SARS‐CoV‐2‐related bat virus behavior in human‐relevant models sheds light on the origin of COVID‐19. (6th March 2023)

• Record Type: Journal Article
• Authors: Temmam, Sarah; Montagutelli, Xavier; Herate, Cécile; Donati, Flora; Regnault, Béatrice; Attia, Mikael; Baquero Salazar, Eduard; Chretien, Delphine; Conquet, Laurine; Jouvion, Grégory; Pipoli Da Fonseca, Juliana; Cokelaer, Thomas; Amara, Faustine; Relouzat, Francis; Naninck, Thibaut; Lemaitre, Julien; Derreudre‐Bosquet, Nathalie; Pascal, Quentin; Bonomi, Massimiliano; Bigot, Thomas; Munier, Sandie; Rey, Felix A; Le Grand, Roger; van der Werf, Sylvie; Eloit, Marc
• Is Part Of: EMBO reports. Volume 24:Number 4(2023)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2023-03-06
• Subjects: adaptive mutations -- animal model -- bat coronavirus -- pathogenesis -- serology; Molecular biology -- Periodicals; Molecular Biology -- Periodicals; Molecular biology; Periodicals; 572.8
• DOI: 10.15252/embr.202256055
• Languages: English
• ISSNs: 1469-221X

Abstract

Abstract: Bat sarbecovirus BANAL‐236 is highly related to SARS‐CoV‐2 and infects human cells, albeit lacking the furin cleavage site in its spike protein. BANAL‐236 replicates efficiently and pauci‐symptomatically in humanized mice and in macaques, where its tropism is enteric, strongly differing from that of SARS‐CoV‐2. BANAL‐236 infection leads to protection against superinfection by a virulent strain. We find no evidence of antibodies recognizing bat sarbecoviruses in populations in close contact with bats in which the virus was identified, indicating that such spillover infections, if they occur, are rare. Six passages in humanized mice or in human intestinal cells, mimicking putative early spillover events, select adaptive mutations without appearance of a furin cleavage site and no change in virulence. Therefore, acquisition of a furin site in the spike protein is likely a pre‐spillover event that did not occur upon replication of a SARS‐CoV‐2‐like bat virus in humans or other animals. Other hypotheses regarding the origin of the SARS‐CoV‐2 should therefore be evaluated, including the presence of sarbecoviruses carrying a spike with a furin cleavage site in bats. Synopsis: A SARS‐CoV‐2‐related bat virus replicates in human models as an enteric virus and does not circulate in highly exposed human populations. Genomic sequence, tissue tropism, and pathogenicity do not evolve toward SARS‐CoV‐2 characteristics upon passaging. SARS‐CoV‐2 related bat virus BANAL‐236 replicates pauci‐symptomatically and is enterotropic in human models. BANAL‐236 infection confers protection against SARS‐CoV‐2. BANAL‐236 does not spread within human populations. Passaging of BANAL‐236 in human models does not generate a furin site and pathogenicity. Abstract : A SARS‐CoV‐2‐related bat virus replicates in human models as an enteric virus and does not circulate in highly exposed human populations. Genomic sequence, tissue tropism, and pathogenicity do not evolve toward SARS‐CoV‐2 characteristics upon passaging.