Topic modeling for multi-omic integration in the human gut microbiome and implications for Autism

被引:2
|
作者
Tataru, Christine [1 ]
Peras, Marie [3 ]
Rutherford, Erica [3 ]
Dunlap, Kaiti [4 ]
Yin, Xiaochen [3 ]
Chrisman, Brianna S. [4 ]
DeSantis, Todd Z. [3 ]
Wall, Dennis P. [5 ,6 ]
Iwai, Shoko [3 ]
David, Maude M. [1 ,2 ]
机构
[1] Oregon State Univ, Dept Microbiol, SW Campus Way, Corvallis, OR 97331 USA
[2] Oregon State Univ, Sch Pharm, SW Campus Way, Corvallis, OR 97331 USA
[3] Second Genome Inc, 1000 Marina Blvd,Suite 500, Brisbane, CA 94005 USA
[4] Serra Mall, Dept Bioengn, Stanford, CA USA
[5] Serra Mall, Dept Biomed Data Sci, Stanford, CA USA
[6] Dept Pediat Syst Med, 1265 Welch Rd, Stanford, CA USA
关键词
DIAGNOSTIC OBSERVATION SCHEDULE; GAMMA-AMINOBUTYRIC-ACID; ESCHERICHIA-COLI; STEROID SULFATASE; SPECTRUM; CAFFEINE; METABOLITE; PROTEINS; HETEROGENEITY; ASSOCIATION;
D O I
10.1038/s41598-023-38228-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
While healthy gut microbiomes are critical to human health, pertinent microbial processes remain largely undefined, partially due to differential bias among profiling techniques. By simultaneously integrating multiple profiling methods, multi-omic analysis can define generalizable microbial processes, and is especially useful in understanding complex conditions such as Autism. Challenges with integrating heterogeneous data produced by multiple profiling methods can be overcome using Latent Dirichlet Allocation (LDA), a promising natural language processing technique that identifies topics in heterogeneous documents. In this study, we apply LDA to multi-omic microbial data (16S rRNA amplicon, shotgun metagenomic, shotgun metatranscriptomic, and untargeted metabolomic profiling) from the stool of 81 children with and without Autism. We identify topics, or microbial processes, that summarize complex phenomena occurring within gut microbial communities. We then subset stool samples by topic distribution, and identify metabolites, specifically neurotransmitter precursors and fatty acid derivatives, that differ significantly between children with and without Autism. We identify clusters of topics, deemed "cross-omic topics", which we hypothesize are representative of generalizable microbial processes observable regardless of profiling method. Interpreting topics, we find each represents a particular diet, and we heuristically label each cross-omic topic as: healthy/general function, age-associated function, transcriptional regulation, and opportunistic pathogenesis.
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页数:16
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