Thiamethoxam-induced stress responses in Melipona scutellaris: insights into the toxicological effects on Malpighian tubules

IF 2.2 3区 农林科学 Q1 ENTOMOLOGY
Lucas Miotelo, Geovana Maloni, Tatiane Caroline Grella, Roberta Cornélio Ferreira Nocelli, Milene Ferro, Osmar Malaspina
{"title":"Thiamethoxam-induced stress responses in Melipona scutellaris: insights into the toxicological effects on Malpighian tubules","authors":"Lucas Miotelo,&nbsp;Geovana Maloni,&nbsp;Tatiane Caroline Grella,&nbsp;Roberta Cornélio Ferreira Nocelli,&nbsp;Milene Ferro,&nbsp;Osmar Malaspina","doi":"10.1007/s13592-025-01203-x","DOIUrl":null,"url":null,"abstract":"<div><p>The increasing use of pesticides has been identified as a major driver of pollinator decline. Thiamethoxam, a neonicotinoid pesticide, poses a significant threat to neotropical bees by impacting behavior and physiology. Despite the ecological importance of stingless bees, little is known about the effects of pesticides on these species. This study investigated the effects of a sublethal concentration of thiamethoxam on the Malpighian tubules (key organs responsible for excretion and detoxification) in <i>Melipona scutellaris</i>. Using immunolabeling techniques, we analyzed the expression of heat shock proteins (HSP70 and HSP90) and cellular stress biomarkers, and evaluated cell death through the TUNEL method. Results showed an increase in HSP70 expression on day 1 of exposure, followed by a decrease on day 8, while HSP90 exhibited the opposite trend. The observed pattern for HSP70 suggests that the Malpighian tubules initially responded to oxidative stress caused by acute exposure (1 day), while after 8 days, other metabolic responses or pathways may have been activated to counteract cellular stress. In contrast, the pattern for HSP90, which was opposite to that of HSP70, may indicate a compensatory response, with increased HSP90 levels potentially protecting the Malpighian tubules as HSP70 levels declined. Additionally, TUNEL assays revealed minimal DNA fragmentation by the eighth day of exposure. These findings highlight the complex response of <i>M. scutellaris</i> to TMX and underscore the need for further ecotoxicological research on stingless bees to better understand the impacts of pesticides on non-target species.</p></div>","PeriodicalId":8078,"journal":{"name":"Apidologie","volume":"56 5","pages":""},"PeriodicalIF":2.2000,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Apidologie","FirstCategoryId":"97","ListUrlMain":"https://link.springer.com/article/10.1007/s13592-025-01203-x","RegionNum":3,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The increasing use of pesticides has been identified as a major driver of pollinator decline. Thiamethoxam, a neonicotinoid pesticide, poses a significant threat to neotropical bees by impacting behavior and physiology. Despite the ecological importance of stingless bees, little is known about the effects of pesticides on these species. This study investigated the effects of a sublethal concentration of thiamethoxam on the Malpighian tubules (key organs responsible for excretion and detoxification) in Melipona scutellaris. Using immunolabeling techniques, we analyzed the expression of heat shock proteins (HSP70 and HSP90) and cellular stress biomarkers, and evaluated cell death through the TUNEL method. Results showed an increase in HSP70 expression on day 1 of exposure, followed by a decrease on day 8, while HSP90 exhibited the opposite trend. The observed pattern for HSP70 suggests that the Malpighian tubules initially responded to oxidative stress caused by acute exposure (1 day), while after 8 days, other metabolic responses or pathways may have been activated to counteract cellular stress. In contrast, the pattern for HSP90, which was opposite to that of HSP70, may indicate a compensatory response, with increased HSP90 levels potentially protecting the Malpighian tubules as HSP70 levels declined. Additionally, TUNEL assays revealed minimal DNA fragmentation by the eighth day of exposure. These findings highlight the complex response of M. scutellaris to TMX and underscore the need for further ecotoxicological research on stingless bees to better understand the impacts of pesticides on non-target species.

噻虫嗪诱导的黄芩应激反应:对马氏小管毒理学效应的研究
农药使用量的增加已被确定为传粉媒介减少的主要驱动因素。噻虫嗪是一种新烟碱类杀虫剂,通过影响蜜蜂的行为和生理对新热带蜜蜂造成重大威胁。尽管无刺蜜蜂具有重要的生态意义,但人们对农药对这些物种的影响知之甚少。本研究探讨了亚致死浓度噻虫嗪对黄鳝马氏小管(负责排泄和解毒的关键器官)的影响。利用免疫标记技术分析热休克蛋白(HSP70和HSP90)和细胞应激生物标志物的表达,并通过TUNEL方法评估细胞死亡。结果显示,HSP70在暴露第1天表达升高,第8天表达降低,而HSP90则相反。观察到的HSP70模式表明,马尔比氏小管最初对急性暴露引起的氧化应激(1天)做出反应,而在8天后,其他代谢反应或途径可能被激活以抵消细胞应激。相反,HSP90的模式与HSP70相反,可能表明代偿反应,当HSP70水平下降时,HSP90水平升高可能会保护马尔比氏小管。此外,TUNEL分析显示,暴露后第8天,DNA断裂最小。这些发现强调了黄花蜜蜂对TMX的复杂反应,并强调了进一步对无刺蜜蜂进行生态毒理学研究的必要性,以更好地了解农药对非目标物种的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Apidologie
Apidologie 生物-昆虫学
CiteScore
5.10
自引率
8.30%
发文量
64
审稿时长
3 months
期刊介绍: Apidologie is a peer-reviewed journal devoted to the biology of insects belonging to the superfamily Apoidea. Its range of coverage includes behavior, ecology, pollination, genetics, physiology, systematics, toxicology and pathology. Also accepted are papers on the rearing, exploitation and practical use of Apoidea and their products, as far as they make a clear contribution to the understanding of bee biology. Apidologie is an official publication of the Institut National de la Recherche Agronomique (INRA) and Deutscher Imkerbund E.V. (D.I.B.)
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信