Cargando…

Flexibility and resilience of great tit (Parus major) gut microbiomes to changing diets

BACKGROUND: Gut microbial communities play important roles in nutrient management and can change in response to host diets. The extent of this flexibility and the concomitant resilience is largely unknown in wild animals. To untangle the dynamics of avian-gut microbiome symbiosis associated with die...

Descripción completa

Detalles Bibliográficos
Autores principales: Bodawatta, Kasun H., Freiberga, Inga, Puzejova, Katerina, Sam, Katerina, Poulsen, Michael, Jønsson, Knud A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7893775/
https://www.ncbi.nlm.nih.gov/pubmed/33602335
http://dx.doi.org/10.1186/s42523-021-00076-6
_version_ 1783653115030929408
author Bodawatta, Kasun H.
Freiberga, Inga
Puzejova, Katerina
Sam, Katerina
Poulsen, Michael
Jønsson, Knud A.
author_facet Bodawatta, Kasun H.
Freiberga, Inga
Puzejova, Katerina
Sam, Katerina
Poulsen, Michael
Jønsson, Knud A.
author_sort Bodawatta, Kasun H.
collection PubMed
description BACKGROUND: Gut microbial communities play important roles in nutrient management and can change in response to host diets. The extent of this flexibility and the concomitant resilience is largely unknown in wild animals. To untangle the dynamics of avian-gut microbiome symbiosis associated with diet changes, we exposed Parus major (Great tits) fed with a standard diet (seeds and mealworms) to either a mixed (seeds, mealworms and fruits), a seed, or a mealworm diet for 4 weeks, and examined the flexibility of gut microbiomes to these compositionally different diets. To assess microbiome resilience (recovery potential), all individuals were subsequently reversed to a standard diet for another 4 weeks. Cloacal microbiomes were collected weekly and characterised through sequencing the v4 region of the 16S rRNA gene using Illumina MiSeq. RESULTS: Initial microbiomes changed significantly with the diet manipulation, but the communities did not differ significantly between the three diet groups (mixed, seed and mealworm), despite multiple diet-specific changes in certain bacterial genera. Reverting birds to the standard diet led only to a partial recovery in gut community compositions. The majority of the bacterial taxa that increased significantly during diet manipulation decreased in relative abundance after reversion to the standard diet; however, bacterial taxa that decreased during the manipulation rarely increased after diet reversal CONCLUSIONS: The gut microbial response and partial resilience to dietary changes support that gut bacterial communities of P. major play a role in accommodating dietary changes experienced by wild avian hosts. This may be a contributing factor to the relaxed association between microbiome composition and the bird phylogeny. Our findings further imply that interpretations of wild bird gut microbiome analyses from single-time point sampling, especially for omnivorous species or species with seasonally changing diets, should be done with caution. The partial community recovery implies that ecologically relevant diet changes (e.g., seasonality and migration) open up gut niches that may be filled by previously abundant microbes or replaced by different symbiont lineages, which has important implications for the integrity and specificity of long-term avian-symbiont associations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-021-00076-6.
format Online
Article
Text
id pubmed-7893775
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-78937752021-02-22 Flexibility and resilience of great tit (Parus major) gut microbiomes to changing diets Bodawatta, Kasun H. Freiberga, Inga Puzejova, Katerina Sam, Katerina Poulsen, Michael Jønsson, Knud A. Anim Microbiome Research Article BACKGROUND: Gut microbial communities play important roles in nutrient management and can change in response to host diets. The extent of this flexibility and the concomitant resilience is largely unknown in wild animals. To untangle the dynamics of avian-gut microbiome symbiosis associated with diet changes, we exposed Parus major (Great tits) fed with a standard diet (seeds and mealworms) to either a mixed (seeds, mealworms and fruits), a seed, or a mealworm diet for 4 weeks, and examined the flexibility of gut microbiomes to these compositionally different diets. To assess microbiome resilience (recovery potential), all individuals were subsequently reversed to a standard diet for another 4 weeks. Cloacal microbiomes were collected weekly and characterised through sequencing the v4 region of the 16S rRNA gene using Illumina MiSeq. RESULTS: Initial microbiomes changed significantly with the diet manipulation, but the communities did not differ significantly between the three diet groups (mixed, seed and mealworm), despite multiple diet-specific changes in certain bacterial genera. Reverting birds to the standard diet led only to a partial recovery in gut community compositions. The majority of the bacterial taxa that increased significantly during diet manipulation decreased in relative abundance after reversion to the standard diet; however, bacterial taxa that decreased during the manipulation rarely increased after diet reversal CONCLUSIONS: The gut microbial response and partial resilience to dietary changes support that gut bacterial communities of P. major play a role in accommodating dietary changes experienced by wild avian hosts. This may be a contributing factor to the relaxed association between microbiome composition and the bird phylogeny. Our findings further imply that interpretations of wild bird gut microbiome analyses from single-time point sampling, especially for omnivorous species or species with seasonally changing diets, should be done with caution. The partial community recovery implies that ecologically relevant diet changes (e.g., seasonality and migration) open up gut niches that may be filled by previously abundant microbes or replaced by different symbiont lineages, which has important implications for the integrity and specificity of long-term avian-symbiont associations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s42523-021-00076-6. BioMed Central 2021-02-18 /pmc/articles/PMC7893775/ /pubmed/33602335 http://dx.doi.org/10.1186/s42523-021-00076-6 Text en © The Author(s) 2021 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/.
spellingShingle Research Article
Bodawatta, Kasun H.
Freiberga, Inga
Puzejova, Katerina
Sam, Katerina
Poulsen, Michael
Jønsson, Knud A.
Flexibility and resilience of great tit (Parus major) gut microbiomes to changing diets
title Flexibility and resilience of great tit (Parus major) gut microbiomes to changing diets
title_full Flexibility and resilience of great tit (Parus major) gut microbiomes to changing diets
title_fullStr Flexibility and resilience of great tit (Parus major) gut microbiomes to changing diets
title_full_unstemmed Flexibility and resilience of great tit (Parus major) gut microbiomes to changing diets
title_short Flexibility and resilience of great tit (Parus major) gut microbiomes to changing diets
title_sort flexibility and resilience of great tit (parus major) gut microbiomes to changing diets
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7893775/
https://www.ncbi.nlm.nih.gov/pubmed/33602335
http://dx.doi.org/10.1186/s42523-021-00076-6
work_keys_str_mv AT bodawattakasunh flexibilityandresilienceofgreattitparusmajorgutmicrobiomestochangingdiets
AT freibergainga flexibilityandresilienceofgreattitparusmajorgutmicrobiomestochangingdiets
AT puzejovakaterina flexibilityandresilienceofgreattitparusmajorgutmicrobiomestochangingdiets
AT samkaterina flexibilityandresilienceofgreattitparusmajorgutmicrobiomestochangingdiets
AT poulsenmichael flexibilityandresilienceofgreattitparusmajorgutmicrobiomestochangingdiets
AT jønssonknuda flexibilityandresilienceofgreattitparusmajorgutmicrobiomestochangingdiets