Acyl-Coa Thioesterases: A Rheostat That Controls Activated Fatty Acids Modulates Dengue Virus Serotype 2 Replication

Viruses. 2022 Jan 25;14(2):240. doi: 10.3390/v14020240.

Abstract

During infection with dengue viruses (DENVs), the lipid landscape within host cells is significantly altered to assemble membrane platforms that support viral replication and particle assembly. Fatty acyl-CoAs are key intermediates in the biosynthesis of complex lipids that form these membranes. They also function as key signaling lipids in the cell. Here, we carried out loss of function studies on acyl-CoA thioesterases (ACOTs), a family of enzymes that hydrolyze fatty acyl-CoAs to free fatty acids and coenzyme A, to understand their influence on the lifecycle of DENVs. The loss of function of the type I ACOTs 1 (cytoplasmic) and 2 (mitochondrial) together significantly increased DENV serotype 2 (DENV2) viral replication and infectious particle release. However, isolated knockdown of mitochondrial ACOT2 significantly decreased DENV2 protein translation, genome replication, and infectious virus release. Furthermore, loss of ACOT7 function, a mitochondrial type II ACOT, similarly suppressed DENV2. As ACOT1 and ACOT2 are splice variants, these data suggest that functional differences and substrate specificities due to the location (cytosol and mitochondria, respectively) of these proteins may account for the differences in DENV2 infection phenotype. Additionally, loss of mitochondrial ACOT2 and ACOT7 expression also altered the expression of several ACOTs located in multiple organelle compartments within the cell, highlighting a complex relationship between ACOTs in the DENV2 virus lifecycle.

Keywords: acyl-CoA; acyl-CoA thioesterase; dengue virus; fatty acids; fatty acyl-CoA; lipids; membranes; rheostat.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cell Line, Tumor
  • Cytosol / enzymology
  • Dengue Virus / genetics
  • Dengue Virus / physiology*
  • Fatty Acids / metabolism*
  • Gene Knockdown Techniques
  • Genome, Viral
  • Humans
  • Mitochondria / enzymology
  • Palmitoyl-CoA Hydrolase / genetics
  • Palmitoyl-CoA Hydrolase / metabolism*
  • RNA, Small Interfering
  • Thiolester Hydrolases / genetics
  • Thiolester Hydrolases / metabolism*
  • Virus Release
  • Virus Replication

Substances

  • Fatty Acids
  • RNA, Small Interfering
  • ACOT1 protein, human
  • Thiolester Hydrolases
  • ACOT2 protein, human
  • ACOT7 protein, human
  • Palmitoyl-CoA Hydrolase