| Literature DB >> 30269970 |
Pierre M Jean Beltran1, Katelyn C Cook1, Yutaka Hashimoto1, Cyril Galitzine2, Laura A Murray1, Olga Vitek2, Ileana M Cristea3.
Abstract
Viral proteins have evolved to target cellular organelles and usurp their functions for virus replication. Despite the knowledge of these critical functions for several organelles, little is known about peroxisomes during infection. Peroxisomes are primarily metabolic organelles with important functions in lipid metabolism. Here, we discovered that the enveloped viruses human cytomegalovirus (HCMV) and herpes simplex virus type 1 (HSV-1) induce the biogenesis of and unique morphological changes to peroxisomes to support their replication. Targeted proteomic quantification revealed a global virus-induced upregulation of peroxisomal proteins. Mathematical modeling and microscopy structural analysis show that infection triggers peroxisome growth and fission, leading to increased peroxisome numbers and irregular disc-like structures. HCMV-induced peroxisome biogenesis increased the phospholipid plasmalogen, thereby enhancing virus production. Peroxisome regulation and dependence were not observed for the non-enveloped adenovirus. Our findings uncover a role of peroxisomes in viral pathogenesis, with likely implications for multiple enveloped viruses.Entities:
Keywords: PRM; herpesvirus; human cytomegalovirus; inference; mass spectrometry; mathematical model; organelle; peroxisome; proteomics; viral infection
Mesh:
Year: 2018 PMID: 30269970 PMCID: PMC6195127 DOI: 10.1016/j.chom.2018.09.002
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023