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

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 B...

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Publié dans:Ecotoxicology (London, England). - 1992. - 29(2020), 9 vom: 09. Nov., Seite 1347-1357
Auteur principal: Guilin, Zhang (Auteur)
Autres auteurs: Pengyu, Zhang, Wei, Li, Fengqi, Hao, Chen, Fangmei, Yu, Yang, Yue, Hou, Yuting, Tao
Format: Article en ligne
Langue:English
Publié: 2020
Accès à la collection:Ecotoxicology (London, England)
Sujets:Journal Article Gut microbiota Metagenomics Microcystin Short-chain fatty acid Fatty Acids, Volatile Marine Toxins Microcystins cyanoginosin LR EQ8332842Y
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Résumé: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
Description:Date Completed 28.10.2020
Date Revised 10.12.2020
published: Print-Electronic
Citation Status MEDLINE
ISSN:1573-3017
DOI:10.1007/s10646-020-02254-9