Integrating high-throughput sequencing and metabolomics to investigate the stereoselective responses of soil microorganisms to chiral fungicide cis-epoxiconazole

• Published in: Chemosphere (Oxford) Vol. 300; p. 134198
• Main Authors: Xue, Pengfei, Liu, Xiaowei, Zhao, Liuqing, Zhang, Jingran, He, Zeying
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.08.2022
• Subjects: Cis-epoxiconazole; Epoxy Compounds; Fungicides, Industrial - analysis; Fungicides, Industrial - toxicity; High-Throughput Nucleotide Sequencing; High-throughput sequencing; Metabolomics; Metabolomics - methods; Soil - chemistry; Soil microorganism; Stereoisomerism; Stereoselectivity; Triazoles - chemistry; Stereoselectivity; Metabolomics; High-throughput sequencing; Soil microorganism; Cis-epoxiconazole
• ISSN: 0045-6535; 1879-1298
• DOI: 10.1016/j.chemosphere.2022.134198

The use of the chiral triazole fungicide cis-epoxiconazole in agricultural production continues to increase; however, little is known about the stereoselective and toxic responses of soil microorganisms to cis-epoxiconazole in the soil microenvironment. High-throughput sequencing and metabolomics were integrated to investigate the stereoselective response of soil microbial community structure, metabolic profile to cis-epoxiconazole exposure, and the correlation between the microbiomes and different metabolites. Soil microbial community structure and soil metabolic profile were significantly altered and exhibited significant enantioselectivity. The alpha diversity (Chao, Shannon, and Simpson diversity) of bacterial and fungus was not significantly affected, whereas the beta diversity (Bray-Curtis dissimilarity and PLS-DA) of bacterial and fungus was significantly altered in treatment of cis-epoxiconazole and its enantiomers (p-value < 0.05). The variation in bacterial and fungus community structure was the highest under (+)-enantiomer exposure, followed by exposure to racemate and (−)-enantiomer. Soil metabolomic analysis revealed that exposure to high or low doses of cis-epoxiconazole and its enantiomers resulted in different degrees of reprogramming of the soil metabolic pool. The 39 significantly changed metabolites mainly included small molecular organic acids, amino acids and their intermediates, and purine and adenosine intermediates. Six metabolic pathways were significantly disrupted. Different correlation patterns were observed between the significantly altered metabolites and microbes (p-value < 0.05) by Pearson correlation-based analysis. In conclusion, as xenobiotic pollutant, epoxiconazole altered the structure and metabolism of soil microorganisms with significant stereoselectivity mainly driven by 2R, 3S-(+)-cis-epoxiconazole. This study provided a more robust assessment of the risks of epoxiconazole exposure to soil microorganisms. Given the importance of the soil environment in agricultural production, characterization of the soil microbiome and metabolome can provide new insights into the ecological risks posed by exposure to the chiral triazole pesticide cis-epoxiconazole and its enantiomers. [Display omitted] •Cis-epoxiconazole showed stereoselective response in soil microbial community.•Cis-epoxiconazole showed stereoselective response in soil metabolic profile.•This study provided new insights for the microbiota stereoselective response.•The interdependence of soil metabolites and the microbiota was verified.