EnteroBase
EnteroBase provides a curated repository and analysis framework for bacterial pathogen genomes to support genomic surveillance, population-structure analysis, cgMLST-based typing, and antimicrobial-resistance detection.
Key Features:
- Comprehensive Database: Manually curated genome sequence data and metadata for over 1.1 million bacterial isolates including Salmonella, Escherichia/Shigella, Mycobacterium tuberculosis, Streptococcus spp., Clostridioides, Vibrio, Helicobacter, Yersinia, Moraxella, and Clostridioides difficile.
- Antimicrobial Resistance Detection: Tools for detection of antimicrobial-resistance determinants directly from genomic data.
- Genomic Population Structure Visualization: A bubble-plot graphical tool visualizes bacterial genomic population structures based on pre-computed hierarchical clusters.
- Clostridioides difficile Specific Tools: Automatic retrieval and assembly of short reads from public databases, core-genome multilocus sequence typing (cgMLST), and organization of 18,254 quality-controlled C. difficile genomes into hierarchical clusters.
- Hierarchical Clustering for Epidemiology: cgMLST-based hierarchical clustering identifies and names populations of C. difficile across contexts from local transmission chains to epidemic strains.
- Statistical Associations with Epidemiological Data: Cluster assignments have been statistically associated with specific hospitals or wards and used to identify inter-hospital transmission in retrospective analyses.
- Integration with Existing Surveillance Methods: Hierarchical clustering correlates with k-mer-based classification and PCR ribotyping to enable comparisons with historical surveillance data.
Scientific Applications:
- Genomic surveillance and outbreak detection: Place newly collected isolates within a phylogenetic and epidemiological framework to identify transmission chains and outbreaks.
- Antimicrobial-resistance surveillance: Detect and track resistance determinants across populations and time.
- Population genetics and microbial diversity: Analyze population structure and diversity across multiple bacterial species.
- Epidemiological investigations: Associate genomic clusters with hospitals, wards, and inter-hospital transmission for retrospective and prospective studies.
- Comparative surveillance: Compare cgMLST-based hierarchical clusters with k-mer-based classification and PCR ribotyping for integration with historical datasets.
Methodology:
Automatic retrieval and assembly of short reads from public databases; core-genome multilocus sequence typing (cgMLST); pre-computed hierarchical clustering; k-mer-based classification comparisons; and statistical association analyses linking clusters to epidemiological metadata.
Topics
Details
- Tool Type:
- web application
- Added:
- 11/14/2019
- Last Updated:
- 1/23/2025
Operations
Publications
Dyer NP, Päuker B, Baxter L, Gupta A, Bunk B, Overmann J, Diricks M, Dreyer V, Niemann S, Holt KE, Rahman M, Brown PE, Stark R, Zhou Z, Ott S, Nübel U. EnteroBase in 2025: exploring the genomic epidemiology of bacterial pathogens. Nucleic Acids Research. 2024;53(D1):D757-D762. doi:10.1093/nar/gkae902. PMID:39441072. PMCID:PMC11701629.
Frentrup M, Zhou Z, Steglich M, Meier-Kolthoff JP, Göker M, Riedel T, Bunk B, Spröer C, Overmann J, Blaschitz M, Indra A, von Müller L, Kohl TA, Niemann S, Seyboldt C, Klawonn F, Kumar N, Lawley TD, García-Fernández S, Cantón R, del Campo R, Zimmermann O, Groß U, Achtman M, Nübel U. A publicly accessible database for Clostridioides difficile genome sequences supports tracing of transmission chains and epidemics. Microbial Genomics. 2020;6(8). doi:10.1099/mgen.0.000410. PMID:32726198. PMCID:PMC7641423.
Frentrup M, Zhou Z, Steglich M, Meier-Kolthoff JP, Göker M, Riedel T, Bunk B, Spröer C, Overmann J, Blaschitz M, Indra A, von Müller L, Kohl TA, Niemann S, Seyboldt C, Klawonn F, Kumar N, Lawley TD, García-Fernández S, Cantón R, del Campo R, Zimmermann O, Groß U, Achtman M, Nübel U. Global genomic population structure of <i>Clostridioides difficile</i>. Unknown Journal. 2019. doi:10.1101/727230.