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Novel insights into the insect trancriptome response to a natural DNA virus

BACKGROUND: Little is known about invertebrate responses to DNA viruses. Here, we infect a commercially important pest moth species Plodia interpunctella with its naturally infecting DNA virus. We sequenced, assembled and annotated the complete transcriptome of the moth, and a partial transcriptome...

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Autores principales: McTaggart, Seanna J, Hannah, Tidbury, Bridgett, Stephen, Garbutt, Jennie S, Kaur, Gaganjot, Boots, Mike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415287/
https://www.ncbi.nlm.nih.gov/pubmed/25924671
http://dx.doi.org/10.1186/s12864-015-1499-z
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author McTaggart, Seanna J
Hannah, Tidbury
Bridgett, Stephen
Garbutt, Jennie S
Kaur, Gaganjot
Boots, Mike
author_facet McTaggart, Seanna J
Hannah, Tidbury
Bridgett, Stephen
Garbutt, Jennie S
Kaur, Gaganjot
Boots, Mike
author_sort McTaggart, Seanna J
collection PubMed
description BACKGROUND: Little is known about invertebrate responses to DNA viruses. Here, we infect a commercially important pest moth species Plodia interpunctella with its naturally infecting DNA virus. We sequenced, assembled and annotated the complete transcriptome of the moth, and a partial transcriptome of the virus. We then tested for differential gene expression between moths that were exposed to the virus and controls. RESULTS: We found 51 genes that were differentially expressed in moths exposed to a DNA baculovirus compared to controls. Gene set enrichment analysis revealed that cuticle proteins were significantly overrepresented in this group of genes. Interestingly, 6 of the 7 differentially expressed cuticle proteins were downregulated, suggesting that baculoviruses are able to manipulate its host’s response. In fact, an additional 29 of the 51 genes were also downregulated in exposed compared with control animals, including a gram-negative binding protein. In contrast, genes involved in transposable element movement were upregulated after infection. CONCLUSIONS: We present the first experiment to measure genome-wide gene expression in an insect after infection with a natural DNA virus. Our results indicate that cuticle proteins might be key genes underpinning the response to DNA viruses. Furthermore, the large proportion of genes that were downregulated after viral exposure suggests that this virus is actively manipulating the insect immune response. Finally, it appears that transposable element activity might increase during viral invasion. Combined, these results provide much needed host candidate genes that respond to DNA viral invaders.
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spelling pubmed-44152872015-05-01 Novel insights into the insect trancriptome response to a natural DNA virus McTaggart, Seanna J Hannah, Tidbury Bridgett, Stephen Garbutt, Jennie S Kaur, Gaganjot Boots, Mike BMC Genomics Research Article BACKGROUND: Little is known about invertebrate responses to DNA viruses. Here, we infect a commercially important pest moth species Plodia interpunctella with its naturally infecting DNA virus. We sequenced, assembled and annotated the complete transcriptome of the moth, and a partial transcriptome of the virus. We then tested for differential gene expression between moths that were exposed to the virus and controls. RESULTS: We found 51 genes that were differentially expressed in moths exposed to a DNA baculovirus compared to controls. Gene set enrichment analysis revealed that cuticle proteins were significantly overrepresented in this group of genes. Interestingly, 6 of the 7 differentially expressed cuticle proteins were downregulated, suggesting that baculoviruses are able to manipulate its host’s response. In fact, an additional 29 of the 51 genes were also downregulated in exposed compared with control animals, including a gram-negative binding protein. In contrast, genes involved in transposable element movement were upregulated after infection. CONCLUSIONS: We present the first experiment to measure genome-wide gene expression in an insect after infection with a natural DNA virus. Our results indicate that cuticle proteins might be key genes underpinning the response to DNA viruses. Furthermore, the large proportion of genes that were downregulated after viral exposure suggests that this virus is actively manipulating the insect immune response. Finally, it appears that transposable element activity might increase during viral invasion. Combined, these results provide much needed host candidate genes that respond to DNA viral invaders. BioMed Central 2015-04-17 /pmc/articles/PMC4415287/ /pubmed/25924671 http://dx.doi.org/10.1186/s12864-015-1499-z Text en © McTaggart et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
McTaggart, Seanna J
Hannah, Tidbury
Bridgett, Stephen
Garbutt, Jennie S
Kaur, Gaganjot
Boots, Mike
Novel insights into the insect trancriptome response to a natural DNA virus
title Novel insights into the insect trancriptome response to a natural DNA virus
title_full Novel insights into the insect trancriptome response to a natural DNA virus
title_fullStr Novel insights into the insect trancriptome response to a natural DNA virus
title_full_unstemmed Novel insights into the insect trancriptome response to a natural DNA virus
title_short Novel insights into the insect trancriptome response to a natural DNA virus
title_sort novel insights into the insect trancriptome response to a natural dna virus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415287/
https://www.ncbi.nlm.nih.gov/pubmed/25924671
http://dx.doi.org/10.1186/s12864-015-1499-z
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