Helen K Feord, Christoph Keuschnig, Christopher B Trivedi, Rey Mourot, Athanasios Zervas, Thomas Turpin-Jelfs, Martyn Tranter, Alexandre M Anesio, Lorenz Adrian, Liane G Benning
{"title":"将格陵兰冰盖上以藻类为主的群落的极端光可用性与细胞功能联系起来。","authors":"Helen K Feord, Christoph Keuschnig, Christopher B Trivedi, Rey Mourot, Athanasios Zervas, Thomas Turpin-Jelfs, Martyn Tranter, Alexandre M Anesio, Lorenz Adrian, Liane G Benning","doi":"10.1093/femsec/fiaf095","DOIUrl":null,"url":null,"abstract":"<p><p>Glacier ice algae of the streptophyte genus Ancylonema bloom on glaciers globally, including the Greenland Ice Sheet. These algae survive under extreme high light conditions in the summer, as well as under very low light or total darkness during (polar) winters and winter burial under snow. However, little is known about the cellular mechanisms underpinning glacier ice algae ecophysiological plasticity in response to extreme light availability. To address this knowledge gap, we evaluated the response of Ancylonema-dominated taxa in samples from the Greenland Ice Sheet to light and dark conditions during a 12-day period using combined multi-omics analyses. The microbial community was not substantially altered during the 12 days of dark incubation, however transcriptomic analysis demonstrated that the algae-associated heterotrophs became more active in the dark. In contrast, we identified a striking algal transcriptome stability in light conditions, in addition to high oxidative stress responses and evidence for high photosystem protein turnover. We also identified transcriptional reprogramming linked to sugar uptake and phytohormone signalling during dark incubation. These results provide crucial clues into the ability of glacier ice algae to adapt and survive in a harsh and extremely variable light environment.</p>","PeriodicalId":12312,"journal":{"name":"FEMS microbiology ecology","volume":" ","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2025-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12501423/pdf/","citationCount":"0","resultStr":"{\"title\":\"Linking extreme light availability to cellular function in algae-dominated communities on the Greenland Ice Sheet.\",\"authors\":\"Helen K Feord, Christoph Keuschnig, Christopher B Trivedi, Rey Mourot, Athanasios Zervas, Thomas Turpin-Jelfs, Martyn Tranter, Alexandre M Anesio, Lorenz Adrian, Liane G Benning\",\"doi\":\"10.1093/femsec/fiaf095\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Glacier ice algae of the streptophyte genus Ancylonema bloom on glaciers globally, including the Greenland Ice Sheet. These algae survive under extreme high light conditions in the summer, as well as under very low light or total darkness during (polar) winters and winter burial under snow. However, little is known about the cellular mechanisms underpinning glacier ice algae ecophysiological plasticity in response to extreme light availability. To address this knowledge gap, we evaluated the response of Ancylonema-dominated taxa in samples from the Greenland Ice Sheet to light and dark conditions during a 12-day period using combined multi-omics analyses. The microbial community was not substantially altered during the 12 days of dark incubation, however transcriptomic analysis demonstrated that the algae-associated heterotrophs became more active in the dark. In contrast, we identified a striking algal transcriptome stability in light conditions, in addition to high oxidative stress responses and evidence for high photosystem protein turnover. We also identified transcriptional reprogramming linked to sugar uptake and phytohormone signalling during dark incubation. These results provide crucial clues into the ability of glacier ice algae to adapt and survive in a harsh and extremely variable light environment.</p>\",\"PeriodicalId\":12312,\"journal\":{\"name\":\"FEMS microbiology ecology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2025-09-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12501423/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"FEMS microbiology ecology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1093/femsec/fiaf095\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"FEMS microbiology ecology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/femsec/fiaf095","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Linking extreme light availability to cellular function in algae-dominated communities on the Greenland Ice Sheet.
Glacier ice algae of the streptophyte genus Ancylonema bloom on glaciers globally, including the Greenland Ice Sheet. These algae survive under extreme high light conditions in the summer, as well as under very low light or total darkness during (polar) winters and winter burial under snow. However, little is known about the cellular mechanisms underpinning glacier ice algae ecophysiological plasticity in response to extreme light availability. To address this knowledge gap, we evaluated the response of Ancylonema-dominated taxa in samples from the Greenland Ice Sheet to light and dark conditions during a 12-day period using combined multi-omics analyses. The microbial community was not substantially altered during the 12 days of dark incubation, however transcriptomic analysis demonstrated that the algae-associated heterotrophs became more active in the dark. In contrast, we identified a striking algal transcriptome stability in light conditions, in addition to high oxidative stress responses and evidence for high photosystem protein turnover. We also identified transcriptional reprogramming linked to sugar uptake and phytohormone signalling during dark incubation. These results provide crucial clues into the ability of glacier ice algae to adapt and survive in a harsh and extremely variable light environment.
期刊介绍:
FEMS Microbiology Ecology aims to ensure efficient publication of high-quality papers that are original and provide a significant contribution to the understanding of microbial ecology. The journal contains Research Articles and MiniReviews on fundamental aspects of the ecology of microorganisms in natural soil, aquatic and atmospheric habitats, including extreme environments, and in artificial or managed environments. Research papers on pure cultures and in the areas of plant pathology and medical, food or veterinary microbiology will be published where they provide valuable generic information on microbial ecology. Papers can deal with culturable and non-culturable forms of any type of microorganism: bacteria, archaea, filamentous fungi, yeasts, protozoa, cyanobacteria, algae or viruses. In addition, the journal will publish Perspectives, Current Opinion and Controversy Articles, Commentaries and Letters to the Editor on topical issues in microbial ecology.
- Application of ecological theory to microbial ecology
- Interactions and signalling between microorganisms and with plants and animals
- Interactions between microorganisms and their physicochemical enviornment
- Microbial aspects of biogeochemical cycles and processes
- Microbial community ecology
- Phylogenetic and functional diversity of microbial communities
- Evolutionary biology of microorganisms