4.7 Article

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

期刊

出版社

MDPI
DOI: 10.3390/ijms22073568

关键词

baculovirus; hemolymph; chitin metabolism; extracellular matrix organization; cuticle development; biopesticides

资金

  1. USDA Agriculture & Food Research Initiative Competitive, joint USDA-NSF-NIH-BBSRC-BSF-NNSFC Ecology and Evolution of Infectious Diseases program [2019-67014-29919, 1019862]
  2. National Science Foundation [MCB 1616827]
  3. Next-Generation BioGreen21 Program of Republic of Korea [PJ01317301]
  4. Louisiana State University

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The study describes the transcriptional responses of two major pests, Spodoptera frugiperda and Trichoplusia ni, to AcMNPV, revealing transcriptional suppression of chitin metabolism and tracheal development in infected hosts, as well as viral transcript abundance associated with replication, structure, and movement. Additionally, the research found overlapping biological processes in both hosts, highlighting the target genes of AcMNPV that are also targeted by chemical insecticides used for pest control.
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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