Neuroinvasion of SARS-CoV-2 in human and mouse brain

Eric Song(Yale University), Ce Zhang(Yale University), Benjamin Israelow(Yale University), Alice Lu-Culligan(Yale University), Alba Vieites‐Prado(Inserm), Sophie Skriabine(Inserm), Peiwen Lu(Yale University), Orr-El Weizman(Yale University), Feimei Liu(Yale University), Yile Dai(Yale University), Klara Szigeti‐Buck(Yale University), Yuki Yasumoto(Yale University), Guilin Wang(Yale Cancer Center), Christopher Castaldi(Yale Cancer Center), Jaime Heltke(Yale Cancer Center), Evelyn Ng(Yale Cancer Center), John F. Wheeler(Yale Cancer Center), Mia Madel Alfajaro(Yale University), Etienne Levavasseur(Inserm), Benjamin Fontes(Yale University), Neal G. Ravindra(Yale University), David van Dijk(Yale University), Shrikant Mane(Yale Cancer Center), Murat Günel(Yale University), Aaron M. Ring(Yale University), Syed A. Jaffar Kazmi(Geisinger Medical Center), Kai Zhang(Geisinger Medical Center), Craig B. Wilen(Yale University), Tamás L. Horváth(Yale University), Isabelle Plu(Inserm), Stéphane Haı̈k(Inserm), Jean‐Léon Thomas(Inserm), Angeliki Louvi(Yale University), Shelli Farhadian(Yale University), Anita Hüttner(Yale University), Danielle Seilhean(Inserm), Nicolas Renier(Inserm), Kaya Bilgüvar(Yale Cancer Center), Akiko Iwasaki(Howard Hughes Medical Institute)
The Journal of Experimental Medicine
December 11, 2020
Cited by 1,032Open Access
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Abstract

Although COVID-19 is considered to be primarily a respiratory disease, SARS-CoV-2 affects multiple organ systems including the central nervous system (CNS). Yet, there is no consensus on the consequences of CNS infections. Here, we used three independent approaches to probe the capacity of SARS-CoV-2 to infect the brain. First, using human brain organoids, we observed clear evidence of infection with accompanying metabolic changes in infected and neighboring neurons. However, no evidence for type I interferon responses was detected. We demonstrate that neuronal infection can be prevented by blocking ACE2 with antibodies or by administering cerebrospinal fluid from a COVID-19 patient. Second, using mice overexpressing human ACE2, we demonstrate SARS-CoV-2 neuroinvasion in vivo. Finally, in autopsies from patients who died of COVID-19, we detect SARS-CoV-2 in cortical neurons and note pathological features associated with infection with minimal immune cell infiltrates. These results provide evidence for the neuroinvasive capacity of SARS-CoV-2 and an unexpected consequence of direct infection of neurons by SARS-CoV-2.


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