A Critical Reexamination of Recovered SARS-CoV-2 Sequencing Data

In 2021, Jesse Bloom published a study addressing why the earliest SARS-CoV-2 sequences in Wuhan from late December 2019 were not those most similar to viruses sampled in bats. The study concluded that recovered partial sequences from Wuhan and annotation of Wuhan links for other sequences increased support for one genotype as the progenitor of the SARS-CoV-2 pandemic. However, we show that the collection date for the recovered sequences was January 30, 2020, later than that of hundreds of other SARS-CoV-2 sequences. Mutations in these sequences also exhibit diversity consistent with SARS-CoV-2 sequences collected in late January 2020. Furthermore, we found that Wuhan exposure history was common for early samples, so Bloom's annotation for a single familial cluster does not support that an early genotype was undersampled in Wuhan. Both the recovered partial sequences and additional annotation align with contemporaneous data rather than increase support for a progenitor. Our findings clarify the significance of the recovered sequences and are supported by additional data and analysis published since mid-2021.

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Institutions

Publication Details

Journal
Molecular Biology and Evolution
Published
2025-05-15
DOI
https://doi.org/10.1093/molbev/msaf109
Citations
4
Primary Topic
SARS-CoV-2 and COVID-19 Research
Type
article
Field-Weighted Citation Impact
5.58

Funders

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article

A Critical Reexamination of Recovered SARS-CoV-2 Sequencing Data

Zach Hensel, Florence Débarre
4 citations
Molecular Biology and Evolution
SARS-CoV-2 and COVID-19 Research
5.58
article

A Critical Reexamination of Recovered SARS-CoV-2 Sequencing Data

Zach Hensel, Florence Débarre
article en
4 citations

Abstract

In 2021, Jesse Bloom published a study addressing why the earliest SARS-CoV-2 sequences in Wuhan from late December 2019 were not those most similar to viruses sampled in bats. The study concluded that recovered partial sequences from Wuhan and annotation of Wuhan links for other sequences increased support for one genotype as the progenitor of the SARS-CoV-2 pandemic. However, we show that the collection date for the recovered sequences was January 30, 2020, later than that of hundreds of other SARS-CoV-2 sequences. Mutations in these sequences also exhibit diversity consistent with SARS-CoV-2 sequences collected in late January 2020. Furthermore, we found that Wuhan exposure history was common for early samples, so Bloom's annotation for a single familial cluster does not support that an early genotype was undersampled in Wuhan. Both the recovered partial sequences and additional annotation align with contemporaneous data rather than increase support for a progenitor. Our findings clarify the significance of the recovered sequences and are supported by additional data and analysis published since mid-2021.

Molecular Biology and EvolutionVol. 42(6)
Centre National de la Recherche Scientifique (FR), Université Paris-Est Créteil (FR), Sorbonne Université (FR), Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement (FR), Institut d'écologie et des sciences de l'environnement de Paris (FR), Institut de Recherche pour le Développement (FR), Universidade Nova de Lisboa (PT)
Fundação para a Ciência e a Tecnologia
Good health and well-being
Openalex Percentile: Top 4%
SARS-CoV-2 and COVID-19 Research
5.58
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A Critical Reexamination of Recovered SARS-CoV-2 Sequencing Data — Zach Hensel, Florence Débarre · Molecular Biology and Evolution (2025) | TGRS Research Map | TGRS