Non-human primate model of long-COVID identifies immune associates of hyperglycemia

Hyperglycemia, and exacerbation of pre-existing deficits in glucose metabolism, are manifestations of the post-acute sequelae of SARS-CoV-2. Our understanding of metabolic decline after acute COVID-19 remains unclear due to the lack of animal models. Here, we report a non-human primate model of metabolic post-acute sequelae of SARS-CoV-2 using SARS-CoV-2 infected African green monkeys. Using this model, we identify a dysregulated blood chemokine signature during acute COVID-19 that correlates with elevated and persistent hyperglycemia four months post-infection. Hyperglycemia also correlates with liver glycogen levels, but there is no evidence of substantial long-term SARS-CoV-2 replication in the liver and pancreas. Finally, we report a favorable glycemic effect of the SARS-CoV-2 mRNA vaccine, administered on day 4 post-infection. Together, these data suggest that the African green monkey model exhibits important similarities to humans and can be utilized to assess therapeutic candidates to combat COVID-related metabolic defects.

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Publication Details

Journal
Nature Communications
Published
2024-08-20
DOI
https://doi.org/10.1038/s41467-024-50339-4
Citations
12
Primary Topic
Long-Term Effects of COVID-19
Type
article
Field-Weighted Citation Impact
4.43

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article

Non-human primate model of long-COVID identifies immune associates of hyperglycemia

Prasun K. Datta, Linh Hellmers, Tracy Fischer, Cecily C. Midkiff et al.
12 citations
Nature Communications
Long-Term Effects of COVID-19
4.43
article

Non-human primate model of long-COVID identifies immune associates of hyperglycemia

Prasun K. Datta, Linh Hellmers, Tracy Fischer, Cecily C. Midkiff, Angela K. Birnbaum, Rafael Tibúrcio, Jay Rappaport, Jason Dufour, Carys Kenway, Ahmad Saied, Kasi Russell‐Lodrigue, Chrysostomos Perdios, Kristyn Moore Green, Clovis S. Palmer, Robert V. Blair, Gabrielle Lehmicke, Kelsey Williams, Carol Coyne, Mohamed Abdel‐Mohsen, Nicholas J. Maness, Marissa Fahlberg, Nadia Golden, Joseph C. Mudd, Rudolf Bohm, Kyndal Boykin
article en
12 citations

Abstract

Hyperglycemia, and exacerbation of pre-existing deficits in glucose metabolism, are manifestations of the post-acute sequelae of SARS-CoV-2. Our understanding of metabolic decline after acute COVID-19 remains unclear due to the lack of animal models. Here, we report a non-human primate model of metabolic post-acute sequelae of SARS-CoV-2 using SARS-CoV-2 infected African green monkeys. Using this model, we identify a dysregulated blood chemokine signature during acute COVID-19 that correlates with elevated and persistent hyperglycemia four months post-infection. Hyperglycemia also correlates with liver glycogen levels, but there is no evidence of substantial long-term SARS-CoV-2 replication in the liver and pancreas. Finally, we report a favorable glycemic effect of the SARS-CoV-2 mRNA vaccine, administered on day 4 post-infection. Together, these data suggest that the African green monkey model exhibits important similarities to humans and can be utilized to assess therapeutic candidates to combat COVID-related metabolic defects.

Nature CommunicationsVol. 15(1)
The Wistar Institute (US), Oregon National Primate Research Center (US), Tulane University (US), Oregon Health & Science University (US), University of San Francisco (US)
National Institutes of Health, Office of Research Infrastructure Programs, National Institutes of Health
Good health and well-being
Openalex Percentile: Top 5%
Long-Term Effects of COVID-19
4.43
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