Host genetics and gut microbiota jointly regulate blood biochemical indicators in chickens

被引:7
作者
Jiang, Xinwei [1 ]
Zhang, Boxuan [1 ]
Lan, Fangren [1 ]
Zhong, Conghao [1 ]
Jin, Jiaming [1 ]
Li, Xiaochang [1 ]
Zhou, Qianqian [1 ]
Li, Junying [1 ]
Yang, Ning [1 ]
Wen, Chaoliang [1 ]
Sun, Congjiao [1 ]
机构
[1] China Agr Univ, Coll Anim Sci & Technol, Dept Anim Genet & Breeding, Beijing 100193, Peoples R China
基金
中国国家自然科学基金;
关键词
Chicken; Blood biochemical indicators; Host genetic variations; Gut microbiota; Joint regulation; WHOLE-GENOME ASSOCIATION; HIGH-DENSITY-LIPOPROTEIN; CHAIN FATTY-ACIDS; CHOLESTEROL; RISK; METABOLITES; PARAMETERS; INFERENCE; VARIANTS; QUALITY;
D O I
10.1007/s00253-023-12814-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Blood biochemical indicators play a crucial role in assessing an individual's overall health status and metabolic function. In this study, we measured five blood biochemical indicators, including total cholesterol (CHOL), low-density lipoprotein cholesterol (LDL-CH), triglycerides (TG), high-density lipoprotein cholesterol (HDL-CH), and blood glucose (BG), as well as 19 growth traits of 206 male chickens. By integrating host whole-genome information and 16S rRNA sequencing of the duodenum, jejunum, ileum, cecum, and feces microbiota, we assessed the contributions of host genetics and gut microbiota to blood biochemical indicators and their interrelationships. Our results demonstrated significant negative phenotypic and genetic correlations (r = - 0.20 similar to - 0.67) between CHOL and LDL-CH with growth traits such as body weight, abdominal fat content, muscle content, and shin circumference. The results of heritability and microbiability indicated that blood biochemical indicators were jointly regulated by host genetics and gut microbiota. Notably, the heritability of HDL-CH was estimated to be 0.24, while the jejunal microbiability for BG and TG reached 0.45 and 0.23. Furthermore, by conducting genome-wide association study (GWAS) with the single-nucleotide polymorphism (SNPs), insertion/deletion (indels), and structural variation (SV), we identified RAP2C, member of the RAS oncogene family (RAP2C), dedicator of cytokinesis 11 (DOCK11), neurotensin (NTS) and BOP1 ribosomal biogenesis factor (BOP1) as regulators of HDL-CH, and glycerophosphodiester phosphodiesterase domain containing 5 (GDPD5), dihydrodiol dehydrogenase (DHDH), and potassium voltage-gated channel interacting protein 1 (KCNIP1) as candidate genes of BG. Moreover, our findings suggest that cecal RF39 and Clostridia_UCG_014 may be linked to the regulation of CHOL, and jejunal Streptococcaceae may be involved in the regulation of TG. Additionally, microbial GWAS results indicated that the presence of gut microbiota was under host genetic regulation. Our findings provide valuable insights into the complex interaction between host genetics and microbiota in shaping the blood biochemical profile of chickens.
引用
收藏
页码:7601 / 7620
页数:20
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