Evidence map›Paper›PMID 40027795›Full record

ArticlebioRxiv : the preprint server for biology2025

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.

Kristin A Sauter, Gabriela M Webb, Lindsay Bader, Craig N Kreklywich, Diana L Takahashi, Cicely Zaro, Casey M McGuire, Anne D Lewis, Lois M A Colgin, Melissa A Kirigiti and 18 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

28 authors.

Kristin A SauterDivision of Metabolic Health and Disease, Oregon National Primate Research Center (ONPRC), Beaverton, OR, USA.
Gabriela M WebbDivision of Pathobiology and Immunology, ONPRC.
Lindsay BaderDivision of Metabolic Health and Disease, Oregon National Primate Research Center (ONPRC), Beaverton, OR, USA.
Craig N KreklywichVaccine and Gene Therapy Institute, Oregon Health and Science University (OHSU), Beaverton, OR, USA.
Diana L TakahashiDivision of Metabolic Health and Disease, Oregon National Primate Research Center (ONPRC), Beaverton, OR, USA.
Cicely ZaroDivision of Metabolic Health and Disease, Oregon National Primate Research Center (ONPRC), Beaverton, OR, USA.
Casey M McGuireDivision of Metabolic Health and Disease, Oregon National Primate Research Center (ONPRC), Beaverton, OR, USA.
Anne D LewisDivision of Comparative Medicine, ONPRC.
Lois M A ColginDivision of Comparative Medicine, ONPRC.
Melissa A KirigitiDivision of Metabolic Health and Disease, Oregon National Primate Research Center (ONPRC), Beaverton, OR, USA.
Hannah BlomenkampDivision of Metabolic Health and Disease, Oregon National Primate Research Center (ONPRC), Beaverton, OR, USA.
Cleiton PessoaDivision of Pathobiology and Immunology, ONPRC.
Matthew HumkeyDivision of Pathobiology and Immunology, ONPRC.
Jesse HulahanDepartment of Pathology and Laboratory Medicine and University of Pennsylvania, Philadelphia, PA, USA.
Madeleine SleemanDepartment of Microbiology, University of Pennsylvania, Philadelphia, PA, USA.
Robert C ZweigDivision of Comparative Medicine, ONPRC.
Sarah ThomasDivision of Neuroscience, ONPRC.
Archana ThomasDivision of Neuroscience, ONPRC.
Lina GaoKnight Cancer Institute, OHSU, Portland, OR, USA.
Alec J HirschVaccine and Gene Therapy Institute, Oregon Health and Science University (OHSU), Beaverton, OR, USA.
Mayaan LevyDepartment of Microbiology, University of Pennsylvania, Philadelphia, PA, USA.
Sara R CherryDepartment of Pathology and Laboratory Medicine and University of Pennsylvania, Philadelphia, PA, USA.
Steven E KahnDivision of Metabolism, Endocrinology and Nutrition, Department of Medicine, VA Puget Sound Health Care System and University of Washington, Seattle, WA, USA.
Mark K SlifkaDivision of Neuroscience, ONPRC.
Daniel N StreblowDivision of Pathobiology and Immunology, ONPRC.
Jonah B SachaDivision of Pathobiology and Immunology, ONPRC.
Paul KievitDivision of Metabolic Health and Disease, Oregon National Primate Research Center (ONPRC), Beaverton, OR, USA.
Charles T RobertsDivision of Metabolic Health and Disease, Oregon National Primate Research Center (ONPRC), Beaverton, OR, USA.ORCID 0000-0003-1756-5772

Funding

Upgrade of confocal microscopy at the Oregon National Primate Research CenterP51OD011092 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI Bonnie J. Nagel · 2012 to 2026
$203.9M
Post-acute metabolic sequelae of SARS-CoV-2 infection in nonhuman primatesR01DK122843 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI KIEVIT, PAUL, ROBERTS, CHARLES T · 2019 to 2023
$6.6M
Impact of obesity on SARS-CoV-2 infection and reciprocal effects of SARS-CoV-2 on metabolic diseaseR01DK132225 · NIDDK · OREGON HEALTH & SCIENCE UNIVERSITY · PI KIEVIT, PAUL · 2023 to 2025
$2.9M
Slide Scanner for the ONPRC Imaging and Morphology CoreS10OD025002 · OD · OREGON HEALTH & SCIENCE UNIVERSITY · PI SRINIVASAN, SATHYA · 2018 to 2018
$146k
NIDDK NIH HHS R01 DK122843NIDDK NIH HHS R01 DK132225NIH HHS P51 OD011092NIH HHS S10 OD025002
6 · The paper itself

Abstract

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.

Identifiers

PMID40027795
PMCPMC11870618

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.