to be a prebiotic and for which a clear increase of this ratio was obtained during incubation. Quantitative real-time PCR showed that EPS exerted a moderate bifidogenic effect, which was comparable to that of inulin for some polymers but which was lower than that found for glucose. PCR-denaturing gradient gel electrophoresis of 16S rRNA gene fragments using universal primers was employed to analyze microbial groups other than bifidobacteria. Changes in banding patterns during incubation with EPS indicated microbial rearrangements of Bacteroides and Escherichia coli relatives. Moreover, the use of EPS from B. pseudocatenulatum in fecal cultures from some individuals accounted for the prevalence of Desulfovibrio and Faecalibacterium prausnitzii, whereas incubation with EPS from B. longum supported populations close to Anaerostipes, Prevotella, and/or OSCILLOSPIRA: Thus, EPS synthesized by intestinal bifidobacteria could act as fermentable substrates for microorganisms in the human gut environment, modifying interactions among intestinal populations.</abstract><cop>Washington, DC</cop><pub>American Society for Microbiology</pub><pmid>18539803</pmid><doi>10.1128/AEM.00325-08</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Bacteria Bacteroides Batch culture Bifidobacterium - genetics Bifidobacterium - isolation & purification Bifidobacterium - metabolism Biological and medical sciences Digestive system DNA, Bacterial - genetics Fatty acids Feces Fermentation Fundamental and applied biological sciences. Psychology Glucose Humans Intestines - microbiology Meeting Presentations Microbiology Polymerase Chain Reaction Polysaccharides, Bacterial - biosynthesis Polysaccharides, Bacterial - metabolism RNA, Bacterial - genetics RNA, Ribosomal, 16S - genetics Substrate Specificity |
title | Exopolysaccharides Produced by Intestinal Bifidobacterium Strains Act as Fermentable Substrates for Human Intestinal Bacteria |
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