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With a pinch of extra salt—Did predatory protists steal genes from their food?

The cellular adjustment of Bacteria and Archaea to high-salinity habitats is well studied and has generally been classified into one of two strategies. These are to accumulate high levels either of ions (the “salt-in” strategy) or of physiologically compliant organic osmolytes, the compatible solute...

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Detalles Bibliográficos
Autores principales: Czech, Laura, Bremer, Erhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796728/
https://www.ncbi.nlm.nih.gov/pubmed/29394244
http://dx.doi.org/10.1371/journal.pbio.2005163
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author Czech, Laura
Bremer, Erhard
author_facet Czech, Laura
Bremer, Erhard
author_sort Czech, Laura
collection PubMed
description The cellular adjustment of Bacteria and Archaea to high-salinity habitats is well studied and has generally been classified into one of two strategies. These are to accumulate high levels either of ions (the “salt-in” strategy) or of physiologically compliant organic osmolytes, the compatible solutes (the “salt-out” strategy). Halophilic protists are ecophysiological important inhabitants of salt-stressed ecosystems because they are not only very abundant but also represent the majority of eukaryotic lineages in nature. However, their cellular osmostress responses have been largely neglected. Recent reports have now shed new light on this issue using the geographically widely distributed halophilic heterotrophic protists Halocafeteria seosinensis, Pharyngomonas kirbyi, and Schmidingerothrix salinarum as model systems. Different approaches led to the joint conclusion that these unicellular Eukarya use the salt-out strategy to cope successfully with the persistent high salinity in their habitat. They accumulate various compatible solutes, e.g., glycine betaine, myo-inositol, and ectoines. The finding of intron-containing biosynthetic genes for ectoine and hydroxyectoine, their salt stress–responsive transcription in H. seosinensis, and the production of ectoine and its import by S. salinarum come as a considerable surprise because ectoines have thus far been considered exclusive prokaryotic compatible solutes. Phylogenetic considerations of the ectoine/hydroxyectoine biosynthetic genes of H. seosinensis suggest that they have been acquired via lateral gene transfer by these bacterivorous Eukarya from ectoine/hydroxyectoine-producing food bacteria that populate the same habitat.
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spelling pubmed-57967282018-02-16 With a pinch of extra salt—Did predatory protists steal genes from their food? Czech, Laura Bremer, Erhard PLoS Biol Primer The cellular adjustment of Bacteria and Archaea to high-salinity habitats is well studied and has generally been classified into one of two strategies. These are to accumulate high levels either of ions (the “salt-in” strategy) or of physiologically compliant organic osmolytes, the compatible solutes (the “salt-out” strategy). Halophilic protists are ecophysiological important inhabitants of salt-stressed ecosystems because they are not only very abundant but also represent the majority of eukaryotic lineages in nature. However, their cellular osmostress responses have been largely neglected. Recent reports have now shed new light on this issue using the geographically widely distributed halophilic heterotrophic protists Halocafeteria seosinensis, Pharyngomonas kirbyi, and Schmidingerothrix salinarum as model systems. Different approaches led to the joint conclusion that these unicellular Eukarya use the salt-out strategy to cope successfully with the persistent high salinity in their habitat. They accumulate various compatible solutes, e.g., glycine betaine, myo-inositol, and ectoines. The finding of intron-containing biosynthetic genes for ectoine and hydroxyectoine, their salt stress–responsive transcription in H. seosinensis, and the production of ectoine and its import by S. salinarum come as a considerable surprise because ectoines have thus far been considered exclusive prokaryotic compatible solutes. Phylogenetic considerations of the ectoine/hydroxyectoine biosynthetic genes of H. seosinensis suggest that they have been acquired via lateral gene transfer by these bacterivorous Eukarya from ectoine/hydroxyectoine-producing food bacteria that populate the same habitat. Public Library of Science 2018-02-02 /pmc/articles/PMC5796728/ /pubmed/29394244 http://dx.doi.org/10.1371/journal.pbio.2005163 Text en © 2018 Czech, Bremer http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Primer
Czech, Laura
Bremer, Erhard
With a pinch of extra salt—Did predatory protists steal genes from their food?
title With a pinch of extra salt—Did predatory protists steal genes from their food?
title_full With a pinch of extra salt—Did predatory protists steal genes from their food?
title_fullStr With a pinch of extra salt—Did predatory protists steal genes from their food?
title_full_unstemmed With a pinch of extra salt—Did predatory protists steal genes from their food?
title_short With a pinch of extra salt—Did predatory protists steal genes from their food?
title_sort with a pinch of extra salt—did predatory protists steal genes from their food?
topic Primer
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796728/
https://www.ncbi.nlm.nih.gov/pubmed/29394244
http://dx.doi.org/10.1371/journal.pbio.2005163
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