4.7 Article

Comprehensive functional core microbiome comparison in genetically obese and lean hosts under the same environment

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COMMUNICATIONS BIOLOGY
卷 4, 期 1, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s42003-021-02784-w

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  1. Spanish National research plan [AGL2017-86083-C2-1-P]
  2. Generalitat Valenciana [APOSTD/2017/060]

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This study provides a comprehensive comparison of microbiome core functionalities between hosts with different genotypes for intramuscular lipid deposition. The differential abundances of microbial genes were found to be influenced by host genetics, shedding light on the impact of host genetic determination on lipid accretion in muscle. The results have implications for the development of strategies targeting obesity.
Our study provides an exhaustive comparison of the microbiome core functionalities (captured by 3,936 microbial gene abundances) between hosts with divergent genotypes for intramuscular lipid deposition. After 10 generations of divergent selection for intramuscular fat in rabbits and 4.14 phenotypic standard deviations (SD) of selection response, we applied a combination of compositional and multivariate statistical techniques to identify 122 cecum microbial genes with differential abundances between the lines (ranging from -0.75 to +0.73 SD). This work elucidates that microbial biosynthesis lipopolysaccharides, peptidoglycans, lipoproteins, mucin components, and NADH reductases, amongst others, are influenced by the host genetic determination for lipid accretion in muscle. We also differentiated between host-genetically influenced microbial mechanisms regulating lipid deposition in body or intramuscular reservoirs, with only 28 out of 122 MGs commonly contributing to both. Importantly, the results of this study are of relevant interest for the efficient development of strategies fighting obesity. Martinez-alvaro et al. employ metagenomic sequencing to compare the differences in caecum microbiome between lean and genetically obese rabbits exhibiting different levels of intramuscular fat. Lipid aggregation in muscle can be attributed to host genetic interactions with microbial biosynthetic products.

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