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Long Term Development of Gut Microbiota Composition in Atopic Children: Impact of Probiotics
Imbalance of the human gut microbiota in early childhood is suggested as a risk factor for immune-mediated disorders such as allergies. With the objective to modulate the intestinal microbiota, probiotic supplementation during infancy has been used for prevention of allergic diseases in infants, wit...
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Published in: | PloS one 2015-09, Vol.10 (9), p.e0137681-e0137681 |
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description | Imbalance of the human gut microbiota in early childhood is suggested as a risk factor for immune-mediated disorders such as allergies. With the objective to modulate the intestinal microbiota, probiotic supplementation during infancy has been used for prevention of allergic diseases in infants, with variable success. However, not much is known about the long-term consequences of neonatal use of probiotics on the microbiota composition. The aim of this study was to assess the composition and microbial diversity in stool samples of infants at high-risk for atopic disease, from birth onwards to six years of age, who were treated with probiotics or placebo during the first year of life.
In a double-blind, randomized, placebo-controlled trial, a probiotic mixture consisting of B. bifidum W23, B. lactis W52 and Lc. Lactis W58 (Ecologic® Panda) was administered to pregnant women during the last 6 weeks of pregnancy and to their offspring during the first year of life. During follow-up, faecal samples were collected from 99 children over a 6-year period with the following time points: first week, second week, first month, three months, first year, eighteen months, two years and six years. Bacterial profiling was performed by IS-pro. Differences in bacterial abundance and diversity were assessed by conventional statistics.
The presence of the supplemented probiotic strains in faecal samples was confirmed, and the probiotic strains had a higher abundance and prevalence in the probiotic group during supplementation. Only minor and short term differences in composition of microbiota were found between the probiotic and placebo group and between children with or without atopy. The diversity of Bacteroidetes was significantly higher after two weeks in the placebo group, and at the age of two years atopic children had a significantly higher Proteobacteria diversity (p < 0.05). Gut microbiota development continued between two and six years, whereby microbiota composition at phylum level evolved more and more towards an adult-like configuration.
Perinatal supplementation with Ecologic® Panda, to children at high-risk for atopic disease, had minor effects on gut microbiota composition during the supplementation period. No long lasting differences were identified. Regardless of intervention or atopic disease status, children had a shared microbiota development over time determined by age that continued to develop between two and six years. |
doi_str_mv | 10.1371/journal.pone.0137681 |
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In a double-blind, randomized, placebo-controlled trial, a probiotic mixture consisting of B. bifidum W23, B. lactis W52 and Lc. Lactis W58 (Ecologic® Panda) was administered to pregnant women during the last 6 weeks of pregnancy and to their offspring during the first year of life. During follow-up, faecal samples were collected from 99 children over a 6-year period with the following time points: first week, second week, first month, three months, first year, eighteen months, two years and six years. Bacterial profiling was performed by IS-pro. Differences in bacterial abundance and diversity were assessed by conventional statistics.
The presence of the supplemented probiotic strains in faecal samples was confirmed, and the probiotic strains had a higher abundance and prevalence in the probiotic group during supplementation. Only minor and short term differences in composition of microbiota were found between the probiotic and placebo group and between children with or without atopy. The diversity of Bacteroidetes was significantly higher after two weeks in the placebo group, and at the age of two years atopic children had a significantly higher Proteobacteria diversity (p < 0.05). Gut microbiota development continued between two and six years, whereby microbiota composition at phylum level evolved more and more towards an adult-like configuration.
Perinatal supplementation with Ecologic® Panda, to children at high-risk for atopic disease, had minor effects on gut microbiota composition during the supplementation period. No long lasting differences were identified. Regardless of intervention or atopic disease status, children had a shared microbiota development over time determined by age that continued to develop between two and six years.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0137681</identifier><identifier>PMID: 26378926</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Abundance ; Age ; Allergic diseases ; Allergies ; Allergy ; Asthma ; Atopy ; Babies ; Bacteria ; Bacterial Typing Techniques ; Bifidobacterium ; Biodiversity ; Child ; Child, Preschool ; Children ; Children & youth ; Chronology ; Composition effects ; Dermatitis ; Dietary Supplements ; Digestive system ; Digestive tract ; Disease control ; Disease prevention ; Double-Blind Method ; Eczema ; Families & family life ; Family medical history ; Female ; Food allergies ; Gastrointestinal Microbiome - drug effects ; Gastrointestinal Microbiome - genetics ; Gastrointestinal tract ; Gene expression ; Health risks ; Hospitals ; Humans ; Hypersensitivity - immunology ; Infant ; Infant, Newborn ; Infants ; Infections ; Intestinal microflora ; Intestine ; Lactobacillus ; Male ; Metagenome - genetics ; Microbiota ; Microbiota (Symbiotic organisms) ; Microorganisms ; Neonates ; Offspring ; Pandas ; Pediatric diseases ; Pediatrics ; Placebos - therapeutic use ; Pregnancy ; Pregnant women ; Probiotics ; Probiotics - therapeutic use ; Risk factors ; RNA, Ribosomal, 16S - genetics ; RNA, Ribosomal, 23S - genetics ; Statistical analysis ; Statistical methods ; Strains (organisms) ; Studies ; Supplementation ; Supplements</subject><ispartof>PloS one, 2015-09, Vol.10 (9), p.e0137681-e0137681</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Rutten et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Rutten et al 2015 Rutten et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c758t-a7edb08283c9cabce45c81817c1b740c45b573e57e59944d52fa0e65da0aec743</citedby><cites>FETCH-LOGICAL-c758t-a7edb08283c9cabce45c81817c1b740c45b573e57e59944d52fa0e65da0aec743</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1719287217/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1719287217?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26378926$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Suchodolski, Jan S</contributor><creatorcontrib>Rutten, N B M M</creatorcontrib><creatorcontrib>Gorissen, D M W</creatorcontrib><creatorcontrib>Eck, A</creatorcontrib><creatorcontrib>Niers, L E M</creatorcontrib><creatorcontrib>Vlieger, A M</creatorcontrib><creatorcontrib>Besseling-van der Vaart, I</creatorcontrib><creatorcontrib>Budding, A E</creatorcontrib><creatorcontrib>Savelkoul, P H M</creatorcontrib><creatorcontrib>van der Ent, C K</creatorcontrib><creatorcontrib>Rijkers, G T</creatorcontrib><title>Long Term Development of Gut Microbiota Composition in Atopic Children: Impact of Probiotics</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Imbalance of the human gut microbiota in early childhood is suggested as a risk factor for immune-mediated disorders such as allergies. With the objective to modulate the intestinal microbiota, probiotic supplementation during infancy has been used for prevention of allergic diseases in infants, with variable success. However, not much is known about the long-term consequences of neonatal use of probiotics on the microbiota composition. The aim of this study was to assess the composition and microbial diversity in stool samples of infants at high-risk for atopic disease, from birth onwards to six years of age, who were treated with probiotics or placebo during the first year of life.
In a double-blind, randomized, placebo-controlled trial, a probiotic mixture consisting of B. bifidum W23, B. lactis W52 and Lc. Lactis W58 (Ecologic® Panda) was administered to pregnant women during the last 6 weeks of pregnancy and to their offspring during the first year of life. During follow-up, faecal samples were collected from 99 children over a 6-year period with the following time points: first week, second week, first month, three months, first year, eighteen months, two years and six years. Bacterial profiling was performed by IS-pro. Differences in bacterial abundance and diversity were assessed by conventional statistics.
The presence of the supplemented probiotic strains in faecal samples was confirmed, and the probiotic strains had a higher abundance and prevalence in the probiotic group during supplementation. Only minor and short term differences in composition of microbiota were found between the probiotic and placebo group and between children with or without atopy. The diversity of Bacteroidetes was significantly higher after two weeks in the placebo group, and at the age of two years atopic children had a significantly higher Proteobacteria diversity (p < 0.05). Gut microbiota development continued between two and six years, whereby microbiota composition at phylum level evolved more and more towards an adult-like configuration.
Perinatal supplementation with Ecologic® Panda, to children at high-risk for atopic disease, had minor effects on gut microbiota composition during the supplementation period. No long lasting differences were identified. Regardless of intervention or atopic disease status, children had a shared microbiota development over time determined by age that continued to develop between two and six years.</description><subject>Abundance</subject><subject>Age</subject><subject>Allergic diseases</subject><subject>Allergies</subject><subject>Allergy</subject><subject>Asthma</subject><subject>Atopy</subject><subject>Babies</subject><subject>Bacteria</subject><subject>Bacterial Typing Techniques</subject><subject>Bifidobacterium</subject><subject>Biodiversity</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Children & youth</subject><subject>Chronology</subject><subject>Composition effects</subject><subject>Dermatitis</subject><subject>Dietary Supplements</subject><subject>Digestive system</subject><subject>Digestive tract</subject><subject>Disease control</subject><subject>Disease prevention</subject><subject>Double-Blind Method</subject><subject>Eczema</subject><subject>Families & family life</subject><subject>Family medical history</subject><subject>Female</subject><subject>Food allergies</subject><subject>Gastrointestinal Microbiome - drug effects</subject><subject>Gastrointestinal Microbiome - genetics</subject><subject>Gastrointestinal tract</subject><subject>Gene expression</subject><subject>Health risks</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Hypersensitivity - immunology</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Infants</subject><subject>Infections</subject><subject>Intestinal microflora</subject><subject>Intestine</subject><subject>Lactobacillus</subject><subject>Male</subject><subject>Metagenome - genetics</subject><subject>Microbiota</subject><subject>Microbiota (Symbiotic organisms)</subject><subject>Microorganisms</subject><subject>Neonates</subject><subject>Offspring</subject><subject>Pandas</subject><subject>Pediatric diseases</subject><subject>Pediatrics</subject><subject>Placebos - therapeutic use</subject><subject>Pregnancy</subject><subject>Pregnant women</subject><subject>Probiotics</subject><subject>Probiotics - therapeutic use</subject><subject>Risk factors</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>RNA, Ribosomal, 23S - genetics</subject><subject>Statistical analysis</subject><subject>Statistical methods</subject><subject>Strains (organisms)</subject><subject>Studies</subject><subject>Supplementation</subject><subject>Supplements</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk12L1DAUhoso7rr6D0QLgujFjPlsEi-EYdR1YGRFV6-EkKanM1napjbtov_ezEx3mcpeSC9STp73PcnJOUnyFKM5pgK_ufJD15hq3voG5iiGMonvJadYUTLLCKL3j_5PkkchXCHEqcyyh8kJyaiQimSnyc-1bzbpJXR1-h6uofJtDU2f-jI9H_r0s7Odz53vTbr0deuD651vUteki963zqbLrauKDpq36apujd0LvxwkzobHyYPSVAGejOtZ8v3jh8vlp9n64ny1XKxnVnDZz4yAIkeSSGqVNbkFxq3EEguLc8GQZTznggIXwJVirOCkNAgyXhhkwApGz5LnB9-28kGPhQkaC6yIFASLSKwOROHNlW47V5vuj_bG6X3AdxttunjkCnSplERUMcoKyqgoFM2wKjJT5tYQCSh6vRuzDXkNhY316kw1MZ3uNG6rN_5aMy6YEiQavBoNOv9rgNDr2gULVWUa8MP-3DE_ZxmN6It_0LtvN1IbEy_gmtLHvHZnqheMSMWFlCpS8zuo-BVQOxu7qHQxPhG8nggi08PvfmOGEPTq29f_Zy9-TNmXR-wWTNVvg6-GXW-FKcgOYOzCEDoob4uMkd4NwU019G4I9DgEUfbs-IFuRTddT_8CJOgBYg</recordid><startdate>20150917</startdate><enddate>20150917</enddate><creator>Rutten, N B M M</creator><creator>Gorissen, D M W</creator><creator>Eck, A</creator><creator>Niers, L E M</creator><creator>Vlieger, A M</creator><creator>Besseling-van der Vaart, I</creator><creator>Budding, A E</creator><creator>Savelkoul, P H M</creator><creator>van der Ent, C K</creator><creator>Rijkers, G T</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150917</creationdate><title>Long Term Development of Gut Microbiota Composition in Atopic Children: Impact of Probiotics</title><author>Rutten, N B M M ; Gorissen, D M W ; Eck, A ; Niers, L E M ; Vlieger, A M ; Besseling-van der Vaart, I ; Budding, A E ; Savelkoul, P H M ; van der Ent, C K ; Rijkers, G T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c758t-a7edb08283c9cabce45c81817c1b740c45b573e57e59944d52fa0e65da0aec743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Abundance</topic><topic>Age</topic><topic>Allergic diseases</topic><topic>Allergies</topic><topic>Allergy</topic><topic>Asthma</topic><topic>Atopy</topic><topic>Babies</topic><topic>Bacteria</topic><topic>Bacterial Typing Techniques</topic><topic>Bifidobacterium</topic><topic>Biodiversity</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Children</topic><topic>Children & youth</topic><topic>Chronology</topic><topic>Composition effects</topic><topic>Dermatitis</topic><topic>Dietary Supplements</topic><topic>Digestive system</topic><topic>Digestive tract</topic><topic>Disease control</topic><topic>Disease prevention</topic><topic>Double-Blind Method</topic><topic>Eczema</topic><topic>Families & family life</topic><topic>Family medical history</topic><topic>Female</topic><topic>Food allergies</topic><topic>Gastrointestinal Microbiome - drug effects</topic><topic>Gastrointestinal Microbiome - genetics</topic><topic>Gastrointestinal tract</topic><topic>Gene expression</topic><topic>Health risks</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Hypersensitivity - immunology</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Infants</topic><topic>Infections</topic><topic>Intestinal microflora</topic><topic>Intestine</topic><topic>Lactobacillus</topic><topic>Male</topic><topic>Metagenome - genetics</topic><topic>Microbiota</topic><topic>Microbiota (Symbiotic organisms)</topic><topic>Microorganisms</topic><topic>Neonates</topic><topic>Offspring</topic><topic>Pandas</topic><topic>Pediatric diseases</topic><topic>Pediatrics</topic><topic>Placebos - therapeutic use</topic><topic>Pregnancy</topic><topic>Pregnant women</topic><topic>Probiotics</topic><topic>Probiotics - therapeutic use</topic><topic>Risk factors</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>RNA, Ribosomal, 23S - genetics</topic><topic>Statistical analysis</topic><topic>Statistical methods</topic><topic>Strains (organisms)</topic><topic>Studies</topic><topic>Supplementation</topic><topic>Supplements</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rutten, N B M M</creatorcontrib><creatorcontrib>Gorissen, D M W</creatorcontrib><creatorcontrib>Eck, A</creatorcontrib><creatorcontrib>Niers, L E M</creatorcontrib><creatorcontrib>Vlieger, A M</creatorcontrib><creatorcontrib>Besseling-van der Vaart, I</creatorcontrib><creatorcontrib>Budding, A E</creatorcontrib><creatorcontrib>Savelkoul, P H M</creatorcontrib><creatorcontrib>van der Ent, C K</creatorcontrib><creatorcontrib>Rijkers, G T</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rutten, N B M M</au><au>Gorissen, D M W</au><au>Eck, A</au><au>Niers, L E M</au><au>Vlieger, A M</au><au>Besseling-van der Vaart, I</au><au>Budding, A E</au><au>Savelkoul, P H M</au><au>van der Ent, C K</au><au>Rijkers, G T</au><au>Suchodolski, Jan S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long Term Development of Gut Microbiota Composition in Atopic Children: Impact of Probiotics</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2015-09-17</date><risdate>2015</risdate><volume>10</volume><issue>9</issue><spage>e0137681</spage><epage>e0137681</epage><pages>e0137681-e0137681</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Imbalance of the human gut microbiota in early childhood is suggested as a risk factor for immune-mediated disorders such as allergies. With the objective to modulate the intestinal microbiota, probiotic supplementation during infancy has been used for prevention of allergic diseases in infants, with variable success. However, not much is known about the long-term consequences of neonatal use of probiotics on the microbiota composition. The aim of this study was to assess the composition and microbial diversity in stool samples of infants at high-risk for atopic disease, from birth onwards to six years of age, who were treated with probiotics or placebo during the first year of life.
In a double-blind, randomized, placebo-controlled trial, a probiotic mixture consisting of B. bifidum W23, B. lactis W52 and Lc. Lactis W58 (Ecologic® Panda) was administered to pregnant women during the last 6 weeks of pregnancy and to their offspring during the first year of life. During follow-up, faecal samples were collected from 99 children over a 6-year period with the following time points: first week, second week, first month, three months, first year, eighteen months, two years and six years. Bacterial profiling was performed by IS-pro. Differences in bacterial abundance and diversity were assessed by conventional statistics.
The presence of the supplemented probiotic strains in faecal samples was confirmed, and the probiotic strains had a higher abundance and prevalence in the probiotic group during supplementation. Only minor and short term differences in composition of microbiota were found between the probiotic and placebo group and between children with or without atopy. The diversity of Bacteroidetes was significantly higher after two weeks in the placebo group, and at the age of two years atopic children had a significantly higher Proteobacteria diversity (p < 0.05). Gut microbiota development continued between two and six years, whereby microbiota composition at phylum level evolved more and more towards an adult-like configuration.
Perinatal supplementation with Ecologic® Panda, to children at high-risk for atopic disease, had minor effects on gut microbiota composition during the supplementation period. No long lasting differences were identified. Regardless of intervention or atopic disease status, children had a shared microbiota development over time determined by age that continued to develop between two and six years.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26378926</pmid><doi>10.1371/journal.pone.0137681</doi><tpages>e0137681</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2015-09, Vol.10 (9), p.e0137681-e0137681 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1719287217 |
source | Open Access: PubMed Central; ProQuest - Publicly Available Content Database |
subjects | Abundance Age Allergic diseases Allergies Allergy Asthma Atopy Babies Bacteria Bacterial Typing Techniques Bifidobacterium Biodiversity Child Child, Preschool Children Children & youth Chronology Composition effects Dermatitis Dietary Supplements Digestive system Digestive tract Disease control Disease prevention Double-Blind Method Eczema Families & family life Family medical history Female Food allergies Gastrointestinal Microbiome - drug effects Gastrointestinal Microbiome - genetics Gastrointestinal tract Gene expression Health risks Hospitals Humans Hypersensitivity - immunology Infant Infant, Newborn Infants Infections Intestinal microflora Intestine Lactobacillus Male Metagenome - genetics Microbiota Microbiota (Symbiotic organisms) Microorganisms Neonates Offspring Pandas Pediatric diseases Pediatrics Placebos - therapeutic use Pregnancy Pregnant women Probiotics Probiotics - therapeutic use Risk factors RNA, Ribosomal, 16S - genetics RNA, Ribosomal, 23S - genetics Statistical analysis Statistical methods Strains (organisms) Studies Supplementation Supplements |
title | Long Term Development of Gut Microbiota Composition in Atopic Children: Impact of Probiotics |
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