fusiform shaped
METPO:1000690 · CLASS · REVIEWED
A cell shape that is wide in the middle and tapers at both ends.
Fusiform-shape tapered polar growth
Edge evidence
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graded polar peptidoglycan growth
has output
end-cap taper
RO:0002234Graded PG growth produces reduced end-cap radius.
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DOI:10.1146/annurev-cellbio-101011-155745polar growth
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end-cap taper
causes
tapered geometry
biolink:causesEnd-cap taper at both poles yields the fusiform body geometry.
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DOI:10.1146/annurev-cellbio-101011-155745cell shape is genetically determined
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tapered geometry
manifests as
fusiform shaped
METPO:2007400Tapered geometry at both poles manifests the fusiform-shaped trait.
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DOI:10.1111/1462-2920.13731Fusobacterium nucleatum
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MreB
guides
lateral peptidoglycan synthesis
MreB filaments orient lateral PG synthesis to maintain rod-like cell shape.
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DOI:10.1038/s41579-020-0366-3
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RodZ
regulates
MreB polymer localization/assembly
RO:0002211RodZ modulates geometric localization and assembly of MreB.
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DOI:10.1186/s12964-025-02373-y
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RodZ
scaffolds
elongasome complex
RodZ provides a scaffold for the elongasome via MreB, RodA, PBP2, PBP1A/1B.
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DOI:10.1038/s41579-020-0366-3
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MreC
activates
PBP2
RO:0002213MreC induces a structural change in PBP2 promoting its TPase activity.
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DOI:10.1038/s41579-020-0366-3
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RodA
required for
lateral peptidoglycan synthesis
SEDS protein RodA with cognate bPBP mediates lateral PG incorporation.
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DOI:10.1016/j.mib.2021.01.011
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FtsW
required for
septal peptidoglycan incorporation
FtsW with cognate bPBP mediates septal PG incorporation.
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DOI:10.1016/j.mib.2021.01.011
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Provenance
- Source
- METPO (2025-11-25)
- Definition source
- DOI:10.1146/annurev-cellbio-101011-155745
Parent traits (1)
Synonyms (1)
- fusiform
kg-microbe context
Matched 1 kg-microbe node via direct_metpo.
METPO:1000690[-2.797, -1.128, -4.645, -0.791, …]
Nearest neighbors in embedding space
- morphology tailed shaped 0.606
- morphology triangular shaped 0.554
- morphology crescent shaped 0.544
- morphology spindle shaped 0.541
- morphology spirochete shaped 0.535
- morphology streptococcus arrangement 0.534
- morphology sarcina arrangement 0.534
- morphology tetrad arrangement 0.534
Deep research
# Curation report: microbial fusiform shape ## Executive assessment **Target:** `METPO:1000690` (“fusiform shaped”), a reviewed morphology class defined as a cell that is wide in the middle and tapers at both ends. The literature strongly supports fusiform shape as a recognizable whole-cell phenotype, but direct mechanism-to-phenotype evidence remains sparse. The strongest current TraitMech candidates fall into two taxon-specific branches: 1. **Spatial peptidoglycan branch:** altered nucleotide-binding states of MreB drive polar localization and are associated with extremely tapered, pointed poles in *Caulobacter crescentus*. This is compelling evidence for formation of the tapered-pole component of fusiform geometry, although the mutant phenotype is not explicitly classified as `METPO:1000690`. (randich2015molecularmechanismsfor pages 7-9) 2. **Energy/metabolism branch:** deletion of `rnfC` in the naturally elongated *Fusobacterium nucleatum* produces short/stubby cells, sharply reduced ATP production, premature growth cessation, and broad amino-acid-metabolism defects. This establishes Rnf as necessary for normal fusobacterial morphology, but not yet as a fusiform-specific morphogen. (britton2024therespiratoryenzyme pages 5-7, britton2024therespiratoryenzyme media caddd5ad) Accordingly, a conservative graph should curate the direct perturbation edges while marking the final links to `METPO:1000690` as **taxon-specific or uncertain**. ## 1. Trait scope ### Operational meaning For microbial curation, fusiform should mean a **spindle-like whole cell whose transverse width reaches a maximum near midcell and declines toward both poles**. The phenotype should ideally be established by microscopy of intact cells rather than inferred from a genus name. A 2023 review provides a clear exemplar: *Helicobacter cetorum* has a “slightly helical, fusiform cell body that is tapered at both ends.” (bansil2023motilityofdifferent pages 1-2) *Tannerella forsythia* is independently described as a Gram-negative, anaerobic fusiform bacterium, and its historical designation was “fusiform Bacteroides.” (posch2012glycobiologyaspectsof pages 1-3, veith2015tannerellaforsythiaouter pages 1-2) ### Boundary cases Exclude or annotate separately: - **Ordinary rods:** approximately parallel lateral walls with rounded or blunt poles. - **Filamentous cells:** length alone does not imply fusiform shape. - **Vibrioid, curved, or helical cells:** curvature/helicity is an independent axis. *H. cetorum* can be both slightly helical and fusiform. (bansil2023motilityofdifferent pages 1-2) - **Unipolar tapering, prosthecae, or stalks:** fusiform requires narrowing at both ends of the cell body. - **Club-shaped or pleomorphic cells:** asymmetric width distributions do not meet the strict definition. - **Spores, fungal conidia, and transient division intermediates:** these should not be merged automatically with vegetative bacterial cell shape. - **Drug-induced or moribund shapes:** retain as assay-specific phenotypes unless normal growth and viability are demonstrated. - **“Extremely tapered and pointed poles” in MreB mutants:** highly relevant mechanistically, but curate as fusiform-like or tapered-pole morphology unless the source explicitly establishes maximum midcell width and bilateral tapering. (randich2015molecularmechanismsfor pages 7-9) ## 2. Current mechanistic understanding Peptidoglycan is the principal load-bearing bacterial cell-wall polymer, while MreB organizes elongation-associated wall synthesis in many rod-shaped bacteria. Fluorescent labeling shows that nascent peptidoglycan synthesis resembles MreB/Mbl distributions; MreB-associated synthetic and degradative proteins organize wall synthesis and normally enforce a cylindrical shape. This is authoritative background, not direct evidence for fusiform morphology. (egan2020regulationofpeptidoglycan pages 8-9) The more specific evidence comes from *C. crescentus*. MreB depletion produces lemon-shaped cells, whereas nucleotide-binding-pocket substitutions E213G, D16G, N21D, and A325P cause variable width with “extremely tapered and pointed” ends. In these mutants MreB localizes at the poles rather than dispersing laterally or condensing at the division plane. The review states that this behavior “presumably drives aberrant peptidoglycan synthesis,” and that wild-type tapered poles develop in the following cell cycle rather than during septation or medial elongation. The resulting model is that MreB nucleotide/ATPase state controls polar localization, which redirects polar wall remodeling and creates tapering. Because “presumably” and “could participate” are used, the localization-to-wall-synthesis edge is interpretive rather than fully demonstrated. (randich2015molecularmechanismsfor pages 7-9) The principal recent development is the 2024 *F. nucleatum* Rnf study. A non-polar, in-frame `rnfC` deletion drastically reduced ATP, caused premature cessation of culture growth, and converted elongated parental cells into short/stubby forms by electron microscopy. Viable counts remained comparable, arguing that the optical-density and morphology effects were not simply caused by cell death. Complementation restored relevant phenotypes. (britton2024therespiratoryenzyme pages 5-7, britton2024therespiratoryenzyme media caddd5ad) The same mutant had reduced `kamA`/`kamD` expression and extracellular lysine accumulation; 15 mM lysine blocked RadD-mediated coaggregation. It also showed reduced MegL, `cysK1`, and `cysK2` expression, deficient H₂S production, altered abundance of 17 of more than 80 detected metabolites, and reduced butyrate. These results connect ion-gradient-dependent energy conservation and amino-acid metabolism to envelope growth and morphology, but the study does not isolate which metabolic lesion causes the short/stubby phenotype. (britton2024therespiratoryenzyme pages 2-5, britton2024therespiratoryenzyme pages 5-7) ## 3. Candidate nodes grouped by type ### Trait and taxa - **fusiform shaped** — `METPO:1000690` - *Fusobacterium* — `NCBITaxon:851` - *Fusobacterium nucleatum* — `NCBITaxon:203492` - *Tannerella forsythia* — `NCBITaxon:28112` - *Helicobacter cetorum* — label-only pending curator verification of the taxon CURIE - *Caulobacter crescentus* — label-only pending curator verification of the strain/taxon CURIE ### Genes and proteins - **MreB**, including E213G, D16G, N21D, and A325P variants — label-only; species-specific identifiers should be assigned from the exact strain record. - **Rnf respiratory complex** and `rnfC`, `rnfD` — label-only pending exact strain-specific protein accessions. - **FtsZ**, elongasome, and divisome — contextual nodes only; no direct fusiform-specific perturbation was retrieved.
Curation history
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SEEDED_FROM_METPO · seed_from_metpo
imported from data/raw/metpo.owl (CLASS)
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CURATED_CAUSAL_GRAPH · claude
Added DOI-backed causal graph linking graded polar peptidoglycan growth and end-cap taper to fusiform morphology.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2000202×1).
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2007400×1).
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RENAME_PREDICATE_LABELS · claude
Renamed 1 causal-edge predicate label(s) to align with existing groundings: shapes → causes ×1.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (biolink:causes×1).
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ENRICH_CAUSAL_GRAPH · claude
Added 6 evidence-backed generic edges (10 new nodes) from the deep-research report.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 2 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002211×1, RO:0002213×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (UniProtKB:A0A1B1UYY2×1).
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GROUND_CAUSAL_NODES · claude
Grounded 5 causal-node grounding field(s) via mappings/node_grounding.tsv (UniProtKB:H1XNL6×1, UniProtKB:A0A1L9R356×1, UniProtKB:A0A2D2D7X6×1, UniProtKB:A0A0H2X1V4×1, UniProtKB:A0A0E1R950×1).
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RETRACT_DEAD_UNIPROT_GROUNDINGS · claude
Retracted 4 UniProtKB grounding(s) whose accessions are deleted from UniProt; nodes demoted to label-only pending re-grounding (docs/GROUNDING_POLICY.md)
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MIGRATE_MICROBE_DOMAIN_EDGES · claude
Re-grounded 1 causal edge(s) off microbe-domain METPO predicates (1 to has output), issue 301. The previous predicates are transitively rdfs:subPropertyOf METPO:2000001, whose rdfs:domain is METPO:1000525 (microbe), so a causal-graph subject entailed that the subject IS a microbe; CausalNodeTypeEnum has no organism member, so no such edge could ever satisfy the domain. Edge directions are unchanged - this pass only relabels and re-grounds. RO:0002234 (has output) is used where the subject is an activity, since biolink gives it the domain 'biological process or activity'; the METPO replacements are proposed in proposals/metpo_traitmech_v8 and v9 and are placeholder ids until METPO mints them.