Key Laboratory of Freshwater Aquatic Genetic Resources Certificated by the Ministry of Agriculture and Rural Affairs, National Demonstration Centre for Experimental Fisheries Science Education, Shanghai Engineering Research Center of Aquaculture, Shanghai Ocean University, Shanghai 201306, China.
J Appl Microbiol. 2024 Sep 2;135(9). doi: 10.1093/jambio/lxae226.
Beyond the pivotal roles of the gut microbiome in initiating physiological processes and modulating genetic factors, a query persists: Can a single gene mutation alter the abundance of the gut microbiome community? Not only this, but the intricate impact of gut microbiome composition on skin pigmentation has been largely unexplored.
Based on these premises, our study examines the abundance of lipase-producing gut microbes about differential gene expression associated with bile acid synthesis and lipid metabolism-related blood metabolites in red (whole wild) and white (whole white wild and SCARB1-/- mutant) Oujiang colour common carp. Following the disruption of the SCARB1 gene in the resulting mutant fish with white body colour (SCARB1-/-), there is a notable decrease in the abundance of gut microbiomes (Bacillus, Staphylococcus, Pseudomonas, and Serratia) associated with lipase production. This reduction parallels the downregulation seen in wild-type white body colour fish (WW), as contrasting to the wild-type red body colour fish (WR). Meanwhile, in SCARB1-/- fish, there was a downregulation noted not only at the genetic and metabolic levels but also a decrease in lipase-producing bacteria. This consistency with WW contrasts significantly with WR. Similarly, genes involved in the bile acid synthesis pathway, along with blood metabolites related to lipid metabolism, exhibited downregulation in SCARB1-/- fish.
The SCARB1 knockout gene blockage led to significant alterations in the gut microbiome, potentially influencing the observed reduction in carotenoid-associated skin pigmentation. Our study emphasizes that skin pigmentation is not only impacted by genetic factors but also by the gut microbiome. Meanwhile, the gut microbiome's adaptability can be rapidly shaped and may be driven by specific single-gene variations.
除了肠道微生物群在启动生理过程和调节遗传因素方面的关键作用外,还有一个问题仍然存在:单一基因突变是否会改变肠道微生物群落的丰度?不仅如此,肠道微生物群落组成对皮肤色素沉着的复杂影响在很大程度上还未被探索。
基于这些前提,我们的研究检查了产生脂肪酶的肠道微生物的丰度,以及与胆汁酸合成和脂质代谢相关的血液代谢物相关的差异基因表达,在红色(全野生)和白色(全野生和 SCARB1-/-突变体)瓯江彩色鲤鱼中。在产生白色体色(SCARB1-/-)的突变鱼中破坏 SCARB1 基因后,与脂肪酶产生相关的肠道微生物群(芽孢杆菌、葡萄球菌、假单胞菌和沙雷氏菌)的丰度显著降低。这种减少与野生型白色体色鱼(WW)的下调相平行,而与野生型红色体色鱼(WR)形成对比。同时,在 SCARB1-/-鱼中,不仅在遗传和代谢水平上观察到下调,而且还观察到产脂肪酶细菌的减少。这种与 WW 的一致性与 WR 形成鲜明对比。同样,参与胆汁酸合成途径的基因以及与脂质代谢相关的血液代谢物在 SCARB1-/-鱼中也表现出下调。
SCARB1 敲除基因阻断导致肠道微生物群发生显著变化,可能影响观察到的与类胡萝卜素相关的皮肤色素沉着减少。我们的研究强调,皮肤色素沉着不仅受遗传因素影响,还受肠道微生物群影响。同时,肠道微生物群的适应性可以迅速形成,并且可能由特定的单基因突变驱动。