High-Fat Diet Consumption Induces Microbiota Dysbiosis and Intestinal Inflammation in Zebrafish

被引:0
作者
Nerea Arias-Jayo
Leticia Abecia
Laura Alonso-Sáez
Andoni Ramirez-Garcia
Alfonso Rodriguez
Miguel A. Pardo
机构
[1] Azti,Food research
[2] CIC bioGUNE,Marine research
[3] Azti,Departmento de Immunología, Microbiología y Parasitología, Facultad de Ciencia y Tecnología
[4] Universidad del País Vasco (UPV/EHU),undefined
[5] St Luke’s General Hospital,undefined
来源
Microbial Ecology | 2018年 / 76卷
关键词
Zebrafish; Microbiota; Inflammation; High-fat diet;
D O I
暂无
中图分类号
学科分类号
摘要
Energy-dense foods and overnutrition represent major starting points altering lipid metabolism, systemic inflammation and gut microbiota. The aim of this work was to investigate the effects of a high-fat diet (HFD) over a period of 25 days on intestinal microbiota and inflammation in zebrafish. Microbial composition of HFD-fed animals was analysed and compared to controls by 16S rRNA sequencing and quantitative PCR. The expression level on several genes related to inflammation was tested. Furthermore, microscopic assessment of the intestine was performed in both conditions. The consumption of the HFD resulted in microbial dysbiosis, characterised by an increase in the relative abundance of the phylum Bacteroidetes. Moreover, an emerging intestinal inflammation via NF-κβ activation was confirmed by the overexpression of several genes related to signalling receptors, antimicrobial metabolism and the inflammatory cascade. The intestinal barrier was also damaged, with an increase of goblet cell mucin production. This is the first study performed in zebrafish which suggests that the consumption of a diet enriched with 10% fat changes the intestinal microbial community composition, which was correlated with low-grade inflammation.
引用
收藏
页码:1089 / 1101
页数:12
相关论文
共 391 条
[31]  
Burcelin R(2012)A new zebrafish model of oro-intestinal pathogen colonization reveals a key role for adhesion in protection by probiotic bacteria PLoS Pathog 8 e1-80
[32]  
Landgraf K(2013)Evaluation of general 16S ribosomal RNA gene PCR primers for classical and next-generation sequencing-based diversity studies Nucleic Acids Res 41 2957-408
[33]  
Schuster S(2011)FLASH: fast length adjustment of short reads to improve genome assemblies Bioinformatics 27 7537-1032
[34]  
Meusel A(2009)Introducing mothur: open-source, platform-independent, community-supported software for describing and comparing microbial communities Appl Environ Microbiol 75 1889-299
[35]  
Garten A(2010)Ironing out the wrinkles in the rare biosphere through improved OTU clustering Environ Microbiol 12 e27310-188
[36]  
Riemer T(2011)Reducing the effects of PCR amplification and sequencing artifacts on 16S rRNA-based studies PLoS One 6 5261-125
[37]  
Schleinitz D(2007)Naïve Bayesian classifier for rapid assignment of rRNA sequences into the new bacterial taxonomy Appl Environ Microbiol 73 7560-300
[38]  
Kiess W(2013)Galacto-oligosaccharides derived from lactulose exert a selective stimulation on the growth of Bifidobacterium animalis in the large intestine of growing rats J Agric Food Chem 61 1601-300
[39]  
Korner A(2006)Comparison of relative mRNA quantification models and the impact of RNA integrity in quantitative real-time RT-PCR Biotechnol Lett 28 71-1772
[40]  
Stephens WZ(2015)Use of gnotobiotic zebrafish to study Vibrio anguillarum pathogenicity Zebrafish 12 402-28