Evidence map›Paper›PMID 32772242›Full record

ArticleEcotoxicology (London, England)2020

Reduction of gut microbial diversity and short chain fatty acids in BALB/c mice exposure to microcystin-LR.

Zhang Guilin, Zhang Pengyu, Li Wei, Hao Fengqi, Fangmei Chen, Yang Yu, Hou Yue, Tao Yuting

Abstract read
PubMed Publisher
In one paragraph

Article in Ecotoxicology (London, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 25 citations in OpenAlex.

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  5. Activation of P2Y1R impedes intestinal mucosa repair during colitis.International journal of biological sciences · 2023
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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

8 authors at 1 institution in 1 country.

Zhang GuilinChangchun University of Science and Technology, School of Life Science and Technology, Changchun, 130022, China.ORCID http://orcid.org/0000-0003-4924-1772
Zhang PengyuChangchun University of Science and Technology, School of Life Science and Technology, Changchun, 130022, China.
Li WeiChangchun University of Science and Technology, School of Life Science and Technology, Changchun, 130022, China. liwei5695084@163.com.
Hao FengqiChangchun University of Science and Technology, School of Life Science and Technology, Changchun, 130022, China.
Fangmei ChenChangchun University of Science and Technology, School of Life Science and Technology, Changchun, 130022, China.
Yang YuChangchun University of Science and Technology, School of Life Science and Technology, Changchun, 130022, China.
Hou YueChangchun University of Science and Technology, School of Life Science and Technology, Changchun, 130022, China.
Tao YutingChangchun University of Science and Technology, School of Life Science and Technology, Changchun, 130022, China.
Changchun University of Science and Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gut microbiota has been shown to play critical roles in host health. The present study was to determine the toxicological effects of microcystin-LR (MCLR) on gut microbial community and metabolites using 16S rDNA sequencing and gas chromatography-mass spectrometry (GC-MS). MCLR was administered to BALB/c mice by gavage for eight weeks. Results of the microbial alpha-diversity (Sobs, Chao1, ACE and Shannon indexes) decreased in MCLR-treated group versus controls. Phylum Candidatus Saccharibacteria decreased significantly in MCLR-treated group versus controls. Correspondingly, more than thirties genera in relative abundance decreased, especially short chain fatty acid (SCFA)-producing bacteria (e.g., Alistipes and Ruminococcus). These results indicated that the gut microbial community structure was remarkably changed by MCLR. Furthermore, concentrations of SCFAs were significantly decreased after MCLR exposure (P < 0.01), where butyrate decreased as high as 4.9-fold. Consequently, sub-chronic exposure to MCLR could not only alter the microbial composition but metabolites. This study offered novel insights into the toxic mechanism of MCs from gut microbiota, and facilitated further clarification of risks to human health from MCs exposure.

Indexed as

AnimalsBiodiversityFatty Acids, VolatileGastrointestinal MicrobiomeMarine ToxinsMiceMice, Inbred BALB CMicrocystinscyanoginosin LRFatty Acids, VolatileMarine ToxinsMicrocystinsGut microbiotaMetagenomicsMicrocystinShort-chain fatty acid

Identifiers

PMID32772242
OpenAlexW3047678113

What OpenQuestion holds

Textmetadata
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.