Strategies employed by viruses to manipulate autophagy

Nilima Dinesh Kumar, Jolanda M Smit, Fulvio Reggiori

Research output: Contribution to journal/Conference contribution in journal/Contribution to newspaperReviewResearchpeer-review

16 Citations (Scopus)

Abstract

Autophagy, originally described as a conserved bulk degradation pathway important to maintain cellular homeostasis during starvation, has also been implicated in playing a central role in multiple physiological processes. For example, autophagy is part of our innate immunity by targeting intracellular pathogens to lysosomes for degradation in a process called xenophagy. Coevolution and adaptation between viruses and autophagy have armed viruses with a multitude of strategies to counteract the antiviral functions of the autophagy pathway. In addition, some viruses have acquired mechanisms to exploit specific functions of either autophagy or the key components of this process, the autophagy-related (ATG) proteins, to promote viral replication and pathogenesis. In this chapter, we describe several examples where the strategy employed by a virus to subvert autophagy has been described with molecular detail. Their stratagems positively or negatively target practically all the steps of autophagy, including the signaling pathways regulating this process. This highlights the intricate relationship between autophagy and viruses and how by commandeering autophagy, viruses have devised ways to fine-tune their replication.

Original languageEnglish
Book seriesProgress in Molecular Biology and Translational Science
Volume172
Pages (from-to)203-237
Number of pages35
ISSN1877-1173
DOIs
Publication statusPublished - 2020
Externally publishedYes

Keywords

  • Animals
  • Apoptosis
  • Autophagosomes/virology
  • Autophagy-Related Proteins/physiology
  • Autophagy/immunology
  • Cytokines/physiology
  • Endoplasmic Reticulum Stress/physiology
  • Endosomes/virology
  • Energy Metabolism/physiology
  • Eukaryotic Initiation Factor-2/physiology
  • Host-Pathogen Interactions
  • Humans
  • Immune Evasion
  • Immunity, Innate
  • Lysosomes/enzymology
  • Mechanistic Target of Rapamycin Complex 1/physiology
  • Membrane Fusion
  • Signal Transduction
  • Stress, Physiological
  • Viral Proteins/physiology
  • Virus Diseases/immunology
  • Virus Physiological Phenomena
  • Virus Replication

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