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Water Dispersal of Methanotrophic Bacteria Maintains Functional Methane Oxidation in Sphagnum Mosses

It is known that Sphagnum associated methanotrophy (SAM) changes in relation to the peatland water table (WT) level. After drought, rising WT is able to reactivate SAM. We aimed to reveal whether this reactivation is due to activation of indigenous methane (CH(4)) oxidizing bacteria (MOB) already pr...

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Autores principales: Putkinen, Anuliina, Larmola, Tuula, Tuomivirta, Tero, Siljanen, Henri M. P., Bodrossy, Levente, Tuittila, Eeva-Stiina, Fritze, Hannu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263434/
https://www.ncbi.nlm.nih.gov/pubmed/22291695
http://dx.doi.org/10.3389/fmicb.2012.00015
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author Putkinen, Anuliina
Larmola, Tuula
Tuomivirta, Tero
Siljanen, Henri M. P.
Bodrossy, Levente
Tuittila, Eeva-Stiina
Fritze, Hannu
author_facet Putkinen, Anuliina
Larmola, Tuula
Tuomivirta, Tero
Siljanen, Henri M. P.
Bodrossy, Levente
Tuittila, Eeva-Stiina
Fritze, Hannu
author_sort Putkinen, Anuliina
collection PubMed
description It is known that Sphagnum associated methanotrophy (SAM) changes in relation to the peatland water table (WT) level. After drought, rising WT is able to reactivate SAM. We aimed to reveal whether this reactivation is due to activation of indigenous methane (CH(4)) oxidizing bacteria (MOB) already present in the mosses or to MOB present in water. This was tested through two approaches: in a transplantation experiment, Sphagna lacking SAM activity were transplanted into flark water next to Sphagna oxidizing CH(4). Already after 3 days, most of the transplants showed CH(4) oxidation activity. Microarray showed that the MOB community compositions of the transplants and the original active mosses had become more similar within 28 days thus indicating MOB movement through water between mosses. Methylocystis-related type II MOB dominated the community. In a following experiment, SAM inactive mosses were bathed overnight in non-sterile and sterile-filtered SAM active site flark water. Only mosses bathed with non-sterile flark water became SAM active, which was also shown by the pmoA copy number increase of over 60 times. Thus, it was evident that MOB present in the water can colonize Sphagnum mosses. This colonization could act as a resilience mechanism for peatland CH(4) dynamics by allowing the re-emergence of CH(4) oxidation activity in Sphagnum.
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spelling pubmed-32634342012-01-30 Water Dispersal of Methanotrophic Bacteria Maintains Functional Methane Oxidation in Sphagnum Mosses Putkinen, Anuliina Larmola, Tuula Tuomivirta, Tero Siljanen, Henri M. P. Bodrossy, Levente Tuittila, Eeva-Stiina Fritze, Hannu Front Microbiol Microbiology It is known that Sphagnum associated methanotrophy (SAM) changes in relation to the peatland water table (WT) level. After drought, rising WT is able to reactivate SAM. We aimed to reveal whether this reactivation is due to activation of indigenous methane (CH(4)) oxidizing bacteria (MOB) already present in the mosses or to MOB present in water. This was tested through two approaches: in a transplantation experiment, Sphagna lacking SAM activity were transplanted into flark water next to Sphagna oxidizing CH(4). Already after 3 days, most of the transplants showed CH(4) oxidation activity. Microarray showed that the MOB community compositions of the transplants and the original active mosses had become more similar within 28 days thus indicating MOB movement through water between mosses. Methylocystis-related type II MOB dominated the community. In a following experiment, SAM inactive mosses were bathed overnight in non-sterile and sterile-filtered SAM active site flark water. Only mosses bathed with non-sterile flark water became SAM active, which was also shown by the pmoA copy number increase of over 60 times. Thus, it was evident that MOB present in the water can colonize Sphagnum mosses. This colonization could act as a resilience mechanism for peatland CH(4) dynamics by allowing the re-emergence of CH(4) oxidation activity in Sphagnum. Frontiers Research Foundation 2012-01-23 /pmc/articles/PMC3263434/ /pubmed/22291695 http://dx.doi.org/10.3389/fmicb.2012.00015 Text en Copyright © 2012 Putkinen, Larmola, Tuomivirta, Siljanen, Bodrossy, Tuittila and Fritze. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Microbiology
Putkinen, Anuliina
Larmola, Tuula
Tuomivirta, Tero
Siljanen, Henri M. P.
Bodrossy, Levente
Tuittila, Eeva-Stiina
Fritze, Hannu
Water Dispersal of Methanotrophic Bacteria Maintains Functional Methane Oxidation in Sphagnum Mosses
title Water Dispersal of Methanotrophic Bacteria Maintains Functional Methane Oxidation in Sphagnum Mosses
title_full Water Dispersal of Methanotrophic Bacteria Maintains Functional Methane Oxidation in Sphagnum Mosses
title_fullStr Water Dispersal of Methanotrophic Bacteria Maintains Functional Methane Oxidation in Sphagnum Mosses
title_full_unstemmed Water Dispersal of Methanotrophic Bacteria Maintains Functional Methane Oxidation in Sphagnum Mosses
title_short Water Dispersal of Methanotrophic Bacteria Maintains Functional Methane Oxidation in Sphagnum Mosses
title_sort water dispersal of methanotrophic bacteria maintains functional methane oxidation in sphagnum mosses
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263434/
https://www.ncbi.nlm.nih.gov/pubmed/22291695
http://dx.doi.org/10.3389/fmicb.2012.00015
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