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Symbiosis between nanohaloarchaeon and haloarchaeon is based on utilization of different polysaccharides

Nano-sized archaeota, with their small genomes and limited metabolic capabilities, are known to associate with other microbes, thereby compensating for their own auxotrophies. These diminutive and yet ubiquitous organisms thrive in hypersaline habitats that they share with haloarchaea. Here, we reve...

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Autores principales: La Cono, Violetta, Messina, Enzo, Rohde, Manfred, Arcadi, Erika, Ciordia, Sergio, Crisafi, Francesca, Denaro, Renata, Ferrer, Manuel, Giuliano, Laura, Golyshin, Peter N., Golyshina, Olga V., Hallsworth, John E., La Spada, Gina, Mena, Maria C., Merkel, Alexander Y., Shevchenko, Margarita A., Smedile, Francesco, Sorokin, Dimitry Y., Toshchakov, Stepan V., Yakimov, Michail M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443923/
https://www.ncbi.nlm.nih.gov/pubmed/32759215
http://dx.doi.org/10.1073/pnas.2007232117
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author La Cono, Violetta
Messina, Enzo
Rohde, Manfred
Arcadi, Erika
Ciordia, Sergio
Crisafi, Francesca
Denaro, Renata
Ferrer, Manuel
Giuliano, Laura
Golyshin, Peter N.
Golyshina, Olga V.
Hallsworth, John E.
La Spada, Gina
Mena, Maria C.
Merkel, Alexander Y.
Shevchenko, Margarita A.
Smedile, Francesco
Sorokin, Dimitry Y.
Toshchakov, Stepan V.
Yakimov, Michail M.
author_facet La Cono, Violetta
Messina, Enzo
Rohde, Manfred
Arcadi, Erika
Ciordia, Sergio
Crisafi, Francesca
Denaro, Renata
Ferrer, Manuel
Giuliano, Laura
Golyshin, Peter N.
Golyshina, Olga V.
Hallsworth, John E.
La Spada, Gina
Mena, Maria C.
Merkel, Alexander Y.
Shevchenko, Margarita A.
Smedile, Francesco
Sorokin, Dimitry Y.
Toshchakov, Stepan V.
Yakimov, Michail M.
author_sort La Cono, Violetta
collection PubMed
description Nano-sized archaeota, with their small genomes and limited metabolic capabilities, are known to associate with other microbes, thereby compensating for their own auxotrophies. These diminutive and yet ubiquitous organisms thrive in hypersaline habitats that they share with haloarchaea. Here, we reveal the genetic and physiological nature of a nanohaloarchaeon–haloarchaeon association, with both microbes obtained from a solar saltern and reproducibly cultivated together in vitro. The nanohaloarchaeon Candidatus Nanohalobium constans LC1Nh is an aerotolerant, sugar-fermenting anaerobe, lacking key anabolic machinery and respiratory complexes. The nanohaloarchaeon cells are found physically connected to the chitinolytic haloarchaeon Halomicrobium sp. LC1Hm. Our experiments revealed that this haloarchaeon can hydrolyze chitin outside the cell (to produce the monosaccharide N-acetylglucosamine), using this beta-glucan to obtain carbon and energy for growth. However, LC1Hm could not metabolize either glycogen or starch (both alpha-glucans) or other polysaccharides tested. Remarkably, the nanohaloarchaeon’s ability to hydrolyze glycogen and starch to glucose enabled growth of Halomicrobium sp. LC1Hm in the absence of a chitin. These findings indicated that the nanohaloarchaeon–haloarchaeon association is both mutualistic and symbiotic; in this case, each microbe relies on its partner’s ability to degrade different polysaccharides. This suggests, in turn, that other nano-sized archaeota may also be beneficial for their hosts. Given that availability of carbon substrates can vary both spatially and temporarily, the susceptibility of Halomicrobium to colonization by Ca. Nanohalobium can be interpreted as a strategy to maximize the long-term fitness of the host.
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spelling pubmed-74439232020-09-01 Symbiosis between nanohaloarchaeon and haloarchaeon is based on utilization of different polysaccharides La Cono, Violetta Messina, Enzo Rohde, Manfred Arcadi, Erika Ciordia, Sergio Crisafi, Francesca Denaro, Renata Ferrer, Manuel Giuliano, Laura Golyshin, Peter N. Golyshina, Olga V. Hallsworth, John E. La Spada, Gina Mena, Maria C. Merkel, Alexander Y. Shevchenko, Margarita A. Smedile, Francesco Sorokin, Dimitry Y. Toshchakov, Stepan V. Yakimov, Michail M. Proc Natl Acad Sci U S A Biological Sciences Nano-sized archaeota, with their small genomes and limited metabolic capabilities, are known to associate with other microbes, thereby compensating for their own auxotrophies. These diminutive and yet ubiquitous organisms thrive in hypersaline habitats that they share with haloarchaea. Here, we reveal the genetic and physiological nature of a nanohaloarchaeon–haloarchaeon association, with both microbes obtained from a solar saltern and reproducibly cultivated together in vitro. The nanohaloarchaeon Candidatus Nanohalobium constans LC1Nh is an aerotolerant, sugar-fermenting anaerobe, lacking key anabolic machinery and respiratory complexes. The nanohaloarchaeon cells are found physically connected to the chitinolytic haloarchaeon Halomicrobium sp. LC1Hm. Our experiments revealed that this haloarchaeon can hydrolyze chitin outside the cell (to produce the monosaccharide N-acetylglucosamine), using this beta-glucan to obtain carbon and energy for growth. However, LC1Hm could not metabolize either glycogen or starch (both alpha-glucans) or other polysaccharides tested. Remarkably, the nanohaloarchaeon’s ability to hydrolyze glycogen and starch to glucose enabled growth of Halomicrobium sp. LC1Hm in the absence of a chitin. These findings indicated that the nanohaloarchaeon–haloarchaeon association is both mutualistic and symbiotic; in this case, each microbe relies on its partner’s ability to degrade different polysaccharides. This suggests, in turn, that other nano-sized archaeota may also be beneficial for their hosts. Given that availability of carbon substrates can vary both spatially and temporarily, the susceptibility of Halomicrobium to colonization by Ca. Nanohalobium can be interpreted as a strategy to maximize the long-term fitness of the host. National Academy of Sciences 2020-08-18 2020-08-05 /pmc/articles/PMC7443923/ /pubmed/32759215 http://dx.doi.org/10.1073/pnas.2007232117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
La Cono, Violetta
Messina, Enzo
Rohde, Manfred
Arcadi, Erika
Ciordia, Sergio
Crisafi, Francesca
Denaro, Renata
Ferrer, Manuel
Giuliano, Laura
Golyshin, Peter N.
Golyshina, Olga V.
Hallsworth, John E.
La Spada, Gina
Mena, Maria C.
Merkel, Alexander Y.
Shevchenko, Margarita A.
Smedile, Francesco
Sorokin, Dimitry Y.
Toshchakov, Stepan V.
Yakimov, Michail M.
Symbiosis between nanohaloarchaeon and haloarchaeon is based on utilization of different polysaccharides
title Symbiosis between nanohaloarchaeon and haloarchaeon is based on utilization of different polysaccharides
title_full Symbiosis between nanohaloarchaeon and haloarchaeon is based on utilization of different polysaccharides
title_fullStr Symbiosis between nanohaloarchaeon and haloarchaeon is based on utilization of different polysaccharides
title_full_unstemmed Symbiosis between nanohaloarchaeon and haloarchaeon is based on utilization of different polysaccharides
title_short Symbiosis between nanohaloarchaeon and haloarchaeon is based on utilization of different polysaccharides
title_sort symbiosis between nanohaloarchaeon and haloarchaeon is based on utilization of different polysaccharides
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443923/
https://www.ncbi.nlm.nih.gov/pubmed/32759215
http://dx.doi.org/10.1073/pnas.2007232117
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