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Analysis of genes expression of Spodoptera exigua Larvae upon AcMNPV infection

  • Jae Young Choi
  • , Jong Yul Roh
  • , Yong Wang
  • , Zou Zhen
  • , Xue Ying Tao
  • , Joo Hyun Lee
  • , Qin Liu
  • , Jae Su Kim
  • , Sang Woon Shin
  • , Yeon Ho Je
  • Seoul National University
  • Korea National Institute of Health
  • Lanzhou University
  • CAS - Institute of Zoology
  • University of California at Riverside

Research output: Contribution to journalJournal articlepeer-review

Abstract

Background: The impact of Autographa californica multicapsid nucleopolyhedrovirus (AcMNPV) infection on host gene expression in Spodoptera exigua 4th instar larvae was investigated through the use of 454 sequencing-based RNA-seq of cDNA libraries developed from insects challenged with active AcMNPV or heat-inactivated AcMNPV. Methodology/Principal Findings: By comparing the two cDNA libraries, we show that 201 host genes are significantly up-regulated and 234 genes are significantly down-regulated by active AcMNPV infection. Down-regulated host genes included genes encoding antimicrobial peptides, namely three gloverin isoforms and an attacin, indicating that the viral infection actively repressed the expression of a portion of the host immune gene repertoire. Another interesting group of down-regulated host genes included genes encoding two juvenile hormone binding proteins and a hexamerin, all of which are involved in juvenile hormone regulation. The expression of these genes was enhanced by the topical application of Juvenile Hormone III (JHIII) in the insects challenged with heat-inactivated AcMNPV. However, infection with the active virus strongly suppresses the expression of these three genes, regardless of the absence or presence of JHIII. Conclusions/Significance: Using RNA-seq, we have identified groups of immune-regulated and juvenile hormone-regulated genes that are suppressed by infection with active AcMNPV. This information and further studies on the regulation of host gene expression by AcMNPV will provide the tools needed to enhance the utility of the virus as an effective protein expression system and as an insecticide.

Original languageEnglish
Article numbere42462
JournalPLoS ONE
Volume7
Issue number7
DOIs
StatePublished - 2012.07.31

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