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

Evidence-backed causal sketch linking helical cell shape to H. pylori shape proteins, peptidoglycan crosslink relaxation, and curvature plus twist.

Helical-shape peptidoglycan relaxation mechanism Interactive directed graph showing evidence-backed causal relationships for helical shaped.

Edge evidence

  • Csd shape proteins promotes peptidoglycan crosslink relaxation RO:0002213

    Csd peptidoglycan endopeptidase homologs contribute to reduced crosslinking in helical-shape generation.

    • DOI:10.1016/j.cell.2010.03.046 three LytM peptidoglycan endopeptidase homologs Supports Csd proteins as required genes in the H. pylori helical shape pathway.
  • CcmA contributes to peptidoglycan crosslink relaxation RO:0002326

    CcmA contributes to the shape-generating pathway for helical morphology.

    • DOI:10.1016/j.cell.2010.03.046 three LytM peptidoglycan endopeptidase homologs ... and a ccmA homolog Supports CcmA as one of the proteins required for helical shape.
  • peptidoglycan crosslink relaxation enables helical curvature and twist RO:0002327

    Relaxed peptidoglycan crosslinking enables curvature and twist.

    • DOI:10.1016/j.cell.2010.03.046 relaxes peptidoglycan crosslinking, enabling helical cell curvature and twist Direct evidence for PG crosslink relaxation causing helical geometry.
  • helical curvature and twist confers helical shaped METPO:2007700

    Helical curvature and twist produce the helical-shaped trait.

    • DOI:10.1016/j.cell.2010.03.046 helical cell curvature and twist Supports the morphology endpoint of the graph.
  • peptidoglycan DL-carboxypeptidase activity causes peptidoglycan stem peptide trimming biolink:causes

    DL-carboxypeptidase activity trims monomeric tripeptides to dipeptides in the peptidoglycan stem.

    • DOI:10.1371/journal.ppat.1002602 Pgp1 is a novel peptidoglycan DL-carboxypeptidase cleaving monomeric tripeptides to dipeptides.
  • peptidoglycan stem peptide trimming promotes helical shaped RO:0002213

    Peptidoglycan stem peptide trimming supports generation of the helical cell shape.

    • DOI:10.1371/journal.ppat.1002602 Pgp1 DL-carboxypeptidase activity on peptidoglycan stem peptides is required for helical cell shape.
  • loss of peptidoglycan-modifying enzyme causes rod-shaped morphology biolink:causes

    Loss of a peptidoglycan-modifying enzyme produces a straight rod-shaped morphology.

    • DOI:10.1371/journal.ppat.1002602 Deletion of pgp1 resulted in a striking, rod-shaped morphology.
  • rod-shaped morphology negatively regulates helical shaped RO:0002212

    Rod-shaped morphology represents loss of the helical-shaped trait.

    • DOI:10.1371/journal.ppat.1002602 pgp1 deletion converts helical cells to rod-shaped cells, i.e., loss of helical shape.
  • localized peptidoglycan crosslink hydrolysis enables helical curvature and twist RO:0002327

    Localized peptidoglycan crosslink hydrolysis generates the curvature and twist underlying helical shape.

    • DOI:10.1016/j.cell.2010.03.046 Coordinated action of multiple proteins relaxes peptidoglycan crosslinking, enabling helical cell curvature and twist.

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 RELATED_SYNONYM · metpo.owl

kg-microbe context

Matched 1 kg-microbe node via direct_metpo.

  • METPO:1000676 [-1.491, -3.251, -3.052, +1.582, …]

512-dim DeepWalkSkipGramEnsmallen embedding from kg-microbe (2026-04-25).

Nearest neighbors in embedding space

Top-8 cosine-similar METPO traits from the 2026-04-25 deepwalk (512-D).

Deep research

Generated by just research-trait; source: research/traits/morphology/helical_shaped-deep-research-falcon.md

Unreviewed literature output — not curated TraitMech content Ontology identifiers suggested below have not been resolved against their ontologies, and some are known to be wrong. Check any CURIE against the source before using it.
# 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

Showing the first 60 of 364 lines of findings; the linked file also carries the run's front matter and the prompt it was given — read the full report.

Curation history

  1. · SEEDED_FROM_METPO · seed_from_metpo

    imported from data/raw/metpo.owl (CLASS)

  2. · CURATED_WITH_LITERATURE · codex

    Reviewed helical shape and added DOI-backed causal graph for Csd proteins, CcmA, peptidoglycan crosslink relaxation, and helical curvature.

  3. · 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).

  4. · GROUND_CAUSAL_NODES · claude

    Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (UniProtKB:E0X6H3×1).

  5. · GROUND_CAUSAL_PREDICATES · claude

    Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002213×1).

  6. · ENRICH_CAUSAL_GRAPH · claude

    Added 5 evidence-backed generic edges (5 new nodes) from the deep-research report.

  7. · 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).

  8. · 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)

  9. · GROUND_CAUSAL_PREDICATES · claude

    Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002212×1).

  10. · 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.