Allometry and Ecology of the Bilaterian Gut Microbiome

ABSTRACT Classical ecology provides principles for construction and function of biological communities, but to what extent these apply to the animal-associated microbiota is just beginning to be assessed. Here, we investigated the influence of several well-known ecological principles on animal-assoc...

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Autores principales: Scott Sherrill-Mix, Kevin McCormick, Abigail Lauder, Aubrey Bailey, Laurie Zimmerman, Yingying Li, Jean-Bosco N. Django, Paco Bertolani, Christelle Colin, John A. Hart, Terese B. Hart, Alexander V. Georgiev, Crickette M. Sanz, David B. Morgan, Rebeca Atencia, Debby Cox, Martin N. Muller, Volker Sommer, Alexander K. Piel, Fiona A. Stewart, Sheri Speede, Joe Roman, Gary Wu, Josh Taylor, Rudolf Bohm, Heather M. Rose, John Carlson, Deus Mjungu, Paul Schmidt, Celeste Gaughan, Joyslin I. Bushman, Ella Schmidt, Kyle Bittinger, Ronald G. Collman, Beatrice H. Hahn, Frederic D. Bushman
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Publicado: American Society for Microbiology 2018
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spelling oai:doaj.org-article:8ce2e460419144ca8074efe69634a3ee2021-11-15T15:53:27ZAllometry and Ecology of the Bilaterian Gut Microbiome10.1128/mBio.00319-182150-7511https://doaj.org/article/8ce2e460419144ca8074efe69634a3ee2018-05-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mBio.00319-18https://doaj.org/toc/2150-7511ABSTRACT Classical ecology provides principles for construction and function of biological communities, but to what extent these apply to the animal-associated microbiota is just beginning to be assessed. Here, we investigated the influence of several well-known ecological principles on animal-associated microbiota by characterizing gut microbial specimens from bilaterally symmetrical animals (Bilateria) ranging from flies to whales. A rigorously vetted sample set containing 265 specimens from 64 species was assembled. Bacterial lineages were characterized by 16S rRNA gene sequencing. Previously published samples were also compared, allowing analysis of over 1,098 samples in total. A restricted number of bacterial phyla was found to account for the great majority of gut colonists. Gut microbial composition was associated with host phylogeny and diet. We identified numerous gut bacterial 16S rRNA gene sequences that diverged deeply from previously studied taxa, identifying opportunities to discover new bacterial types. The number of bacterial lineages per gut sample was positively associated with animal mass, paralleling known species-area relationships from island biogeography and implicating body size as a determinant of community stability and niche complexity. Samples from larger animals harbored greater numbers of anaerobic communities, specifying a mechanism for generating more-complex microbial environments. Predictions for species/abundance relationships from models of neutral colonization did not match the data set, pointing to alternative mechanisms such as selection of specific colonists by environmental niche. Taken together, the data suggest that niche complexity increases with gut size and that niche selection forces dominate gut community construction. IMPORTANCE The intestinal microbiome of animals is essential for health, contributing to digestion of foods, proper immune development, inhibition of pathogen colonization, and catabolism of xenobiotic compounds. How these communities assemble and persist is just beginning to be investigated. Here we interrogated a set of gut samples from a wide range of animals to investigate the roles of selection and random processes in microbial community construction. We show that the numbers of bacterial species increased with the weight of host organisms, paralleling findings from studies of island biogeography. Communities in larger organisms tended to be more anaerobic, suggesting one mechanism for niche diversification. Nonselective processes enable specific predictions for community structure, but our samples did not match the predictions of the neutral model. Thus, these findings highlight the importance of niche selection in community construction and suggest mechanisms of niche diversification.Scott Sherrill-MixKevin McCormickAbigail LauderAubrey BaileyLaurie ZimmermanYingying LiJean-Bosco N. DjangoPaco BertolaniChristelle ColinJohn A. HartTerese B. HartAlexander V. GeorgievCrickette M. SanzDavid B. MorganRebeca AtenciaDebby CoxMartin N. MullerVolker SommerAlexander K. PielFiona A. StewartSheri SpeedeJoe RomanGary WuJosh TaylorRudolf BohmHeather M. RoseJohn CarlsonDeus MjunguPaul SchmidtCeleste GaughanJoyslin I. BushmanElla SchmidtKyle BittingerRonald G. CollmanBeatrice H. HahnFrederic D. BushmanAmerican Society for Microbiologyarticlebacteriabilateriamicrobiomemicrobiotaneutral modelspecies-areaMicrobiologyQR1-502ENmBio, Vol 9, Iss 2 (2018)
institution DOAJ
collection DOAJ
language EN
topic bacteria
bilateria
microbiome
microbiota
neutral model
species-area
Microbiology
QR1-502
spellingShingle bacteria
bilateria
microbiome
microbiota
neutral model
species-area
Microbiology
QR1-502
Scott Sherrill-Mix
Kevin McCormick
Abigail Lauder
Aubrey Bailey
Laurie Zimmerman
Yingying Li
Jean-Bosco N. Django
Paco Bertolani
Christelle Colin
John A. Hart
Terese B. Hart
Alexander V. Georgiev
Crickette M. Sanz
David B. Morgan
Rebeca Atencia
Debby Cox
Martin N. Muller
Volker Sommer
Alexander K. Piel
Fiona A. Stewart
Sheri Speede
Joe Roman
Gary Wu
Josh Taylor
Rudolf Bohm
Heather M. Rose
John Carlson
Deus Mjungu
Paul Schmidt
Celeste Gaughan
Joyslin I. Bushman
Ella Schmidt
Kyle Bittinger
Ronald G. Collman
Beatrice H. Hahn
Frederic D. Bushman
Allometry and Ecology of the Bilaterian Gut Microbiome
description ABSTRACT Classical ecology provides principles for construction and function of biological communities, but to what extent these apply to the animal-associated microbiota is just beginning to be assessed. Here, we investigated the influence of several well-known ecological principles on animal-associated microbiota by characterizing gut microbial specimens from bilaterally symmetrical animals (Bilateria) ranging from flies to whales. A rigorously vetted sample set containing 265 specimens from 64 species was assembled. Bacterial lineages were characterized by 16S rRNA gene sequencing. Previously published samples were also compared, allowing analysis of over 1,098 samples in total. A restricted number of bacterial phyla was found to account for the great majority of gut colonists. Gut microbial composition was associated with host phylogeny and diet. We identified numerous gut bacterial 16S rRNA gene sequences that diverged deeply from previously studied taxa, identifying opportunities to discover new bacterial types. The number of bacterial lineages per gut sample was positively associated with animal mass, paralleling known species-area relationships from island biogeography and implicating body size as a determinant of community stability and niche complexity. Samples from larger animals harbored greater numbers of anaerobic communities, specifying a mechanism for generating more-complex microbial environments. Predictions for species/abundance relationships from models of neutral colonization did not match the data set, pointing to alternative mechanisms such as selection of specific colonists by environmental niche. Taken together, the data suggest that niche complexity increases with gut size and that niche selection forces dominate gut community construction. IMPORTANCE The intestinal microbiome of animals is essential for health, contributing to digestion of foods, proper immune development, inhibition of pathogen colonization, and catabolism of xenobiotic compounds. How these communities assemble and persist is just beginning to be investigated. Here we interrogated a set of gut samples from a wide range of animals to investigate the roles of selection and random processes in microbial community construction. We show that the numbers of bacterial species increased with the weight of host organisms, paralleling findings from studies of island biogeography. Communities in larger organisms tended to be more anaerobic, suggesting one mechanism for niche diversification. Nonselective processes enable specific predictions for community structure, but our samples did not match the predictions of the neutral model. Thus, these findings highlight the importance of niche selection in community construction and suggest mechanisms of niche diversification.
format article
author Scott Sherrill-Mix
Kevin McCormick
Abigail Lauder
Aubrey Bailey
Laurie Zimmerman
Yingying Li
Jean-Bosco N. Django
Paco Bertolani
Christelle Colin
John A. Hart
Terese B. Hart
Alexander V. Georgiev
Crickette M. Sanz
David B. Morgan
Rebeca Atencia
Debby Cox
Martin N. Muller
Volker Sommer
Alexander K. Piel
Fiona A. Stewart
Sheri Speede
Joe Roman
Gary Wu
Josh Taylor
Rudolf Bohm
Heather M. Rose
John Carlson
Deus Mjungu
Paul Schmidt
Celeste Gaughan
Joyslin I. Bushman
Ella Schmidt
Kyle Bittinger
Ronald G. Collman
Beatrice H. Hahn
Frederic D. Bushman
author_facet Scott Sherrill-Mix
Kevin McCormick
Abigail Lauder
Aubrey Bailey
Laurie Zimmerman
Yingying Li
Jean-Bosco N. Django
Paco Bertolani
Christelle Colin
John A. Hart
Terese B. Hart
Alexander V. Georgiev
Crickette M. Sanz
David B. Morgan
Rebeca Atencia
Debby Cox
Martin N. Muller
Volker Sommer
Alexander K. Piel
Fiona A. Stewart
Sheri Speede
Joe Roman
Gary Wu
Josh Taylor
Rudolf Bohm
Heather M. Rose
John Carlson
Deus Mjungu
Paul Schmidt
Celeste Gaughan
Joyslin I. Bushman
Ella Schmidt
Kyle Bittinger
Ronald G. Collman
Beatrice H. Hahn
Frederic D. Bushman
author_sort Scott Sherrill-Mix
title Allometry and Ecology of the Bilaterian Gut Microbiome
title_short Allometry and Ecology of the Bilaterian Gut Microbiome
title_full Allometry and Ecology of the Bilaterian Gut Microbiome
title_fullStr Allometry and Ecology of the Bilaterian Gut Microbiome
title_full_unstemmed Allometry and Ecology of the Bilaterian Gut Microbiome
title_sort allometry and ecology of the bilaterian gut microbiome
publisher American Society for Microbiology
publishDate 2018
url https://doaj.org/article/8ce2e460419144ca8074efe69634a3ee
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