Evidence map›Paper›PMID 30187502›Full record

ArticleJournal of applied toxicology : JAT2019

Irreversible effects of trichloroethylene on the gut microbial community and gut-associated immune responses in autoimmune-prone mice.

Sangeeta Khare, Kuppan Gokulan, Katherine Williams, Shasha Bai, Kathleen M Gilbert, Sarah J Blossom

Open access · greenAbstract read
In one paragraph

Article in Journal of applied toxicology : JAT, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 26% of its field
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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Exploring the relationship betweenFrontiers in neuroscience · 2025
    Article
  3. Review
  4. Parkinson's Disease Progression and Exposure to Contaminated Water at Camp Lejeune.Movement disorders : official journal of the Movement Disorder Society · 2024
    Article
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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

6 authors at 2 institutions in 1 country.

Sangeeta KhareDivision of Microbiology, National Center for Toxicological Research, 3900 NCTR Road, Jefferson, AR, 72079, USA.ORCID 0000-0002-9496-6636
Kuppan GokulanDivision of Microbiology, National Center for Toxicological Research, 3900 NCTR Road, Jefferson, AR, 72079, USA.
Katherine WilliamsDivision of Microbiology, National Center for Toxicological Research, 3900 NCTR Road, Jefferson, AR, 72079, USA.
Shasha BaiUniversity of Arkansas for Medical Sciences, Arkansas Children's Research Institute, Little Rock, AR, 72202, USA.
Kathleen M GilbertUniversity of Arkansas for Medical Sciences, Arkansas Children's Research Institute, Little Rock, AR, 72202, USA.
Sarah J BlossomUniversity of Arkansas for Medical Sciences, Arkansas Children's Research Institute, Little Rock, AR, 72202, USA.
Arkansas Children's Hospital · USNational Center for Toxicological Research · US

Funding

Developmental programming of TCE induced autoimmune diseaseR01ES021484 · NIEHS · ARKANSAS CHILDREN'S HOSPITAL RES INST · PI BLOSSOM, SARAH J, GILBERT, KATHLEEN M · 2013 to 2016
$1.4M
NIEHS NIH HHS R01 ES021484
6 · The paper itself

Abstract

The developing immune system is particularly sensitive to immunotoxicants. This study assessed trichloroethylene (TCE)-induced effects on the gut microbiome and cytokine production during the development in mice. Mice were exposed to TCE (0.05 or 500 μg/mL) at the levels that approximate to environmental or occupational exposure, respectively. Mice were subjected to a continuous developmental exposure to these doses encompassing gestation, lactation and continuing directly in the drinking water postnatally for 154 days (PND154) or PND259. To observe persistence of the effect TCE was removed from the drinking water in a subset of mice on PND154 and were provided regular drinking water until the study terminus (PND259). Abundance of total tissue-associated bacteria reduced only in mice exposed to TCE until PND259. The ratio of Firmicutes/Bacteroidetes did not alter during this continuos exposure; however, cessation of high-dose TCE at PND154 resulted in the increased abundance Bacteroidetes at PND259. Furthermore, high-dose TCE exposure until PND259 resulted in a lower abundance of the genera Bacteroides and Lactobaccilus and increased abundance of genus Bifidobactrium and bacterial family Enterobacteriaceae. TCE exposure until PND154 showed significant changes in the production of interleukin-33; that might play a dual role in maintaining the balance and homeostasis between commensal microbiota and mucosal health. At PND259, interleukin-3, granulocyte-macrophage colony-stimulating factor and Eotaxin were altered in both, the continuous exposure and cessation groups, whereas only a cessation group had a higher level of KC that may facilitate infiltration of neutrophils. The irreversible effects of TCE after a period of exposure cessation suggested a unique programming and potential toxicity of TCE even at the environmental level exposure.

Indexed as

AnimalsAnimals, NewbornAutoimmune DiseasesCytokinesDose-Response Relationship, DrugFemaleGastrointestinal MicrobiomeIleumImmunity, MucosalMaternal ExposureMiceMice, Inbred StrainsMicrobiotaPregnancyTrichloroethyleneWater Pollutants, ChemicalCytokinesTrichloroethyleneWater Pollutants, ChemicalbacteriaBacteroidetesFirmicutesgastrointestinalimmuneintestinemicrobiomeTCEtoxicityxenobiotic

Identifiers

PMID30187502
PMCPMC6338528
OpenAlexW2891695407

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.