Considering they have been finding evidence/genetic signature of the original strain from 2019, that is unlikely
It was a pretty hot topic a year ago and I remember an article a while ago, who came up with pretty good reasons why it's not likely a bioweapon leak.
Primarily, bioweapons are usually developed with an antidote or some other preventative protection ... unless the group wants global depopulation as the target
Even if they didn't develop an antidote, it should be designed that an antidote could not be developed easily.
There are dozens of vaccines developed using every technique known to mitigate the spread
They already had an antidote. Dr. Todd Rider's DRACO, a.k.a. Double-stranded RNA-Activated Caspase Oligomerizer, developed at MIT with DARPA funding, tested successfully
in vivo on mice in the US, and also further tested
in vitro on pig cells in China.
Currently there are relatively few antiviral therapeutics, and most which do exist are highly pathogen-specific or have other disadvantages. We have developed a new broad-spectrum antiviral approach, dubbed Double-stranded RNA (dsRNA) Activated Caspase Oligomerizer (DRACO) that selectively...
journals.plos.org
Porcine reproductive and respiratory syndrome virus (PRRSV) continues to cause substantial economic losses to the pig industry worldwide. Current vaccination strategies and antiviral drugs against PRRSV are still inadequate. Therefore, there is an urgent need for new antiviral strategies to...
pubmed.ncbi.nlm.nih.gov
DRACO was big in popsci mags in the US back around ten years ago, and then suddenly, all the funding for the research dried up. Dr. Rider's grant money ran out, even though the one single published paper showed very promising results, and he resorted to E-begging for crowdfunding.
DRACO is a fusion protein that, in its most typical formulation, consists of Protein Kinase R bound end-to-end with Apoptotic Activating Factor 1 in a configuration not found in nature. It's cultured by inserting the gene into a culture of living cells, like E. Coli bacteria or spirulina or whatever, and then growing tons of it in a bioreactor, collecting the protein, and then purifying it. Basically, it could be made the same exact way as recombinant insulin.
The way DRACO defeats viruses is actually rather simple. PKR is a protein that, in nature, hunts down and binds to viral dsRNA. Pretty much all major viruses (including coronaviruses) make long strands of double-stranded RNA as part of their replication process. Therefore, the presence of viral dsRNA in a cell is basically proof positive that it's been infected by something. There is no other way for dsRNA to end up in there.
DRACO proteins have HIV TAT, a cell-penetrating peptide, that let them slip right in past the membrane of a cell. Once inside, if there's no dsRNA, they do absolutely nothing, so they're non-toxic to uninfected cells.
If there is some dsRNA in there, they do something completely different. They start binding to the dsRNA one after another. Then, the cell's own procaspases start binding to the exposed APAF-1 ends of the DRACOs, initiating the end-phase of apoptosis, or programmed cell death.
Viruses have ways of "zombifying" cells, suppressing death signals and forcing cells to work on replicating virus particles until they fall apart. Viruses never evolved a defense against this. There is no protein in nature that goes "If viral dsRNA is present in this cell, commit sudoku
immediately!"
DRACO is so effective, it basically functions like a universal vaccine. If you inject a mouse with DRACO proteins, and then inject them with lethal quantities of influenza virus, nothing will happen. The mice will remain healthy, their cells basically unaffected. The DRACOs last for about a week before they're eliminated. The only real adverse effects occur if DRACOs are administered late, with a large population of cells already infected. In that case, you see a bit of extra inflammation from the cells that DRACO commands to immediately die and stop replicating viruses.
DARPA supposedly wanted an antivirus for soldiers that could stop
any pathogen. Even unidentified bioweapons. However, even though DRACO was shown to work in mice, development stopped right there. They never actually manufactured it or issued it to soldiers.
What do you wanna bet the Illuminati have an underground base somewhere with equipment to make large quantities of DRACO?
They already had the antidote. They've had it for ten years.
It acts too slow to be effective ... they would have experimented on both highly virulent "and" fast acting, from the get go.
The majority of people are asymptomatic, especially the fit and healthy, and they recover.
Even if you design in asymptomatic spread, it should eventually affect the carrier.
Not if the goal is to destroy an economy, rather than killing lots of people. COVID-19 is slow-acting, with symptoms appearing after 5 days and hyperinflammation setting in about 10 days post-exposure, with recovery usually around day 21. That is perfect for creating terror and isolation without killing large numbers of people.
It is targeting the wrong groups (old/morbidly ill people) ... you want to target fit and healthy
It is targeting the
right group. China is aging out. They have a massive demographic problem with lots and lots of old people hanging around too long.
By 2029, China's population will age into 'unstoppable' decline
time.com
In the West, governments have raided pension funds and basically just want old people to die before they retire and start cashing in.
News, analysis and comment from the Financial Times, the worldʼs leading global business publication
www.ft.com
There is a mutual goal, to eliminate the old, the infirm, the welfare recipients. "Undesirables" who are a drain on the system. Not the young and healthy. They were never the target.
After the end of the die-off, who is left? Fresh meat for the power elite.
