Showing posts with label Biological Weapons. Show all posts
Showing posts with label Biological Weapons. Show all posts

Monday, November 10, 2014

U.S. contemplated viral weapons in 1969 by Wayne Madsen




U.S. contemplated viral weapons in 1969


At a hearing on June 9, 1969, the U.S. House of Representatives Subcommittee on Defense Appropriations heard testimony from Pentagon chemical and biological warfare officials calling for the inclusion of funds in the 1970 Defense Appropriations bill for the creation of "a new infective microorganism" that would be invulnerable to human immune systems. Dr. Donald M. MacArthur, the Deputy Director of the Department of Defense's Research and Engineering branch, testified that his efforts to create such a microorganism weapon that could defeat human immune defenses would cost $10 million over a five to ten year period. MacArthur was in charge of 76 Department of Defense laboratories at the time of his testimony.

Some ten years later, the world would be plagued by the Human Immondeficiency Virus (HIV)/A
cquired Immune Deficiency Syndrome (AIDS), which plagued Africa, the gay community, heroin addicts, and hemophiliacs. More, recently, Ebola reached epidemic proportions in West Africa, with the virus being called "AIDS on steroids." The first case of Ebola was recorded in Zaire, now the Democratic Republic of Congo, in 1976.

MacArthur stated, on the record:
"Molecular biology is a field that is advancing very rapidly, and eminent biologists believe that within a period of 5 to 10 years it would be possible to produce a synthetic biological agent, an agent that does not naturally exist and for which no natural immunity could have been acquired."

The official also stated, "Within a period of 5 to 10 years it would probably be possible to make a new infective microorganism which could differ in certain important aspects from any known disease-causing organisms. Most important of these is that it might be refractory to the immunological and therapeutic processes upon which we depend to maintain our relative freedom from infectious disease…. A research program to explore the feasibility of this could be completed in approximately 5 years at a total cost of $10 million."

The program to jointly develop a synthetic microorganism weapon by the Department of Defense and the National Academy of Sciences/National Research Council (NAS/NRC)was postponed over the previous two years because of decreasing funding for the chemical and biological weapons program, "growing criticism" of the program, and a reluctance to involve the civilian NAS and NRC in the project.

MacArthur was joined in providing testimony to the subcommittee by Dr. B. Harris, Deputy Assistant Director for Chemical Technology within the Research and Engineering office; Dr. K. C. Emerson, Acting Deputy Assistant Secretary of the Army for Research and Engineering; Brig. Gen. W. S. Stone, Jr., Director of Materiel Requirement for the Army Materiel Command; and Col. J. J. Osick, Chief of the Systems and Requirements Divsion of the Directorate of Chemical, Biological, Radiological and Nuclear Operations of the office of the Army Assistant Chief of Staff for Force Development.

MacArthur's information was in answer to questions posed by Representative Robert Sikes (D-FL). Sikes represented the Florida panhandle where a number of military bases were located, including Pensacola Naval Air Station, Hurlburt Field, and Eglin Air Force Base. Sikes was known as a corrupt king of pork barrel projects and he was reprimanded in 1976 by the House for owning stock in defense companies that benefited from contracts he earmarked for his district.
  
Was the U.S. Army Medical Research Institute of Infectious Diseases (USAMRIID) at Fort Detrick ground zero for the viral weapons of HIV/AIDS, Ebola, and deadly E-Z measles vaccine?


In addition to HIV/AIDS first being detected in Cuban troops returning from Angola, where they were fighting against Central Intelligence Agency-supported guerrillas, and in Zaire and Sudan in 1976, the Edmonston-Zagreb (E-Z) vaccine for measles administered 
by the World Health Organization in the late 1980s and early 1990s to infants in Guinea, Guinea-Bissau, Senegal, Burkina Faso, Haiti, Vietnam, Mexico, Philippines, Egypt, and Argentina. Infant girls in Africa were given twice the dose as boys and, because their immune systems were suppressed from 6 months to years, many of the female infants died. At the same time, the Centers for Disease Control (CDC) and Kaiser Permanente administered the E-Z vaccine to largely African American and Latino infants in Los Angeles. The parents of the infants in Los Angeles were never told that the measles vaccine was experimental. Dr. David Satcher, the director of the CDC, said, "a mistake was made," adding, "it shocked me." The U.S. military's development of microorganism weapons in the 1970s may have behind Satcher's reaction of shock to such testing programs on unwary individuals in Los Angeles and in Third World countries around the world.

As WMR reported on October 22, 
a leaked December 15, 2009 cable from the U.S. embassy in Berlin to the U.S. State and Defense Departments revealed that German authorities hesitated to permit the transfer of hemorrhagic fever cultures from a German bio-research firm to the suspected biological warfare laboratory at the U.S. Army Medical Research Institute of Infectious Diseases (USAMRIID) in Fort Detrick, Maryland because the Germans feared the Army might "weaponize" the cultures. The German government specifically stated that the ability of Fort Detrick to "create replicating recombinant infectious species" of dangerous hemorrhagic viruses could violate international controls on the export of dangerous weapons of mass destruction that are enforced by the Australia Group of signatories to biological, chemical, and nuclear export treaties.
On October 16, the White House announced that it was cutting off funding to risky government experimentation that studied certain infectious agents by making them more dangerous.







Monday, December 21, 2009

Obama's Bioweapons Program




The Obama administration's recent declaration on bioweapons would simply be another run-of-the-mill example of our "change" president's duplicity were it not such an unmitigated disaster.

Recapitulating sinister Cold War practices that informed American ruling class consensus when it came to secretly toying with nature's most deadly pathogens, (a) because they could, (b) because it was, and is, highly profitable and (c) because they got with it, the profound failure by the administration to rein-in out-of-control corporate grifters, militarists and scientists thirsting after an endless flow of taxpayer dollars, have put us all on a potential glide path towards the abyss.

Since the roll-out of the Obama product-line January 21, on issues ranging from war and peace to economic justice and from civil liberties to healthcare, the "change" team exhibit the same callous disregard for disarmament proposals that characterized their Bushist predecessors in the Oval Office.

Nowhere is this reality so transparently delineated than by the administration's continuing efforts to derail plans to revitalize the moribund Biological Weapons Convention (BWC), rejecting binding verification protocols that would finally give the 1972 treaty teeth.

"Strengthening" the BWC: Killing it with Kindness

From her perch as U.S. Undersecretary of State for Arms Control and International Security, Ellen Tauscher, a former Democratic congresswoman from the San Francisco Bay Area (in other words, a feckless "liberal" who spent her career paying lip-service to the antiwar sentiments of her constituents--and then voting in favor of every blood-soaked imperialist adventure undertaken by the Bush regime) rejected international monitoring of military and pharmaceutical sites that might employ research for illicit purposes, e.g., the fabrication of banned biological weapons.

"The Obama administration will not seek to revive negotiations on a verification protocol to the convention," Tauscher told delegates December 9 at the annual meeting of the States Parties to the Biological Weapons Convention in Geneva.

The position outlined last week by the administration eerily follows in the footsteps of the previous government. In 2001, there was broad support internationally for revitalizing the BWC draft Protocol; a long, circuitous process undertaken back in 1991.

But during these earlier negotiations, the U.S. Pharmaceutical Research and Manufacturers of America (PhRMA) released a position paper opposing the routine inspection of laboratories and other research facilities on the grounds of safeguarding "confidential business information," a position they have reiterated today.

This, along with U.S. Defense Department opposition killed the deal after the American delegation, under instructions from arch neocon John Bolton who then held Tauscher's brief, argued that an international inspections regime would put U.S. "national security" at "risk" by allowing spot checks of suspected U.S. weapons sites.

Revealing a warmer and fuzzier, though no less obstructionist side than blustery Bolton, the Undersecretary mounted a charm offensive in Geneva, touting the National Security Council's (NSC) "National Strategy for Countering Biological Threats" as a major transformation of the U.S. position. It wasn't. Tauscher told delegates: "The United States intends to implement this [NSC] strategy through renewed cooperation and more thorough consultations with our international counterparts in order to prevent the misuse and abuse of science while working together to strengthen health security around the world."

However, not a single word in the 23-page NSC document addresses the vital issue of verification. Indeed, while no-holds-barred inspections of nuclear weapons' facilities undergird international treaties governing the destruction of warheads and missiles, thus ensuring compliance with treaty obligations by states, when it comes to biological weapons the "National Strategy" skirts the question entirely. Why?

While the United States claims that it will "advance policies and practices that establish and reinforce norms against the misuse of the knowledge and capabilities that arise from the life sciences while encouraging their free and open availability for peaceful and beneficial use," a call to "develop and employ complementary and multi-layered systems for influencing, identifying, inhibiting, and interdicting biological threats" does nothing to constrain state or corporate actors from exploiting the life sciences for nefarious ends, to wit, work with dual use select agents that can be diverted into surreptitious weapons' programs.

This is crucial. While the document asserts that America's "relationships with the United Nations, international organizations, foreign governments, and the private sector are critical to the success of our efforts" the fact is, the "private sector" and the secret state's own Defense Department are dead-set against any initiative that give international arms' control monitors access to their facilities.

Claiming that the United States "has carefully reviewed previous efforts to develop a verification protocol," the administration has "determined that a legally binding protocol would not achieve meaningful verification or greater security."

Echoing Tauscher and the NSC's lame reasoning, Barry Kellman, president of the International Security and Biopolicy Institute told The Hill he "agreed," and told the publication "that given the rapid evolution of the biological market, technologies that once could only be made in a laboratory can now be made anywhere, so it would be impossible to verify that a country is holding true to the convention protocols."

Really? Perhaps then, Mr. Kellman would care to enlighten us as to which select agent was used in the first and to date, only, bioterrorist attack of the 21st century, and where pray tell it might have come from.

Editing Out the Secret State: The 2001 Anthrax Attacks

As has generally been accepted by scientific experts and as The Baltimore Sun revealed back in 2001, "for nearly a decade, U.S. Army scientists at Dugway Proving Ground in Utah have made small quantities of weapons-grade anthrax that is virtually identical to the powdery spores used in the [October 2001] mail attacks."

Investigative journalist Scott Shane disclosed that Dugway's Life Sciences Division "made hundreds of kilograms of anthrax for bombs designed to kill enemy troops over hundreds of square miles" during the Cold War.

Indeed, the "extraordinary concentration" of the finely-milled powdered anthrax mailed to the media and members of Congress was "in the range of 1 trillion spores per gram" which "meant that the letter could have contained 200 million times the average dose necessary to kill a person."

Researchers at Northern Arizona University determined that "the genetic fingerprint of the mailed anthrax is indistinguishable from that of the Ames 'reference strain,' which is the strain used most often at Fort Detrick and Dugway, according to a scientist familiar with the genetic work," the Sun reported.

Years later, former Ft. Detrick deputy commander Richard Spertzel told investigative journalists Bob Coen and Eric Nadler that "the material that was in the Daschle/Leahy letter was "1.5 to 3 microns in particle size" and characterized the refinement "as super sophisticated ... phenomenal." When investigators attempted to examine samples under a microscope, "it readily floated off the slides."

In other words, the "genetic fingerprint" and "extraordinary concentration" of the weaponized anthrax used in the attack would require a team of individuals, and not a proverbial "lone nut" to produce a biotoxin possessing such exquisitely lethal characteristics. The inescapable conclusion is that the anthrax used to murder five people, sicken dozens of others and terrorize the rest of us, could only have come from a state program or one operating under contract to a government agency.

Could the deadly biotoxin have been diverted from a U.S. defense facility or corporate lab by a group of "black box" scientists operating under the radar for their own nefarious ends, i.e. strengthening the state's repressive hand within the social-political context of the 9/11 attacks? It is certainly possible and cannot be ruled out.

As I previously reported, Global Security Newswire (GSN) disclosed in June that "a recently completed inventory at a major U.S. Army biodefense facility found nearly 10,000 more vials of potentially lethal pathogens than were known to be stored at the [Ft. Detrick] site."

According to reporter Martin Matishak, the 9,220 samples discovered "included the bacterial agents that cause plague, anthrax and tularemia; Venezuelan, Eastern and Western equine encephalitis viruses; Rift valley fever virus; Junin virus; Ebola virus; and botulinum neurotoxins."

While Ft. Detrick's deputy commander Col. Mark Kortepeter claimed there are "multiple layers of security" and that "a lot of buffers [would] prevent anyone who shouldn't be in the laboratory from getting in in the first place and then preventing them taking something out with them," this dodges the question of whether someone who was authorized to be inside Ft. Detrick or any of the other 400 U.S. facilities that have Biosafety Level-3 or Biosafety Level-4 laboratories, could smuggle out deadly toxic substances.

The New York Times reported December 9, that Tauscher rejects a strict regulatory regimen that would monitor state bioweapons research and development because of the "regulatory burdens that verification would place on the American pharmaceutical industry and on the military's bio-defense research activities."

Given the available facts surrounding the 2001 anthrax terrorist incident and the FBI's subsequent cover-up, Tauscher's fear of "regulatory burdens" on the "pharmaceutical industry" and the state's own "bio-defense research activities" are certainly misplaced and should be viewed with suspicion.

Big Pharma and Congress: Best Friends Forever!

While journalists and researchers have explored ethically-challenged relationships amongst former Defense Department officials and the weapons' industry, most recently by USA Today, and have described the oft-cited revolving door as entrée to an exclusive and highly lucrative good 'ol boys club; call it a Beltway version of a retirement village for Pentagon clock-punchers.

Inquiring minds can't help but wonder: does the same clubby atmosphere pervade, and inform, the policy decisions made by denizens of the Bioweapons-Industrial-Complex? Let's take a look!

Take the Alliance for Biosecurity, a Big Pharma lobby shop aligned with the Center for Biosecurity of the University of Pittsburgh Medical Center (UPMC), as a starting point. Self-described as "a collaboration among the Center for Biosecurity and 13 pharmaceutical and biotechnology companies," one "whose mission is to work in the public interest to improve prevention and treatment of severe infectious diseases--particularly those diseases that present global security challenges," one discovers that similar relationships between academia, industry and government abound.

Since Antifascist Calling first reported on Alliance efforts to increase state funding of biotechnology and "biodefense" research in August, all references to the Alliance for Biosecurity have been scrubbed from UPMC's web site. Indeed, all traces of the lobby shop's activities, including group policy statements and testimony before relevant congressional committees have simply vanished.

But why, pray tell, would they take evasive action in the first place? And more importantly, what do they have to hide? As it turns out, quite a lot.

According to The Washington Times, when the Center for Biosecurity's director, Dr. Tara O'Toole, was nominated for her current post as Undersecretary of Science and Technology at the Department of Homeland Security, she had "served as a key adviser for a lobbying group funded by the pharmaceutical industry that has asked the government to spend more money for anthrax vaccines and biodefense research."

Reporter Tim McElhatton disclosed that O'Toole "never reported her involvement with the lobbying group called the Alliance for Biosecurity in a recent government ethics filing." The Washington Times further reported that the Alliance "has spent more than $500,000 lobbying Congress and federal agencies--including Homeland Security--since 2005, congressional records show."

"In written testimony to Congress" according to McElhatton, "Dr. O'Toole said the alliance was 'created to protect the Center for Biosecurity's status as an honest broker between the biopharma companies and the U.S. government'." As is well known, $500,000 buys much in the way of "honesty" in the halls of Congress!

In an October 31 letter to House Speaker Nancy Pelosi (D-CA) "signed by Dr. O'Toole and two other alliance officials, the group called on Congress to include more than $900 million for the 'advanced development of medical countermeasures' to be administered by the Biomedical Advanced Research and Development Authority."

The Washington Times revealed that the letter was also "signed by the chief executive officer of member company PharmAthene, David Wright, who was one of the two first co-chairmen for the alliance after its creation in 2005."

McElhatton reported that according to a Securities and Exchange Commission filing "Mr. Wright's company has a big financial interest in securing work from the authority," and that "PharmAthene has been trying to win a contract administered by the authority to supply 25 million doses of an anthrax vaccine to the national stockpile."

According to a press release, the firm announced that PharmAthene "will participate in and present data at the HHS Public Health Emergency Medical Countermeasures Enterprise (PHEMCE) workshop and BARDA Industry Day taking place in Washington, DC Dec. 2-4, 2009."

Indeed, the PHEMCE work shop "will bring together public and private sector stakeholders for a dynamic dialogue on the current state of medical countermeasure preparedness, PHEMCE initiatives in the past year, and plans for moving forward to enhance national capabilities to respond to a public health emergency."

When "moving forward" entails the expenditure of nearly one billion dollars for "countermeasure preparedness," one can be sure that companies on the make will be all ears!

Former Bushist Secretary of Health and Human Services, Tommy Thompson, averred that the PHEMCE workshop "is very timely given the WMD Commission's conclusion that terrorists are much more likely to attack America with a biological weapon than a nuclear weapon."

Despite the fact that weapons' experts have not reached a consensus on the Commission's alarmist report, given the extreme difficulty faced by "terrorists" to fabricate biotoxins into an effective weapon, Thompson claims, "now that our national experts have made this warning clear, we need to take the immediate steps necessary to protect against potential biological attacks against the U.S. homeland. In particular, we need to move forward efforts to build and stockpile appropriate biological countermeasures, such as next-generation anthrax vaccines, recombinant influenza vaccines, and novel antivirals."

Among the "experts" consulted by the WMD Commission were none other than Dr. O'Toole's Center for Biosecurity who have called for the expenditure of some $3.4 billion annually on "countermeasure development to reach 90 percent chance of success defending the country against bioterrorism threats."

Nowhere however, in the PharmAthene press release is it disclosed that the former HHS Secretary has a proprietary interest in securing federal dollars allegedly to "enhance national capabilities" to better respond "to a public health emergency." Currently, Thompson is the President of Logistics Health, Inc., a firm that does extensive business with the U.S. Department of Defense for what it euphemistically calls "military readiness."

Craig Holman, the legislative director of the watchdog group Public Citizen, said that O'Toole's lack of transparency "definitely and clearly runs counter to the intent of the law."

What was the response by Senate Democrats, quick to denounce the "culture of corruption" of their coconspirators across the aisle? According to The New York Times, Senate Majority Leader Harry Reid "slammed Republicans for slowing down, and in some cases, blocking the confirmation of nominees for various posts in the Obama administration."

Neither Reid, nor for that matter the Times, breathed a word about O'Toole's obvious conflict of interest and cosy relationships with biodefense firms she would presumably oversee from her perch at DHS.

Instead, we are lavished with empty rhetoric from Reid who told the Times: "'For that position, [DHS Undersecretary] President Obama nominated an expert in combating both pandemics and bioterror attacks,' Mr. Reid said, adding: 'Imagine that: Americans are bracing against a flu epidemic here at home and threats of terrorism from abroad, the President nominated someone highly experienced in both of those areas, and Republicans are saying no'."

Despite revelations of serious ethical breaches, O'Toole was confirmed by the Senate November 4.

The Ties that Bind (And Pay Handsomely!)

The close proximity of O'Toole, the Center for Biosecurity and now, the Department of Homeland Security to Alliance members such as Bavarian Nordic; Cangene Corporation; DOR BioPharma, Inc.; DynPort Vaccine Company LLC; Elusys Therapeutics, Inc.; Emergent BioSolutions; Hematech, Inc.; Human Genome Sciences, Inc.; NanoViricides, Inc.; Pfizer Inc.; PharmAthene; Siga Technologies, Inc.; Unither Virology LLC, , as well as associate Alliance member, the spooky, CIA-connected Battelle Memorial Institute, might just help explain the Obama administration's opposition to strengthening the BWC.

According to the Center for Responsive Politic's OpenSecrets.org database, the Alliance for Biosecurity have contributed some $600,000 to congressional grifters since 2005 through the Philadelphia law firm Drinker, Biddle & Reath.

While chump change when it comes to assuring that the best congresspeople money can buy stay "on-message," OpenSecrets reports that since 1990, Big Pharma and their allies in the health products industry have spent a whopping $177,030,005 on "influence and lobbying." Breaking down the numbers, the watchdog group avers that the bulk of contributions have benefited Republicans ($111,405,078 or 63%) vs. Democrats ($65,056,643 or 37%).

In The Washington Times piece cited above, ethics groups have said that the Alliance's set-up "is an example of what critics call "stealth lobbying," in which like-minded companies form a loosely knit compact and spend lots of money lobbying the government. The arrangement is legal, but it exposes loopholes that prevent the public from finding out how much money each company pays and whether one business exerts more control over the others."

Alliance legal counsel Anita Cicero told the paper, "the group is complying with all applicable federal laws" and that the group "does not generate income, does not have a bank account and does not owe taxes." She told the paper the organization "was formed so companies, academic institutions and the government" could work together to "accelerate the development of therapeutic and vaccine countermeasures."

"Countermeasures" that markedly add to the corporatist bottom line.

As Antifascist Calling previously reported, the National Biodefense Science Board (NBSB), chock-a-block with industry insiders and academic shills, posted an August 11 notice buried in the Federal Register.

Rescued from oblivion by the whistleblowing intelligence and security web site Cryptome, we were informed that NBSB's "Market & Sustainability Work Group" seek to hand over even more cash to industry partners.

Seeking public comment on the group's working document, "Inventory of Issues Constraining or Enabling Industry Involvement in Medical Countermeasure Efforts," NBSB is seeking to further "streamline" the Food and Drug Administration's already lax review process in a move meant to further "incentivize" industry by "increased federal funding for advanced development, in the form of cost-reimbursement contracts and rewarding private-capital investments with milestone payments at procurement."

Under NBSB's proposal, the drug industry stands to grab "reimbursement of development costs + 15%, with return-on-working-capital at 22%, and cost-of-money-for-capital at 15%."

If said corporate patriots swing into action during a national emergency, then "compensation if commercial product(s) during emergencies (e.g., lost sales, market share, delayed licensing" are fully paid by the federal government. Talk about a robust "public-private partnership" in action!

But wait, there's more!

GSN reported in October that Alliance member Human Genome Sciences Inc. had earned $160 million from the federal government for sales of its ABthrax vaccine, despite a Food and Drug Administration report that stated although the product performed better than a placebo (!) "it is still unknown how well these models and results predict efficacy in humans." Despite these equivocal findings, "Washington has placed an order for 65,000 doses of ABthrax for the country's emergency medicines reserve."

Now that's what I call a streamlined review process!

Earlier in October, GSN disclosed that Alliance member Emergent BioSolutions won $4.9 million in funding from the U.S. National Institute of Allergy and Infectious Diseases, a branch of the National Institutes of Health, "for the development of a new anthrax vaccine that could require only two doses to provide protection."

As investigative journalists and filmmakers Bob Coen and Eric Nadler revealed in Anthrax War and a companion book, Dead Silence: Fear and Terror on the Anthrax Trail, Emergent BioSolutions has a very interesting pedigree indeed.

When the State of Michigan auctioned off the Michigan Biological Products Institute (MBPI) in 1998, standing in the wings with a check for $24 million were Lebanese financiers Ibrahim El-Hibri and son Fuad, "an international telecom magnate" according to Coen and Nadler. During this period, the firm the El-Hibri's had founded after scooping-up MBPI for a song, BioPort, "held the exclusive contract to provide the U.S. government with the anthrax vaccine, and that in addition to the physical plant, the Michigan sale included $130 million in contracts with the Department of Defense."

During their investigation, Coen and Nadler learned "that the El-Hibris had participated in the privatization of portions of the United Kingdom's leading biodefense facility, Porton Down, a decade earlier" and that "with the acquisition of the Michigan plant, the family had planted stakes in the only two leading anthrax vaccine producers in the West." What makes this particularly troubling according to Coen and Nadler, is the fact that the "El-Hibri's did not have science backgrounds or biotech business experience before the Porton takeover--but were clearly canny investors."

Alarmingly, "the troubling fact [was] that the sale of MBPI to BioPort had transferred control of a sensitive government program to a network of companies, one of which was headquartered in the Dutch Caribbean."

Indeed, "Fuad El-Hibri himself informed Congress in 1999 that the controlling shareholder in BioPort--Intervac LLC--was partly owned by I and F Holdings NV, a Netherlands Antilles investment company owned by his father."

None of this troubled Congress in the least since, as Coen and Nadler relate "no one on the House Committee on Government Reform asked him if El-Hibri senior had any partners in I and F Holdings." These disturbing facts led the investigative journalists to wonder: "Who actually owned the largest anthrax vaccine manufacturing plant in the West, if not the world? Who really knew."

Fast forward a decade and according to GSN BioPort, now Emergent BioSolutions, "is the producer of BioThrax, the only vaccine licensed by the Food and Drug Administration for the prevention of anthrax disease. The company is also developing other anthrax treatments and countermeasures against diseases such as botulism and hepatitis B." Funds for developing the vaccine were provided "through the American Recovery and Reinvestment Act of 2009."

Last month, GSN revealed that Alliance member, Danish firm Bavarian Nordic will receive some $40 million for a freeze-dried version of the firm's Imvamune vaccine for smallpox. GSN reported that "Bavarian Nordic has received $680 million in contracts for Imvamune from the U.S. government. Washington has ordered 20 million doses of the vaccine in its liquid-frozen form and has the option of buying another 60 million," according to a company press release.

This, despite the fact that smallpox has disappeared as an international public health threat. However as the Sunshine Project's Edward Hammond revealed in Emerging Technologies: Genetic Engineering and Biological Weapons, when a U.S. research team at the State University of New York in Stony Brook synthesized poliovirus "from scratch," the responsible bioresearch community were alarmed.

Hammond commented that "the experiment exemplifies possibilities that generate real problems if similar techniques become applicable to agents such as smallpox. Today it is unlikely (though not completely impossible) that countries apart from Russia and the USA have access to smallpox virus. This is the basis of the current threat assessments with regard to smallpox, which rate the likelihood of a smallpox attack very low. Should it become possible in a few years to build smallpox virus in the laboratory, the situation would be turned upside down. The relative security that can be assumed today (at least for most countries in the world) will evaporate."

Since Hammond's piece first appeared in 2003, is it plausible that synthetic smallpox could have been ginned-up in a top secret U.S. research facility, hence contingency planning by secret state officials to have a freeze-dried, hence longer-lived vaccine on hand? We don't know.

Examining only the three above-named firms, OpenSecrets reports that since 2000, Human Genome Sciences has expended some $24 million since 2002 for lobbying; Emergent BioSolutions has spent some $10.9 on lobbying efforts since 2003, and Bavarian Nordic has spent some $21.7 lobbying Congress since 2002.

Given the enormous outlay of taxpayer largesse to firms that have profited handily under the Project BioShield Act of 2004, a grotesque piece of Bushist legislative flotsam, and the nearly $60 billion dollars reported by the Center for Arms Control and Non-Proliferation spent on so-called biodefense by the federal government, one can only conclude that lobbying activities by Big Pharma is an investment well-spent!

Keep in mind too, that the expenditure of federal dollars for Project BioShield and related programs do not include black budget allocations concealed by the CIA and Pentagon under a welter of above top secret Special Access Programs, a subject that Antifascist Calling will explore in future reports.

Conclusion

As the Sunshine Project's Edward Hammond has warned: "Rapid developments in biotechnology, genetics and genomics pose a variety of environmental, ethical, political, and social questions. And because they open up tremendous new possibilities for biological warfare, these technological developments have grave implications for peace and security."

We must view the Obama administration's cynical opposition to strengthening the Biological Weapons Convention because of the "regulatory burdens that verification would place on the American pharmaceutical industry and on the military's bio-defense research activities" as a dire international public health emergency, one which University of Illinois constitutional law professor Francis Boyle, the author of the 1989 Bioweapons Anti-Terrorism Act, has called "a catastrophe waiting to happen."

We proceed blindly along this path at our own peril.

Tom Burghardt is a researcher and activist based in the San Francisco Bay Area. In addition to publishing in Covert Action Quarterly and Global Research, his articles can be read on Dissident Voice, The Intelligence Daily, Pacific Free Press, Uncommon Thought Journal, Information Clearing House and the whistleblowing website Wikileaks. He is the editor of Police State America: U.S. Military "Civil Disturbance" Planning, distributed by AK Press.

Tuesday, May 12, 2009

SPECIAL REPORT. The history of the synthetic H1N1 flu virus, the resurrection of the 1918 flu virus and a not-so-rosy future

The history of the extraction of the genetic material from the corpses of victims of the 1918 Spanish influenza virus who were buried in Arctic permafrost is part "X-Files" and part "Jurassic Park." After an unsuccessful 1951 mission, that involved U.S. biological warfare specialists, to extract 1918 Spanish flu genetic material in 1951 from a cemetery in the Inupiat Eskimo village of Brevig Mission, Alaska, scientists made another attempt, a successful one it turns out, in 1997. Dr. Johan Hultin, from the State University of Iowa, successfully extracted genetic material from the corpse of an obese thirty-something female who died from the Spanish flu in 1918, along with 85 percent of Brevig Mission's (called Teller Mission in 1918) villagers in a single week. The pandemic killed at least 50 million people around the world.

Once the Spanish flu genetic material was obtained from the lungs, spleen, liver, and heart of the Eskimo woman's corpse, scientists, in a scene reminiscent of the fictional movie "Jurassic Park," in which genetic material from extinct dinosaurs is used to bring the creatures back to life, recreated the long-since dead 1918 Spanish flu in a U.S.-government funded laboratory. The woman's organs were cut into one-inch cubes and shipped to the Armed Forces Institute of Pathology in Rockville, Maryland where the virus's genetic RNA material was identified and the 1918 Spanish flu was successfully brought back to life.

The search for the frozen bodies of 1918 flu victims was not limited to Alaska. Another team of scientists, acting like Dr. Frankenstein's "Igor," set out to dig up the graves of miners who died from the flu in the remote Norwegian mining village of Longyearbyen in Spitsbergen, which lies north of the Arctic Circle.

WMR has learned from a research scientist who has been working on the recreation of the 1918 flu that the genetic material has been re-engineered to synthetically create what is now known as the A/H1N1 virus, or as the Centers for Disease Control (CDC) calls it, the "novel flu."

The A/H1N1 influenza, which contains genetic material from two strains of swine flu, two strains of human flu, and a single strain of avian flu, has, according to the World Health Organization (WHO), infected a total of 4880 people in North America: 2,059 in Mexico; 2,535 in the United States, and 286 in Canada. There have been 56 reported deaths from the flu in Mexico, three in the United States, and one in Canada.

WMR has learned from an A/H1N1 researcher that the current "novel" flu strain is mutating rapidly in humans but no animals have contracted the virus. The enzyme in A/H1N1, as with all influenza A viruses, is called a polymerase. Scientists have calculated the molecular clock of A/H1N1 form the virus's polymerase rate. Because of the rapid mutation of the virus and the fact that, unlike 1918, rapid global transportation is now the norm, scientists are predicting that the molecular clock of the A/H1N1 virus, coupled with modern transportation, means that almost all the countries of the world will experience an A/H1N1 outbreak within the next few months.

What is different about A/H1N1 is that, unlike other new strains of viruses that rapidly mutate upon emerging and then slow down mutation and then stop entirely, the "novel" or incorrectly-named "swine flu" is showing no signs yet of slowing down its mutation rate and that, according to scientists who worry about A/H1N1 being synthetically-generated, does not happen in nature.

In 2006, at a summit meeting in Cancun, Mexico, President George W. Bush, Canadian Prime Minister Stephen Harper, and Mexican President Vicente Fox agreed for their nations to coordinate their response to avian flu, which was spreading in Asia. National Public Radio, on April 2, 2006, ran a segment on how bird flu wreaked havoc in 1918 in Brevig Mission. NPR's Weekend Edition ran a report from Brevig Mission by Lori Townsend of Alaska Public Radio:

"The grave has been opened twice by the same pathologist. In 1951, Johann Hultin convinced village elders to allow him to take tissue samples from bodies buried in permafrost. His lab attempts to map the virus were unsuccessful, but he returned in 1997, and when he did, he was once again given permission to re-open the grave."

WMR has learned from a journalist from Anchorage who covered the 1997 grave exhumation that there was CIA personnel with the team of scientists. Inuit elders of Brevig Mission argued against digging up the graves of the flu victims would release evil spirits. However, money allegedly changed hands between the U.S. government research team and some of the elders, so permission to dig up the graves was granted.

NPR and Alaska Public Radio was reporting what was extracted from the 1918 flu victim's corpse was the H5N1 avian flu virus, but that was erroneous. Or was it? If what was extracted from the dead woman's body in Brevig Mission was used to synthetically create the current A/H1N1 virus, there is a strain of avian flu in the virus. But the current A/H1N1 virus also contains swine and human flu strains.

What has been relayed by the researcher is that the original 1918 virus was the H1N1 virus. In Bio-safety level 3 (BSL-s) laboratory work that was largely classified, the virus was artifically combined with common H3N2 and a minor gene splice from the H5N1 Eurasian avian flu strain.

The avian flu or H5N1 virus that struck Asia in 2006 contained some genetic mutations of the 1918 virus. And scientists researching pandemic flu strains have, since the recreation of the 1918 flu, been playing fast and loose with flu samples. On April, 17, 2005, The Washington Post reported that Meridian Bioscience, which was under contract to the College of American Pathologists, accidentally distributed the pandemic H2N2/Japan flu strain, as part of a flu testing kit, to influenza laboratories around the world. WHO ordered the labs to immediately destroy the flu sample because it was worried about an accidental release of the pandemic virus, resulting in a global health crisis. In 1957, H2N2 killed a million people around the world.

The Post'sarticle, by Wendy Orent, states that scientists were working to create an artificial strain of the 1918 virus: "[Scientists] can combine some 1918 genes either with laboratory strains that have been adapted to grow in mice, which don't normally catch human flu, or with ordinary human flu strains to yield new artificial strains. Then the researcher infects mice with his new strain. Strains using three of the 1918 genes are already known to kill mice."

The same Postarticle quotes Peter B. Jahrling, the chief scientist at the National Institute of Allergy and Infectious Diseases, about the danger of the virus recreation research. Jahrling stated the research was like "looking for a gas leak with a lighted match." The article continues: "What concerns Jahrling and Brown, among others, is that experiments involving 1918 genes are not being carried out under the highest biosafety level, BSL-4. While most of the scientists use what is known as BSL-3 plus, or enhanced, conditions, they do not use space suits, chemical showers or gas-tight cabinets in their work."

Lastly, the article has a stark warning regarding the 1918 flu reconstruction at the military laboratory in Rockville, research led by Dr. Jeffery Taubenberger. The article states: "Even more disturbing is what may happen when Taubenberger publishes the remaining three gene sequences. Then the entire 1918 flu could be built from scratch by anyone, anywhere, who has sufficient resources and skill. It is quite conceivable that resurrected 1918 flu could someday be used as a bioterrorist agent."

In a January 29, 2006, New York Times article by Jamie Shreeve, titled "Why Revive a Deadly Flu Virus?," it is reported that the 1918 flu had been successfully revived. The article states: "In October, a team of scientists, [CDC's Terrence] Tumpey among them, announced that they had recreated the extinct organism from its genetic code -- essentially the scenario played out in the movie ''Jurassic Park,'' albeit on a microbial scale. In the movie, the scientists' self-serving revivification of dinosaurs leads to mayhem and death . . . . How dangerous is the 1918 virus to today's population? Its genetic code is now in public databases, where other researchers can download it to conduct experiments. Scientists from the University of Wisconsin and the National Microbiology Laboratory in Canada have already collaborated to reconstruct the virus from the publicly available sequence. How easy would it be for a bioterrorist to exploit the same information for malevolent ends?"

The article details how the 1918 genetic material was extracted and who worked on the project: "The resurrection of the 1918 influenzavirus was a team effort engaging the resources of the C.D.C. in Atlanta, an obscure military pathology lab outside Washington, D.C., an esteemed group of influenza experts at Mount Sinai School of Medicine in New York and one elderly Swede. Though the story has been told before, it is impossible not to begin with the Swede. In 1950, Johan Hultin, then a 25-year-old graduate student at the University of Iowa, was searching for a Ph.D. topic when he heard a visiting virologist say that the only way to solve the mystery of the 1918 pandemic would be to recover the virus from a victim who had been buried in permafrost."

There has been yet another secretive U.S. government group involved in researching bio-warfare agents like influenza. Known simply as JASON, the group consists of civilian scientists, the top experts in their fields and a number of Nobel laureates, who meet periodically and issue reports, many of which are classified. JASON has been in existence for 40 years and is thought to be a follow-on to the Manhattan Project, the top secret scientific group that created the atomic bomb during World War II. In fact, some of JASON's earliest members helped to design both the atomic and hydrogen bombs. Its first three members were scientists at Los Alamos National Laboratory, the home of the Manhattan Project.

Operating under the aegis of the MITRE Corporation, a federally-funded contracting entity, JASON scientists primarily met in the highly-secured Building 29 at 3550 General Atomics Court in San Diego. The location is the address of the Torrey Pines Institute. Funded by the Defense Advanced Research Projects Agency (DARPA), JASON also has links, according to distribution lists on JASON reports, to the CIA. The CIA maintains an element called the IC [Intelligence Community] JASON Program under the Chief Technical Officer. Traditionally, JASON self-selects its members from a number of academic disciplines. However, JASON almost lost its funding a few years ago, when, after issuing a report critical of the Bush administration's ballistic missile defense program, DARPA attempted to force three new members, obviously political overseers, on to the JASON membership rolls. DARPA's chief Tony Tether pulled funding for JASON, forcing the group for the first time since its inception in 1959 to look for another Pentagon sponsor. The ballistic missile defense program, also called Star Wars II, was a personal pet project of Secretary of Defense Donald Rumsfeld.

JASON survived when DARPA's parent orgzniation, the Pentagon's Directorate for Defense Research and Engineering (DDR&E), provided JASON with direct funding, an indication of the power enjoyed by the secretive JASON organization. JASON also has other federal government sponsors, including the Department of Energy.

JASON is also very much involved in issues of biological warfare. JASON produced a report on Civilian Biodefense in January 2000, which was highly-redacted when released. Even the names of the report's authors and the information on four bio-warfare scenarios is completely blacked out, except for a discussion of a 1947 smallpox incident in Scenario Two. The report also states that the CIA's Clandestine Measurement and Signatures Intelligence (MASINT) Operations Center and Counter-Proliferation Center were interested in biological weapons intelligence collection and signatures. A section of the report on "Managing Civilian Response" to a bio-war attack is also completely redacted, as is a section on domestic intelligence. A page on the anthrax threat references "psychological BW [biological weapons] warfare." The JASON report was completed almost two years before anthrax attacks all but suspended the work of Congress after 9/11 and saw the quick passage of the US Patriot Act.

The JASON report also discusses the mining of medical data, including patient billing records, to find out if a disease outbreak has occurred and how far and what direction it is spreading by examining "spatiotemporal patterns," including "averaging statistics for humans traveling globally."

In fact, the JASON Civilian Biodefense report mirrors, in many respects, the analysis being currently conducted by medical intelligence (MEDINT) agencies around the world on the outbreak and spread of A/H1N1. And that begs the question: is A/H1N1, artificially-developed by U.S. government scientists, the real thing or a test run for something much worse?

---

SIDEBAR:

The Jason report on bio-war discusses "managing civilian response." That also appears be a major concern of the CDC on A/H1N1 at the present time judging from the following internal CDC memo obtained by WMR (note that "swine flu" is being referred to as the "novel H1N1 flu"):

From: CDC Announcements
Sent: Monday, May 11, 2009 10:31 AM
To: CDC All - [REDACTED]
Subject: Public Inquires Regarding Novel H1N1 Flu – CDC-INFO
Public Inquires Regarding Novel H1N1 Flu – CDC-INFO

The CDC National Contact Center, CDC-INFO, is available to assist CDC programs in responding to calls and emails related to the novel H1N1 flu. CDC-INFO maintains current content for phone and email responses; maintains records of calls/emails; collects and analyzes quality assurance and customer satisfaction data; and provides on-demand reports for program partners.

If the general public is contacting you with questions related to the novel H1N1 outbreak, we encourage you to direct those inquires you receive to CDC-INFO. CDC-INFO representatives are available to respond to inquiries 24 hours, 7 days a week via email and phone, in English and Spanish. Emails should be forwarded to cdcinfo@cdc.gov. Telephone inquiries may be routed to 1-800-CDC-INFO (1-800-232-4636).

If you have any questions regarding this email, or for assistance in routing public inquiries, please contact eocjiccdcinfo@cdc.gov.

CDC-INFO’s Novel H1N1 Flu Response

Since April 22, 2009, CDC-INFO has answered more than 29,000 phone and email inquiries from the general public and health care professionals in support of CDC’s novel H1N1 flu response. As of Friday, May 8, 2009, the average hold time for phone calls related to novel H1N1 flu was less than 5 seconds. To date, the states with the highest number of phone inquiries are: California, Texas, New York, Florida, and Georgia.

On Thursday, April 30, 2009, CDC-INFO answered the highest number of inquiries on a single topic in its 4-year history, with 3,127 calls and emails answered related to the novel H1N1 outbreak.

As of May 5, 2009, 75 percent of survey respondents gave CDC-INFO their highest satisfaction rating for the novel H1N1 flu-related services they received.

Supporting CDC’s Mission

The CDC-INFO National Contact Center (1800-CDC-INFO or cdcinfo@cdc.gov) supports CDC’s mission by providing a single trusted source of accurate, timely, consistent, and science-based information for the general public, healthcare providers and public health partners. Information is available on more than 400 CDC health and safety topics, disease prevention, and health promotion information through phone, TTY, and email. CDC-INFO provides critical health information to vulnerable populations, including those without access to CDC’s internet resources or those with low health literacy.

Wednesday, May 06, 2009

More evidence emerges that H1N1 was engineered in "Jurassic Park" bio-labs

Informed sources have revealed to WMR that the H1N1 virus, which the World Health Organization (WHO) has warned could become a global pandemic, was reverse engineered from genetic material obtained from the remains of victims of the deadly 1918 "Spanish flu" influenza pandemic that killed 50 million people worldwide.

WMR has obtained information from biological researchers that the 1918 Spanish flu genetic sequences were "manipulated" in order to effect transmission capability. The current H1N1 virus, called "swine flu," is reportedly a combination of two forms of human flu, two forms of swine flu (North American and Eurasian), and avian or bird flu. There are now reports of species hopping from humans to pigs in Canada.

The scientific name for the current H1N1 virus that was manipulated is "Influenza A virus (strain A/Brevig Mission/1/1918 H1N1)." It is called Brevig Mission because, as WMR previously reported, U.S. Army biological warfare specialists recovered the genetic material from the fairly intact corpse of an Inuit woman who died from the 1918 flu in Brevig Mission, Alaska. WMR has learned that work on manipulation of the Brevig Mission flu strain began in 1997.

Two bio-safety laboratories have been associated with the genetic reverse engineering of not only A-H1N1, the current "swine flu" strain, but also the deadly Ebola virus. They are the University of Wisconsin-Madison and the National Microbiology Laboratory in Winnipeg, Canada. The Associated Press reported on September 20, 2007, that the Madison laboratory was cited for safety violations: "University of Wisconsin-Madison research on the deadly Ebola virus was conducted for a year in a less-secure laboratory than required, until the National Institutes of Health alerted the school to the problem. The deadly virus itself was never present in the laboratory, said Jan Klein, UW-Madison biological safety officer. Instead, DNA copies of the virus were being studied to better understand one of the world's most dangerous pathogens."

The report also stated that the Madison research facility was involved with combining "materials": "Klein said no one was ever at risk, though an infectious virus could have been produced if the research material had been combined with other components. But that was not part of any planned experiment and would not be done by accident,' she said."

The National Institutes of Health (NIH) reportedly shut down the Ebola research at Madison but it was reportedly moved to a Level 4 Bio-Safety Laboratory at the National Microbiology Laboratory at the Canadian Science Center for Human and Animal Health in Winnipeg, Manitoba. In 2007, macaque monkeys were infected with the 1981 flu virus at the Canadian laboratory by some of the same researchers who were involved in the risky Ebola research in Madison.

The research in Madison on Ebola had been conducted in a Bio Safety Level 2 laboratory when it should have been conducted in a Bio Safety Level 4 laboratory, the most stringent for pathogens like Ebola and H1N1. At the time of the safety violations, Madison has less stringent Level 3 labs but no Level 4 labs. In early 2008, Madison again conducted work on Ebola, but in a Level 4 lab.

Science Daily reported the following from Madison on October 7, 2004: "Using a gene resurrected from the virus that caused the 1918 Spanish influenza pandemic, recorded history's most lethal outbreak of infectious disease, scientists have found that a single gene may have been responsible for the devastating virulence of the virus."

The Winnipeg laboratory figures into the November 15, 2001 disappearance of noted Harvard University virologist Dr. Don C. Wiley in Memphis, Tennessee after his attendance at a banquet honoring his service as a scientific advisory board member of St. Jude's Hospital. Wiley's body was found one month later in the Mississippi River in Vidalia, Louisiana. The Shelby County medical examiner ruled Wiley's death a "suicide" from jumping into the Mississippi River from the west bound lane of the I-40 Hernando de Soto bridge. Wiley was heading back to his father's residence in Millington, northeast of Memphis at the time of his disappearance.

This editor reported on the Wiley death extensively at the time. And the Canadian facility became involved in the investigation. From "Mystery in Memphis," published in "Abuse Your Illusions, 2003, edited by Russ Kick: "While the Memphis Police and the FBI continued to handle the Wiley case as just another distraught "jumper" hurling himself 135 feet into the Mississippi River, other law enforcement agencies were not as sanguine.

On November30 [2001], [Memphis Police Sergeant Robert 'Bubba' Shemwell received a call from Detective Paul McKemmie of the National Security Investigation Unit of the Royal Canadian Mounted Police (RCMP) in Ottawa. McKemmie advised Shemwell that his unit was responsible for protecting scientists with Level-3 and Level-4 clearance at the Canadian Science Center for Human and Animal Health in Winnipeg, Manitoba.

The Canadian center houses the National Microbiology Laboratory, where scientists deal with the most dangerous and contagious human and animal pathogens and diseases, which are categorized as Level-4. These include hantavirus, hepatitis, influenza, and hemorrhagic fevers such as the Ebola virus, Marburg virus, and Lassa Fever. In another hghly-protected laboratory, scientists work with Level-3 agents, which include bacteria such as anthrax that, although not contagious, can be transmitted through the air and can cause death or serious illness. The center's tight security is overseen by the RCMP and Canadian Security and Intelligence Service.

McKemmie told Shemwell that someone had posted an email suggesting that Dr. Wiley was not the target for a kidnapping to obtain anthrax but that a scientist working at the Winnipeg laboratory was a more likely target for a kidnapping by bioterrorists.

Nevertheless, the RCMP wanted to know if Memphis hadany information that would indicate that Wiley was the target for an abduction by terrorists. Shockingly, Shemwell fed te RCMP the same line he was feeding the Wiley family and the media: There was no evidence to support the theory that Wiley's disappearance was the result of foul play and that suggestions to the contrary were being mentioned only in the media.

Obviously, not buying Shemwell's line, the Mountie indicated that the RCMP, like the FBI, also would continue to monitor Wiley's disappearance and check out any leads from Canada."

The idea that Wiley's body could have been in the fast-raging Mississippi for a month seems fanciful. When his body was discovered in Louisiana, Wiley's clothing was intact. Recovered from Wiley's clothing were his watch, wedding band, belt, wallet, and even a piece of hard candy that managed not have dissolved after an entire month in water.

Wiley co-wrote a paper on the structures of H5 avian flu and H9 swine flu that was published in the Journal of the National Academy of Sciences in September 18, 2001, just some two months before he went missing in Memphis. However, Wiley's expertise on the 1918 influenza was longstanding. In 1981, Wiley co-wrote a paper, titled "X-ray structures of H5 avian and H9 swine influenza virus hemagglutinins bound to avian and human receptor analogs," that defined the crystal structure of the 1918 influenza virus, a step that made it easier to conduct "forensic" analysis on the origin of precursor viruses and their naturally-occurring or man-made genetic off-shoots.

Although virology, not bacteriology, was Wiley's area of expertise, it was revealed during my investigation of Wiley's death that he had become quite concerned about the mailing of anthrax through the postal system. A week before his disappearance, Wiley attended a session on "Bioethics and Research" at a meeting of the Howard Hughes Medical Institute in Chevy Chase, Maryland. At the time of the conference, four people had already been killed from being exposed to anthrax-laden letters sent through the mail. It was later discovered that the anthrax originated from the U.S. Army Medical Research Institute for Infectious Diseases at Fort Detrick, Maryland.

Wiley had also received a letter from a failed PhD student at University College in Dublin, Ireland that sought to warn him about the origins of anthrax. In October 2001, a series of "white powder" samples were discovered at University College. Irish Army specialists transferred all the samples to Britain's Porton Down bio-warfare facility, the UK's equivalent of Fort Detrick.

Based on Dr. Wiley's expertise in tracking down the origins of viruses and, with his speciality in crystallization of samples, bacteria like anthrax, as well, it is clear that whoever is benefiting from the outbreak of a A-H1N1 flu that has been resurrected and genetically "manipulated" in a "Jurassic Park" laboratory had a very good reason to murder Dr. Wiley and make it appear to be a suicide.

Saturday, April 25, 2009

Swine Flu Kills The Torture Memos By Lori Price

Citizens For Legitimate Government is a multi-partisan activist group established to expose and resist US imperialism, corpora-terrorism, and the New World Order.

Flu Kills The Torture Memos By Lori Price, www.legitgov.org
26 April 2009

In a 'Holy convenience, Batman!' moment, a 'unique' flu virus (one likely concocted in US Army labs) overtakes media coverage of revelations that the highest levels of the US government instructed the CIA (and private contractors) to torture terror suspects.

Scientists said the virus combines genetic material from pigs, birds and humans in a way researchers have not seen before. “We are very, very concerned,” World Health Organization spokesman Thomas Abraham said. “We have what appears to be a novel virus and it has spread from human to human,” he said. “It’s all hands on deck at the moment.”

Guess where the first swine flu outbreak occurred? That's right, Fort Dix, New Jersey, in 1976. Also likely created in a US Army lab. Thirteen soldiers died, leading the US government to force a questionable vaccine on the population -- backed by a legal liability escape clause mandated by and for the pharma-terrorists. Next, people started dying not from the flu -- but from the *vaccine.*

Every major media outlet has reported the fact that US/UK bioterrorists have been manipulating the avian flu virus in university and Army labs. This new flu strain, one that 'no one has ever seen,' contains avian flu. Now, how does *that* happen?

CLG has been covering flu 'oddities' for eight years. See: Flu 'Oddities' and Flu 'Oddities' News Archives.

*****

U.S. denies producing biological weapons from bird flu samples --Media: U.S. denies Indonesia's allegation on bird flu virus 17 Mar 2008 The United States has flatly denied allegations it was producing biological weapons from bird flu samples sent by Indonesia to the World Health Organization, the English daily The Jakarta Post reported Monday. Michael H. Anderson, counselor for Public Affairs at the U.S. Embassy in Indonesia, [has issued the denial]. However, Indonesian senior biodefense researcher Isro Samihardjo said the U.S. could use bird flu virus samples from Indonesia to develop weapons at the Los Alamos Laboratory. Isro was speaking at a meeting about Health Minister Siti Fadilah Supari's newly released book here Saturday. In her book "It's Time for the World to Change, Divine Hands behind Bird Flu," Siti writes of her suspicions about a conspiracy between the U.S. and the WHO.

Experts identify genes for bird flu replication 09 Jul 2008 Scientists have identified around 100 genes that the H5N1 bird flu virus needs in a host in order to replicate, and this finding may help in the hunt for ways to block foment its proliferation.

Army: 3 vials of virus samples missing from Maryland facility 22 Apr 2009 Missing vials of a potentially dangerous virus have prompted an Army investigation into the disappearance from a lab in Maryland. The Army's Criminal Investigation Command agents have been visiting Fort Detrick in Frederick, Maryland, to investigate the disappearance of the vials. The vials contained samples of Venezuelan Equine Encephalitis... In 97 percent of cases, humans with the virus suffer flu-like symptoms, but it can be deadly in about 1 out of 100 cases, according to Caree Vander Linden, a spokeswoman for the U.S. Army Medical Research Institute of Infectious Diseases.

Scientists isolate genes that made 1918 flu lethal 29 Dec 2008 By mixing and matching a contemporary flu virus with the "Spanish flu" -- a virus that killed between 20 and 50 million people 90 years ago in history's most devastating outbreak of infectious disease -- researchers have identified a set of three genes that helped underpin the extraordinary virulence of the 1918 virus. Writing today (Dec. 29) in the Proceedings of the National Academy of Sciences, a team led by University of Wisconsin-Madison virologists Yoshihiro Kawaoka and Tokiko Watanabe identifies genes that gave the 1918 virus the capacity to reproduce in lung tissue, a hallmark of the pathogen that claimed more lives than all the battles of World War I combined.

Venture capital firm set to reap rewards on swine flu 24 Apr 2009 The swine flu outbreak is likely to benefit one of the most prolific and successful venture capital firms in the United States: Kleiner Perkins Caufield & Byers, Thomson Reuters Private Equity Week reported on Friday. Shares of the two public companies in the firm's portfolio of eight Pandemic and Bio Defense companies -- BioCryst Pharmaceuticals and Novavax -- jumped Friday on news that the swine flu killed a reported 60 people in Mexico and has infected people in the United States. The World Health Organization said the [unique] virus appears to be susceptible to Roche's flu drug Tamiflu, also known as oseltamivir, but not to older flu drugs such as amantadine.

Rumsfeld's growing stake in Tamiflu --Defense Secretary, ex-chairman of flu treatment rights holder, sees portfolio value growing. 31 Oct 2005 The prospect of a bird flu outbreak may be panicking people around the globe, but it's proving to be very good news for Defense Secretary Donald Rumsfeld and other politically connected investors in Gilead Sciences, the California biotech company that owns the rights to Tamiflu, the influenza remedy that's now the most-sought after drug in the world. Rumsfeld served as Gilead (Research)'s chairman from 1997 until he joined the Bush administration in 2001, and he still holds a Gilead stake valued at between $5 million and $25 million, according to federal financial disclosures filed by Rumsfeld.

Deadly new flu strain erupts in Mexico, U.S. 24 Apr 2009 A strain of flu never seen before has killed up to 60 people in Mexico and also appeared in the United States, where eight people were infected but recovered, health officials said on Friday. Mexico's government said at least 20 people have died of the flu and it may also be responsible for 40 other deaths. The WHO said the virus appears to be susceptible to Roche AG's flu drug Tamiflu, also known as oseltamivir, but not to older flu drugs such as amantadine. [Lucky Rumsfeld!]

Swine Flu May Be Named Event of International Concern 25 Apr 2009 The World Health Organization is set to declare the deadly swine flu virus outbreak in Mexico and the U.S. a global concern, potentially prompting travel advisories, said a person familiar with the matter. An emergency committee of the WHO in Geneva will declare the outbreak "a public health event of international concern" in a teleconference that began at 4 p.m. today, said the person, who spoke on condition of anonymity because the meeting is confidential.

WHO chief says swine flu has pandemic potential 25 Apr 2009 --WHO emergency committee to advise on changing alert level --All countries urged to be vigilant for unusual cases --Premature to issue travel advisories, WHO head says --Too soon to switch to production of new flu vaccine

WHO worries Mexico flu deaths could mark pandemic 25 Apr 2009 Mexico closed its schools across its capital Friday after at least 16 otherwise healthy people died and more than 900 others fell ill from what could be a new strain of swine flu. The World Health Organization worried that it could mark the start of a flu pandemic.

Outbreak in Mexico, U.S. tied to new swine flu --Source of unique virus a mystery; CDC expects more cases 24 Apr 2009 The unique strain of swine flu found in seven people in California and Texas has been connected to the deadly flu that has broken out in Mexico, killing as many as 61 people. The strain has never been seen before and is raising fears of a possible pandemic across North America. The World Health Organization said the virus that killed at least 12 of the victims in Mexico had the same genetic structure as an outbreak discovered in California. [See: Flu 'Oddities'.]

Navy Experimenting With Flu at Mexican Border --Mexico Shuts Schools Amid Deadly Flu Outbreak 25 Apr 2009 Mexican officials, scrambling to control a swine flu outbreak that has killed at least 16 people and possibly dozens more in recent weeks... The unusual strain this year was noticed, said Dr. Anne Schuchat, director of respiratory diseases the Centers for Disease Control and Prevention, only because the agency was trying out a new diagnostic test at a Navy laboratory and doing more testing than usual through a new Border Infectious Disease Surveillance Project along the Mexican border. [See: The U.S.-Mexico Border Infectious Disease Surveillance Project: Establishing Bi-national Border Surveillance (cdc.gov)]

Possible Swine Flu Outbreak At NYC Prep School --Department of Health Officials Testing 75 Students At St. Francis Preparatory School In Queens 24 Apr 2009 New York City health officials say that about 75 students at a Queens high school have fallen ill with flu-like symptoms and testing is under way to rule out the strain of swine flu that has killed dozens in Mexico. The Health Department's Dr. Don Weiss said Friday that a team of agency doctors and investigators were dispatched to the private St. Francis Preparatory School the previous day after students reported fever, sore throat, cough, aches and pains.

Mexico flu deaths raise fears of global epidemic --Unique virus connected to cases in Calif. and Texas; source still a mystery 24 Apr 2009 Mexico shut down schools, museums, libraries and state-run theaters across its overcrowded capital Friday in hopes of containing a swine flu outbreak that authorities say killed at least 20 people -- and perhaps dozens more. World health authorities worried openly that the strange new virus could become a global epidemic. The U.S. Centers for Disease Control and Prevention said tests show some of the Mexico victims died from the same new strain of swine flu that sickened eight people in Texas and California. Of the 14 samples tested from Mexico, seven were matches, said the CDC's acting director Dr. Richard Besser.

'Laboratory testing showed that the virus does not match any known flu strains.' In California and Texas, 5 New Swine Flu Cases 24 Apr 2009 Government scientists have identified five more people who have been infected with swine flu, apparently confirming suspicions that the unusual strain of the respiratory infection is spreading from person to person, federal health officials said yesterday. Three new cases were found in California and two in Texas, bringing the total number of confirmed cases to seven, officials at the federal Centers for Disease Control and Prevention in Atlanta said... Genetic analysis of the virus indicates it is highly unusual: It is a hybrid that resulted from a [Fort Detrick?] combination of four different viruses.'

Troops Could Be Sent to Border --Under $350M plan, National Guard would be aimed at drug war 24 Apr 2009 The Pentagon and Homeland Security Department are developing contingency plans to send National Guard troops to the U.S.-Mexican border under a $350 million initiative that would expand the U.S. military's role in [fomenting] the drug war, according to Obama administration officials.

In 2002, Military Agency Warned Against 'Torture' --Extreme Duress Could Yield Unreliable Information, It Said 24 Apr 2009 The military agency that provided advice on harsh interrogation techniques for use against terrorism suspects referred to the application of extreme duress as "torture" in a July 2002 document sent to the Pentagon's chief lawyer and warned that it would produce "unreliable information." "The unintended consequence of a U.S. policy that provides for the torture of prisoners is that it could be used by our adversaries as justification for the torture of captured U.S. personnel," says the document, an unsigned two-page attachment to a memo by the military's Joint Personnel Recovery Agency. Parts of the attachment, obtained in full by The Washington Post, were quoted in a Senate report on harsh interrogation released this week. [Oops! Looks like the PentaPost will have to stop calling torture 'enhanced interrogation techniques' because the Pentagon itself calls torture torture. --LRP]

Memo From the Joint Personnel Recovery Agency 24 Apr 2009

Cheney Requests Release of 2 CIA Reports on Interrogations 25 Apr 2009 Former vice president [sic] Richard B. Cheney is asking for the release of two CIA reports in his bid to marshal evidence that coercive interrogation tactics such as waterboarding helped thwart terrorist plots, according to documents released yesterday by the National Archives and Records Administration.

UK High Court demands U.S. torture documents 22 Apr 2009 The chief justice of the British High Court on Wednesday gave the British government one week to obtain the U.S. release of classified information about the alleged torture of a British resident [Binyam Mohamed] who'd been detained at the U.S. military prison in Guantanamo Bay, Cuba. The court indicated that it would issue its own order if the government doesn't respond or justify why continued secrecy is warranted.

*****