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Microbiomes of ant castes implicate new microbial roles in the fungus-growing ant Trachymyrmex septentrionalis

Fungus-growing ants employ several defenses against diseases, including disease-suppressing microbial biofilms on their integument and in fungal gardens. Here, we compare the phenology of microbiomes in natural nests of the temperate fungus-growing ant Trachymyrmex septentrionalis using culture-depe...

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Autores principales: Ishak, Heather D., Miller, Jessica L., Sen, Ruchira, Dowd, Scot E., Meyer, Eli, Mueller, Ulrich G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3244503/
https://www.ncbi.nlm.nih.gov/pubmed/22355719
http://dx.doi.org/10.1038/srep00204
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author Ishak, Heather D.
Miller, Jessica L.
Sen, Ruchira
Dowd, Scot E.
Meyer, Eli
Mueller, Ulrich G.
author_facet Ishak, Heather D.
Miller, Jessica L.
Sen, Ruchira
Dowd, Scot E.
Meyer, Eli
Mueller, Ulrich G.
author_sort Ishak, Heather D.
collection PubMed
description Fungus-growing ants employ several defenses against diseases, including disease-suppressing microbial biofilms on their integument and in fungal gardens. Here, we compare the phenology of microbiomes in natural nests of the temperate fungus-growing ant Trachymyrmex septentrionalis using culture-dependent isolations and culture-independent 16S-amplicon 454-sequencing. 454-sequencing revealed diverse actinobacteria associated with ants, including most prominently Solirubrobacter (12.2–30.9% of sequence reads), Pseudonocardia (3.5–42.0%), and Microlunatus (0.4–10.8%). Bacterial abundances remained relatively constant in monthly surveys throughout the annual active period (late winter to late summer), except Pseudonocardia abundance declined in females during the reproductive phase. Pseudonocardia species found on ants are phylogenetically different from those in gardens and soil, indicating ecological separation of these Pseudonocardia types. Because the pathogen Escovopsis is not known to infect gardens of T. septentrionalis, the ant-associated microbes do not seem to function in Escovopsis suppression, but could protect against ant diseases, help in nest sanitation, or serve unknown functions.
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spelling pubmed-32445032011-12-22 Microbiomes of ant castes implicate new microbial roles in the fungus-growing ant Trachymyrmex septentrionalis Ishak, Heather D. Miller, Jessica L. Sen, Ruchira Dowd, Scot E. Meyer, Eli Mueller, Ulrich G. Sci Rep Article Fungus-growing ants employ several defenses against diseases, including disease-suppressing microbial biofilms on their integument and in fungal gardens. Here, we compare the phenology of microbiomes in natural nests of the temperate fungus-growing ant Trachymyrmex septentrionalis using culture-dependent isolations and culture-independent 16S-amplicon 454-sequencing. 454-sequencing revealed diverse actinobacteria associated with ants, including most prominently Solirubrobacter (12.2–30.9% of sequence reads), Pseudonocardia (3.5–42.0%), and Microlunatus (0.4–10.8%). Bacterial abundances remained relatively constant in monthly surveys throughout the annual active period (late winter to late summer), except Pseudonocardia abundance declined in females during the reproductive phase. Pseudonocardia species found on ants are phylogenetically different from those in gardens and soil, indicating ecological separation of these Pseudonocardia types. Because the pathogen Escovopsis is not known to infect gardens of T. septentrionalis, the ant-associated microbes do not seem to function in Escovopsis suppression, but could protect against ant diseases, help in nest sanitation, or serve unknown functions. Nature Publishing Group 2011-12-22 /pmc/articles/PMC3244503/ /pubmed/22355719 http://dx.doi.org/10.1038/srep00204 Text en Copyright © 2011, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareALike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Article
Ishak, Heather D.
Miller, Jessica L.
Sen, Ruchira
Dowd, Scot E.
Meyer, Eli
Mueller, Ulrich G.
Microbiomes of ant castes implicate new microbial roles in the fungus-growing ant Trachymyrmex septentrionalis
title Microbiomes of ant castes implicate new microbial roles in the fungus-growing ant Trachymyrmex septentrionalis
title_full Microbiomes of ant castes implicate new microbial roles in the fungus-growing ant Trachymyrmex septentrionalis
title_fullStr Microbiomes of ant castes implicate new microbial roles in the fungus-growing ant Trachymyrmex septentrionalis
title_full_unstemmed Microbiomes of ant castes implicate new microbial roles in the fungus-growing ant Trachymyrmex septentrionalis
title_short Microbiomes of ant castes implicate new microbial roles in the fungus-growing ant Trachymyrmex septentrionalis
title_sort microbiomes of ant castes implicate new microbial roles in the fungus-growing ant trachymyrmex septentrionalis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3244503/
https://www.ncbi.nlm.nih.gov/pubmed/22355719
http://dx.doi.org/10.1038/srep00204
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