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A Tale of Two Transcriptomic Responses in Agricultural Pests via Host Defenses and Viral Replication

Autographa californica Multiple Nucleopolyhedrovirus (AcMNPV) is a baculovirus that causes systemic infections in many arthropod pests. The specific molecular processes underlying the biocidal activity of AcMNPV on its insect hosts are largely unknown. We describe the transcriptional responses in tw...

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Autores principales: Pantha, Pramod, Chalivendra, Subbaiah, Oh, Dong-Ha, Elderd, Bret D., Dassanayake, Maheshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8037200/
https://www.ncbi.nlm.nih.gov/pubmed/33808210
http://dx.doi.org/10.3390/ijms22073568
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author Pantha, Pramod
Chalivendra, Subbaiah
Oh, Dong-Ha
Elderd, Bret D.
Dassanayake, Maheshi
author_facet Pantha, Pramod
Chalivendra, Subbaiah
Oh, Dong-Ha
Elderd, Bret D.
Dassanayake, Maheshi
author_sort Pantha, Pramod
collection PubMed
description Autographa californica Multiple Nucleopolyhedrovirus (AcMNPV) is a baculovirus that causes systemic infections in many arthropod pests. The specific molecular processes underlying the biocidal activity of AcMNPV on its insect hosts are largely unknown. We describe the transcriptional responses in two major pests, Spodoptera frugiperda (fall armyworm) and Trichoplusia ni (cabbage looper), to determine the host–pathogen responses during systemic infection, concurrently with the viral response to the host. We assembled species-specific transcriptomes of the hemolymph to identify host transcriptional responses during systemic infection and assessed the viral transcript abundance in infected hemolymph from both species. We found transcriptional suppression of chitin metabolism and tracheal development in infected hosts. Synergistic transcriptional support was observed to suggest suppression of immune responses and induction of oxidative stress indicating disease progression in the host. The entire AcMNPV core genome was expressed in the infected host hemolymph with a proportional high abundance detected for viral transcripts associated with replication, structure, and movement. Interestingly, several of the host genes that were targeted by AcMNPV as revealed by our study are also targets of chemical insecticides currently used commercially to control arthropod pests. Our results reveal an extensive overlap between biological processes represented by transcriptional responses in both hosts, as well as convergence on highly abundant viral genes expressed in the two hosts, providing an overview of the host–pathogen transcriptomic landscape during systemic infection.
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spelling pubmed-80372002021-04-12 A Tale of Two Transcriptomic Responses in Agricultural Pests via Host Defenses and Viral Replication Pantha, Pramod Chalivendra, Subbaiah Oh, Dong-Ha Elderd, Bret D. Dassanayake, Maheshi Int J Mol Sci Article Autographa californica Multiple Nucleopolyhedrovirus (AcMNPV) is a baculovirus that causes systemic infections in many arthropod pests. The specific molecular processes underlying the biocidal activity of AcMNPV on its insect hosts are largely unknown. We describe the transcriptional responses in two major pests, Spodoptera frugiperda (fall armyworm) and Trichoplusia ni (cabbage looper), to determine the host–pathogen responses during systemic infection, concurrently with the viral response to the host. We assembled species-specific transcriptomes of the hemolymph to identify host transcriptional responses during systemic infection and assessed the viral transcript abundance in infected hemolymph from both species. We found transcriptional suppression of chitin metabolism and tracheal development in infected hosts. Synergistic transcriptional support was observed to suggest suppression of immune responses and induction of oxidative stress indicating disease progression in the host. The entire AcMNPV core genome was expressed in the infected host hemolymph with a proportional high abundance detected for viral transcripts associated with replication, structure, and movement. Interestingly, several of the host genes that were targeted by AcMNPV as revealed by our study are also targets of chemical insecticides currently used commercially to control arthropod pests. Our results reveal an extensive overlap between biological processes represented by transcriptional responses in both hosts, as well as convergence on highly abundant viral genes expressed in the two hosts, providing an overview of the host–pathogen transcriptomic landscape during systemic infection. MDPI 2021-03-30 /pmc/articles/PMC8037200/ /pubmed/33808210 http://dx.doi.org/10.3390/ijms22073568 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pantha, Pramod
Chalivendra, Subbaiah
Oh, Dong-Ha
Elderd, Bret D.
Dassanayake, Maheshi
A Tale of Two Transcriptomic Responses in Agricultural Pests via Host Defenses and Viral Replication
title A Tale of Two Transcriptomic Responses in Agricultural Pests via Host Defenses and Viral Replication
title_full A Tale of Two Transcriptomic Responses in Agricultural Pests via Host Defenses and Viral Replication
title_fullStr A Tale of Two Transcriptomic Responses in Agricultural Pests via Host Defenses and Viral Replication
title_full_unstemmed A Tale of Two Transcriptomic Responses in Agricultural Pests via Host Defenses and Viral Replication
title_short A Tale of Two Transcriptomic Responses in Agricultural Pests via Host Defenses and Viral Replication
title_sort tale of two transcriptomic responses in agricultural pests via host defenses and viral replication
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8037200/
https://www.ncbi.nlm.nih.gov/pubmed/33808210
http://dx.doi.org/10.3390/ijms22073568
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