Dietary Fatty Acid Intake and the Colonic Gut Microbiota in Humans

被引:39
作者
Xu, Anthony A. [1 ]
Kennedy, Luke K. [1 ]
Hoffman, Kristi [2 ]
White, Donna L. [1 ,3 ,4 ]
Kanwal, Fasiha [1 ,3 ,4 ,5 ]
El-Serag, Hashem B. [1 ,3 ,4 ,5 ]
Petrosino, Joseph F. [2 ]
Jiao, Li [1 ,6 ]
机构
[1] Baylor Coll Med, Dept Med, Houston, TX 77030 USA
[2] Baylor Coll Med, Alkek Ctr Metagen & Microbiome Res, Dept Mol Virol & Microbiol, Houston, TX 77030 USA
[3] Michael E DeBakey VA Med Ctr, Ctr Innovat Qual Effectiveness & Safety, Houston, TX 77030 USA
[4] Texas Med Ctr Digest Dis Ctr, Houston, TX 77030 USA
[5] Michael E DeBakey VA Med Ctr, Sect Gastroenterol, Houston, TX 77030 USA
[6] Harris Cty Publ Hlth, Houston, TX 77030 USA
关键词
diet; fat; microbiome; mucosa; human; epidemiology; Sutterella; CARDIOVASCULAR-DISEASE; ASSOCIATIONS; MORTALITY; SUPPORT; RISK;
D O I
10.3390/nu14132722
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
A high-fat diet has been associated with systemic diseases in humans and alterations in gut microbiota in animal studies. However, the influence of dietary fatty acid intake on gut microbiota in humans has not been well studied. In this cross-sectional study, we examined the association between intake of total fatty acids (TFAs), saturated fatty acids (SFAs), trans fatty acids (TrFAs), monounsaturated fatty acids (MUFAs), polyunsaturated fatty acids (PUFAs), n3-FAs, and n6-FAs, and the community composition and structure of the adherent colonic gut microbiota. We obtained 97 colonic biopsies from 34 participants with endoscopically normal colons. Microbial DNA was used to sequence the 16S rRNA V4 region. The DADA2 and SILVA database were used for amplicon sequence variant assignment. Dietary data were collected using the Block food frequency questionnaire. The biodiversity and the relative abundance of the bacterial taxa by higher vs. lower fat intake were compared using the Mann-Whitney test followed by multivariable negative binomial regression model. False discovery rate-adjusted p-values (q value) < 0.05 indicated statistical significance. The beta diversity of gut bacteria differed significantly by intake of all types of fatty acids. The relative abundance of Sutterella was significantly higher with higher intake of TFAs, MUFAs, PUFAs, and n6-FAs. The relative abundance of Tyzzerella and Fusobacterium was significantly higher with higher intake of SFAs. Tyzzerella was also higher with higher intake of TrFA. These observations were confirmed by multivariate analyses. Dietary fat intake was associated with bacterial composition and structure. Sutterella, Fusobacterium, and Tyzzerella were associated with fatty acid intake.
引用
收藏
页数:13
相关论文
共 64 条
[1]   Habitual Sleep Duration and the Colonic Mucosa-Associated Gut Microbiota in Humans-A Pilot Study [J].
Agrawal, Ritwick ;
Ajami, Nadim J. ;
Malhotra, Sonal ;
Chen, Liang ;
White, Donna L. ;
Sharafkhaneh, Amir ;
Hoffman, Kristi L. ;
Graham, David Y. ;
El-Serag, Hashem B. ;
Petrosino, Joseph F. ;
Li Jiao .
CLOCKS & SLEEP, 2021, 3 (03) :387-397
[2]   Quantitative trait loci analysis using the false discovery rate [J].
Benjamini, Y ;
Yekutieli, D .
GENETICS, 2005, 171 (02) :783-789
[3]   Gut Microbiome in Down Syndrome [J].
Biagi, Elena ;
Candela, Marco ;
Centanni, Manuela ;
Consolandi, Clarissa ;
Rampelli, Simone ;
Turroni, Silvia ;
Severgnini, Marco ;
Peano, Clelia ;
Ghezzo, Alessandro ;
Scurti, Maria ;
Salvioli, Stefano ;
Franceschi, Claudio ;
Brigidi, Patrizia .
PLOS ONE, 2014, 9 (11)
[4]   Gut dysbiosis: a potential link between increased cancer risk in ageing and inflammaging [J].
Biragyn, Arya ;
Ferrucci, Luigi .
LANCET ONCOLOGY, 2018, 19 (06) :E295-E304
[5]   Dietary Fat and Cancer-Which Is Good, Which Is Bad, and the Body of Evidence [J].
Bojkova, Bianka ;
Winklewski, Pawel J. ;
Wszedybyl-Winklewska, Magdalena .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (11) :1-56
[6]   Analysis of Fusobacterium persistence and antibiotic response in colorectal cancer [J].
Bullman, Susan ;
Pedamallu, Chandra S. ;
Sicinska, Ewa ;
Claney, Thomas E. ;
Zhang, Xiaoyang ;
Cai, Diana ;
Neuberg, Donna ;
Huang, Katherine ;
Guevara, Fatima ;
Nelson, Timothy ;
Chipashvili, Otari ;
Hagan, Timothy ;
Walker, Mark ;
Ramachandran, Aruna ;
Diosdado, Begona ;
Serna, Garazi ;
Mulet, Nuria ;
Landolfi, Stefania ;
Ramon y Cajal, Santiago ;
Fasani, Roberta ;
Aguirre, Andrew J. ;
Ng, Kimmie ;
Elez, Elena ;
Ogino, Shuji ;
Tabernero, Josep ;
Fuchs, Charles S. ;
Hahn, William C. ;
Nuciforo, Paolo ;
Meyerson, Matthew .
SCIENCE, 2017, 358 (6369) :1443-+
[7]   Metabolic fate and function of dietary glutamate in the gut [J].
Burrin, Douglas G. ;
Stoll, Barbara .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2009, 90 (03) :850S-856S
[8]   TLR4 mediates high-fat diet induced physiological changes in mice via attenuating PPARγ/ABCG1 signaling pathway [J].
Cao, Xiao-Jie ;
Zhang, Ming-Jie ;
Zhang, Li-Li ;
Yu, Ke ;
Xiang, Yang ;
Ding, Xin ;
Fan, Jin ;
Li, Jing-Cheng ;
Wang, Qing-Song .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2018, 503 (03) :1356-1363
[9]   Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms [J].
Caporaso, J. Gregory ;
Lauber, Christian L. ;
Walters, William A. ;
Berg-Lyons, Donna ;
Huntley, James ;
Fierer, Noah ;
Owens, Sarah M. ;
Betley, Jason ;
Fraser, Louise ;
Bauer, Markus ;
Gormley, Niall ;
Gilbert, Jack A. ;
Smith, Geoff ;
Knight, Rob .
ISME JOURNAL, 2012, 6 (08) :1621-1624
[10]   Diet Dominates Host Genotype in Shaping the Murine Gut Microbiota [J].
Carmody, Rachel N. ;
Gerber, Georg K. ;
Luevano, Jesus M., Jr. ;
Gatti, Daniel M. ;
Somes, Lisa ;
Svenson, Karen L. ;
Turnbaugh, Peter J. .
CELL HOST & MICROBE, 2015, 17 (01) :72-84