Covid 2.0 doesn't even have spike proteins and is mutating in the population

[Snowball]

Here's what most people will be getting now or very soon:


- Covid-19 vax, or Bivalent Vax


AND


- Influenza Vax

Now, here's the danger or the "plan" with taking Covid to the next level. Moving past the spike protein mutations to cellular mutation itself.

The spike-protein dependent vaccine approach has taught the virus to mutate internally, instead of in its periphery spike proteins, as it has not been surviving long enough with its spike proteins no longer defending it. In order to live longer in the host, it is combining and mutating not on the periphery but rather inside the envelope.

This means spike-protein based vaccinations won't protect anyone. They will merely infect you with harmful spike proteins and misdirect your immune system.

The distributed covid variants will combine their inside-DNA with a strain of Influenza and/or other diseases that, without spike proteins, willl not trigger antibodies fast enough, and will spread through the host readily, especially in the vaccinated who have trained their immune systems to be hyper-defensive about spike proteins... it is exactly that reaction that is driving a new mutation that has potential to be worse than Covid-19.


Yet Another Curveball in the COVID Mutation Nightmare
https://news.yahoo.com/yet-another-curveball-covid-mutation-084446293.html

 

[Snowball]

Who woulda thunk it ?

Oh, wait..

9/28/21: Human coronavirus replicates in bats without using the spike protein

Researchers in Singapore have conducted a study showing active replication of a human coronavirus in bats that occurred without the viral spike protein binding to host cell receptors.

One key interaction required for coronaviruses to enter host cells is the binding of the viral spike protein to host receptors such as angiotensin-converting enzyme 2 (ACE2) in the cases of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) or aminopeptidase N in the case of HCoV-229E.

Now, researchers from Duke-NUS Medical School and the Bioinformatics Institute have reported extensive mutations in the genome of HCoV-229E viruses that resulted in the loss of spike protein expression, without any loss in the ability to infect bat cells.

https://www.news-medical.net/news/2...-in-bats-without-using-the-spike-protein.aspx

 

[Snowball]

Evidently, whether by full mutation or by covert introduction into the host population (as tested on bats), the Covid is starting to mutate completely, rather than merely modifying its spike proteins. This is bad news for all, vaccinated or not, it doesn't matter. Why? The IS of the vaccinated is sensitised to mount a quick defense against the spikes and it is by those spikes that Covid is identifiable to the IS. Without the spikes at all, Covid can shade itself against the IS. The IS of the unvaccinated, 95%+ of whom have already been naturally vaccinated to Covid, via infection (symptomatic or unsymptomatic), and/or shedding of the vaccinated, are also looking for spike proteins to ward off again. So, their IS have been faked too. An integrally-mutated Covid, without spikes, is mutated inside the envelope. This internal base is called the capsid. The capsid is where the DNA of the Covid virion mass is housed. Covid is already a hybrid of a coronavirus type and other virions, some studies suggest HIV, influenza. That is how Covid leaped ito humans BUT it is more apparent Covid did not naturally cross the species boundary, it was engineered with other human coronavirus virions. In the same manner, but slower, Covid can mutate with other viruses in host or in the ecosphere to cause new symptoms if it is able to infect new individuals, especially if it establishes initial cross-species infection and those infections spread into the human population like swine flu, bird flu, zika, etc.

Only those who have been infected with live Covid - not merely by exposure to shedding dead spike proteins, and not merely by most vaccination types (there are exceptions in the larger world, but almost all Americans vaccinated were vaccinated with spike-proteins, not whole, de-activated virus) - have the stronger chance of immuity response because it will be Covid in some ways... although that might not work either, and eventually this ability to detect the Covid in the capsid will also be mutated against. If that happens, it will be a new pathogen. Here is an example of this, from just a couple weeks ago: (link)
https://www.msn.com/en-us/health/me...ovid-19-identified-in-russian-bat/ar-AA12afxe

Notice in the link, that this Khosta-2 / sarbecovirus obtained cross-species infection in areas where the U.S. black ops had biowarfare laboratories. The sarbecovirus/Khosta-2 would be a new pandemic from base one. Perhaps it was designed to infect Russians like Covid was designed to infect Chinese. It is suggested, because the Khosta-2 is a human and animal coronavirus that was somehow mixed with animal sarbecovirus. Perhaps that was done in the Ukrainian biolabs.

As Covid morphs its structural layers to find ways to attach to human cells without the spikes, and tests spike structures that experience longevity in the host, the hosts will have longer infections. Much longer. These longer infections are not mere symptomatic stresses. They turn your body into a living petri dish that allows the mutating Covid to exchange RNA and perhaps intra-capsid DNA with other viruses AND also into bacterias in the intestinal tract resulting in bacterial and viral infections, and viral loads being carried by bacteria, and by parasites if any are present. Making this even more dangerous, the fraudulent scientists are putting synthetic mRNA into edible plants and in livestock, and in insects that cross the blood-barrier. They have plans far beyond Covid-19 spike proteins in this manufactured mRNA. If they place it into our food chain it will enhance and expedite cross-species transmissibility of viral pathogens, and possess other advantages such as increasing the load counts in a host and getting into the stomach and intestinal tract.