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

被引:0
作者
Niu, Yonggang [1 ]
Zhang, Xuejing [2 ]
Zhang, Haiying [1 ]
Men, Shengkang [2 ]
Xu, Tisen [1 ]
Ding, Li [3 ]
Li, Xiangyong [1 ]
Wang, Lei [1 ]
Wang, Huisong [1 ]
Storey, Kenneth B. [4 ]
Chen, Qiang [2 ]
机构
[1] Dezhou Univ, Sch Life Sci, Dezhou 253023, Shandong, Peoples R China
[2] Lanzhou Univ, Sch Life Sci, Lanzhou 730000, Peoples R China
[3] Southwest Univ Sci & Technol, Sch Life Sci & Engn, Mianyang 621010, Peoples R China
[4] Carleton Univ, Dept Biol, Ottawa, ON K1S 5B6, Canada
基金
中国国家自然科学基金;
关键词
Bufo gargarizans; Altitudinal gradient; Phenotypic traits; Transcriptome; Adaptation; OXIDATIVE STRESS; TREE FROG; SKIN; HYPOXIA; MECHANISMS; LIFE; ELEVATION; MEMBRANES; EXPOSURE; REPTILES;
D O I
10.1186/s12915-024-02033-6
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Organisms 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. Results Comparison 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 beta-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. Conclusions Collectively, 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.
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