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Comparative Transcriptomics of Cold Growth and Adaptive Features of a Eury- and Steno-Psychrophile

Permafrost subzero environments harbor diverse, active communities of microorganisms. However, our understanding of the subzero growth, metabolisms, and adaptive properties of these microbes remains very limited. We performed transcriptomic analyses on two subzero-growing permafrost isolates with di...

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Autores principales: Raymond-Bouchard, Isabelle, Tremblay, Julien, Altshuler, Ianina, Greer, Charles W., Whyte, Lyle G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080646/
https://www.ncbi.nlm.nih.gov/pubmed/30108551
http://dx.doi.org/10.3389/fmicb.2018.01565
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author Raymond-Bouchard, Isabelle
Tremblay, Julien
Altshuler, Ianina
Greer, Charles W.
Whyte, Lyle G.
author_facet Raymond-Bouchard, Isabelle
Tremblay, Julien
Altshuler, Ianina
Greer, Charles W.
Whyte, Lyle G.
author_sort Raymond-Bouchard, Isabelle
collection PubMed
description Permafrost subzero environments harbor diverse, active communities of microorganisms. However, our understanding of the subzero growth, metabolisms, and adaptive properties of these microbes remains very limited. We performed transcriptomic analyses on two subzero-growing permafrost isolates with different growth profiles in order to characterize and compare their cold temperature growth and cold-adaptive strategies. The two organisms, Rhodococcus sp. JG3 (-5 to 30°C) and Polaromonas sp. Eur3 1.2.1 (-5 to 22°C), shared several common responses during low temperature growth, including induction of translation and ribosomal processes, upregulation of nutrient transport, increased oxidative and osmotic stress responses, and stimulation of polysaccharide capsule synthesis. Recombination appeared to be an important adaptive strategy for both isolates at low temperatures, likely as a mechanism to increase genetic diversity and the potential for survival in cold systems. While Rhodococcus sp. JG3 favored upregulating iron and amino acid transport, sustaining redox potential, and modulating fatty acid synthesis and composition during growth at -5°C compared to 25°C, Polaromonas sp. Eur3 1.2.1 increased the relative abundance of transcripts involved in primary energy metabolism and the electron transport chain, in addition to signal transduction and peptidoglycan synthesis at 0°C compared to 20°C. The increase in energy metabolism may explain why Polaromonas sp. Eur3 1.2.1 is able to sustain growth rates at 0°C comparable to those at higher temperatures. For Rhodococcus sp. JG3, flexibility in use of carbon sources, iron acquisition, control of membrane fatty acid composition, and modulating redox and co-factor potential may be ways in which this organism is able to sustain growth over a wider range of temperatures. Increasing our understanding of the microbes in these habitats helps us better understand active pathways and metabolisms in extreme environments. Identifying novel, thermolabile, and cold-active enzymes from studies such as this is also of great interest to the biotechnology and food industries.
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spelling pubmed-60806462018-08-14 Comparative Transcriptomics of Cold Growth and Adaptive Features of a Eury- and Steno-Psychrophile Raymond-Bouchard, Isabelle Tremblay, Julien Altshuler, Ianina Greer, Charles W. Whyte, Lyle G. Front Microbiol Microbiology Permafrost subzero environments harbor diverse, active communities of microorganisms. However, our understanding of the subzero growth, metabolisms, and adaptive properties of these microbes remains very limited. We performed transcriptomic analyses on two subzero-growing permafrost isolates with different growth profiles in order to characterize and compare their cold temperature growth and cold-adaptive strategies. The two organisms, Rhodococcus sp. JG3 (-5 to 30°C) and Polaromonas sp. Eur3 1.2.1 (-5 to 22°C), shared several common responses during low temperature growth, including induction of translation and ribosomal processes, upregulation of nutrient transport, increased oxidative and osmotic stress responses, and stimulation of polysaccharide capsule synthesis. Recombination appeared to be an important adaptive strategy for both isolates at low temperatures, likely as a mechanism to increase genetic diversity and the potential for survival in cold systems. While Rhodococcus sp. JG3 favored upregulating iron and amino acid transport, sustaining redox potential, and modulating fatty acid synthesis and composition during growth at -5°C compared to 25°C, Polaromonas sp. Eur3 1.2.1 increased the relative abundance of transcripts involved in primary energy metabolism and the electron transport chain, in addition to signal transduction and peptidoglycan synthesis at 0°C compared to 20°C. The increase in energy metabolism may explain why Polaromonas sp. Eur3 1.2.1 is able to sustain growth rates at 0°C comparable to those at higher temperatures. For Rhodococcus sp. JG3, flexibility in use of carbon sources, iron acquisition, control of membrane fatty acid composition, and modulating redox and co-factor potential may be ways in which this organism is able to sustain growth over a wider range of temperatures. Increasing our understanding of the microbes in these habitats helps us better understand active pathways and metabolisms in extreme environments. Identifying novel, thermolabile, and cold-active enzymes from studies such as this is also of great interest to the biotechnology and food industries. Frontiers Media S.A. 2018-07-31 /pmc/articles/PMC6080646/ /pubmed/30108551 http://dx.doi.org/10.3389/fmicb.2018.01565 Text en Copyright © 2018 Raymond-Bouchard, Tremblay, Altshuler, Greer and Whyte. 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
Raymond-Bouchard, Isabelle
Tremblay, Julien
Altshuler, Ianina
Greer, Charles W.
Whyte, Lyle G.
Comparative Transcriptomics of Cold Growth and Adaptive Features of a Eury- and Steno-Psychrophile
title Comparative Transcriptomics of Cold Growth and Adaptive Features of a Eury- and Steno-Psychrophile
title_full Comparative Transcriptomics of Cold Growth and Adaptive Features of a Eury- and Steno-Psychrophile
title_fullStr Comparative Transcriptomics of Cold Growth and Adaptive Features of a Eury- and Steno-Psychrophile
title_full_unstemmed Comparative Transcriptomics of Cold Growth and Adaptive Features of a Eury- and Steno-Psychrophile
title_short Comparative Transcriptomics of Cold Growth and Adaptive Features of a Eury- and Steno-Psychrophile
title_sort comparative transcriptomics of cold growth and adaptive features of a eury- and steno-psychrophile
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080646/
https://www.ncbi.nlm.nih.gov/pubmed/30108551
http://dx.doi.org/10.3389/fmicb.2018.01565
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