Transcriptome Analysis of the Harmful Dinoflagellate Heterocapsa bohaiensis Under Varied Nutrient Stress Conditions

The increasing prevalence of harmful algal blooms (HABs) driven by eutrophication, particularly in China's nearshore waters, is a growing concern. Dinoflagellate <i>Heterocapsa bohaiensis</i> blooms have caused significant ecological and economic damage, as well as mass mortality, in cultivated species. Nutrients are one of the primary inducers of <i>H. bohaiensis</i> blooms. However, the transcriptomic studies of <i>H. bohaiensis</i> remain sparse, and its metabolic pathways are unknown. This study analyzed the transcriptome of <i>H. bohaiensis</i> under varying nutrient conditions (nitrogen at 128, 512, and 880 μM; phosphate at 8, 6, and 32 μM), focusing on differential gene expression. The results indicated that deviations in nutrient conditions (higher or lower N:P ratios) led to a higher number of differentially expressed genes compared to the control (N:P ratios = 27.5), thereby underscoring their pivotal role in growth. Gene Ontology (GO) enrichment analyses showed that nutrient limitation upregulated the biosynthesis and catabolism processes while downregulating the cell cycle and division functions. The Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis revealed that, under nitrogen limitation, the proteasome pathways were upregulated, while photosynthesis and carbon fixation were downregulated; under phosphorus limitation, the proteasome pathways were upregulated and nitrogen metabolism was downregulated. These findings suggest that <i>H. bohaiensis</i> adapts to nutrient stress by adjusting its metabolic processes.

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Publication Details

Journal
Microorganisms
Published
2024-12-22
DOI
https://doi.org/10.3390/microorganisms12122665
Citations
1
Primary Topic
Microbial Community Ecology and Physiology
Type
article
Field-Weighted Citation Impact
0.46

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article

Transcriptome Analysis of the Harmful Dinoflagellate Heterocapsa bohaiensis Under Varied Nutrient Stress Conditions

Ying Su, Jingjing Zhan, Xiaofeng Guo, Yiwen Zhang et al.
1 citations
Microorganisms
Microbial Community Ecology and Physiology
0.46
article

Transcriptome Analysis of the Harmful Dinoflagellate Heterocapsa bohaiensis Under Varied Nutrient Stress Conditions

Ying Su, Jingjing Zhan, Xiaofeng Guo, Yiwen Zhang, Fei Han, Xue Gong, Peng Peng
article en
1 citations

Abstract

The increasing prevalence of harmful algal blooms (HABs) driven by eutrophication, particularly in China's nearshore waters, is a growing concern. Dinoflagellate <i>Heterocapsa bohaiensis</i> blooms have caused significant ecological and economic damage, as well as mass mortality, in cultivated species. Nutrients are one of the primary inducers of <i>H. bohaiensis</i> blooms. However, the transcriptomic studies of <i>H. bohaiensis</i> remain sparse, and its metabolic pathways are unknown. This study analyzed the transcriptome of <i>H. bohaiensis</i> under varying nutrient conditions (nitrogen at 128, 512, and 880 μM; phosphate at 8, 6, and 32 μM), focusing on differential gene expression. The results indicated that deviations in nutrient conditions (higher or lower N:P ratios) led to a higher number of differentially expressed genes compared to the control (N:P ratios = 27.5), thereby underscoring their pivotal role in growth. Gene Ontology (GO) enrichment analyses showed that nutrient limitation upregulated the biosynthesis and catabolism processes while downregulating the cell cycle and division functions. The Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis revealed that, under nitrogen limitation, the proteasome pathways were upregulated, while photosynthesis and carbon fixation were downregulated; under phosphorus limitation, the proteasome pathways were upregulated and nitrogen metabolism was downregulated. These findings suggest that <i>H. bohaiensis</i> adapts to nutrient stress by adjusting its metabolic processes.

MicroorganismsVol. 12(12)
Dalian University of Technology (CN)
National Natural Science Foundation of China
Life below water
Openalex Percentile: Top 27%
Microbial Community Ecology and Physiology
0.46
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