2018/06/15 by Mathieu Dubé, Alain Le Coupanec, Alan H. M. Wong +3 · 470 citations
Agricultural and Biological Sciences · Medicine · Neuroscience · #Animal Virus Infections Studies #Biology #Central nervous system #Coronavirus #Coronavirus disease 2019 (COVID-19) #Disease #Long-Term Effects of COVID-19 #Medicine #Neuron #Neuroscience #Olfactory bulb #Pathology #SARS-CoV-2 and COVID-19 Research #Virology
paper · doi:10.1128/jvi.00404-18
published in Journal of Virology 92(17) (American Society for Microbiology)
openalex publication_date 2018/06/15 · openalex created_date 2025/10/10 · openalex updated_date 2026/08/06
Coronaviruses may invade the CNS, disseminate, and participate in the induction of neurological diseases. Their neuropathogenicity is being increasingly recognized in humans, and the presence and persistence of human coronaviruses (HCoV) in human brains have been proposed to cause long-term sequelae. Using our mouse model relying on natural susceptibility to HCoV OC43 and neuronal cell cultures, we have defined the most relevant path taken by HCoV OC43 to access and spread to and within the CNS toward the brain stem and spinal cord and studied in cell culture the underlying modes of intercellular propagation to better understand its neuropathogenesis. Our data suggest that axonal transport governs HCoV OC43 egress in the CNS, leading to the exacerbation of neuropathogenesis. Exploiting knowledge on neuroinvasion and dissemination will enhance our ability to control viral infection within the CNS, as it will shed light on underlying mechanisms of neuropathogenesis and uncover potential druggable molecular virus-host interfaces.