Suppression of the pelo protein by Wolbachia and its effect on dengue virus in Aedes aegypti

PLoS Negl Trop Dis. 2018 Apr 11;12(4):e0006405. doi: 10.1371/journal.pntd.0006405. eCollection 2018 Apr.

Abstract

The endosymbiont Wolbachia is known to block replication of several important arboviruses, including dengue virus (DENV), in the mosquito vector Aedes aegypti. So far, the exact mechanism of this viral inhibition is not fully understood. A recent study in Drosophila melanogaster has demonstrated an interaction between the pelo gene and Drosophila C virus. In this study, we explored the possible involvement of the pelo protein, that is involved in protein translation, in Wolbachia-mediated antiviral response and mosquito-DENV interaction. We found that pelo is upregulated during DENV replication and its silencing leads to reduced DENV virion production suggesting that it facilities DENV replication. However, in the presence of Wolbachia, specifically in female mosquitoes, the pelo protein is downregulated and its subcellular localization is altered, which could contribute to reduction in DENV replication in Ae. aegypti. In addition, we show that the microRNA aae-miR-2940-5p, whose abundance is highly enriched in Wolbachia-infected mosquitoes, might mediate regulation of pelo. Our data reveals identification of pelo as a host factor that is positively involved in DENV replication, and its suppression in the presence of Wolbachia may contribute to virus blocking exhibited by the endosymbiont.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aedes / genetics
  • Aedes / metabolism
  • Aedes / microbiology*
  • Aedes / virology*
  • Animals
  • Dengue Virus / physiology*
  • Down-Regulation
  • Female
  • Insect Proteins / genetics*
  • Insect Proteins / metabolism
  • Insect Vectors / microbiology*
  • Insect Vectors / virology*
  • MicroRNAs / genetics
  • MicroRNAs / metabolism
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism
  • Virus Replication
  • Wolbachia / physiology*

Substances

  • Insect Proteins
  • MicroRNAs
  • Nuclear Proteins

Grants and funding

This project was funded by the Australian Research Council (DP150101782; www.arc.gov.au) and the National Health and Medical Research Council (APP1062983; www.nhmrc.gov.au). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.