helical shaped
METPO:1000676 · CLASS · REVIEWED
A cell shape in which an organism has a corkscrew-like helical cell body with curvature and twist along its long axis.
Helical-shape peptidoglycan relaxation mechanism
Edge evidence
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Csd shape proteins
promotes
peptidoglycan crosslink relaxation
RO:0002213Csd peptidoglycan endopeptidase homologs contribute to reduced crosslinking in helical-shape generation.
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DOI:10.1016/j.cell.2010.03.046three LytM peptidoglycan endopeptidase homologs
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CcmA
contributes to
peptidoglycan crosslink relaxation
RO:0002326CcmA contributes to the shape-generating pathway for helical morphology.
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DOI:10.1016/j.cell.2010.03.046three LytM peptidoglycan endopeptidase homologs ... and a ccmA homolog
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peptidoglycan crosslink relaxation
enables
helical curvature and twist
RO:0002327Relaxed peptidoglycan crosslinking enables curvature and twist.
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DOI:10.1016/j.cell.2010.03.046relaxes peptidoglycan crosslinking, enabling helical cell curvature and twist
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helical curvature and twist
confers
helical shaped
METPO:2007700Helical curvature and twist produce the helical-shaped trait.
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DOI:10.1016/j.cell.2010.03.046helical cell curvature and twist
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peptidoglycan DL-carboxypeptidase activity
causes
peptidoglycan stem peptide trimming
biolink:causesDL-carboxypeptidase activity trims monomeric tripeptides to dipeptides in the peptidoglycan stem.
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DOI:10.1371/journal.ppat.1002602
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peptidoglycan stem peptide trimming
promotes
helical shaped
RO:0002213Peptidoglycan stem peptide trimming supports generation of the helical cell shape.
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DOI:10.1371/journal.ppat.1002602
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loss of peptidoglycan-modifying enzyme
causes
rod-shaped morphology
biolink:causesLoss of a peptidoglycan-modifying enzyme produces a straight rod-shaped morphology.
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DOI:10.1371/journal.ppat.1002602
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rod-shaped morphology
negatively regulates
helical shaped
RO:0002212Rod-shaped morphology represents loss of the helical-shaped trait.
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DOI:10.1371/journal.ppat.1002602
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localized peptidoglycan crosslink hydrolysis
enables
helical curvature and twist
RO:0002327Localized peptidoglycan crosslink hydrolysis generates the curvature and twist underlying helical shape.
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DOI:10.1016/j.cell.2010.03.046
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Provenance
- Source
- METPO (2025-11-25)
- Author
- Jed Dongjin Kim-Ozaeta
- Definition source
- DOI:10.1016/j.cell.2010.03.046
Parent traits (1)
Synonyms (1)
- helical-shaped
kg-microbe context
Matched 1 kg-microbe node via direct_metpo.
METPO:1000676[-1.491, -3.251, -3.052, +1.582, …]
Nearest neighbors in embedding space
- morphology crescent shaped 0.583
- morphology tetrad arrangement 0.573
- morphology streptococcus arrangement 0.573
- morphology staphylococcus arrangement 0.573
- morphology cell shape 0.573
- morphology sarcina arrangement 0.573
- morphology diplococcus shaped 0.569
- morphology spore shaped 0.552
Deep research
# Curation report: microbial “helical shaped” ## Executive summary **Target:** “METPO:1000676” (`helical shaped`), morphology class, reviewed. The trait should denote a **cell-body** geometry having longitudinal curvature plus twist, yielding a corkscrew or true helical centerline. It should not be assigned merely because an organism has a helical flagellar filament, follows a helical swimming trajectory, is a single-plane curved rod, or transiently becomes coccoid or filamentous. Two mechanistically distinct graph branches are warranted: 1. **Peptidoglycan (PG)-sculpted helicity** in *Helicobacter pylori* and *Campylobacter jejuni*: regulated PG endopeptidase/carboxypeptidase activity and cytoskeletal/scaffolding proteins alter peptide stems and crosslinks, producing anisotropic wall mechanics and stable curvature/twist. 2. **Periplasmic-flagella-imposed morphology** in spirochetes: elastic forces between internal flagella and the cell cylinder impose species-specific waves or helices. This branch needs tighter phenotype qualification because *Borrelia burgdorferi* is usually described as **flat-wave**, not a true three-dimensional helical cell body. (charon2012theuniqueparadigm pages 2-4, charon2012theuniqueparadigm pages 4-5, nakamura2020spirocheteflagellaand pages 1-3) The strongest immediately curatable backbone is therefore: **shape proteins/PG hydrolases → altered PG peptide stems and crosslinks → asymmetric sacculus mechanics → cell curvature plus twist → helical cell body → enhanced movement or colonization in host-associated environments.** --- ## 1. Trait scope and boundaries ### 1.1 Positive operational definition Curate “METPO:1000676” when microscopy or isolated-sacculus analysis demonstrates a stable corkscrew-like cell body with curvature and axial twist. Useful measurements include centerline torsion, helical pitch, radius, handedness, and three-dimensional reconstruction. In *H. pylori*, mutant sacculi reproduce the morphology of intact cells, directly identifying the PG sacculus as the shape-bearing structure. (sycuro2010peptidoglycancrosslinkingrelaxation pages 7-8, sycuro2010peptidoglycancrosslinkingrelaxation pages 6-7, sycuro2010peptidoglycancrosslinkingrelaxation pages 5-6) ### 1.2 Boundary cases - **Curved rod:** curvature without clear axial twist is a nearby but distinct phenotype. Deletion of *H. pylori csd1/csd2/ccmA* or *C. jejuni pgp3* produces curved rods rather than wild-type helices. These mutant phenotypes are useful negative or intermediate states, not instances of full helicity. (frirdich2023multiplecampylobacterjejuni pages 2-3, sycuro2010peptidoglycancrosslinkingrelaxation pages 2-4) - **Flat-wave spirochete:** *B. burgdorferi* has a planar waveform—reported amplitude 0.78 µm and wavelength 2.83 µm—rather than an unambiguous three-dimensional helix. It should be included only if TraitMech intentionally treats “spiral/wavy” as within scope; otherwise map it to a separate waveform trait. (charon2012theuniqueparadigm pages 2-4) - **Helical flagellum:** the flagellar filament is an appendage, not the cell body. In *B. burgdorferi*, purified periplasmic flagella are left-handed helices with approximately 0.28-µm diameter and 1.48-µm pitch, whereas the cell body is a flat wave. (charon2012theuniqueparadigm pages 2-4) - **Helical swimming trajectory:** circular or corkscrew movement is an assay outcome and cannot alone establish cell-body helicity. - **Coccoid transition:** aged or stressed *Helicobacter/Campylobacter* cells may become spherical; this is a morphological transition away from the target trait, not another expression of helicity. - **External flagella on helical rods:** *H. pylori* and *C. jejuni* body shape is principally encoded by PG architecture; their external flagella primarily generate propulsion. In spirochetes, internal flagella can additionally determine body shape. ### 1.3 Recommended trait-assignment rule Require evidence for the **cell body**, preferably from three-dimensional imaging or a combination of phase/DIC microscopy and isolated sacculi. Record `curved rod`, `flat wave`, and `helical` separately whenever the source does so. Do not infer the target from a genus name such as *Spirillum* or from “spiral-shaped” wording without inspection of the authors’ morphology definition. --- ## 2. Candidate nodes grouped by type ### 2.1 Trait and taxon nodes - **helical shaped:** “METPO:1000676” - **parent morphology:** “METPO:1000666” - *Helicobacter pylori* — taxon label; verify the current NCBITaxon CURIE during ingestion. - *Campylobacter jejuni* — taxon label; verify NCBITaxon CURIE during ingestion. - *Borrelia burgdorferi*, *Leptospira interrogans*, *Treponema pallidum* — label-only here pending accession validation. - Boundary phenotypes: `curved rod`, `straight rod`, `flat-wave cell body`, `coccoid cell`. ### 2.2 Cellular structures and localizations - Peptidoglycan sacculus / cell wall — **GO:0009274** is a suitable general bacterial PG-based cell-wall term, subject to ontology-version confirmation. - Periplasmic space — **GO:0042597**. - Cytoplasmic membrane / inner membrane. - Cytoskeleton and bactofilin polymers. - Periplasmic flagellum/endoflagellum; flagellar ribbon; motor, hook and filament. - Membrane-associated *H. pylori* “shapeosome/shapesome” complex—candidate label-only complex. ### 2.3 *H. pylori* genes and proteins
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
Reviewed helical shape and added DOI-backed causal graph for Csd proteins, CcmA, peptidoglycan crosslink relaxation, and helical curvature.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 3 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002326×1, RO:0002327×1, METPO:2000202×1).
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GROUND_CAUSAL_NODES · claude
Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (UniProtKB:E0X6H3×1).
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002213×1).
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ENRICH_CAUSAL_GRAPH · claude
Added 5 evidence-backed generic edges (5 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 (biolink:causes×2, RO:0002213×1, RO:0002327×1).
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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)
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GROUND_CAUSAL_PREDICATES · claude
Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002212×1).
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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.