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Combined transcriptome and metabolite profiling analyses provide insights into the chronic toxicity of carbaryl and acetamiprid to Apis mellifera larvae

Despite many studies have revealed that developing honey bee (Apis mellifera) larvae are posting a high risk on exposure to insecticides, the toxicology information on bee larvae remain limited. The present study demonstrated the first assessment of the effects of no observed adverse effect concentr...

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Autores principales: Gao, Jing, Yang, Yang, Ma, Shilong, Liu, Feng, Wang, Qiang, Wang, Xing, Wu, Yanyan, Zhang, Li, Liu, Yongjun, Diao, Qingyun, Dai, Pingli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543932/
https://www.ncbi.nlm.nih.gov/pubmed/36207421
http://dx.doi.org/10.1038/s41598-022-21403-0
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author Gao, Jing
Yang, Yang
Ma, Shilong
Liu, Feng
Wang, Qiang
Wang, Xing
Wu, Yanyan
Zhang, Li
Liu, Yongjun
Diao, Qingyun
Dai, Pingli
author_facet Gao, Jing
Yang, Yang
Ma, Shilong
Liu, Feng
Wang, Qiang
Wang, Xing
Wu, Yanyan
Zhang, Li
Liu, Yongjun
Diao, Qingyun
Dai, Pingli
author_sort Gao, Jing
collection PubMed
description Despite many studies have revealed that developing honey bee (Apis mellifera) larvae are posting a high risk on exposure to insecticides, the toxicology information on bee larvae remain limited. The present study demonstrated the first assessment of the effects of no observed adverse effect concentration (NOAEC) of carbaryl (CR) and acetamiprid (ACE) on transcriptome and metabolome in honeybee larvae reared in vitro. Chronic exposure to carbaryl caused transcriptional disorders associated with oxidative stress. In addition, a series of metabolic homeostasis were disrupted by carbaryl stress, such amino acid metabolism, purine and pyrimidine metabolism and flavone and flavonol biosynthesis. The activities of enzymic biomarkers including GST, P450, CAT, AChE and SOD were not influenced by ACE stress, while the CR exposure slightly decreased the activity of CAT and SOD. Our results clearly show that ACE and CR display different potential to modulate transcriptome and metabolome associated with their different toxicity against bee larvae.
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spelling pubmed-95439322022-10-09 Combined transcriptome and metabolite profiling analyses provide insights into the chronic toxicity of carbaryl and acetamiprid to Apis mellifera larvae Gao, Jing Yang, Yang Ma, Shilong Liu, Feng Wang, Qiang Wang, Xing Wu, Yanyan Zhang, Li Liu, Yongjun Diao, Qingyun Dai, Pingli Sci Rep Article Despite many studies have revealed that developing honey bee (Apis mellifera) larvae are posting a high risk on exposure to insecticides, the toxicology information on bee larvae remain limited. The present study demonstrated the first assessment of the effects of no observed adverse effect concentration (NOAEC) of carbaryl (CR) and acetamiprid (ACE) on transcriptome and metabolome in honeybee larvae reared in vitro. Chronic exposure to carbaryl caused transcriptional disorders associated with oxidative stress. In addition, a series of metabolic homeostasis were disrupted by carbaryl stress, such amino acid metabolism, purine and pyrimidine metabolism and flavone and flavonol biosynthesis. The activities of enzymic biomarkers including GST, P450, CAT, AChE and SOD were not influenced by ACE stress, while the CR exposure slightly decreased the activity of CAT and SOD. Our results clearly show that ACE and CR display different potential to modulate transcriptome and metabolome associated with their different toxicity against bee larvae. Nature Publishing Group UK 2022-10-07 /pmc/articles/PMC9543932/ /pubmed/36207421 http://dx.doi.org/10.1038/s41598-022-21403-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gao, Jing
Yang, Yang
Ma, Shilong
Liu, Feng
Wang, Qiang
Wang, Xing
Wu, Yanyan
Zhang, Li
Liu, Yongjun
Diao, Qingyun
Dai, Pingli
Combined transcriptome and metabolite profiling analyses provide insights into the chronic toxicity of carbaryl and acetamiprid to Apis mellifera larvae
title Combined transcriptome and metabolite profiling analyses provide insights into the chronic toxicity of carbaryl and acetamiprid to Apis mellifera larvae
title_full Combined transcriptome and metabolite profiling analyses provide insights into the chronic toxicity of carbaryl and acetamiprid to Apis mellifera larvae
title_fullStr Combined transcriptome and metabolite profiling analyses provide insights into the chronic toxicity of carbaryl and acetamiprid to Apis mellifera larvae
title_full_unstemmed Combined transcriptome and metabolite profiling analyses provide insights into the chronic toxicity of carbaryl and acetamiprid to Apis mellifera larvae
title_short Combined transcriptome and metabolite profiling analyses provide insights into the chronic toxicity of carbaryl and acetamiprid to Apis mellifera larvae
title_sort combined transcriptome and metabolite profiling analyses provide insights into the chronic toxicity of carbaryl and acetamiprid to apis mellifera larvae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543932/
https://www.ncbi.nlm.nih.gov/pubmed/36207421
http://dx.doi.org/10.1038/s41598-022-21403-0
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