Evidence map›Paper›PMID 40825928›Full record

ArticleScience China. Life sciences2025

Cell-supporting cytoskeletons and phagocytic acquisition of compatible solutes emerge as common strategies for high-salt adaptation in different ciliates.

Fengchao Li, Wenying Zhang, Shuai Luo, Ning Ma, Jing Zhang, Weiwei Qin, Che Hu, Xinxin Gao, Yuan Xiao, Chuanqi Jiang and 8 more

Abstract read
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Article in Science China. Life sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Study of Unconventional Cytoskeleton Components Regulating Actin Contraction.Methods in molecular biology (Clifton, N.J.) · 2026
    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

18 authors.

Fengchao Li *College of Life Sciences, Hebei University, Baoding, 071002, China.
Wenying Zhang *College of Life Sciences, Hebei University, Baoding, 071002, China.
Shuai Luo *Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China.
Ning MaCollege of Life Sciences, Hebei University, Baoding, 071002, China.
Jing ZhangInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China.
Weiwei QinInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China.
Che HuInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China.
Xinxin GaoInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China.
Yuan XiaoInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China.
Chuanqi JiangInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China.
Xiaocui ChaiInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China.
Qiukun WangCollege of Life Sciences, Hebei University, Baoding, 071002, China.
Yuwen JiangCollege of Life Sciences, Hebei University, Baoding, 071002, China.
Fang ZhouInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China.
Kai ChenInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China.
Feng GeInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China.
Wei MiaoInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China. miaowei@ihb.ac.cn.
Jie XiongInstitute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China. xiongjie@ihb.ac.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding the adaptation of organisms to extreme environments is a fascinating topic in biology. Ciliated eukaryotes (ciliates) that inhabit high-salinity environments exhibit remarkable diversity. We revealed various structural and molecular adaptations through a comprehensive investigation of Schmidingerothrix, a ciliate tolerant to salinity levels of up to 25%. One key finding was the presence of a unique microtubule cytoskeleton under the pellicle of Schmidingerothrix, which significantly contributed to its high-salt adaptation. Our results highlight the essential role of coexisting halophilic bacteria in supporting the thriving of ciliates in culture. Contrary to previous studies, our findings indicated an inability to synthesize glycine betaine and ectoine in Schmidingerothrix. However, Schmidingerothrix appears to have expanded its repertoire of phagocytosis-related genes, suggesting a robust mechanism for the uptake and accumulation of compatible solutes via phagocytosis of halophilic bacteria. We expanded our investigation to other high-salt ciliates from different clades and discovered that microtubule cell-shape-supporting cytoskeletons and the phagocytic acquisition of compatible solutes were common strategies for high-salt adaptation. These findings significantly enhance our understanding of how ciliates adapt to high-salt environments and provide valuable insights into the high diversity of heterotrophic protists.

Indexed as

Adaptation, PhysiologicalCiliophoraCytoskeletonPhagocytosisSalt ToleranceAmino Acids, DiaminoBetaineMicrotubulesPhylogenySalinityAmino Acids, DiaminoBetaineectoineectoineglycine betainehalophile ciliatehypersaline adaptationmacronuclear genomeSchmidingerothrix

Identifiers

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Registered trials

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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.