AI summary · arXiv: 2610.33881v1 · q-bio.NC

Sensorimotor behaviour from an untrained brain-and-nerve-cord connectome

John R. Minnick, Jesus Gonzalez-Ferrer, Jinghui Geng, Jason K. Eshraghian, Mohammed A. Mostajo-Radji, David Haussler, Mircea Teodorescu
Original paper Submitted to arXiv on 24 Oct. 2026 42 pages: the manuscript with six figures, and the Supplementary Information (4 figures, 8 tables) appended License: NONEXCLUSIVE-DISTRIB 1.0 Also in: fr

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The essentials

An untrained fly connectome supports simulated odour navigation through fixed sensorimotor rules, while associative learned avoidance requires correcting odour-dependent activity and using a signed output readout.

Question

How much sensorimotor function follows from the measured wiring of an adult fly’s brain and nerve cord without task-specific parameter fitting? Can that wiring support navigation and learned behavioural reversal inside a simulated body?

Method

The authors built a leaky integrate-and-fire network from the female BANC connectome: 172,433 units, 11.75 million connections and 35.7 million synapses, using unchanged parameters from a published brain model. They tested 15 known pathways and coupled the network to NeuroMechFly through fixed sensory and motor rules, comparing intact, degree-and-sign-preserving rewired and mushroom-body-lesioned networks across nine arenas containing 32 sources, with 20 simulation seeds per condition. Learning experiments imposed dopamine-gated depression on 8,377 Kenyon-cell-to-output-neuron connections and compared paired reinforcement, reinforcement alone and no plasticity, including a variant with cholinergic local-neuron output scaled to 0.15.

Findings

  • Result In the identified-target tests, pathways supplying at least 2% of their target’s input conducted at some stimulation rate, whereas seven pathways supplying 0.03% or less did not.
    See the passage in the paper
    Every pathway tested onto an identified neuron conducts at some drive if it supplies at least 2% of that neuron’s input, and the seven supplying 0.03% or less do not (Fig. 2f).
  • Result Across the nine arenas, the intact network reached 95% of odour sources, compared with 18% after rewiring that preserved neuronal degrees and signs.
    See the passage in the paper
    In the NeuroMechFly body[38], coupled through two fixed rules, the network reaches 95% of 32 odour sources across nine arenas, where a network rewired to keep every neuron’s degrees and signs reaches 18%.
  • Result Replaying recorded motor commands without sensory feedback reduced source acquisition to 2%, compared with 94% for closed-loop runs from the same rotated starting orientation.
    See the passage in the paper
    The replays reach 0.07 sources per run against 3.29 for the closed loop from the same rotated start (2.0% against 94.0% of the sources, per fly).
  • Result The as-read olfactory network produced dense, persistent Kenyon-cell activity, while scaling one excitatory synapse class to 0.15 brought the tested odour code into the fly’s measured range.
    See the passage in the paper
    This closes a loop between projection and local neurons that sustains itself once started, and two thirds of the Kenyon cells then fire to every odour. Scaling that one class of synapse to 0.15 of its face value brings the Kenyon-cell code into the fly’s range.
  • Result In the scaled variant, paired reinforcement produced avoidance in all 20 flies, whereas reinforcement alone preserved approach in all 20, unlike the non-associative reversal in the as-read network.
    See the passage in the paper
    Pairing takes the weight to 0.195 mV and the valence to $-0.53$, and none of 20 trained flies reaches the source (median closest approach 21.1 mm). Reinforcement alone leaves the weight at 0.508 mV and the valence at 1.38, and all 20 flies reach the source, as they do without plasticity (paired against reinforcement alone, $P=6.8\times 10^{-8}$, $\delta=+1.00$) (Fig. 6h, i).

Limitations

  • Odour-directed turning is partly supplied by a hand-written interface, so the rescue experiments identify a required output signal rather than demonstrate that the connectome computes the turn.
    See the passage in the paper
    The rescue locates the deficit of both manipulations at the mushroom-body output. It does not show that the connectome computes the turn.
  • The model uses one animal’s wiring and simplified neuronal dynamics, omitting electrical synapses, spontaneous activity and endogenous neuromodulation.
    See the passage in the paper
    The model makes as few assumptions as a spiking network can: point neurons with one sign each, chemical synapses only, no neuromodulation, no spontaneous activity, one animal.
  • Learned avoidance depends on the chosen signed output readout and restriction of reinforcement to aversive compartments.
    See the passage in the paper
    The trained fly turns away only when the readout is signed and the reinforcement is confined to the aversive compartments, where 41 of the 50 MBONs drive approach.

Why it matters

The authors present an unfitted baseline for separating contributions of measured wiring from those of the body interface and sensory feedback. Its successes and identifiable failures provide fixed tests for adding missing physiology and motivate experimental predictions about pathway input share, activity-dependent steering and associative learning.

Written by AI from the paper. Passages are checked word for word against the text we analysed; the rest may contain errors.

AI-generated keywords: Fruit fly connectome; Sensorimotor function; Leaky integrate-and-fire network; Embodied navigation; Associative learning

Read further

  • Comprehensive Summary
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  • Original abstract
This paper investigates how much sensorimotor function can emerge from a fruit fly’s measured neural wiring without training the network to perform a task. The authors examine whether an adult brain-and-ventral-nerve-cord connectome can reproduce known neural pathways, support navigation in a simulated body, and enable learned avoidance. They distinguish functions supported by anatomical connectivity under simple modelling assumptions from those requiring additional physiological information or explicitly designed interfaces. The authors converted the female BANC connectome into a leaky integrate-and-fire network comprising 172,433 simulated neurons, 11.75 million connections, and 35.7 million synapses. Connection strengths were proportional to synapse counts, with excitatory or inhibitory signs assigned according to predicted neurotransmitters. Neuronal parameters were adopted unchanged from an earlier fly-brain model. The authors first tested 15 experimentally characterized pathways, then coupled the network to NeuroMechFly using fixed sensory-input and motor-output rules. Odour and visual signals activated selected sensory populations, while leg motor-neuron activity adjusted an existing gait controller. The balance between approach- and avoidance-associated mushroom-body output neurons modulated a hand-coded odour-steering rule. Seven of the 15 tested pathways transmitted signals, lost their effects after connectivity shuffling, and reproduced the direction of experimentally observed responses. These included sugar-driven feeding, bitter-induced suppression, escape-related pathways, and selected steering and grooming commands. Identified targets could be activated when a tested pathway supplied approximately 2% or more of their input synapses, whereas seven pathways supplying 0.03% or less failed. This threshold is specific to the model rather than an established biological law. Some failures highlighted missing physiology: adding a connection representing electrical coupling restored transmission from the giant fibre to its motor target, while background activity enabled inhibitory steering effects that were absent in a silent network. Across nine simulated arenas containing 32 odour sources, 20 independently seeded flies with intact connectivity reached an average of 30.25 sources, or approximately 95%. A shuffled network preserving connection degrees and signs reached 5.80 sources, or 18%; mushroom-body lesions reduced performance to 3.45 sources, while a correlated random walk reached 2.20. In a separate three-source arena, lesions preserved walking but abolished approach. Artificially restoring the mushroom-body valence signal rescued approach, locating the deficit in the signal supplied to the controller. Sensory feedback was also essential: from a rotated starting orientation, closed-loop runs reached 94% of sources, whereas replaying previously successful motor commands reached only 2%. Dopamine-gated weakening of Kenyon-cell connections onto selected mushroom-body output neurons reversed approach into avoidance. After paired training, mean plastic connection weights decreased from 0.513 to 0.138 mV, and none of the 20 flies reached the source, compared with all 20 before training. However, the original network also learned avoidance from reinforcement without odour because its olfactory circuit remained active. Reducing cholinergic local-neuron output to 15% produced more biologically realistic odour coding and restored associative learning: paired training induced avoidance in all 20 flies, whereas reinforcement alone left all 20 approaching. The study concludes that measured wiring can support substantial neural signal propagation and contribute to behaviour without task-specific network training. However, connectivity alone did not generate navigation: explicit steering rules and a pre-existing gait controller performed important computations. Learned avoidance also depended on a signed output readout and compartment-specific reinforcement. Further limitations include simplified neurons, neurotransmitter-prediction errors, missing electrical synapses and endogenous modulation, and reliance on a single animal’s connectome. The findings therefore demonstrate both the explanatory value of connectivity and the physiological and interface assumptions required to translate it into behaviour.

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Weekly letter Presented in "Brain and behaviour this week" of 2 November 2026. Brain and behaviour this week: What wiring explains—and what context changes

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