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/
We showed that the Re values of XBB lineages are comparable with or slightly higher than those of BQ.1 lineages, and notably, XBB and BQ.1 lineages are becoming dominants in Eastern and Western Hemisphere, respectively. 4/
Neutralization assay revealed that XBB is the most profoundly resistant variant to BA.2/5 breakthrough infection sera ever (!!). >30-fold more resistant to BA.2 breakthrough infection sera than BA.2, and >13-fold more resistant to BA.5 breakthrough infection sera than BA.2😵 5/
XBB spike is more fusogenic than BA.2.75 spike. Notably, the recombination breakpoint is located in the receptor-binding domain of spike, and each region of recombined spike respectively conferred both immune evasion and augmented fusogenicity to the XBB spike. 6/
Finally, we demonstrated that the intrinsic pathogenicity of XBB in hamsters is comparable to or even lower than that of BA.2.75, an ancestral lineage of XBB. 7/
Our multiscale investigation provided evidence suggesting that #XBB is the first documented example of a SARS-CoV-2 variant that increased its fitness (Re) through an recombination event rather than substitutions. 8/8
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BREAKING🔔 The 14th preprint from G2P-Japan🇯🇵 is out @biorxivpreprint. We illuminated the evolutionary rule underlying the convergent evolution of #Omicron and the virological characteristics of one of the latest lineages of concern, BQ.1.1. Please RT. 1/ biorxiv.org/content/10.110…
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/
BREAKING🔔 The 15th paper from G2P-Japan🇯🇵 is out at iScience @iScience_CP. We revealed that the virological features of #Omicron BA.1 variant are determined by the spike #S375F mutation. Please RT. 1/6 cell.com/iscience/fullt…
We have demonstrated that the Omicron BA.1 spike exhibits 1) decreased efficiency of spike cleavage and 2) attenuated fusogenicity:
Cf. The 5th paper from G2P-Japan🇯🇵↓ nature.com/articles/s4158…
However, it remained unclear which mutation(s) determine these BA.1’s features. 2/6
1️⃣Our comprehensive screening experiments revealed that these BA.1's features are determined by its receptor binding domain and particularly, only #S375F mutation is responsible. 3/6
BREAKING🔔 The 14th paper from G2P-Japan🇯🇵 is out at Cell Host & Microbe @cellhostmicrobe. #Omicron BA.2.75 (aka #Centaurus) seems to be more contagious than BA.5 and more pathogenic than the original BA.2. Please RT. 1/16 cell.com/cell-host-micr…
BA.2.75, emerged in India🇮🇳, is classified as VOC-LUM (variant of concern linage under monitoring) by WHO on July 7. Here we elucidated the transmissibility, sensitivity to antiviral immunity & drugs, and intrinsic pathogenicity of BA.2.75. 2/16 who.int/activities/tra…
BA.2.75 is a descendant of BA.2. However, BA.2.75 is phylogenetically different from BA.5, the currently predominant BA.2 descendant. BA.2.75 spike bears nine substitutions, but only a substitution is shared with BA.5 spike. 3/16