In a recent interview with Maria Zeee on Zeee Media, I discussed another very troubling discovery about the mRNA bioweapons technology. Maria Zeee asked me to shed more light on the Doherty Institutes involvement with the US biolabs in Ukraine.
Russian reports revealed that 350 cryocontainers with blood serum samples were transferred from the Public Health Centre of the Ministry of Health of Ukraine to a reference laboratory for infectious diseases at the Doherty Institute in Australia.
Under the guise of tackling Placental Malaria, the Doherty Institute has been directly involved in research using insects such as mosquitos and tics as bioweapons carriers. The Doherty Institute also developed a “vaccine” that uses a parasite to target the placenta of pregnant women to abort their babies in utero, under the pretext of “antibody research”.
During the testing of this novel technology, mosquitos were developed as carriers of a genetically attenuated parasite called the P. falciparum which is the most deadly of the 5 Malaria causing parasites. The World Health Organization (WHO) and the U.S. Government were also directly involved in this research to “immunize” via mosquito bite using radiation-attenuated Sporozoites.
The female Anopheles mosquito inject a minimum of Sporozoites (Spz) (~ 100) during its bite. It was tested on adolescents, children and infants aged 6 months old. 1 out of the 6 volunteers developed parasitaemia 12 days after exposure. Parasitaemia means parasites in the blood.
The parasite “vaccines” use radiation-attenuated Sporozoite, administered under drug coverage. Genetically-attenuated Sporozoite “vaccines” and recombinant protein “vaccines” (RTS,S and R21) and recombinant viral vectors “vaccines” (Chad63 MVA ME-TRAP, CSVAC, ChAd63 METRAP and MVA METRAP with the matrix-M adjuvant) are all used.
Sporozoite recombinant proteins, DNA or viral vectored protein fragments (mRNA) and attenuated Sporozoite “vaccines” induce malaria reactive CD4+ and CD8+ T-lymphocyte counts. Radiation-attenuated Sporozoite (RAS), genetically-attenuated parasite (GAP) and Sporozoite are administered under drug coverage, according to the WHO study. Here’s another WHO study from 2021.
By 2021, they had a P. falciparum Sporozoite (PfSPZ) “vaccine” as the main candidate containing live, radiation-attenuated, whole, aseptic and metabolically active Sporozoite which have been isolated from the salivary glands of mosquitos infected by P. falciparum. They tested their novel “vaccine” on infants in Kenya.
Another study conducted by the NIAID in 2022, used Malian children 6-10 years old and injected them with three doses of the PfSpz “vaccine” to induce an “infection” by “parasitic disease” of a “vector borne disease” using the P. falciparum.
Another study in 2021 carried out by the U.S. Government, experimented on 336 infants aged 5-12 months, in Kenya, inoculating them with the P. falciparum “vaccine”. This is not in fact a “vaccine” but a weapons system for the murder of babies in utero and this is a bioweapon which is transmissible to others, according to the WHO research.
In addition, the WHO’s P. falciparumresearch helped in the development of monoclonal antibodies. In fact, the P. falciparum parasite is a critical component in the monoclonal antibodies bioweapon system.
Children’s Health Defence reported in Augustthat the Covid-19 injections are dangerous for mothers and babies. According to former Chief Scientist of Pfizer, Dr. Mike Yeadon, the injected ingredients is building up in the ovaries and attacking the placenta of pregnant women.
A recent report released in March of this year, shows that fetal deaths due to “covid vaccines” are almost 2,000% greater than deaths associated with other vaccines.
“Viral vectors represent promising tools for vaccine development, because they enable intracellular antigens to be expressed by increasing the ability to generate robust cytotoxic T-lymphocyte responses and proinflammatory interferon and cytokine production without the need for an adjuvant. However, there is great concern regarding their genotoxicity due to possible viral genome integration; this has led to many efforts aimed at finding a high level of safety and efficacy.”
“Several viral, bacterial, and parasite vectors have been used in anti-malarial vaccine candidates; currently, many clinical trials are exploring their advantages to increase their potential and accelerate their use in vaccines.”
CHAD63 MVA ME-TRAP
“This anti-malarial vaccine was developed using chimpanzee adenovirus 63 (Chad63) and modified Vaccinia virus Ankara (MVA) into which were inserted genes encoding the thrombospondin-related adhesion protein (TRAP) multiple epitope (ME) chain.”
“The ME-TRAP hybrid is thus a 2398 base pair (bp) insert encoding a single 789 aa-long peptide, covering the complete P. falciparum TRAP sequence, fused to a chain of 20 malaria T- and B-cell epitopes (14 targeting MHC class I, 3 MHC class II and 1 murine).”
PCR
“A trial involving adults in Senegal to assess vaccine efficacy using a polymerase chain reaction (PCR) assay was able to detect > 10 parasites/μl blood. PCR was positive for 12 out of 57 participants vaccinated with ChAd63 ME-TRAP with a booster dose of MVA ME-TRAP and 13 out of 58 control patients who received an anti-rabies vaccine were positive by PCR, giving 8% efficacy (which was not statistically significant). They thus grouped the results with the 67% efficacy obtained in a study in Kenya and, using Cox regression, showed 50% overall vaccine efficacy in both populations.”
CSVAC
“CSVAC, a vaccine from Chad63 and MVA to encode the P. falciparum CS protein, continued such line of research into plasmid DNA anti-malarial vaccines; the CS insert was a codon-optimized cDNA encoding the CS protein truncated at the C-terminal extreme thereby lacking 14 C-terminal aa and thus omitting the GPI anchor.”
FUTURE DIRECTIONS
“Nanovaccinology” with Self-Assembling Protein Nanoparticles (SAPNs)… The next major challenge concerns the host’s genetic variability and parasite proteins’ interaction with the human immune system.”
“The choice of antigen to be used is quite complicated due to factors such as the parasite’s complex life-cycle involving two reproduction cycles (sexual and asexual), different development stages and two hosts (the Anopheles mosquito and human beings). All this can be added to the multiple invasion routes described so far for each of its target cells(hepatocytes and/or erythrocytes), the parasite’s ability to modify its gene expression and the genetic variability between P. falciparum circulating strains.”
“The next major challenge concerns the host’s genetic variability, particularly major histocompatibility class II (MHCII) complex molecules exerting their mechanism by synthesizing proteins encoded by the HLA-DR regions β1*, β3*, β4* and β5* where the HLA-DR β1* region encodes more than 1500 genetic variants grouped into 16 allele families called HLA-DRβ1*01, *03, *04, *07, etc. Parasite proteins’ interaction with the human immune system should be analysed by predicting B and T epitopes (using NetMHCIIpan 3.2 or other predictors).”
La Quinta Columna just told us the extermination of Humans could be complete in a few months. My ears are still ringing but this information is solid and sound! God be with us all!
After 20,000 hours of research by scientific teams, the University of Almeria and The Fifth Column release a comprehensive report outlining the mechanism of Telephoresis and 5G, a Bluetooth connectivity both found in patents and science labs in Europe.
Evidence proves that Covid-19 is induced by Graphene Oxide, a bioligical weapon.
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 alreadyknown 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.
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,andSARS. 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.
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 Hydraallows in vivotracking 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”processcalled transfection. A new generation of transgenic Hydra polyps continues reproducing the chimeric genetic expression in their offspring.
These GMO Hydra polyps are now genetically codedvectors, 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.
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 Projectdeveloped 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 proteincalled 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 genesin 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 andmerge 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. Thetransplanting 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.
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.
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 24/7but 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 anew neural networkin 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 fromHSV (herpes simplex virus) which is being used for “reduced gene expression” in humans. This uses the chimeric E. coli bacteria and Lentivirus.
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.
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 cellsin 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 (shRNAsilencing 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 humansis encoded by the WNT3gene. 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 embryosand 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.
“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.
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
