TY - JOUR
T1 - Effect of obesity on the acute response to SARS-CoV-2 infection and development of post-acute sequelae of COVID-19 (PASC) in nonhuman primates
AU - Sauter, Kristin A.
AU - Webb, Gabriela M.
AU - Bader, Lindsay
AU - Kreklywich, Craig N.
AU - Takahashi, Diana L.
AU - Zaro, Cicely
AU - McGuire, Casey M.
AU - Lewis, Anne D.
AU - Colgin, Lois M.A.
AU - Kirigiti, Melissa A.
AU - Blomenkamp, Hannah
AU - Pessoa, Cleiton
AU - Humkey, Matthew
AU - Hulahan, Jesse
AU - Sleeman, Madeleine
AU - Zweig, Robert C.
AU - Thomas, Sarah
AU - Thomas, Archana
AU - Gao, Lina
AU - Hirsch, Alec J.
AU - Levy, Maayan
AU - Cherry, Sara
AU - Kahn, Steven E.
AU - Slifka, Mark K.
AU - Streblow, Daniel N.
AU - Sacha, Jonah B.
AU - Kievit, Paul
AU - Roberts, Charles T.
N1 - Publisher Copyright:
© 2025 Sauter et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2025/7/1
Y1 - 2025/7/1
N2 - Long-term adverse consequences of SARS-CoV-2 infection, termed “long COVID” or post-acute sequelae of COVID (PASC), are a major component of overall COVID-19 disease burden. Prior obesity and metabolic disease increase the severity of acute disease, but SARS-CoV-2 infection also contributes to the development of new-onset metabolic disease. Since the COVID pandemic occurred in the context of the global obesity epidemic, an important question is the extent to which pre-existing obesity modifies long-term responses to SARS-CoV-2 infection. We utilized a nonhuman primate model to compare the effects of infection with the SARS-CoV-2 delta variant in lean and obese/insulin-resistant adult male rhesus macaques over a 6-month time course. While some longitudinal responses to SARS-CoV-2 infection, including overall viral dynamics, SARS-CoV-2-specific IgG induction, cytokine profiles, and tissue persistence of viral RNA, did not appreciably differ between lean and obese animals, other responses, including neutralizing Ab dynamics, lung pathology, body weight, degree of insulin sensitivity, adipocytokine profiles, body temperature, and nighttime activity levels were significantly different in lean versus obese animals. Furthermore, several parameters in lean animals were altered following SARS-CoV-2 infection to resemble those in obese animals. Notably, persistent changes in multiple parameters were present in most animals, suggesting that PASC may be more prevalent than estimated from self-reported symptoms in human studies.
AB - Long-term adverse consequences of SARS-CoV-2 infection, termed “long COVID” or post-acute sequelae of COVID (PASC), are a major component of overall COVID-19 disease burden. Prior obesity and metabolic disease increase the severity of acute disease, but SARS-CoV-2 infection also contributes to the development of new-onset metabolic disease. Since the COVID pandemic occurred in the context of the global obesity epidemic, an important question is the extent to which pre-existing obesity modifies long-term responses to SARS-CoV-2 infection. We utilized a nonhuman primate model to compare the effects of infection with the SARS-CoV-2 delta variant in lean and obese/insulin-resistant adult male rhesus macaques over a 6-month time course. While some longitudinal responses to SARS-CoV-2 infection, including overall viral dynamics, SARS-CoV-2-specific IgG induction, cytokine profiles, and tissue persistence of viral RNA, did not appreciably differ between lean and obese animals, other responses, including neutralizing Ab dynamics, lung pathology, body weight, degree of insulin sensitivity, adipocytokine profiles, body temperature, and nighttime activity levels were significantly different in lean versus obese animals. Furthermore, several parameters in lean animals were altered following SARS-CoV-2 infection to resemble those in obese animals. Notably, persistent changes in multiple parameters were present in most animals, suggesting that PASC may be more prevalent than estimated from self-reported symptoms in human studies.
UR - https://www.scopus.com/pages/publications/105011384777
UR - https://www.scopus.com/pages/publications/105011384777#tab=citedBy
U2 - 10.1371/journal.ppat.1012988
DO - 10.1371/journal.ppat.1012988
M3 - Article
C2 - 40705709
AN - SCOPUS:105011384777
SN - 1553-7366
VL - 21
JO - PLoS pathogens
JF - PLoS pathogens
IS - 7 July
M1 - e1012988
ER -