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Varicella zoster virus-induced autophagy in human neuronal and hematopoietic cells exerts antiviral activity

Heinz, Johanna L. (author)
Hinke, Daniela M. (author)
Maimaitili, Muyesier (author)
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Wang, Jiayi (author)
Sabli, Ira K. D. (author)
Thomsen, Michelle (author)
Farahani, Ensieh (author)
Ren, Fanghui (author)
Hu, Lili (author)
Zillinger, Thomas (author)
Grahn, Anna, 1973 (author)
Gothenburg University,Göteborgs universitet,Institutionen för biomedicin, avdelningen för infektionssjukdomar,Institute of Biomedicine, Department of Infectious Medicine
von Hofsten, Joanna, 1976 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för klinisk neurovetenskap,Institute of Neuroscience and Physiology, Department of Clinical Neuroscience
Verjans, Georges M. G. M. (author)
Paludan, Soren R. (author)
Viejo-Borbolla, Abel (author)
Sancho-Shimizu, Vanessa (author)
Mogensen, Trine H. (author)
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 (creator_code:org_t)
2024
2024
English.
In: JOURNAL OF MEDICAL VIROLOGY. - 0146-6615 .- 1096-9071. ; 96:6
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Autophagy is a degradational pathway with pivotal roles in cellular homeostasis and survival, including protection of neurons in the central nervous system (CNS). The significance of autophagy as antiviral defense mechanism is recognized and some viruses hijack and modulate this process to their advantage in certain cell types. Here, we present data demonstrating that the human neurotropic herpesvirus varicella zoster virus (VZV) induces autophagy in human SH-SY5Y neuronal cells, in which the pathway exerts antiviral activity. Productively VZV-infected SH-SY5Y cells showed increased LC3-I-LC3-II conversion as well as co-localization of the viral glycoprotein E and the autophagy receptor p62. The activation of autophagy was dependent on a functional viral genome. Interestingly, inducers of autophagy reduced viral transcription, whereas inhibition of autophagy increased viral transcript expression. Finally, the genotype of patients with severe ocular and brain VZV infection were analyzed to identify potential autophagy-associated inborn errors of immunity. Two patients expressing genetic variants in the autophagy genes ULK1 and MAP1LC3B2, respectively, were identified. Notably, cells of both patients showed reduced autophagy, alongside enhanced viral replication and death of VZV-infected cells. In conclusion, these results demonstrate a neuro-protective role for autophagy in the context of VZV infection and suggest that failure to mount an autophagy response is a potential predisposing factor for development of severe VZV disease.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Infektionsmedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Infectious Medicine (hsv//eng)

Keyword

acute retinal necrosis
autophagy
CNS infection
innate immunity
varicella zoster virus

Publication and Content Type

ref (subject category)
art (subject category)

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