Cargando…
The Seasonal Metabolic Activity Cycle of Antarctic Krill (Euphausia superba): Evidence for a Role of Photoperiod in the Regulation of Endogenous Rhythmicity
Antarctic krill (Euphausia superba), a key species in the Southern Ocean, reduce their metabolism as an energy saving mechanism in response to the harsh environmental conditions during the Antarctic winter. Although the adaptive significance of this seasonal metabolic shift seems obvious, the drivin...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307472/ https://www.ncbi.nlm.nih.gov/pubmed/30618779 http://dx.doi.org/10.3389/fphys.2018.01715 |
_version_ | 1783383008239157248 |
---|---|
author | Piccolin, Fabio Suberg, Lavinia King, Robert Kawaguchi, So Meyer, Bettina Teschke, Mathias |
author_facet | Piccolin, Fabio Suberg, Lavinia King, Robert Kawaguchi, So Meyer, Bettina Teschke, Mathias |
author_sort | Piccolin, Fabio |
collection | PubMed |
description | Antarctic krill (Euphausia superba), a key species in the Southern Ocean, reduce their metabolism as an energy saving mechanism in response to the harsh environmental conditions during the Antarctic winter. Although the adaptive significance of this seasonal metabolic shift seems obvious, the driving factors are still unclear. In particular, it is debated whether the seasonal metabolic cycle is driven by changes in food availability, or if an endogenous timing system entrained by photoperiod might be involved. In this study, we used different long-term photoperiodic simulations to examine the influence of light regime and endogenous rhythmicity on the regulation of krill seasonal metabolic cycle. Krill showed a seasonal cycle of growth characterized by null-to-negative growth rates during autumn-winter and positive growth rates during spring-summer, which was manifested also in constant darkness, indicating strong endogenous regulation. Similar endogenous cycles were observed for the activity of the key-metabolic enzyme malate dehydrogenase (MDH) and for the expression levels of a selection of metabolic-related genes, with higher values in spring-summer and lower values in autumn-winter. On the other side, a seasonal cycle of oxygen consumption was observed only when krill were exposed to simulated seasonal changes in photoperiod, indicating that light-related cues might play a major role in the regulation of krill oxygen consumption. The influence of light-regime on oxygen consumption was minimal during winter, when light-phase duration was below 8 h, and it was maximal during summer, when light-phase duration was above 16 h. Significant upregulation of the krill clock genes clk, cry2, and tim1, as well as of the circadian-related opsins rh1a and rrh, was observed after light-phase duration had started to decrease in early autumn, suggesting the presence of a signaling cascade linking specific seasonal changes in the Antarctic light regime with clock gene activity and the regulation of krill metabolic dormancy over the winter. |
format | Online Article Text |
id | pubmed-6307472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63074722019-01-07 The Seasonal Metabolic Activity Cycle of Antarctic Krill (Euphausia superba): Evidence for a Role of Photoperiod in the Regulation of Endogenous Rhythmicity Piccolin, Fabio Suberg, Lavinia King, Robert Kawaguchi, So Meyer, Bettina Teschke, Mathias Front Physiol Physiology Antarctic krill (Euphausia superba), a key species in the Southern Ocean, reduce their metabolism as an energy saving mechanism in response to the harsh environmental conditions during the Antarctic winter. Although the adaptive significance of this seasonal metabolic shift seems obvious, the driving factors are still unclear. In particular, it is debated whether the seasonal metabolic cycle is driven by changes in food availability, or if an endogenous timing system entrained by photoperiod might be involved. In this study, we used different long-term photoperiodic simulations to examine the influence of light regime and endogenous rhythmicity on the regulation of krill seasonal metabolic cycle. Krill showed a seasonal cycle of growth characterized by null-to-negative growth rates during autumn-winter and positive growth rates during spring-summer, which was manifested also in constant darkness, indicating strong endogenous regulation. Similar endogenous cycles were observed for the activity of the key-metabolic enzyme malate dehydrogenase (MDH) and for the expression levels of a selection of metabolic-related genes, with higher values in spring-summer and lower values in autumn-winter. On the other side, a seasonal cycle of oxygen consumption was observed only when krill were exposed to simulated seasonal changes in photoperiod, indicating that light-related cues might play a major role in the regulation of krill oxygen consumption. The influence of light-regime on oxygen consumption was minimal during winter, when light-phase duration was below 8 h, and it was maximal during summer, when light-phase duration was above 16 h. Significant upregulation of the krill clock genes clk, cry2, and tim1, as well as of the circadian-related opsins rh1a and rrh, was observed after light-phase duration had started to decrease in early autumn, suggesting the presence of a signaling cascade linking specific seasonal changes in the Antarctic light regime with clock gene activity and the regulation of krill metabolic dormancy over the winter. Frontiers Media S.A. 2018-12-20 /pmc/articles/PMC6307472/ /pubmed/30618779 http://dx.doi.org/10.3389/fphys.2018.01715 Text en Copyright © 2018 Piccolin, Suberg, King, Kawaguchi, Meyer and Teschke. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Piccolin, Fabio Suberg, Lavinia King, Robert Kawaguchi, So Meyer, Bettina Teschke, Mathias The Seasonal Metabolic Activity Cycle of Antarctic Krill (Euphausia superba): Evidence for a Role of Photoperiod in the Regulation of Endogenous Rhythmicity |
title | The Seasonal Metabolic Activity Cycle of Antarctic Krill (Euphausia superba): Evidence for a Role of Photoperiod in the Regulation of Endogenous Rhythmicity |
title_full | The Seasonal Metabolic Activity Cycle of Antarctic Krill (Euphausia superba): Evidence for a Role of Photoperiod in the Regulation of Endogenous Rhythmicity |
title_fullStr | The Seasonal Metabolic Activity Cycle of Antarctic Krill (Euphausia superba): Evidence for a Role of Photoperiod in the Regulation of Endogenous Rhythmicity |
title_full_unstemmed | The Seasonal Metabolic Activity Cycle of Antarctic Krill (Euphausia superba): Evidence for a Role of Photoperiod in the Regulation of Endogenous Rhythmicity |
title_short | The Seasonal Metabolic Activity Cycle of Antarctic Krill (Euphausia superba): Evidence for a Role of Photoperiod in the Regulation of Endogenous Rhythmicity |
title_sort | seasonal metabolic activity cycle of antarctic krill (euphausia superba): evidence for a role of photoperiod in the regulation of endogenous rhythmicity |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307472/ https://www.ncbi.nlm.nih.gov/pubmed/30618779 http://dx.doi.org/10.3389/fphys.2018.01715 |
work_keys_str_mv | AT piccolinfabio theseasonalmetabolicactivitycycleofantarctickrilleuphausiasuperbaevidenceforaroleofphotoperiodintheregulationofendogenousrhythmicity AT suberglavinia theseasonalmetabolicactivitycycleofantarctickrilleuphausiasuperbaevidenceforaroleofphotoperiodintheregulationofendogenousrhythmicity AT kingrobert theseasonalmetabolicactivitycycleofantarctickrilleuphausiasuperbaevidenceforaroleofphotoperiodintheregulationofendogenousrhythmicity AT kawaguchiso theseasonalmetabolicactivitycycleofantarctickrilleuphausiasuperbaevidenceforaroleofphotoperiodintheregulationofendogenousrhythmicity AT meyerbettina theseasonalmetabolicactivitycycleofantarctickrilleuphausiasuperbaevidenceforaroleofphotoperiodintheregulationofendogenousrhythmicity AT teschkemathias theseasonalmetabolicactivitycycleofantarctickrilleuphausiasuperbaevidenceforaroleofphotoperiodintheregulationofendogenousrhythmicity AT piccolinfabio seasonalmetabolicactivitycycleofantarctickrilleuphausiasuperbaevidenceforaroleofphotoperiodintheregulationofendogenousrhythmicity AT suberglavinia seasonalmetabolicactivitycycleofantarctickrilleuphausiasuperbaevidenceforaroleofphotoperiodintheregulationofendogenousrhythmicity AT kingrobert seasonalmetabolicactivitycycleofantarctickrilleuphausiasuperbaevidenceforaroleofphotoperiodintheregulationofendogenousrhythmicity AT kawaguchiso seasonalmetabolicactivitycycleofantarctickrilleuphausiasuperbaevidenceforaroleofphotoperiodintheregulationofendogenousrhythmicity AT meyerbettina seasonalmetabolicactivitycycleofantarctickrilleuphausiasuperbaevidenceforaroleofphotoperiodintheregulationofendogenousrhythmicity AT teschkemathias seasonalmetabolicactivitycycleofantarctickrilleuphausiasuperbaevidenceforaroleofphotoperiodintheregulationofendogenousrhythmicity |