TY - JOUR
T1 - Effects of COVID-19 virus-like particles on the behavioral and cognitive performance of human apolipoprotein E targeted replacement mice
AU - O’Niel, Abigail
AU - Pederson, Alexandra
AU - Saltontall, Elizabeth
AU - Nguyen, Kayla
AU - Pantoja, Monzerrat
AU - Chaudhari, Mitali
AU - Sandholm, Phoebe
AU - Yoon, Eric
AU - Harrison, Henry F.
AU - Boutros, Sydney
AU - Hirsch, Alec J.
AU - Raber, Jacob
N1 - Publisher Copyright:
Copyright © 2024 O’Niel, Pederson, Saltontall, Nguyen, Pantoja, Chaudhari, Sandholm, Yoon, Harrison, Boutros, Hirsch and Raber.
PY - 2024
Y1 - 2024
N2 - Introduction: The effects of viral infections might be apolipoprotein E (apoE) isoform-dependent. In humans, there are three major apoE isoforms, E2, E3, and E4. E4 is associated with the enhanced entry of several viruses into the brain and their disease progression. A concern of infection by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the development of post-acute COVID-19 syndrome, also known as long COVID. Genetic risk factors for developing long COVID were reported. Methods: In this study, we used virus-like particles (VLPs) that include expression of the SARS-CoV-2 nucleocapsid (N), membrane (M), and envelope (E) structural proteins together with S. In the current study, we used human E2, E3, and E4 targeted replacement mice to assess whether these VLPs affect body weight, behavioral and cognitive performance, and circadian body temperatures. Using VLPs allow working outside an ABSL-3 facility. Results: The effects of VLPs on some behavioral measures were apoE isoform-dependent, with the E2 mice being more affected than E3 or E4 mice. The overall decreased activity in the open field containing objects in week 2 indicate that VLPs can also reduce activity levels in an apoE isoform-independent fashion. Discussion: The results of the current study indicate that even in the absence of viral replication, detrimental effects of VLPs on behavioral measures and circadian body temperatures are seen.
AB - Introduction: The effects of viral infections might be apolipoprotein E (apoE) isoform-dependent. In humans, there are three major apoE isoforms, E2, E3, and E4. E4 is associated with the enhanced entry of several viruses into the brain and their disease progression. A concern of infection by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the development of post-acute COVID-19 syndrome, also known as long COVID. Genetic risk factors for developing long COVID were reported. Methods: In this study, we used virus-like particles (VLPs) that include expression of the SARS-CoV-2 nucleocapsid (N), membrane (M), and envelope (E) structural proteins together with S. In the current study, we used human E2, E3, and E4 targeted replacement mice to assess whether these VLPs affect body weight, behavioral and cognitive performance, and circadian body temperatures. Using VLPs allow working outside an ABSL-3 facility. Results: The effects of VLPs on some behavioral measures were apoE isoform-dependent, with the E2 mice being more affected than E3 or E4 mice. The overall decreased activity in the open field containing objects in week 2 indicate that VLPs can also reduce activity levels in an apoE isoform-independent fashion. Discussion: The results of the current study indicate that even in the absence of viral replication, detrimental effects of VLPs on behavioral measures and circadian body temperatures are seen.
KW - apolipoprotein E
KW - behavioral testing
KW - cognitive testing
KW - COVID-19
KW - virus-like particles
UR - http://www.scopus.com/inward/record.url?scp=85211244140&partnerID=8YFLogxK
U2 - 10.3389/fimmu.2024.1473366
DO - 10.3389/fimmu.2024.1473366
M3 - Article
C2 - 39660133
AN - SCOPUS:85211244140
VL - 15
JO - Frontiers in Immunology
JF - Frontiers in Immunology
M1 - 1473366
ER -