Microbial colony sequencing combined with metabolomics revealed the effects of chronic hexavalent chromium and nickel combined exposure on intestinal inflammation in mice

被引:9
作者
Gu, Yueming [1 ]
Zheng, Shuangyan [1 ,2 ]
Huang, Cheng [1 ]
Cao, Xianhong [1 ]
Liu, Ping [1 ]
Zhuang, Yu [1 ]
Li, Guyue [1 ]
Hu, Guoliang [1 ]
Gao, Xiaona [1 ]
Guo, Xiaoquan [1 ]
机构
[1] Jiangxi Agr Univ, Inst Anim Populat Hlth, Coll Anim Sci & Technol, Jiangxi Prov Key Lab Anim Hlth, Nanchang 330045, Peoples R China
[2] Nanchang Univ, Sino German Joint Res Inst, Nanchang 330047, Peoples R China
基金
国家重点研发计划;
关键词
Hexavalent chromium; Nickel; Inflammatory response; Microbiome; Metabolomics; GUT MICROBIOTA; TRACE-ELEMENTS; TOXICITY;
D O I
10.1016/j.scitotenv.2023.169853
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The pollution and toxic effects of hexavalent chromium [Cr(VI)] and divalent nickel [Ni(II)] have become worldwide public health issues. However, the potential detailed effects of chronic combined Cr(VI) and Ni exposure on colonic inflammation in mice have not been reported. In this study, 16S rDNA sequencing, metabolomics data analysis, qPCR and other related experimental techniques were used to comprehensively explore the mechanism of toxic damage and the inflammatory response of the colon in mice under the co-toxicity of chronic hexavalent chromium and nickel. The results showed that long-term exposure to Cr(VI) and/or Ni resulted in an imbalance of trace elements in the colon of mice with significant inflammatory infiltration of tissues. Moreover, Cr(VI) and/or Ni poisoning upregulated the expression levels of IL -6, IL -18, IL-1 beta, TNF-alpha, IFN gamma, JAK2 and STAT3 mRNA, and downregulated IL -10 mRNA, which was highly consistent with the trend in protein expression. Combined with multiomics analysis, Cr(VI) and/or Ni could change the alpha diversity and beta diversity of the gut microbiota and induce significant differential changes in metabolites such as Pyroglu-Glu-Lys, Val -Asp -Arg, stearidonic acid, and 20-hydroxyarachidonic acid. They are also associated with disorders of important metabolic pathways such as lipid metabolism and amino acid metabolism. Correlation analysis revealed that there was a significant correlation between gut microbes and metabolites (P < 0.05). In summary, based on the advantages of comprehensive analysis of high -throughput sequencing sets, these results suggest that chronic exposure to Cr(VI) and Ni in combination can cause microbial flora imbalances, induce metabolic disorders, and subsequently cause colonic damage in mice. These data provide new insights into the toxicology and molecular mechanisms of Cr(VI) and Ni.
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页数:14
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