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Microbiota-Based Interventions Differentially Rescue Gut and Social Behavior Phenotypes in <italic>Drosophila</italic> with Kdm5 Deficiency.

Overview

Authors: Natalia A. Peta Martinez1, Melanie Reinoso Arnaldi1, Tasha M. Santiago-Rodriguez2,3, Imilce A. Rodriguez-Fernandez1
  1. Department of Biology, University of Puerto Rico Rio Piedras, San Juan, PR, USA
  2. Department of Molecular Virology and Microbiology, The Alkek Center for Metagenomics and Microbiome Research, Baylor College of Medicine, Houston, TX, USA
  3. Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, TX, USA
Institutions: University of Puerto Rico at Río Piedras (Puerto Rico); Baylor College of Medicine (United States)
Journal: Developmental neuroscience, pages 1-21
Dates: received 10 January 2026; accepted 18 May 2026; published online 21 May 2026; in print May 2026
Type: Other · Language: English
License: CC BY-NC
Identifiers: DOI 10.1159/000552681 · PMID 42166402 · PMCID PMC13412211 · OpenAlex W7161975342
Open access: hybrid, a free copy (OpenAlex)
Status: data only
Categories: drosophila (organism), clinical / translational (subfield)
Methods: Statistics, Machine learning, fMRI & imaging
Keywords: Microbiome, Gut-brain axis, Kdm5, Drosophila, Probiotics, FMT
Topic: Invertebrate Immune Response Mechanisms (Immunology, Immunology and Microbiology), according to OpenAlex
Funding: NIGMS NIH HHS (P20 GM103642, P30 GM149367)
Citations: not cited yet (Europe PMC); 61 references in the paper

Abstract

Introduction: Autism spectrum disorder (ASD) is a lifelong neurological and developmental disorder that is often accompanied by gastrointestinal (GI) issues. The bidirectional communication system known as the gut microbiota-brain axis may help explain how GI dysfunction contributes to neurological symptoms. Loss-of-function mutations in the histone demethylases KDM5A, KDM5B, or KDM5C are found in patients with intellectual disability and ASD. Here, we use a genetically tractable Drosophila model of loss-of-function of the ASD-associated chromatin regulator Kdm5 to investigate how host genetic disruption influences gut microbial composition and social behavior. Previous studies using a Drosophila Kdm5 loss-of-function (Kdm5LOF) revealed gut microbial dysbiosis, reduced abundance of Lactiplantibacillus plantarum, and impaired social behavior. While L. plantarum supplementation rescued intestinal abnormalities, it did not restore social behavior.

Methods: We evaluated multiple microbiota-based interventions, including probiotic supplementation with L. plantarum, Lactobacillus helveticus, their combination, and fecal microbiota transplantation (FMT), to determine their capacity to modulate gut microbial composition and behavior in adult Kdm5LOF flies. Gut bacterial abundance was quantified using colony-forming unit assays and full-length 16S rRNA gene sequencing. Social behavior was assessed using the social distance assay, while anxiety-like behavior and locomotion were evaluated using the open field test. Gut-specific Kdm5 knockdown was used to assess tissue-specific contributions to microbiota and behavioral phenotypes.

Results: Kdm5 deficiency resulted in reduced abundance of culturable Lactobacillus, Acetobacter, and Enterobacter species, accompanied by impaired social behavior. L. plantarum supplementation restored gut microbial abundance in both whole-body Kdm5LOF and gut-specific Kdm5 knockdown models but did not significantly rescue social behavior. In contrast, L. helveticus significantly improved social interaction in Kdm5LOF flies despite minimal effects on gut bacterial abundance, revealing a dissociation between microbial restoration and behavioral outcomes. Gut-specific Kdm5 knockdown phenocopied both microbial and social defects observed in Kdm5LOF mutants. Notably, FMT from healthy donors partially restored Lactobacillus abundance, reshaped gut microbial community structure, and partially improved social behavior in Kdm5LOF recipient flies.

Conclusion: Together, these findings identify Kdm5 as a key regulator of gut microbial viability and social behavior and demonstrate that microbiota-based interventions exert strain- and phenotype-specific effects. Our results reveal that restoration of microbial abundance alone is insufficient to rescue social behavior and highlight the importance of functional host-microbe interactions in gut-brain communication. This work establishes Drosophila as a tractable platform for dissecting epigenetic regulation of microbiota-behavior relationships in the context of disruption of an ASD-associated gene and for studying microbiota-based modulation of host physiology and behavior. All experiments were conducted in adult flies, and thus, these findings reflect post-developmental effects of Kdm5 disruption.

Reproduced under the paper's license (CC BY-NC), from the paper cited above.

Code

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Data

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Data Availability Statement

16S sequencing data are available in the NCBI Sequence Read Archive under BioProject Accession No.: PRJNA1365331. Additional data generated during this study are available from the corresponding author upon reasonable request.

Reproduced under the paper's license (CC BY-NC), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 2, 28 September 2026

  • Publisher: — → Karger Publishers

Version 1, 28 September 2026: the first record

Recorded: type, language, journal, pages, dates, 4 authors, 6 keywords, 1 funder, 59 references.

Cite

This paper

Peta Martinez, N. A., Reinoso Arnaldi, M., Santiago-Rodriguez, T. M., & Rodriguez-Fernandez, I. A. (2026). Microbiota-Based Interventions Differentially Rescue Gut and Social Behavior Phenotypes in <italic>Drosophila</italic> with Kdm5 Deficiency. Developmental neuroscience, 1-21. https://doi.org/10.1159/000552681

BibTeX

@article{petamartinez2026microbiota,
author = {Peta Martinez, Natalia A. and Reinoso Arnaldi, Melanie and Santiago-Rodriguez, Tasha M. and Rodriguez-Fernandez, Imilce A.},
title = {{Microbiota-Based Interventions Differentially Rescue Gut and Social Behavior Phenotypes in \<italic\>Drosophila\</italic\> with Kdm5 Deficiency}},
journal = {Developmental neuroscience},
year = {2026},
month = may,
pages = {1--21},
publisher = {Karger Publishers},
issn = {0378-5866},
doi = {10.1159/000552681},
url = {https://doi.org/10.1159/000552681},
pmid = {42166402},
pmcid = {PMC13412211}
}

RIS

TY - JOUR
AU - Peta Martinez, Natalia A.
AU - Reinoso Arnaldi, Melanie
AU - Santiago-Rodriguez, Tasha M.
AU - Rodriguez-Fernandez, Imilce A.
TI - Microbiota-Based Interventions Differentially Rescue Gut and Social Behavior Phenotypes in <italic>Drosophila</italic> with Kdm5 Deficiency
T2 - Developmental neuroscience
J2 - Dev Neurosci
PY - 2026
DA - 2026/05/21
SP - 1
EP - 21
SN - 0378-5866
PB - Karger Publishers
DO - 10.1159/000552681
UR - https://doi.org/10.1159/000552681
LA - en
ER -

CSL-JSON

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