Cargando…

Herbivorous turtle ants obtain essential nutrients from a conserved nitrogen-recycling gut microbiome

Nitrogen acquisition is a major challenge for herbivorous animals, and the repeated origins of herbivory across the ants have raised expectations that nutritional symbionts have shaped their diversification. Direct evidence for N provisioning by internally housed symbionts is rare in animals; among...

Descripción completa

Detalles Bibliográficos
Autores principales: Hu, Yi, Sanders, Jon G., Łukasik, Piotr, D’Amelio, Catherine L., Millar, John S., Vann, David R., Lan, Yemin, Newton, Justin A., Schotanus, Mark, Kronauer, Daniel J. C., Pierce, Naomi E., Moreau, Corrie S., Wertz, John T., Engel, Philipp, Russell, Jacob A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840417/
https://www.ncbi.nlm.nih.gov/pubmed/29511180
http://dx.doi.org/10.1038/s41467-018-03357-y
_version_ 1783304574209097728
author Hu, Yi
Sanders, Jon G.
Łukasik, Piotr
D’Amelio, Catherine L.
Millar, John S.
Vann, David R.
Lan, Yemin
Newton, Justin A.
Schotanus, Mark
Kronauer, Daniel J. C.
Pierce, Naomi E.
Moreau, Corrie S.
Wertz, John T.
Engel, Philipp
Russell, Jacob A.
author_facet Hu, Yi
Sanders, Jon G.
Łukasik, Piotr
D’Amelio, Catherine L.
Millar, John S.
Vann, David R.
Lan, Yemin
Newton, Justin A.
Schotanus, Mark
Kronauer, Daniel J. C.
Pierce, Naomi E.
Moreau, Corrie S.
Wertz, John T.
Engel, Philipp
Russell, Jacob A.
author_sort Hu, Yi
collection PubMed
description Nitrogen acquisition is a major challenge for herbivorous animals, and the repeated origins of herbivory across the ants have raised expectations that nutritional symbionts have shaped their diversification. Direct evidence for N provisioning by internally housed symbionts is rare in animals; among the ants, it has been documented for just one lineage. In this study we dissect functional contributions by bacteria from a conserved, multi-partite gut symbiosis in herbivorous Cephalotes ants through in vivo experiments, metagenomics, and in vitro assays. Gut bacteria recycle urea, and likely uric acid, using recycled N to synthesize essential amino acids that are acquired by hosts in substantial quantities. Specialized core symbionts of 17 studied Cephalotes species encode the pathways directing these activities, and several recycle N in vitro. These findings point to a highly efficient N economy, and a nutritional mutualism preserved for millions of years through the derived behaviors and gut anatomy of Cephalotes ants.
format Online
Article
Text
id pubmed-5840417
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-58404172018-03-09 Herbivorous turtle ants obtain essential nutrients from a conserved nitrogen-recycling gut microbiome Hu, Yi Sanders, Jon G. Łukasik, Piotr D’Amelio, Catherine L. Millar, John S. Vann, David R. Lan, Yemin Newton, Justin A. Schotanus, Mark Kronauer, Daniel J. C. Pierce, Naomi E. Moreau, Corrie S. Wertz, John T. Engel, Philipp Russell, Jacob A. Nat Commun Article Nitrogen acquisition is a major challenge for herbivorous animals, and the repeated origins of herbivory across the ants have raised expectations that nutritional symbionts have shaped their diversification. Direct evidence for N provisioning by internally housed symbionts is rare in animals; among the ants, it has been documented for just one lineage. In this study we dissect functional contributions by bacteria from a conserved, multi-partite gut symbiosis in herbivorous Cephalotes ants through in vivo experiments, metagenomics, and in vitro assays. Gut bacteria recycle urea, and likely uric acid, using recycled N to synthesize essential amino acids that are acquired by hosts in substantial quantities. Specialized core symbionts of 17 studied Cephalotes species encode the pathways directing these activities, and several recycle N in vitro. These findings point to a highly efficient N economy, and a nutritional mutualism preserved for millions of years through the derived behaviors and gut anatomy of Cephalotes ants. Nature Publishing Group UK 2018-03-06 /pmc/articles/PMC5840417/ /pubmed/29511180 http://dx.doi.org/10.1038/s41467-018-03357-y Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hu, Yi
Sanders, Jon G.
Łukasik, Piotr
D’Amelio, Catherine L.
Millar, John S.
Vann, David R.
Lan, Yemin
Newton, Justin A.
Schotanus, Mark
Kronauer, Daniel J. C.
Pierce, Naomi E.
Moreau, Corrie S.
Wertz, John T.
Engel, Philipp
Russell, Jacob A.
Herbivorous turtle ants obtain essential nutrients from a conserved nitrogen-recycling gut microbiome
title Herbivorous turtle ants obtain essential nutrients from a conserved nitrogen-recycling gut microbiome
title_full Herbivorous turtle ants obtain essential nutrients from a conserved nitrogen-recycling gut microbiome
title_fullStr Herbivorous turtle ants obtain essential nutrients from a conserved nitrogen-recycling gut microbiome
title_full_unstemmed Herbivorous turtle ants obtain essential nutrients from a conserved nitrogen-recycling gut microbiome
title_short Herbivorous turtle ants obtain essential nutrients from a conserved nitrogen-recycling gut microbiome
title_sort herbivorous turtle ants obtain essential nutrients from a conserved nitrogen-recycling gut microbiome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5840417/
https://www.ncbi.nlm.nih.gov/pubmed/29511180
http://dx.doi.org/10.1038/s41467-018-03357-y
work_keys_str_mv AT huyi herbivorousturtleantsobtainessentialnutrientsfromaconservednitrogenrecyclinggutmicrobiome
AT sandersjong herbivorousturtleantsobtainessentialnutrientsfromaconservednitrogenrecyclinggutmicrobiome
AT łukasikpiotr herbivorousturtleantsobtainessentialnutrientsfromaconservednitrogenrecyclinggutmicrobiome
AT dameliocatherinel herbivorousturtleantsobtainessentialnutrientsfromaconservednitrogenrecyclinggutmicrobiome
AT millarjohns herbivorousturtleantsobtainessentialnutrientsfromaconservednitrogenrecyclinggutmicrobiome
AT vanndavidr herbivorousturtleantsobtainessentialnutrientsfromaconservednitrogenrecyclinggutmicrobiome
AT lanyemin herbivorousturtleantsobtainessentialnutrientsfromaconservednitrogenrecyclinggutmicrobiome
AT newtonjustina herbivorousturtleantsobtainessentialnutrientsfromaconservednitrogenrecyclinggutmicrobiome
AT schotanusmark herbivorousturtleantsobtainessentialnutrientsfromaconservednitrogenrecyclinggutmicrobiome
AT kronauerdanieljc herbivorousturtleantsobtainessentialnutrientsfromaconservednitrogenrecyclinggutmicrobiome
AT piercenaomie herbivorousturtleantsobtainessentialnutrientsfromaconservednitrogenrecyclinggutmicrobiome
AT moreaucorries herbivorousturtleantsobtainessentialnutrientsfromaconservednitrogenrecyclinggutmicrobiome
AT wertzjohnt herbivorousturtleantsobtainessentialnutrientsfromaconservednitrogenrecyclinggutmicrobiome
AT engelphilipp herbivorousturtleantsobtainessentialnutrientsfromaconservednitrogenrecyclinggutmicrobiome
AT russelljacoba herbivorousturtleantsobtainessentialnutrientsfromaconservednitrogenrecyclinggutmicrobiome