gliding

METPO:1000706 · CLASS · REVIEWED

A motile in which an organism moves smoothly along solid surfaces without flagella or pili.

Gliding surface motility mechanism

Evidence-backed causal sketch linking gliding to solid surfaces, cell-envelope motors, surface adhesins, and type IX secretion/gliding systems.

Gliding surface motility mechanism Interactive directed graph showing evidence-backed causal relationships for gliding.

Edge evidence

  • solid surface enables context for gliding

    Gliding is a mode of active bacterial movement over surfaces.

    • DOI:10.1146/annurev.micro.55.1.49 move actively over surfaces Supports surface movement as defining context for gliding.
  • gliding motility machinery confers gliding METPO:2007700

    Specialized machinery drives bacterial surface movement without flagella.

    • DOI:10.1016/j.cub.2016.12.035 without using flagella, pili, or other external appendages Supports gliding as a distinct motility mode.
  • surface adhesins transmit force for gliding

    Surface adhesins couple internal motors to external substrates.

    • DOI:10.1038/s41579-021-00626-4 moves adhesins along the cell surface Review summarizes gliding models using moving surface adhesins.
  • type IX secretion system contributes to gliding motility machinery RO:0002326

    Type IX secretion-associated components contribute to some gliding systems.

    • DOI:10.1038/s41579-021-00626-4 type 9 secretion and gliding motility Supports linkage between type IX secretion and gliding machinery.
  • proton motive force powers gliding motility machinery METPO:2007900

    Proton motive force can power gliding motility motors.

    • DOI:10.1038/s41579-021-00626-4 proton-driven motor that powers type 9 secretion and gliding motility Supports proton-driven gliding machinery in reviewed systems.
  • helical conveyor track guides surface adhesins

    Adhesins are translocated along an envelope-associated filamentous track during gliding.

    • DOI:10.1038/s42003-023-04472-3 Filamentous multirail structures in the cell envelope are associated with the gliding machinery and SprB adhesin translocation.
  • surface adhesins enables substratum coupling and traction RO:0002327

    Surface adhesins engage the substratum to generate traction.

    • DOI:10.1126/sciadv.abq0619 Surface adhesin at bacterial focal adhesions immobilizes motility complexes against the substratum to generate traction.
  • substratum coupling and traction causes cell propulsion biolink:causes

    Traction at substratum-coupled adhesins drives forward movement of the cell body.

    • DOI:10.1371/journal.pbio.3001443 Proton-dependent motors power adhesin surface translocation that propels the cell during gliding.
  • cell propulsion realizes gliding

    Propulsion of the cell body along a surface constitutes the gliding phenotype.

    • DOI:10.1371/journal.pbio.3001443 Adhesin surface translocation produces the smooth surface movement characteristic of gliding.
  • gliding machinery gene complement predicts gliding

    Presence of the core gliding/secretion machinery gene set predicts gliding capacity from genomes.

    • DOI:10.1021/acsomega.3c05155 T9GPred predicts gliding motility from an 11-protein mandatory component set across Bacteroidetes genomes.

Provenance

Source
METPO (2025-11-25)
Definition source
DOI:10.1146/annurev.micro.55.1.49

Parent traits (1)

kg-microbe context

Matched 1 kg-microbe node via direct_metpo.

  • METPO:1000706 [-1.115, +0.741, -2.784, -0.615, …]

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/gliding-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 gliding

## 1. Scope and recommended interpretation

**Target:** `METPO:1000706`  
**Category:** MORPHOLOGY; **term kind:** CLASS; **parent:** `METPO:1000702`; **mapping:** REVIEWED.

For TraitMech, gliding should denote **active, energy-dependent translocation of a microbial cell along a solid or semisolid interface without flagellar propulsion**. Canonical *Flavobacterium* gliding uses moving cell-surface adhesins, whereas *Myxococcus xanthus* adventurous/A-motility uses a trans-envelope Agl–Glt focal-adhesion system. These systems are mechanistically nonhomologous and should be represented as separate branches converging on `METPO:1000706`. *F. columnare* glides on fish tissue, glass, agar, and other surfaces and forms spreading colonies on agar, illustrating both the biological phenotype and common assays. (vincent2022dynamicprotondependentmotors pages 1-2, thunes2024glidingmotilityproteins pages 1-2, jolivet2023integrinlikeadhesincgld pages 1-3)

The supplied wording—“moves smoothly along solid surfaces without flagella or pili”—is appropriate for canonical *Flavobacterium* motility and *M. xanthus* A-motility. It should **not** be applied indiscriminately to every historical use of “gliding,” because some cyanobacterial literature uses that label for type-IV-pilus-related movement.

### Boundary cases

- **Exclude swimming:** movement through liquid driven by flagella or other swimming machinery.
- **Exclude twitching/social motility:** type IV pilus extension–retraction. In *M. xanthus*, S-motility is twitching, whereas A-motility is the gliding branch. (chen2022flagellarmotortransformed pages 1-2)
- **Exclude passive sliding:** colony expansion driven chiefly by growth, surfactants, or reduced friction without an active cell-autonomous motor.
- **Do not equate colony spreading with gliding automatically:** spreading can combine growth, environmental conditions, collective organization, and several adhesins. Agar and glucose strongly alter *F. johnsoniae* colony morphology, and glucose can permit SprB-independent spreading on soft agar. (sato2021colonyspreadingof pages 1-3)
- **Swarming is separate:** normally a coordinated, flagellum-dependent surface behavior.
- **Mycoplasma gliding:** a genuine but mechanistically distinct ATP-driven branch. Because adequate full-text evidence was not recovered here, its machinery should not be added to this graph from this report alone.

## 2. Current mechanistic understanding

### Bacteroidota/*Flavobacterium* branch

The best-supported causal chain is:

**transmembrane proton gradient → GldL/GldM motor → T9SS-dependent SprB export and surface motion → transient SprB–substratum adhesion → cell-body displacement → gliding.**

Vincent et al. directly showed that the pH-gradient component of proton motive force powers *F. johnsoniae* gliding. GldL and GldM form dynamic membrane channels; conserved glutamates in GldL TMH2 are required; and PMF-dissipating inhibitors prevent secretion and halt cell displacement. SprB follows a closed helical path, and its substrate binding converts relative adhesin motion into screw-like forward displacement. The paper was published **25 March 2022**. (vincent2022dynamicprotondependentmotors pages 1-2)

The apparatus is intertwined with the type IX secretion system (T9SS). GldK, GldL, GldM, and GldN are shared core components, while some factors are branch-specific. PorV can be required for secretion of many type-A CTD substrates without eliminating SprB-dependent movement, whereas SprB is principally a motility adhesin. Thus, “T9SS activity” and “gliding” should be separate nodes rather than treated as equivalent phenotypes. (thunes2024glidingmotilityproteins pages 2-5, thunes2024glidingmotilityproteins pages 1-2)

### *Myxococcus xanthus* A-motility branch

The approximately 20-component Agl–Glt apparatus spans the cell envelope. Its AglR/Q/S energy-harvesting unit is homologous to MotA/B-family flagellar stators and operates as a proton-channel motor. Motors move helically in an MreB-dependent manner and become stationary relative to the substratum at force-generating bacterial focal adhesions. MreB disruption abolishes helical motor motion and blocks gliding, although whether MreB is a direct track remains unresolved. Motor aggregation also increases on harder substrates, supporting a mechanosensing model. These conclusions were synthesized in a peer-reviewed perspective published **6 May 2022**. (chen2022flagellarmotortransformed pages 1-2)

A **19 October 2023 bioRxiv preprint** proposed that CglB engagement immobilizes the Agl–Glt complex at focal-adhesion sites, enabling force transmission. It further identified CglD as a calcium-dependent, integrin-like outer-membrane lipoprotein that anchors and stabilizes the Glt–CglB assembly. The work used traction-force, bead-force, TIRF microscopy, and biochemical methods, but its preprint status requires an uncertainty flag. (jolivet2023integrinlikeadhesincgld pages 1-3)

## 3. Candidate nodes

### Trait and processes

- gliding — `METPO:1000706`
- cell motility — `GO:0048870`
- surface-associated locomotion — label-only
- bacterial focal-adhesion assembly — label-only
- trans-envelope force transduction — label-only
- mechanosensing — label-only
- type IX secretion — label-only pending curator verification of an exact ontology term
- colony spreading — label-only; assay readout, not synonymous with gliding
- virulence in fish — label-only; downstream application phenotype

### Energy, chemicals, and experimental factors

- proton — `CHEBI:15378`
- transmembrane proton gradient / proton motive force — label-only
- calcium(2+) — `CHEBI:33070`
- glucose — `CHEBI:17234` should be curator-verified before use; retain label-only if not verified locally
- carbonyl cyanide *m*-chlorophenyl hydrazone (CCCP) — label-only pending identifier verification
- solid substratum, glass, agar, fish tissue — label-only or ENVO-grounded after exact-term verification

Showing the first 60 of 205 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 gliding trait and added DOI-backed causal graph for surface gliding machinery, adhesins, type IX secretion, and proton motive force.

  3. · GROUND_CAUSAL_PREDICATES · claude

    Grounded 2 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002327×1, RO:0002326×1).

  4. · GROUND_CAUSAL_NODES · claude

    Grounded 1 causal-node grounding field(s) via mappings/node_grounding.tsv (METPO:1007500×1).

  5. · RETYPE_CAUSAL_NODES · claude

    Re-typed 1 causal-node node_type field(s) to align with CausalNodeTypeEnum semantics: proton motive force: BIOLOGICAL_PROCESS → STATE ×1.

  6. · RENAME_PREDICATE_LABELS · claude

    Renamed 1 causal-edge predicate label(s) to align with existing groundings: powers → enables ×1.

  7. · GROUND_CAUSAL_PREDICATES · claude

    Grounded 1 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002327×1).

  8. · REMOVE_REDUNDANT_SYNONYM · claude

    Removed 1 synonym(s) whose text duplicated the label (seeder redundancy; no information lost).

  9. · ENRICH_CAUSAL_GRAPH · claude

    Added 5 evidence-backed generic edges (4 new nodes) from the deep-research report.

  10. · GROUND_CAUSAL_PREDICATES · claude

    Grounded 2 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002327×1, biolink:causes×1).

  11. · MIGRATE_ENABLES_TRAIT_EDGES · claude

    Migrated 1 causal edge(s) off enables/RO:0002327 with a TRAIT object (1 to confers), issue 302. RO:0002327 has range 'biological process or activity', which a trait (a disposition) cannot satisfy, so the previous form entailed trait is-a BiologicalProcessOrActivity. The replacements are proposed in proposals/metpo_traitmech_v8 and are placeholder ids until METPO mints them.

  12. · REGROUND_CAUSAL_EDGE · claude

    Re-grounded causal edge(s) off enables/RO:0002327 onto contributes to (RO:0002326), 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.

  13. · REGROUND_CAUSAL_EDGE · claude

    Reverted the motive-force edge from contributes to back to enables/RO:0002327, issue 334 review. biolink defines contributes to as holding where one entity contributes to the occurrence or GENERATION of the other. A motive force does not generate the motor or machinery - it powers rotation, which is what the edge description says. That is the same energy-powers-a-machine idiom this work deferred for molecular_oxygen and cytoplasmic_na, so deferring it here too is the consistent call. The edge stays baselined under issue 334 until it is modelled as an input to the machine or pointed at the rotation process, either of which is range-correct.

  14. · REGROUND_CAUSAL_EDGE · claude

    Edge proton_motive_force -> gliding_motility_machinery in graph gliding_surface_motility: re-grounded it from enables/RO:0002327 to powers/METPO:2007900. Issue 334. biolink declares enables range 'biological process or activity', which of CausalNodeTypeEnum only BIOLOGICAL_PROCESS, PATHWAY and MOLECULAR_FUNCTION satisfy, so this edge entailed a false type on its object. 'Proton motive force can POWER gliding motility motors.'