评估土壤环境中戊硫磷的立体选择性生物活性和生物毒性,以提高药效和减少危害。

Kuan Fang, Tong Liu, Guo Tian, Wei Sun, Xiangwei You, Xiuguo Wang
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引用次数: 0

摘要

Penthiopyrad 是一种手性杀虫剂,已被广泛应用于农业生产。然而,对戊噻菌胺在土壤环境中的立体选择性生物活性和生物毒性的系统评价尚不充分。本研究考察了苯噻菌胺对三种土传病原菌的立体选择性生物活性及其对土壤非靶标生物的立体选择性生物毒性。结果表明,由于 S-penthiopyrad 与不同目标病原体中 SDH 的作用模式不同,其生物活性分别是 R-penthiopyrad 的 546 倍、76 倍和 1.1 倍。与 R-penthiopyrad 相比,S-penthiopyrad 在土壤环境中的持久性更强,生物累积性也更强。苯噻菌胺在蚯蚓体内的积累诱导了解毒系统的反应,导致 GST、CarE 和 CYP450 等解毒酶的活性显著增加。此外,S-吡噻菌胺和 R-吡噻菌胺都能诱导蚯蚓细胞凋亡、肠道损伤和不同基因的表达,尤其是 S-吡噻菌胺。此外,S-吡蚜酮与 COL6A 和 ACE 蛋白的结合能力更强,而 R-吡蚜酮与 CYP450 家族蛋白的结合能力更强,这可能是 PEN 对映体之间生物毒性不同的主要原因。考虑到 Penthiopyrad 对映体在生物活性和生物毒性方面的差异,以及农药对目标生物和非目标生物的作用模式,S-penthiopyrad 具有更大的未来开发潜力。
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Assessing the stereoselective bioactivity and biotoxicity of penthiopyrad in soil environment for efficacy improvement and hazard reduction.

Penthiopyrad, a chiral pesticide, has been widely used in agricultural production. However, systematic evaluation of stereoselective bioactivity and biotoxicity of penthiopyrad in soil environment is insufficient. In this study, the stereoselective bioactivity of penthiopyrad against three soil-borne disease pathogens and its stereoselective biotoxicity to soil non-target organisms were investigated. The present results showed that the bioactivities of S-penthiopyrad were 546, 76 and 1.1-fold higher than those of R-penthiopyrad due to their different interaction modes with SDH in different target pathogens. S-penthiopyrad was more persistent in the soil environment and had stronger bioaccumulation than R-penthiopyrad. The accumulation of penthiopyrad in earthworms induced the response of detoxification system, resulting in the significant increases in the activity of detoxifying enzymes, such as GST, CarE, and CYP450. Additionally, both S-penthiopyrad and R-penthiopyrad induced cell apoptosis, intestinal damage and differentially expressed genes in earthworms, especially S-penthiopyrad. Furthermore, S-penthiopyrad has stronger binding capacity with COL6A and ACE proteins, while R-penthiopyrad has stronger binding capacity with CYP450 family proteins, which may be the main reason for the differences in biotoxicity between PEN enantiomers. Considering the differences in bioactivity and biotoxicity of penthiopyrad enantiomers, as well as the modes of action of pesticides on target and non-target organisms, S-penthiopyrad has greater potential for future development.

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