In vitro shared transcriptomic responses of Aedes aegypti to arboviral infections: example of dengue and Rift Valley fever viruses

Parasit Vectors. 2020 Aug 5;13(1):395. doi: 10.1186/s13071-020-04253-5.

Abstract

Background: Arthropod borne virus infections are the cause of severe emerging diseases. Among the diseases due to arboviruses, dengue (DEN) and Rift Valley fever (RVF) are in the top ten in the list of diseases responsible of severe human cases worldwide. Understanding the effects of viral infection on gene expression in competent vectors is a challenge for the development of early diagnostic tools and may enable researchers and policy makers to better anticipate outbreaks in the next future.

Methods: In this study, alterations in gene expression across the entire Aedes aegypti genome during infection with DENV and RVFV were investigated in vitro at two time points of infection, the early phase (24 h) and the late phase (6 days) of infection using the RNA sequencing approach RESULTS: A total of 10 upregulated genes that share a similar expression profile during infection with both viruses at early and late phases of infection were identified. Family B and D clip-domain serine proteases (CLIP) were clearly overrepresented as well as C-type lectins and transferrin.

Conclusions: Our data highlight the presence of 10 viral genes upregulated in Ae. aegypti during infection. They may also be targeted in the case of the development of broad-spectrum anti-viral diagnostic tools focusing the mosquito vectors rather than the mammalian hosts as they may predict the emergence of outbreaks.

Keywords: Aedes aegypti; Dengue; In vitro; Rift Valley fever; Transcriptomic responses.

MeSH terms

  • Aedes* / genetics
  • Aedes* / virology
  • Animals
  • Arbovirus Infections / transmission
  • Arboviruses
  • Dengue / transmission
  • Dengue Virus*
  • Gene Expression Profiling
  • Genes, Insect
  • Host Microbial Interactions
  • Humans
  • Lectins, C-Type / genetics
  • Mosquito Vectors / genetics
  • Mosquito Vectors / virology
  • Rift Valley Fever / transmission
  • Rift Valley fever virus*
  • Serine Proteases / genetics
  • Transcriptome*
  • Transferrin / genetics

Substances

  • Lectins, C-Type
  • Transferrin
  • Serine Proteases