Design of Specific Primer Set for Detection of B.1.1.7 SARS-CoV-2 Variant using Deep Learning

Author:

Lopez-Rincon AlejandroORCID,Perez-Romero Carmina A.ORCID,Tonda AlbertoORCID,Mendoza-Maldonado LuceroORCID,Claassen EricORCID,Garssen JohanORCID,Kraneveld Aletta D.ORCID

Abstract

ABSTRACTThe SARS-CoV-2 variant B.1.1.7 lineage, also known as clade GR from Global Initiative on Sharing All Influenza Data (GISAID), Nextstrain clade 20B, or Variant Under Investigation in December 2020 (VUI – 202012/01), appears to have an increased transmissability in comparison to other variants. Thus, to contain and study this variant of the SARS-CoV-2 virus, it is necessary to develop a specific molecular test to uniquely identify it. Using a completely automated pipeline involving deep learning techniques, we designed a primer set which is specific to SARS-CoV-2 variant B.1.1.7 with >99% accuracy, starting from 8,923 sequences from GISAID. The resulting primer set is in the region of the synonymous mutation C16176T in the ORF1ab gene, using the canonical sequence of the variant B.1.1.7 as a reference. Furtherin-silicotesting shows that the primer set’s sequences do not appear in different viruses, using 20,571 virus samples from the National Center for Biotechnology Information (NCBI), nor in other coronaviruses, using 487 samples from National Genomics Data Center (NGDC). In conclusion, the presented primer set can be exploited as part of a multiplexed approach in the initial diagnosis of Covid-19 patients, or used as a second step of diagnosis in cases already positive to Covid-19, to identify individuals carrying the B.1.1.7 variant.

Publisher

Cold Spring Harbor Laboratory

Reference24 articles.

1. Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding;The Lancet,2020

2. Chand, M. , Hopkins, S. & Dabrera, G. Investigation of novel SARS-COV-2 variant: Variant of Concern 202012/01 (2020).

3. for Disease Prevention, E. C. & Control. Rapid increase of a sars-cov-2 variant with multiple spike protein mutations observed in the united kingdom (2020).

4. Arambaut, Garmstrong & Isabel. Preliminary genomic characterisation of an emergent sars-cov-2 lineage in the uk defined by a novel set of spike mutations (2020).

5. Nextstrain: real-time tracking of pathogen evolution;Bioinformatics,2018

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