Evidence map›Paper›PMID 39520540›Full record

ArticleArchives of toxicology2025

Maternal probiotic supplementation protects against PBDE-induced developmental, behavior and metabolic reprogramming in a sexually dimorphic manner: Role of gut microbiome.

Maximillian E Denys, Elena V Kozlova, Rui Liu, Anthony E Bishay, Elyza A Do, Varadh Piamthai, Yash V Korde, Crystal N Luna, Artha A Lam, Ansel Hsiao and 1 more

Abstract read
In one paragraph

Article in Archives of toxicology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
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

11 authors.

Maximillian E Denys *Department of Molecular Cell and Systems Biology, University of California, Riverside, CA, 92521, USA.ORCID 0000-0002-7423-6265
Elena V Kozlova *Department of Molecular Cell and Systems Biology, University of California, Riverside, CA, 92521, USA.ORCID 0000-0002-4691-6618
Rui LiuDepartment of Microbiology and Plant Pathology, University of California, Riverside, CA, USA.
Anthony E BishayDepartment of Molecular Cell and Systems Biology, University of California, Riverside, CA, 92521, USA.ORCID 0000-0002-6057-3770
Elyza A DoDepartment of Microbiology and Plant Pathology, University of California, Riverside, CA, USA.ORCID 0000-0003-3264-8138
Varadh PiamthaiDepartment of Microbiology and Plant Pathology, University of California, Riverside, CA, USA.ORCID 0009-0008-8273-8653
Yash V KordeDepartment of Molecular Cell and Systems Biology, University of California, Riverside, CA, 92521, USA.
Crystal N LunaDepartment of Molecular Cell and Systems Biology, University of California, Riverside, CA, 92521, USA.ORCID 0009-0003-3003-0665
Artha A LamDepartment of Molecular Cell and Systems Biology, University of California, Riverside, CA, 92521, USA.ORCID 0009-0001-1023-5204
Ansel HsiaoDepartment of Microbiology and Plant Pathology, University of California, Riverside, CA, USA.
Margarita Currás-CollazoDepartment of Molecular Cell and Systems Biology, University of California, Riverside, CA, 92521, USA. mcur@ucr.edu.ORCID 0000-0002-0189-4179

Funding

Gut microbiome-mediated small-molecule signaling and resistance to invading microorganismsR35GM124724 · NIGMS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI HSIAO, ANSEL · 2017 to 2021
$1.8M
Interpersonal variation in microbiome structure modulates inter-individual immune responses to Vibrio choleraeF31AI179030 · NIAID · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI Elyza Amber Do · 2023 to 2026
$98k
Maternal Transfer of Oxytocin and Thyroid-disrupting Indoor Flame Retardants Affecting Offspring Social BrainF31ES034304 · NIEHS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI KOZLOVA, ELENA V · 2023 to 2024
$83k
Foundation for the National Institutes of Health F31AI179030Foundation for the National Institutes of Health F31ES034304Foundation for the National Institutes of Health R35GM124724NIAID NIH HHS F31 AI179030NIEHS NIH HHS F31 ES034304NIGMS NIH HHS R35 GM124724
6 · The paper itself

Abstract

Polybrominated diphenyl ethers (PBDEs) are endocrine-disrupting persistent organic pollutants (POPs) used as flame retardants in a wide range of commercial applications. We have previously reported neurobehavioral and metabolic reprogramming produced by developmental PBDEs. PBDEs perturb the microbiome, an influencer of life-long health, while probiotic supplementation with Limosilactobacillus reuteri (LR) can avert neurobehavioral and endocrine disruption. We, therefore, tested the hypothesis that perinatal maternal LR supplementation would protect gut microbiome richness and diversity, developmental milestones, adult neurobehavior and metabolic homeostasis in PBDE-exposed offspring. C57BL/6N dams were orally exposed to a commercial penta-mixture of PBDEs, DE-71, at 0.1 mg/kg/day, or corn oil vehicle (VEH/CON) during gestation and lactation. Mice offspring received DE-71 or VEH/CON with or without co-administration of LR (ATCC-PTA-6475) indirectly via their mother from gestational day (GD) 0 until postnatal day (P)21 (Cohort 1), or continued to receive LR directly from P22 through adulthood (Cohort 2). Results of fecal 16S rRNA sequencing indicated age- and sex-dependent effects of DE-71 on gut microbial communities. Maternal LR treatment protected against DE-71-induced reduction in α-diversity in P22 females and against β-diversity alterations in P30 males. In females, DE-71 changed the relative abundance of specific bacterial taxa, such as Tenericutes and Cyanobacteria (elevated) and Deferribacterota (reduced). In males, several Firmicutes taxa were elevated, while Proteobacteria, Chlamydiae, and several Bacteroidota taxa were reduced. The number of disrupted taxa normalized by maternal LR supplementation was as follows: 100% in P22 females and 33% in males at P22 and 25% at P30. Maternal LR treatment protected against DE-71-induced delay of postnatal body weight gain in males and ameliorated the abnormal timing of incisor eruption in both sexes. Further, DE-71 produced exaggerated digging in both sexes as well as locomotor hyperactivity in females, effects that were mitigated by maternal LR only in females. Other benefits of LR therapy included normalization of glucose tolerance, insulin-to-glucose ratio and plasma leptin in adult DE-71 females (Cohort 2). This study provides evidence that probiotic supplementation can mitigate POP-induced reprogramming of neurodevelopment, adult neurobehavior, and glucose metabolism in association with modified gut microbial community structure in a sex-dependent manner.

Indexed as

Endocrine DisruptorsFlame RetardantsGastrointestinal MicrobiomeHalogenated Diphenyl EthersPrenatal Exposure Delayed EffectsProbioticsAnimalsBehavior, AnimalDietary SupplementsFemaleMaleMaternal ExposureMetabolic ReprogrammingMiceMice, Inbred C57BLPregnancyEndocrine DisruptorsFlame RetardantsHalogenated Diphenyl EthersBody weightDE-71Endocrine-disrupting chemicalsEye openingGlucoseIncisor eruptionLactobacillus reuteriLimosilactobacillus reuteriThyroid

Identifiers

PMID39520540
PMCPMC11748483

What Socratic holds

Textmetadata
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 Socratic graph.