Evidence map›Paper›PMID 42558671›Full record

ReviewFrontiers in neural circuits2026

Transsynaptic viral tools in neural circuit analysis: from anatomical mapping to functional interrogation.

Zsolt Boldogkői, Gábor Torma, Zsolt Csabai, Zoltán Máté, Rebeka Fekete, Máté Mizik, Ferenc Erdélyi, Dóra Tombácz, Ádám Dénes

Abstract readReview
In one paragraph

Review in Frontiers in neural circuits, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Zsolt BoldogkőiDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Gábor TormaDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Zsolt CsabaiDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Zoltán MátéMedical Gene Technology Unit, HUN-REN Institute of Experimental Medicine, Budapest, Hungary.
Rebeka FeketeDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Máté MizikDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Ferenc ErdélyiMedical Gene Technology Unit, HUN-REN Institute of Experimental Medicine, Budapest, Hungary.
Dóra TombáczDepartment of Medical Biology, Albert Szent-Györgyi Medical School, University of Szeged, Szeged, Hungary.
Ádám DénesLaboratory of Neuroimmunology, HUN-REN Institute of Experimental Medicine, Budapest, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The application of transsynaptic viruses has transformed neural circuit analysis, enabling increasingly precise mapping of neuronal connectivity. These approaches can be broadly divided into polysynaptic and monosynaptic strategies. Polysynaptic retrograde tracers based on pseudorabies virus, including the classically selected Bartha strain and genetically engineered retrograde variants have provided important insights into multisynaptic circuit organization in rodents. For polysynaptic anterograde tracing, herpes simplex virus strain H129 and its derivatives have been used to map output pathways, with later genetic modifications improving detectability and experimental control. Over the past few years, growing attention has shifted toward monosynaptic tracing based on engineered rabies virus platforms used in combination with adeno-associated virus helper systems, which enable genetically restricted spread to direct presynaptic partners. Viral tracing is increasingly integrated with functional approaches, including calcium and voltage imaging, optogenetics, chemogenetics, and recombinase-based genetic strategies, thereby extending circuit analysis from anatomical mapping to causal interrogation of the function of defined neuronal populations. Looking forward, improved control of polysynaptic spread, together with large transgene capacity, suitability for tracing hierarchical circuit architecture, and the ability to incorporate functional readouts, is expected to revive interest in multisynaptic tracing.

Indexed as

Nerve NetNeuroanatomical Tract-Tracing TechniquesNeuronsSynapsesAnimalsDependovirusHumansNeural PathwaysOptogeneticsadeno-associated virusfluorescent activity markerinducible systemsneural tracingoptogeneticspseudorabies virusrabies virus

Identifiers

PMID42558671
PMCPMC13438269

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.