Comparative Transcriptome Analysis Reveals That WSSV IE1 Protein Plays a Crucial Role in DNA Replication Control

Int J Mol Sci. 2022 Jul 25;23(15):8176. doi: 10.3390/ijms23158176.

Abstract

For DNA viruses, the immediate-early (IE) proteins are generally essential regulators that manipulate the host machinery to support viral replication. Recently, IE1, an IE protein encoded by white spot syndrome virus (WSSV), has been demonstrated to function as a transcription factor. However, the target genes of IE1 during viral infection remain poorly understood. Here, we explored the host target genes of IE1 using RNAi coupled with transcriptome sequencing analysis. A total of 429 differentially expressed genes (DEGs) were identified from penaeid shrimp, of which 284 genes were upregulated and 145 genes were downregulated after IE1 knockdown. GO and KEGG pathway enrichment analysis revealed the identified DEGs are significantly enriched in the minichromosome maintenance (MCM) complex and DNA replication, indicating that IE1 plays a critical role in DNA replication control. In addition, it was found that Penaeus vannamei MCM complex genes were remarkably upregulated after WSSV infection, while RNAi-mediated knockdown of PvMCM2 reduced the expression of viral genes and viral loads at the early infection stage. Finally, we demonstrated that overexpression of IE1 promoted the expression of MCM complex genes as well as cellular DNA synthesis in insect High-Five cells. Collectively, our current data suggest that the WSSV IE1 protein is a viral effector that modulates the host DNA replication machinery for viral replication.

Keywords: DNA replication; IE protein; MCM complex; WSSV; shrimp.

MeSH terms

  • Animals
  • DNA Replication / genetics
  • Gene Expression Profiling
  • Gene Expression Regulation, Viral
  • Immediate-Early Proteins* / genetics
  • Immediate-Early Proteins* / metabolism
  • Penaeidae* / metabolism
  • Transcriptome
  • White spot syndrome virus 1* / genetics

Substances

  • Immediate-Early Proteins

Grants and funding

This work was funded by the National Natural Science Foundation of China (Nos. 31702387 and 32173017), Science and Technology Planning Project of Guangdong Province (STKJ2021188) and Shantou University Scientific Research Foundation for Talents (No. NTF20008).