Cargando…
Lactobacillus acidophilus DDS-1 Modulates Intestinal-Specific Microbiota, Short-Chain Fatty Acid and Immunological Profiles in Aging Mice
Distribution of the microbiota varies according to the location in the gastrointestinal (GI) tract. Thus, dysbiosis during aging may not be limited to faecal microbiota and extend to the other parts of the GI tract, especially the cecum and colon. Lactobacillus acidophilus DDS-1, a probiotic strain,...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627711/ https://www.ncbi.nlm.nih.gov/pubmed/31181695 http://dx.doi.org/10.3390/nu11061297 |
_version_ | 1783434800667820032 |
---|---|
author | Vemuri, Ravichandra Gundamaraju, Rohit Shinde, Tanvi Perera, Agampodi Promoda Basheer, Waheedha Southam, Benjamin Gondalia, Shakuntla V. Karpe, Avinash V. Beale, David J. Tristram, Stephen Ahuja, Kiran D. K. Ball, Madeleine Martoni, Christopher J. Eri, Rajaraman |
author_facet | Vemuri, Ravichandra Gundamaraju, Rohit Shinde, Tanvi Perera, Agampodi Promoda Basheer, Waheedha Southam, Benjamin Gondalia, Shakuntla V. Karpe, Avinash V. Beale, David J. Tristram, Stephen Ahuja, Kiran D. K. Ball, Madeleine Martoni, Christopher J. Eri, Rajaraman |
author_sort | Vemuri, Ravichandra |
collection | PubMed |
description | Distribution of the microbiota varies according to the location in the gastrointestinal (GI) tract. Thus, dysbiosis during aging may not be limited to faecal microbiota and extend to the other parts of the GI tract, especially the cecum and colon. Lactobacillus acidophilus DDS-1, a probiotic strain, has been shown to modulate faecal microbiota and its associated metabolic phenotype in aging mice. In the present study, we investigated the effect of L. acidophilus DDS-1 supplementation on caecal- and mucosal-associated microbiota, short-chain fatty acids (SCFAs) and immunological profiles in young and aging C57BL/6J mice. Besides differences in the young and aging control groups, we observed microbial shifts in caecal and mucosal samples, leading to an alteration in SCFA levels and immune response. DDS-1 treatment increased the abundances of beneficial bacteria such as Akkermansia spp. and Lactobacillus spp. more effectively in caecal samples than in mucosal samples. DDS-1 also enhanced the levels of butyrate, while downregulating the production of inflammatory cytokines (IL-6, IL-1β, IL-1α, MCP-1, MIP-1α, MIP-1β, IL-12 and IFN-γ) in serum and colonic explants. Our findings suggest distinct patterns of intestinal microbiota, improvements in SCFA and immunological profiles with DDS-1 supplementation in aging mice. |
format | Online Article Text |
id | pubmed-6627711 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66277112019-07-23 Lactobacillus acidophilus DDS-1 Modulates Intestinal-Specific Microbiota, Short-Chain Fatty Acid and Immunological Profiles in Aging Mice Vemuri, Ravichandra Gundamaraju, Rohit Shinde, Tanvi Perera, Agampodi Promoda Basheer, Waheedha Southam, Benjamin Gondalia, Shakuntla V. Karpe, Avinash V. Beale, David J. Tristram, Stephen Ahuja, Kiran D. K. Ball, Madeleine Martoni, Christopher J. Eri, Rajaraman Nutrients Article Distribution of the microbiota varies according to the location in the gastrointestinal (GI) tract. Thus, dysbiosis during aging may not be limited to faecal microbiota and extend to the other parts of the GI tract, especially the cecum and colon. Lactobacillus acidophilus DDS-1, a probiotic strain, has been shown to modulate faecal microbiota and its associated metabolic phenotype in aging mice. In the present study, we investigated the effect of L. acidophilus DDS-1 supplementation on caecal- and mucosal-associated microbiota, short-chain fatty acids (SCFAs) and immunological profiles in young and aging C57BL/6J mice. Besides differences in the young and aging control groups, we observed microbial shifts in caecal and mucosal samples, leading to an alteration in SCFA levels and immune response. DDS-1 treatment increased the abundances of beneficial bacteria such as Akkermansia spp. and Lactobacillus spp. more effectively in caecal samples than in mucosal samples. DDS-1 also enhanced the levels of butyrate, while downregulating the production of inflammatory cytokines (IL-6, IL-1β, IL-1α, MCP-1, MIP-1α, MIP-1β, IL-12 and IFN-γ) in serum and colonic explants. Our findings suggest distinct patterns of intestinal microbiota, improvements in SCFA and immunological profiles with DDS-1 supplementation in aging mice. MDPI 2019-06-07 /pmc/articles/PMC6627711/ /pubmed/31181695 http://dx.doi.org/10.3390/nu11061297 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Vemuri, Ravichandra Gundamaraju, Rohit Shinde, Tanvi Perera, Agampodi Promoda Basheer, Waheedha Southam, Benjamin Gondalia, Shakuntla V. Karpe, Avinash V. Beale, David J. Tristram, Stephen Ahuja, Kiran D. K. Ball, Madeleine Martoni, Christopher J. Eri, Rajaraman Lactobacillus acidophilus DDS-1 Modulates Intestinal-Specific Microbiota, Short-Chain Fatty Acid and Immunological Profiles in Aging Mice |
title | Lactobacillus acidophilus DDS-1 Modulates Intestinal-Specific Microbiota, Short-Chain Fatty Acid and Immunological Profiles in Aging Mice |
title_full | Lactobacillus acidophilus DDS-1 Modulates Intestinal-Specific Microbiota, Short-Chain Fatty Acid and Immunological Profiles in Aging Mice |
title_fullStr | Lactobacillus acidophilus DDS-1 Modulates Intestinal-Specific Microbiota, Short-Chain Fatty Acid and Immunological Profiles in Aging Mice |
title_full_unstemmed | Lactobacillus acidophilus DDS-1 Modulates Intestinal-Specific Microbiota, Short-Chain Fatty Acid and Immunological Profiles in Aging Mice |
title_short | Lactobacillus acidophilus DDS-1 Modulates Intestinal-Specific Microbiota, Short-Chain Fatty Acid and Immunological Profiles in Aging Mice |
title_sort | lactobacillus acidophilus dds-1 modulates intestinal-specific microbiota, short-chain fatty acid and immunological profiles in aging mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6627711/ https://www.ncbi.nlm.nih.gov/pubmed/31181695 http://dx.doi.org/10.3390/nu11061297 |
work_keys_str_mv | AT vemuriravichandra lactobacillusacidophilusdds1modulatesintestinalspecificmicrobiotashortchainfattyacidandimmunologicalprofilesinagingmice AT gundamarajurohit lactobacillusacidophilusdds1modulatesintestinalspecificmicrobiotashortchainfattyacidandimmunologicalprofilesinagingmice AT shindetanvi lactobacillusacidophilusdds1modulatesintestinalspecificmicrobiotashortchainfattyacidandimmunologicalprofilesinagingmice AT pereraagampodipromoda lactobacillusacidophilusdds1modulatesintestinalspecificmicrobiotashortchainfattyacidandimmunologicalprofilesinagingmice AT basheerwaheedha lactobacillusacidophilusdds1modulatesintestinalspecificmicrobiotashortchainfattyacidandimmunologicalprofilesinagingmice AT southambenjamin lactobacillusacidophilusdds1modulatesintestinalspecificmicrobiotashortchainfattyacidandimmunologicalprofilesinagingmice AT gondaliashakuntlav lactobacillusacidophilusdds1modulatesintestinalspecificmicrobiotashortchainfattyacidandimmunologicalprofilesinagingmice AT karpeavinashv lactobacillusacidophilusdds1modulatesintestinalspecificmicrobiotashortchainfattyacidandimmunologicalprofilesinagingmice AT bealedavidj lactobacillusacidophilusdds1modulatesintestinalspecificmicrobiotashortchainfattyacidandimmunologicalprofilesinagingmice AT tristramstephen lactobacillusacidophilusdds1modulatesintestinalspecificmicrobiotashortchainfattyacidandimmunologicalprofilesinagingmice AT ahujakirandk lactobacillusacidophilusdds1modulatesintestinalspecificmicrobiotashortchainfattyacidandimmunologicalprofilesinagingmice AT ballmadeleine lactobacillusacidophilusdds1modulatesintestinalspecificmicrobiotashortchainfattyacidandimmunologicalprofilesinagingmice AT martonichristopherj lactobacillusacidophilusdds1modulatesintestinalspecificmicrobiotashortchainfattyacidandimmunologicalprofilesinagingmice AT erirajaraman lactobacillusacidophilusdds1modulatesintestinalspecificmicrobiotashortchainfattyacidandimmunologicalprofilesinagingmice |