Early introductions and transmission of SARS-CoV-2 variant B.1.1.7 in the United States
The emergence and spread of SARS-CoV-2 lineage B.1.1.7, first detected in the United Kingdom, has become a global public health concern because of its increased transmissibility. Over 2,500 COVID-19 cases associated with this variant have been detected in the United States (US) since December 2020,...
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Veröffentlicht in: | Cell 2021-05, Vol.184 (10), p.2595-2604.e13, Article 13 |
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Sprache: | eng |
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Zusammenfassung: | The emergence and spread of SARS-CoV-2 lineage B.1.1.7, first detected in the United Kingdom, has become a global public health concern because of its increased transmissibility. Over 2,500 COVID-19 cases associated with this variant have been detected in the United States (US) since December 2020, but the extent of establishment is relatively unknown. Using travel, genomic, and diagnostic data, we highlight that the primary ports of entry for B.1.1.7 in the US were in New York, California, and Florida. Furthermore, we found evidence for many independent B.1.1.7 establishments starting in early December 2020, followed by interstate spread by the end of the month. Finally, we project that B.1.1.7 will be the dominant lineage in many states by mid- to late March. Thus, genomic surveillance for B.1.1.7 and other variants urgently needs to be enhanced to better inform the public health response.
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•Flight data identify that NY, CA, and FL were high risk for importing B.1.1.7•B.1.1.7 was introduced separately to multiple US states starting in December 2020•Phylogenetic analysis shows evidence for domestic spread between regions in US•Exponential growth of B.1.1.7 projects that it will be the dominant lineage
The SARS-CoV-2 variant B.1.1.7 was introduced to the US in early December 2020 and soon became established within many communities. The primary points of entry into the US are identified as New York, California, and Florida, and exponential growth in these states resulted in spread to neighboring states. |
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ISSN: | 0092-8674 1097-4172 1097-4172 |
DOI: | 10.1016/j.cell.2021.03.061 |