Full vaccination suppresses SARS-CoV-2 delta variant mutation frequency
medrxiv.org
medrxiv.org
We recommend that: 1) universal vaccination should be administered as soon as possible to suppress the generation of virulent mutations;
Wait, I’m being punked.. right?
How is universal vaccination the solution, if it is literally the cause of the more contagious strain?
The logic is a bit circular, no?
Yeah the paper is littered with these kinds of gaps in reasoning, see my other comment for a more detailed critique.
>The OP alleges it can't sufficiently mutate among the vaccinated, so their recommendation of full vaccination to eliminate the virus is perfectly consistent.
From the study:
"We conclude that the virus becomes more contagious as it is screened through the vaccinated population and the resultant strain becomes the dominant strain and able to infect the entire population."
The main takeaway from the paper is that the vaccinated are driving new variants.
>Opening up and letting everyone get delta, vaccinated or not, is going to happen sooner and is not good because passing through the unvaccinated will cause many new mutations some of which might start new waves.
Again, the paper states the vaccinated are driving new mutations. Technically due to natural immunity, the unvaccinated who have been previously infected are now in a better position than the vaccinated. They don't contract, get sick or spread whereas the vaccinated do. The big exception is unvaccinated who have never been infected by this coronavirus or any other past coronavirus. They are still susceptible to infection, spread, etc.
Filtering is the takeaway, one dominant strain and orders of magnitude less variations since most variation is not viable in a vaccinated public.
If we have a highly variable virus that never goes away. That is the flu.
Covid transmits in animals. CDC says based on current data, transmission to human is low (but not impossible) but more studies are needed. The fact they can get it is already not on the same scale as smallpox or polio.
https://www.cdc.gov/coronavirus/2019-ncov/daily-life-coping/...
You’re attempting to tie these mutations to only the unvaccinated. They likely shed mutations as well but that’s not what this paper highlights.
Not only can the vaccinated spread the virus but they’re likely making it more pathogenic in the process. See here:
https://journals.plos.org/plosbiology/article/info:doi/10.13...
This is a relatively low quality paper that presents very tenuous supporting evidence of it's claims & conclusions.
There is no randomization, placebo-control, or blinding - nor any serious consideration or analysis of confounding factors such as natural immunity, comorbidities, and other demographic biases. Evidence that doesn't fit their hypothesis (eg Australia) is dismissed with barely a hand wave. The P-values & correlation coefficients are borderline statistically insignificant, the citations are comically sparse, and the conclusions lack a critical & balanced evaluation with respect to the existing literature.
We shall see if the paper passes any legitimate peer review - I'd bet against it.
Quoting from OP:
> we first analyzed the correlation between the rates of full vaccination and the point mutation frequency (Mf) of COVID-19 delta variants’ genome in 20 countries
> Complete SARS-CoV-2 genome sequences with high coverage from June 20 to July 3 2021 in 20 countries were collected from the Global Initiative on Sharing All Influenza Data (GISAID)
> We found that Mf was logarithmically reduced as the full vaccination rate increased in 16 of the 20 countries (R2=0.878, Figure 1A)
> With 10.8% vaccinated rate, Mf was exceptionally low in Australia, likely as a result of the national lockdown restrictions.
> In contrast, Mf is higher in Japan, Switzerland, and United States, suggesting that their mitigation strategies have been less successful
> We chronologically analyzed SARS-CoV-2 delta variant sequences in the UK (N=27,344), India (N=4,451) and Australia (N=305) from 13 February to 3 July 2021, respectively in the GISAID
> Genome alignments and analysis using the Tajima D test, a neutrality statistic widely used in population genetics, were carried out
> The Tajima D test (D’) compares pairwise nucleotide diversity (π, the average number of nucleotide differences per site between two sequences) and total polymorphism to infer selection and demographic events
> We observed that π was significantly lower in the UK (π< 1.5 × 10−4) than others which emerged after April 24, 2021 (π> 2.0 × 10−4; p<0.01)
> we recommend that: 1) universal vaccination should be administered as soon as possible to suppress the generation of deadly mutations
I’m sorry to say, but its not ever going be eradicated, especially with vaccines that don’t stop you getting the virus, or transmitting it.
Very interesting. My thesis for the new highly contagious variants is they are from the vaccinated because of the virus's escape mechanism. And on cue here we have a mention of the phenomenon in a medical study.
Oh well, postponing all judgement until it's peer reviewed. And while we're at it, how about study on head to head vaccinated vs unvaccinated mutation frequency.
Hopefully you're aware that viruses accumulate mutations randomly by chance over time. The only way mutations can be outright stopped is through an immune response that completely neutralizes the SARS-CoV-2 virus. Determining if mutations originated in a vaccinated or unvaccinated host is a pretty useless endeavor that would only serve as fodder for divisive discussion. The fact is that mutations are expected to exist in high numbers due to neutral genetic variation alone.
With that said, worrying about viral evolution undermining the efficacy of the vaccine is a valid concern.
In general a leaky vaccine is one that keeps the host alive without necessarily stopping further infection and transmission. These conditions contribute to an environment that can allow the virus to accumulate mutations which eventually lead to immune escape [1][2].
Because the current mRNA vaccines are leaky and also induce an immune response highly targeted toward the spike protein RBD, there is concern that mass vaccination may create tremendous selective pressure which further enhances the fitness of the virus [3]. It's difficult to predict if such selective pressure will lead to enhanced virulence or infectiousness, but so far many variants of concern have mutations impacting the spike protein RBD. These mutations result in partial immune escape and manifest as increased infectiousness, reduced vaccine efficiency, and also reduced immunity in naturally infected individuals [4][5][6].
[1] The adaptive evolution of virulence: a review of theoretical predictions and empirical tests https://pubmed.ncbi.nlm.nih.gov/26302775/
[2] Why does drug resistance readily evolve but vaccine resistance does not? https://royalsocietypublishing.org/doi/pdf/10.1098/rspb.2016...
[3] Risk of rapid evolutionary escape from biomedical interventions targeting SARS-CoV-2 spike protein https://pubmed.ncbi.nlm.nih.gov/33909660/
[4] SARS-CoV-2 immune evasion by the B.1.427/B.1.429 variant of concern https://science.sciencemag.org/content/early/2021/06/30/scie...
[5] mRNA vaccine-elicited antibodies to SARS-CoV-2 and circulating variants https://www.nature.com/articles/s41586-021-03324-6
[6] Reduced sensitivity of SARS-CoV-2 variant Delta to antibody neutralization https://www.nature.com/articles/s41586-021-03777-9
If vaccinated people also keep wearing masks and social distancing, dangerous mutations should be much less likely.
Selection among these mutations will occur. The virus with the pre-vaccine, spike protein will be largely blocked from replicating, and mutations which have spike proteins that better enable infection will be selected for. Welcome to evolution ;)
That doesn't smell right. It's also a pre-print without peer review yet.