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Microbial cells can cooperate to resist high-level chronic ionizing radiation

Understanding chronic ionizing radiation (CIR) effects is of utmost importance to protecting human health and the environment. Diverse bacteria and fungi inhabiting extremely radioactive waste and disaster sites (e.g. Hanford, Chernobyl, Fukushima) represent new targets of CIR research. We show that...

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Autores principales: Shuryak, Igor, Matrosova, Vera Y., Gaidamakova, Elena K., Tkavc, Rok, Grichenko, Olga, Klimenkova, Polina, Volpe, Robert P., Daly, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738026/
https://www.ncbi.nlm.nih.gov/pubmed/29261697
http://dx.doi.org/10.1371/journal.pone.0189261
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author Shuryak, Igor
Matrosova, Vera Y.
Gaidamakova, Elena K.
Tkavc, Rok
Grichenko, Olga
Klimenkova, Polina
Volpe, Robert P.
Daly, Michael J.
author_facet Shuryak, Igor
Matrosova, Vera Y.
Gaidamakova, Elena K.
Tkavc, Rok
Grichenko, Olga
Klimenkova, Polina
Volpe, Robert P.
Daly, Michael J.
author_sort Shuryak, Igor
collection PubMed
description Understanding chronic ionizing radiation (CIR) effects is of utmost importance to protecting human health and the environment. Diverse bacteria and fungi inhabiting extremely radioactive waste and disaster sites (e.g. Hanford, Chernobyl, Fukushima) represent new targets of CIR research. We show that many microorganisms can grow under intense gamma-CIR dose rates of 13–126 Gy/h, with fungi identified as a particularly CIR-resistant group of eukaryotes: among 145 phylogenetically diverse strains tested, 78 grew under 36 Gy/h. Importantly, we demonstrate that CIR resistance can depend on cell concentration and that certain resistant microbial cells protect their neighbors (not only conspecifics, but even radiosensitive species from a different phylum), from high-level CIR. We apply a mechanistically-motivated mathematical model of CIR effects, based on accumulation/removal kinetics of reactive oxygen species (ROS) and antioxidants, in bacteria (3 Escherichia coli strains and Deinococcus radiodurans) and in fungi (Candida parapsilosis, Kazachstania exigua, Pichia kudriavzevii, Rhodotorula lysinophila, Saccharomyces cerevisiae, and Trichosporon mucoides). We also show that correlations between responses to CIR and acute ionizing radiation (AIR) among studied microorganisms are weak. For example, in D. radiodurans, the best molecular correlate for CIR resistance is the antioxidant enzyme catalase, which is dispensable for AIR resistance; and numerous CIR-resistant fungi are not AIR-resistant. Our experimental findings and quantitative modeling thus demonstrate the importance of investigating CIR responses directly, rather than extrapolating from AIR. Protection of radiosensitive cell-types by radioresistant ones under high-level CIR is a potentially important new tool for bioremediation of radioactive sites and development of CIR-resistant microbiota as radioprotectors.
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spelling pubmed-57380262017-12-29 Microbial cells can cooperate to resist high-level chronic ionizing radiation Shuryak, Igor Matrosova, Vera Y. Gaidamakova, Elena K. Tkavc, Rok Grichenko, Olga Klimenkova, Polina Volpe, Robert P. Daly, Michael J. PLoS One Research Article Understanding chronic ionizing radiation (CIR) effects is of utmost importance to protecting human health and the environment. Diverse bacteria and fungi inhabiting extremely radioactive waste and disaster sites (e.g. Hanford, Chernobyl, Fukushima) represent new targets of CIR research. We show that many microorganisms can grow under intense gamma-CIR dose rates of 13–126 Gy/h, with fungi identified as a particularly CIR-resistant group of eukaryotes: among 145 phylogenetically diverse strains tested, 78 grew under 36 Gy/h. Importantly, we demonstrate that CIR resistance can depend on cell concentration and that certain resistant microbial cells protect their neighbors (not only conspecifics, but even radiosensitive species from a different phylum), from high-level CIR. We apply a mechanistically-motivated mathematical model of CIR effects, based on accumulation/removal kinetics of reactive oxygen species (ROS) and antioxidants, in bacteria (3 Escherichia coli strains and Deinococcus radiodurans) and in fungi (Candida parapsilosis, Kazachstania exigua, Pichia kudriavzevii, Rhodotorula lysinophila, Saccharomyces cerevisiae, and Trichosporon mucoides). We also show that correlations between responses to CIR and acute ionizing radiation (AIR) among studied microorganisms are weak. For example, in D. radiodurans, the best molecular correlate for CIR resistance is the antioxidant enzyme catalase, which is dispensable for AIR resistance; and numerous CIR-resistant fungi are not AIR-resistant. Our experimental findings and quantitative modeling thus demonstrate the importance of investigating CIR responses directly, rather than extrapolating from AIR. Protection of radiosensitive cell-types by radioresistant ones under high-level CIR is a potentially important new tool for bioremediation of radioactive sites and development of CIR-resistant microbiota as radioprotectors. Public Library of Science 2017-12-20 /pmc/articles/PMC5738026/ /pubmed/29261697 http://dx.doi.org/10.1371/journal.pone.0189261 Text en © 2017 Shuryak et al 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 Research Article
Shuryak, Igor
Matrosova, Vera Y.
Gaidamakova, Elena K.
Tkavc, Rok
Grichenko, Olga
Klimenkova, Polina
Volpe, Robert P.
Daly, Michael J.
Microbial cells can cooperate to resist high-level chronic ionizing radiation
title Microbial cells can cooperate to resist high-level chronic ionizing radiation
title_full Microbial cells can cooperate to resist high-level chronic ionizing radiation
title_fullStr Microbial cells can cooperate to resist high-level chronic ionizing radiation
title_full_unstemmed Microbial cells can cooperate to resist high-level chronic ionizing radiation
title_short Microbial cells can cooperate to resist high-level chronic ionizing radiation
title_sort microbial cells can cooperate to resist high-level chronic ionizing radiation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5738026/
https://www.ncbi.nlm.nih.gov/pubmed/29261697
http://dx.doi.org/10.1371/journal.pone.0189261
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