MassIVE MSV000095094

Partial Public PXD053258

HCMV strain- and cell type-specific alterations in membrane contact sites point to the convergent regulation of organelle remodeling

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Description

Data-independent acquisition assessment of human fibroblasts and epithelial cells infected with different strains of human cytomegalovirus (HCMV). Viruses are ubiquitous entities that infect organisms across the kingdoms of life. While viruses can infect a range of cells, tissues, and organisms, this aspect is often not explored in cell culture analyses. There is limited information about which infection-induced changes are shared or distinct in different cellular environments. The prevalent pathogen HCMV remodels the structure and function of subcellular organelles and their interconnected networks formed by membrane contact sites (MCSs). A large portion of this knowledge has been derived from fibroblasts infected with a lab-adapted HCMV strain. Here, we assess strain- and cell type-specific alterations in MCSs and organelle remodeling induced by HCMV. Integrating quantitative mass spectrometry, super-resolution microscopy, and molecular virology assays, we compare infections with lab-adapted and low-passage HCMV strains in fibroblast and epithelial cells. We determine that, despite baseline proteome disparities between uninfected fibroblast and epithelial cells, infection induces convergent changes and is remarkably similar. We show that hallmarks of HCMV infection in fibroblasts, mitochondria-ER encapsulations (MENCs) and peroxisome proliferation, are also conserved in infected epithelial and macrophage-like cells. Exploring cell type-specific differences, we demonstrate that fibroblasts rely on endosomal cholesterol transport while epithelial cells rely on cholesterol from the Golgi. Despite these mechanistic differences, infections in both cell types result in phenotypically similar cholesterol accumulation at the viral assembly complex. Our findings highlight the adaptability of HCMV, in that infections can be tailored to the initial cell state by inducing both shared and unique proteome alterations, ultimately promoting a unified pro-viral environment. [doi:10.25345/C52B8VP8S] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: Proteomics, HCMV, Herpesvirus, Organelle remodeling, Membrane Contact Sites, Data-independent acquisition

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Principal Investigators:
(in alphabetical order) 		Ileana M. Cristea, Princeton University, United States of America
Submitting User: Krystallum
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