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Quantitative Modeling of Microbial Population Responses to Chronic Irradiation Combined with Other Stressors
Microbial population responses to combined effects of chronic irradiation and other stressors (chemical contaminants, other sub-optimal conditions) are important for ecosystem functioning and bioremediation in radionuclide-contaminated areas. Quantitative mathematical modeling can improve our unders...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726741/ https://www.ncbi.nlm.nih.gov/pubmed/26808049 http://dx.doi.org/10.1371/journal.pone.0147696 |
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author | Shuryak, Igor Dadachova, Ekaterina |
author_facet | Shuryak, Igor Dadachova, Ekaterina |
author_sort | Shuryak, Igor |
collection | PubMed |
description | Microbial population responses to combined effects of chronic irradiation and other stressors (chemical contaminants, other sub-optimal conditions) are important for ecosystem functioning and bioremediation in radionuclide-contaminated areas. Quantitative mathematical modeling can improve our understanding of these phenomena. To identify general patterns of microbial responses to multiple stressors in radioactive environments, we analyzed three data sets on: (1) bacteria isolated from soil contaminated by nuclear waste at the Hanford site (USA); (2) fungi isolated from the Chernobyl nuclear-power plant (Ukraine) buildings after the accident; (3) yeast subjected to continuous γ-irradiation in the laboratory, where radiation dose rate and cell removal rate were independently varied. We applied generalized linear mixed-effects models to describe the first two data sets, whereas the third data set was amenable to mechanistic modeling using differential equations. Machine learning and information-theoretic approaches were used to select the best-supported formalism(s) among biologically-plausible alternatives. Our analysis suggests the following: (1) Both radionuclides and co-occurring chemical contaminants (e.g. NO(2)) are important for explaining microbial responses to radioactive contamination. (2) Radionuclides may produce non-monotonic dose responses: stimulation of microbial growth at low concentrations vs. inhibition at higher ones. (3) The extinction-defining critical radiation dose rate is dramatically lowered by additional stressors. (4) Reproduction suppression by radiation can be more important for determining the critical dose rate, than radiation-induced cell mortality. In conclusion, the modeling approaches used here on three diverse data sets provide insight into explaining and predicting multi-stressor effects on microbial communities: (1) the most severe effects (e.g. extinction) on microbial populations may occur when unfavorable environmental conditions (e.g. fluctuations of temperature and/or nutrient levels) coincide with radioactive contamination; (2) an organism’s radioresistance and bioremediation efficiency in rich laboratory media may be insufficient to carry out radionuclide bioremediation in the field—robustness against multiple stressors is needed. |
format | Online Article Text |
id | pubmed-4726741 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-47267412016-02-03 Quantitative Modeling of Microbial Population Responses to Chronic Irradiation Combined with Other Stressors Shuryak, Igor Dadachova, Ekaterina PLoS One Research Article Microbial population responses to combined effects of chronic irradiation and other stressors (chemical contaminants, other sub-optimal conditions) are important for ecosystem functioning and bioremediation in radionuclide-contaminated areas. Quantitative mathematical modeling can improve our understanding of these phenomena. To identify general patterns of microbial responses to multiple stressors in radioactive environments, we analyzed three data sets on: (1) bacteria isolated from soil contaminated by nuclear waste at the Hanford site (USA); (2) fungi isolated from the Chernobyl nuclear-power plant (Ukraine) buildings after the accident; (3) yeast subjected to continuous γ-irradiation in the laboratory, where radiation dose rate and cell removal rate were independently varied. We applied generalized linear mixed-effects models to describe the first two data sets, whereas the third data set was amenable to mechanistic modeling using differential equations. Machine learning and information-theoretic approaches were used to select the best-supported formalism(s) among biologically-plausible alternatives. Our analysis suggests the following: (1) Both radionuclides and co-occurring chemical contaminants (e.g. NO(2)) are important for explaining microbial responses to radioactive contamination. (2) Radionuclides may produce non-monotonic dose responses: stimulation of microbial growth at low concentrations vs. inhibition at higher ones. (3) The extinction-defining critical radiation dose rate is dramatically lowered by additional stressors. (4) Reproduction suppression by radiation can be more important for determining the critical dose rate, than radiation-induced cell mortality. In conclusion, the modeling approaches used here on three diverse data sets provide insight into explaining and predicting multi-stressor effects on microbial communities: (1) the most severe effects (e.g. extinction) on microbial populations may occur when unfavorable environmental conditions (e.g. fluctuations of temperature and/or nutrient levels) coincide with radioactive contamination; (2) an organism’s radioresistance and bioremediation efficiency in rich laboratory media may be insufficient to carry out radionuclide bioremediation in the field—robustness against multiple stressors is needed. Public Library of Science 2016-01-25 /pmc/articles/PMC4726741/ /pubmed/26808049 http://dx.doi.org/10.1371/journal.pone.0147696 Text en © 2016 Shuryak, Dadachova 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 Dadachova, Ekaterina Quantitative Modeling of Microbial Population Responses to Chronic Irradiation Combined with Other Stressors |
title | Quantitative Modeling of Microbial Population Responses to Chronic Irradiation Combined with Other Stressors |
title_full | Quantitative Modeling of Microbial Population Responses to Chronic Irradiation Combined with Other Stressors |
title_fullStr | Quantitative Modeling of Microbial Population Responses to Chronic Irradiation Combined with Other Stressors |
title_full_unstemmed | Quantitative Modeling of Microbial Population Responses to Chronic Irradiation Combined with Other Stressors |
title_short | Quantitative Modeling of Microbial Population Responses to Chronic Irradiation Combined with Other Stressors |
title_sort | quantitative modeling of microbial population responses to chronic irradiation combined with other stressors |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4726741/ https://www.ncbi.nlm.nih.gov/pubmed/26808049 http://dx.doi.org/10.1371/journal.pone.0147696 |
work_keys_str_mv | AT shuryakigor quantitativemodelingofmicrobialpopulationresponsestochronicirradiationcombinedwithotherstressors AT dadachovaekaterina quantitativemodelingofmicrobialpopulationresponsestochronicirradiationcombinedwithotherstressors |