Chronic sub-lethal exposure to clothianidin triggers organismal and sub-organismal-level health hazards in a non-target organism, Drosophila melanogaster

噻虫胺 生物 毒理 有机体 新烟碱 黑腹果蝇 脂质过氧化 幼虫 杀虫剂 噻虫嗪 氧化应激 益达胺 生物化学 生态学 基因 古生物学
作者
Sayantani Nanda,Abhratanu Ganguly,Moutushi Mandi,Kanchana Das,Siddhartha Ghanty,Gopal Biswas,Prem Rajak
出处
期刊:Science of The Total Environment [Elsevier BV]
卷期号:: 172783-172783
标识
DOI:10.1016/j.scitotenv.2024.172783
摘要

Neonicotinoids are extensively used systemic pesticides across the globe. These chemicals have gathered significant attention for their potential adverse impacts on non-target organisms. Clothianidin is a novel neonicotinoid pesticide, widely used to control sucking and chewing types of pests. In nature, various non-target organisms can be exposed to this chemical. Nonetheless, extensive investigations demonstrating the sub-lethal impacts of clothianidin on non-targets are limited. Hence, the present study aimed to unravel the chronic sub-lethal impacts (LC50 0.74 μg/mL) of clothianidin on a non-target organism, Drosophila melanogaster. The study parameters involved multiple tiers of life covering from organism level to the sub-cellular level. 1st instar larvae were exposed to the six sub-lethal concentrations viz. 0.05, 0.06, 0.07, 0.08, 0.09, and 0.1 μg/mL of clothianidin till their 3rd larval instar. Investigations involving organism level have revealed clothianidin-induced significant reduction in the developmental duration, life span, phototaxis, and physical activities of the treated individuals. Interestingly, the tested compound has also altered the compound eye morphology of treated flies. Study was extended to the tissue and cellular levels where reduced cell viability in gut, brain, and fat body was apparent. Additionally, increased ROS production, nuclear disorganization, and higher lipid deposition were evident in gut of treated larvae. Study was further extended to the sub-cellular level where chronic exposure to clothianidin up-regulated the major oxidative stress markers such as lipid peroxidation, protein carbonylation, HSP-70, SOD, catalase, GSH, and thioredoxin reductase. Furthermore, the activities of detoxifying enzymes such as CYP4501A1 and GST were also altered. Chronic exposure to clothianidin also favored DNA fragmentation in treated larvae. In essence, results of this multi-level study depict the ROS-mediated toxicity of clothianidin on a non-target organism, D. melanogaster.
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