With the XEC variant on the way to dominance in most places, and XEC waves starting to show in COVID metrics, it is time to ponder which variant will drive the next wave after XEC.
Here are the leading contenders: LP.8.1, MC.10.2, MV.1, and XEC.4.
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They are shown above using a log scale, so you can compare their growth rates vs OG XEC.
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LP.8.1 is descended from FLiRT KP.1.1.3. LP.8 adds the Spike:Q493E mutation (featured in FLuQE) and also H445R and F186L – a potent example of convergent evolution. Then LP.8.1 adds R190S.
LP.8.1 has had some success in Taiwan, Japan, Singapore and lately in the US.
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Globally, LP.8.1 is showing a growth advantage of 6% per day (42% per week) vs XEC, so any crossover looks like happening in December.
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MC.10.2 is descended from DeFLuQE KP.3.1.1, so boosts the resistance of the dominant DeFLuQE clan. MC.10.2 adds the Spike I101T and A376D mutations.
MC.10.2 has had some success in NZ and Ontario, Canada.
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Before you say “oh Ontario huh, just like XEM”, please note that there was a wide geographic distribution before it took hold there.
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Globally, MC.10.2 is showing a striking growth advantage of 11.1% per day (78% per week) vs XEC, which predicts a crossover in late November.
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MV.1 is descended from JN.1.49.1 via MB.1.1.1. MV.1 adds the Spike:K478T mutation.
Singapore is at around 50% frequency, and it seems quite prevalent in Mauritius. It is also growing strongly in Australia and the US.
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Globally, MV.1 is showing an accelerating growth advantage of 3.5% per day (25% per week) vs XEC, so any crossover looks like December or later.
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XEC.4 adds the Spike T572I mutation.
XEC.4 has been most successful in New Zealand and Australia, and is also growing strongly in Sweden, the UK and Canada.
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Globally, XEC.4 is showing an accelerating growth advantage of 4.9% per day (34% per week) vs XEC, so any crossover looks like December or later.
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So in summary, the most obvious contenders to challenge XEC at this point are MV.1, LP.8.1 and MC.10.2. I will continue to back MV.1, with it's high growth rate and it's success in undersampled regions.
I will continue to monitor the other contenders.
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The usual caveats apply - recent sample sizes are smaller which might skew these results, and “global” sequencing data is dominated by wealthy countries, with many under-sampled regions.
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Interactive genomic sequencing dataviz, code, acknowledgements and more info here:
A recent scientific paper compared long-term mortality by vaccination status.
I noticed that Table 2 drew a lot of attention, but was actually included in the paper as a static image. So I built a quick dataviz project to explore.
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On the first page, I've added a % Incidence change (vaccinated vs unvaccinated) and emphasised that with data bars. This is quicker for general readers to grasp than hazard ratios.
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You can click on any column header to sort the rows, e.g. as shown by % Incidence change. The starkest difference was deaths from COVID-19 at +372%.
Other causes with significant differences were diseases of the skin & blood, pregnancy and childbirth.
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A recent scientific paper included an antigenic map, comparing the immune status of individuals vaccinated with a range of vaccines "… vaccinated sera", against a collection of significant variants "Virus …".
The map was very informative, so I built a quick dataviz project.
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The map shows starkly that BA.3.2 "Cicada" is a wild outlier, way out on its own in the south-west corner. This suggests the current vaccines and/or disease-acquired immunity will not offer strong protection against infection.
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Another point of note is how the XFG "Stratus" variant is the furthest away from BA.3.2, at the extreme south, compared to other recent variants.
This might help explain how BA.3.2 has been able to drive significant waves in Europe, following their recent waves of XFG
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Here's the latest variant picture for Europe (excluding the UK), to late November.
BA.3.2.* "Cicada" is showing a very strong growth advantage of 7.9% per day (55% per week) over XFG.* "Stratus", which predicts a crossover in late December.
#COVID19 #EUR #BA_3_2 #Cicada #XFG
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To include the latest BA.3.2.* samples, I have rolled my reporting window forward an extra week or so. So the most recent data is even less representative than usual. The picture for those dates might change as more data is shared.
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Here are the leading European countries reporting BA.3.2.* .
The Netherlands leapfrogged Germany to report the highest frequency at 31%. Germany also grew sharply to 25%. Denmark grew to 16%.
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Here's the latest variant picture for the United Kingdom, to late November.
For the UK, BA.3.2.* "Cicada" is showing a strong growth advantage of 5% per day (35% per week) over XFG.* "Stratus", which predicts an imminent crossover.
#COVID19 #SARSCoV2 #UK #BA_3_2 #Cicada
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To include the latest BA.3.2.* samples, I have rolled my reporting window forward an extra week. So the most recent data is even less representative than usual. The picture for those dates might change as more data is shared.
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BA.3.2.* accelerated sharply in Scotland to 16% of recent samples.
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A recent scientific paper explored the impact of mass SARS-CoV-2 infections on Lymphocytes (crucial to the body’s immune system).
I noticed the authors had shared the data behind their charts in the Appendix Supplementary materials, so I built a quick dataviz project.
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Above, I’ve re-cast the data behind their Figures 3 and 5 in terms of % change from the baseline. Hopefully this is useful to help compare the subsets, whose results vary in scale.
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I added interactive filter controls and a trend line (dashed pink). You can use those to explore for example the trends in the last 12 months measured in the paper, for the CD3, 4 & 8 series.
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It became clear during November that a unusual second wave is underway in Australia, driven by the new "clade K" (H3N2 clade 2a.3a.1, subclade K).
Tasmania, New South Wales and South Australia are currently the hardest-hit.
#Influenza #Australia
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Western Australia had been spared the worst of this second wave until the last week or so. But now there’s a signal of a sharp change in case momentum there also.
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The latest Australian Respiratory Surveillance Report confirms my earlier speculation that the new "clade K" (H3N2 clade 2a.3a.1, subclade K) is driving the "unusual" second wave of influenza in Australia.