AI-based decoding of long covid cognitive impairments in mice using automated behavioral system and comparative transcriptomic analysis
Heba M. AmeriD, Mohamed M. ShamseldiniD, Sarah FaberiD, Mostafa M. EltobgyiD, Amy WebbiD, Rabab ElMergawy, Michelle ChambleeiD, Richard Perez, Owen D. Whitham, Asmaa BadriD, Gauruv A. Gupta, Jihad I. OmraniD, Destiny Bissel, Jacob S. YountiD, Estelle Cormet‐BoyakaiD, Prosper N. BoyakaiD, Jiànróng LǐiD, Xiaoli ZhangiD, Mark E. PeeplesiD, KC Mahesh, Maciej PietrzakiD, Stephanie M. SeveauiD, Olga N. Kokiko‐CochraniD, Magdi Amer, Ruth M. BarrientosiD, , Amal O. AmeriD
Abstract
Long COVID (LC) following SARS-CoV-2 infection affects millions of individuals world-wide and manifests with a variety of symptoms including cognitive dysfunction also known as "brain fog". This is characterized by difficulties in executive functions, planning, decision-making, working memory, impairments in complex attention, loss of ability to learn new skills and perform sophisticated brain tasks. No effective treatment options currently exist for LC-related cognitive dysfunction. Here, we use the IntelliCage, which is an automated tracking system of cognitive functions, following SARS-CoV-2 infection in mice, measuring the ability of each mouse within a group to perform tasks that mimic complex human behaviors, such as planning, decision-making, cognitive flexibility, and working memory. Artificial intelligence and machine learning analyses of the tracking data classified LC mice into distinct behavioral categories from non-infected control mice, permitting precise identification and quantification of complex cognitive dysfunction in a controlled, replicable manner. Importantly, we find that brains from LC mice with cognitive dysfunction exhibit transcriptomic alterations similar to those observed in humans suffering from LC-related cognitive impairments, including altered expression of genes involved in learning, executive functions, synaptic functions, neurotransmitters and memory. Together, our findings establish a validated murine model and an automated unbiased approach to study LC-related cognitive dysfunction for the first time, and providing a valuable tool for screening potential treatments and therapeutic interventions.
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