Drinking alcohol is associated with variation in the human oral microbiome in a large study of American adults

被引:177
作者
Fan, Xiaozhou [1 ]
Peters, Brandilyn A. [1 ]
Jacobs, Eric J. [2 ]
Gapstur, Susan M. [2 ]
Purdue, Mark P. [3 ]
Freedman, Neal D. [3 ]
Alekseyenko, Alexander V. [4 ,5 ]
Wu, Jing [1 ]
Yang, Liying [6 ]
Pei, Zhiheng [7 ,8 ,9 ]
Hayes, Richard B. [1 ,7 ]
Ahn, Jiyoung [1 ,7 ]
机构
[1] NYU, Dept Populat Hlth, Sch Med, 650 First Ave,Room 518, New York, NY 10016 USA
[2] Amer Canc Soc, Epidemiol Res Program, 250 Williams St NW, Atlanta, GA 30303 USA
[3] NCI, Div Canc Epidemiol & Genet, 9609 Med Ctr Dr, Rockville, MD 20850 USA
[4] Med Univ South Carolina, Program Human Microbiome Res, Biomed Informat Ctr, Dept Publ Hlth Sci, Charleston, SC 29425 USA
[5] Med Univ South Carolina, Program Human Microbiome Res, Biomed Informat Ctr, Dept Oral Hlth Sci, Charleston, SC 29425 USA
[6] NYU, Dept Med, Sch Med, 423 East 23rd St, New York, NY 10010 USA
[7] NYU, Laura & Isaac Perlmutter Canc Inst, 522 First Ave, New York, NY 10016 USA
[8] NYU, Dept Pathol, Sch Med, 550 First Ave, New York, NY 10016 USA
[9] Dept Vet Affairs New York Harbor Healthcare Syst, New York, NY 10010 USA
关键词
Oral microbiome; 16s rRNA genes; Alcohol consumption; Large population-based study; HUMAN PERIODONTAL-DISEASE; SISTER-CHROMATID EXCHANGES; ACTINOBACILLUS-ACTINOMYCETEMCOMITANS; PROBIOTIC LACTOBACILLUS; ACETALDEHYDE PRODUCTION; CONSUMPTION; ETHANOL; ENDOCARDITIS; SALIVA; METABOLISM;
D O I
10.1186/s40168-018-0448-x
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Dysbiosis of the oral microbiome can lead to local oral disease and potentially to cancers of the head, neck, and digestive tract. However, little is known regarding exogenous factors contributing to such microbial imbalance. Results: We examined the impact of alcohol consumption on the oral microbiome in a cross-sectional study of 1044 US adults. Bacterial 16S rRNA genes from oral wash samples were amplified, sequenced, and assigned to bacterial taxa. We tested the association of alcohol drinking level (non-drinker, moderate drinker, or heavy drinker) and type (liquor, beer, or wine) with overall microbial composition and individual taxon abundance. The diversity of oral microbiota and overall bacterial profiles differed between heavy drinkers and non-drinkers (alpha-diversity richness p = 0.0059 and beta-diversity unweighted UniFrac p = 0.0036), and abundance of commensal order Lactobacillales tends to be decreased with higher alcohol consumption (fold changes = 0.89 and 0.94 for heavy and moderate drinkers, p trend = 0.005 [q = 0.064]). Additionally, certain genera were enriched in subjects with higher alcohol consumption, including Actinomyces, Leptotrichia, Cardiobacterium, and Neisseria; some of these genera contain oral pathogens, while Neisseria can synthesize the human carcinogen acetaldehyde from ethanol. Wine drinkers may differ from non-drinkers in microbial diversity and profiles (alpha-diversity richness p = 0.048 and beta-diversity unweighted UniFrac p = 0.059) after controlling for drinking amount, while liquor and beer drinkers did not. All significant differences between drinkers and non-drinkers remained after exclusion of current smokers. Conclusions: Our results, from a large human study of alcohol consumption and the oral microbiome, indicate that alcohol consumption, and heavy drinking in particular, may influence the oral microbiome composition. These findings may have implications for better understanding the potential role that oral bacteria play in alcohol-related diseases.
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页数:15
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