BREAKING🔔 The 53th paper from G2P-Japan🇯🇵 is out at Lancet Infectious Diseases @TheLancetInfDis. We elucidated the virological characteristics of SARS-CoV-2 NB.1.8.1. Please repost🔥 1/ thelancet.com/journals/lanin…
NB.1.8.1 is a descendant strain of XDV (XDV is a recombinant of XDE, FL.13.4 and JN.1) and is currently spreading in Asian countries. 2/
NB.1.8.1 has 7 mutations in spike and 23 mutations in the non-spike region compared to JN.1. Compared to XEC spike, NB.1.8.1 spike has 4 substitutions, G184S, K478I, A435S and L1104V. 3/
Transmissibility (Re, relative effective reproduction number):
The Re of NB.1.8.1 was ~1.1-1.2-fold higher than that of LP.8.1, a major variant recently. This suggests that NB.1.8.1 has the potential to become the major variant in the near future. 4/
Pseudovirus infectivity:
The infectivity of NB.1.8.1 was higher than that of LP.8.1 but lower than that of XEC. Compared to XEC, K478I and L1104V were the substitutions contributing to lower infectivity. 5/
Immune resistance:
50% neutralizing titer of NB.1.8.1 in both XEC convalescent sera and JN.1 vaccine sera was similar to that of XEC and LP.8.1🤔 6/
In sum, the advantage of NB.1.8.1 over LP.8.1 may be attributed to its higher infectivity. However,
1, Some data are inconsistent with another paper by @yunlong_cao
2, There are many mutations other than spike.
Therefore, more detailed study will be required. 7/
BREAKING🔔 The 50th🎉 paper from G2P-Japan🇯🇵 is out at Lancet Infectious Diseases
@TheLancetInfDis. We elucidated the virological characteristics of SARS-CoV-2 LP.8.1. Please repost🔥 1/ thelancet.com/journals/lanin…
In spike, LP.8.1 has 9 mutations (S31del, F186L, R190S, R346T, V445R, F456L, Q493E, K1086R, and V1104L) compared with JN.1; and 8 amino acid residues (T22N, S31del, F59S, F186L, R190S, R346T, H445R, and K1086R) differ between the spike proteins of LP.8.1 and XEC. 2/
Transmissibility/fitness (Re):
Epidemic dynamics modeling led by Jumpei @jampei2 and Kaho showed that the Re of LP.8.1 is ~1.1-fold higher than that of XEC in 🇺🇸. However, the Re of LP.8.1 and XEC were almost comparable in 🇯🇵. Difference between countries🤔?? 3/
BREAKING🔔 A new study from G2P-Japan🇯🇵, led by Keiya @Keiya717, is out at @biorxivpreprint. We assessed the humoral immunity induced by JN.1 mRNA vaccines against a broad range of SARS-CoV-2 variants including JN.1, KP.3.1.1 & XEC. Please repost🔥 1/ biorxiv.org/content/10.110…
In this study, we used 2 mRNA vaccines, one is from Pfizer/BioNTech🇺🇸🇩🇪, while another is from Daiichi-Sankyo🇯🇵. The good news is that there are no significant differences between them and both broadly neutralized a variety of SARS-CoV-2 including JN.1, KP.3.1.1 and XEC. 2/
But there are two scientific interests.
First, compared to our recent study using JN.1 and KP.3.3 breakthrough (i.e. natural) infection sera, antiviral humoral immunity against KP.3 and XEC was weakly induced. However, JN.1 mNRA vaccine can. Why🤔?? 3/
BREAKING🔔 A new study from G2P-Japan🇯🇵, led by Yu in my lab, is out at bioRxiv @biorxivpreprint. We elucidated the virological characteristics of SARS-CoV-2 #XEC. Please repost🔥 1/ biorxiv.org/content/10.110…
Compared with KP.3, #XEC harbors two spike substitutions, S:T22N and S:F59S. Recombination analysis by Shusuke @KawakuboShusuke showed that XEC is a recombinant lineage of KS.1.1 (JN.13.1.1.1) and KP.3.3 (JN.1.11.1.3.3) with a breakpoint at genomic position 21,738–22,599. 2/
Transmissibility/fitness (Re):
Molecular phylogenetic-epidemic dynamics modeling led by Jumpei @jampei2 and Kaho showed that the Re of #XEC is greater than that of KP.3.1.1, the most predominant variant in the world. 3/
BREAKING🔔 Here I want to quickly report our new results from G2P-Japan🇯🇵 before the preprint publication. We have elucidated the virological characteristics of SARS-CoV-2 KP.3.1.1 - a progeny of JN.1. Please RT🔥 1/
Cf.1 A new one, KP.2 (JN.1.11.1.2), has been already elucidated. 2/