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Spiking Pandemic Potential: Structural and Immunological Aspects of SARS-CoV-2

  • Ying Ting Wang
    ,
  • Sara Landeras-Bueno
    ,
  • Li En Hsieh
    ,
  • Yutaka Terada
    ,
  • Kenneth Kim
    ,
*Corresponding author for this work
Scholary Output:
Contribution to journal
Review article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

SARS-Coronavirus-2 (SARS-CoV-2) causes Coronavirus disease 2019 (COVID-19), an infectious respiratory disease causing thousands of deaths and overwhelming public health systems. The international spread of SARS-CoV-2 is associated with the ease of global travel, and societal dynamics, immunologic naiveté of the host population, and muted innate immune responses. Based on these factors and the expanding geographic scale of the disease, the World Health Organization (WHO) declared the COVID-19 outbreak a pandemic–the first caused by a coronavirus. In this review, we summarize the current epidemiological status of COVID-19 and consider the virological and immunological lessons, animal models, and tools developed in response to prior SARS-CoV and MERS-CoV outbreaks that can serve as resources for development of SARS-CoV-2 therapeutics and vaccines. In particular, we discuss structural insights into the SARS-CoV-2 spike protein, a major determinant of transmissibility, and discuss key molecular aspects that will aid in understanding and fighting this new global threat.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 605-618 (14 pages)

Journal (Volume, Issue Number)

Trends in Microbiology (Volume 28, Issue 8)

Publication milestones

  • Published - 08/2020

Publication status

Published - 08/2020

ISSN

0966-842X

Publication IDs

  • Scopus: 85085923286
  • PubMed: 32507543

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8
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0.89
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1
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1
Scopus
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Funding Details

We thank Sharon Schendel for critical reading of the manuscript and numerous helpful suggestions. This research was funded by Bill and Melinda Gates Foundation grant # INV-006133 .
FunderFunding number
BMGF
INV-006133