Herbivorous turtle ants obtain essential nutrients from a conserved nitrogen-recycling gut microbiome.
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Hu Y
Department of Biology, Drexel University, Philadelphia, PA, 19104, USA. yh332@drexel.edu.
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Sanders JG
Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, 02138, USA.
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Łukasik P
Department of Biology, Drexel University, Philadelphia, PA, 19104, USA.
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D'Amelio CL
Department of Biology, Drexel University, Philadelphia, PA, 19104, USA.
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Millar JS
Department of Medicine, Institute of Diabetes, Obesity and Metabolism, University of Pennsylvania, Philadelphia, PA, 19104, USA.
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Vann DR
Department of Earth and Environmental Science, University of Pennsylvania, Philadelphia, PA, 19104, USA.
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Lan Y
School of Biomedical Engineering, Science and Health systems, Drexel University, Philadelphia, PA, 19104, USA.
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Newton JA
Department of Biology, Drexel University, Philadelphia, PA, 19104, USA.
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Schotanus M
Department of Biology, Calvin College, Grand Rapids, MI, 49546, USA.
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Kronauer DJC
Laboratory of Social Evolution and Behavior, The Rockefeller University, New York, NY, 10065, USA.
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Pierce NE
Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, 02138, USA.
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Moreau CS
Department of Science and Education, Field Museum of Natural History, Chicago, IL, 60605, USA.
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Wertz JT
Department of Biology, Calvin College, Grand Rapids, MI, 49546, USA.
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Engel P
Department of Fundamental Microbiology, University of Lausanne, 1015, Lausanne, Switzerland.
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Russell JA
Department of Biology, Drexel University, Philadelphia, PA, 19104, USA.
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Published in:
- Nature communications. - 2018
English
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.
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Language
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Open access status
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gold
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Identifiers
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Persistent URL
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https://sonar.ch/global/documents/20408
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