SARS-CoV-2 D614G variant exhibits efficient replication ex vivo and transmission in vivo

Author:

Hou Yixuan J.1ORCID,Chiba Shiho2ORCID,Halfmann Peter2ORCID,Ehre Camille3ORCID,Kuroda Makoto2,Dinnon Kenneth H.4ORCID,Leist Sarah R.1ORCID,Schäfer Alexandra1ORCID,Nakajima Noriko5ORCID,Takahashi Kenta5,Lee Rhianna E.3ORCID,Mascenik Teresa M.3ORCID,Graham Rachel1ORCID,Edwards Caitlin E.1ORCID,Tse Longping V.1ORCID,Okuda Kenichi3ORCID,Markmann Alena J.6ORCID,Bartelt Luther6ORCID,de Silva Aravinda4ORCID,Margolis David M.146ORCID,Boucher Richard C.3,Randell Scott H.3ORCID,Suzuki Tadaki5ORCID,Gralinski Lisa E.1ORCID,Kawaoka Yoshihiro27ORCID,Baric Ralph S.14ORCID

Affiliation:

1. Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

2. Influenza Research Institute, Department of Pathobiological Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI, USA.

3. Marsico Lung Institute, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

4. Department of Microbiology and Immunology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

5. Department of Pathology, National Institute of Infectious Diseases, Tokyo, Japan.

6. Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

7. Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.

Abstract

Changing with the times Pandemic spread of a virus in naïe populations can select for mutations that alter pathogenesis, virulence, and/or transmissibility. The ancestral form of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) that emerged from China has now been largely replaced by strains containing the mutation D614G (Asp 614 -to-Gly) in the viral spike protein. Hou et al. compared the characteristics of the new variant against the ancestral form in a series of experiments in human cells and animal models. The variant is better at infecting upper-airway epithelial cells and replicates in greater numbers than the ancestral virus. Evidence indicates modest, if any, significant changes to virulence in animal models. Therefore, the virus appears to have evolved for greater transmissibility in humans rather than for greater pathogenicity. The mutation renders the new virus variant more susceptible to neutralizing antisera without altering the efficacy of vaccine candidates currently under development. Science , this issue p. 1464

Funder

National Institutes of Health

Japan Agency for Medical Research and Development

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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