I DON’T APPRECIATE BEING DEPENDENT ON ANYTHING, BE IT BIG GOVERNMENT, BIG PHARMA OR BIG FOOD SOURCES.
MY INTEREST IS NOT FROM A PLACE OF FEAR.
MY INTEREST IS FROM A PLACE OF FREEDOM.
Don’t confuse my personality with my attitude.
My personality is who I am. My attitude depends on you.
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Despite mainstream attempts to downplay the alarming contamination problem plaguing COVID-19 vaccines, the Gates Foundation has awarded $3.3 million to a team of scientists at New York’s Rensselaer Polytechnic Institute (RPI) to develop “breakthrough purification technologies” for producing mRNA-based vaccines.
A September Autoimmunity study confirms that both Pfizer-BioNTech and Moderna’s mRNA COVID-19 injections contain many hundreds of times more contamination than the FDA and WHO limit.
The grant is an implicit admission that contamination is in fact a problem posed by mRNA vaccines, as well as a sign that the platform is here to stay.
Gates is funding the project because of the “impurities” and “inefficien[cy]” related to mRNA vaccines.
According to an RPI announcement:
The research team aims to address a critical bottleneck in the production of mRNA therapeutics: the purification process that removes impurities while maintaining the integrity of the therapeutic molecule.
“This project represents a paradigm shift in how we think about mRNA purification,” Belfort said. “Current technologies are prohibitively expensive and inefficient, creating barriers to access for the populations that need them most. Our goal is to develop a purification platform that is not only more cost-effective but also more productive and scalable.”
The researchers aim to accomplish this by “replacing conventional resin-based purification systems with advanced membrane technologies and innovative binding molecules.”
The RPI announcement also admits that current mRNA-based vaccine impurities are linked to side effects and that the injectables are not effective enough, more revelations that cut against mainstream counterclaims.
Higher purity mRNA vaccines with lower immunogenic impurities could lead to improved clinical outcomes, including reduced side effects and enhanced therapeutic efficacy.
The announcement predicts the rise of self-replicating vaccine technology, which this website was the first to warn about in December 2023.
Additionally, the technology being developed could prove particularly valuable for self-amplifying RNA (saRNA) therapeutics, which require lower doses than traditional mRNA vaccines and represent the next generation of RNA-based medicines.
Gates has been developing self-copying mRNA vaccines for COVID (here, here) as well as for bird flu (here), which is the pathogen this website has been predicting will fuel the next orchestrated pandemic.
The billionaire’s latest investment is made in the name of strengthening Big Pharma infrastructure, as well as “equity” and “pandemic preparedness.”
If successful, this technology could enable local production of mRNA vaccines in regions that currently lack access to affordable biomanufacturing infrastructure, supporting global health equity and pandemic preparedness.
Despite the disease, hospitalizations, and deaths linked to mRNA jabs, the technology isn’t going anywhere.
U.S. Representative Chris Smith (R-NJ) has successfully included his amendment to investigate whether the U.S. military weaponized ticks with Lyme disease into the 2026 National Defense Authorization Act (NDAA).
The ordeal underscores the national security threat posed by laboratory pathogen manipulation.
Rep. Smith, who is Co-Chair of the Congressional Lyme and Tick-Borne Disease Caucus, had offered similar amendments—one in 2019 and the other in 2021—which passed the House, but failed in the Senate.
The successful addition of the amendment follows FDA Chief Dr. Marty Makary’s statements during a November podcast, in which Makary expressed his belief that Lyme disease was created in U.S. military Lab 257 on Plum Island, New Jersey.
A Thursday press release from Smith’s office reads:
A critical amendment authored by Rep. Chris Smith (R-NJ) to investigate whether the U.S. military weaponized ticks with Lyme disease has been included in the National Defense Authorization Act for Fiscal Year 2026 (FY26 NDAA) (S. 1071), which has cleared the U.S. House of Representatives, headed to the Senate, and is expected to be signed by President Trump upon its final passage.
Smith’s amendment—now Sec. 1068 of the bill—directs the Government Accountability Office (GAO)—the Congressional “watchdog”—to investigate the Cold War-era Department of Defense (Department of War) bioweapons program and determine whether they ever used ticks as hosts or delivery mechanisms for biological warfare agents.
In the press release, Smith emphasized that “New Jersey has one of the highest Lyme rates in the United States—the disease is present in all 21 counties.”
“The pervasive presence of Lyme disease in New Jersey not only carries concerns for civilians, but also for the military personnel stationed in the state—especially and including those serving at Joint Base McGuire-Dix-Lakehurst, part of which is located within my congressional district,” the republican added.
The press release explained that Smith’s amendments were inspired by Kris Newby’s book, Bitten: The Secret History of Lyme Disease and Biological Weapons.
The book includes interviews with Dr. Willy Burgdorfer, the federal researcher and U.S. bioweapons specialist credited with discovering Lyme disease.
Dr. Burgdorfer has revealed that “he and other bio-weapons specialists injected ticks with pathogens in order to cause severe disability, disease, and even death to potential enemies in unsuspecting ways.”
Smith’s amendment in the NDAA would compel the Comptroller General of the United States “to conduct an exhaustive review of research conducted by the military, the National Institutes of Health (NIH), the U.S. Department of Agriculture (USDA), and other federal agencies between the period of January 1, 1945 and December 31, 1972, regarding experiments involving Spirochaetales and Rickettsiales—two forms of tick-borne bacteria.”
Smith says we are now “one step closer to finally determining whether the U.S. government’s bioweapons program contributed to the proliferation of Lyme disease.”
“The hundreds of thousands of New Jerseyans suffering from Lyme disease—in addition to the millions across the United States—deserve to know the truth about the origins of their illness. An enhanced understanding of how Lyme came to be will only assist in finding a cure for this debilitating disease,” said Smith.
Rep. Smith’s amendment reads:
SEC. 1068. GAO REVIEW AND REPORT ON BIOLOGICAL WEAPONS EXPERIMENTS ON AND IN RELATION TO TICKS, TICK-BORNE DISEASE.
(a) REVIEW.— The Comptroller General of the United States shall, to the extent practicable, conduct a review of research conducted during the period beginning on January 1, 1945, and ending on December 31, 1972, by the Department of Defense, including by the Department of Defense in consultation with the National Institutes of Health, the Department of Agriculture, or any other Federal department or agency on—
(1) the use of ticks as hosts or delivery mechanisms for biological warfare agents, including experiments involving Spirochaetales or Rickettsiales; and
(2) any efforts to improve the effectiveness and viability of Spirochaetales or Rickettsiales as biological weapons through combination with other diseases or viruses.
(b) LOCATION OF RESEARCH.— In conducting the review under subsection (a), the Comptroller General shall review research conducted at facilities located inside the United States and, if feasible, facilities located outside the United States, including laboratories and field work locations.
(c) INFORMATION TO BE REVIEWED.—
(1) CLASSIFIED INFORMATION.— In conducting the review under subsection (a), the Comptroller General shall review any relevant classified information.
(2) MATTERS FOR REVIEW.— In conducting the review under subsection (a), the Comptroller General shall review, among other sources, the following:
(A) Technical Reports related to The Summary of Major Events and Problems, US Army Chemical Corps, FY 1951–FY 1969.
(B) Site Holding: CB DT DW 48158
Title: Virus and Rickettsia Waste Disposal Study.
Technical Report No. 103, January 1969.
Corp Author Name: Fort Detrick, Frederick, MD.
Report Number: SMUFD-TR-103.
Publish Date: 1969-01-01.(C) Site Holding: CB DT DW 60538
Title: A Plaque Assay System for Several Species of Rickettsia.
Corp Author Name: Fort Detrick, Frederick, MD.
Report Number: SMUFD-TM-538.
Publish Date: 1969-06-01.(D) Site Holding: CB DW 531493
Title: Progress Report for Ecology and Epidemiology and Biological Field Test Technology, Third Quarter FY 1967.
Corp Author Name: Army Dugway Proving Ground, UT.
Publish Date: 1967-05-08.(E) Any relevant scientific research on the history of Lyme disease in the United States.
(d) REPORT.—
(1) IN GENERAL.— Not later than two years after the date of the enactment of this Act, the Comptroller General shall submit to the Committees on Armed Services of the House of Representatives or the Senate a report that includes the following:
(A) A list of the research projects reviewed under subsection (a) and an assessment of the scope of such research.
(B) A finding by the Comptroller General as to whether such review could lead to a determination that any ticks used in such research were released outside of any facility (including any ticks that were released unintentionally).
(C) A finding by the Comptroller General as to whether such review could lead to a determination that any records related to such research were destroyed, and whether such destruction was intentional or unintentional.
(2) FORM OF REPORT.— The report required under paragraph (1) shall be submitted in unclassified form, but may contain a classified annex.
If the GAO does its job and follows the paper trail where it leads, this amendment may finally force the U.S. government to answer a question it has avoided for decades: whether a taxpayer-funded Cold War bioweapons program left millions of Americans paying the price with their health.
No U.S. agency has ever verified that the COVID-19 pathogen’s (SARS-CoV-2) genetic code that a Chinese government biolab supplied at the beginning of the COVID-19 pandemic—said to have been sequenced from a pneumonia patient’s lung wash—actually originated from that clinical sample before it was encoded into hundreds of millions of mRNA vaccine doses.
China never provided the physical patient sample to any U.S. institution.
In fact, Beijing issued an official directive forbidding the sharing of any samples and ordering the destruction of those samples.
And the U.S. never demanded or required an analysis of those samples before allowing its citizens to be injected with China’s pathogenic spike protein-producing code.
This critical step in verification was—and still has been—skipped, despite earlier warnings that China’s military had been exploring bioweapons development that integrates biotechnology and genetic engineering into a “new domain of warfare.”
It was also skipped despite EcoHealth Alliance’s 2018 ‘DEFUSE’ proposal to DARPA to collaborate with China to create chimeric coronavirus spike proteins with furin cleavage sites, receptor-binding domain upgrades, and two proline insertions—the defining characteristics of the COVID-19 pathogen and mRNA vaccines.
Congress, the White House, the Department of Energy, the FBI, the CIA, and Germany’s Federal Intelligence Service (BND) have confirmed that the COVID-19 pandemic was likely the result of lab-engineered pathogen manipulation—meaning billions were injected with a genetic drug that codes for a Chinese government-constructed, lab-altered spike protein.
The SARS-CoV-2 genetic code was created in a biosafety level 3 (BSL-3) laboratory at the Chinese government-run Shanghai Public Health Clinical Center, using long-debunked (here) reverse-transcription PCR (RT–PCR) technology.
A February 2020 Nature publication explains how China created the SARS-CoV-2 sequence:
Here we study a single patient who was a worker at the market and who was admitted to the Central Hospital of Wuhan on 26 December 2019 while experiencing a severe respiratory syndrome that included fever, dizziness and a cough. Metagenomic RNA sequencing4 of a sample of bronchoalveolar lavage fluid from the patient identified a new RNA virus strain from the family Coronaviridae, which is designated here ‘WH-Human 1’ coronavirus (and has also been referred to as ‘2019-nCoV’). Phylogenetic analysis of the complete viral genome (29,903 nucleotides) revealed that the virus was most closely related (89.1% nucleotide similarity) to a group of SARS-like coronaviruses (genus Betacoronavirus, subgenus Sarbecovirus) that had previously been found in bats in China5. This outbreak highlights the ongoing ability of viral spill-over from animals to cause severe disease in humans.
To investigate the possible aetiological agents associated with this disease, we collected bronchoalveolar lavage fluid (BALF) and performed deep meta-transcriptomic sequencing. The clinical specimen was handled in a biosafety level 3 laboratory at Shanghai Public Health Clinical Center. Total RNA was extracted from 200 μl of BALF and a meta-transcriptomic library was constructed for pair-end (150-bp reads) sequencing using an Illumina MiniSeq as previously described4,6,7,8. In total, we generated 56,565,928 sequence reads that were de novo-assembled and screened for potential aetiological agents. Of the 384,096 contigs assembled by Megahit9, the longest (30,474 nucleotides (nt)) had a high abundance and was closely related to a bat SARS-like coronavirus (CoV) isolate—bat SL-CoVZC45 (GenBank accession number MG772933)—that had previously been sampled in China, with a nucleotide identity of 89.1% (Supplementary Tables 1, 2). The genome sequence of this virus, as well as its termini, were determined and confirmed by reverse-transcription PCR (RT–PCR)10 and 5′/3′ rapid amplification of cDNA ends (RACE), respectively. This virus strain was designated as WH-Human 1 coronavirus (WHCV) (and has also been referred to as ‘2019-nCoV’) and its whole genome sequence (29,903 nt) has been assigned GenBank accession number MN908947. Remapping the RNA-sequencing data to the complete genome of WHCV resulted in an assembly of 123,613 reads, providing 99.99% genome coverage at a mean depth of 6.04× (range, 0.01–78.84×) (Extended Data Fig. 3). The viral load in the BALF sample was estimated by qPCR to be 3.95 × 108 copies per ml (Extended Data Fig. 4).
China handed the world a genetic code in computer form (in silico).
And governments all over the world accepted that code without scrutiny.
They allowed billions of people to be injected with a vaccine that creates the Chinese government’s foreign protein in the body for more than 700 days.
A January 2024 U.S. House Energy & Commerce press release confirms China possessed the SARS-CoV-2 sequence “days before the CCP acknowledged an outbreak, and more than two weeks before the China CDC release[d] their sequence.”
The congressional body said that fact “calls into question how early the CCP knew about the virus and how long they withheld this information from the world.”
This significant discovery further underscores why we cannot trust any of the so-called ‘facts’ or data provided by the CCP and calls into serious question the legitimacy of any scientific theories based on such information. The American people deserve to know the truth about the origins of SARS-CoV-2, and our investigation has uncovered numerous causes for concern, including how taxpayers’ dollars are spent, how our government’s public health agencies operate, and the need for more oversight into research grants to foreign scientists,” said Chairs Rodgers, Guthrie, and Griffith.
My report from last month revealed that before the pandemic, DARPA had developed a program to synthesize viruses purely from digital sequences within in 60 days.
In the end, the world was locked down and injected on the honor system of a hostile foreign government, and not one U.S. agency has yet produced the single piece of evidence that should have come first: independent proof that China’s digital code ever came from a real human sample.
Will the same national security concern-raising strategy be used in the apparently incoming bird flu pandemic?
A recent WHO-funded study published in Health Policy and Planning outlines in direct operational terms the governance model the organization expects countries to activate during an influenza pandemic.
For years, this website has been documenting avian influenza gain-of-function experiments and countermeasures development carried out by governments all over the world in an apparent instigation/orchestration of a coming bird flu pandemic.
The WHO-backed document is framed around influenza specifically, describing it as the catalyst for restructuring national systems into a unified, multisector authority.
The paper establishes influenza as the justification:
“Zoonotic influenzas have high pandemic potential, having caused four pandemics over the past 100 years.”
“We focus on zoonotic influenza because of the urgency to respond to the ongoing influenza panzootic and reduce its pandemic potential.”
From that premise, the authors build out a governance architecture designed to take effect during conditions of influenza-driven crisis, uncertainty, or sector failure.
The study defines the activation conditions for these multisector structures:
“MSPs rarely arise due to common goals. Instead, different actors come together under conditions of uncertainty, crisis, or sector failure—when no single sector has the knowledge or resources to address the challenge.”
According to the framework, a severe zoonotic influenza outbreak meets all of these criteria.
Under those circumstances, governments are expected to transition from sector-specific decision-making to coordinated, collaborative, and ultimately consolidated control.
The study provides explicit definitions of the governance levels intended for pandemic response.
Under the “Consolidation” and “Integration” stages, the paper states:
“Integration—merger of assets.”
“United governance—All governance functions assumed by a single entity.”
In the context of an influenza pandemic, this means:
These are the document’s literal terms.
Because the authors tie their influenza governance model directly to the One Health Theory of Change, the sectors incorporated into pandemic decision-making expand far outside traditional public health.
The One Health scope is explicitly stated:
“Collective need for clean water, energy and air, safe and nutritious food, taking action on climate change, and contributing to sustainable development.”
During an influenza pandemic, this framework places climate policy, food systems, water resources, agriculture, environmental management, and human health under a unified command structure, justified by zoonotic transmission risk.
The study acknowledges that governance under this model lacks transparency:
“There is a black-box approach to the governance of MSPs around zoonotic influenza.”
The document offers no mechanisms for public oversight during such a consolidation.
The authors state that the same governance framework used during a pandemic should remain active between outbreaks:
“We expect the ToA to be used in preparedness and inter-outbreak periods when program managers have the opportunity for reflection.”
The governance model triggered by a pandemic is not temporary. It becomes the template for both emergency response and routine administration.
The authors note that One Health structures do not embed easily in “peacetime”:
“One Health remains difficult to implement in ‘peacetime.’”
In this context, a pandemic acts as the operational doorway through which One Health governance can be implemented.
The authors acknowledge that different ministries and sectors have diverging priorities, especially during influenza outbreaks:
“Their ‘preferred outcomes’ likely promote their individual interests over shared goals.”
“The commercial, economic, and political dynamics of zoonotic influenza-related MSPs… have not always been addressed in operational guidance.”
The solution offered in the paper is to consolidate these interests under a unified authority rather than allow them to operate independently.
The study’s language is straightforward.
An influenza pandemic creates the conditions—crisis, uncertainty, and sector failure—under which national ministries are expected to merge their operations, assets, decision-making processes, and governance structures into a single integrated authority.
The resulting system extends far beyond healthcare, embedding climate, agriculture, food systems, and environmental management directly into pandemic command operations.
Supranational bird flu pandemic orchestration is well underway.
What follows is a documented sequence showing how the World Health Organization (WHO) seized operational control of the COVID-19 response from day one—and how it is now positioning itself to run the avian influenza pandemic the same way.
Will America follow the WHO into pandemic peril again?
On December 31, 2019, the Chinese government reported a cluster of pneumonia cases in Wuhan, Hubei Province.
On the same day, the WHO commandeered the international vaccine response, issuing its first “emergency use validation for a COVID-19 vaccine” emphasizing the “need for equitable global access” and declaring governments all over the world must “expedite their own regulatory approval processes to import and administer the vaccine”:
“The World Health Organization (WHO) today listed the Comirnaty COVID-19 mRNA vaccine for emergency use, making the Pfizer/BioNTech vaccine the first to receive emergency validation from WHO since the outbreak began a year ago,” reads the organization’s Dec 31 press release.
“The WHO’s Emergency Use Listing (EUL) opens the door for countries to expedite their own regulatory approval processes to import and administer the vaccine. It also enables UNICEF and the Pan-American Health Organization to procure the vaccine for distribution to countries in need.”
“‘This is a very positive step towards ensuring global access to COVID-19 vaccines. But I want to emphasize the need for an even greater global effort to achieve enough vaccine supply to meet the needs of priority populations everywhere,’ said Dr Mariângela Simão, WHO Assistant-Director General for Access to Medicines and Health Products. ‘WHO and our partners are working night and day to evaluate other vaccines that have reached safety and efficacy standards. We encourage even more developers to come forward for review and assessment. It’s vitally important that we secure the critical supply needed to serve all countries around the world and stem the pandemic.’”
“Regulatory experts convened by (the) WHO from around the world and (the) WHO’s own teams reviewed the data on the Pfizer/BioNTech vaccine.”
(The) “WHO is working to support countries in assessing their [COVID vaccine] delivery plans and preparing for use where possible.”
“The emergency use listing (EUL) procedure assesses the suitability of novel health products during public health emergencies. The objective is to make medicines, vaccines and diagnostics available as rapidly as possible to address the emergency while adhering to stringent criteria of safety, efficacy and quality.”
“Once a vaccine has been listed for WHO emergency use, WHO engages its regional regulatory networks and partners to inform national health authorities on the vaccine and its anticipated benefits based on data from clinical studies to date.”
“As part of the EUL process, the company producing the vaccine must commit to continue to generate data to enable full licensure and WHO prequalification of the vaccine. The WHO prequalification process will assess additional clinical data generated from vaccine trials and deployment on a rolling basis to ensure the vaccine meets the necessary standards of quality, safety and efficacy for broader availability.”
The very next day, January 1, 2020, the WHO set up its IMST (Incident Management Support Team), putting the organization “on an emergency footing for dealing with the outbreak,” according to the WHO’s own published timeline.
On January 5, the WHO published its first “Disease Outbreak News” on the new purported virus, which represented a “flagship technical publication to the scientific and public health community as well as global media” and gave “a risk assessment and advice” to governments, public health officials, and the mainstream international scientific community.
On January 7, the Chinese government claimed to have identified a brand new coronavirus as the causative agent of the outbreak.
On January 10, China’s Center for Disease Control and Prevention (China CDC) publicly released what they said was the genetic sequence for the SARS-CoV-2 pathogen, named Wuhan-Hu-1.
On the same day (Jan 10), the WHO began using the phrase “2019 Novel Coronavirus” or “2019-nCoV” to refer to the disease.
On January 11, the WHO announced that it had received the Chinese government’s SARS-CoV-2 genetic sequences.
On January 12, the WHO officially endorsed China’s in silico coronavirus sequence:
“On 11 and 12 January 2020, WHO received further detailed information from the National Health Commission about the outbreak,” a press release reads.
“WHO is reassured of the quality of the ongoing investigations and the response measures implemented in Wuhan, and the commitment to share information regularly.”
Vaccine developers, including those at Moderna and Pfizer-BioNTech, initiated vaccine design within hours of the sequence becoming available, and diagnostic assays were developed within days.
The transnational scientific community accepted the sequence, leading to immediate action in diagnostics, vaccine development, and surveillance, with minimal skepticism or delay.
On January 22, the WHO convened an emergency committee to assess the outbreak.
By January 30, it declared the outbreak a Public Health Emergency of International Concern (PHEIC), advising all countries to prepare for containment, which included doomed social distancing and isolation measures, as well as the “rapid development and access” to vaccines.
On March 11, the WHO became the first international body to officially declare the COVID-19 outbreak a global “pandemic” and, despite being a foreign and unelected body, began dictating what countries should do:
“We have called every day for countries to take urgent and aggressive action.”
Countries should “detect, test, treat, isolate, trace and mobilise their people in the response.”
“We’re calling on you to activate and scale up your emergency response mechanisms.”
“Communicate with your people about the risks and how they can protect themselves.”
“Find, isolate, test and treat every case and trace every contact.”
“Ready your hospitals, protect and train your health workers.”
“Countries must take a whole-of-government, all-of-society approach.”
“We cannot say this loudly enough or clearly enough or often enough; all countries can still change the course of this pandemic.”
“We are not suggesting to shift from containment to mitigation; we are not, we underline that.”
“All countries need to review their strategies right now.”
“Surveillance systems have to improve.”
“There’s no excuse to say that we cannot do this.”
“Countries must… take urgent and aggressive action.”
In short, the WHO declared what would be the “scientific consensus” regarding COVID-19, and the international mainstream scientific community followed suit.
After its two-year investigation into the COVID-19 pandemic, the Congressional Select Subcommittee on the Coronavirus Pandemic confirmed that the WHO’s draconian authoritarianism throughout the pandemic “was an abject failure,” writing:
“The WHO’s response to the COVID-19 pandemic was an abject failure because it caved to pressure from the Chinese Communist Party and placed China’s political interests ahead of its international duties. Further, the WHO’s newest effort to solve the problems exacerbated by the COVID-19 pandemic—via a “Pandemic Treaty”—may harm the United States.”
But there is no need for a treaty, no matter how national-sovereignty-degrading, when the world’s public health leaders and self-appointed scientific elite unquestioningly carry out the WHO’s bidding.
The WHO is right now orchestrating a coming avian influenza “bird flu” pandemic.
The WHO has already:
Simultaneously, governments all over the world are performing reverse-genetics gain-of-function (GOF) experiments on- and developing countermeasures (vaccines, etc.) for bird flu (see links below).
Just as they were before the COVID pandemic.
The Trump administration has been “actively participating” in WHO bird flu seminars despite the president’s January 2025 executive order to withdraw from the organization.
The admin’s $500 million ‘Generation Gold Standard’ platform is focused on bird flu vaccine development.
If the WHO repeats its COVID plan with avian influenza, we will see the same rapid lockstep activation of a prebuilt command system—instant acceptance of an unverified digital genome, accelerated vaccine deployment, suppressed dissent, and a global population maneuvered once again into mandatory genetic countermeasures before independent validation is possible.
U.S. officials and American citizens must decide now whether they will permit this system to run again, or whether they will finally impose the oversight and resistance that were absent the first time.
Yes, sometimes young people have strokes. Sometimes they get cancer. Mostly they don’t. And when well-established population incidence of something such as ALS or stroke or infertility or cancer or lupus, etc., suddenly shoots up, there is always a cause. It is the work of epidemiology, forensics, pathology and similar to look at the pattern and find the cause so it can be remedied.
If, that is, there is any real desire to fix the problem. When the problem is that there is a concerted effort to cause, not fix, the problem because the problem is seen, by someone at the controls, as the solution to some other problem, well, Houston, we most certainly do have a problem.
Here is Aussie 17’s remarkable Part 2 which was promised:
PharmaFiles by Aussie17
The Jab That Keeps on Giving: Part 2. Stroke drug skyrockets 200%!
Before proceeding with this article, it is strongly recommended reading Part 1 first.
Bioweapons, like the ones disguised as mRNA jabs, for example, are designed to maim and kill. Otherwise, they are not effective. They are designed to cloak their presence and impact in mystery. Otherwise, they are not safe for those who made and deployed them. So, yes, the jabs are safe and effective, in those terms, but most certainly not safe and effective as health measures.
Depopulation of a hardy and resilient species with a lot of members living under widely divergent situations takes a LOT of effort and generates a LOT of money.
A LOT of money.
Sicker populations are easier to control and easier to finish off. Sicker populations do not mount effective resistances, or not for long. Sicker populations are more obedient to orders directing and deflecting them.
And sicker populations generate massive wealth before being disposed of.
Pandemic? Chronic illness? What’s not to love, at least if you are a psychopathic predator, serving at the whim of the central parasite, the UN/globalist parasite, that is
Get out of the United Nations, yes, but that action means nothing unless the parasitic, and deadly, regulations, programs, policies, protocols, guidelines, etc., infesting every part of our public and civic lives are extracted, examined and either replaced with ones that support and follow Constitutional law or just discarded if they are, in fact, unnecessary.
You know, like a government of the people, by the people and for the people instead of one that is of the controllagarchs, by the billionaires and for the destructocrats.
Visit PreventGenocide2030,org to learn more and mobilize.
Frankly, we are at the Detox or Die stage, as unpleasant a thought as that might be. We are being killed and, if we leave the parasite in place, that can only accelerate. There really is no option.
The World Health Organization (WHO) has released a “new strategic plan for the management of coronavirus disease threats,” according to a Wednesday press release.
The announcement comes after the WHO, with Gates Foundation funding, published its blueprint for a supranational digital ID system that tracks every person on Earth from birth, merges vaccine status with income, ethnicity, and religion, and deploys AI-driven surveillance to identify, target, and monitor entire populations.
Per today’s press release, the WHO wants to control how sovereign nations respond to “COVID-19, Middle East respiratory syndrome (MERS), and potential new coronavirus diseases.”
The plan “encompasses both routine management as well as emergency scenarios” involving the “emergence of a new coronavirus with pandemic potential.”
The unelected international foreign body emphasizes that the move represents “the first such unified plan.”
The goal is “sustained, long-term, and integrated management.”
WHO says it’s doing this in the name of “advancing integration, sustainability, and equity,” common globalist-tied tropes.
The plan is part of the organization’s “2025–2030” agenda for national health authorities to participate in an “action-oriented approach to managing coronavirus disease threats in the broader context of infectious disease management.”
WHO’s justification is the coronavirus’s alleged “capacity to trigger epidemics and pandemics.”
WHO insists that “uncertainties persist around virus evolution and long-term impacts of COVID-19.”
One WHO director explained that the plan also lumps in efforts regarding influenza, the pathogen that this website has been warning readers is currently being dangerously manipulated in government-funded laboratories all over the world.
The director urged government leaders to prepare for “future” pathogenic threats by falling in line with the WHO:
“Coronaviruses remain one of the most consequential infectious disease threats today,” said Dr Maria Van Kerkhove, WHO Acting Director for Epidemic and Pandemic Management. “Integrating their management into broader respiratory disease and infectious threat prevention and control programmes, including for influenza, is essential. While each country will have its own approach tailored to its national context, WHO urges Member States to use the strategic directions set out in the plan to build resilient health systems that can effectively manage current threats while preparing for future ones.”
The WHO is expanding its CoViNet “sentinel surveillance” network, now comprised of 45 laboratories.
Eleven labs were added this year alone, signifying the magnitude of the operation.
“To strengthen global coronavirus monitoring, WHO has also expanded its Coronavirus Network (CoViNet), a network of disease surveillance programmes and reference laboratories for SARS-CoV-2, MERS-CoV, and emerging coronaviruses of public health significance. CoViNet now includes 45 national reference laboratories across the human, animal, and environmental health sectors, with 11 laboratories added in 2025. CoViNet complements WHO’s Global Influenza Surveillance and Response System (GISRS), which conducts global sentinel surveillance, including for SARS-CoV-2.”
Despite President Donald Trump’s January executive order withdrawing the U.S. from the WHO, CoViNet includes labs belonging to Emory University, Ohio State University, and the Centers for Disease Control and Prevention (CDC).
In short, the WHO’s new “strategic plan” represents an international effort to centralize pandemic authority under an unelected foreign body, erode national sovereignty, override accountability, and collapse public-health decision-making into a global command structure.
And it comes even after President Trump formally withdrew the United States from the WHO, underscoring how deeply these surveillance and biosecurity networks remain embedded—and how ripe they are for further abuse.
Universe 25 was not a fable about rodents; it was a behavioral model of what happens when structure, hierarchy, and purpose are replaced by unlimited external provisioning. Dr. John Calhoun observed that when mice lived in a habitat where every material need was met automatically, their social roles collapsed. Male withdrawal, weakened parental investment, falling fertility, and eventually a complete demographic crash followed. It is tempting to think humans would behave differently, but the striking parallels to what happened under LBJ’s Great Society suggest otherwise. This claim seems bold at first glance. Yet careful reflection shows it to be tragically plausible.
To understand the parallel, we must first remind ourselves what Calhoun found. Universe 25 provided abundance without effort. Food appeared without foraging. Shelter required no construction. Predators were removed. At first, the population expanded rapidly. Then something surprising occurred. As resources remained stable, the social structure atrophied. Dominant males withdrew or fixated on repetitive, self-soothing behavior. Females stopped caring for offspring. Infanticide increased. Fertility collapsed. Eventually, the final generation, the so-called “Beautiful Ones,” ceased to reproduce, withdrew from contact, and spent their days grooming or eating in isolation. Abundance without purpose created behavioral degradation so deep that the population could not recover even when conditions remained materially perfect.
If this seems remote from human affairs, consider what Black Americans had achieved before Washington intervened. Despite the severe constraints imposed by segregation, Black families were intact and resilient. More than 85% of Black children were born to married parents in the early 1960s, an astonishing rate for any urban poor population. Poverty existed, but social cohesion was strong. Churches, fraternal organizations, and family networks created structure and responsibility. There was purpose, and there were roles. These institutions helped people navigate unjust external conditions and provided the scaffolding for upward mobility.
Then the Great Society arrived. Washington attempted to replace family, church, and community with federal programs. The intent was compassionate. Yet intent does not override human nature. Welfare incentives rewarded the absence of fathers. Public assistance replaced the reciprocal obligations that had sustained families. The cultural norm that linked marriage, sex, and child rearing was severed. The numbers show how quickly the damage spread. Prior to 1965 fewer than 2% of black women received any form of public assistance. By 1970 roughly 36% did. An eighteen-fold increase in five years reveals not gradual social evolution but a policy driven shock.
Fertility followed a similar arc. In 1965 the General Fertility Rate for black women ages 15 to 44 stood at 140.3 births per 1,000 women. By 1970 it had fallen to 123.5. Today it has collapsed to 45.8. A two thirds decline in sixty years is not an ordinary demographic adjustment. It is the signature of a community losing its social structure. Calhoun observed that once parental roles erode, fertility does not rebound simply because material conditions are comfortable. The behavioral patterns produced by disrupted roles persist across generations. In short, once the social fabric tears, later generations cannot easily repair it.
The expansion of SNAP reinforced the pattern. Food stamps did not reach every county until 1974. Yet by 1980 roughly 35% of black households used them. Today that figure is 52%. More than half of black households now rely on a federal provisioning system to meet basic nutritional needs. Calhoun found that abundant food provided without effort weakened social behaviors related to care, discipline, and responsibility. We see a disturbing parallel. Federal provisioning was meant to provide relief. Instead, it displaced the social norms that sustain families.
The collapse of marriage tells the same story. In 1965 over 85% of black children were born to married parents. By 1970 fewer than 63% were. By 1980 that figure had fallen below 50%. Today it sits below 30%. No developed society has ever seen such a fast decline in marriage without accompanying social dysfunction. When marriage collapses, so does the structure that teaches children discipline, reciprocity, and responsibility. Calhoun would not have been surprised by these outcomes. When a system replaces organic roles with external provisioning, social roles dissolve.
Some readers may resist this interpretation. Perhaps they believe social structures collapsed because of lingering discrimination or economic shocks. These factors matter, but they cannot explain the timing. The most dramatic changes occurred precisely when Great Society programs expanded. Nor can they explain why black families remained stable during far harsher periods before the 1960s. When we look at the causal chain, the policies come first, followed by the collapse in marriage, the surge in welfare use, the decline in fertility, and the rise of multi-generational dependency.
Consider Calhoun’s central insight. A system that removes incentives for productive behavior while failing to reinforce social norms does not create flourishing. It creates a behavioral sink. In Universe 25 the sink emerged not because conditions were harsh but because they were artificially easy. The mice did not need each other, so they stopped forming healthy bonds. They did not need to protect or nurture, so parental roles decayed. They did not need to cooperate, so hierarchy collapsed. What remained was isolation, withdrawal, and the slow erosion of purpose.
Translate this into human social terms. When the state displaces fathers, fathers withdraw. When bureaucracies replace parental responsibility with monthly checks, parental investment declines. When food appears without effort, the link between work and provision breaks. When norms collapse, marriage becomes optional, then rare. The social ecosystem enters a downward spiral. This is precisely what happened in many black communities after the 1960s. The Great Society redistributed material goods while undermining the structures that gave life meaning.
Why does this matter today? Because Democrats still treat the Great Society as an untouchable legacy. They defend it with quasi-religious devotion. Their attachment persists even as the data show catastrophic outcomes. If the goal was to alleviate poverty, they failed. If the goal was to strengthen families, they failed. If the goal was to promote flourishing, they failed. And yet they demand more of the same policies. Calhoun would call this expansion of provisioning a deepening of the behavioral sink.
A reasonable reader might now ask how we should respond. We begin by recovering the insight that material assistance without social norms destroys the very communities it claims to help. Next, we must restore the institutions that originally sustained black families. Churches, civic groups, and strong families cannot be replaced by bureaucracies. Finally, we must ask why a political movement insists on maintaining policies that corrode family life. How do we save America if our policies are designed to destroy the structures that make America possible?
The lesson of Universe 25 is sobering. When abundance is provided without structure, communities decline. The Great Society followed the same script. Calhoun’s experiment warned us. We ignored it. We still have time to reverse course, but doing so requires the courage to admit that our social experiment failed and that the path to renewal runs through responsibility, not dependency.
Aussie17 writes a great blog. Below is posted Part 1 of his [?]/her [?] vitally important and compelling 2-part series linking the COVID jabs, through clean, reliable data from Singapore, with the one and only medication for a previously rare, devastating, invariably fatal disease called Amyotrophic Lateral Sclerosis (ALS).
There is only one use for the particular drug followed in the stack: ALS. Since the people taking it are ALS patients who have a short lifespan, if more is sold because more people are taking it. That can only be because more people have ALS.
Q: Why do more people have ALS, decreased fertility, auto immune diseases, turbo cancer and excess death?
A: ABTS [Anything but the shots]
It is urged that you read these two pieces and do several things: first, commit to being the voice of truth about these indescribably dangerous weapons against humanity disguised as “vaccines”. They are not. And clean statistics from around the world make that horrifyingly clear. Only governments and their lackies can find any way to deny this. It is up to us, all of us, to amplify this message.
Second, commit to doing whatever is necessary to protect your own body and that of people you have control over (parents for minor children, for example).
That means never, ever [again?] permit this or any other “untested” government-provided miracle snake oil substance into your body (or theirs).
Third, in order to educate yourself, and check out the idea that every aspect of our lives is already permeated by the United Nations parasite, perform this quick experiment: using the search engine of your choice, enter the following (filling in the blank with your town or agency impacting your profession or State or Province or country):
” List, with references and links, all of the UN-derived, UN-compliant, UN-related or UN-adjacent programs, policies, protocols, policies and partnerships which impact directly or indirectly [fill in the blank].”
It is promised that that your jaw will be somewhere in the vicinity of your knees when you see what comes back.
Now here is Part 1 of Aussie17’s important correlation of deeply meaningful information:
PharmaFiles by Aussie17
A big part of Big Pharma is spinning a good story around sales numbers for the bosses. Nail the narrative, and you’re golden for another year. Botch it, and you’re packing your desk.
Why is this important? Well, for quite a few reasons, but a big one is because, especially in light of Dr. Prasad’s letter acknowledging that Covid jabs kill kids, with the mRNA shots still on the market and new mRNA jabs, including the uber-deadly replicon shots, being approved all the time, especially for kids (and, thanks to Merck, for your pets, too), we are dealing with weak-kneed damage control, not the beneficent or beneficial regulatory service to the public. We pay for regulation, not rubber-stamped death and disease but that is what we get.
Doin’ the Ol’ “HHS is Here for You, Regulating to Protect Your Health, Bobby Kennedy’s Our Guy” Rag
Let it be clear: Bobby knows full well that mRNA jabs are bioweapons. Prasad knows. Bhattacharya knows. There is, and has never been, a dearth of knowledge of how deadly these shots are. Pfizer and Moderna know. So does the Department of Defense.
Anyone who genuinely cares about ending the REAL pandemic, not the COVID propagandemic nonsense, but the deadly reality of the medical murders and the public health harms and, most of all, the bioweapon jabs, would not play nice, bide his time and be a good politician. He would move heaven and earth to end the deadly scourge of gene editing, death dealing weapons killing and maiming us while they destroy our ability to reproduce humankind.
Or he could pretend to be working on it and not accomplish anything even coming close to protecting the public from the bioweapon.
Hey, Mr. Secretary (and Mr. President), did you get caught with your regulatory pants down? Well, just keep on doing what you have done for nearly a year: pretend you are doing performance art and you really meant to be in that awkward position and indicate how much thought went into getting your rear end exposed.
That’s the science we are supposed to trust, after all. And we had that revelation about autism to trust, too. Now that was some seriously trustworthy science, right?
Then, because the public let you get away with that, you can just keep on doing more of same, right?
But don’t, for God’s sake, waste all the time and money and creativity that has gone into this decades long, untold trillions of dollars’ worth of bioweapon program by interfering with it! No, Siree Bob! Cover your tracks first, lie out of every orifice you and your associates can make any sounds out and keep the bioweapons in the rapid approval pipeline.
Most important of all, of course, cover your own ass if you can manage it, and keep on doing what you’re doing.
Maybe nobody will notice while they are exterminated from the bioweapons on the shelves and in the clinics.
Or maybe we will. And maybe we will eject the deadly UN parasite from every cell in the Body Politic and make some real headway to recovery
Nothing less.
And neither the head of the Executive Branch of the US government nor his appointee over at Health and Human Services has done so. Meanwhile, we suffer and die through an entirely man-made plague.
As it turns out, hiding it in Singapore is quite difficult. Thus, this outstanding two-part revelation.
Who is behind it? The genocidal maniacs who think you and I are disposable at their whim and pleasure. That’s right: the globalist parasites who operate the United Nations for their pleasure and profit, and for our pain and punishment. We, after all, are the carbon they intend to eliminate.
The solution? a good, comprehensive detox to get the UN and its bits and pieces out of our lives, our bodies, our government, our schools, our town halls, our clinics and hospitals, our airports, our banks and everywhere else.
Learn more, a lot more, at PreventGenocide2030.org.
In a document published in the October Bulletin of the World Health Organization and funded by the Gates Foundation, the World Health Organization (WHO) is proposing a globally interoperable digital-identity infrastructure that permanently tracks every individual’s vaccination status from birth.
The dystopian proposal raises far more than privacy and autonomy concerns: it establishes the architecture for government overreach, cross-domain profiling, AI-driven behavioral targeting, conditional access to services, and a globally interoperable surveillance grid tracking individuals from birth.
It also creates unprecedented risks in data security, accountability, and mission creep, enabling a digital control system that reaches into every sector of life.
The proposed system:
To establish the framework, the authors define the program as nothing less than a restructuring of how governments govern:
“Digital transformation is the intentional, systematic implementation of integrated digital applications that change how governments plan, execute, measure and monitor programmes.”
They openly state the purpose:
“This transformation can accelerate progress towards the Immunization agenda 2030, which aims to ensure that everyone, everywhere, at every age, fully benefits from vaccines.”
This is the context for every policy recommendation that follows: a global vaccination compliance system, digitally enforced.
The document describes a system in which a newborn is automatically added to a national digital vaccine-tracking registry the moment their birth is recorded.
“When birth notification triggers the set-up of a personal digital immunization record, health workers know who to vaccinate before the child’s first contact with services.”
They specify that this digital identity contains personal identifiers:
“A newborn whose electronic immunization record is populated with personally identifiable information benefits because health workers can retrieve their records through unique identifiers or demographic details, generate lists of unvaccinated children and remind parents to bring them for vaccination.”
This is automated, cradle-to-grave traceability.
The system also enables surveillance across all locations:
“[W]ith a national electronic immunization record, a child can be followed up anywhere within the country and referred electronically from one health facility to another.”
This is mobility tracking tied to medical compliance.
The document explicitly endorses merging vaccine status with socioeconomic data.
“Registers that record household asset data for social protection programmes enable monitoring of vaccination coverage by socioeconomic status such as household income, ethnicity and religion.”
This is demographic stratification attached to a compliance database.
The WHO acknowledges and encourages systems that require vaccine passes for core civil functions:
“Some countries require proof of vaccination for children to access daycare and education, and evidence of other vaccinations is often required for international travel.”
They then underline why digital formats are preferred:
“Digital records and certificates are traceable and shareable.”
Digital traceability means enforceability.
The authors describe a key rationale:
“Children’s vaccination status is not checked during campaigns, a practice that wastes vaccine on already immune children and exposes them to the risk of adverse events.”
Their solution is automated verification to maximize vaccination throughput.
The digital system is positioned as both a logistical enhancer and a compliance enforcer:
“National electronic immunization records could transform how measles campaigns and supplementary immunization activities are conducted by enabling on-site confirmation of vaccination status.”
The WHO document openly promotes artificial intelligence to shape public behavior:
“AI… demonstrate[s] its utility in identifying and targeting the unreached, identifying critical service bottlenecks, combating misinformation and optimizing task management.”
They explain additional planned uses:
“Additional strategic applications include analysing population-level data, predicting service needs and spread of disease, identifying barriers to immunization, and enhancing nutrition and health status assessments via mobile technology.”
This is predictive analytics paired with influence operations.
The authors call for a unified international data standard:
“Recognize fast healthcare interoperability resources… as the global standard for exchange of health data.”
Translated: vaccine-linked personal identity data must be globally shareable.
They describe the need for “digital public infrastructure”:
“Digital public infrastructure is a foundation and catalyst for the digital transformation of primary health care.”
This is the architecture of a global vaccination-compliance network.
The WHO outlines a surveillance model that activates whenever a child interacts with any health or community service:
“CHWs who identify children during home visits and other community activities can refer them for vaccination through an electronic immunization registry or electronic child health record.”
This means non-clinical community actors participating in vaccination-compliance identification.
The authors also describe cross-service integration:
“Under-vaccinated children can be reached when CHWs and facility-based providers providing other services collaborate and communicate around individual children in the same electronic child health records.”
Every point of contact becomes a checkpoint.
The WHO endorses using digital messaging to overcome “intention–action gaps”:
“Direct communication with parents in the form of alerts, reminders and information helps overcome the intention–action gap.”
They also prescribe digital surveillance of public sentiment:
“Active detection and response to misinformation in social media build trust and demand.”
This is official justification for monitoring and countering speech.
At the very end of the article, the financial architect is stated plainly:
“This work was supported by the Gates Foundation [INV-016137].”
This confirms the alignment with Gates-backed global ID and vaccine-registry initiatives operating through Gavi, the World Bank, UNICEF, and WHO.
In the WHO’s own words:
“Digital transformation is a unique opportunity to address many longstanding challenges in immunization… now is the time for bold, new approaches.”
And:
“Stakeholders… should embrace digital transformation as an enabler for achieving the ambitious Immunization agenda 2030 goals.”
This is a comprehensive proposal for a global digital-identity system, permanently linked to vaccine status, integrated with demographic and socioeconomic data, enforced through AI-driven surveillance, and designed for international interoperability.
It is not speculative, but written in plain language, funded by the Gates Foundation, and published in the World Health Organization’s own journal.
Researchers from the U.S. Centers for Disease Control and Prevention (CDC) and Pfizer Inc. have created new, engineered H5 bird flu influenza genetic constructs, including a codon-optimized hemagglutinin (HA) gene with a synthetically altered cleavage site, as documented in a Saturday npj Vaccines publication.
According to the authors, the stated purpose of the study was to evaluate an mRNA-based H5 vaccine, which they describe as “a nucleoside-modified mRNA construct encoding the full-length, codon-optimized HA protein with the polybasic cleavage site deleted from A/Astrakhan/3212/2020 A(H5N8).”
The paper confirms that the engineered HA used in the study was genetically modified beyond its purported natural form.
The authors state that the cleavage site was synthetically altered, writing that the polybasic amino acids were “mutated from ‘REKRRKR’ to ‘RETR’.”
The cleavage site is like a switch that must be cut to turn the flu pathogen “on” so it can infect cells, and if this site can be cut by many types of enzymes in the body, the virus can spread more and cause worse disease.
The engineered constructs were then formulated into lipid nanoparticles following “the same platform methods used for Pfizer’s COVID-19 and seasonal influenza mRNA vaccines.”
The work was conducted by multiple CDC branches, including the Influenza Division, the Division of High-Consequence Pathogens and Pathology, and the Office of Advanced Molecular Detection.
It was carried out by Pfizer scientists at the company’s Pearl River, NY facility, with additional involvement from ORISE.
The authors specify that “all research involving HPAI A(H5N1) viruses was conducted within Biosafety Level 3 enhanced (BSL-3E) or ABSL-3 facilities at the CDC.”
To test the performance of the engineered constructs, the CDC–Pfizer team conducted live-virus challenge experiments using human-derived H5N1 isolates.
The ferrets were infected with virus formations “A/Chile/25945/2023” and “A/Michigan/90/2024… from a farm worker exposed to infected cattle.”
Using these human isolates, the researchers documented efficient mammal-to-mammal spread, reporting a “100% transmission rate” in unvaccinated ferrets.
The funding disclosures indicate direct federal and corporate sponsorship.
The authors state: “This work was funded by the US Centers for Disease Control and Prevention and by Pfizer Inc.”
The authors also disclose full corporate participation in the scientific process, writing: “Pfizer was involved in the design, analysis, and interpretation of the data in these research studies, the writing of this report, and the decision to publish.”
Additionally, the paper notes that Pfizer researchers associated with the project are “inventors on patent applications relating to influenza mRNA compositions.”
The new study documents that CDC and Pfizer jointly engineered new H5 constructs through codon optimization and cleavage-site mutation, formulated them using Pfizer’s mRNA-LNP platform, and then tested them against recent human H5N1 isolates inside CDC BSL-3E laboratories.
The result is a federally backed, corporate-driven program in which U.S. authorities and Pfizer quietly engineered H5 influenza genetics and tested them with human-infecting H5N1—blurring the line between vaccine development and high-risk pathogen manipulation.
The dangerous experiments raise national security concerns.
In a federally funded experiment conducted by Iowa State University and the USDA Agricultural Research Service, researchers created genetically engineered, chimeric H5N1 influenza viruses using reverse genetics.
They demonstrated that these lab-built viruses possess the ability to bind to the mammary-gland tissue of cattle, pigs, sheep, goats, alpacas, and—critically—to human breast epithelium containing the receptors needed for viral attachment.
The foundation of this study is not observation of natural viruses, but the deliberate engineering of new viral constructs.
Lab-Built Virus #1: Reverse-Engineered H5N1–PR8 Chimera
The team constructed a synthetic H5N1 influenza virus consisting of:
The paper describes it plainly:
“A reverse engineered… H5N1 that contained an engineered low pathogenicity 2.3.4.4b H5… wild type N1, and 6 internal segments from A/Puerto Rico/8/1943 (H1N1)… .”
This is a designed chimeric virus, intentionally altered for experimental use.
Lab-Built Virus #2: Twist-Biosciences HA/NA Recombinant
For replication and confirmation, the team constructed a second engineered H5N1, using:
The paper states:
“These 2 plasmids were then combined with reverse genetic plasmids encoding the 6 internal genes of the laboratory-adapted A/Puerto Rico/8/34 (H1N1).”
The study is fundamentally about manufacturing H5N1 hybrids, not characterizing natural spillover.
Everything that follows is a property of the viruses they created.
These outcomes describe what the engineered constructs were capable of, not what wild H5N1 has proven to do.
The Engineered Viruses Bound to Human Breast Tissue
When the researchers exposed their synthetic H5N1 to human breast sections, the virus demonstrated binding to multiple epithelial regions.
This is possible because human breast ducts and alveoli contain both avian-type (α2,3) and human-adapted (α2,6) influenza receptors, which the engineered virus exploited:
“Human sections of the interlobular duct and secretory alveoli (Ciii, Diii, Giii, and Hiii) showed multifocal to diffuse apical epithelial labeling for both SNA and MAL-II. Teat and gland cistern are uncommon in the human breast.”
Thus, the lab-built virus displayed binding compatibility with human mammary epithelium.
b. The Engineered Viruses Bound to Livestock Mammary Glands Across Species
The engineered H5N1 constructs also bound strongly to:
“The current study showed that the mammary tissues from ruminants (cattle, sheep, and goat) and nonruminants (alpaca, pig, and human) exhibited labeled SA α2,3-gal and SA α2,6-gal receptors along the mammary epithelium, suggesting that both mammalian and avian IAV have the potential to bind.”
The Engineered Viruses Exhibit Mammary Tropism
The results show that the viruses they designed can attach throughout the entire mammary architecture:
The authors explicitly acknowledge implications for infection:
“The mammary gland could serve as an alternative replication site for IAV.”
Again: This is what their lab-built H5N1 is capable of.
The engineered-virus work was funded and executed by:
Funding disclosure:
“This work was also supported in part by the USDA ARS (project number 5030-32000-231-000-D).”
Virus engineering, tissue-binding analysis, and outbreak-response authority sit inside the same federal architecture.
Laboratory-Engineered Mammary Tropism
The ability of an engineered H5N1 construct to bind to human mammary tissue creates direct concerns for:
Engineered Cross-Species Compatibility
The synthetic viruses exhibit mammary binding across multiple agricultural species, suggesting the constructs have broad mammalian attachment potential—a trait with dual-use implications.
The Virus’ Characteristics Are Lab-Derived, Not Naturally Observed
Every feature described in the paper—especially mammary binding—is a trait expressed by the engineered constructs they built.
This distinction is essential for policy and oversight.
This study is not an examination of wild H5N1 behavior.
It is an examination of engineered viral behavior.
The researchers created new chimeric H5N1 viruses using synthetic genetics and a PR8 backbone, and these lab-built constructs showed binding abilities in human breast tissue and the mammary glands of multiple livestock species.
The national-security implications stem directly from these engineered viral traits—not from natural evolution.
fox files 
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