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Disentangling factors that shape the gut microbiota in German Shepherd dogs
The aim of this study was to explore the development of the gut microbiota in 168 German Shepherd dogs (30 litters) from 7 weeks to 18 months of age and furthermore, to study the effect of relatedness, maternal microbiota composition and living environment in a large and well-defined population of d...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865712/ https://www.ncbi.nlm.nih.gov/pubmed/29570709 http://dx.doi.org/10.1371/journal.pone.0193507 |
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author | Vilson, Åsa Ramadan, Ziad Li, Qinghong Hedhammar, Åke Reynolds, Arleigh Spears, Julie Labuda, Jeff Pelker, Robyn Björkstén, Bengt Dicksved, Johan Hansson-Hamlin, Helene |
author_facet | Vilson, Åsa Ramadan, Ziad Li, Qinghong Hedhammar, Åke Reynolds, Arleigh Spears, Julie Labuda, Jeff Pelker, Robyn Björkstén, Bengt Dicksved, Johan Hansson-Hamlin, Helene |
author_sort | Vilson, Åsa |
collection | PubMed |
description | The aim of this study was to explore the development of the gut microbiota in 168 German Shepherd dogs (30 litters) from 7 weeks to 18 months of age and furthermore, to study the effect of relatedness, maternal microbiota composition and living environment in a large and well-defined population of dogs. Using 454 pyrosequencing, we assessed the effects of pre- and postnatal probiotic supplementation (Lactobacillus johnsonii NCC533 (La1)) and analysed whether administration of the probiotic strain influenced fecal microbiota composition in a placebo controlled double-blinded study. The bitches were treated with probiotics or placebo during last trimester of pregnancy and until their puppies were 8 weeks old, the puppies received the same treatment as their mothers between 3–12 weeks of age. Samples from bitches were collected at pregnancy day 42, partum, 4 weeks postpartum and 7 weeks postpartum and from puppies at the age 4 weeks, 7 weeks, 12–13 months and 15–18 months. Serum IgA, total serum IgE, fecal IgA and IgG antibody responses against canine distemper virus were analysed by ELISA in order to detect any immune stimulating effects of the probiotic strain. Analysis of the fecal microbiota composition showed that the predominant phyla were the same in 7 weeks old puppies as in pregnant and lactating bitches (Firmicutes, Fusobacteria, Bacteroidetes). Proportions among different bacteria as well as diversity varied from 7 weeks old puppies up to 15–18 months of age. Litter mates had a more similar fecal microbiota compared to unrelated dogs and 7 weeks old puppies were more similar to their mothers than to unrelated bitches at 7 weeks postpartum but not at partum. We observed a change in the relative abundance of different bacteria during lactation, and an increase in diversity from pregnancy to end of lactation. The microbial diversity was affected by living area where dogs living in big cities had higher diversity compared to dogs living at the countryside. However, we were not able to demonstrate an effect by pre and postnatal exposure to Lactobacillus johnsonii NCC533 (La1) upon the diversity or composition of the microbiota or the levels of serum IgA, total serum IgE, fecal IgA or vaccine response. Our findings provide a better understanding of the canine fecal microbiota in growing dogs as well as in pregnant and lactating bitches. This information forms a basis for further research on the connection between early gut colonization and immune function later in life. |
format | Online Article Text |
id | pubmed-5865712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58657122018-03-28 Disentangling factors that shape the gut microbiota in German Shepherd dogs Vilson, Åsa Ramadan, Ziad Li, Qinghong Hedhammar, Åke Reynolds, Arleigh Spears, Julie Labuda, Jeff Pelker, Robyn Björkstén, Bengt Dicksved, Johan Hansson-Hamlin, Helene PLoS One Research Article The aim of this study was to explore the development of the gut microbiota in 168 German Shepherd dogs (30 litters) from 7 weeks to 18 months of age and furthermore, to study the effect of relatedness, maternal microbiota composition and living environment in a large and well-defined population of dogs. Using 454 pyrosequencing, we assessed the effects of pre- and postnatal probiotic supplementation (Lactobacillus johnsonii NCC533 (La1)) and analysed whether administration of the probiotic strain influenced fecal microbiota composition in a placebo controlled double-blinded study. The bitches were treated with probiotics or placebo during last trimester of pregnancy and until their puppies were 8 weeks old, the puppies received the same treatment as their mothers between 3–12 weeks of age. Samples from bitches were collected at pregnancy day 42, partum, 4 weeks postpartum and 7 weeks postpartum and from puppies at the age 4 weeks, 7 weeks, 12–13 months and 15–18 months. Serum IgA, total serum IgE, fecal IgA and IgG antibody responses against canine distemper virus were analysed by ELISA in order to detect any immune stimulating effects of the probiotic strain. Analysis of the fecal microbiota composition showed that the predominant phyla were the same in 7 weeks old puppies as in pregnant and lactating bitches (Firmicutes, Fusobacteria, Bacteroidetes). Proportions among different bacteria as well as diversity varied from 7 weeks old puppies up to 15–18 months of age. Litter mates had a more similar fecal microbiota compared to unrelated dogs and 7 weeks old puppies were more similar to their mothers than to unrelated bitches at 7 weeks postpartum but not at partum. We observed a change in the relative abundance of different bacteria during lactation, and an increase in diversity from pregnancy to end of lactation. The microbial diversity was affected by living area where dogs living in big cities had higher diversity compared to dogs living at the countryside. However, we were not able to demonstrate an effect by pre and postnatal exposure to Lactobacillus johnsonii NCC533 (La1) upon the diversity or composition of the microbiota or the levels of serum IgA, total serum IgE, fecal IgA or vaccine response. Our findings provide a better understanding of the canine fecal microbiota in growing dogs as well as in pregnant and lactating bitches. This information forms a basis for further research on the connection between early gut colonization and immune function later in life. Public Library of Science 2018-03-23 /pmc/articles/PMC5865712/ /pubmed/29570709 http://dx.doi.org/10.1371/journal.pone.0193507 Text en © 2018 Vilson et al http://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/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Vilson, Åsa Ramadan, Ziad Li, Qinghong Hedhammar, Åke Reynolds, Arleigh Spears, Julie Labuda, Jeff Pelker, Robyn Björkstén, Bengt Dicksved, Johan Hansson-Hamlin, Helene Disentangling factors that shape the gut microbiota in German Shepherd dogs |
title | Disentangling factors that shape the gut microbiota in German Shepherd dogs |
title_full | Disentangling factors that shape the gut microbiota in German Shepherd dogs |
title_fullStr | Disentangling factors that shape the gut microbiota in German Shepherd dogs |
title_full_unstemmed | Disentangling factors that shape the gut microbiota in German Shepherd dogs |
title_short | Disentangling factors that shape the gut microbiota in German Shepherd dogs |
title_sort | disentangling factors that shape the gut microbiota in german shepherd dogs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5865712/ https://www.ncbi.nlm.nih.gov/pubmed/29570709 http://dx.doi.org/10.1371/journal.pone.0193507 |
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