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Influence of protozoan grazing on magnetotactic bacteria on intracellular and extracellular iron content

Magnetotactic bacteria (MTB) ubiquitously inhabit the oxic–anoxic interface or anaerobic areas of aquatic environments. MTB biomineralize magnetite or greigite crystals and synthesize an organelle known as magnetosome. This intrinsic ability of MTB allows them to accumulate iron to levels 100–1000 t...

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Detalles Bibliográficos
Autores principales: Seki, Yusuke, Eguchi, Yukako, Taoka, Azuma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464679/
https://www.ncbi.nlm.nih.gov/pubmed/36779255
http://dx.doi.org/10.1111/1758-2229.13140
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author Seki, Yusuke
Eguchi, Yukako
Taoka, Azuma
author_facet Seki, Yusuke
Eguchi, Yukako
Taoka, Azuma
author_sort Seki, Yusuke
collection PubMed
description Magnetotactic bacteria (MTB) ubiquitously inhabit the oxic–anoxic interface or anaerobic areas of aquatic environments. MTB biomineralize magnetite or greigite crystals and synthesize an organelle known as magnetosome. This intrinsic ability of MTB allows them to accumulate iron to levels 100–1000 times higher than those in non‐magnetotactic bacteria (non‐MTB). Therefore, MTB considerably contributes to the global iron cycle as primary iron suppliers in the aquatic environmental food chain. However, to the best of our knowledge, there have been no reports describing the effects of trophic interactions between MTB and their protist grazers on the iron distributions in MTB grazers and the extracellular milieu. Herein, we evaluated the effects of MTB grazing using a model species of protist (Tetrahymena pyriformis) and a model species of MTB (Magnetospirillum magneticum AMB‐1). MTB‐fed T. pyriformis exhibited a magnetic response and contained magnetite crystals in their vacuoles. Fluorescence imaging using a ferrous ion‐specific fluorescent dye revealed that the cellular ferrous ion content was five times higher in MTB‐fed T. pyriformis than in non‐MTB grazers. Moreover, soluble iron concentrations in the spent media increased with time during MTB predation. This study provides experimental evidence to delineate the importance of trophic interactions of MTB on iron distributions.
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spelling pubmed-104646792023-08-30 Influence of protozoan grazing on magnetotactic bacteria on intracellular and extracellular iron content Seki, Yusuke Eguchi, Yukako Taoka, Azuma Environ Microbiol Rep Brief Reports Magnetotactic bacteria (MTB) ubiquitously inhabit the oxic–anoxic interface or anaerobic areas of aquatic environments. MTB biomineralize magnetite or greigite crystals and synthesize an organelle known as magnetosome. This intrinsic ability of MTB allows them to accumulate iron to levels 100–1000 times higher than those in non‐magnetotactic bacteria (non‐MTB). Therefore, MTB considerably contributes to the global iron cycle as primary iron suppliers in the aquatic environmental food chain. However, to the best of our knowledge, there have been no reports describing the effects of trophic interactions between MTB and their protist grazers on the iron distributions in MTB grazers and the extracellular milieu. Herein, we evaluated the effects of MTB grazing using a model species of protist (Tetrahymena pyriformis) and a model species of MTB (Magnetospirillum magneticum AMB‐1). MTB‐fed T. pyriformis exhibited a magnetic response and contained magnetite crystals in their vacuoles. Fluorescence imaging using a ferrous ion‐specific fluorescent dye revealed that the cellular ferrous ion content was five times higher in MTB‐fed T. pyriformis than in non‐MTB grazers. Moreover, soluble iron concentrations in the spent media increased with time during MTB predation. This study provides experimental evidence to delineate the importance of trophic interactions of MTB on iron distributions. John Wiley & Sons, Inc. 2023-02-13 /pmc/articles/PMC10464679/ /pubmed/36779255 http://dx.doi.org/10.1111/1758-2229.13140 Text en © 2023 The Authors. Environmental Microbiology Reports published by Applied Microbiology International and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Reports
Seki, Yusuke
Eguchi, Yukako
Taoka, Azuma
Influence of protozoan grazing on magnetotactic bacteria on intracellular and extracellular iron content
title Influence of protozoan grazing on magnetotactic bacteria on intracellular and extracellular iron content
title_full Influence of protozoan grazing on magnetotactic bacteria on intracellular and extracellular iron content
title_fullStr Influence of protozoan grazing on magnetotactic bacteria on intracellular and extracellular iron content
title_full_unstemmed Influence of protozoan grazing on magnetotactic bacteria on intracellular and extracellular iron content
title_short Influence of protozoan grazing on magnetotactic bacteria on intracellular and extracellular iron content
title_sort influence of protozoan grazing on magnetotactic bacteria on intracellular and extracellular iron content
topic Brief Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10464679/
https://www.ncbi.nlm.nih.gov/pubmed/36779255
http://dx.doi.org/10.1111/1758-2229.13140
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AT taokaazuma influenceofprotozoangrazingonmagnetotacticbacteriaonintracellularandextracellularironcontent