Stool microbiome, pH and short/branched chain fatty acids in infants receiving extensively hydrolyzed formula, amino acid formula, or human milk through two months of age

Background: Early infant feeding with intact or extensively hydrolyzed (EH) proteins or free amino acids (AA) may differentially affect intestinal microbiota composition and immune reactivity. This multicenter, double-blind, controlled, parallel-group, pilot study compared stool microbiota from Base...

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Veröffentlicht in:BMC microbiology 2020-11, Vol.20 (1), p.337-337, Article 337
Hauptverfasser: Kok, Car Reen, Brabec, Bradford, Chichlowski, Maciej, Harris, Cheryl L., Moore, Nancy, Wampler, Jennifer L., Vanderhoof, Jon, Rose, Devin, Hutkins, Robert
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container_end_page 337
container_issue 1
container_start_page 337
container_title BMC microbiology
container_volume 20
creator Kok, Car Reen
Brabec, Bradford
Chichlowski, Maciej
Harris, Cheryl L.
Moore, Nancy
Wampler, Jennifer L.
Vanderhoof, Jon
Rose, Devin
Hutkins, Robert
description Background: Early infant feeding with intact or extensively hydrolyzed (EH) proteins or free amino acids (AA) may differentially affect intestinal microbiota composition and immune reactivity. This multicenter, double-blind, controlled, parallel-group, pilot study compared stool microbiota from Baseline (1-7 days of age) up to 60 days of age in healthy term infants who received mother's own milk (assigned to human milk [HM] reference group) (n = 25) or were randomized to receive one of two infant formulas: AA-based (AAF; n = 25) or EH cow's milk protein (EHF; n = 28). Stool samples were collected (Baseline, Day 30, Day 60) and 16S rRNA genes were sequenced. Alpha (Shannon, Simpson, Chao1) and beta diversity (Bray Curtis) were analyzed. Relative taxonomic enrichment and fold changes were analyzed (Wilcoxon, DESEq2). Short/branched chain fatty acids (S/BCFA) were quantified by gas chromatography. Mean S/BCFA and pH were analyzed (repeated measures ANOVA). Results: At baseline, alpha diversity measures were similar among all groups; however, both study formula groups were significantly higher versus the HM group by Day 60. Significant group differences in beta diversity at Day 60 were also detected, and study formula groups were compositionally more similar compared to HM. The relative abundance of Bifidobacterium increased over time and was significantly enriched at Day 60 in the HM group. In contrast, a significant increase in members of Firmicutes for study formula groups were detected at Day 60 along with butyrate-producing species in the EHF group. Stool pH was significantly higher in the AAF group at Days 30 and 60. Butyrate increased significantly from Baseline to Day 60 in the EHF group and was significantly higher in study formula groups vs HM at Day 60. Propionate was also significantly higher for EHF and AAF at Day 30 and AAF at Day 60 vs HM. Total and individual BCFA were higher for AAF and EHF groups vs HM through Day 60. Conclusions: Distinct patterns of early neonatal microbiome, pH, and microbial metabolites were demonstrated for infants receiving mother's own milk compared to AA-based or extensively hydrolyzed protein formula. Providing different sources of dietary protein early in life may influence gut microbiota and metabolites.
doi_str_mv 10.1186/s12866-020-01991-5
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This multicenter, double-blind, controlled, parallel-group, pilot study compared stool microbiota from Baseline (1-7 days of age) up to 60 days of age in healthy term infants who received mother's own milk (assigned to human milk [HM] reference group) (n = 25) or were randomized to receive one of two infant formulas: AA-based (AAF; n = 25) or EH cow's milk protein (EHF; n = 28). Stool samples were collected (Baseline, Day 30, Day 60) and 16S rRNA genes were sequenced. Alpha (Shannon, Simpson, Chao1) and beta diversity (Bray Curtis) were analyzed. Relative taxonomic enrichment and fold changes were analyzed (Wilcoxon, DESEq2). Short/branched chain fatty acids (S/BCFA) were quantified by gas chromatography. Mean S/BCFA and pH were analyzed (repeated measures ANOVA). Results: At baseline, alpha diversity measures were similar among all groups; however, both study formula groups were significantly higher versus the HM group by Day 60. Significant group differences in beta diversity at Day 60 were also detected, and study formula groups were compositionally more similar compared to HM. The relative abundance of Bifidobacterium increased over time and was significantly enriched at Day 60 in the HM group. In contrast, a significant increase in members of Firmicutes for study formula groups were detected at Day 60 along with butyrate-producing species in the EHF group. Stool pH was significantly higher in the AAF group at Days 30 and 60. Butyrate increased significantly from Baseline to Day 60 in the EHF group and was significantly higher in study formula groups vs HM at Day 60. Propionate was also significantly higher for EHF and AAF at Day 30 and AAF at Day 60 vs HM. Total and individual BCFA were higher for AAF and EHF groups vs HM through Day 60. Conclusions: Distinct patterns of early neonatal microbiome, pH, and microbial metabolites were demonstrated for infants receiving mother's own milk compared to AA-based or extensively hydrolyzed protein formula. Providing different sources of dietary protein early in life may influence gut microbiota and metabolites.</description><identifier>ISSN: 1471-2180</identifier><identifier>EISSN: 1471-2180</identifier><identifier>DOI: 10.1186/s12866-020-01991-5</identifier><identifier>PMID: 33167908</identifier><language>eng</language><publisher>LONDON: Springer Nature</publisher><subject>Age ; Amino acids ; Antigens ; Bifidobacterium ; Breast milk ; Chain branching ; Cow's milk ; Diet ; Extremely high frequencies ; Fatty acids ; Gas chromatography ; Gene expression ; Host-bacteria relationships ; Identification and classification ; Infant formula ; Infant formulas ; Infant microbiota ; Infant nutrition ; Infants ; Intestinal microflora ; Intestine ; Life Sciences &amp; Biomedicine ; Metabolites ; Microbiology ; Microbiomes ; Microbiota ; Microbiota (Symbiotic organisms) ; Microorganisms ; Milk ; Neonates ; Nutrition ; pH effects ; Physiological aspects ; Properties ; Propionic acid ; Proteins ; Relative abundance ; rRNA 16S ; Science &amp; Technology ; Short chain fatty acids ; Taxonomy ; Variance analysis</subject><ispartof>BMC microbiology, 2020-11, Vol.20 (1), p.337-337, Article 337</ispartof><rights>COPYRIGHT 2020 BioMed Central Ltd.</rights><rights>2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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This multicenter, double-blind, controlled, parallel-group, pilot study compared stool microbiota from Baseline (1-7 days of age) up to 60 days of age in healthy term infants who received mother's own milk (assigned to human milk [HM] reference group) (n = 25) or were randomized to receive one of two infant formulas: AA-based (AAF; n = 25) or EH cow's milk protein (EHF; n = 28). Stool samples were collected (Baseline, Day 30, Day 60) and 16S rRNA genes were sequenced. Alpha (Shannon, Simpson, Chao1) and beta diversity (Bray Curtis) were analyzed. Relative taxonomic enrichment and fold changes were analyzed (Wilcoxon, DESEq2). Short/branched chain fatty acids (S/BCFA) were quantified by gas chromatography. Mean S/BCFA and pH were analyzed (repeated measures ANOVA). Results: At baseline, alpha diversity measures were similar among all groups; however, both study formula groups were significantly higher versus the HM group by Day 60. Significant group differences in beta diversity at Day 60 were also detected, and study formula groups were compositionally more similar compared to HM. The relative abundance of Bifidobacterium increased over time and was significantly enriched at Day 60 in the HM group. In contrast, a significant increase in members of Firmicutes for study formula groups were detected at Day 60 along with butyrate-producing species in the EHF group. Stool pH was significantly higher in the AAF group at Days 30 and 60. Butyrate increased significantly from Baseline to Day 60 in the EHF group and was significantly higher in study formula groups vs HM at Day 60. Propionate was also significantly higher for EHF and AAF at Day 30 and AAF at Day 60 vs HM. Total and individual BCFA were higher for AAF and EHF groups vs HM through Day 60. Conclusions: Distinct patterns of early neonatal microbiome, pH, and microbial metabolites were demonstrated for infants receiving mother's own milk compared to AA-based or extensively hydrolyzed protein formula. Providing different sources of dietary protein early in life may influence gut microbiota and metabolites.</description><subject>Age</subject><subject>Amino acids</subject><subject>Antigens</subject><subject>Bifidobacterium</subject><subject>Breast milk</subject><subject>Chain branching</subject><subject>Cow's milk</subject><subject>Diet</subject><subject>Extremely high frequencies</subject><subject>Fatty acids</subject><subject>Gas chromatography</subject><subject>Gene expression</subject><subject>Host-bacteria relationships</subject><subject>Identification and classification</subject><subject>Infant formula</subject><subject>Infant formulas</subject><subject>Infant microbiota</subject><subject>Infant nutrition</subject><subject>Infants</subject><subject>Intestinal microflora</subject><subject>Intestine</subject><subject>Life Sciences &amp; Biomedicine</subject><subject>Metabolites</subject><subject>Microbiology</subject><subject>Microbiomes</subject><subject>Microbiota</subject><subject>Microbiota (Symbiotic organisms)</subject><subject>Microorganisms</subject><subject>Milk</subject><subject>Neonates</subject><subject>Nutrition</subject><subject>pH effects</subject><subject>Physiological aspects</subject><subject>Properties</subject><subject>Propionic acid</subject><subject>Proteins</subject><subject>Relative abundance</subject><subject>rRNA 16S</subject><subject>Science &amp; 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Biomedicine</topic><topic>Metabolites</topic><topic>Microbiology</topic><topic>Microbiomes</topic><topic>Microbiota</topic><topic>Microbiota (Symbiotic organisms)</topic><topic>Microorganisms</topic><topic>Milk</topic><topic>Neonates</topic><topic>Nutrition</topic><topic>pH effects</topic><topic>Physiological aspects</topic><topic>Properties</topic><topic>Propionic acid</topic><topic>Proteins</topic><topic>Relative abundance</topic><topic>rRNA 16S</topic><topic>Science &amp; Technology</topic><topic>Short chain fatty acids</topic><topic>Taxonomy</topic><topic>Variance analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kok, Car Reen</creatorcontrib><creatorcontrib>Brabec, Bradford</creatorcontrib><creatorcontrib>Chichlowski, Maciej</creatorcontrib><creatorcontrib>Harris, Cheryl L.</creatorcontrib><creatorcontrib>Moore, Nancy</creatorcontrib><creatorcontrib>Wampler, Jennifer L.</creatorcontrib><creatorcontrib>Vanderhoof, Jon</creatorcontrib><creatorcontrib>Rose, Devin</creatorcontrib><creatorcontrib>Hutkins, Robert</creatorcontrib><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; 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This multicenter, double-blind, controlled, parallel-group, pilot study compared stool microbiota from Baseline (1-7 days of age) up to 60 days of age in healthy term infants who received mother's own milk (assigned to human milk [HM] reference group) (n = 25) or were randomized to receive one of two infant formulas: AA-based (AAF; n = 25) or EH cow's milk protein (EHF; n = 28). Stool samples were collected (Baseline, Day 30, Day 60) and 16S rRNA genes were sequenced. Alpha (Shannon, Simpson, Chao1) and beta diversity (Bray Curtis) were analyzed. Relative taxonomic enrichment and fold changes were analyzed (Wilcoxon, DESEq2). Short/branched chain fatty acids (S/BCFA) were quantified by gas chromatography. Mean S/BCFA and pH were analyzed (repeated measures ANOVA). Results: At baseline, alpha diversity measures were similar among all groups; however, both study formula groups were significantly higher versus the HM group by Day 60. Significant group differences in beta diversity at Day 60 were also detected, and study formula groups were compositionally more similar compared to HM. The relative abundance of Bifidobacterium increased over time and was significantly enriched at Day 60 in the HM group. In contrast, a significant increase in members of Firmicutes for study formula groups were detected at Day 60 along with butyrate-producing species in the EHF group. Stool pH was significantly higher in the AAF group at Days 30 and 60. Butyrate increased significantly from Baseline to Day 60 in the EHF group and was significantly higher in study formula groups vs HM at Day 60. Propionate was also significantly higher for EHF and AAF at Day 30 and AAF at Day 60 vs HM. Total and individual BCFA were higher for AAF and EHF groups vs HM through Day 60. Conclusions: Distinct patterns of early neonatal microbiome, pH, and microbial metabolites were demonstrated for infants receiving mother's own milk compared to AA-based or extensively hydrolyzed protein formula. Providing different sources of dietary protein early in life may influence gut microbiota and metabolites.</abstract><cop>LONDON</cop><pub>Springer Nature</pub><pmid>33167908</pmid><doi>10.1186/s12866-020-01991-5</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0001-6116-711X</orcidid><oa>free_for_read</oa></addata></record>
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subjects Age
Amino acids
Antigens
Bifidobacterium
Breast milk
Chain branching
Cow's milk
Diet
Extremely high frequencies
Fatty acids
Gas chromatography
Gene expression
Host-bacteria relationships
Identification and classification
Infant formula
Infant formulas
Infant microbiota
Infant nutrition
Infants
Intestinal microflora
Intestine
Life Sciences & Biomedicine
Metabolites
Microbiology
Microbiomes
Microbiota
Microbiota (Symbiotic organisms)
Microorganisms
Milk
Neonates
Nutrition
pH effects
Physiological aspects
Properties
Propionic acid
Proteins
Relative abundance
rRNA 16S
Science & Technology
Short chain fatty acids
Taxonomy
Variance analysis
title Stool microbiome, pH and short/branched chain fatty acids in infants receiving extensively hydrolyzed formula, amino acid formula, or human milk through two months of age
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