Early innate immune response and evolution of a SARS-CoV-2 furin cleavage site inactive variant in bat cells.

Publication date: Jul 01, 2025

SARS-CoV-2 has caused the largest known coronavirus pandemic and is believed to have emerged from insectivorous bats. Little is known about the evolution of these viruses in their reservoir bat species. In this study, we investigate the SARS-CoV-2-host interaction using human and bat cells. Bat cells mount a robust and early antiviral response but elicit a dampened proinflammatory response upon SARS-CoV-2 infection compared to human cells. Furthermore, an inactivating R685P mutation within the furin cleavage site (FCS) of the SARS-CoV-2 spike protein is naturally selected for in infected bat cells. Taken together, our data demonstrate that insectivorous Eptesicus fuscus bat cells have evolved a differential antiviral immune response against SARS-CoV-2 infection, likely contributing to their disease tolerance ability. Our study sheds light on the evolution of sarbecoviruses in bats and extends molecular evidence to data from field studies that have demonstrated that SARS-CoV-2-related viruses in wild-caught bats lack an intact FCS.

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Concepts Keywords
Antiviral antiviral response
Bat bats
Cleavage coronavirus
Host CP: Immunology
Sarbecoviruses CP: Microbiology
furin cleavage site
proteomics
reservoir host
SARS-CoV-2
transcriptomics
zoonosis

Semantics

Type Source Name
disease IDO innate immune response
disease IDO site
disease IDO host
disease MESH SARS-CoV-2 infection
pathway REACTOME SARS-CoV-2 Infection
disease IDO immune response
drug DRUGBANK Coenzyme M
disease MESH Abiotic Stress
disease IDO process
drug DRUGBANK Pentaerythritol tetranitrate
drug DRUGBANK Zinc
drug DRUGBANK Polyethylene glycol
drug DRUGBANK Salicylic acid
drug DRUGBANK Water
drug DRUGBANK Carboxyamidotriazole
disease IDO protein
disease MESH fungal infections
disease IDO pathogen
drug DRUGBANK Nitrogen
disease IDO reagent
drug DRUGBANK Mannitol
drug DRUGBANK Ethanol
drug DRUGBANK Kanamycin
drug DRUGBANK Rifampicin
disease IDO assay
drug DRUGBANK Amino acids
drug DRUGBANK Spinosad
disease MESH polyploidy
disease MESH tetraploid
drug DRUGBANK Guanosine
pathway REACTOME Signal Transduction
drug DRUGBANK (S)-Des-Me-Ampa
drug DRUGBANK Oxygen
drug DRUGBANK Hydrogen peroxide
disease MESH oxidative damage
disease IDO production
disease MESH death
disease MESH necrosis
disease IDO cell
drug DRUGBANK Phencyclidine
pathway REACTOME Metabolism
pathway REACTOME Reproduction
disease IDO zoonosis

Original Article

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