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63 changes: 50 additions & 13 deletions NEXT_TASKS.md
Original file line number Diff line number Diff line change
Expand Up @@ -360,19 +360,56 @@ errors, e.g. sulfite → CHEBI:16731 *(E)-cinnamaldehyde* instead of CHEBI:17359
the primary full text isn't retrievable, keep edges to abstract-supported/directly-implied
claims and file the rest as a KNOWLEDGE_GAP (000176 is the worked example).

**PENDING — enrich the single-edge records via a full causal-graph run.** Six 2-node
records already carry one hand-authored `downstream` edge (donor→acceptor) from original
curation but have not had an Edison causal-graph pass: the DIET trio
`Geobacter_Clostridium_DIET` (000031, PMID:28287150),
`Geobacter_Methanosaeta_DIET` (000032, doi:10.1039/C3EE42189A),
`Geobacter_Methanosarcina_DIET` (000033, PMID:24837373); and the syntrophies
`Syntrophobacter_Methanobacterium_Syntrophy` (000068), `Syntrophobacter_Methanospirillum_Syntrophy`
(000069), `Syntrophomonas_Methanospirillum_Syntrophy` (000070). A full run could add
mechanistic nodes/edges (e.g. conductive pili / OmcS-OmcZ cytochromes, conductive-material
mediation, formate-vs-H2 routes, reverse/feedback edges) beyond the single existing edge.
Run `just research-community-causal CommunityMech:0000NN` per record, then curate
conservatively as usual. NB: stray untracked `*.yaml.bak` backups exist alongside these in
`kb/communities/` (gitignored, not in the repo) — target the `.yaml` files.
**DONE — single-edge record enrichment (#254).** All six 2-node records got an Edison
causal-graph pass and conservative curation. What actually landed, per record:

- **000070 `Syntrophomonas_Methanospirillum`** — reverse feedback edge (methanogen H2
scavenging → enables butyrate β-oxidation). Best evidence was already in the cached
abstract, not in the Edison report: PMID:16345745 reports both the dependency
("Growth and degradation of fatty acids occur only in syntrophic association with
H(2)-using bacteria") and the perturbation ("The addition of H(2) … stopped growth and
butyrate degradation"). No new reference needed.
- **000069 `Syntrophobacter_Methanospirillum`** — reverse feedback edge, on the
axenic-vs-syntrophic contrast in PMID:9828440 (exact pair: M. hungateii).
- **000068 `Syntrophobacter_Methanobacterium`** — reverse feedback edge + **fixed a real
misattribution**: two evidence items quoted the Harmsen M. *hungateii* passage but were
explained as establishing M. *formicicum* (this record's partner). Downgraded to PARTIAL,
added exact-pair support from PMID:29611893, and filed discussion
`kg-syntrophobacter-methanobacterium-partner-attribution`.
- **000033 `Geobacter_Methanosarcina`** — new `T6SS-Associated Delay of DIET Establishment`
interaction + NEGATIVE edge to the DIET node (>30 d lag wild-type vs very little lag for
the Hcp-deficient mutant, PMID:37650614, OA full text cached). Curated as *T6SS-associated*,
not T6SS-caused: the mutant is pleiotropic (also reduces Fe(III) oxide faster).
- **000031 `Geobacter_Clostridium`** — no new edge; filed CONTROVERSY discussion
`kg-geobacter-clostridium-contact-dependence-contested`. **This record's core framing is
contested**: the follow-up study (PMID:34939136) concludes the interaction is *mediated*
(putative cobamide), and its full text reports that 0.22-µm-filtered cell-free spent
medium reproduces the metabolic shift — which would make pili contact unnecessary.
Curator decision still open on whether to re-scope the record away from `community_category:
DIET`; not applied unilaterally.
- **000032 `Geobacter_Methanosaeta`** — no new edge (000176 precedent). Edison proposed an
acetate cross-feeding node, but its quotations came from secondary reviews; the primary
(doi:10.1039/C3EE42189A) is cached abstract-only and is silent on acetate. Filed as
`kg-geobacter-methanosaeta-acetate-route-unresolved`.

Verification: all 6 `just validate` clean; snippet audit MATCH 4086→4101 (all 12 new
snippets match, zero new mismatches) and caching PMID:29611893 OA full text also cleared the
3 pre-existing 000068 Methods-snippet mismatches (169→166 repo-wide); network-integrity audit
clean for all 6. New reference caches: PMID:34939136, PMID:37650614.

**Follow-ups this batch surfaced:**
1. **000031 re-scoping decision** (above) — the highest-value open item.
2. **Li et al. 2024** (`doi:10.3390/w16243551`, *Water*) has exact-pair graded-formate
perturbation data for 000068 (5–10 mM promotes, ≥30 mM inhibits; FDH/hydrogenase
transcript downregulation). **Not ingested**: the journal is not in PubMed and has no PMC
record, so `scripts/cache_fulltext.py` can't verify its snippets. Would need a
DOI-based full-text cache path.
3. `just validate-references` is a **no-op** — it reports `Total checks: 0` even on untouched
files. `scripts/evidence_snippet_audit.py` is what actually validates snippets. Worth
fixing or documenting, since the justfile recipe implies coverage it isn't providing.

NB: stray untracked `*.yaml.bak` backups still exist alongside these in `kb/communities/`
(gitignored, not in the repo).

**Edison auth (resolved 2026-07-21):** the key was refreshed in `.env`
(`EDISON_API_KEY`) and authenticates (HTTP 200). The stale-key shadowing footgun is
Expand Down
52 changes: 52 additions & 0 deletions kb/communities/Geobacter_Clostridium_DIET.yaml
Original file line number Diff line number Diff line change
Expand Up @@ -498,3 +498,55 @@ related_ingredients:
metals_present: []
metal_relevance: SIGNIFICANT
metal_notes: Metal/REE detected via environmental factor measurements
discussions:
- discussion_id: kg-geobacter-clostridium-contact-dependence-contested
prompt: >
Is the G. sulfurreducens-induced metabolic shift in C. pasteurianum actually caused by
contact-dependent direct interspecies electron transfer along conductive pili, or by a
diffusible mediator (candidate: a cobamide) released by G. sulfurreducens?
kind: CONTROVERSY
status: OPEN
attaches_to:
- ecological_interactions#Acetate Oxidation and Direct Electron Transfer
- ecological_interactions#Glycerol Fermentation with DIET-Induced Metabolic Shift
rationale: >
This record asserts contact-dependent DIET through electrically conductive pili
(nanowires) as the established mechanism, following the original coculture study
(PMID:28287150), which inferred interspecies electron transfer rather than
demonstrating contact dependence. A follow-up study by the same group
(PMID:34939136) set out to identify the mechanism and concluded that the interaction
is MEDIATED: it proposes that G. sulfurreducens releases cobamide molecules that act
on the C. pasteurianum glycerol dehydratase, with electron entry via a transmembrane
flavin-bound polyferredoxin / cytochrome b5-rubredoxin route offered only as a
putative reinforcement. The published full text (not open access, so only the
abstract is snippet-verifiable here) additionally reports that 0.22-um-filtered,
cell-free G. sulfurreducens spent medium reproduces the metabolic shift, which would
make Geobacter cells - and therefore pili contact - unnecessary for the shift.
Until that contrast is verified against the full text, the nanowire/contact-dependent
framing in this record's description, its `Acetate Oxidation and Direct Electron
Transfer` interaction, and its DIET `community_category` should be treated as
CONTESTED rather than established. Resolving this may require re-scoping the record
away from DIET; that is a curator decision, not applied here.
evidence:
- reference: PMID:34939136
supports: PARTIAL
evidence_source: IN_VITRO
snippet: It was assumed that this metabolic shift of the fermentative species resulted
from an interspecies electron transfer
explanation: The follow-up study characterizes the interspecies-electron-transfer reading
of the original experiment as an assumption, not a demonstrated mechanism.
- reference: PMID:34939136
supports: REFUTE
evidence_source: IN_VITRO
snippet: 'C. pasteurianum-G. sulfurreducens interaction inducing a metabolic shift is
mediated'
explanation: Key-point conclusion that the interaction is mediated (via a diffusible
molecule), contradicting the contact-dependent nanowire mechanism asserted by this record.
- reference: PMID:34939136
supports: SUPPORT
evidence_source: IN_VITRO
snippet: 'a putative interaction model was proposed: G. sulfurreducens produces cobamide
molecules that possibly modify C. pasteurianum metabolic pathway at the key enzyme
glycerol dehydratase'
explanation: States the competing diffusible-cobamide mechanism, and marks it as putative -
so it must not be asserted as an interaction in place of the current one.
34 changes: 34 additions & 0 deletions kb/communities/Geobacter_Methanosaeta_DIET.yaml
Original file line number Diff line number Diff line change
Expand Up @@ -372,3 +372,37 @@ metals_present: []
metal_relevance: SIGNIFICANT
metal_notes: Metal/REE detected via environmental factor measurements; Metal/REE detected
via keyword matching in description (context-validated)
discussions:
- discussion_id: kg-geobacter-methanosaeta-acetate-route-unresolved
prompt: >
Alongside DIET-driven CO2 reduction, does M. harundinacea also cross-feed on the
acetate generated by G. metallireducens ethanol oxidation, and what fraction of
methane comes from each route in this defined coculture?
kind: KNOWLEDGE_GAP
status: OPEN
attaches_to:
- ecological_interactions#Ethanol Oxidation and Direct Electron Transfer
- ecological_interactions#Direct Electron Acceptance and Methanogenesis
rationale: >
A causal-graph pass on this record proposed an additional acetate cross-feeding node
and an acetate -> methanogenesis edge, on the reasoning that Methanosaeta is
classically an acetoclastic genus and that ethanol oxidation by G. metallireducens
yields acetate, giving an overall stoichiometry near 1.5 mol CH4 per mol ethanol.
That claim is NOT curated here as an interaction: the primary source
(doi:10.1039/C3EE42189A) is cached abstract-only and its full text was not
retrievable, and the abstract states only that M. harundinacea "accepted electrons
via DIET for the reduction of carbon dioxide to methane" - it does not report acetate
cross-feeding, the acetate/DIET split, or the per-route methane stoichiometry. The
supporting quotations offered for the acetate route came from secondary reviews
attributing findings to this study, which per this repo's conservative-curation rule
(see CommunityMech:000176) is not a sufficient basis for an exact-system causal edge.
Resolving this needs the primary full text or a radiotracer/isotope partition
experiment in this exact coculture.
evidence:
- reference: doi:10.1039/C3EE42189A
supports: PARTIAL
evidence_source: IN_VITRO
snippet: Transcriptomic, radiotracer, and genetic analysis demonstrated that M. harundinacea
accepted electrons via DIET for the reduction of carbon dioxide to methane
explanation: The abstract demonstrates only the DIET/CO2-reduction route; it is silent on an
acetate cross-feeding route, which is why that edge is filed as a gap rather than curated.
60 changes: 60 additions & 0 deletions kb/communities/Geobacter_Methanosarcina_DIET.yaml
Original file line number Diff line number Diff line change
Expand Up @@ -201,6 +201,66 @@ ecological_interactions:
evidence_source: IN_VITRO
snippet: Direct interspecies electron transfer (DIET) is potentially an effective
form of syntrophy in methanogenic communities, but little is known about the
- name: T6SS-Associated Delay of DIET Establishment
Comment on lines 202 to +204
description: 'Geobacter metallireducens expresses a type VI secretion system (T6SS) during
the initiation of DIET cocultures, and this is associated with a long delay before the
partnership becomes productive. Cocultures started with wild-type G. metallireducens showed
a lag of more than 30 days before methane production, whereas cocultures started with an
Hcp-deficient (T6SS structural protein) mutant had very little lag and established DIET
with M. barkeri faster. The sign of this edge is NEGATIVE: the wild-type T6SS-expressing
state suppresses the rate at which the DIET partnership is established. The molecular
attribution is confounded and must not be curated as demonstrated antagonism toward the
archaeon - the same mutant also reduced Fe(III) oxide faster than wild type, a phenotype
not expected from loss of the T6SS, and the authors state that the effect of T6SSs on
archaeal cells still requires study. Encoded as a delay of establishment, not as
predation, killing, or toxin delivery to M. barkeri.

'
interaction_type: COMPETITION
source_taxon:
preferred_term: Geobacter metallireducens
term:
id: NCBITaxon:28232
label: Geobacter metallireducens
biological_processes:
- preferred_term: protein secretion by the type VI secretion system
term:
id: GO:0033103
label: protein secretion by the type VI secretion system
downstream:
- target: Ethanol Oxidation and Direct Electron Transfer
description: NEGATIVE edge - the wild-type T6SS-expressing state of G. metallireducens
delays establishment of the DIET partnership (>30 d lag vs very little lag for the
Hcp-deficient mutant). Demonstrated by knockout phenotype in this exact coculture, but
the mutant is pleiotropic, so the causal attribution to the T6SS specifically is
HYPOTHESIZED rather than proven.
evidence:
- reference: PMID:37650614
supports: SUPPORT
evidence_source: IN_VITRO
snippet: there was a lag period of more than 30 d in co-cultures initiated with wild-type
G. metallireducens
explanation: Wild-type baseline for the delay, measured in the G. metallireducens-M. barkeri
ethanol coculture that this record describes.
- reference: PMID:37650614
supports: SUPPORT
evidence_source: IN_VITRO
snippet: In contrast, there was very little lag in co-cultures initiated with the Hcp-deficient
G. metallireducens strain
explanation: Knockout arm of the perturbation - removing the T6SS structural protein Hcp
largely removes the lag, which is the basis for the negative causal edge.
- reference: PMID:37650614
supports: SUPPORT
evidence_source: IN_VITRO
snippet: The hcp-deficient mutant also established DIET quicker with Methanosarcina barkeri
explanation: Confirms the phenotype specifically for the M. barkeri partner of this community.
- reference: PMID:37650614
supports: PARTIAL
evidence_source: IN_VITRO
snippet: the mutant also reduced Fe(III) oxide faster than the wild-type strain, a phenotype
not expected from the loss of the T6SS
explanation: Records the pleiotropy confounder - the reason this edge is curated as
T6SS-associated rather than T6SS-caused.
environmental_factors:
- name: Anaerobic Conditions
value: Strict anaerobic
Expand Down
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