coccobacillus shaped
METPO:1000688 · CLASS · REVIEWED
A cell shape intermediate between spherical cocci and elongated bacilli, typically appearing as short or plump rods.
Coccobacillus short-rod morphogenesis mechanism
Edge evidence
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MreB
controls
peptidoglycan synthesis
RO:0002211MreB contributes to control of peptidoglycan synthetic complexes.
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DOI:10.1128/JB.187.1.54-64.2005control of the peptidoglycan synthetic complexes
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peptidoglycan synthesis
causes
short-rod geometry
biolink:causesWall synthesis patterns determine whether cells remain rod-like or become short coccobacilli.
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DOI:10.1128/JB.187.1.54-64.2005conditions causing changes in cell shape
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septal growth
contributes to
short-rod geometry
RO:0002326Division-associated septal growth contributes to the short-rod intermediate geometry.
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DOI:10.1128/JB.187.1.54-64.2005role at mid-cell ... in early septation
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short-rod geometry
confers
coccobacillus shaped
METPO:2007700Short-rod geometry produces the coccobacillus-shaped trait.
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DOI:10.1128/JB.187.1.54-64.2005from a rod to coccobacillus
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RodA/PBP3 elongasome
increases
cell length-to-width ratio
RO:0002213Elongasome-driven lateral wall synthesis increases the long-to-short axis ratio, opposing a coccoid shape.
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DOI:10.1128/mBio.03235-23
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cell length-to-width ratio
determines
short-rod geometry
A reduced but non-coccoid length-to-width ratio defines the short-rod geometry of coccobacilli.
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DOI:10.1128/mBio.03235-23
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GpsB
regulates
PBP2 localization
RO:0002211GpsB regulates the localization of PBP2 between cell periphery and division septum.
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DOI:10.1128/mBio.03235-23
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PBP2 localization
controls
peptidoglycan synthesis
RO:0002211Spatial localization of PBP2 controls where peptidoglycan insertion and crosslinking occur, biasing cells toward elongation or rounding.
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DOI:10.1128/mBio.03235-23
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FtsZ filament properties
directs
peptidoglycan synthesis
RO:0002211FtsZ filament geometry directs asymmetric, helical patterns of cell-wall insertion.
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DOI:10.1128/mBio.00908-16
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PBP2 (elongasome transpeptidase)
required for
short-rod geometry
PBP2 transpeptidase activity within the RodA-PBP2 elongasome is required to maintain non-spherical rod/short-rod geometry.
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DOI:10.1073/pnas.2215237120
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Provenance
- Source
- METPO (2025-11-25)
- Definition source
- DOI:10.1128/JB.187.1.54-64.2005
Parent traits (1)
Synonyms (1)
- coccobacillus
kg-microbe context
Matched 1 kg-microbe node via direct_metpo.
METPO:1000688[-20.154, -47.811, +18.193, -1.988, …]
Nearest neighbors in embedding space
- morphology ovoid shaped 0.438
- environment extremely halophilic 0.303
- environment non halophilic 0.238
- physiology autotrophic 0.206
- environment NaCl optimum mid2 0.189
- morphology non motile 0.176
- morphology branched shaped 0.174
- morphology disc shaped 0.170
Deep research
# Curation report: coccobacillus-shaped morphology ## Executive summary **Target:** **coccobacillus shaped** (`METPO:1000688`), morphology class, reviewed; parent `METPO:1000666`. The trait denotes a cell whose longitudinal axis remains discernible but is only modestly longer than its width—a short, squat, or plump rod intermediate between a bacillus and a coccus. It is a geometric phenotype, not a single conserved pathway. The strongest mechanistic evidence supports at least three context-specific routes: 1. **Physiological remodeling:** *Rhodobacter sphaeroides* changes from rods during aerobic growth to coccobacilli during photoheterotrophic growth; lower light increases the spherical character. 2. **Maintenance of an intrinsic short-rod state:** in *Acinetobacter baumannii*, zinc-stabilized PBP2 and the RodA–PBP2 elongasome maintain the characteristic short, squat rod. Loss of this machinery moves cells beyond the target state toward spheres. 3. **Evolutionary reduction of elongation:** stepwise loss of `yacF` and elongasome genes can drive rod/coccobacillus-to-coccus transitions in Neisseriaceae and Moraxellaceae. Accordingly, the best TraitMech model should represent **balanced lateral peptidoglycan elongation relative to septal growth** as the proximal shape mechanism, while keeping physiological, genetic, and evolutionary branches taxon-scoped. Peptidoglycan principally determines cell shape, and RodA/PBP2 extend the longitudinal axis by inserting lateral-wall material. (slovak2005localizationofmreb pages 1-2, micelli2023aconservedzincbinding pages 1-2) ## 1. Trait scope and boundaries ### Operational definition Curate `METPO:1000688` when microscopy or an authoritative taxonomic description identifies cells as **coccobacilli, short rods, squat rods, or plump rods**, ideally with images or length/width measurements. The phenotype may be constitutive or conditional. In *A. baumannii*, the experimentally described wild-type state is “short, squat rods”; in *R. sphaeroides*, photoheterotrophic cells are expressly “coccobacillus shaped.” (slovak2005localizationofmreb pages 1-2, micelli2023aconservedzincbinding pages 4-6) ### Boundary cases - **Coccus/spherical:** no sustained long axis. The spherical Δ`pbp2` phenotype in *A. baumannii* is an **out-of-class endpoint**, useful as loss-of-trait evidence but not as a positive instance of `METPO:1000688`. (micelli2023aconservedzincbinding pages 4-6) - **Ordinary bacillus/rod:** clearly elongated cells with a larger aspect ratio. Aerobic *R. sphaeroides* is the contrasting rod state. (slovak2005localizationofmreb pages 1-2) - **Filament:** excessive length or failed septation; not coccobacillary. Piperacillin–tazobactam-associated filamentation should not be mapped to this trait. (micelli2023aconservedzincbinding pages 4-6) - **Localized bulging/swelling:** amdinocillin produces mid-cell bulges in *R. sphaeroides*. This is evidence about PBP2-directed side-wall elongation, but it is not itself evidence for a uniform coccobacillus phenotype. (slovak2005localizationofmreb pages 7-10) - **Pleomorphism:** a heterogeneous population should receive the coccobacillus trait only if that state is explicitly observed and its frequency or growth condition is recorded. - **Taxonomic label versus measured state:** calling a genus “coccobacillary” does not prove that every strain or growth condition has the same morphology. ### Recommended assay representation Record growth phase, medium, oxygen regime, illumination, temperature, perturbation, imaging method, cell count, median length, median width, and aspect-ratio distribution. “Short rod” without measurements is acceptable but weaker. A universal numerical aspect-ratio cutoff is not supported by the retrieved literature and should not be invented. ## 2. Candidate graph nodes ### Trait and phenotype nodes - **coccobacillus shaped** — `METPO:1000688` - short/squat rod — label-only synonym or narrower assay description - rod-shaped cell — label-only unless an approved METPO identifier is verified - spherical/coccal cell — label-only contrasting phenotype - increased cell width — label-only quantitative phenotype - bacterial cell morphogenesis — `GO:0000902` ### Taxa - *Acinetobacter baumannii* — `NCBITaxon:470` - *Rhodobacter sphaeroides* — `NCBITaxon:1063` - *Neisseria elongata* — use label-only until the intended strain-level taxon is verified - Neisseriaceae and Moraxellaceae — label-only unless exact taxonomic CURIEs are validated during YAML curation ### Genes, proteins, and complexes - `pbp2` / penicillin-binding protein 2 (PBP2; class-B PBP transpeptidase) — label-only; use a strain-specific UniProt identifier only after sequence verification - `rodA` / RodA, SEDS-family peptidoglycan glycosyltransferase — label-only - RodA–PBP2 complex — label-only complex - elongasome/rod system — label-only cellular machinery - `mreB`, `mreC`, `mreD`, `rodZ` — label-only - `yacF` / ZapD — label-only; note nomenclature and taxon dependence - `pbpC` — label-only because gene naming can be taxon-specific
Curation history
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SEEDED_FROM_METPO · seed_from_metpo
imported from data/raw/metpo.owl (CLASS)
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CURATED_WITH_LITERATURE · codex
Added DOI-backed definition and causal graph for MreB, peptidoglycan synthesis, septal growth, and short-rod coccobacillus geometry.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 2 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002326×1, METPO:2000202×1).
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002211×1).
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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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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (GO:0009252×1).
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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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ENRICH_CAUSAL_GRAPH · claude
Added 6 evidence-backed generic edges (6 new nodes) from the deep-research report.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 4 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002211×3, RO:0002213×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (UniProtKB:A0A060RK42×1).
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RETRACT_DEAD_UNIPROT_GROUNDINGS · claude
Retracted 2 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 confers), 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.