Skip to main navigation Skip to search Skip to main content

Cholesterol shuttling is important for RNA replication of coxsackievirus B3 and encephalomyocarditis virus

    Research output: Contribution to journal › Article › Academic › peer-review

    Abstract

    Picornaviruses are a family of positive-strand RNA viruses that represent important human and animal pathogens. Upon infection, picornaviruses induce an extensive remodeling of host cell membranes into replication organelles, which is critical for replication. Membrane lipids and lipid remodeling processes are at the base of RO formation, yet their involvement remains largely obscure. Recently, phosphatidylinositol-4-phosphate (PI4P) was the first lipid discovered to be important for the replication of a number of picornaviruses. Here, we investigate the role of the lipid cholesterol in picornavirus replication. We show that two picornaviruses from distinct genera that rely on different host factors for replication, namely the enterovirus coxsackievirus B3 (CVB3) and the cardiovirus encephalomyocarditis virus (EMCV), both recruited cholesterol to their ROs. Although CVB3 and EMCV both required cholesterol for efficient genome replication, the viruses appeared to rely on different cellular cholesterol pools. Treatments that altered the distribution of endosomal cholesterol inhibited replication of both CVB3 and EMCV, showing the importance of endosomal cholesterol shuttling for the replication of these viruses. Summarizing, we here demonstrate the importance of cholesterol homeostasis for efficient replication of CVB3 and EMCV.

    Original languageEnglish
    Pages (from-to)1144-1156
    Number of pages12
    JournalCellular Microbiology
    Volume17
    Issue number8
    Early online date10 Mar 2015
    DOIs
    Publication statusPublished - Aug 2015

    Bibliographical note

    This article is protected by copyright. All rights reserved.

    Fingerprint

    Dive into the research topics of 'Cholesterol shuttling is important for RNA replication of coxsackievirus B3 and encephalomyocarditis virus'. Together they form a unique fingerprint.

    Cite this