4.7 Article

Comparing infectivity and virulence of emerging SARS-CoV-2 variants in Syrian hamsters

期刊

EBIOMEDICINE
卷 68, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.ebiom.2021.103403

关键词

Emergence; Hamster model; SARS-CoV-2; Variants of concern (VoC)

资金

  1. Flemish Research Foundation (FWO) emergency Covid19 fund [G0G4820N]
  2. FWO Excellence of Science (EOS) program [30981113]
  3. European Union [101003627, 733176]
  4. Bill and Melinda Gates Foundation [INV00636]
  5. KU Leuven Internal Funds [C3/19/057, C24/17/061]
  6. FWO [1186121N]
  7. China Scholarship Council [201906170033]
  8. KU Leuven/UZ Leuven Covid19 Fund (COVAX-PREC project)

向作者/读者索取更多资源

The global COVID-19 pandemic has resulted in over 108 million infections and 2.4 million deaths within a year, with new variants of concern emerging. Research on prototypic VoC from B.1.1.7 and B.1.351 variants in hamsters revealed efficient infection of the lower respiratory tract and highlighted the need for assessing vaccine and therapeutic efficacy against these variants.
Background: Within one year after its emergence, more than 108 million people acquired SARS-CoV-2 and almost 2.4 million succumbed to COVID-19. New SARS-CoV-2 variants of concern (VoC) are emerging all over the world, with the threat of being more readily transmitted, being more virulent, or escaping naturally acquired and vaccine-induced immunity. At least three major prototypic VoC have been identified, i.e. the United Kingdom, UK (B.1.1.7), South African (B.1.351) and Brazilian (B.1.1.28.1) variants. These are replacing formerly dominant strains and sparking new COVID-19 epidemics. Methods: We studied the effect of infection with prototypic VoC from both B.1.1.7 and B.1.351 variants in female Syrian golden hamsters to assess their relative infectivity and virulence in direct comparison to two basal SARS-CoV-2 strains isolated in early 2020. Findings: A very efficient infection of the lower respiratory tract of hamsters by these VoC is observed. In line with clinical evidence from patients infected with these VoC, no major differences in disease outcome were observed as compared to the original strains as was quantified by (i) histological scoring, (ii) micro-computed tomography, and (iii) analysis of the expression profiles of selected antiviral and pro-inflammatory cytokine genes. Noteworthy however, in hamsters infected with VoC B.1.1.7, a particularly strong elevation of proin-flammatory cytokines was detected. Interpretation: We established relevant preclinical infection models that will be pivotal to assess the efficacy of current and future vaccine(s) (candidates) as well as therapeutics (small molecules and antibodies) against two important SARS-CoV-2 VoC. (C) 2021 The Authors. Published by Elsevier B.V.

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