| Autor: |
Havranek KE; Department of Infectious Diseases, College of Veterinary Medicine, University of Georgia, Athens, GA 30602, USA., Reyes Ballista JM; Department of Infectious Diseases, College of Veterinary Medicine, University of Georgia, Athens, GA 30602, USA., Hines KM; Department of Chemistry, Franklin College of Arts and Sciences, University of Georgia, Athens, GA 30602, USA., Brindley MA; Department of Infectious Diseases, Department of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA 30602, USA. |
| Abstrakt: |
The viral lifecycle is critically dependent upon host lipids. Enveloped viral entry requires fusion between viral and cellular membranes. Once an infection has occurred, viruses may rely on host lipids for replication and egress. Upon exit, enveloped viruses derive their lipid bilayer from host membranes during the budding process. Furthermore, host lipid metabolism and signaling are often hijacked to facilitate viral replication. We employed an untargeted HILIC-IM-MS lipidomics approach and identified host lipid species that were significantly altered during vesicular stomatitis virus (VSV) infection. Many glycerophospholipid and sphingolipid species were modified, and ontological enrichment analysis suggested that the alterations to the lipid profile change host membrane properties. Lysophosphatidylcholine (LPC), which can contribute to membrane curvature and serve as a signaling molecule, was depleted during infection, while several ceramide sphingolipids were augmented during infection. Ceramide and sphingomyelin lipids were also enriched in viral particles, indicating that sphingolipid metabolism is important during VSV infection. |
