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Epidemiological, clinical and genomic snapshot of the first 100 B.1.1.7 SARS-CoV-2 cases in Madrid

Authors :
Darío García de Viedma
Pilar Catalán Pharmacy
Agustín Estévez
Pedro J Sola Campoy
Laura Pérez-Lago
Julia Suárez-González
Mariana G. López
Patricia Muñoz
Iñaki Comas
Fernando González-Candelas
Víctor Manuel de la Cueva Technician
Luis Alcalá
Marta Herranz Tecnichian
Sergio Buenestado-Serrano
Instituto de Salud Carlos III
Consejo Superior de Investigaciones Científicas (España)
Source :
Digital.CSIC. Repositorio Institucional del CSIC, instname, Journal of Travel Medicine
Publication Year :
2021
Publisher :
University of Oxford, 2021.

Abstract

A new SARS-CoV-2 variant, B.1.1.7, emerged in September in the UK, and is responsible for 76.6% of COVID-19 cases.1 This variant has also been reported in another 45 countries, 17 of them European.2,3 B.1.1.7 is considered to have higher transmissibility.4 It carries an unusually high number of specific mutations/deletions, 18, mostly non-synonymous and eight concentrate in the S gene,5 including several which might have relevant functional roles. The 69/70 deletion may be associated to immune response evasion6 and the N501Y substitution increases the affinity to the ACE2 receptor.7 These findings have raised the alarm of having to face a new variant with the potential to accelerate the spread of the pandemic. A recent report finds a realistic possibility that B.1.1.7 is associated with an increased risk of death.<br />This work was supported by Instituto de Salud Carlos III (Ref COV20/00140: SeqCOVID—Consorcio para la epidemiología genómica de SARS-CoV-2 en España) and by Consejo Superior de Investigaciones Científicas (CSIC) (PTI Salud Global). LPL holds a Miguel Servet Contract CP15/00075).

Details

Database :
OpenAIRE
Journal :
Digital.CSIC. Repositorio Institucional del CSIC, instname, Journal of Travel Medicine
Accession number :
edsair.doi.dedup.....91c19f2ce7ecb7012d2eca09e2734b5f