Understanding the Passport


This guide explains the data fields and nomenclature used within the Microbial Clinical Atlas (MCA) Taxon Passports.

Identity

Passport ID
A stable, unique identifier for each taxon entry following the format MCA-[DOMAIN]-[NNNNNN].

[DOMAIN] prefixes indicate the organism type:

  • BAC: Bacteria
  • FUN: Fungi
  • VIR: Viruses
  • ARC: Archaea

[NNNNNN] is a unique six-digit numeric identifier that ensures permanent reference regardless of taxonomic updates.

TaxID
The official NCBI Taxonomy database identifier, linking each entry to a globally recognised taxonomic record. Clicking the TaxID opens the corresponding NCBI Taxonomy page.
BacDive ID
Identifier linking to the BacDive entry for this taxon's type strain. BacDive is a standardised microbiological culture collection database maintained by DSMZ, providing curated microbiological metadata including culture conditions, physiology, and isolation sources. Available at species level and below.
Rank
The taxonomic level of the entry, such as family, genus, species, or strain.
Lineage
The full taxonomic hierarchy from domain down to the specific rank of the entry.
Synonyms
Alternative scientific names and historical nomenclature sourced from NCBI Taxonomy.

Biology

Gram Status
Gram stain classification (positive, negative, or variable) for bacterial taxa. Sourced from BacDive.
Oxygen Tolerance
Classification of metabolic oxygen requirements (e.g., aerobe, obligate anaerobe, facultative anaerobe). Sourced from BacDive.
Morphology
Typical physical cell structure and shape (e.g., rod, coccus, spiral). Sourced from BacDive.
Key Traits
Biologically relevant features such as spore formation, biofilm production, or toxin production. Sourced from BacDive.

Ecology

Primary Niches
The specific body sites or environments where the organism is most commonly found (e.g., gut, oral cavity, skin). Sourced from BacDive.
Reservoir
The natural hosts or environments where the taxon persists: human, animal, or environment. Sourced from BacDive.
Transmission
The routes through which the organism is typically acquired (e.g., contact, foodborne, waterborne). Sourced from the curated literature.

Clinical Profile

Pathobiont
Whether this taxon is considered a pathobiont — a resident commensal that can cause disease under specific conditions. Values:
  • Yes — organism is a recognised pathobiont
  • Context dependent — pathobiont status depends on host factors, clinical setting, or taxonomic level
  • No — organism is not considered a pathobiont
  • Unknown — insufficient evidence to classify
Clinical Roles
The clinical characterisation of this taxon, such as opportunistic pathogen, protective commensal, or commensal. Extracted from curated literature.
Typical Specimen
Common specimen types in which the organism is identified in a clinical context (e.g., stool, blood, respiratory). Extracted from curated literature.
Risk Contexts
Clinical settings or patient populations where this taxon is most likely to cause harm (e.g., ICU, post-antibiotic, immunocompromised). Extracted from curated literature.
Antimicrobial Resistance
Notable resistance phenotypes that impact clinical management (e.g., ESBL, CRE, VRE). Extracted from curated literature. Where available, linked to the CARD Antibiotic Resistance Ontology (ARO):
multidrug-resistant (MDR) 3004305
Bloom Triggers
Conditions that enable this taxon to expand to clinically relevant abundance (e.g., antibiotic exposure, immunosuppression). Extracted from curated literature. Specific drugs are linked to KEGG Drug (D numbers):
proton pump inhibitor (PPI) use D00455
Virulence Factors
Molecular factors that contribute to pathogenicity (e.g., toxins, adhesins, capsule). Linked to the Virulence Factor Database (VFDB) where available:
Toxin A VF0592

Metabolites

Metabolite Relationships
Documented metabolic interactions between this taxon and specific compounds. Each entry describes the relationship type:
  • Produces — taxon synthesises this metabolite
  • Consumes — taxon degrades or consumes this metabolite
  • Modifies — taxon chemically transforms this metabolite
Compounds are linked to KEGG Compound (C numbers) and ChEBI IDs (CHEBI:XXXXXX) where available. IDs are displayed as clickable badges linking to their respective databases.

Clinical Associations

Association
An individual, evidence-graded claim linking this taxon to a specific clinical condition or outcome, extracted from a peer-reviewed publication. Each association is supported by at least one PMID and assigned an evidence grade:
E3 — Strong human clinical evidence
Supported by systematic reviews, meta-analyses, clinical guidelines, or multiple independent human cohorts reported in a single paper.
E2 — Moderate human evidence
Supported by a single human cohort, RCT, case-control, or cross-sectional study.
E1 — Limited / preliminary
Supported by animal models, in vitro studies, case reports, or mechanistic work only.
MeSH
Standardised Medical Subject Headings (MeSH) terms assigned by NLM to the source paper, filtered to those directly relevant to the association. Clicking a badge opens the NLM MeSH Browser entry.
Cross Infection D003428
KEGG
KEGG Disease identifiers mapping the associated clinical condition to KEGG's disease classification. Clicking a badge opens the corresponding KEGG Disease entry.
Enterococcal infection H01444

Evidence Timeline

Timeline
A chronological summary of the papers that contributed clinical associations to this passport. Each card shows the publication year and study design. Clicking a card opens the source paper on PubMed.

Related Taxa

Related Taxa
Other taxa in the MCA database that share at least one annotated attribute with this entry. Two match types are shown:
  • Shared Niche — both taxa occupy the same primary body site or environment
  • Shared Risk — both taxa are associated with the same clinical risk context or vulnerable population
Clicking a related taxon card opens its passport in a new tab.