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Transcriptome-level assessment of the impact of deformed wing virus on honey bee larvae

Deformed wing virus (DWV) prevalence is high in honey bee (Apis mellifera) populations. The virus infects honey bees through vertical and horizontal transmission, leading to behavioural changes, wing deformity, and early mortality. To better understand the impacts of viral infection in the larval st...

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Autores principales: Chang, Zih-Ting, Huang, Yu-Feng, Chen, Yue-Wen, Yen, Ming-Ren, Hsu, Po-Ya, Chen, Tzu-Han, Li, Yi-Hsuan, Chiu, Kuo-Ping, Nai, Yu-Shin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298419/
https://www.ncbi.nlm.nih.gov/pubmed/34294840
http://dx.doi.org/10.1038/s41598-021-94641-3
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author Chang, Zih-Ting
Huang, Yu-Feng
Chen, Yue-Wen
Yen, Ming-Ren
Hsu, Po-Ya
Chen, Tzu-Han
Li, Yi-Hsuan
Chiu, Kuo-Ping
Nai, Yu-Shin
author_facet Chang, Zih-Ting
Huang, Yu-Feng
Chen, Yue-Wen
Yen, Ming-Ren
Hsu, Po-Ya
Chen, Tzu-Han
Li, Yi-Hsuan
Chiu, Kuo-Ping
Nai, Yu-Shin
author_sort Chang, Zih-Ting
collection PubMed
description Deformed wing virus (DWV) prevalence is high in honey bee (Apis mellifera) populations. The virus infects honey bees through vertical and horizontal transmission, leading to behavioural changes, wing deformity, and early mortality. To better understand the impacts of viral infection in the larval stage of honey bees, artificially reared honey bee larvae were infected with DWV (1.55 × 10(10) copies/per larva). No significant mortality occurred in infected honey bee larvae, while the survival rates decreased significantly at the pupal stage. Examination of DWV replication revealed that viral replication began at 2 days post inoculation (d.p.i.), increased dramatically to 4 d.p.i., and then continuously increased in the pupal stage. To better understand the impact of DWV on the larval stage, DWV-infected and control groups were subjected to transcriptomic analysis at 4 d.p.i. Two hundred fifty-five differentially expressed genes (DEGs) (fold change ≥ 2 or ≤ -2) were identified. Of these DEGs, 168 genes were downregulated, and 87 genes were upregulated. Gene Ontology (GO) analysis showed that 141 DEGs (55.3%) were categorized into molecular functions, cellular components and biological processes. One hundred eleven genes (38 upregulated and 73 downregulated) were annotated by KO (KEGG Orthology) pathway mapping and involved metabolic pathways, biosynthesis of secondary metabolites and glycine, serine and threonine metabolism pathways. Validation of DEGs was performed, and the related gene expression levels showed a similar tendency to the DEG predictions at 4 d.p.i.; cell wall integrity and stress response component 1 (wsc1), cuticular protein and myo-inositol 2-dehydrogenase (iolG) were significantly upregulated, and small conductance calcium-activated potassium channel protein (SK) was significantly downregulated at 4 d.p.i. Related gene expression levels at different d.p.i. revealed that these DEGs were significantly regulated from the larval stage to the pupal stage, indicating the potential impacts of gene expression levels from the larval to the pupal stages. Taken together, DWV infection in the honey bee larval stage potentially influences the gene expression levels from larvae to pupae and reduces the survival rate of the pupal stage. This information emphasizes the consequences of DWV prevalence in honey bee larvae for apiculture.
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spelling pubmed-82984192021-07-23 Transcriptome-level assessment of the impact of deformed wing virus on honey bee larvae Chang, Zih-Ting Huang, Yu-Feng Chen, Yue-Wen Yen, Ming-Ren Hsu, Po-Ya Chen, Tzu-Han Li, Yi-Hsuan Chiu, Kuo-Ping Nai, Yu-Shin Sci Rep Article Deformed wing virus (DWV) prevalence is high in honey bee (Apis mellifera) populations. The virus infects honey bees through vertical and horizontal transmission, leading to behavioural changes, wing deformity, and early mortality. To better understand the impacts of viral infection in the larval stage of honey bees, artificially reared honey bee larvae were infected with DWV (1.55 × 10(10) copies/per larva). No significant mortality occurred in infected honey bee larvae, while the survival rates decreased significantly at the pupal stage. Examination of DWV replication revealed that viral replication began at 2 days post inoculation (d.p.i.), increased dramatically to 4 d.p.i., and then continuously increased in the pupal stage. To better understand the impact of DWV on the larval stage, DWV-infected and control groups were subjected to transcriptomic analysis at 4 d.p.i. Two hundred fifty-five differentially expressed genes (DEGs) (fold change ≥ 2 or ≤ -2) were identified. Of these DEGs, 168 genes were downregulated, and 87 genes were upregulated. Gene Ontology (GO) analysis showed that 141 DEGs (55.3%) were categorized into molecular functions, cellular components and biological processes. One hundred eleven genes (38 upregulated and 73 downregulated) were annotated by KO (KEGG Orthology) pathway mapping and involved metabolic pathways, biosynthesis of secondary metabolites and glycine, serine and threonine metabolism pathways. Validation of DEGs was performed, and the related gene expression levels showed a similar tendency to the DEG predictions at 4 d.p.i.; cell wall integrity and stress response component 1 (wsc1), cuticular protein and myo-inositol 2-dehydrogenase (iolG) were significantly upregulated, and small conductance calcium-activated potassium channel protein (SK) was significantly downregulated at 4 d.p.i. Related gene expression levels at different d.p.i. revealed that these DEGs were significantly regulated from the larval stage to the pupal stage, indicating the potential impacts of gene expression levels from the larval to the pupal stages. Taken together, DWV infection in the honey bee larval stage potentially influences the gene expression levels from larvae to pupae and reduces the survival rate of the pupal stage. This information emphasizes the consequences of DWV prevalence in honey bee larvae for apiculture. Nature Publishing Group UK 2021-07-22 /pmc/articles/PMC8298419/ /pubmed/34294840 http://dx.doi.org/10.1038/s41598-021-94641-3 Text en © The Author(s) 2021 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
Chang, Zih-Ting
Huang, Yu-Feng
Chen, Yue-Wen
Yen, Ming-Ren
Hsu, Po-Ya
Chen, Tzu-Han
Li, Yi-Hsuan
Chiu, Kuo-Ping
Nai, Yu-Shin
Transcriptome-level assessment of the impact of deformed wing virus on honey bee larvae
title Transcriptome-level assessment of the impact of deformed wing virus on honey bee larvae
title_full Transcriptome-level assessment of the impact of deformed wing virus on honey bee larvae
title_fullStr Transcriptome-level assessment of the impact of deformed wing virus on honey bee larvae
title_full_unstemmed Transcriptome-level assessment of the impact of deformed wing virus on honey bee larvae
title_short Transcriptome-level assessment of the impact of deformed wing virus on honey bee larvae
title_sort transcriptome-level assessment of the impact of deformed wing virus on honey bee larvae
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298419/
https://www.ncbi.nlm.nih.gov/pubmed/34294840
http://dx.doi.org/10.1038/s41598-021-94641-3
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