Neuropsychiatric sequelae in an experimental model of post-COVID syndrome in mice.

Publication date: Aug 01, 2025

The global impact of the COVID-19 pandemic has been unprecedented, and presently, the world is facing a new challenge known as post-COVID syndrome (PCS). Current estimates suggest that more than 100 million people are grappling with PCS, encompassing several manifestations, including pulmonary, musculoskeletal, metabolic, and neuropsychiatric sequelae (cognitive and behavioral). The mechanisms underlying PCS remain unclear. The present study aimed to: (i) comprehensively characterize the acute effects of pulmonary inoculation of the betacoronavirus MHV-A59 in immunocompetent mice at clinical, cellular, and molecular levels; (ii) examine potential acute and long-term pulmonary, musculoskeletal, and neuropsychiatric sequelae induced by the betacoronavirus MHV-A59; and to (iii) assess sex-specific differences. Male and female C57Bl/6 mice were initially inoculated with varying viral titers (3×10 to 3×10 PFU/30 μL) of the betacoronavirus MHV-A59 via the intranasal route to define the highest inoculum capable of inducing disease without causing mortality. Further experiments were conducted with the 3×10 PFU inoculum. Mice exhibited an altered neutrophil/lymphocyte ratio in the blood in the 2nd and 5th day post-infection (dpi). Marked lung lesions were characterized by hyperplasia of the alveolar walls, infiltration of polymorphonuclear leukocytes (PMN) and mononuclear leukocytes, hemorrhage, increased concentrations of CCL2, CCL3, CCL5, and CXCL1 chemokines, as well as high viral titers until the 5th dpi. While these lung inflammatory signs resolved, other manifestations were observed up to the 60 dpi, including mild brain lesions with gliosis and hyperemic blood vessels, neuromuscular dysfunctions, anhedonic-like behavior, deficits in spatial working memory, and short-term aversive memory. These musculoskeletal and neuropsychiatric complications were exclusive to female mice and prevented after ovariectomy. In summary, our study describes for the first time a novel sex-dependent model of PCS focused on neuropsychiatric and musculoskeletal disorders. This model provides a unique platform for future investigations regarding the effects of acute therapeutic interventions on the long-term sequelae unleashed by betacoronavirus infection.

Concepts Keywords
5th Animals
Betacoronavirus Coronavirus Infections
Global COVID-19
Hemorrhage COVID-19
Mice Disease Models, Animal
Female
Long COVID
Lung
Male
MHV-A59
Mice
Murine hepatitis virus
Neuropsychiatric sequelae
Ovariectomy
Pandemics
Pneumonia, Viral
post-COVID syndrome
SARS-CoV-2

Semantics

Type Source Name
disease MESH sequelae
disease MESH syndrome
disease MESH COVID-19 pandemic
disease IDO blood
disease MESH infection
disease MESH hyperplasia
disease MESH hemorrhage
disease MESH gliosis
disease MESH Coronavirus Infections
disease MESH Disease Models Animal
disease MESH Long COVID
disease MESH Pneumonia Viral

Original Article

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