4.8 Article

Transmission event of SARS-CoV-2 delta variant reveals multiple vaccine breakthrough infections

期刊

BMC MEDICINE
卷 19, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12916-021-02103-4

关键词

SARS-CoV-2; Delta variant; B; 1; 617; 2; COVID-19; Infectious disease

资金

  1. National Institute of Allergy and Infectious Diseases [1U19AI144297]
  2. Baylor College of Medicine

向作者/读者索取更多资源

This study identified a cluster of 6 vaccinated patients infected with the delta variant, suggesting immune evasion in patients who received the Pfizer BNT162b2, Moderna mRNA-1273, and Covaxin BBV152 vaccines. The delta variant may pose the highest risk among currently circulating SARS-CoV-2 variants, with increased transmissibility over the alpha variant and potential vaccine breakthrough.
Background This study aims to identify the causative strain of SARS-CoV-2 in a cluster of vaccine breakthroughs. Vaccine breakthrough by a highly transmissible SARS-CoV-2 strain is a risk to global public health. Methods Nasopharyngeal swabs from suspected vaccine breakthrough cases were tested for SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) by qPCR (quantitative polymerase chain reaction) for Wuhan-Hu1 and alpha variant. Positive samples were then sequenced by Swift Normalase Amplicon Panels to determine the causal variant. GATK (genome analysis toolkit) variants were filtered with allele fraction >= 80 and min read depth 30x. Results Viral sequencing revealed an infection cluster of 6 vaccinated patients infected with the delta (B.1.617.2) SARS-CoV-2 variant. With no history of vaccine breakthrough, this suggests the delta variant may possess immune evasion in patients that received the Pfizer BNT162b2, Moderna mRNA-1273, and Covaxin BBV152. Conclusions Delta variant may pose the highest risk out of any currently circulating SARS-CoV-2 variants, with previously described increased transmissibility over alpha variant and now, possible vaccine breakthrough. Funding Parts of this work was supported by the National Institute of Allergy and Infectious Diseases (1U19AI144297) and Baylor College of Medicine internal funding.

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