Evidence mapPaperPMID 35869388Full record

ArticleThe ISME journal2022

MicroRNA-mediated regulation of lipid metabolism in virus-infected Emiliania huxleyi.

Enquan Zhang, Jingjing Gao, Zehua Wei, Jun Zeng, Jian Li, Guiling Li, Jingwen Liu

Open access · hybridAbstract read
In one paragraph

Article in The ISME journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Enquan ZhangCollege of Ocean Food and Biological Engineering, Jimei University, Xiamen, 361021, China.
Jingjing GaoCollege of Ocean Food and Biological Engineering, Jimei University, Xiamen, 361021, China.
Zehua WeiCollege of Ocean Food and Biological Engineering, Jimei University, Xiamen, 361021, China.
Jun ZengCollege of Ocean Food and Biological Engineering, Jimei University, Xiamen, 361021, China.
Jian LiCollege of Ocean Food and Biological Engineering, Jimei University, Xiamen, 361021, China.
Guiling LiCollege of Ocean Food and Biological Engineering, Jimei University, Xiamen, 361021, China. glli2016@jmu.edu.cn.ORCID 0000-0002-0940-6010
Jingwen LiuCollege of Ocean Food and Biological Engineering, Jimei University, Xiamen, 361021, China. ljwsbch@163.com.ORCID 0000-0001-7231-6483
Jimei University · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 42076086Natural Science Foundation of Fujian Province (Fujian Provincial Natural Science Foundation) 2019J01696
6 · The paper itself

Abstract

The interactions between Emiliania huxleyi and E. huxleyi virus (EhV) regulate marine carbon and sulfur biogeochemical cycles and play a prominent role in global climate change. As a large DNA virus, EhV has developed a novel "virocell metabolism" model to meet its high metabolic needs. Although it has been widely demonstrated that EhV infection can profoundly rewire lipid metabolism, the epigenetic regulatory mechanisms of lipid metabolism are still obscure. MicroRNAs (miRNAs) can regulate biological pathways by targeting hub genes in the metabolic processes. In this study, the transcriptome, lipidome, and miRNAome were applied to investigate the epigenetic regulation of lipid metabolism in E. huxleyi cells during a detailed time course of viral infection. Combined transcriptomic, lipidomic, and physiological experiments revealed reprogrammed lipid metabolism, along with mitochondrial dysfunction and calcium influx through the cell membrane. A total of 69 host miRNAs (including 1 known miRNA) and 7 viral miRNAs were identified, 27 of which were differentially expressed. Bioinformatic prediction revealed that miRNAs involved in the regulation of lipid metabolism and a dual-luciferase reporter assay suggested that phosphatidylinositol 3-kinase (PI3K) gene might be a target of ehx-miR5. Further qPCR and western blot analysis showed a significant negative correlation between the expression of ehx-miR5 and its target gene PI3K, along with the lower activity of its downstream components (p-Akt, p-TOR, SREBP), indicating that lipid metabolism might be regulated by ehx-miR5 through the PI3K-Akt-TOR signaling pathway. Our findings reveal several novel mechanisms of viral strategies to manipulate host lipid metabolism and provide evidence that ehx-miR5 negatively modulates the expression of PI3K and disturbs lipid metabolism in the interactions between E. huxleyi and EhV.

Indexed as

HaptophytaMicroRNAsVirusesCalciumCarbonEpigenesis, GeneticLipid MetabolismPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSterol Regulatory Element Binding Protein 1SulfurCalciumCarbonMicroRNAsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSterol Regulatory Element Binding Protein 1Sulfur

Identifiers

PMID35869388
PMCPMC9561107
OpenAlexW4286487558

What Socratic holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.