2021
DOI: 10.1002/jmv.27235
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Introduction of SARS‐COV‐2 C.37 (WHO VOI lambda) from Peru to Italy

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Cited by 16 publications
(14 citation statements)
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“…Mutations which can also be found in the Delta variant are present in this variant at the higher prevalence and act similarly [ 22 ] 8 B.1.525 21D/20A Eta VOI MUL Q52R, A67V, E484K, Q677H, F888L Q677H and E484K result in reduced neutralization by various antibody treatments [ 119 , 120 ] 9 B.1.526 21F/20C Iota VOI USA L5F, T95I, D253G, E484K Mutations in common with the Beta, Gamma and Delta variants perform similarly 10 C.37 21G/20D Lambda VOI PER G75V, T76I, L452Q, F490S, T859N L452Q and F490S are on the RBD of the S protein. The former is exclusive to C.37 and is responsible for enhancing the affinity for the ACE2 receptor, while the latter is responsible for decreased neutralization by antibodies [ 121 , 122 ]). T76I is also involved in increasing viral infectivity [ 123 ] 11 B.1.621 21H Mu VOI COL T95I, Y144S, Y145N, R346K, E484K, N501Y, P681H Mutations that are also found in the previously mentioned Alpha, Beta, Gamma and Delta variants show similar effects as described previously 12 B.1.427 and B.1.429 21C Epsilon VOI (currently De-escalated) USA S13I, W152C, L452R L452R mutation decreases the activity of multiple RBD specific monoclonal antibodies, while W152C and L452R abrogate the action of the NTD supersite directed antibodies [ 124 ] 13 B.1.1.519 20B/S:...…”
Section: Sars-cov2 Variantsmentioning
confidence: 99%
“…Mutations which can also be found in the Delta variant are present in this variant at the higher prevalence and act similarly [ 22 ] 8 B.1.525 21D/20A Eta VOI MUL Q52R, A67V, E484K, Q677H, F888L Q677H and E484K result in reduced neutralization by various antibody treatments [ 119 , 120 ] 9 B.1.526 21F/20C Iota VOI USA L5F, T95I, D253G, E484K Mutations in common with the Beta, Gamma and Delta variants perform similarly 10 C.37 21G/20D Lambda VOI PER G75V, T76I, L452Q, F490S, T859N L452Q and F490S are on the RBD of the S protein. The former is exclusive to C.37 and is responsible for enhancing the affinity for the ACE2 receptor, while the latter is responsible for decreased neutralization by antibodies [ 121 , 122 ]). T76I is also involved in increasing viral infectivity [ 123 ] 11 B.1.621 21H Mu VOI COL T95I, Y144S, Y145N, R346K, E484K, N501Y, P681H Mutations that are also found in the previously mentioned Alpha, Beta, Gamma and Delta variants show similar effects as described previously 12 B.1.427 and B.1.429 21C Epsilon VOI (currently De-escalated) USA S13I, W152C, L452R L452R mutation decreases the activity of multiple RBD specific monoclonal antibodies, while W152C and L452R abrogate the action of the NTD supersite directed antibodies [ 124 ] 13 B.1.1.519 20B/S:...…”
Section: Sars-cov2 Variantsmentioning
confidence: 99%
“…We report a cluster of B.1.617.2 and E484K occurring in Lombardy, Italy. All cases were first tested by real-time reverse transcription PCR and, if positive, sequenced as previously reported ( 1 ).…”
mentioning
confidence: 99%
“…815 of these 2,622 positive samples underwent sequencing for characterizing the infecting SARS CoV-2 variant, according to the surveillance programme of the Italian National Institute of Health and Ministry of Health. Of these 815, 97 samples were sequenced by Sanger for the entire Spike gene or by next-generation whole-genome sequencing (NGS) as previously reported [ 3 ]. Briefly, Sanger protocol was performed on RT–PCR fragments covering the complete Spike gene of SARS-CoV-2, and directly using the Big Dye Terminator cycle-sequencing kit (Applied Biosystems).…”
Section: Methodsmentioning
confidence: 99%