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Bat-specific adaptations in interferon signaling and GBP1 contribute to enhanced antiviral capacity

Nature Communications. 2025-07; 
Victoria Gonzalez, Briallen Lobb, Jacob Côté, Arkadeb Bhuinya, Adriana G Tubb, Stephen S Nuthalapati, Akarin Asavajaru, Yan Zhou, Vikram Misra, Darryl Falzarano, Trevor R Sweeney, Sophie M C Gobeil, Linfa Wang, Andrew C Doxey, Arinjay Banerjee Laboratory of Zoonotic Viruses and Comparative Immunology, Vaccine and Infectious Disease Organization (VIDO), University of Saskatchewan, Saskatoon, SK, Canada.
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PCR Cloning and Subcloning Human, P. alecto, and E. fuscus GBP1 cDNA was synthesized (GenScript) and cloned into the p3X-FLAG7. Get A Quote

摘要

Bats are reservoirs of emerging zoonotic viruses that may cause severe disease in humans and agricultural animals. However, it is poorly understood how bats can tolerate diverse viral infections. Here, we characterized type I interferon response pathways in kidney cell lines derived from two divergent bat species, Pteropus alecto and Eptesicus fuscus, identifying distinct mechanisms underlying their enhanced control of viral infection. We demonstrate the critical roles of STAT1/STAT2 in IFNβ signaling, along with species-specific adaptations that contribute towards a steady and ready antiviral state. Unlike in humans, bat IFNβ signaling processes resist the immune antagonistic properties of MERS-CoV which fur... More

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