Evidence map›Paper›PMID 39390465›Full record

ArticleBMC biology2024

Ecological adaptations of amphibians to environmental changes along an altitudinal gradient (Case Study: Bufo gargarizans) from phenotypic and genetic perspectives.

Yonggang Niu, Xuejing Zhang, Haiying Zhang, Shengkang Men, Tisen Xu, Li Ding, Xiangyong Li, Lei Wang, Huisong Wang, Kenneth B Storey and 1 more

Abstract read
In one paragraph

Article in BMC biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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

11 authors.

Yonggang NiuSchool of Life Sciences, Dezhou University, Dezhou, Shandong, 253023, China. yonggangniu@126.com.ORCID http://orcid.org/0000-0002-6674-1798
Xuejing ZhangSchool of Life Sciences, Lanzhou University, Lanzhou, 730000, China.
Haiying ZhangSchool of Life Sciences, Dezhou University, Dezhou, Shandong, 253023, China.
Shengkang MenSchool of Life Sciences, Lanzhou University, Lanzhou, 730000, China.
Tisen XuSchool of Life Sciences, Dezhou University, Dezhou, Shandong, 253023, China.
Li DingSchool of Life Science and Engineering, Southwest University of Science and Technology, Mianyang, 621010, China.
Xiangyong LiSchool of Life Sciences, Dezhou University, Dezhou, Shandong, 253023, China.
Lei WangSchool of Life Sciences, Dezhou University, Dezhou, Shandong, 253023, China.
Huisong WangSchool of Life Sciences, Dezhou University, Dezhou, Shandong, 253023, China.
Kenneth B StoreyDepartment of Biology, Carleton University, Ottawa, ON, K1S 5B6, Canada.
Qiang ChenSchool of Life Sciences, Lanzhou University, Lanzhou, 730000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOrganisms have evolved a range of phenotypic and genetic adaptations to live in different environments along an altitudinal gradient. Herein, we studied the widely distributed Chinese toad, Bufo gargarizans, as a model and used an integrated phenotype-genotype approach to assess adaptations to different altitudinal environments.

resultsComparison of populations from four altitudes (50 m, 1200 m, 2300 m, and 3400 m) showed more effective defenses among high-altitude toads. These included thickened epidermis, more epidermal capillaries and granular glands, greater gland size in skin, and higher antioxidant enzyme activities in plasma. High-altitude toads also showed increased erythrocytes and hematocrit and elevated hemoglobin concentration, potentially improving oxygen delivery. Elevated altitude led to a metabolic shift from aerobic to anaerobic metabolism, and high-altitude populations favored carbohydrates over fatty acids to fuel for energy metabolism. Differentially expressed genes were associated with adaptive phenotypic changes. For instance, expression of genes associated with fatty acid metabolism showed greater suppression at high altitude (3400 m), consistent with decreased flux of β-hydroxybutyric acid and lower free fatty acids levels. Moreover, down-regulation of genes involved in carbon metabolism processes at high altitude (3400 m) were coincident with reduced TCA cycle flux. These results suggest that high-altitude toads adopt a metabolic suppression strategy for survival under harsh environmental conditions. Moreover, the hypoxia-inducible factor signaling cascade was activated at high altitude.

conclusionsCollectively, these results advance our comprehension of adaptation to high-altitude environments by revealing physiological and genetic mechanisms at work in Chinese toads living along altitudinal gradients.

Indexed as

Adaptation, PhysiologicalAltitudeBufonidaePhenotypeAcclimatizationAnimalsChinaAdaptationAltitudinal gradientBufo gargarizansPhenotypic traitsTranscriptome

Identifiers

PMID39390465
PMCPMC11465660

What Socratic holds

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LicenceCC BY-NC-ND
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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.