Author
Listed:
- Ibolya Rutkai
(Tulane University School of Medicine)
- Meredith G. Mayer
(Tulane National Primate Research Center)
- Linh M. Hellmers
(Tulane National Primate Research Center)
- Bo Ning
(Tulane University School of Medicine)
- Zhen Huang
(Tulane University School of Medicine)
- Christopher J. Monjure
(Tulane National Primate Research Center)
- Carol Coyne
(Tulane National Primate Research Center)
- Rachel Silvestri
(Tulane National Primate Research Center)
- Nadia Golden
(Tulane National Primate Research Center)
- Krystle Hensley
(Tulane National Primate Research Center)
- Kristin Chandler
(Tulane National Primate Research Center)
- Gabrielle Lehmicke
(Tulane National Primate Research Center)
- Gregory J. Bix
(Tulane University School of Medicine)
- Nicholas J. Maness
(Tulane National Primate Research Center
Tulane University School of Medicine)
- Kasi Russell-Lodrigue
(Tulane National Primate Research Center
Tulane University School of Medicine)
- Tony Y. Hu
(Tulane University School of Medicine)
- Chad J. Roy
(Tulane National Primate Research Center
Tulane University School of Medicine)
- Robert V. Blair
(Tulane National Primate Research Center
Tulane University School of Medicine)
- Rudolf Bohm
(Tulane National Primate Research Center
Tulane University School of Medicine)
- Lara A. Doyle-Meyers
(Tulane National Primate Research Center
Tulane University School of Medicine)
- Jay Rappaport
(Tulane National Primate Research Center
Tulane University School of Medicine)
- Tracy Fischer
(Tulane National Primate Research Center
Tulane University School of Medicine)
Abstract
Neurological manifestations are a significant complication of coronavirus disease (COVID-19), but underlying mechanisms aren’t well understood. The development of animal models that recapitulate the neuropathological findings of autopsied brain tissue from patients who died from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection are critical for elucidating the neuropathogenesis of infection and disease. Here, we show neuroinflammation, microhemorrhages, brain hypoxia, and neuropathology that is consistent with hypoxic-ischemic injury in SARS-CoV-2 infected non-human primates (NHPs), including evidence of neuron degeneration and apoptosis. Importantly, this is seen among infected animals that do not develop severe respiratory disease, which may provide insight into neurological symptoms associated with “long COVID”. Sparse virus is detected in brain endothelial cells but does not associate with the severity of central nervous system (CNS) injury. We anticipate our findings will advance our current understanding of the neuropathogenesis of SARS-CoV-2 infection and demonstrate SARS-CoV-2 infected NHPs are a highly relevant animal model for investigating COVID-19 neuropathogenesis among human subjects.
Suggested Citation
Ibolya Rutkai & Meredith G. Mayer & Linh M. Hellmers & Bo Ning & Zhen Huang & Christopher J. Monjure & Carol Coyne & Rachel Silvestri & Nadia Golden & Krystle Hensley & Kristin Chandler & Gabrielle Le, 2022.
"Neuropathology and virus in brain of SARS-CoV-2 infected non-human primates,"
Nature Communications, Nature, vol. 13(1), pages 1-13, December.
Handle:
RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-29440-z
DOI: 10.1038/s41467-022-29440-z
Download full text from publisher
Citations
Citations are extracted by the
CitEc Project, subscribe to its
RSS feed for this item.
Cited by:
- Benedict D. Michael & Cordelia Dunai & Edward J. Needham & Kukatharmini Tharmaratnam & Robyn Williams & Yun Huang & Sarah A. Boardman & Jordan J. Clark & Parul Sharma & Krishanthi Subramaniam & Greta , 2023.
"Para-infectious brain injury in COVID-19 persists at follow-up despite attenuated cytokine and autoantibody responses,"
Nature Communications, Nature, vol. 14(1), pages 1-15, December.
- Changli Wei & Prasun K. Datta & Florian Siegerist & Jing Li & Sudhini Yashwanth & Kwi Hye Koh & Nicholas W. Kriho & Anis Ismail & Shengyuan Luo & Tracy Fischer & Kyle T. Amber & David Cimbaluk & Alan , 2023.
"SuPAR mediates viral response proteinuria by rapidly changing podocyte function,"
Nature Communications, Nature, vol. 14(1), pages 1-12, December.
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-29440-z. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.