Cargando…

A double-blind, 377-subject randomized study identifies Ruminococcus, Coprococcus, Christensenella, and Collinsella as long-term potential key players in the modulation of the gut microbiome of lactose intolerant individuals by galacto-oligosaccharides

Background. Our recent publication (Chey et al., Nutrients 2020) showed that a 30-day administration of pure galacto-oligosaccharides (GOS) significantly reduced symptoms and altered the fecal microbiome in patients with lactose intolerance (LI). Results. In this addendum, we performed an in-depth a...

Descripción completa

Detalles Bibliográficos
Autores principales: Azcarate-Peril, M. A., Roach, J., Marsh, A., Chey, William D., Sandborn, William J., Ritter, Andrew J., Savaiano, Dennis A., Klaenhammer, T. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8354614/
https://www.ncbi.nlm.nih.gov/pubmed/34365905
http://dx.doi.org/10.1080/19490976.2021.1957536
_version_ 1783736627116376064
author Azcarate-Peril, M. A.
Roach, J.
Marsh, A.
Chey, William D.
Sandborn, William J.
Ritter, Andrew J.
Savaiano, Dennis A.
Klaenhammer, T. R.
author_facet Azcarate-Peril, M. A.
Roach, J.
Marsh, A.
Chey, William D.
Sandborn, William J.
Ritter, Andrew J.
Savaiano, Dennis A.
Klaenhammer, T. R.
author_sort Azcarate-Peril, M. A.
collection PubMed
description Background. Our recent publication (Chey et al., Nutrients 2020) showed that a 30-day administration of pure galacto-oligosaccharides (GOS) significantly reduced symptoms and altered the fecal microbiome in patients with lactose intolerance (LI). Results. In this addendum, we performed an in-depth analysis of the fecal microbiome of the 377 LI patients randomized to one of two GOS doses (Low, 10–15 grams/day or High, 15–20 grams/day), or placebo in a multi-center, double-blinded, placebo-controlled trial. Sequencing of 16S rRNA amplicons was done on GOS or placebo groups at weeks zero (baseline), four (end of treatment), nine, 16 and 22. Taxa impacted by treatment and subsequent dairy consumption included lactose-fermenting species of Bifidobacterium, Lactobacillus, Lactococcus, and Streptococcus. Increased secondary fermentation microorganisms included Coprococcus and Ruminococcus species, Blautia producta, and Methanobrevibacterium. Finally, tertiary fermenters that use acetate to generate butyrate were also increased, including Faecalibacterium prausnitzii, Roseburia faecis, and C. eutactus. Conclusions. Results confirmed and expanded data on GOS microbiome modulation in LI individuals. Microbiome analysis at 16 and 22 weeks after treatment further suggested relatively long-term benefits when individuals continued consumption of dairy products.
format Online
Article
Text
id pubmed-8354614
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-83546142021-08-13 A double-blind, 377-subject randomized study identifies Ruminococcus, Coprococcus, Christensenella, and Collinsella as long-term potential key players in the modulation of the gut microbiome of lactose intolerant individuals by galacto-oligosaccharides Azcarate-Peril, M. A. Roach, J. Marsh, A. Chey, William D. Sandborn, William J. Ritter, Andrew J. Savaiano, Dennis A. Klaenhammer, T. R. Gut Microbes Addendum Background. Our recent publication (Chey et al., Nutrients 2020) showed that a 30-day administration of pure galacto-oligosaccharides (GOS) significantly reduced symptoms and altered the fecal microbiome in patients with lactose intolerance (LI). Results. In this addendum, we performed an in-depth analysis of the fecal microbiome of the 377 LI patients randomized to one of two GOS doses (Low, 10–15 grams/day or High, 15–20 grams/day), or placebo in a multi-center, double-blinded, placebo-controlled trial. Sequencing of 16S rRNA amplicons was done on GOS or placebo groups at weeks zero (baseline), four (end of treatment), nine, 16 and 22. Taxa impacted by treatment and subsequent dairy consumption included lactose-fermenting species of Bifidobacterium, Lactobacillus, Lactococcus, and Streptococcus. Increased secondary fermentation microorganisms included Coprococcus and Ruminococcus species, Blautia producta, and Methanobrevibacterium. Finally, tertiary fermenters that use acetate to generate butyrate were also increased, including Faecalibacterium prausnitzii, Roseburia faecis, and C. eutactus. Conclusions. Results confirmed and expanded data on GOS microbiome modulation in LI individuals. Microbiome analysis at 16 and 22 weeks after treatment further suggested relatively long-term benefits when individuals continued consumption of dairy products. Taylor & Francis 2021-08-07 /pmc/articles/PMC8354614/ /pubmed/34365905 http://dx.doi.org/10.1080/19490976.2021.1957536 Text en © 2021 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Addendum
Azcarate-Peril, M. A.
Roach, J.
Marsh, A.
Chey, William D.
Sandborn, William J.
Ritter, Andrew J.
Savaiano, Dennis A.
Klaenhammer, T. R.
A double-blind, 377-subject randomized study identifies Ruminococcus, Coprococcus, Christensenella, and Collinsella as long-term potential key players in the modulation of the gut microbiome of lactose intolerant individuals by galacto-oligosaccharides
title A double-blind, 377-subject randomized study identifies Ruminococcus, Coprococcus, Christensenella, and Collinsella as long-term potential key players in the modulation of the gut microbiome of lactose intolerant individuals by galacto-oligosaccharides
title_full A double-blind, 377-subject randomized study identifies Ruminococcus, Coprococcus, Christensenella, and Collinsella as long-term potential key players in the modulation of the gut microbiome of lactose intolerant individuals by galacto-oligosaccharides
title_fullStr A double-blind, 377-subject randomized study identifies Ruminococcus, Coprococcus, Christensenella, and Collinsella as long-term potential key players in the modulation of the gut microbiome of lactose intolerant individuals by galacto-oligosaccharides
title_full_unstemmed A double-blind, 377-subject randomized study identifies Ruminococcus, Coprococcus, Christensenella, and Collinsella as long-term potential key players in the modulation of the gut microbiome of lactose intolerant individuals by galacto-oligosaccharides
title_short A double-blind, 377-subject randomized study identifies Ruminococcus, Coprococcus, Christensenella, and Collinsella as long-term potential key players in the modulation of the gut microbiome of lactose intolerant individuals by galacto-oligosaccharides
title_sort double-blind, 377-subject randomized study identifies ruminococcus, coprococcus, christensenella, and collinsella as long-term potential key players in the modulation of the gut microbiome of lactose intolerant individuals by galacto-oligosaccharides
topic Addendum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8354614/
https://www.ncbi.nlm.nih.gov/pubmed/34365905
http://dx.doi.org/10.1080/19490976.2021.1957536
work_keys_str_mv AT azcarateperilma adoubleblind377subjectrandomizedstudyidentifiesruminococcuscoprococcuschristensenellaandcollinsellaaslongtermpotentialkeyplayersinthemodulationofthegutmicrobiomeoflactoseintolerantindividualsbygalactooligosaccharides
AT roachj adoubleblind377subjectrandomizedstudyidentifiesruminococcuscoprococcuschristensenellaandcollinsellaaslongtermpotentialkeyplayersinthemodulationofthegutmicrobiomeoflactoseintolerantindividualsbygalactooligosaccharides
AT marsha adoubleblind377subjectrandomizedstudyidentifiesruminococcuscoprococcuschristensenellaandcollinsellaaslongtermpotentialkeyplayersinthemodulationofthegutmicrobiomeoflactoseintolerantindividualsbygalactooligosaccharides
AT cheywilliamd adoubleblind377subjectrandomizedstudyidentifiesruminococcuscoprococcuschristensenellaandcollinsellaaslongtermpotentialkeyplayersinthemodulationofthegutmicrobiomeoflactoseintolerantindividualsbygalactooligosaccharides
AT sandbornwilliamj adoubleblind377subjectrandomizedstudyidentifiesruminococcuscoprococcuschristensenellaandcollinsellaaslongtermpotentialkeyplayersinthemodulationofthegutmicrobiomeoflactoseintolerantindividualsbygalactooligosaccharides
AT ritterandrewj adoubleblind377subjectrandomizedstudyidentifiesruminococcuscoprococcuschristensenellaandcollinsellaaslongtermpotentialkeyplayersinthemodulationofthegutmicrobiomeoflactoseintolerantindividualsbygalactooligosaccharides
AT savaianodennisa adoubleblind377subjectrandomizedstudyidentifiesruminococcuscoprococcuschristensenellaandcollinsellaaslongtermpotentialkeyplayersinthemodulationofthegutmicrobiomeoflactoseintolerantindividualsbygalactooligosaccharides
AT klaenhammertr adoubleblind377subjectrandomizedstudyidentifiesruminococcuscoprococcuschristensenellaandcollinsellaaslongtermpotentialkeyplayersinthemodulationofthegutmicrobiomeoflactoseintolerantindividualsbygalactooligosaccharides
AT azcarateperilma doubleblind377subjectrandomizedstudyidentifiesruminococcuscoprococcuschristensenellaandcollinsellaaslongtermpotentialkeyplayersinthemodulationofthegutmicrobiomeoflactoseintolerantindividualsbygalactooligosaccharides
AT roachj doubleblind377subjectrandomizedstudyidentifiesruminococcuscoprococcuschristensenellaandcollinsellaaslongtermpotentialkeyplayersinthemodulationofthegutmicrobiomeoflactoseintolerantindividualsbygalactooligosaccharides
AT marsha doubleblind377subjectrandomizedstudyidentifiesruminococcuscoprococcuschristensenellaandcollinsellaaslongtermpotentialkeyplayersinthemodulationofthegutmicrobiomeoflactoseintolerantindividualsbygalactooligosaccharides
AT cheywilliamd doubleblind377subjectrandomizedstudyidentifiesruminococcuscoprococcuschristensenellaandcollinsellaaslongtermpotentialkeyplayersinthemodulationofthegutmicrobiomeoflactoseintolerantindividualsbygalactooligosaccharides
AT sandbornwilliamj doubleblind377subjectrandomizedstudyidentifiesruminococcuscoprococcuschristensenellaandcollinsellaaslongtermpotentialkeyplayersinthemodulationofthegutmicrobiomeoflactoseintolerantindividualsbygalactooligosaccharides
AT ritterandrewj doubleblind377subjectrandomizedstudyidentifiesruminococcuscoprococcuschristensenellaandcollinsellaaslongtermpotentialkeyplayersinthemodulationofthegutmicrobiomeoflactoseintolerantindividualsbygalactooligosaccharides
AT savaianodennisa doubleblind377subjectrandomizedstudyidentifiesruminococcuscoprococcuschristensenellaandcollinsellaaslongtermpotentialkeyplayersinthemodulationofthegutmicrobiomeoflactoseintolerantindividualsbygalactooligosaccharides
AT klaenhammertr doubleblind377subjectrandomizedstudyidentifiesruminococcuscoprococcuschristensenellaandcollinsellaaslongtermpotentialkeyplayersinthemodulationofthegutmicrobiomeoflactoseintolerantindividualsbygalactooligosaccharides