HCV Interplay with Lipoproteins: Inside or Outside the Cells?

Viruses

CIRI-Centre International de Recherche en Infectiologie, Univ Lyon, Université Claude Bernard Lyon 1, Inserm, U1111, CNRS, UMR5308, ENS Lyon, F-69007 Lyon, France.

Published: April 2020

AI Article Synopsis

  • Hepatitis C virus (HCV) infection leads to chronic liver diseases and involves unique particles with special lipid compositions that include neutral lipids and apolipoproteins.
  • The relationship between HCV particles and these lipoproteins is not fully understood, particularly how it affects viral entry into cells and other stages of the viral life cycle.
  • Understanding this association is crucial for developing a protective vaccine, as HCV particle structure influences their entry into cells and their resistance to neutralizing antibodies.

Article Abstract

Hepatitis C virus (HCV) infection is a major public health issue leading to chronic liver diseases. HCV particles are unique owing to their particular lipid composition, namely the incorporation of neutral lipids and apolipoproteins. The mechanism of association between HCV virion components and these lipoproteins factors remains poorly understood as well as its impact in subsequent steps of the viral life cycle, such as entry into cells. It was proposed that the lipoprotein biogenesis pathway is involved in HCV morphogenesis; yet, recent evidence indicated that HCV particles can mature and evolve biochemically in the extracellular medium after egress. In addition, several viral, cellular and blood components have been shown to influence and regulate this specific association. Finally, this specific structure and composition of HCV particles was found to influence entry into cells as well as their stability and sensitivity to neutralizing antibodies. Due to its specific particle composition, studying the association of HCV particles with lipoproteins remains an important goal towards the rational design of a protective vaccine.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7232430PMC
http://dx.doi.org/10.3390/v12040434DOI Listing

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