PUBLICATION

Intranasal delivery of SARS-CoV-2 Spike protein is sufficient to cause olfactory damage, inflammation and olfactory dysfunction in zebrafish

Authors
Kraus, A., Huertas, M., Ellis, L., Boudinot, P., Levraud, J.P., Salinas, I.
ID
ZDB-PUB-220323-8
Date
2022
Source
Brain, behavior, and immunity   102: 341-359 (Journal)
Registered Authors
Levraud, Jean-Pierre
Keywords
EOG, SARS-CoV-2, animal models, olfactory damage, olfactory receptor expression, spike protein, zebrafish (Danio rerio)
MeSH Terms
  • Animals
  • Anosmia
  • COVID-19*
  • COVID-19 Vaccines
  • Humans
  • Inflammation/metabolism
  • Olfactory Mucosa/metabolism
  • SARS-CoV-2
  • Spike Glycoprotein, Coronavirus*/metabolism
  • Zebrafish
PubMed
35307504 Full text @ Brain Behav. Immun.
Abstract
Anosmia, loss of smell, is a prevalent symptom of SARS-CoV-2 infection. Anosmia may be explained by several mechanisms driven by infection of non-neuronal cells and damage in the nasal epithelium rather than direct infection of olfactory sensory neurons (OSNs). Previously, viral proteins have been shown to be sufficient to cause neuroimmune responses in the olfactory organ (OO) by our group. We hypothesize that SARS-CoV-2 spike (S) protein is sufficient to cause olfactory damage and olfactory dysfunction. Using an adult zebrafish model, we report that intranasally delivered SARS-CoV-2 S RBD mostly binds to the non-sensory epithelium of the olfactory organ and causes severe olfactory histopathology characterized by loss of cilia, hemorrhages and edema. Electrophysiological recordings reveal impaired olfactory function to both food and bile odorants in animals treated intranasally with SARS-CoV-2 S RBD. However, no loss of behavioral preference for food was detected in SARS-CoV-2 S RBD treated fish. Single cell RNA-Seq of the adult zebrafish olfactory organ indicated widespread loss of olfactory receptor expression and inflammatory responses in sustentacular, endothelial, and myeloid cell clusters along with reduced numbers of Tregs. Combined, our results demonstrate that intranasal SARS-CoV-2 S RBD is sufficient to cause structural and functional damage to the zebrafish olfactory system. These findings may have implications for intranasally delivered vaccines against SARS-CoV-2.
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