The Truth Is Out There

Posts tagged ‘avian-influenza’

U.S. Military Aerosolizes Hantavirus with 30% Fatality Rate in Nebraska: Journal ‘Pathogens’


Pentagon-funded study confirms scientists deliberately created airborne hantavirus particles and carried out stabilization trials to prolong their survival.

The U.S. military has funded research, published in July in the journal Pathogens, in which scientists deliberately aerosolized Sin Nombre virus (SNV)—the hantavirus that kills roughly 30% of those infected—in order to study how long the virus can survive in the air and under what conditions it remains infectious.

Why is the Pentagon commissioning experiments that turn a rodent-borne virus with a 30% kill rate into an airborne particle?

Why are U.S. defense labs probing how to stabilize lethal aerosols?

The study would say it aerosolized hantavirus because “gaining insight into the SNV bioaerosol decay profile is fundamental to the prevention of SNV infections,” but the deeper concern is whether such work risks accidental release or could be harnessed intentionally for pandemic potential.

This new study fits the same disturbing pattern: taxpayer-funded projects that blur the line between “biodefense” and the step-by-step recipe for a future bioweapon.

Dr. Richard Bartlett didn’t mince words as he raised alarm over Pentagon-backed hantavirus aerosol experiments:

“How much longer will We the People tolerate our government using our tax dollars to do deadly experiments in our homeland? Has anyone heard that the COVID pandemic might have been caused by a lab leak? We have no guarantee that another lab leak might happen on our own soil. Remember: Dr. Anthony Fauci and a 2016 NIH-led biosecurity report identified insider leaks as the “most probable” risk in gain-of-function research.”


A Lethal Virus

The authors admit the severity of the pathogen upfront:

“Later symptoms involve respiratory distress that requires immediate medical attention and has a 30% fatality rate.”

In other words, this is not a mild virus.

If contracted, nearly one in three patients will die, and there is no approved treatment or vaccine.

The Pentagon’s Involvement

This wasn’t purely academic work.

The study declares its sponsor:

“This research was funded by the Defense Threat Reduction Agency (DTRA), under grant number DTRA/CBS-NSRI CB1099.”

That means the Pentagon’s weapons division paid for scientists to aerosolize and study the airborne stability of a lethal hantavirus—a clear overlap with bioweapons research.

Aerosolizing a Killer

The researchers describe how they turned the virus into an aerosol:

“Suspensions were aerosolized via a 120 kHz ultrasonic nozzle… with 3 lpm of carrier air.”

Put plainly, they deliberately converted liquid hantavirus into airborne particles small enough to reach deep into human lungs.

This step—aerosolization—is the foundation of making a respiratory bioweapon.

Measuring Airborne Survival

They then tracked how long these particles remained infectious under different conditions:

“At 49.1 ± 0.8% RH, the addition of 1.0 ppm ozone caused a significant increase in the amount of SNV decay at 2.6 ± 0.1 log/min.”

In other words, in normal humidity, the virus survives in the air unless destroyed by ozone.

Sunlight weakened it but did not fully eliminate infectivity.

This proves SNV is stable enough to persist airborne indoors—such as in barns, sheds, or attics—precisely where human infections are known to occur.

Comparison to Other Pandemic Viruses

The researchers themselves compared SNV to avian influenza and Lassa virus:

“This transmission route is similar to other viruses that have an environmental transmission route, such as avian influenza (e.g., H5N1) and Lassa virus.”

This places hantavirus in the same category as pathogens with known pandemic potential.

The implication is clear: if SNV ever adapted to spread person-to-person, as Andes virus already does, the results would be catastrophic.

Particle Sizes Optimized for Lung Infection

The team also measured the size of the particles they created:

“The results indicated a bimodal distribution… with a peak at under a micron in size and a second peak under two microns.”

Translated, these are exactly the particle sizes most dangerous to humans, capable of bypassing upper airways and embedding deep inside the lungs.

Where the Experiments Took Place

The aerosolization experiments were conducted at the University of Nebraska Medical Center (UNMC) in Omaha, Nebraska, using the Biological Aerosol Reaction Chamber (Bio-ARC).

This is a specialized flow-through system designed to expose bioaerosols to controlled conditions such as simulated sunlight, ozone, and humidity.

Institutional Affiliations

The authors are affiliated with the following institutions:

  1. Department of Pathology, Microbiology, and Immunology, University of Nebraska Medical Center (UNMC), Omaha, NE
  2. The Global Center for Health Security, University of Nebraska Medical Center (UNMC), Omaha, NE
  3. National Strategic Research Institute (NSRI), Omaha, NE
  4. Center for Global Health, Department of Internal Medicine, University of New Mexico, Albuquerque, NM

Full List of Scientists

  • Elizabeth A. Klug
  • Danielle N. Rivera
  • Vicki L. Herrera
  • Ashley R. Ravnholdt
  • Daniel N. Ackerman
  • Yangsheng Yu
  • Chunyan Ye
  • Steven B. Bradfute
  • St. Patrick Reid
  • Joshua L. Santarpia

Bottom Line

The Pentagon has funded scientists to take a hantavirus with a 30% fatality rate, aerosolize it into tiny lung-penetrating particles, and measure how long it stays infectious in the air.

This kind of research, while framed as biodefense, is indistinguishable from steps needed to weaponize a virus.

With no vaccine or treatment available, the knowledge produced here doesn’t just help “protect”—it creates a blueprint for how to turn hantavirus into a bioweapon.

U.S. and South Korean Scientists Lab-Engineer Frankenstein Bird Flu Viruses in Georgia: Journal ‘Virology’


Georgia State University is creating pandemic-capable mutant avian influenza pathogens with NIH funding.

This month, the journal Virology published a study confirming that U.S. researchers at Georgia State University and South Korean collaborators from Jeju National University and Sungshin Women’s University are using reverse genetics to create chimeric H5N1 “Frankenstein” bird flu viruses.

The study was supported by the National Institutes of Health (NIH) and National Institute of Allergy and Infectious Diseases (NIAID) grant AI154656.

Researchers combined purported highly pathogenic avian influenza genes with a laboratory H1N1 backbone.

This is not happening in isolation.

It’s unfolding amid international “pandemic preparedness” efforts, where the creation of dangerous bird flu pathogens goes hand-in-hand with the rollout of vaccines as the supposed solution, which no mainstream or non-mainstream sources are warning about—except this website.

It follows the same playbook as COVID-19, which multiple U.S. agencies have said most likely came from a lab incident.

The new bird flu pathogen creation comes as the United Nations has staged its first-ever global bird flu summit, mobilizing 500 officials and scientists to coordinate “control strategies,” surveillance, and vaccination campaigns—confirming that the very governments engineering these Frankenstein viruses are simultaneously organizing the policies and vaccines that will follow.Subscribe


Building Hybrid Pathogens

The paper openly admits to constructing synthetic flu viruses:

“Reverse genetically engineered reassortant H5N1 influenza viruses were generated using hemagglutinin (HA) and neuraminidase genes derived from either A/Vietnam/1203/2004 (Vietnam rgH5N1) or A/Indonesia/05/2005 (Indonesia rgH5N1), with the remaining seven gene segments derived from A/PR/8/34 (H1N1).”

In plain terms: they spliced bird flu proteins from Asian outbreaks onto a lab H1N1 backbone.

That’s a lab-born hybrid that doesn’t exist in nature.

The very definition of engineered pathogen creation.

Inflammatory Collapse

The experiments revealed catastrophic immune reactions:

“Vaccinated AG129 mice demonstrated significantly higher levels of IL-6, IL-1β, the regulatory cytokine IL-10, and the neutrophil-attracting chemokine KC (CXCL-1) compared to vaccinated A129 mice.”

This translates to runaway lung inflammation—a cytokine storm–like collapse that mirrors the reportedly lethal immune overactivation seen in severe flu and COVID cases.

The Authors

Here are all of the authors, some also holding affiliations in South Korea:

  • Ki-Hye Kim
  • Hye Suk Hwang
  • Youri Lee
  • Yu-Jin Jung
  • Eun-Ju Ko
  • Jae Min Song
  • Sang-Moo Kang.

But all of them are affiliated with Georgia State University in Atlanta, which you can contact here.

Bottom Line

The paper proves two damning facts:

  1. Engineered bird flu hybrids were built in a U.S. lab with help from South Korea, using reverse genetics.
  2. These constructs triggered lethal inflammatory outcomes when combined with vaccination.

This is not preparation, but orchestration.

It’s the same pattern we saw before the COVID-19 pandemic, now being repeated with bird flu.

This isn’t isolated “basic science.”

It’s a pipeline: build dangerous pathogens, then promote vaccines as the “solution.”

The COVID-19 pandemic was said to have been caused by this very thing.

U.N. Stages First-Ever ‘Global Dialogue’ for Bird Flu, Mobilizes 500 International ‘Experts and Decision-Makers’ for Pandemic Coordination


Prioritizing “control strategies” for backyard poultry systems, early warning systems, vaccination strategies, and biosecurity measures.

In another unprecedented instance of worldwide bird flu pandemic coordination, the Food and Agriculture Organization of the United Nations (FAO) has mobilized “around 500 experts and decision-makers to galvanize multisectoral collaboration and investment” at a three-day meeting in Foz do Iguaçu, Brazil.

The FAO’s latest move comes as scientists in Brazil’s Butantan Institute recently engineered never-before-seen H5 bird flu pathogens using reverse genetics—chimeric lab-built viruses that never existed in nature, created under the banner of “pandemic vaccine preparedness.”

Led by Secretary-General António Guterres of Portugal, the United Nations is a highly influential body that can shape international laws, economies, and policies, as many critics view its push for centralized global governance as a dangerous step toward eroding national sovereignty.

The U.N. exploited its unprecedented power during the COVID-19 pandemic by endorsing harsh emergency measures that led to widespread human rights abuses, including repression, censorship, and excessive force against vulnerable populations under the guise of crisis control.

As this website has exclusively been reporting, Brazil, the United States, Japan, South Korea, Egypt, and several countries in Europe are all coordinating bird flu gain-of-function research, reverse-genetics experiments, and vaccine development.

Together, these developments show a coordinated global apparatus in which the same governments engineering new bird flu pathogens are simultaneously assembling under the U.N. to dictate the vaccines and policies that will follow.


Unprecedented International Bird Flu Mobilization

For the first time in history, the United Nations has staged a worldwide bird flu summit, bringing together hundreds of handpicked government officials, scientists, corporate executives, and bureaucrats in one room to coordinate pandemic policy.

Just like they did before the COVID-19 outbreak with the infamous “Event 201” exercise, conducted by the Johns Hopkins Center for Health Security in partnership with the World Economic Forum and the Bill and Melinda Gates Foundation.

This is unprecedented.

The U.N. has never before convened this level of global multisectoral coordination on avian influenza.

But it confirms my warning that governments and global institutions aren’t just preparing for pandemics—they’re actively building the infrastructure for them.

While the U.S. is telling the public that it’s about “protecting food security” and “backyard poultry systems,” the deeper reality is clear: the very same governments funding bird flu gain-of-function, reverse genetics, and Frankenstein chimera experiments are now organizing the response framework—and pre-positioning vaccines as the solution.

‘Surveillance, Biosecurity, and Vaccination’

This is pandemic planning.

Beth Bechdol, FAO Deputy Director-General, declared: “Failure is not an option.”

What she did not say is that many of the “solutions” already on the table are vaccine campaigns waiting to be rolled out, designed in lockstep with the engineered crisis itself.

The official agenda is revealing:

  • Targeting backyard poultry systems in low-income countries
  • Building global early warning systems for outbreak detection
  • Expanding vaccination strategies as central to control
  • Hardening biosecurity measures across poultry operations
  • Integrating animal and human health policy under the U.N.’s “One Health” framework
  • Locking in surveillance tools for rapid outbreak response.

Brazil’s Agriculture Minister Carlos Favaro praised his country’s “swift and effective response” to bird flu detection earlier this year, framing it as proof of a “credible sanitary system.”

FAO’s Chief Veterinarian Thanawat Tiensin doubled down on the vaccine-surveillance model, saying: “Improved surveillance, biosecurity, and vaccination when appropriate… are keys to controlling this disease.”

Bottom Line

This was not just another conference.

The U.N. has openly staged a first-of-its-kind global command center for bird flu, aligning governments, corporations, and scientists under one pandemic framework.

While labs around the world continue to manufacture the threat through reckless genetic engineering, the U.N. is setting the stage for mass-coordinated countermeasures—vaccines and surveillance systems—before the next intentional or accidental outbreak even begins.

China Lab Engineers Two New Bird Flu Constructs: One Binds to Host Cells 64x Stronger, the Other Is 100% Lethal in Mammals


Chinese scientists use reverse genetics to build Frankenstein H5N1/H1N1 hybrids inside government-run labs.

In a new study published last month in the journal Virology, Chinese government-linked scientists at the Changchun Institute of Biological Products (Sinopharm) say they have engineered two new H5N1 influenza constructs: a virus-like particle (VLP) that binds to host cells 64 times stronger than controls, and a recombinant chimera virus that killed 100% of mammals (mice) in challenge tests.

In plain terms, China’s Sinopharm lab built one bird flu construct that grabs onto cells 64 times harder, and another that wiped out every single mammal it infected.

The creation of these brand-new viral constructs comes after Congress, the White House, the Department of Energy, the FBI, and the CIA acknowledged that a lab-related incident involving gain-of-function research is most likely the origin of COVID-19, raising concerns that ongoing government experiments like these could trigger another deadly pandemic.

High-risk bird flu experiments are being conducted all over the world as governments invest billions of dollars into bird flu pandemic measures—and no one’s talking about it.Subscribe


Who Did the Work

The study’s lead author is Yongbo Qiao from the Changchun Institute of Biological Products Co., Ltd, Changchun, China, under the State Key Laboratory of Novel Vaccines for Emerging Infectious Diseases, China National Biotec Group Company Limited (Sinopharm), Beijing, China.

Other contributors include Mengru Tang, Mo Du, Chen Zhao, Yuan Lv, Junjun Zhou, Ying Liu, Yutian Wang, Shuang Li, and Yehong Wu.

Construct 1: Virus-Like Particles (VLPs)—64x Stronger Binding

The authors describe how their engineered VLPs displayed dramatically enhanced binding to host cells:

“Functional analysis through hemagglutination assays demonstrated superior RBC binding capacity of HA-VLPs, exhibiting 64-fold higher titers (1:512) compared to HA-Mono (1:8) and HA-T4 (1:32).”

These virus-like particles, built from H5N1 hemagglutinin (HA) and H1N1 matrix protein (M1), bound 64 times more strongly to red blood cells than the HA protein alone.

That is a clear gain-of-function in host binding—the pseudo-virus behaves more like a fully infectious virion, even though it lacks a genome.

Construct 2: Recombinant Chimera Virus—100% Lethal in Mammals

The study also engineered a recombinant chimera virus using reverse genetics: H5N1 HA + NA genes spliced with H1N1 internal genes.

Reverse genetics is a lab technique that lets scientists build purported viruses entirely from cloned DNA, piece by piece, instead of isolating them from nature.

The researchers tested it in mice at 10x LD50 (the dose that kills 50% of test animals):

“All of the mice treated with PBS or HA-Mono died within 8 days post challenge, with considerable body weight loss (over 25%).”

Every mouse infected with this engineered chimera virus died within 8 days.

This shows the construct was 100% lethal in mammals, making it a true Frankenstein hybrid virus created under the banner of “vaccine research.”

Where the Experiments Took Place

The work was carried out at:

  • Changchun Institute of Biological Products Co., Ltd (Sinopharm), Changchun, China
  • State Key Laboratory of Novel Vaccines for Emerging Infectious Diseases, Beijing, China.

Bottom Line

China’s state-run Sinopharm lab engineered two alarming H5N1 constructs:

  • A virus-like particle (VLP) that binds to host cells 64x stronger than controls.
  • A recombinant chimera virus that proved universally lethal in mammals.

Both represent dangerous gain-of-function experiments cloaked as vaccine development.

With H5N1 already carrying a human fatality rate of ~52%, these engineered constructs show how Chinese labs are building Frankenstein viruses with enhanced binding and lethality.

If COVID-19 taught us anything, it’s that weaponizing bird flu in the name of “vaccine research” is a gamble with humanity’s survival—and China’s new Frankenstein constructs prove they’re still rolling the dice.