Cargando…
Metatranscriptomic Signatures Associated With Phytoplankton Regime Shift From Diatom Dominance to a Dinoflagellate Bloom
Diatoms and dinoflagellates dominate coastal marine phytoplankton communities as major players of marine biogeochemical cycles and their seasonal succession often leads to harmful algal blooms (HABs). What regulates their respective dominances and the development of the HABs remains elusive. Here we...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439486/ https://www.ncbi.nlm.nih.gov/pubmed/30967855 http://dx.doi.org/10.3389/fmicb.2019.00590 |
_version_ | 1783407272993488896 |
---|---|
author | Zhang, Yaqun Lin, Xin Shi, Xinguo Lin, Lingxiao Luo, Hao Li, Ling Lin, Senjie |
author_facet | Zhang, Yaqun Lin, Xin Shi, Xinguo Lin, Lingxiao Luo, Hao Li, Ling Lin, Senjie |
author_sort | Zhang, Yaqun |
collection | PubMed |
description | Diatoms and dinoflagellates dominate coastal marine phytoplankton communities as major players of marine biogeochemical cycles and their seasonal succession often leads to harmful algal blooms (HABs). What regulates their respective dominances and the development of the HABs remains elusive. Here we conducted time-sequential metatranscriptomic profiling on a natural assemblage that evolved from diatom dominance to a dinoflagellate bloom to interrogate the underlying major metabolic and ecological drivers. Data reveals similarity between diatoms and dinoflagellates in exhibiting high capacities of energy production, nutrient acquisition, and stress protection in their respective dominance stages. The diatom-to-dinoflagellate succession coincided with an increase in turbidity and sharp declines in silicate and phosphate availability, concomitant with the transcriptomic shift from expression of silicate uptake and urea utilization genes in diatoms to that of genes for light harvesting, diversified phosphorus acquisition and autophagy-based internal nutrient recycling in dinoflagellates. Furthermore, the diatom-dominant community featured strong potential to carbohydrate metabolism and a strikingly high expression of trypsin potentially promoting frustule building. In contrast, the dinoflagellate bloom featured elevated expression of xanthorhodopsin, and antimicrobial defensin genes, indicating potential importance of energy harnessing and microbial defense in bloom development. This study sheds light on mechanisms potentially governing diatom- and dinoflagellate-dominance and regulating bloom development in the natural environment and raises new questions to be addressed in future studies. |
format | Online Article Text |
id | pubmed-6439486 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64394862019-04-09 Metatranscriptomic Signatures Associated With Phytoplankton Regime Shift From Diatom Dominance to a Dinoflagellate Bloom Zhang, Yaqun Lin, Xin Shi, Xinguo Lin, Lingxiao Luo, Hao Li, Ling Lin, Senjie Front Microbiol Microbiology Diatoms and dinoflagellates dominate coastal marine phytoplankton communities as major players of marine biogeochemical cycles and their seasonal succession often leads to harmful algal blooms (HABs). What regulates their respective dominances and the development of the HABs remains elusive. Here we conducted time-sequential metatranscriptomic profiling on a natural assemblage that evolved from diatom dominance to a dinoflagellate bloom to interrogate the underlying major metabolic and ecological drivers. Data reveals similarity between diatoms and dinoflagellates in exhibiting high capacities of energy production, nutrient acquisition, and stress protection in their respective dominance stages. The diatom-to-dinoflagellate succession coincided with an increase in turbidity and sharp declines in silicate and phosphate availability, concomitant with the transcriptomic shift from expression of silicate uptake and urea utilization genes in diatoms to that of genes for light harvesting, diversified phosphorus acquisition and autophagy-based internal nutrient recycling in dinoflagellates. Furthermore, the diatom-dominant community featured strong potential to carbohydrate metabolism and a strikingly high expression of trypsin potentially promoting frustule building. In contrast, the dinoflagellate bloom featured elevated expression of xanthorhodopsin, and antimicrobial defensin genes, indicating potential importance of energy harnessing and microbial defense in bloom development. This study sheds light on mechanisms potentially governing diatom- and dinoflagellate-dominance and regulating bloom development in the natural environment and raises new questions to be addressed in future studies. Frontiers Media S.A. 2019-03-22 /pmc/articles/PMC6439486/ /pubmed/30967855 http://dx.doi.org/10.3389/fmicb.2019.00590 Text en Copyright © 2019 Zhang, Lin, Shi, Lin, Luo, Li and Lin. 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 | Microbiology Zhang, Yaqun Lin, Xin Shi, Xinguo Lin, Lingxiao Luo, Hao Li, Ling Lin, Senjie Metatranscriptomic Signatures Associated With Phytoplankton Regime Shift From Diatom Dominance to a Dinoflagellate Bloom |
title | Metatranscriptomic Signatures Associated With Phytoplankton Regime Shift From Diatom Dominance to a Dinoflagellate Bloom |
title_full | Metatranscriptomic Signatures Associated With Phytoplankton Regime Shift From Diatom Dominance to a Dinoflagellate Bloom |
title_fullStr | Metatranscriptomic Signatures Associated With Phytoplankton Regime Shift From Diatom Dominance to a Dinoflagellate Bloom |
title_full_unstemmed | Metatranscriptomic Signatures Associated With Phytoplankton Regime Shift From Diatom Dominance to a Dinoflagellate Bloom |
title_short | Metatranscriptomic Signatures Associated With Phytoplankton Regime Shift From Diatom Dominance to a Dinoflagellate Bloom |
title_sort | metatranscriptomic signatures associated with phytoplankton regime shift from diatom dominance to a dinoflagellate bloom |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6439486/ https://www.ncbi.nlm.nih.gov/pubmed/30967855 http://dx.doi.org/10.3389/fmicb.2019.00590 |
work_keys_str_mv | AT zhangyaqun metatranscriptomicsignaturesassociatedwithphytoplanktonregimeshiftfromdiatomdominancetoadinoflagellatebloom AT linxin metatranscriptomicsignaturesassociatedwithphytoplanktonregimeshiftfromdiatomdominancetoadinoflagellatebloom AT shixinguo metatranscriptomicsignaturesassociatedwithphytoplanktonregimeshiftfromdiatomdominancetoadinoflagellatebloom AT linlingxiao metatranscriptomicsignaturesassociatedwithphytoplanktonregimeshiftfromdiatomdominancetoadinoflagellatebloom AT luohao metatranscriptomicsignaturesassociatedwithphytoplanktonregimeshiftfromdiatomdominancetoadinoflagellatebloom AT liling metatranscriptomicsignaturesassociatedwithphytoplanktonregimeshiftfromdiatomdominancetoadinoflagellatebloom AT linsenjie metatranscriptomicsignaturesassociatedwithphytoplanktonregimeshiftfromdiatomdominancetoadinoflagellatebloom |