Closed ryhisner closed 11 months ago
2 more seqs (France+1 Scotland, UK+1)
NSP14_G44C, E_S68F, Spike_Q218R
which query are you using?
A22215G, T25902A,T23042C finds 4 changing it in the main proposal
This jumped to 10 reaching also Quebec and NY and one new region in France.
one more from England
Description
Sub-lineage of: XBB.1.17.1 Earliest sequence: 2023-8-21, France, Ile-de-France, Bobigny, — EPI_ISL_18221906, EPI_ISL_18221907 Most recent sequence: 2023-8-21, France, Ile-de-France, Bobigny — EPI_ISL_18221906, EPI_ISL_18221907 Countries circulating: France (2) Number of Sequences: 2 GISAID AA Query: NSP14_G44C, E_S68F, Spike_Q218R Alternative Query : A22215G, T25902A,T23042C (4/4) or C8140T, C9298T, C26447T (3/4)(EDITED) GISAID Nucleotide Query: T12655C, A22215G, T25902A (2/4) CovSpectrum Query: Nextcladepangolineage:XBB.1.17.1* & [2-of: T12655C, A22215G, T25902A] Substitutions/Deletions on top of XBB.1.17.1: Spike: N148T, ∆177-181, Q218R, S494P, P521S N: ORF1a:E622G, T1422I (NSP2_E442G, NSP3_T611I) ORF1b: G1568C (NSP14_G44C) Nucleotide: A2130G, C4511T, C8140T, C9298T, T12655C, G18169T, ∆22091-22105, A22005C, A22215G, T23042C, C23123T, T25902A, C26447T
Phylogenetic Order of Mutations: A2130G, C4511T (ORF1a:E622G, ORF1a: T1429I) → C23123T (S:P521S) → A22005C, T23042C (S:N148T, S:S494P) → C8140T, C9298T, T12655C, G18169T, ∆22091-22105, A22215G, T25902A, C26447T
USHER Tree https://nextstrain.org/fetch/raw.githubusercontent.com/ryhisner/jsons/main/XBB.1.17.1__N148T_177-181del_Q218R_S494P_P521S.json?c=gt-S_218&gmax=25384&gmin=21563&label=id:node_7051983
Evidence This lineage consists, so far, of only two sequences from separate hospitalized patients in France, both collected on August 21. I'm posting it here because XBB.1.17.1 seems likely to have originated in western Africa and is presumably still most common there. We get so few sequences from that region that it's impossible to know what is circulating in recent weeks. These two identical sequences have a large number of mutations, particularly in spike, so I think it's conceivable it evolved in a stepwise manner through fairly wide circulation in some part of Africa. Most likely it will disappear soon, but it seems worth tracking to me, particularly with its very unusual (perhaps unique) deletion in the N4 NTD loop (S:∆177-181).
Genomes
Genomes
EPI_ISL_18221906, EPI_ISL_18221907