Olfactory Bulb and Amygdala Gene Expression Changes in Subjects Dying with COVID-19.


Journal

medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986

Informations de publication

Date de publication:
15 Sep 2021
Historique:
pubmed: 22 9 2021
medline: 22 9 2021
entrez: 21 9 2021
Statut: epublish

Résumé

In this study we conducted RNA sequencing on two brain regions (olfactory bulb and amygdala) from subjects who died from COVID-19 or who died of other causes. We found several-fold more transcriptional changes in the olfactory bulb than in the amygdala, consistent with our own work and that of others indicating that the olfactory bulb may be the initial and most common brain region infected. To some extent our results converge with pseudotime analysis towards common processes shared between the brain regions, possibly induced by the systemic immune reaction following SARS-CoV-2 infection. Changes in amygdala emphasized upregulation of interferon-related neuroinflammation genes, as well as downregulation of synaptic and other neuronal genes, and may represent the substrate of reported acute and subacute COVID-19 neurological effects. Additionally, and only in olfactory bulb, we observed an increase in angiogenesis and platelet activation genes, possibly associated with microvascular damages induced by neuroinflammation. Through coexpression analysis we identified two key genes (

Identifiants

pubmed: 34545375
doi: 10.1101/2021.09.12.21263291
pmc: PMC8452114
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIA NIH HHS
ID : U01 AG046152
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG030146
Pays : United States
Organisme : NIA NIH HHS
ID : RC2 AG036547
Pays : United States
Organisme : NIA NIH HHS
ID : RF1 AG057473
Pays : United States
Organisme : NIA NIH HHS
ID : U01 AG046161
Pays : United States
Organisme : NIA NIH HHS
ID : U01 AG061356
Pays : United States
Organisme : NIA NIH HHS
ID : U01 AG032984
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG017917
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG072980
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG036042
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG010161
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG019610
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG048015
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG036836
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG015819
Pays : United States

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Auteurs

Ignazio S Piras (IS)

Translational Genomics Research Institute, Neurogenomics Division.

Matthew J Huentelman (MJ)

Translational Genomics Research Institute, Neurogenomics Division.

Jessica E Walker (JE)

Banner Sun Health Research Institute, Sun City, AZ.

Richard Arce (R)

Banner Sun Health Research Institute, Sun City, AZ.

Michael J Glass (MJ)

Banner Sun Health Research Institute, Sun City, AZ.

Daisy Vargas (D)

Banner Sun Health Research Institute, Sun City, AZ.

Lucia I Sue (LI)

Banner Sun Health Research Institute, Sun City, AZ.

Anthony J Intorcia (AJ)

Banner Sun Health Research Institute, Sun City, AZ.

Courtney M Nelson (CM)

Banner Sun Health Research Institute, Sun City, AZ.

Katsuko E Suszczewicz (KE)

Banner Sun Health Research Institute, Sun City, AZ.

Claryssa L Borja (CL)

Banner Sun Health Research Institute, Sun City, AZ.

Marc Desforges (M)

Centre Hospitalier Universitaire Sainte-Justine, Laboratory of Virology, Montreal, Canada.

Michael Deture (M)

Mayo Clinic College of Medicine, Mayo Clinic Florida, Jacksonville, FL.

Dennis W Dickson (DW)

Mayo Clinic College of Medicine, Mayo Clinic Florida, Jacksonville, FL.

Thomas G Beach (TG)

Banner Sun Health Research Institute, Sun City, AZ.

Geidy E Serrano (GE)

Banner Sun Health Research Institute, Sun City, AZ.

Classifications MeSH