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Thiamethoxam exposure deregulates short ORF gene expression in the honey bee and compromises immune response to bacteria

Maximizing crop yields relies on the use of agrochemicals to control insect pests. One of the most widely used classes of insecticides are neonicotinoids that interfere with signalling of the neurotransmitter acetylcholine, but these can also disrupt crop-pollination services provided by bees. Here,...

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Autores principales: Decio, Pâmela, Ustaoglu, Pinar, Derecka, Kamila, Hardy, Ian C. W., Roat, Thaisa C., Malaspina, Osmar, Mongan, Nigel, Stöger, Reinhard, Soller, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7811001/
https://www.ncbi.nlm.nih.gov/pubmed/33452318
http://dx.doi.org/10.1038/s41598-020-80620-7
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author Decio, Pâmela
Ustaoglu, Pinar
Derecka, Kamila
Hardy, Ian C. W.
Roat, Thaisa C.
Malaspina, Osmar
Mongan, Nigel
Stöger, Reinhard
Soller, Matthias
author_facet Decio, Pâmela
Ustaoglu, Pinar
Derecka, Kamila
Hardy, Ian C. W.
Roat, Thaisa C.
Malaspina, Osmar
Mongan, Nigel
Stöger, Reinhard
Soller, Matthias
author_sort Decio, Pâmela
collection PubMed
description Maximizing crop yields relies on the use of agrochemicals to control insect pests. One of the most widely used classes of insecticides are neonicotinoids that interfere with signalling of the neurotransmitter acetylcholine, but these can also disrupt crop-pollination services provided by bees. Here, we analysed whether chronic low dose long-term exposure to the neonicotinoid thiamethoxam alters gene expression and alternative splicing in brains of Africanized honey bees, Apis mellifera, as adaptation to altered neuronal signalling. We find differentially regulated genes that show concentration-dependent responses to thiamethoxam, but no changes in alternative splicing. Most differentially expressed genes have no annotated function but encode short Open Reading Frames, a characteristic feature of anti-microbial peptides. As this suggested that immune responses may be compromised by thiamethoxam exposure, we tested the impact of thiamethoxam on bee immunity by injecting bacteria. We show that intrinsically sub-lethal thiamethoxam exposure makes bees more vulnerable to normally non-pathogenic bacteria. Our findings imply a synergistic mechanism for the observed bee population declines that concern agriculturists, conservation ecologists and the public.
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spelling pubmed-78110012021-01-21 Thiamethoxam exposure deregulates short ORF gene expression in the honey bee and compromises immune response to bacteria Decio, Pâmela Ustaoglu, Pinar Derecka, Kamila Hardy, Ian C. W. Roat, Thaisa C. Malaspina, Osmar Mongan, Nigel Stöger, Reinhard Soller, Matthias Sci Rep Article Maximizing crop yields relies on the use of agrochemicals to control insect pests. One of the most widely used classes of insecticides are neonicotinoids that interfere with signalling of the neurotransmitter acetylcholine, but these can also disrupt crop-pollination services provided by bees. Here, we analysed whether chronic low dose long-term exposure to the neonicotinoid thiamethoxam alters gene expression and alternative splicing in brains of Africanized honey bees, Apis mellifera, as adaptation to altered neuronal signalling. We find differentially regulated genes that show concentration-dependent responses to thiamethoxam, but no changes in alternative splicing. Most differentially expressed genes have no annotated function but encode short Open Reading Frames, a characteristic feature of anti-microbial peptides. As this suggested that immune responses may be compromised by thiamethoxam exposure, we tested the impact of thiamethoxam on bee immunity by injecting bacteria. We show that intrinsically sub-lethal thiamethoxam exposure makes bees more vulnerable to normally non-pathogenic bacteria. Our findings imply a synergistic mechanism for the observed bee population declines that concern agriculturists, conservation ecologists and the public. Nature Publishing Group UK 2021-01-15 /pmc/articles/PMC7811001/ /pubmed/33452318 http://dx.doi.org/10.1038/s41598-020-80620-7 Text en © The Author(s) 2021 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/.
spellingShingle Article
Decio, Pâmela
Ustaoglu, Pinar
Derecka, Kamila
Hardy, Ian C. W.
Roat, Thaisa C.
Malaspina, Osmar
Mongan, Nigel
Stöger, Reinhard
Soller, Matthias
Thiamethoxam exposure deregulates short ORF gene expression in the honey bee and compromises immune response to bacteria
title Thiamethoxam exposure deregulates short ORF gene expression in the honey bee and compromises immune response to bacteria
title_full Thiamethoxam exposure deregulates short ORF gene expression in the honey bee and compromises immune response to bacteria
title_fullStr Thiamethoxam exposure deregulates short ORF gene expression in the honey bee and compromises immune response to bacteria
title_full_unstemmed Thiamethoxam exposure deregulates short ORF gene expression in the honey bee and compromises immune response to bacteria
title_short Thiamethoxam exposure deregulates short ORF gene expression in the honey bee and compromises immune response to bacteria
title_sort thiamethoxam exposure deregulates short orf gene expression in the honey bee and compromises immune response to bacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7811001/
https://www.ncbi.nlm.nih.gov/pubmed/33452318
http://dx.doi.org/10.1038/s41598-020-80620-7
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