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Two Chloroflexi classes independently evolved the ability to persist on atmospheric hydrogen and carbon monoxide

Most aerobic bacteria exist in dormant states within natural environments. In these states, they endure adverse environmental conditions such as nutrient starvation by decreasing metabolic expenditure and using alternative energy sources. In this study, we investigated the energy sources that suppor...

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Autores principales: Islam, Zahra F., Cordero, Paul R. F., Feng, Joanna, Chen, Ya-Jou, Bay, Sean K., Jirapanjawat, Thanavit, Gleadow, Roslyn M., Carere, Carlo R., Stott, Matthew B., Chiri, Eleonora, Greening, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776052/
https://www.ncbi.nlm.nih.gov/pubmed/30872805
http://dx.doi.org/10.1038/s41396-019-0393-0
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author Islam, Zahra F.
Cordero, Paul R. F.
Feng, Joanna
Chen, Ya-Jou
Bay, Sean K.
Jirapanjawat, Thanavit
Gleadow, Roslyn M.
Carere, Carlo R.
Stott, Matthew B.
Chiri, Eleonora
Greening, Chris
author_facet Islam, Zahra F.
Cordero, Paul R. F.
Feng, Joanna
Chen, Ya-Jou
Bay, Sean K.
Jirapanjawat, Thanavit
Gleadow, Roslyn M.
Carere, Carlo R.
Stott, Matthew B.
Chiri, Eleonora
Greening, Chris
author_sort Islam, Zahra F.
collection PubMed
description Most aerobic bacteria exist in dormant states within natural environments. In these states, they endure adverse environmental conditions such as nutrient starvation by decreasing metabolic expenditure and using alternative energy sources. In this study, we investigated the energy sources that support persistence of two aerobic thermophilic strains of the environmentally widespread but understudied phylum Chloroflexi. A transcriptome study revealed that Thermomicrobium roseum (class Chloroflexia) extensively remodels its respiratory chain upon entry into stationary phase due to nutrient limitation. Whereas primary dehydrogenases associated with heterotrophic respiration were downregulated, putative operons encoding enzymes involved in molecular hydrogen (H(2)), carbon monoxide (CO), and sulfur compound oxidation were significantly upregulated. Gas chromatography and microsensor experiments showed that T. roseum aerobically respires H(2) and CO at a range of environmentally relevant concentrations to sub-atmospheric levels. Phylogenetic analysis suggests that the hydrogenases and carbon monoxide dehydrogenases mediating these processes are widely distributed in Chloroflexi genomes and have probably been horizontally acquired on more than one occasion. Consistently, we confirmed that the sporulating isolate Thermogemmatispora sp. T81 (class Ktedonobacteria) also oxidises atmospheric H(2) and CO during persistence, though further studies are required to determine if these findings extend to mesophilic strains. This study provides axenic culture evidence that atmospheric CO supports bacterial persistence and reports the third phylum, following Actinobacteria and Acidobacteria, to be experimentally shown to mediate the biogeochemically and ecologically important process of atmospheric H(2) oxidation. This adds to the growing body of evidence that atmospheric trace gases are dependable energy sources for bacterial persistence.
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spelling pubmed-67760522019-10-04 Two Chloroflexi classes independently evolved the ability to persist on atmospheric hydrogen and carbon monoxide Islam, Zahra F. Cordero, Paul R. F. Feng, Joanna Chen, Ya-Jou Bay, Sean K. Jirapanjawat, Thanavit Gleadow, Roslyn M. Carere, Carlo R. Stott, Matthew B. Chiri, Eleonora Greening, Chris ISME J Article Most aerobic bacteria exist in dormant states within natural environments. In these states, they endure adverse environmental conditions such as nutrient starvation by decreasing metabolic expenditure and using alternative energy sources. In this study, we investigated the energy sources that support persistence of two aerobic thermophilic strains of the environmentally widespread but understudied phylum Chloroflexi. A transcriptome study revealed that Thermomicrobium roseum (class Chloroflexia) extensively remodels its respiratory chain upon entry into stationary phase due to nutrient limitation. Whereas primary dehydrogenases associated with heterotrophic respiration were downregulated, putative operons encoding enzymes involved in molecular hydrogen (H(2)), carbon monoxide (CO), and sulfur compound oxidation were significantly upregulated. Gas chromatography and microsensor experiments showed that T. roseum aerobically respires H(2) and CO at a range of environmentally relevant concentrations to sub-atmospheric levels. Phylogenetic analysis suggests that the hydrogenases and carbon monoxide dehydrogenases mediating these processes are widely distributed in Chloroflexi genomes and have probably been horizontally acquired on more than one occasion. Consistently, we confirmed that the sporulating isolate Thermogemmatispora sp. T81 (class Ktedonobacteria) also oxidises atmospheric H(2) and CO during persistence, though further studies are required to determine if these findings extend to mesophilic strains. This study provides axenic culture evidence that atmospheric CO supports bacterial persistence and reports the third phylum, following Actinobacteria and Acidobacteria, to be experimentally shown to mediate the biogeochemically and ecologically important process of atmospheric H(2) oxidation. This adds to the growing body of evidence that atmospheric trace gases are dependable energy sources for bacterial persistence. Nature Publishing Group UK 2019-03-14 2019-07 /pmc/articles/PMC6776052/ /pubmed/30872805 http://dx.doi.org/10.1038/s41396-019-0393-0 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Islam, Zahra F.
Cordero, Paul R. F.
Feng, Joanna
Chen, Ya-Jou
Bay, Sean K.
Jirapanjawat, Thanavit
Gleadow, Roslyn M.
Carere, Carlo R.
Stott, Matthew B.
Chiri, Eleonora
Greening, Chris
Two Chloroflexi classes independently evolved the ability to persist on atmospheric hydrogen and carbon monoxide
title Two Chloroflexi classes independently evolved the ability to persist on atmospheric hydrogen and carbon monoxide
title_full Two Chloroflexi classes independently evolved the ability to persist on atmospheric hydrogen and carbon monoxide
title_fullStr Two Chloroflexi classes independently evolved the ability to persist on atmospheric hydrogen and carbon monoxide
title_full_unstemmed Two Chloroflexi classes independently evolved the ability to persist on atmospheric hydrogen and carbon monoxide
title_short Two Chloroflexi classes independently evolved the ability to persist on atmospheric hydrogen and carbon monoxide
title_sort two chloroflexi classes independently evolved the ability to persist on atmospheric hydrogen and carbon monoxide
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776052/
https://www.ncbi.nlm.nih.gov/pubmed/30872805
http://dx.doi.org/10.1038/s41396-019-0393-0
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