bacillus shaped
METPO:1000667 · CLASS · REVIEWED
A cell shape characterized by an elongated, rod cylindrical morphology with relatively parallel sides and rounded ends.
Bacillus-shape rod elongation mechanism
Edge evidence
-
MreB
interacts with
Rod complex
biolink:interacts_withMreB filaments interact with the Rod complex that elongates the cell wall.
-
DOI:10.1146/annurev-cellbio-010521-010834MreB filaments interact with Rod complexes
-
-
Rod complex
directs
peptidoglycan synthesis
RO:0002211Rod complexes direct sidewall peptidoglycan synthesis.
-
DOI:10.1146/annurev-cellbio-010521-010834Rod complexes drive cell wall insertion
-
-
peptidoglycan synthesis
has output
lateral cell-wall elongation
RO:0002234Directed peptidoglycan synthesis supports cylindrical elongation.
-
DOI:10.1038/nrmicro2677peptidoglycan synthesis to bacterial growth and morphology
-
-
lateral cell-wall elongation
regulates
bacillus shaped
RO:0002211Lateral wall elongation maintains bacillus-like rod morphology.
-
DOI:10.1016/j.tim.2011.11.004restores its rod shape
-
-
FtsZ
coordinates with
peptidoglycan synthesis
FtsZ coordinates division-associated peptidoglycan synthesis with rod-cell growth.
-
DOI:10.1038/nrmicro1205FtsZ collaborates with penicillin binding proteins
-
-
peptidoglycan cell wall
determines
bacillus shaped
The peptidoglycan cell wall protects against osmotic lysis and determines cell shape.
-
DOI:10.1038/s41467-023-39037-9
-
-
RodA-PBP2 synthase (Rod complex)
required for
bacterial cell elongation
RodA-PBP2 is the essential synthase responsible for bacterial elongation.
-
DOI:10.1038/s41467-023-39037-9
-
-
circumferential glycan strand insertion
gives rise to
bacillus shaped
Elongasome inserts long glycan strands as barrel-hoop reinforcement, giving rise to a rod-shaped cell.
-
DOI:10.1038/s41467-024-49785-x
-
-
moenomycin
inhibits
class A penicillin-binding proteins
RO:0002212Moenomycin inhibits class A penicillin-binding proteins, a family of PG synthases.
-
DOI:10.1038/s41467-023-41082-3
-
-
RodZ
causally upstream of, negative effect
spherical cell morphology
Loss of RodZ causes cells to become spherical, indicating RodZ maintains rod shape.
-
DOI:10.3389/fmicb.2024.1400434
-
Provenance
- Source
- METPO (2025-11-25)
- Author
- Anthea Guo
- Definition source
- DOI:10.1146/annurev-cellbio-010521-010834
Parent traits (1)
Synonyms (1)
- bacillus
kg-microbe context
Matched 1 kg-microbe node via direct_metpo.
METPO:1000667[-93.971, +37.913, +150.959, -201.986, …]
Nearest neighbors in embedding space
- environment facultatively aerobic 0.630
- morphology non-spore forming 0.602
- morphology gram negative 0.592
- morphology swarming motility 0.578
- morphology twitching motility 0.578
- morphology motile 0.578
- morphology non motile 0.496
- morphology gram positive 0.420
Deep research
# Curation report: bacillus-shaped morphology ## Trait record and scope - **Trait:** bacillus shaped - **Identifier:** **“METPO:1000667”** - **Category/kind/status:** MORPHOLOGY / CLASS / REVIEWED - **Parent:** METPO:1000666 - **Operational meaning:** a single microbial cell with an elongated cylindrical body, approximately parallel lateral sides, and rounded ends. Here, **bacillus** denotes morphology, not membership in the genus *Bacillus*. The trait should be assigned from an observed cell-shape phenotype, ideally during a specified growth phase and condition. It is not itself a physiological capacity or growth preference. In canonical bacteria, rod shape is propagated as the peptidoglycan (PG) sacculus expands: the Rod complex directs lateral PG insertion, whereas the divisome makes septal wall. A 2023 review states that the elongasome directs lateral insertion “along the long axis, enabling cylindrical growth,” with RodA and FtsW supporting elongation and division, respectively (galinier2023recentadvancesin pages 3-5). ### Boundaries - **Include:** straight rods and ordinary rod-length variants whose sides remain approximately parallel. - **Curved rods:** retain rod architecture but may merit an additional curvature trait; curvature-specific modules such as CrvA, crescentin, or porin–PapS should not define the generic bacillus-shaped graph. - **Coccobacilli/ovococci:** borderline where length-to-width ratio and parallel sidewalls are weak; require an explicit assay rule. - **Filaments:** elongated rods without normal septation should additionally receive a filamentous phenotype; filamentation is not equivalent to ordinary bacillus shape. - **Spheres, disks, L-forms, and pleomorphic cells:** exclude unless documenting a transition into or out of the rod state. Wall-deficient *Vibrio cholerae* spheroplasts lose rod organization and later regenerate branches of normal rod diameter, making this a useful regeneration assay rather than a constitutive trait (goudin2023recoveryofvibrio pages 1-2). - **Archaeal rods:** phenotypically in scope but mechanistically separate. *Haloferax volcanii* lacks bacterial PG and changes between rods and disks according to growth phase and swimming state; bacterial elongasome edges must not be projected onto it (schiller2024identificationofstructural pages 1-2). - **Noncanonical bacterial rods:** some Rhizobiales produce rods through unipolar growth without the standard MreB-mediated dispersed-growth program (williams2019mechanismsofpolar pages 57-61). ## Current mechanistic model The strongest general model is **distributed envelope synthesis plus mechanical feedback**, not “MreB alone specifies a cylinder.” MreB filaments orient active Rod complexes approximately around the circumference; RodA polymerizes glycan and PBP2 cross-links peptide stems. This yields anisotropic sidewall expansion while septal synthesis closes and rounds the ends. MreC, MreD, RodZ, hydrolases, aPBPs, precursor supply, and envelope mechanics regulate this core process (fivenson2023arolefor pages 1-2, galinier2023recentadvancesin pages 3-5). Recent work expands the model beyond PG alone. In Gram-negative *E. coli*, strengthening the outer membrane rescued growth and rod-shape defects of hypomorphic Rod-complex mutants and restored proper orientation of MreB-directed synthesis. Thus, rod propagation depends on the mechanical state of the whole envelope, although this result is taxon-specific (fivenson2023arolefor pages 1-2, fivenson2023arolefor media 0289c886). ## Candidate nodes grouped by type ### Trait and processes - bacillus shaped — **METPO:1000667** - cell morphogenesis — candidate **GO:0000902** - regulation of cell shape — candidate **GO:0008360** - peptidoglycan-based cell-wall biogenesis — candidate **GO:0009273** - cell-wall organization or biogenesis — candidate **GO:0071554** - lateral PG synthesis / cylindrical cell elongation — label-only until the project’s preferred process term is verified - septal PG synthesis / cell division - circumferential glycan insertion - sacculus mechanical anisotropy - cell diameter control - de novo rod-shape recovery ### Complexes and cellular structures - Rod complex / elongasome — MreB, MreC, MreD, RodZ, RodA, PBP2 - divisome — FtsZ-associated apparatus including FtsW–FtsI - peptidoglycan sacculus - cytoplasmic membrane - periplasm — candidate **GO:0042597** - Gram-negative outer membrane — candidate **GO:0009279** - MreB cytoskeletal filaments - FtsZ ring ### Genes and proteins - **mreB / MreB:** actin-like organizer of circumferential Rod-complex activity - **mreC / MreC:** Rod-complex regulator; evidence supports activation through PBP2–RodA in *E. coli* - **mreD / MreD:** core component, but its precise causal function remains incompletely resolved
Curation history
-
·
SEEDED_FROM_METPO · seed_from_metpo
imported from data/raw/metpo.owl (CLASS)
-
·
CURATED_WITH_LITERATURE · codex
Reviewed bacillus shape as rod-like morphology and added DOI-backed causal graph for MreB, Rod complex, peptidoglycan synthesis, lateral wall elongation, and FtsZ coupling.
-
·
GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (METPO:2000202×1).
-
·
GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002211×1).
-
·
RENAME_PREDICATE_LABELS · claude
Renamed 1 causal-edge predicate label(s) to align with existing groundings: maintains → regulates ×1.
-
·
GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002211×1).
-
·
GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (GO:0009252×1).
-
·
GROUND_CAUSAL_NODES · claude
Grounded 2 causal-node grounding field(s) via mappings/node_grounding.tsv (UniProtKB:A0A1B1UYY2×1, UniProtKB:C0LUM8×1).
-
·
RENAME_PREDICATE_LABELS · claude
Renamed 1 causal-edge predicate label(s) to align with existing groundings: organizes → enables ×1.
-
·
GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002327×1).
-
·
ENRICH_CAUSAL_GRAPH · claude
Added 5 evidence-backed generic edges (8 new nodes) from the deep-research report.
-
·
GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002212×1).
-
·
GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (CHEBI:28908×1).
-
·
GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (UniProtKB:H1XNL6×1).
-
·
RETRACT_DEAD_UNIPROT_GROUNDINGS · claude
Retracted 1 UniProtKB grounding(s) whose accessions are deleted from UniProt; nodes demoted to label-only pending re-grounding (docs/GROUNDING_POLICY.md)
-
·
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.
-
·
REGROUND_CAUSAL_EDGE · claude
Re-grounded causal edge(s) off enables/RO:0002327 onto part of (biolink:part_of), issue 334. biolink declares enables range 'biological process or activity', which only BIOLOGICAL_PROCESS, PATHWAY and MOLECULAR_FUNCTION satisfy, so an edge pointing at a GENE_OR_PROTEIN entailed a false type. The replacements are chosen per idiom rather than swept: a gene cluster ENCODES its product, a subunit is PART OF the complex it belongs to, and an energy source or acquired repertoire CONTRIBUTES TO the machine it powers or composes. All three declare no rdfs:domain or rdfs:range, so none can reintroduce the class of defect being removed.
-
·
REGROUND_CAUSAL_EDGE · claude
Corrected the mreB edge from part of to interacts with (biolink:interacts_with), issue 334 review. The first pass over-claimed: the edge's own snippet says MreB filaments INTERACT WITH Rod complexes, and the target node is described as machinery associated with MreB, so parthood is not what the evidence supports. The corpus is also split on it - cell_shape.yaml types rod_complex a PATHWAY with MreB inside it, while this file types it GENE_OR_PROTEIN with MreB outside - which makes parthood exactly the kind of modelling decision this work defers elsewhere. interacts with says what the quoted sentence says and needs no such decision. The edge description was rephrased to match the predicate.