Zhao Xiuxin, Liu Peimin, Xia Zhenglong, Cai Miuying, Tang Qiongying, Yang Guoliang, Gao Quanxin, Yi Shaokui
Huzhou University, College of Life Sciences, Key Laboratory of Aquatic Biological Resources Conservation and Development Technology of Zhejiang Province/Chines Academy of Fishery Sciences, Key Laboratory of Aquatic Animal Breeding and Nutrition, Huzhou 313000, Zhejiang, China.
Jiangsu Shufeng Prawn Breeding Co. LTD, Gaoyou 225654, Jiangsu, China.
Comp Biochem Physiol Part D Genomics Proteomics. 2025 Jun;54:101432. doi: 10.1016/j.cbd.2025.101432. Epub 2025 Jan 29.
Macrobrachium rosenbergii (giant freshwater prawn; GFP) holds considerable importance in aquaculture due to its high market demand and economic significance. Female GFP growth varies significantly, however, the processes responsible for these growth disparities remain unknown. In this study, intestinal and hemolymph samples of large (FL), medium (FM), and small (FS) female GFPs were collected to investigate the molecular mechanism of female GFP growth. Through the utilization of 16S rRNA sequencing and liquid chromatography-mass spectrometry metabolomics, significant intestinal flora and metabolites linked to the growth performance of female GFPs were identified. The dominant phyla of the three groups were the same, namely Firmicutes and Proteobacteria. Among groups, small females exhibited the lowest abundance of Proteobacteria (27.26 %) and the highest abundance of Firmicutes (70.10 %). The most abundant genus in each group was Lactococcus. Liquid chromatography-mass spectrometry identified 115 annotated differential metabolites, and essential metabolites related to female GFP growth performance were screened. The concentration of serum metabolites in the larger females exhibited a statistically significant variance compared to that of the smaller females. Through association analysis, we identified key genes, metabolites, and gut microbiota that influence the growth of female GFPs. Likewise, we used multi-omics techniques to establish two relationship models ("gut microbiota-GFP phenotype-metabolite", "gut microbiota-GFP phenotype-transcript"), and three important network association models ("DN5520_c0_g1-CW1-Bacteroides", "DN537746_c0_g1-BW-Roseburia" and "Picolinic acid-phenotype-Roseburia") were further developed. The present study provides novel insights into the mechanisms underlying the variability in individual growth among female GFPs. Our findings offer valuable information for future investigations exploring the correlation between gut flora and host organisms in aquatic environments.
罗氏沼虾(巨型淡水虾;GFP)因其高市场需求和经济意义在水产养殖中具有相当重要的地位。然而,雌性罗氏沼虾的生长差异显著,而导致这些生长差异的过程仍不清楚。在本研究中,采集了大型(FL)、中型(FM)和小型(FS)雌性罗氏沼虾的肠道和血淋巴样本,以研究雌性罗氏沼虾生长的分子机制。通过利用16S rRNA测序和液相色谱 - 质谱代谢组学,鉴定出了与雌性罗氏沼虾生长性能相关的重要肠道菌群和代谢产物。三组的优势菌门相同,即厚壁菌门和变形菌门。在各组中,小型雌性变形菌门的丰度最低(27.26%),厚壁菌门的丰度最高(70.10%)。每组中最丰富的属是乳球菌属。液相色谱 - 质谱鉴定出115种注释的差异代谢产物,并筛选出了与雌性罗氏沼虾生长性能相关的必需代谢产物。与较小雌性相比,较大雌性血清代谢产物的浓度表现出统计学上的显著差异。通过关联分析,我们确定了影响雌性罗氏沼虾生长的关键基因、代谢产物和肠道微生物群。同样,我们使用多组学技术建立了两个关系模型(“肠道微生物群 - GFP表型 - 代谢产物”,“肠道微生物群 - GFP表型 - 转录本”),并进一步建立了三个重要的网络关联模型(“DN5520_c0_g1 - CW1 - 拟杆菌属”,“DN537746_c0_g1 - BW - 罗斯氏菌属”和“吡啶甲酸 - 表型 - 罗斯氏菌属”)。本研究为雌性罗氏沼虾个体生长差异的潜在机制提供了新的见解。我们的研究结果为未来探索水生环境中肠道菌群与宿主生物之间相关性提供了有价值的信息。