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Fluvalinate-Induced Changes in MicroRNA Expression Profile of Apis mellifera ligustica Brain Tissue
Fluvalinate is a widely used and relatively safe acaricide for honeybees, but it still has a negative impact on honeybee colonies. Such negative effects may be related to fluvalinate-induced brain nerve tissue damage, but the detailed molecular regulatory mechanism of this phenomenon is still poorly...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039055/ https://www.ncbi.nlm.nih.gov/pubmed/35495168 http://dx.doi.org/10.3389/fgene.2022.855987 |
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author | Tianle, Chao Liuxu, Yang Delong, Lou Yunhan, Fan Yu, He Xueqing, Shan Haitao, Xia Guizhi, Wang |
author_facet | Tianle, Chao Liuxu, Yang Delong, Lou Yunhan, Fan Yu, He Xueqing, Shan Haitao, Xia Guizhi, Wang |
author_sort | Tianle, Chao |
collection | PubMed |
description | Fluvalinate is a widely used and relatively safe acaricide for honeybees, but it still has a negative impact on honeybee colonies. Such negative effects may be related to fluvalinate-induced brain nerve tissue damage, but the detailed molecular regulatory mechanism of this phenomenon is still poorly understood. In this study, we analyzed the miRNA expression profile changes in the brain tissue of Apis mellifera ligustica by miRNA sequencing after fluvalinate treatment. A total of 1,350 miRNAs were expressed in Apis mellifera ligustica brain tissue, of which only 180 were previously known miRNAs in honeybees. Among all known and novel miRNAs, 15 were differentially expressed between at least two of the four time periods before and after fluvalinate administration. Further analysis revealed five significantly enriched KEGG pathways of the differentially expressed miRNA (DEM) potential target genes, namely, “Hippo signaling pathway-fly,” “Phototransduction-fly,” “Apoptosis-fly,” “Wnt signaling pathway,” and “Dorso-ventral axis formation,” which indicates that differentially expressed miRNA function may be related to cell apoptosis and memory impairment in the fluvalinate-treated Apis mellifera ligustica brain. Ame-miR-3477-5p, ame-miR-375-3p, and miR-281-x were identified as key miRNAs. Overall, our research provides new insights into the roles of miRNAs in brain tissue during the process of fluvalinate-induced Apis mellifera ligustica poisoning. |
format | Online Article Text |
id | pubmed-9039055 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90390552022-04-27 Fluvalinate-Induced Changes in MicroRNA Expression Profile of Apis mellifera ligustica Brain Tissue Tianle, Chao Liuxu, Yang Delong, Lou Yunhan, Fan Yu, He Xueqing, Shan Haitao, Xia Guizhi, Wang Front Genet Genetics Fluvalinate is a widely used and relatively safe acaricide for honeybees, but it still has a negative impact on honeybee colonies. Such negative effects may be related to fluvalinate-induced brain nerve tissue damage, but the detailed molecular regulatory mechanism of this phenomenon is still poorly understood. In this study, we analyzed the miRNA expression profile changes in the brain tissue of Apis mellifera ligustica by miRNA sequencing after fluvalinate treatment. A total of 1,350 miRNAs were expressed in Apis mellifera ligustica brain tissue, of which only 180 were previously known miRNAs in honeybees. Among all known and novel miRNAs, 15 were differentially expressed between at least two of the four time periods before and after fluvalinate administration. Further analysis revealed five significantly enriched KEGG pathways of the differentially expressed miRNA (DEM) potential target genes, namely, “Hippo signaling pathway-fly,” “Phototransduction-fly,” “Apoptosis-fly,” “Wnt signaling pathway,” and “Dorso-ventral axis formation,” which indicates that differentially expressed miRNA function may be related to cell apoptosis and memory impairment in the fluvalinate-treated Apis mellifera ligustica brain. Ame-miR-3477-5p, ame-miR-375-3p, and miR-281-x were identified as key miRNAs. Overall, our research provides new insights into the roles of miRNAs in brain tissue during the process of fluvalinate-induced Apis mellifera ligustica poisoning. Frontiers Media S.A. 2022-04-12 /pmc/articles/PMC9039055/ /pubmed/35495168 http://dx.doi.org/10.3389/fgene.2022.855987 Text en Copyright © 2022 Tianle, Liuxu, Delong, Yunhan, Yu, Xueqing, Haitao and Guizhi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Genetics Tianle, Chao Liuxu, Yang Delong, Lou Yunhan, Fan Yu, He Xueqing, Shan Haitao, Xia Guizhi, Wang Fluvalinate-Induced Changes in MicroRNA Expression Profile of Apis mellifera ligustica Brain Tissue |
title | Fluvalinate-Induced Changes in MicroRNA Expression Profile of Apis mellifera ligustica Brain Tissue |
title_full | Fluvalinate-Induced Changes in MicroRNA Expression Profile of Apis mellifera ligustica Brain Tissue |
title_fullStr | Fluvalinate-Induced Changes in MicroRNA Expression Profile of Apis mellifera ligustica Brain Tissue |
title_full_unstemmed | Fluvalinate-Induced Changes in MicroRNA Expression Profile of Apis mellifera ligustica Brain Tissue |
title_short | Fluvalinate-Induced Changes in MicroRNA Expression Profile of Apis mellifera ligustica Brain Tissue |
title_sort | fluvalinate-induced changes in microrna expression profile of apis mellifera ligustica brain tissue |
topic | Genetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039055/ https://www.ncbi.nlm.nih.gov/pubmed/35495168 http://dx.doi.org/10.3389/fgene.2022.855987 |
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