Microbial Co-Occurrence Patterns and Keystone Species in the Gut Microbial Community of Mice in Response to Stress and Chondroitin Sulfate Disaccharide

被引:20
|
作者
Liu, Fang [1 ]
Li, Zhaojie [1 ]
Wang, Xiong [1 ]
Xue, Changhu [1 ]
Tang, Qingjuan [1 ]
Li, Robert W. [2 ]
机构
[1] Ocean Univ China, Coll Food Sci & Engn, Qingdao 266003, Shandong, Peoples R China
[2] ARS, USDA, Anim Genom & Improvement Lab, Beltsville, MD 20705 USA
基金
中国国家自然科学基金;
关键词
16S rRNA gene; chondroitin sulfate disaccharide; co-occurrence network; global network; microbial interactions; microbiome; modularity; superoxide dismutase; BLOOD UREA NITROGEN; LOCAL SIMILARITY ANALYSIS; OXIDATIVE STRESS; ANALYSIS REVEALS; EXERCISE; ENVIRONMENT; LEVEL;
D O I
10.3390/ijms20092130
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Detecting microbial interactions is essential to the understanding of the structure and function of the gut microbiome. In this study, microbial co-occurrence patterns were inferred using a random matrix theory based approach in the gut microbiome of mice in response to chondroitin sulfate disaccharide (CSD) under healthy and stressed conditions. The exercise stress disrupted the network composition and microbial co-occurrence patterns. Thirty-four Operational Taxonomic Units (OTU) were identified as module hubs and connectors, likely acting as generalists in the microbial community. Mucispirillum schaedleri acted as a connector in the stressed network in response to CSD supplement and may play a key role in bridging intimate interactions between the host and its microbiome. Several modules correlated with physiological parameters were detected. For example, Modules M02 (under stress) and S05 (stress + CSD) were strongly correlated with blood urea nitrogen levels (r = 0.90 and -0.75, respectively). A positive correlation between node connectivity of the OTUs assigned to Proteobacteria with superoxide dismutase activities under stress (r = 0.57, p < 0.05) provided further evidence that Proteobacteria can be developed as a potential pathological marker. Our findings provided novel insights into gut microbial interactions and may facilitate future endeavor in microbial community engineering.
引用
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页数:15
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