BREAKING🔔 The 20th paper from G2P-Japan🇯🇵 is out at Nature Communications @NatureComms. We illuminated the convergent evolution of #Omicron and characteristics of BQ.1.1 (aka #Cerberos). Please RT
In late 2022, the Omicron subvariants have highly diversified. However, some lineages have convergently acquired amino acid substitutions at five critical residues in the spike protein: R346, K444, L452, N460 and F486. 2/
Omicron BQ.1.1 (aka #Cerberus), a descendant of BA.5, bears all five substitutions at the convergent sites: R346T, K444T, L452R, N460K, F486V. 3/
Here, we, particularly two young shining stars, @jampei2 & @SpyrosLytras, performed phylogenetic and epidemic dynamics analyses and showed that Omicron subvariants independently increased their viral fitness by acquiring the convergent substitutions. 4/
All five convergent substitutions (R346T, K444T, L452R, N460K & F486V) contributed to increase relative effective reproduction number (Re), and BQ.1.1, which harbors all five convergent substitutions, showed the highest fitness among the viruses investigated. 5/
Neutralization assay showed that BQ.1.1 is more resistant to breakthrough BA.2 and BA.5 infection sera than BA.5. 6/
We showed lines of data suggesting the close association of viral fusogenicity and intrinsic pathogenicity. For instance, both BA.5 and BA.2.75, descendants of BA.2, are more fusogenic and pathogenic than BA.2. 7/
Notably, the BQ.1.1 spike exhibited greater fusogenicity than the BA.5 spike, suggesting that BQ.1.1 is more pathogenic than BA.5. 8/
However, unexpectedly, experiments using hamsters showed that the pathogenicity of BQ.1.1 in hamsters is comparable to or even lower than that of BA.5.
Our multiscale investigations provide insights into the evolutionary trajectory of Omicron subvariants. 9/9
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BREAKING🔔 The 19th paper from G2P-Japan🇯🇵 is out at Lancet Infectious Diseases @TheLancetInfDis . We elucidated the virological characteristics of new SARS-CoV-2 variant of interest, XBB.1.16 (aka #Arcturus) Please RT🔥 1/ thelancet.com/journals/lanin…
XBB.1.16 = XBB.1 + #F486P, #E180V, and #T478K in spike.
cf. XBB.1.5 = XBB.1 + #F486P in spike (i.e., XBB.1.16 = XBB.1.5 + #E180V and #T478K in spike). 2/
A phylogenetic tree shows that XBB.1.16 is a descendant of XBB.1, not of XBB.1.5. 3/
BREAKING🔔 We introduce the latest work from G2P-Japan🇯🇵 focusing on the virological characteristics of new SARS-CoV-2 lineage of concern, XBB.1.5 (aka #Kraken), which is rapidly spreading in the US🇺🇸 Please RT! Preprint/peer-review paper will come soon🔥 1/
XBB.1.5 = XBB.1 + #F486P in spike. We also found that a part of XBB.1.5 has reversion mutation in Y144del (=XBB.1.5 + #ins144Y) in spike. Because #Y144del evades antiviral immunity and decreases pseudovirus infectivity, its reversion might be also critical. 2/
First, a brilliant young talent, @jampei2, showed that the relative basic reproduction number (Re) of XBB.1.5 is >1.2-fold greater than the parental XBB.1 (❗️). Importantly the "1.2-fold difference" is similar to the differences between BA.1 versus BA.2 and BA.2 versus BA.5. 3/
BREAKING🔔 The 15th preprint from G2P-Japan🇯🇵 is out @biorxivpreprint. We illuminated the virological characteristics of one of the latest SARS-CoV-2 lineages of concern, XBB, which was generated by recombination of two #Omicron subvariants. Please RT. 1/ biorxiv.org/content/10.110…
In late 2022, the Omicron subvariants have highly diversified. An example is BQ.1.1, which has convergently acquired amino acid substitutions at five critical residues in the spike protein: R346T, K444T, L452R, N460K & F486V. We reported it as below⬇️ 2/
Another variant of concern is XBB (aka #gryphon). First, two young talents, @jampei2 & @SpyrosLytras, showed that XBB emerged by recombination of two co-circulating BA.2 lineages, BJ.1 & BM.1.1.1 (a progeny of BA.2.75), during 2022 summer in India or its neighboring countries. 3/