Category: E. coli

BREAKING: Anthrax Is The COVID-19 “Vaccine Antigen” And It’s Aerosolized!
Posted on by Ariyana Love

By Dr. Ariyana Love

Covid-19 is a biological and technological weapon system using self-replicating, programmable nanotechnology with synthetic modRNA poisons. We are told that a vaccine antigen is used in the Covid-19 technology to “evoke an immune response” because that’s medical science. But what if the Covid-19 vaccine antigen is ANTHRAX?

“…hardly any natural pathogens are really well suited to being biowarfare agents from a military point of view. Such a bioweapon must fulfill a variety of demands: it needs to be produced in large amounts, it must act fast, it must be environmentally robust, and the disease must be treatable… only a minority of natural pathogens are suitable for military purposes. “Anthrax is of course the first choice because the causative agent, B. anthracis, fulfills nearly all of these specifications.”

The first Anthrax was a biological weapon developed by Russia in 1950. According to the NIH, the USSR’s ‘invisible anthrax’ was created by introducing an “alien gene“ into the highly toxic Bacillus Anthracis bacteria. This means that advanced technologies such as Cross-Species-Genomics capability was acquired by the government before 1950 when a lethal bacteria and an alien gene were genetically altered and blended together to produce the deadly bioweapon known as Anthrax.

Russia’s Anthrax could be treated with antibiotics even several days after exposure and thus it met the requirements under the Biological Weapons Convention. Being the bioweapon of choice, NIH funded Anthony Fauci increased Anthrax’s lethality. Russia’s Anthrax was genetically attenuated by the NIH before 2006. Through GAIN-and-LOSS-of-Function the NIH produced a more drastic and deadly Anthrax that’s resistant to antibiotics and more.

According to a University of Minnesota publication, the United States D.O.D smuggled shipments of live B anthracis spores from the Army’s Dugway Proving Ground in Utah, to other labs in the United States and abroad (Source: USA Today). The U.S. Army sent shipments of live samples of Anthrax to 86 labs outside the U.S. over a period of 10 years (Source: The Daily Beast).

Transfers of samples of live B anthracis and the H5N1 influenza bioweapon were sent from CDC labs to other labs. CDC correspondence released under the Freedom of Information Act shows that labs studying bioterror pathogens “have failed over and over to comply with important safety and security regulations.”

The D.O.D. tried to cover for the CDC, claiming “system failure” was to blame for the lab leaks but we already know that the D.O.D spearheaded this “Covid-19 vaccine” Democide.

Please see: Aerosolized inoculation of Anthrax – Aerosolized Intratracheal Inoculation of Recombinant Protective Antigen (rPA) Vaccine Provides

In 2007, Anthony Fauci created the H7N9 bioweapon, otherwise known as the “influenza vaccine.” The NIH, CCP and the Israeli state collaborated through GAIN-and-LOSS-of-Function to produce the H7N9 “flu vaccine” and the new and improved “Aerosolized Anthrax Vaccine”. Both have just been administered to the world population through inoculations, PCR swabs and aerosolization and self-replication.

Ofir Israeli from the Israel Institute of Biological Research, sequenced the Bacillus anthracis V770-NP1-R Strain in 2014 creating a synthetic chemical bioweapon. The Israeli state oversaw the animal trials for the Anthrax “vaccine” and told us it was safe and effective. Meanwhile, the Israeli company called Sanofi Pasteur developed the first H7N9 “vaccine” and trialed it for the NIH, also in 2014. Also in 2014, the NIH developed the H7N9 “influenza vaccine” to be droplet transmissible. Simultaneously in 2014, China achieved a 99% transmissibility of the H7N9 “flu vaccine”. China also trialed the first aerosolized intratracheal Anthrax “vaccine” on mice. The study admits to severe side effects.

PLEASE SEE: NIH Using DEAD CORPSES To Make “Virus”; Gain Of Function Weaponized Dead Corpses

The Israeli state, NIH and China turned their new and improved Anthrax bioweapon into an attenuated antigen to be used in “vaccines” under the guise of “evoking an immune response” and “vaccine immunity.” The nations have been intentionally poisoned with biowarfare.

In March of 2022, the Russian military discovered that the Covid-19 bioweapons are being developed in U.S. biolabs in Ukraine. This includes the plague, Ebola, Filoviruses’, Anthrax and more.

Ebola is used in the J&J and Sinovax jabs while Filovirus is used in Moderna. Ebola and Marburg are both Anthrax. The H7N9 is used in all “flu vaccines” while Anthrax is being used as a “vaccine adjuvant” in all Covid-19 jabs and swabs!

Here’s how they did it. Through Loss-Of-Function, genetic deletions were performed inside the B. anthracis bacteria to improve replication of the bacteria in vivo. This ensured hospital protocols would not work to stop it from replicating inside the human body due to it being antibiotic resistant.

The B. anthracis bacteria was also genetically modified to survive in insect hosts so as not to sporulate before it’s injected into the human host by a Bill Gates GMO mosquitoes which is part of DARPA’s weaponized insect project called The Sentinels.

Incidentally, the CDC owns the Anthrax isolate patent that was funded by the U.S. Government. This is treason. The CDC also says that a bioterrorist attack would most likely be Anthrax.

Please see: Malaria Parasites In “Vaccines” Target Placenta, Kill Babies In Utero

SPIKE PROTEIN IS AEROSOLIZED ANTHRAX!

There’s 232 B. anthracis genomes that are currently available in the GenBank database. There’s an Anthrax “vaccine” for cattle and two strains are licensed for use in humans. There exist two patents for an “Aerosolized Anthrax Vaccine.”

The first Anthrax “vaccine” patent for humans is partly owned by the U.S. Government. The second is a “Recombinant Anthrax Vaccine“.

“The spores of the toxigenic, nonencapsulated B. anthracis STI-1 strain and the cell-free PA-based “vaccines” consisting of aluminum hydroxide-adsorbed supernatant material from cultures of the toxigenic, nonencapsulated B. anthracis strain V770-NPI-R or alum-precipitated culture filtrate from the Sterne strain. Each of these Anthrax toxins are being used for “cellular entry in humans“. The LF is a metalloprotease recently shown to cleave the amino termini of the mitogen-activated protein kinase kinases 1 and 2, which results in their inactivation.”

In layman’s terms, the poisonous Anthrax “antigen” is being used in the genetic modification of the human genome and it’s literally being encoded into the genome, after knockouts (deletions) of the genome.

The molecular basis of Anthrax “vaccines” contains “spores and DNA plasmids.“ This is a targeted weapon system. The following quote about the Anthrax “protective antigen” is particularly revealing:

“PA (protective antigen) is the common receptor binding domain of the toxins and can interact with the two different effector domains, EF and LF, to mediate their entry into target cells (14).”

Anthrax is being used to “regulate gene expression by binding to DNA sequences and modulating transcriptional activity through their effector domains”. Pharma has essentially found a way to encode any synthetic proteins into the human genome from any species they want.

Luciferase is insect DNA and that’s going into the genome. The “Aerosolized Anthrax Antigen” is being encoded into target cells to make those cells produce the chemical drug called Anthrax. This is how the Anthrax “vaccine” is aerosolized. Once a person is inoculated with the Covid-19 bioweapon through subcutaneous injection or nasopharyngeal delivery (aerosolization), the weapon system will begin genetic deletions and encoding the genome of target cells with the Anthrax spike protein. A person begins producing the toxic spike protein and shedding Anthrax into the air, exposing everyone to Inhalation Anthrax. It’s a weapon system that is intentionally aerosolized.

This study admits that the Anthrax spores from B. anthracis STI-1 strain and B. anthracis strain V770-NPI-R used in the “aerosolized Anthrax vaccines” are toxigenic. The Sterne strain which is used to inoculate our food supply (animals) is also genotoxic.

This NIH study explains how a “replicon” of the Bacillus anthracis bacteria was cloned into an Escherichia coli (E. coli) “vector” using cross-species-genomics. These two bacteria were synthetically fused together to enhance lethality.

ALHYDROGEL

The hydrogel technology was developed over many years during a collaboration between DARPA and Profusa, a private biotech company specializing in the development of tissue-integrated biosensors. In 2018, DARPA published a video revealing their intention to use this biosensing technology for both military and public health.

According to the “aerosolized Anthrax vaccine” patents, the so-called “vaccine adjuvant” used is Alhydrogel. The Alhydrogel is infused with 750 μg of aluminum, making it magnetic. In the Alhydrogel invention, Anthrax was fused together into this nanogel called Alhydrogel, consisting of fibrous nanoparticles (Nanofibers) that are “antigen specific to CD4+ T cells”.

Again in layman’s terms, the nanorobots are intentionally programmed to target and alter the genome of CD4-T cells, inducing cell death. This essential part of our immune system (T-cells) stop foreign invaders from entering our cells. Destroying our T-cells enables the government’s operating system to take root in the body and quicken death.

Nanofibers are used for self-assembly and electrospinning, for tissue engineering and delivery of drugs and chemicals into the brain. Being magnetic and nanotech based, the Alhydrogel can replicate everywhere in the body and wire a new neural network, which is what I believe some eugenicists were trying to achieve.

Astonishingly, Alhydrogel is already the most widely used vaccine adjuvant! There’s many Alhydrogel patents that contain toxic cocktails that will overwhelm anyone’s immune system.

This Alhydrogel patent demonstrates its use of the B anthracis bacteria, E. coli, N. gonorrhoeae, Chlamydia, Staphylococcus, TB and more. It also contains the H5N1 influenza bioweapon, RNA, DNA synthesis and Polysorbate 80 for Blood Brain Barrier (BBB) permeability.

It begs the question, where do venereal diseases come from? But I digress.

This Nature article reveals that 2% Alhydrogel is used in all Covid-19 “vaccines”. Previously, aluminum salts were the only adjuvants licensed for vaccine use in humans in the U.S. In recent decades however, nanoparticle adjuvants in hydrated gels were introduced. The article continues by saying that the “influenza vaccine” was the first to use Alhydrogel.

“Aluminum salt-based adjuvants such as alhydrogel have been a mainstay of vaccines for decades” boasts Christopher B. Fox and colleagues at the Infectious Disease Research Institute in Seattle, USA.

So, both nanoparticles and Anthrax have been used in vaccines for decades already, without Informed Consent of the public.

Alhydrogel was improved and transformed into the Nanoalum adjuvant.

Here, we introduce a top-down manufacturing process—high-pressure microfluidization—to generate aluminum oxyhydroxide nanoparticles, hereupon referred to as nanoalum, using the clinically approved Alhydrogel adjuvant as the precursor.

The “Aerosolized Anthrax Vaccines” also contain SEQ ID NO: 1 which is owned by the Pirbright Institute (Bill & Melinda Gates). SEQ ID NO: 1 contains the world’s most deadly genetically modified parasites.

Please see: MEGA BOMBS! GMO Parasites Are The mRNA Vector!

ANTHRAX SYMPTOMS AND TREATMENT

Anthrax has been deployed on the population by three methods; injection, inhalation and skin penetration. The mortality rate for Anthrax varies depending on the method of exposure. It’s approximately 20% fatality for cutaneous Anthrax and 25–75% for Gastrointestinal Anthrax. Inhalation Anthrax is by far the worst with a fatality rate that is 80% or higher. Inhalation Anthrax is what we’re all being exposed to from the Covid-19 jabs and swabs which contain delayed release technology that contains a military weapon system.

Antibiotics constitute the mainstay of treatment against Anthrax, despite the fact that they won’t work to stop its replication due to the NIH, China and Israel’s GAIN-and-LOSS-of-Function enhancements.

Pharmaceutical experimental genotoxic drugs such as Oblitoxaximab and Raxibacumab are being touted as Anthrax treatments but these are monoclonal antibodies. We know from the monoclonal antibody patents that they’re also the “mRNA vaccine” weapon system. Anytime you inject recombinant proteins or modRNA into humans it’s EXTREMELY TOXIC.

Please read: Monoclonal Antibodies Is mRNA Gene Knockdown Tech, Encoding HIV – Patent Review

They also say the only known effective “prevention” against Anthrax is the Anthrax “vaccine”. However, the Anthrax “vaccine” inoculation given to U.S. military troops was a complete disaster. U.S. Army statistics that were never published show the Anthrax “vaccine” induces cancers.

The toxicological harms of Anthrax are many. It causes severe heart issues. Could this be a contributing factor to Myocarditis? Anthrax also coagulates the blood. Read more here and here.

“Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.”

Anthrax also causes a person to hemorrhage. So this explains all the excessive bleeding people experience after Covid-19 injections and from aerosolized exposure. In other words, shedding by transmission. Inhalation Anthrax.

Mice “treated” with anthrax lethal toxin (LT) exhibit hemorrhage and liver damage. Monocyte procoagulant responses to anthrax peptidoglycan are reinforced by https://pmc.ncbi.nlm.nih.gov/articles/PMC3124019/proinflammatory cytokine signaling and histological lesions in the spleen.

Anthrax has been tested on the public already. During 9/11 Anthrax spores were intentionally released into “some environments” in NYC, according to the NIH. The FBI launched an investigation called “Amerithrax”. It was “one of the largest and most complex (investigation) in the history of law enforcement”, according to the FBI.

Heroine users in Europe have been tested on with Injection Anthrax.

Our skies are sprayed with smart dust and chemicals daily. Our governments have launched all out war against their constituents. We are being poisoned in a myriad of ways so please keep this in mind:

“Anthrax is easy to produce in large quantities, highly lethal, relatively easy to develop as a weapon, easily spread over a large area, easily stored and dangerous for a long time. Given appropriate weather and wind conditions, 50 kilograms of aerosolised anthrax spores released from an aircraft along a 2 kilometer line could create a lethal cloud of anthrax spores that would extend beyond 20 kilometers downwind. The aerosol cloud would be colorless, odorless and invisible following its release. Given the small size of the spores, people indoors would receive the same amount of exposure as on the street. There are currently no atmospheric warning systems to detect an aerosol cloud of anthrax spores. The first sign of a bioterrorist attack would most likely be patients presenting with symptoms of inhalation anthrax. A 1970 analysis by Whole Health Organization concluded that the release of aerosolized anthrax upwind to a population of 5,000,000 could lead to an estimated 250,000 casualties, of whom as many as 100,000 could be expected to die. A later analysis, by the Office of Technology Assessment of the U.S. Congress estimated that 130,000 to 3 million deaths could occur following the release of 100 kilograms of aerosolized anthrax over Washington D.C., making such an attack as lethal as a hydrogen bomb.”

TREATMENT

If you have been inoculated with Covid-19, or PCR swabbed and you are suffering from heart pain and other severe symptoms, it could be Injection Anthrax. If you are “unvaccinated” and hemorrhaging from being around “vaccinated” then you may have been exposed to Inhalation Anthrax.

Many doctors, including myself, have documented persistent bleeding rectally, violent bleeding vaginally, nasally and in the eyes. If you have been exposed to Inhalation Anthrax, you will feel hot and very flushed, similar and you may break out in big, red splotches on your skin, followed by a completely red eye in the morning.

Although they don’t get much attention, “anti-toxins have long been considered an essential ‘adjunctive’ therapy, and remain so”, according to the NIH. Anti-toxins are the natural medicines that detox poisons. In other words, you need a good doctor with complete protocols.

I have been successfully detoxing people from the Covid-19 bioweapons for two years. I have a complete protocol for Anthrax poisoning. If you would like to schedule a consultation with me, please do so through my online booking system.

If you would like to donate to my research, please do so here.

Posted on by Ariyana Love

By Dr. Ariyana Love

In my latest interview with Stew Peter’s, we discussed how the “Covid-19 vaccine” ingredients listed in the patents, reveal that all these poisonous death shots are deleting genes and genetically modifying Humans for patentability.

GRAPHENE

The Hydrogel patent US8415325B2 is listed in the Moderna patent, here. Hydrogels are also mentioned in a second Moderna patent, here. Hydrogel is listed in the Johnson & Johnson patent, here. Hydrogels are made from Graphene Oxide. Nobody can deny the evidence that Graphene Oxide is in the shots.

GMO HUMANS

All the Covid-19 “vaccine” patents mention gene deletion. All the patents except one, mention “complimentary DNA” (cDNA). cDNA is a chimeric mRNA cocktail that’s being coded into Human cells using artificial genetic sequences in cross-species genomics.

According to the US Supreme Court ruling in 2013, altering Humans with cDNA makes them patent eligible. The court documents show that cDNA is made using modified bacterium and Supreme Court judges ruled it patent eligible. This means that a plant, animal or Human, could be patented and owned if first genetically modified with cDNA.

Mark Steele summarized it perfectly by stating:

In the US, the Supreme Court has ruled that vaccinated people worldwide are products, patented goods, according to US law, no longer human. Through a modified DNA or RNA vaccination, the mRNA vaccination, the person ceases to be human and becomes the OWNER of the holder of the modified GEN vaccination patent, because they have their own genome and are no longer “human” (without natural people), but “trans-human”, so a category that does not exist in Human Rights. The quality of a natural person and all related rights are lost. This applies worldwide and patents are subject to US law.

Since 2013, all people vaccinated with GM-modified mRNAs are legally trans-human and legally identified as trans-human and do not enjoy any human or other rights of a state, and this applies worldwide, because GEN-POINT technology patents are under US jurisdiction and law, where they were registered.”

BACTERIUM, NOT “VIRUSES”

The court document says scientists added 4 plasmids to a bacterium. I already documented in my article entitled, “EPIGENETICS: Vaccines Are deleting Human Genes & Transfecting Cells With Ebola/Marburg,” that E. coli is the base for all these chimeric bioweapons, not viruses.

I found E. coli listed in most of the patents. Mind you, these are genetically enhanced, antibiotic resistant bacterium, made to be them more lethal. They are then transfected into GMO parasites and Hydras. These parasites are more difficult to kill but they can be killed using specific natural protocols.

You can eliminate the entire species with CRISPR-Cas-9 technology or completely remove genetic traits in the Human race. 

FAUCI FUNDED BIOWEAPONS

I previously wrote about the Fauci-funded chimeric bioweapon called the Lentivirus mRNA vector in my article entitled, ” Transgenic Hydras & Parasites A Biological Weapons System For Rapid Human Cloning.” The Lentivirus bioweapon was developed in Wuhan and contains the HIV 1-3, SARS, MERS and the AIDS inducing SRV-1. It can be found in the Moderna, Pfizer, J&J, AstraZeneca and Oxford patents.

The HIV-1 Bioweapon, which contained within the Lentivirus vector, is patented and owned by Anthony Fauci. He is a mass murdering war criminal responsible for this “Vaccine” Holocaust.

PATENT HIGHLIGHTS

The Pfizer patent mentions gene 69-70 deletion and mutation.

Thermo Fischer produced a study revealing that gene deletion mutations is the cause of “vaccine” induced variants. This company is not only profiting from this “Vaccine” Holocaust but Thermo Fischer has a scientific report clearly stating that gene deletion is responsible for the Lambda, Alpha, Beta, Gamma, and Delta variants.

SV-40 vector is a chimeric Bioweapon found in the J&J patent. It’s known to cause rapid cancer growth. The SV-40 vector is provided to J&J by Thermo Fischer. SV-40 contains Human cells, Bovine Growth Hormone (Mad Cow Disease), E. coli, and Herpes. This would explain the Herpes outbreaks after “vaccination”.

The Pfizer patent also mentions gene 144 deletion which causes rapid cancer growth.

I also found a patent for a “Combo kit PCR” that mentions gene deletion! So the PCR is not a test at all but implants the mRNA technology without Informed Consent, into your brain.

The Pfizer patent mentions X / Y Chromosome inversions. Inversion of sex genes cause sterility. Since this is a depopulation/extermination and cloning agenda, the transgender Psyop begins to make sense. They want to sterilize our kids and cross-sex hormones will achieve that.

The Moderna patent mentions folding protein and mutations (thus variants) that result in rapid aging and genetic diseases. The patent literally says this is a “Loss-of-Function” and thus, a gene deleting Bioweapon. 

Moderna’s patents are listed on their website, here. 

The Moderna patent says it’s using the Bovine Growth Hormone which comes from a cow disease known as Mad Cow Disease. Moderna is cloning Humans with a cow disease that becomes deadly when coded into Human cells. This is an animal disease that does NOT even affect Humans so why is Big Pharma transfecting Human cells with Bovine Growth Hormone when it’s known to induce neurological degeneration, dementia and death?

Here’s a PCR kit patent that “tests” Humans for Mad Cow Disease. Or, does it actually transfect Humans with Mad Cow Disease using the Hydrogels?

The Moderna patents makes “add and delete” references to RNA using cDNA templates. It also has starts codons or Open Reading Frame (ORF. These are no stop codons which means there’s no stop to the gene mutations. The variants will continue on indefinitely, passing through the Human race just as Geert Vanden Bosche said would happen.

Without stop codons, an organism is unable to produce specific proteins. The new polypeptide (protein) chain will just grow and grow until the cell bursts or there are no more available amino acids to add to it.

Moderna’s patent also mentions “induce triple helix formation”. This is the third strand that’s being synthetically added to Human DNA. This study shows more about how scientists are creating the triple helix formation in Humans. Here’s another study revealing the artificial triple helix.

The Moderna “Protocol” says one in two of their shots is a Saline. So that’s a 50-50% Russian Roulette chance with your life and your health. The patent also states that Moderna is “encoding HIV-1“. Once again, that’s Fauci’s bioweapon.

The AstraZeneca patent states an E1, E3, E4 gene deletion. As I documented earlier, these gene deletions induce AIDS, unless you get the Saline. Later the pharmaceutical cartel will be removing all Saline shots.

The Novovax patent mentions gene deletion.

The GlaxoSmithKline patent mentions gene deletion and says it uses H1N1, which is the same chimeric bacteria that was used to kill 500 million people in the 1918 Democide, dubbed the “Spanish Flu”, as this study reveals.

“The trimerization domain (foldon) of T4 phage fibritin, a trimeric beta hairpin propeller, was first used in crystallization studies of the 1918 H1N1.”

Bill Gates said to expect a Smallpox Bioweapon terror attack. Smallpox is made from the N1H1 chimeric bacterium proteins. I documented that previously.

The patents back up what Dr. Pablo Campra’s said in his Stew Peter’s interview, that these death jabs contain Nano-biosensors. I’ll be revealing more about this from the patents very soon!

Conclusion

This is not a weapons system of one country against another. This is a weapons system of the NWO against the entire Human population. The only way this ends is when we stand together as one.

Here’s the World Freedom Alliance Notice of Liability. Any regular citizen can serve anyone with a notice of war crimes, if they are mandating or coercing you to take this poisonous shot which is in violation of your basic Human Rights and Nuremberg Codes. Since this is an international case, the Notice of Liability is served in English, country-wide. 

See original interview with Stew Peters and Dr. Ariyana Love on Rumble, here.

PLEASE SEE: Dr. Ariyana Love: Graphene Covid Kill Shots, Let The Evidence Speak For Itself

Follow Red Voice Media, here.

Follow Stew Peters Show, here.

Posted on by Ariyana Love

By Dr. Ariyana Love

(Updated Nov. 23, 2021)

Stockholm University just released a scientific horror. The “spike” protein in the Covid-19 “vaccines” are penetrating the cells of the vaccinated, reaching the cell nuclei, and impairing your cell’s ability to repair damaged DNA.

Pharmaceutical “vaccines” are silencing the genes responsible for DNA repair and deleting them forever in humans.

I joined Stew Peter’s Show once again, to break this shocking discovery on Red Voice Media.

Johnson & Johnson uses Adenovirus 26 (Ad26) in its vaxxine. J&J openly admits that their Ad26 vector “codes your cells to produce a spike protein” but they don’t tell you they’re also deleting your genes.

The U.S. patent #20140017278 for Adenovirus 26 and 35 Filovirus, openly states that it codes your cells with the Ebola and Marburg chimeric proteins.

“The filovirus antigenic protein is usually a glycoprotein from an Ebola virus or a Marburg virus.”

The J&J Adenovirus 26 vector deletes your E1 gene. The patent also states that it deletes the E1 gene in Humans. This is known as the X Chromosome. The E1 gene is required for accurate and instant repair of damaged DNA. Deletion of this gene is lethal.

E1 gene deletion causes embryonic lethality which means permanent sterility for men and women. It causes Lactic Acidosis in children which is the lack of oxygen in the blood. E1 gene deletion causes rapid cancer growth, Thrombosis, and the coagulation of the blood which leads to clotting. Blood clotting is the main reason people are dying from the Covid vaxxines.

E1 gene deletion causes Mitochondrial DNA-Associated Syndrome which is a process of glucose metabolism deficiency that exists in various diseases such as Alzheimer’s, epilepsy, diabetes-associated cognitive decline, and severe neurological disorders such as Leigh’s Syndrome. There’s a progressive loss of mental cognition and typically results in death within two or three years, usually due to respiratory failure.

Without your E1 gene, your cells will literally self-suicide.

U.S. patent #10695417 is the Human Adenovirus 5 vector that contains E1 and E2B gene deletions. The Adenovirus 5 vector is used in Sinovax and it encodes the cells with Ebola Glycoprotein. Glycoprotein-41 andglycoprotein-120 are HIV viral coat Proteins and Glycoprotein plays a key role in reproduction.

Sinovac is used in China, Chile, Brazil, Turkey, and the Philippines.

The Adenovirus 5 vector was developed through Gain-of-Function research.

Knocking out the E2B gene caused sterilization in male mice.

You can order the chimeric messenger RNA of the Lentivirus and the Adenovirus 5 vectors or Baculoviridae online from Thermo Fischer, for recombinant cross-species genomics (cloning).

Thermo Fischer explains how the Adenovirus 5 targets and enters the bronchial epithelial cells (lungs) and deletes the E3 and E4 genes, intentionally inducing Sjögren’ssyndrome which is long-term autoimmunity (AIDS).

Loss of your E4 gene deletes your cognitive function. Deletion of your E3 gene degenerates your brain, causes dementia, gradual loss of memory, judgment, and the overall ability to function.

Here’s a study describing how you knockout the E3 gene.

The knockout of these genes affects the moisture-producing glands of your body. It’s not the “spike protein” that’s causing the blood of the vaxxed to coagulate, it’s the gene silencing (deletion). Without moisture, your blood coagulates and clots. The deletion of these genes also causes gastrointestinal disorders.

Adenovirus 5 also alters the cell signaling pathways and leads to Lymphoma due to destruction to the immune system. This causes cancers to grow and the blood to coagulate.

This is proof positive they’re creating the next “pandemic” with lethal injections that will gradually induce AIDS in the inoculated masses through gene deletion.

The pharmaceutical cartel has not only injected Ebola and Marburg into people but they’re also transfecting people’s cells with these catastrophic chimeric pathogens. The vaxxed will battle chronic infections and lifelong disabilities while the cells of the vaxxed continuously replicate with the synthetic genetic sequences of Ebola and Marburg until it kills them unless they detoxify continuously.

The immune system of the vaxxed is depreciating 5% each week according to a recent UK Government study. Everyone who vaxxed age 30 and above, will have no immunity left by Christmas. But that’s not all.

As the cells of the vaxxed replicate Ebola and Marburg “spike proteins” and their cells decay and die, they will shed the chimeric disease throughout the population via transmission. Therefore it’s crucial for the unvaxxed to continuously detoxify as well.

According to a UK government declaration from the NIH, we are presently in a Phase III clinical trial on Humans using the Adenovirus 5 vector to “fight Covid-19” which began on January 22, 2021.

“This is a global phase III clinical trial to evaluate efficacy, safety, immuogenicity of Ad5-nCoV manufactured by Cansino and Beijing Institute of Biotechnology in health adults aged 18 years old and above.”

So the UK Government is partners with the Chinese Communist Party (CCP) to exterminate Humans.

The World Health Organization (WHO) also published on their website that we are in an Ebola Vaccine Stage III Clinical Trial.

WHO published that we are in an Ebola Vaccine Stage III Clinical Trial

Later the WHO scrubbed it from their website.

Viruses are still an unproven theory. Given the advances in scientific lab equipment and considering that we’re able to observe nanotechnology under microscopy and spectroscopy, would somebody please explain to me why we still can’t identify a virus? Could Germ Theory be the big pharmacopeia lie in modern medicine and Terrain Theory be the more relevant truth?

Governments enhanced the airborne transmissibility in mammals (Humans) of highly virulent avian influenza strains. The history of making pathogens transmissible goes back at least to the synthesis of viable influenza H1N1 from 1918. Incidentally, the 2009 swine flu Pandemic was also induced by inoculation using the H1N1 vaxxine. So this is nothing new under the sun.

Sinister shadow governments have been weaponizing nature, producing diseases through vaxxine injection and genetically manipulating Humans for at least the past 100 years. But where did they get this technology to do it?

The U.S. National Library of Medicine revealed something rather interesting. The USSR’s ‘invisible anthrax’ is a Gain-of-Function bioweapon created by introducing an “alien gene“ into Bacillus anthracis (bacteria). That’s how they made Anthrax. They used an alien gene and genetically altered bacterial immunological properties to produce a deadly pathogen to Humans. Where did they get an alien gene from? A UFO crash perhaps? Negotiations with other beings? Your guess is as good as mine.

The U.S. Government has been testing this germ warfare technology on its own military troops since the 1950s, using Adenovirus 4, Ad5, and Ad7 vectors with HIV encoding Envelope (clade C.1086). The Ad7 vector delivered in enteric capsules has been used to “vaccinate” U.S. military personnel “against respiratory and gastrointestinal illness”, since the 1970s.

Monkeypox is also made from the same bacterial pathogens as Ebola and Marburg. Ebola and Marburg can kill nine out of ten people it infects. Although this is not really an infection, it’s transfection (human cloning).

Ebola and Marburg cause hemorrhagic fevers (VHF). They simultaneously affect multiple organ systems in the body and may be accompanied by hemorrhage, or bleeding. These pathogens cause high fever, chills, muscle aches, and vomiting. The patients worsen rapidly until they bleed from every orifice in their body, including needle puncture wounds. They usually die within 1-3 days.

Bill and Melinda Gates say on their Gavi website to expect the next pandemic to be a Marburg outbreak. These two psychics or psychos also claim that Ebola and Marburg are carried by African Green Monkeys.

The lying CDC claims that people can get “Ebola Virus disease” through direct contact with an infected animal (bat or nonhuman primate). They’re taking the absolute piss out of us! Never in the history of medicine has an animal disease infected Humans! The only possible way to make a Human diseased with an animal disease is through cross-species genomics using Adenvirus or mRNA and Nanotechnology.

Polio vaccines used in the late 1950s and early 1960s were intentionally contaminated with a bacterial pathogen called the “Simian Virus” 40 (SV40) present in monkey kidney cells. The Simian Virus is used for infecting Humans. It was “accidentally administered to Humans” through Polio vaxxines.

The “Vaccinia virus” is similar to the “smallpox virus” but it’s not naturally occurring after all. Scientific Direct reported that “vaccinee-to-cattle and cattle-to-human Transmissions occurred on Farms”, proving the transmission of pathogens between animal to human species is being done by genetic engineering and administered through vaxxines.

Knocking out the E1 and E3 genes is necessary when transfecting cross-species in order to make the pathogen replicate. The Vaccinia pathogen has been used on a wide scale to produce many different kinds of chimeric proteins, including HIV-1 and it encodes approximately 250 genes.

Ebola and Marburg are GAIN-and-Loss-of-Function bioweapons and both are created using the “Green Monkey disease“, a chimeric pathogen that you can purchase online!

Adenovirus’ are from human/monkey clone origin and are used with chimeric Lentiviruses, as well as the Filoviruses. Of course, none of these are actual viruses! All the Adenoviruses and messenger RNA (mRNA) are chimeric weapons used to code your cells to reproduce deadly proteins used to both silence genes and program artificial genetic sequences. They are inducing diseases and making up disease names and syndromes to hide the fact that it’s coming from vaxxines!

Ebola, Marburg, and Monkeypox are Gain-of-Function bioweapons created using the “Green Monkey disease”. It’s an Adenovirus made from E. coli bacteria from the decaying flesh of a human/monkey hybrid’s kidney tissue culture. Adenovirus vectors transfect Humans with monkey DNA, Ebola, and HIV. Adenovirus vectors are transfecting humans with monkey DNA and Human DNA from a Chimpanzee/Human clone to be exact.

There are 49 immunologically distinct types of adenovirus that can cause infection for long-term gene expression. They’re made with Sialic acid which is a group of derivatives of Neuraminic Acid found in animal tissues. Sialic acid is the primary entry receptor used in Adenovirus.

Sialic Acid is an animal DNA from “Species D” Adenovirus which is used in both Adenovirus 5 and Adenovirus 26 (Sinovac and J&J) to transfect Ebola and HIV into Human cells using Sialic acid-bearing glycans (animal DNA) as a primary cell entry receptor. Adenovirus 5 is of “Chimpanzee origin”. There’s that Green Monkey clone again!

Sialic acid proliferates tumor growth and metastases. N-acetylneuraminic acid (Neu5Ac) is made from E. coli bacteria. See the study’s here and here.

Polio vaxxines used in the late 1950s and early 1960s were “contaminated with a virus” or rather a bacterial pathogen called the Simian Virus 40 (SV40) which is present in monkey kidney cells used to grow the vaxxine.

The Pharma death cult is inducing diseases with their vaxxine racket and making up names and syndromes that they can then profit from by “treating” later when people become diseased. What would life be like without the Pharma cartel disabling our children and killing healthy people in the name of science and medicine?

There are no viruses involved in the making of any of the mRNA or Adenovirus vaxxines, only GAIN-and Loss-of-Function chimeric pathogens made from bacteria and other plasmids which Pharma keeps naming “viruses”.

There’s no “spike” from a virus particle being used in any of these vaxxine induced diseases. We should change our language from “spike protein” which is a half-truth with a half-lie and replace it with “chimeric protein” to be medically accurate because that’s what we’re dealing with.

E. coli bacteria are used as the base for all these chimeric diseases because bacteria DNA replicates. They’re also using other plasmids and mixing fungus, yeasts, and “several mammal-based systems” (Human/Chimpanzee clone), then genetically enhancing them to increase lethality.

They’re also using baculovirus-mediated insect cell expression. This means the Pharma cult is transfecting human cells with insect DNA. This could explain the strange mutations and Morgellons.

Marburg is simply Ebola with Ricin added to make it more lethal. Both cause hemorrhagic fevers (VHF) and attack multiple organ systems in the body, accompanied by bleeding.

The Pharma death cartel and the Eugenicists already have a PCR kit for “testing” for Marburg disease and a vaxxine to immunize against, called RiVax. The main component of RiVax is “a genetically altered version of a Ricin Toxin.” Ricin is more toxic than Graphene Oxide, by the way.

I think it’s high time people stop trusting our governments, stop relying on government and take our children out of public schools, as Dr. Zev Zelenko said to Alex Jones on Info Wars. Don’t sacrifice your kids to Satan.

My detox protocol works for the vaxxed and the unvaxxed to kill the Micro-plasmids (parasites, transgenic Hydra’s and bacteria) and reverse the coagulation cascade which leads to blood clots.

PLEASE SEE: DR. LOVE’S DETOX PROTOCOL

For consultations or if you have questions please don’t hesitate to reach out to me: metanutrients@mailfence.com

Posted on by Ariyana Love

By Dr. Ariyana Love

The transhumanist dystopian nightmare we find ourselves in is taking a new turn with the shocking discovery of Hydra Vulgaris and PARASITES in the so-called Covid-19 “vaccines”.

Dr. Carrie Madej revealed her Hydra findings on the Stew Peter’s Show on September 29th, 2021, followed by Dr. Zandre Botha’s stunning discovery of microscopic, self-assembling medical devices in the blood of her vaxxed patients. The red blood cells are dangerously deformed and coagulated, things she says she’s never seen before in her 15 years as a blood doctor.

Hydra Vulgaris identified in Pfizer & Moderna Covid-19 serums

About 10 days later, “That Thing” (Hydra Vulgaris) was also identified in Pfizer vials by Dr. Franc Zalewski. He took the science to a new level and did a chemical analysis of the Hydra, exposing that the chemical compound of the creature contains Aluminum, Carbon, and Bromium. This means the Hydra’s are being genetically modified before they’re injected into humans. The good doctor also identified parasites in the vials.

Dr. Jane Ruby, a pharmaceutical researcher, gave vital commentary on Stew Peter’s Show about Dr. Zalewski’s findings, emphasizing that the dormant Hydra “eggs” become active, grow and multiply when exposed to Graphite tape and heat.

Earlier in August, parasites and other horrors were identified by Dr. Robert Young in four Covid-19 vials. Dr. Jane Ruby again joined Stew Peters to give crucial commentary on Dr. Young’s findings.

Investigative Journalist Ramola D. provided us with further information about the parasites discovered by Dr. Young and did an expose in October.

Back in July, La Quinta Columna studied four “vaccines”; Pfizer, Moderna, AstraZeneca, and Johnson & Johnson, and found toxic nano metallic particulates, particularly nanographene oxide, in significant amounts, as well as lipid nanoparticles and the parasite Trypanosoma cruzii, in the Pfizer-BioNTech serum.

Pfizer whistleblower Karen Kingston appeared on Stew Peter’s Show in July and walked us through a presentation on how Graphene Oxide is in all Covid-19 serums. Graphene Oxide was not listed in the patent filings and was deliberately concealed under a trade secrete because it’s known to be poisonous to humans.

As a result of these horrifying discoveries, I did my own research on Graphene Oxide Nanoparticles and Toxicity and wrote an article entitled “Graphene Oxide The Vector For Covid-19 Democide“. I reveal how humanity is being saturated with Graphene Oxide Nanoparticles in a myriad of ways.

I also wrote an article on protocols for detoxifying Graphene Oxide from your body, here.

The openly declared ingredients in Covid-19 serums should be enough to dissuade anybody from taking them. Now it’s clear there are additional poisonous and other horrors not being disclosed to the public by the Biotech pharma industry.

Karen Kingston has backed up all these terrifying discoveries with the patent filings and receipts, on Stew Peter’s Show. Kingston explains that the vaxxines are a “gateway to an obedience platform and potentially an execution platform if you are not obedient to your score”.

Informed Consent has been waived and therefore people didn’t know they’re being injected with smart devices and bioweapons. The patents also reveal that it was already known by Pfizer that the vaxxed would become “super spreaders” and transmit deadly pathogens to healthy individuals.

There’s an AI component to these vaxxines Kingston explains, “they’re committed to replacing the American people with Artificial Intelligence”. She continues disclosing that “Hong Kong is ready to replace the American people with robots right now”.

Due to the fact that patent filings do not reveal the components to Biotech’s vaxxine ingredients, I began researching scientific peer-reviewed studies involving Hydra Vulgaris and parasites to see if I could identify why they’re being injected into humans.

GAIN-OF-FUNCTION

Everything I’m writing here is based on evidence from open-source, peer-reviewed literature of scientific breakthroughs and technological developments that extend through the past decades and are linked in this article. As sci-fi thrilling as this information may sound, the technology has already been deployed and is being injected into the veins of our children as we speak. You can read the studies for yourself, as I have done.

DNA hybridization began in 1980 with Nadrian C. Seeman who started constructing self-assembled nanostructures. Hydra Vulgaris transgenesis technology was developed over the last 30 years. This is the process of transferring genes and organisms from one species to another which creates a new cloned species.

The Human Genome Project began in the year 2,000. Hydra’s are used in the human genome assembly for gene silencing of humans. Messenger RNA (mRNA), SPIONS (Super Paramagnetic Iron Oxide Nanoparticles), DNA coated lipid-nanoparticles containing drugs and chemicals, transgenic Hydra’s and parasites are all part of an “operating system” which is bypassing the human immune system. You can read more about Moderna’s “operating system” from their own website, here.

Graphene Oxide sheets are used to slice open the membrane of your cells so that programmable Nanorobots can reach the cell nuclei to turn off undesired genes (gene silencing) and code artificial gene sequences. This process is called biohacking.

Graphene Oxide sheets are able to slice open every cell membrane of the human body within 15 minutes after inoculation, according to Dr. Robert Martin.

DARPA partly funded the development of protein-to-genomic sequence alignments for cross-species genomics. Gain-Of-Function and Loss-Of-Function studies using transgenic Hydra were funded by Fauci and the NIH and developed at the Wuhan Institute in China and in universities in the U.S. and China. Their scientific findings were published in 2013.

The Sixth International Workshop on DNA Nanotechnology was held August 26–28, in 2017, in Beijing, China where the forum showcased the applications of self-assembled DNA nanostructures.

CHIMERIC SPIKE PROTEIN

The “spike protein” in the Covid-19 vaxxines that everyone is talking about is called a Lentivirus. The Lentivirus contains a combination of HIV types 1-3, SRV-1/AIDS, MERS, and SARS. These are the most deadly Gain-Of-Function bioweapons ever developed, thanks to mass-murdering Fauci.

A Stanford study reveals that the Lentivirus is a “genus of retroviruses that cause chronic and deadly diseases characterized by long incubation periods, in humans”. It enables long-term transgene expression. The best-known Lentivirus is the human immunodeficiency pathogen, which causes AIDS. This is why we’re seeing an autoimmune and neurodegenerative decline after Covid-19 inoculation. This is an induced condition known as PRION.

The mRNA from the Lentivirus chimeric cocktail is inserted into the DNA of human cells through an invasive procedure that permanently changes the genome of that cell. Once inside the host cell’s cytoplasm, lipid-coated nanobots take the reverse transcriptase enzyme in the Lentivirus to produce DNA from the mRNA genome, the reverse of the usual pattern, thus retro.

HYDRA 2.0 GENOME ASSEMBLY

Hydra’s are used in cross-species genomics. They’re being genetically modified in a lab at the University of Kiel to produce transgenic clonal Hydra lines. Since 2006, thousands of embryos have been microinjected and nearly 200 transgenic lines have been established in the Hydra Transgenic Facility.

Morphogenesis and stem-cell control using the Hydras were developed to learn the neurobiological functions of humans and for in vivo tracing of cells. Transgenic Hydra allows in vivo tracking of individual stem cells during morphogenesis (tissue and cell growth).

Transgenic Hydra lines are generated by embryo microinjection with plasmid DNA from self-replicating DNA found in bacteria. This is a permanent transmissible change of genetic material (DNA) resulting in the decreased production of a protein. The merging of the two species is a “cloning” process called transfection. A new generation of transgenic Hydra polyps continues reproducing the chimeric genetic expression in their offspring.

These GMO Hydra polyps are now genetically coded vectors, carrying a variety of programmed synthetic genomic sequences and mRNA (messenger RNA) for the purpose of transfecting humans. Once inside the human body, these transgenic Hydra polyps serve to rewire and control the ancestral circuitry of human beings.

BLAST Sequence technology is being used to create new DNA sequences and find similar genetic sequences between species, performing alignment functions for same-species and cross-species genetic splicing for the purpose of transcription.

Proteins regulate gene expression. This technology targets the cell organelles of the nuclei which store genetic information; mitochondria, which produce chemical energy; and ribosomes, which assemble proteins, using mRNA to make mitochondrial sequences.

A 2017 Gain-Of-Function research project from Germany, demonstrates how RNA extraction and quantitative reverse transcription-polymerase chain reaction or reverse genetics is used to knockout and knockdown genes using Hydra’s and CRISPR/Cas9.

The genetically modified Hydra lines in the Covid-19 operating system is first coded with chimeric gene sequences (Lentivirus) which is then being coded into human cells using CRISPR-Cas9 technology and electroporation.

Electrodes attached to gold programmable nanorobots transfect human cells, silencing your innate God-given genetic sequences and coding your cells to reproduce the synthetic genetic sequence of the chimeric spike protein (Lentivirus), indefinitely. More simply stated, your cells will continue to replicate themselves over and over again with the new genetic sequence of the chimeric pathogen you were injected with. The same chimeric pathogen was funded by bioterrorist Anthony Fauci and developed in Wuhan, China.

One of the deadly bacteria being chimerically enhanced to transfect Hydra’s for implantation into humans is E. coli, which causes about 36% of the infections in humans.

PARASITES

Parasites are also transfected with bacteria and used as transfection vectors for DNA binding and genetic sequencing in humans. Parasites can evade drugs, escape the immune system and regulate genes.

The human Malaria Genome Project developed at Stanford University, used CRISPR technology and bacterial plasmids which can replicate rapidly inside parasites. They transfected bacterial plasmids into parasites, disrupting a series of gene encoding molecules. In that study, scientists transfected Malaria parasites with Luciferase to use it for gene targeting and transgene expression in humans.

T. gondiiandP. falciparum and other parasites were also used in transfection studies. It’s important to be aware that from the P. falciparum they designed a Chloroquine-resistant transgenic parasite strain called Dd2.

LUCIFERASE

Hydra polyps are also being coded with the overexpressed chimeric protein called Luciferase, which is a Green Florescent Protein derived from the firefly. Transgenic Hydra also carries the Luciferase RNA trigger to code your cells with and silence genes in human cells.

Holstein lab investigated the repressing activity of HySp5 on the HyWnt3 promoter, performing Luciferase reporter assays in human HEK293T cells for DNA-binding and transplanting Hydra into humans by invading human tissues.

The transgenic Hydra and parasites replicate and merge with humans during transfection. They are integrated with the transgenes (Luciferase and Lentivirus) into one of the epithelial cell lineages and assimilated into the human host. The transplanting of Hydra’s into humans is called Homoplastic transplantation using induced Hydranth as “implants”.

Epithelial cells are stem cell lineages responsible for cell signaling. Transgenic Hydra’s reporter genes are cell-signaling with each other inside humans, much like neurons in a neural network. Transgenic Hydra’s cell signaling becomes synthesized with human cell signaling in a process called catenin signaling, which is induced by mutations of genes in humans through upregulation (cell response) to the plasmids expressing activators in the Hydra (HySp5–2992:Luc); aka transfection.

Transgenic Hydra and parasites induce humans to generate a new electrochemical signal by organizing enzymes spatially to create a programmable redox enzymatic cascade pathway, changing the predictable generation of electrochemical signals in humans. The newly established synthetic gene sequences are now shared between the transgenic Hydra’s, parasites, and newly hybridized humans.

In fact, Biotech’s chimeric operating system establishes a new neural network in humans and an artificial brain by re-directing endogenous neural stem cells. Brain implants can erase memories and implant new, artificial memories while Graphene Oxide can “hear your brain whisper”.

A team of scientists from UC Davis and Rice University was boasting back in July about manipulating the nervous system of Hydra Vulgaris and humans to “build a new brain from the bottom up”, in order to control neural pathways and human behavior. This technology was developed over the last decade through the Human Brain Project.

The European Union’s 1.5 billion euro Graphene Flagship project developed graphene-based implants for “future brain-computer interfaces”. I have to wonder if the “implants” they’re referring to contain transgenic Hydra’s?

Graphene implants can record electrical activity in the brain at extremely low frequencies and over large areas, “unlocking the wealth of information found below 0.1 Hz”.

A Russian initiative called 2045 wants to use neural interfaces for an “improvement of man himself” because mankind is “standing at the edge of a total loss of the conceptual guidelines necessary for further evolution”. This demonstrates the anti-human mindset of eugenicists who want to clone the entire human race.

The fluorescent (Luciferase) Hydra’s were also tested with externally applied electrical fields to see how much voltage they could endure, to “facilitate the future use of electric fields as an experimental means to redistribute intracellular constituents in developing tissues”. I presume this was to test Hydra’s ability to survive 5G frequency?

THE OPERATING SYSTEM

Hydra’s and parasites also serve as a reporter system. Luciferase exhibits bright green fluorescence when exposed to light in the blue to the ultraviolet range, enabling the vaxxed to be traced externally. Genes of interest can be turned off occasionally or turned on at will by your patent holders through what’s called transregulation.

This means you’re not only externally traced 24/7 but you’ll also be externally controlled. Your patent holders will be able to upregulate and downregulate your genetic codes through an external database, through the Eukaryotic Genome Annotation Pipeline for transgenic humans.

Did you think the Starlink satellite network’s “Precision Tracking Space System” had something to do with defense? Don’t worry, you’ll be “happy” owning nothing so long as they get your dopamine levels worked out.

ADDGene is selling a variety of CRISPR parasites to be used as gene vectors for human transfection. These are not “vaccines” at all but a WEAPONS SYSTEM (my words) for the RAPID CLONING (their words) of humans, through gene knockout (silencing), artificial gene sequencing (coding) and to monitor transfectants inside of humans (tracing).

ProSplign is a worldwide protein-to-genome alignment tool enabling Human DNA to be easily synthesized from a single-stranded RNA template and catalyzed by an enzyme for reverse transcriptase.

ADDGene also offers a Lentiviral Envelope and Packaging Plasmids for transfecting humans using transgenic Hydra. They offer “Non-overlapping NEURAL NETWORKS” (their words) using Hydra Vulgaris for building a new neural network in Hydra’s. This technology is being deployed in humans through the Coivd-19 Quackccine program now.

Dr. Carrie Madej also disclosed in her latest interview on Stew Peter’s Show that the vaxxine operating system is building an artificial neural network in humans.

ADDGene offers a Tetracycline off system for on/off gene expression, “fusing tetR with the C-terminal domain of VP16 (virion protein 16), an essential transcriptional activation domain from HSV (herpes simplex virus) which is being used for “reduced gene expression” in humans. This uses the chimeric E. coli bacteria and Lentivirus.

The Hydra genome assembly offers a Nano DNA kit called Illumina. Illumina Inc figured out how to reduce the cost ofsequencingahuman genomedown from $1 million to $1,000 USD, back in 2007.

After Luciferase is infused and coded for targeted genes via a computer, it’s then mapped onto the Human through the public Galaxy server to perform “differential expression analysis”. Proteins can be targeted, upregulated, and downregulated.

Then there’s Vector Biolabs whose selling Adenovirus’ for human sp5 shRNA silencing. A Knockout vector system (adenovirus) for knocking down the expression of particular genes (gene silencing), is being marketed online and sold by Vector Builder. You can create artificial genome sequences and merge genomes of different species.

You can preorder DNA sequences for humans on HydraAtlas website.

The Genome Data Viewer (GDV) will help you select genome assemblies (DNA sequences) for humans from primarily finished human clones, that were sequenced as part of the Human Genome Project.

VIGENE offers multiple shRNA cloning options for your gene silencing experiments. They’re packaging transfer Plasmids, Adenovirus’ (AAV) and Lentivirus’ and they guarantee at least a 70% knockdown of your gene of interest. They have a catalog of over 27,000 shRNA plasmid sets targeting the human genome.

This table lists common Lentiviral envelope and packaging plasmids that can be used with 2nd and 3rd generation lentivirus technologies.

ADDGene’s lentiviral genome is delivered to a target cell upon infection using CRISPR gRNA. They explain how the Lentiviral genome encodes genetic material that the “researcher” (or patent holders and Big Pharma) wants to be delivered to specific target cells. The genome is encoded by plasmids called “transfer plasmids,” which can be modified to encode a wide range of gene products.

ADDGene admits their DNA-targeting enzymes very often will delete, insert or otherwise alter the targeted RNA or DNA, so don’t let the fake media fool you.

Lentiviral Plasmids can be ordered through ADDGene here.

BEHAVIOR CONTROL

Vector Biolabs offers an Adenovirus (AAV) expressing shRNA for the knockout (gene silencing) of Human SP5. When developing this technology during the animal trials, social recognition, spatial learning, and memory were impaired after 4 weeks.

In an animal study using reverse transcriptase-polymerase chain reaction (RT-PCR) with an Adenovirus vector and drugs, scientists were able to induce Huntington’s Disease by targeting the Corpus striatum of the brain which resulted in 100 fold neurodegeneration and motor behavioral impairment.

REPRODUCTION & FERTILITY

The transgenic Hydra’s are used to induce gene silencing predominantly targeting embryonic cells in the testes of men and the ovaries of women and also nerve cells. This is why we’re seeing neurological degeneration (PRION) after inoculation. It also explains why 82% of expectant mothers who take the “jab” are having spontaneous abortions.

Microinjection of foreign DNA into the pro-nucleus of single-cell embryos of fertilized mice to control the genetic expression of future generations has been perfected, since 2008.

Proteins control gene expression. Transgenic Hydra is instrumental in encoding the human SP5 (shRNA silencing AAV) which is a gene on chromosome 2q31.1 that encodes a protein that binds to the GC-box promoter elements, thought to play a role in coordinating the intricate changes in transcription which occur in the developing embryo.

Wnt-3 is a protein that in humans is encoded by the WNT3 gene. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis.

The point I’m making here is that the operating system is DNA-binding, downregulation, and upregulating genes using the transgenic Hydra’s, targeting human embryos and embryonic cells, leading to developmental alterations from binding genes to the Wnt/β-catenin signaling pathway.

Do you understand what this means? It’s not only the vaxxed who are being genetically modified, cloned, and hybridized, but SO ARE THEIR OFFSPRING! That is of course if you’re still able to reproduce at all after the jab! Most people will just be sterilized and their babies aborted. This is a human cloning experiment as well as extermination.

Microinjection of Retrovirus transgenes (Lentivirus & Luciferase) integrates randomly into the genome which poses enormous risks for the vaxxed as well as their hybrid offspring. This can create strange and unpredictable mutations of DNA by the addition of one or more base pairs. This is precisely why we’re seeing freaky mutations and why doctors are removing blood clots with Hydra-like tentacles from teenagers!

Dr. Carrie Madej shares an image of a blood clot with Hydra-like mutational growth that was removed from the heart of an early teen who received a Covid vaxx.

If you still aren’t convinced, please listen to Dr. Peter McCullough explain this biotechnology and how the chimeric spike proteins are being coded into human cells, at the 78th Annual Meeting of Association of American Physicians and Surgeons, on October 2, 2021.

“It is a deadly protein” explains Dr. McCullough. “It is the first time in medicine that we are injecting vaccines and asking the human body to make a potentially lethal protein” .

While the Covid-19 serums appear on the surface to be only a clear liquid, under microscopy you can visibly see all the many components of the computer-interface operating system, which is a sophisticated biological weapons system for the cloning and extermination of the human race.

https://www.youtube.com/watch?v=s8e06KfDWMM

FINAL NOTE

If you would like more information on detox protocols and disrupting the blood coagulation cascade which leads to blood clots from the jab or for protocols that will protect you from the adverse effects of transmission, please contact me directly at: metanutrients@mailfence.com