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TaxSEA is an R package designed to enable rapid interpretation of differential abundance analysis or correlation analysis output for microbiota data. TaxSEA takes as input a vector of genus or species names and a rank. For example log2 fold changes or Spearman's rho. TaxSEA then uses a Kolmogorov-Smirnov test to identify if a particular group of species or genera (i.e. a set of taxa such as butyrate producers) are skewed to one end of the distribution .
Simply put, TaxSEA allows users to rapidly convert species/genus level changes to alterations in
- Metabolite producers
- Disease signatures
- Previously published associations
Note: Although TaxSEA in principle can be applied to microbiome data from any source, the databases utilized largely cover human associated microbiomes and the human gut microbiome in particular. As such TaxSEA will likely perform best on human gut microbiome data.
TaxSEA utilizes taxon sets generated from five reference databases (gutMGene, GMrepo v2, MiMeDB, mBodyMap, BugSigDB).
Please cite the appropriate database if using:
- Cheng et al. gutMGene: a comprehensive database for target genes of gut microbes and microbial metabolites Nucleic Acids Res. 2022.
- Dai et al. GMrepo v2: a curated human gut microbiome database with special focus on disease markers and cross-dataset comparison Nucleic Acids Res. 2022.
- Wishart et. al. MiMeDB: the Human Microbial Metabolome Database Nucleic Acids Res. 2023.
- Jin et al. mBodyMap: a curated database for microbes across human body and their associations with health and diseases. Nucleic Acids Res. 2022.
- Geistlinger et al. BugSigDB captures patterns of differential abundance across a broad range of host-associated microbial signatures. Nature Biotech. 2023.
library(devtools)
install_github("feargalr/TaxSEA")
library(TaxSEA)
library(TaxSEA)
# Retrieve taxon sets containing Bifidobacterium longum.
blong.sets <- get_taxon_sets(taxon="Bifidobacterium_longum")
# Run TaxSEA with test data provided
data(TaxSEA_test_data)
taxsea_results <- TaxSEA(taxon_ranks=TaxSEA_test_data)
#Enrichments among metabolite producers from gutMgene and MiMeDB
metabolites.df <- taxsea_results$Metabolite_producers
#Enrichments among health and disease signatures from GMRepoV2 and mBodyMap
disease.df <- taxsea_results$Health_associations
#Enrichments amongh published associations from BugSigDB
bsdb.df <- taxsea_results$BugSigdB
All that is required for TaxSEA is a vector in R containing ranks (e.g. log2 fold changes) and names (E.g. species/genus). TaxSEA will not work for ranks higher than species or genus. The input should be for all taxa tested, and not limited to only a pre-defined set (e.g. do not use a threshold for significance or remove any taxa). See example below for format. TaxSEA will lookup and convert taxon names to NCBI taxonomic identifiers. TaxSEA stores a commonly observed identifiers internally and so will only look up whatever is not covered to save time.
Input IDs should be in the format of like one of the following
- Species name. E.g. "Bifidobacterium longum", "Bifidobacterium_longum"
- Genus name. E.g. "Bifidobacterium"
- NCBI ID E.g. 216816
#Input IDs with the full taxonomic lineage should be split up. E.g.
x <- "d__Bacteria.p__Actinobacteriota.c__Actinomycetes.o__Bifidobacteriales.f__Bifidobacteriaceae.g__Bifidobacterium"
x <- strsplit(x,split="\\.")[[1]][6]
x <- gsub("g__","",x)
## Running this through a vector of IDs may look something like the following
#new_ids <- sapply(as.character(old_ids),function(y) {strsplit(x = y,split="\\.")[[1]][6]})
#new_ids <- gsub("g__","",new_ids)
## Example test data
library(TaxSEA)
data("TaxSEA_test_data")
head(sample(TaxSEA_test_data),4)
data("TaxSEA_test_data")
taxsea_results <- TaxSEA(taxon_ranks=TaxSEA_test_data)
#Enrichments among metabolite producers from gutMgene and MiMeDB
metabolites.df <- taxsea_results$Metabolite_producers
#Enrichments among health and disease signatures from GMRepoV2 and mBodyMap
disease.df <- taxsea_results$Health_associations
#Enrichments among published associations from BugSigDB
bsdb.df <- taxsea_results$BugSigdB
The test data provided with TaxSEA consists of log2 fold changes comparing between healthy and IBD. The count data for this was downloaded from curatedMetagenomeData and fold changes generated with LinDA.
- Hall et al. A novel Ruminococcus gnavus clade enriched in inflammatory bowel disease patients** Genome Med. 2017 Nov 28;9(1):103.
- Pasolli et al. Accessible, curated metagenomic data through ExperimentHub. Nat Methods. 2017 Oct 31;14(11):1023-1024. doi: 10.1038/nmeth.4468.
- Zhou et al. LinDA: linear models for differential abundance analysis of microbiome compositional data. Genome Biol. 2022 Apr 14;23(1):95.
> head(sample(TaxSEA_test_data),4)
Bacteroides_thetaiotaomicron Blautia_sp_CAG_257 Ruminococcus bromii Clostridium_disporicum
1.908 3.650 -5.038 0.300
The output is a list of three data frames providing enrichment results for metabolite produers, health/disease associations, and published signatures from BugSigDB. Each dataframe has 5 columns
- taxonSetName - The name of the taxon set tested
- median_rank - This is simply the median rank across all detected members in the set. This allows you to see the direction of change
- P value - Kolmogorov-Smirnov test P value.
- FDR - P value adjusted for multiple testing.
- TaxonSet - Returns list of taxa in the set to show what is driving the signal
The results above were generated by using TaxSEA on the output of a differential abundance analysis comparing between disease and control. The input was per spcies log2 fold changes between taxa in Inflammatory Bowel disease and control. TaxSEA identified a significant depletion in the producers of certain short chain fatty acids. Using barplots we can show the overall signatures identified as significantly different. We can then highlight the individual species contributing to this signature on a volcano plot.
The format of BugSigDB is that each publication is entered as a "Study", and within this there is different experiments and signatures. For example signature 1 may be taxa increased in an experiment, and signature 2 taxa that are decreased. Users can find out more by querying the BugSigDB. See below for an example.
library(bugsigdbr) #This package is installable via Bioconductor
bsdb <- importBugSigDB() #Import database
#E.g. if the BugSigDB identifier you found enriched was #bsdb:74/1/2_obesity:obese_vs_non-obese_DOWN
#This is Study 74, Experiment 1, Signature 2
bsdb[bsdb$Study=="Study 74" &
bsdb$Experiment=="Experiment 1" &
bsdb$Signature=="Signature 2",]
The TaxSEA function by default uses the Kolmogorov Smirnov test and the original idea was inspired by gene set enrichment analyses from RNASeq. Should users wish to use an alternative gene set enrichment analysis tool the database is formatted in such a way that should be possible. See below for an example with fast gene set enrichment analysis (fgsea).
library(fgsea) #This package is installable via Bioconductor
data(TaxSEA_DB)
#Convert input names to NCBI taxon ids
names(TaxSEA_test_data) = get_ncbi_taxon_ids(names(TaxSEA_test_data))
TaxSEA_test_data = TaxSEA_test_data[!is.na(names(TaxSEA_test_data))]
#Run fgsea
fgsea_results <- fgsea(TaxSEA_db, TaxSEA_test_data, minSize=5, maxSize=500)