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The microbiota of healthy dogs demonstrates individualized responses to synbiotic supplementation in a randomized controlled trial

BACKGROUND: Probiotics have been demonstrated to ameliorate clinical signs of gastrointestinal diseases in dogs in various studies. However, the effect of probiotics in a healthy population, as well as factors contributing individualized responses, remain largely unknown. This trial examined gut mic...

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Autores principales: Tanprasertsuk, Jirayu, Jha, Aashish R., Shmalberg, Justin, Jones, Roshonda B., Perry, LeeAnn M., Maughan, Heather, Honaker, Ryan W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8111948/
https://www.ncbi.nlm.nih.gov/pubmed/33971985
http://dx.doi.org/10.1186/s42523-021-00098-0
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author Tanprasertsuk, Jirayu
Jha, Aashish R.
Shmalberg, Justin
Jones, Roshonda B.
Perry, LeeAnn M.
Maughan, Heather
Honaker, Ryan W.
author_facet Tanprasertsuk, Jirayu
Jha, Aashish R.
Shmalberg, Justin
Jones, Roshonda B.
Perry, LeeAnn M.
Maughan, Heather
Honaker, Ryan W.
author_sort Tanprasertsuk, Jirayu
collection PubMed
description BACKGROUND: Probiotics have been demonstrated to ameliorate clinical signs of gastrointestinal diseases in dogs in various studies. However, the effect of probiotics in a healthy population, as well as factors contributing individualized responses, remain largely unknown. This trial examined gut microbiota (GM) and health outcomes in household dogs after synbiotic (SN) supplementation containing probiotics and inulin (a prebiotic). Healthy dogs were randomized to receive SN (50 mg/d inulin and 20 billion total CFU/d of L. reuteri, P. acidilactici, E. faecium, L. acidophilus, B. animalis, L. fermentum, L. rhamnosus) or placebo (PL) for 4 weeks. Owners completed a health survey and collected stool samples for GM profiling (shotgun metagenomic sequencing) at baseline and week 4 in both groups, and at week 6 in the SN group. RESULTS: A significant shift (p < 0.001) in β-diversity was observed in the SN (n = 24), but not PL group (n = 19), at week 4 relative to baseline. Forty-five bacterial species, 43 (96%) of which were Lactobacillales, showed an increase in the relative abundances (≥2 fold change, adjusted p < 0.05) in the SN group at week 4. E. coli also decreased at week 4 in the SN group (2.8-fold, adjusted p < 0.01). The altered taxa largely returned to baseline at week 6. The degree of changes in β-diversity was associated with GM at baseline. Specifically, dogs with higher Proteobacteria and lower Lactobacillales responded more robustly to supplementation in terms of the change in β-diversity. Dogs fed SN tended to have lower diarrhea incidence (0% vs 16%, p = 0.08). CONCLUSIONS: SN supplement had a short-term impact on the gut microbiota in healthy household dogs as characterized by shotgun metagenomic sequencing. Findings warrant further investigation with longer duration and populations at risk of gastrointestinal diseases. The magnitude of response to the supplement was associated with microbial profile at baseline. To our knowledge, this is the first study documenting such association and may provide a basis for personalized nutrition in companion dogs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-021-00098-0.
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spelling pubmed-81119482021-05-12 The microbiota of healthy dogs demonstrates individualized responses to synbiotic supplementation in a randomized controlled trial Tanprasertsuk, Jirayu Jha, Aashish R. Shmalberg, Justin Jones, Roshonda B. Perry, LeeAnn M. Maughan, Heather Honaker, Ryan W. Anim Microbiome Research Article BACKGROUND: Probiotics have been demonstrated to ameliorate clinical signs of gastrointestinal diseases in dogs in various studies. However, the effect of probiotics in a healthy population, as well as factors contributing individualized responses, remain largely unknown. This trial examined gut microbiota (GM) and health outcomes in household dogs after synbiotic (SN) supplementation containing probiotics and inulin (a prebiotic). Healthy dogs were randomized to receive SN (50 mg/d inulin and 20 billion total CFU/d of L. reuteri, P. acidilactici, E. faecium, L. acidophilus, B. animalis, L. fermentum, L. rhamnosus) or placebo (PL) for 4 weeks. Owners completed a health survey and collected stool samples for GM profiling (shotgun metagenomic sequencing) at baseline and week 4 in both groups, and at week 6 in the SN group. RESULTS: A significant shift (p < 0.001) in β-diversity was observed in the SN (n = 24), but not PL group (n = 19), at week 4 relative to baseline. Forty-five bacterial species, 43 (96%) of which were Lactobacillales, showed an increase in the relative abundances (≥2 fold change, adjusted p < 0.05) in the SN group at week 4. E. coli also decreased at week 4 in the SN group (2.8-fold, adjusted p < 0.01). The altered taxa largely returned to baseline at week 6. The degree of changes in β-diversity was associated with GM at baseline. Specifically, dogs with higher Proteobacteria and lower Lactobacillales responded more robustly to supplementation in terms of the change in β-diversity. Dogs fed SN tended to have lower diarrhea incidence (0% vs 16%, p = 0.08). CONCLUSIONS: SN supplement had a short-term impact on the gut microbiota in healthy household dogs as characterized by shotgun metagenomic sequencing. Findings warrant further investigation with longer duration and populations at risk of gastrointestinal diseases. The magnitude of response to the supplement was associated with microbial profile at baseline. To our knowledge, this is the first study documenting such association and may provide a basis for personalized nutrition in companion dogs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-021-00098-0. BioMed Central 2021-05-10 /pmc/articles/PMC8111948/ /pubmed/33971985 http://dx.doi.org/10.1186/s42523-021-00098-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Tanprasertsuk, Jirayu
Jha, Aashish R.
Shmalberg, Justin
Jones, Roshonda B.
Perry, LeeAnn M.
Maughan, Heather
Honaker, Ryan W.
The microbiota of healthy dogs demonstrates individualized responses to synbiotic supplementation in a randomized controlled trial
title The microbiota of healthy dogs demonstrates individualized responses to synbiotic supplementation in a randomized controlled trial
title_full The microbiota of healthy dogs demonstrates individualized responses to synbiotic supplementation in a randomized controlled trial
title_fullStr The microbiota of healthy dogs demonstrates individualized responses to synbiotic supplementation in a randomized controlled trial
title_full_unstemmed The microbiota of healthy dogs demonstrates individualized responses to synbiotic supplementation in a randomized controlled trial
title_short The microbiota of healthy dogs demonstrates individualized responses to synbiotic supplementation in a randomized controlled trial
title_sort microbiota of healthy dogs demonstrates individualized responses to synbiotic supplementation in a randomized controlled trial
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8111948/
https://www.ncbi.nlm.nih.gov/pubmed/33971985
http://dx.doi.org/10.1186/s42523-021-00098-0
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