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Wolbachia and Virus Alter the Host Transcriptome at the Interface of Nucleotide Metabolism Pathways
Wolbachia is a maternally transmitted bacterium that manipulates arthropod and nematode biology in myriad ways. The Wolbachia strain colonizing Drosophila melanogaster creates sperm-egg incompatibilities and protects its host against RNA viruses, making it a promising tool for vector control. Despit...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7885120/ https://www.ncbi.nlm.nih.gov/pubmed/33563832 http://dx.doi.org/10.1128/mBio.03472-20 |
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author | Lindsey, Amelia R. I. Bhattacharya, Tamanash Hardy, Richard W. Newton, Irene L. G. |
author_facet | Lindsey, Amelia R. I. Bhattacharya, Tamanash Hardy, Richard W. Newton, Irene L. G. |
author_sort | Lindsey, Amelia R. I. |
collection | PubMed |
description | Wolbachia is a maternally transmitted bacterium that manipulates arthropod and nematode biology in myriad ways. The Wolbachia strain colonizing Drosophila melanogaster creates sperm-egg incompatibilities and protects its host against RNA viruses, making it a promising tool for vector control. Despite successful trials using Wolbachia-transfected mosquitoes for dengue control, knowledge of how Wolbachia and viruses jointly affect insect biology remains limited. Using the Drosophila melanogaster model, transcriptomics and gene expression network analyses revealed pathways with altered expression and splicing due to Wolbachia colonization and virus infection. Included are metabolic pathways previously unknown to be important for Wolbachia-host interactions. Additionally, Wolbachia-colonized flies exhibit a dampened transcriptomic response to virus infection, consistent with early blocking of virus replication. Finally, using Drosophila genetics, we show that Wolbachia and expression of nucleotide metabolism genes have interactive effects on virus replication. Understanding the mechanisms of pathogen blocking will contribute to the effective development of Wolbachia-mediated vector control programs. |
format | Online Article Text |
id | pubmed-7885120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-78851202021-02-19 Wolbachia and Virus Alter the Host Transcriptome at the Interface of Nucleotide Metabolism Pathways Lindsey, Amelia R. I. Bhattacharya, Tamanash Hardy, Richard W. Newton, Irene L. G. mBio Research Article Wolbachia is a maternally transmitted bacterium that manipulates arthropod and nematode biology in myriad ways. The Wolbachia strain colonizing Drosophila melanogaster creates sperm-egg incompatibilities and protects its host against RNA viruses, making it a promising tool for vector control. Despite successful trials using Wolbachia-transfected mosquitoes for dengue control, knowledge of how Wolbachia and viruses jointly affect insect biology remains limited. Using the Drosophila melanogaster model, transcriptomics and gene expression network analyses revealed pathways with altered expression and splicing due to Wolbachia colonization and virus infection. Included are metabolic pathways previously unknown to be important for Wolbachia-host interactions. Additionally, Wolbachia-colonized flies exhibit a dampened transcriptomic response to virus infection, consistent with early blocking of virus replication. Finally, using Drosophila genetics, we show that Wolbachia and expression of nucleotide metabolism genes have interactive effects on virus replication. Understanding the mechanisms of pathogen blocking will contribute to the effective development of Wolbachia-mediated vector control programs. American Society for Microbiology 2021-02-09 /pmc/articles/PMC7885120/ /pubmed/33563832 http://dx.doi.org/10.1128/mBio.03472-20 Text en Copyright © 2021 Lindsey et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Lindsey, Amelia R. I. Bhattacharya, Tamanash Hardy, Richard W. Newton, Irene L. G. Wolbachia and Virus Alter the Host Transcriptome at the Interface of Nucleotide Metabolism Pathways |
title | Wolbachia and Virus Alter the Host Transcriptome at the Interface of Nucleotide Metabolism Pathways |
title_full | Wolbachia and Virus Alter the Host Transcriptome at the Interface of Nucleotide Metabolism Pathways |
title_fullStr | Wolbachia and Virus Alter the Host Transcriptome at the Interface of Nucleotide Metabolism Pathways |
title_full_unstemmed | Wolbachia and Virus Alter the Host Transcriptome at the Interface of Nucleotide Metabolism Pathways |
title_short | Wolbachia and Virus Alter the Host Transcriptome at the Interface of Nucleotide Metabolism Pathways |
title_sort | wolbachia and virus alter the host transcriptome at the interface of nucleotide metabolism pathways |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7885120/ https://www.ncbi.nlm.nih.gov/pubmed/33563832 http://dx.doi.org/10.1128/mBio.03472-20 |
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