sars-cov-2-variants / lineage-proposals

Repository to propose and discuss lineages
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XDY + S:A435S, S:A1174T, N:R36Q, ORF7a:P34L, ORF9b:D33N (4 with S:T572I) [10 seq, 5 countries] #2014

Open ryhisner opened 2 weeks ago

ryhisner commented 2 weeks ago

Description Sub-lineage of: XDY Earliest sequence: 2024-7-31, USA, Massachusetts — EPI_ISL_19347338 Most recent sequence: 2024-8-28, USA, South Carolina — EPI_ISL_19394879 Continents circulating: Europe (4), North America (2) Countries circulating: France (2), USA (2), Scotland (1), Sweden (1) Number of Sequences: 6 GISAID Nucleotide Query: C27494T, G28380A, G22865T CovSpectrum Query: [3-of: C27494T, G28380A, G22865T] Substitutions on top of XDY: Spike: A435S, A1174T (+ T572I in further, 3-seq branch) N: R36Q ORF7a: P34L ORF9b: D33N ORF1a: ∆82-84, M85V (only in further, 3-seq branch) Nucleotide: G22865T, G25082A, C27494T, G28380A (+ ∆510-518, C23277T in further branch)

Phylogenetic Order of Mutations: C27494T (ORF7a:P34L) G25082A, G28380A (S:A1174T, N:R36Q, ORF9b:D33N) G22865T (S:A435S) ∆510-518, C23277T (ORF1a:∆82-84, ORF1a:M85V, S:T572I)

USHER Tree https://nextstrain.org/fetch/raw.githubusercontent.com/ryhisner/jsons3/main/XDY_A435S_A1174T.json

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Evidence Seems to be a lot of positive selection in this branch. All mutations here are non-synonymous, and one sequence here has, on top of baseline XDY, eight AA mutations—four in spike—on just seven nuc substitutions (5/6 non-synonymous with one double N/ORF9b mutation + an out-of-frame ORF1a deletion causing ORF1a:M85V). Wide geographic spread and recent collection dates make it worth watching.

Genomes

Genomes EPI_ISL_19344396, EPI_ISL_19347338, EPI_ISL_19357169, EPI_ISL_19372202, EPI_ISL_19389996, EPI_ISL_19394879
FedeGueli commented 2 weeks ago

Very interesting one : Orf7a:P34L/S has been in 50K sequences and mutliple lineages especially in the vocs era. 435S is the only convergent&successful mutation in the rbd recently (beyond 493E,FLiRT, 445X and 478X) S:A1174V (here is T) is convergent (and going) in #1843 and #1997 despite not being widespread it was already in B.1.1.7 and other lineages. Plus double Orf9b/N mutation are always something to watch although this one has not been widesporead

ryhisner commented 2 weeks ago

One showed up in Italy today. Clusters with sequences from France, Scotland, and Sweden.

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FedeGueli commented 1 week ago

+2 FRANCE, ONE FROM GBW pointing to some sort of prevalence there. please propose when it reaches 20

FedeGueli commented 1 week ago

@ryhisner there was at ypo in the title it is Orf9b:D33N as correctly reported in the proposal , right?

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