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Microbiome reduction and endosymbiont gain from a switch in sea urchin life history.

Publication ,  Journal Article
Carrier, TJ; Leigh, BA; Deaker, DJ; Devens, HR; Wray, GA; Bordenstein, SR; Byrne, M; Reitzel, AM
Published in: Proceedings of the National Academy of Sciences of the United States of America
April 2021

Animal gastrointestinal tracts harbor a microbiome that is integral to host function, yet species from diverse phyla have evolved a reduced digestive system or lost it completely. Whether such changes are associated with alterations in the diversity and/or abundance of the microbiome remains an untested hypothesis in evolutionary symbiosis. Here, using the life history transition from planktotrophy (feeding) to lecithotrophy (nonfeeding) in the sea urchin Heliocidaris, we demonstrate that the lack of a functional gut corresponds with a reduction in microbial community diversity and abundance as well as the association with a diet-specific microbiome. We also determine that the lecithotroph vertically transmits a Rickettsiales that may complement host nutrition through amino acid biosynthesis and influence host reproduction. Our results indicate that the evolutionary loss of a functional gut correlates with a reduction in the microbiome and the association with an endosymbiont. Symbiotic transitions can therefore accompany life history transitions in the evolution of developmental strategies.

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Published In

Proceedings of the National Academy of Sciences of the United States of America

DOI

EISSN

1091-6490

ISSN

0027-8424

Publication Date

April 2021

Volume

118

Issue

16

Start / End Page

e2022023118

Related Subject Headings

  • Symbiosis
  • Sea Urchins
  • RNA, Ribosomal, 16S
  • Phylogeny
  • Microbiota
  • Gastrointestinal Tract
  • Biological Evolution
  • Animals
  • Adaptation, Biological
 

Citation

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Carrier, T. J., Leigh, B. A., Deaker, D. J., Devens, H. R., Wray, G. A., Bordenstein, S. R., … Reitzel, A. M. (2021). Microbiome reduction and endosymbiont gain from a switch in sea urchin life history. Proceedings of the National Academy of Sciences of the United States of America, 118(16), e2022023118. https://doi.org/10.1073/pnas.2022023118
Carrier, Tyler J., Brittany A. Leigh, Dione J. Deaker, Hannah R. Devens, Gregory A. Wray, Seth R. Bordenstein, Maria Byrne, and Adam M. Reitzel. “Microbiome reduction and endosymbiont gain from a switch in sea urchin life history.Proceedings of the National Academy of Sciences of the United States of America 118, no. 16 (April 2021): e2022023118. https://doi.org/10.1073/pnas.2022023118.
Carrier TJ, Leigh BA, Deaker DJ, Devens HR, Wray GA, Bordenstein SR, et al. Microbiome reduction and endosymbiont gain from a switch in sea urchin life history. Proceedings of the National Academy of Sciences of the United States of America. 2021 Apr;118(16):e2022023118.
Carrier, Tyler J., et al. “Microbiome reduction and endosymbiont gain from a switch in sea urchin life history.Proceedings of the National Academy of Sciences of the United States of America, vol. 118, no. 16, Apr. 2021, p. e2022023118. Epmc, doi:10.1073/pnas.2022023118.
Carrier TJ, Leigh BA, Deaker DJ, Devens HR, Wray GA, Bordenstein SR, Byrne M, Reitzel AM. Microbiome reduction and endosymbiont gain from a switch in sea urchin life history. Proceedings of the National Academy of Sciences of the United States of America. 2021 Apr;118(16):e2022023118.
Journal cover image

Published In

Proceedings of the National Academy of Sciences of the United States of America

DOI

EISSN

1091-6490

ISSN

0027-8424

Publication Date

April 2021

Volume

118

Issue

16

Start / End Page

e2022023118

Related Subject Headings

  • Symbiosis
  • Sea Urchins
  • RNA, Ribosomal, 16S
  • Phylogeny
  • Microbiota
  • Gastrointestinal Tract
  • Biological Evolution
  • Animals
  • Adaptation, Biological