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Genomic Insights Into the Lifestyles of Thaumarchaeota Inside Sponges

Sponges are among the oldest metazoans and their success is partly due to their abundant and diverse microbial symbionts. They are one of the few animals that have Thaumarchaeota symbionts. Here we compare genomes of 11 Thaumarchaeota sponge symbionts, including three new genomes, to free-living one...

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Autores principales: Haber, Markus, Burgsdorf, Ilia, Handley, Kim M., Rubin-Blum, Maxim, Steindler, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848895/
https://www.ncbi.nlm.nih.gov/pubmed/33537022
http://dx.doi.org/10.3389/fmicb.2020.622824
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author Haber, Markus
Burgsdorf, Ilia
Handley, Kim M.
Rubin-Blum, Maxim
Steindler, Laura
author_facet Haber, Markus
Burgsdorf, Ilia
Handley, Kim M.
Rubin-Blum, Maxim
Steindler, Laura
author_sort Haber, Markus
collection PubMed
description Sponges are among the oldest metazoans and their success is partly due to their abundant and diverse microbial symbionts. They are one of the few animals that have Thaumarchaeota symbionts. Here we compare genomes of 11 Thaumarchaeota sponge symbionts, including three new genomes, to free-living ones. Like their free-living counterparts, sponge-associated Thaumarchaeota can oxidize ammonia, fix carbon, and produce several vitamins. Adaptions to life inside the sponge host include enrichment in transposases, toxin-antitoxin systems and restriction modifications systems, enrichments previously reported also from bacterial sponge symbionts. Most thaumarchaeal sponge symbionts lost the ability to synthesize rhamnose, which likely alters their cell surface and allows them to evade digestion by the host. All but one archaeal sponge symbiont encoded a high-affinity, branched-chain amino acid transporter system that was absent from the analyzed free-living thaumarchaeota suggesting a mixotrophic lifestyle for the sponge symbionts. Most of the other unique features found in sponge-associated Thaumarchaeota, were limited to only a few specific symbionts. These features included the presence of exopolyphosphatases and a glycine cleavage system found in the novel genomes. Thaumarchaeota have thus likely highly specific interactions with their sponge host, which is supported by the limited number of host sponge species to which each of these symbionts is restricted.
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spelling pubmed-78488952021-02-02 Genomic Insights Into the Lifestyles of Thaumarchaeota Inside Sponges Haber, Markus Burgsdorf, Ilia Handley, Kim M. Rubin-Blum, Maxim Steindler, Laura Front Microbiol Microbiology Sponges are among the oldest metazoans and their success is partly due to their abundant and diverse microbial symbionts. They are one of the few animals that have Thaumarchaeota symbionts. Here we compare genomes of 11 Thaumarchaeota sponge symbionts, including three new genomes, to free-living ones. Like their free-living counterparts, sponge-associated Thaumarchaeota can oxidize ammonia, fix carbon, and produce several vitamins. Adaptions to life inside the sponge host include enrichment in transposases, toxin-antitoxin systems and restriction modifications systems, enrichments previously reported also from bacterial sponge symbionts. Most thaumarchaeal sponge symbionts lost the ability to synthesize rhamnose, which likely alters their cell surface and allows them to evade digestion by the host. All but one archaeal sponge symbiont encoded a high-affinity, branched-chain amino acid transporter system that was absent from the analyzed free-living thaumarchaeota suggesting a mixotrophic lifestyle for the sponge symbionts. Most of the other unique features found in sponge-associated Thaumarchaeota, were limited to only a few specific symbionts. These features included the presence of exopolyphosphatases and a glycine cleavage system found in the novel genomes. Thaumarchaeota have thus likely highly specific interactions with their sponge host, which is supported by the limited number of host sponge species to which each of these symbionts is restricted. Frontiers Media S.A. 2021-01-11 /pmc/articles/PMC7848895/ /pubmed/33537022 http://dx.doi.org/10.3389/fmicb.2020.622824 Text en Copyright © 2021 Haber, Burgsdorf, Handley, Rubin-Blum and Steindler. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Haber, Markus
Burgsdorf, Ilia
Handley, Kim M.
Rubin-Blum, Maxim
Steindler, Laura
Genomic Insights Into the Lifestyles of Thaumarchaeota Inside Sponges
title Genomic Insights Into the Lifestyles of Thaumarchaeota Inside Sponges
title_full Genomic Insights Into the Lifestyles of Thaumarchaeota Inside Sponges
title_fullStr Genomic Insights Into the Lifestyles of Thaumarchaeota Inside Sponges
title_full_unstemmed Genomic Insights Into the Lifestyles of Thaumarchaeota Inside Sponges
title_short Genomic Insights Into the Lifestyles of Thaumarchaeota Inside Sponges
title_sort genomic insights into the lifestyles of thaumarchaeota inside sponges
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848895/
https://www.ncbi.nlm.nih.gov/pubmed/33537022
http://dx.doi.org/10.3389/fmicb.2020.622824
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