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Tuesday, May 15, 2007

Millions dead within weeks

I became interested in primate research at the university of Wisconsin in 1997, after learning about some of the research at the Oregon and Washington Regional Primate Research Centers. Since then, I have been a fairly close observer of primate research in the United States.

Among the National Institutes of Health's National Primate Research Centers, Wisconsin stands out for a couple of reasons. Harry Harlow started the lab that bears his name, and he was the first director of the Wisconsin Regional Primate Research Center, which sits next door. (In April 2002, the Regional Primate Research Centers were renamed National Primate Rersearch Centers.) Many people remember Harlow as the scientist associated with the black and white photos of the baby monkeys clinging to a cloth-covered surrogate mother. Harlow was one of the promoters and architects of the country’s current system of publicly funded primate research centers. At Wisconsin, primate research seems homegrown.

Wisconsin’s setting is unique. The other primate centers are shielded from public view. Yerkes, Oregon, California, New England, Tulane, and Southwest are located on large acreages and more or less impossible to see from the road, while Washington presents itself as a single door along one of a labyrinth of hallways in the Magnuson Health Sciences Center (once billed as the largest area under one roof in the world.)

Wisconsin is comprised of two buildings immediately next door to a third monkey lab (Harlow) on the edge of campus. A short street bisects the center; it is sometimes possible to see monkeys being carried between the buildings. At Wisconsin, you can see people working at their desks on the ground floor of one building, although the buildings are otherwise nearly windowless.

All of the centers have closets filled with multiple USDA violations and scandal. But here too, Wisconsin is a stand out. Briefly, they lied in writing repeatedly to the county in regard to their use of protected monkeys at the county zoo; a director was involved in an abusive sex scandal with a graduate student; they paid off a veterinarian to keep quiet about the lack of medical care the monkeys were receiving; USDA inspectors discovered many instances of neglect and lack of oversight. I have detailed these and other unique features of Wisconsin elsewhere.

My observation of the industry has led me to realize that much of what they say publicly is a surreal abstraction of the truth and sometimes has little similarity to reality. I now read anything written by those associated with the Wisconsin animal labs with a skepticism born from their history of lying to the public to protect or promote their own interests.

So I was primed to doubt much in the featured article in the alumni magazine about Yoshiro Kawaoka and his research; especially because he had jut made national news by demonstrating that exposure to the reconstituted previously extinct 1918 Spanish flu quickly leads to an agonizing death in monkeys.

Since I first wrote about seeming contradictions in the article, a letter to the editor appeared in a local paper, and some behind-the-scenes correspondence has taken place between the magazine’s editors and James W. Tracy an official responsible for the university’s select agent program.

Select agents are things like germs or spores that could cause public health problems if they escaped from a laboratory.

In reply to the recent letter to the editor, [Capital Times 5/12/2007] Tracy had this to say:
Dear Editor: Melissa Tedrowe's letter regarding the work of Dr. Yoshihiro Kawaoka contains serious inaccuracies. It misrepresents not only a very important line of research intended to mitigate the effects of potential future flu pandemics, but also the processes and mechanisms in place to oversee work involving serious pathogens such as influenza.

The most serious inaccuracy is the assertion that Dr. Kawaoka's group has been conducting work on campus with live 1918 or Spanish flu virus. Dr. Kawaoka's group has indeed reconstituted the virus, but work with the live, infectious agent has not taken place on the Madison campus. That work was conducted in Canada, in high-level biosafety facilities that do not exist in Wisconsin.

The virus was first reconstituted by researchers at the U.S. Centers for Disease Control in laboratory settings a safety level below the laboratory where Dr. Kawaoka's work was performed. Dr. Kawaoka's experiments, which received considerable international publicity, are critical to understanding the nature of influenza viruses such as the 1918 virus, and insight gleaned from those experiments is already being utilized to help prepare for future flu pandemics, which will inevitably occur.

That the UW-Madison Institutional Biosafety Committee raised questions about Dr. Kawaoka's influenza work simply shows that the oversight process is vigorous and thorough. All such work undergoes scrutiny and must be approved before it is undertaken. We would be concerned if such questions were not raised.

Ms. Tedrowe also implies that the public is somehow uninformed about such work. No doubt the inspiration for her letter was the cover story about Dr. Kawaoka in the winter issues of On Wisconsin, the university's alumni publication. Sharing the important work done by Dr. Kawaoka and his colleagues with 300,000 of our closest friends seems like a good way to make this a part of public conversation.

James W. Tracy, Ph.D., Select Agent Program, University of Wisconsin-Madison
It seems to be true that some experiments with the 1918 Spanish flu were conducted in Canada at a lab with a relatively high level of biosafety and that Kawaoka was associated with them. And, it is true that the experiments received considerable international publicity. And, it is true that an article appeared in On Wisconsin. But on this scaffold of true statements, Tracy has hung a number of misleading claims.

If we were talking about most diseases, this would all be fairly academic; the university’s lies might serve to shine its image, they might serve to deflect public concern over the animals’ suffering, but they would not be putting the public at such a profound risk.

The risk associated with the 1918 Spanish flu is unlike the risks associated with any other infectious agent. Let me repeat that: The risk associated with the 1918 Spanish flu is unlike the risks associated with any other infectious agent.

When the disease first appeared, the United States government was well prepared for an epidemic. Medical experts knew that disease, at that time in history, accounted for more losses during a time of war than did the fighting itself. As the country geared up to fight the Great War, military doctors and public health experts put procedures in place that they felt would be needed when disease broke out, as they knew it would.

When the first cases showed up, quarantine was almost immediate. It is unlikely that such a rapid response would occur today.

By the time people showed any symptoms, they had been infectious for a few days and had already spread the virus. Pre-planned and vigorous quarantine had little affect on the spread of the disease.

John M. Barry, in his book The Great Influenza says:
Although the influenza pandemic stretched over two years, perhaps two-thirds of the deaths occurred in a period of twenty-four weeks, and more than half of those deaths occurred in even less time, from mid-September to early December 1918. Influenza killed more people in a year than the Black Death killed in a century; it killed more people in twenty-four weeks than AIDS has killed in twenty-four years.
Over half of those who died in the 1918 pandemic were in their 20s and 30s, in the prime of their lives, not the elderly.

Keeping in mind the government’s response to hurricane Katrina, it seems unlikely that a response to an outbreak of 1918 Spanish flu would come in time to contain it. Whether we even could contain it, even if we were ready for it, seems like a gamble that only a fool would take.

Estimates of the number of deaths cause by the epidemic vary from 20 to 100 million. This was prior to air travel and among a smaller population. The death toll today could be much higher. Betting it will be lower next time rests on an unwarranted faith in local, state, and world governments' timely and intelligent responses. Some scientists think that the world's population might now have a natural immunity to the virus. Should we test this conjecture?

Government’s wisdom regarding the 1918 Spanish flu is suspect at best. Once the epidemic ran its course, it all but completely disappeared. J. van Aken of the Research Group for Biological Weapons and Arms Control at the University of Hamburg, writes:
Recently, a team of US scientists resurrected a virus that has since been labelled 'perhaps the most effective bioweapons agent now known' (von Bubnoff, 2005). In 1918, a highly virulent strain of influenza virus killed up to 50 million people worldwide. The virus – later dubbed the Spanish Flu – killed more people than any other disease of similar duration in the history of humankind. Until last year, this virus was extinct, preserved only as small DNA fragments in victims buried in Alaskan permafrost, or in tissue specimen of the United States Armed Forces Pathology Institute. Now the full sequence of the Spanish Flu virus has been published (Taubenberger et al., 2005) and the virus itself reconstructed. It proved to be as fatal as the original….[Risks of resurrecting 1918 flu virus outweigh benefits. Heredity. 2007. 98, 1–2; published online 11 October 2006.]

So, with all these encouraging facts before us, look again at James Tracy’s letter. His main assertions are these:

“[W]ork with the live, infectious agent has not taken place on the Madison campus.”

This “work was conducted in Canada, in high-level biosafety facilities that do not exist in Wisconsin.”

The work that took place in Canada was reported in the journal Nature (the journal has been criticized for doing so): Kobasa D, Kawaoka Y. et al. Aberrant innate immune response in lethal infection of macaques with the 1918 influenza virus. Nature. 2007 Jan 18;445(7125):319-23.

But the real question is whether all the experiments leading up to this one were also conducted in the Canadian lab, and what was the nature of those that were conducted at Wisconsin?

In 2004, Kawaoka reported that inserting genes from the 1918 Spanish flu into contemporary flu viruses caused them to become deadly in mice: “these highly virulent recombinant viruses expressing the 1918 viral HA could infect the entire lung and … resulted in infiltration of inflammatory cells and severe haemorrhage, hallmarks of the illness produced during the original pandemic.” [Enhanced virulence of influenza A viruses with the haemagglutinin of the 1918 pandemic virus. Nature. 2004 Oct 7;431(7009):703-7.] This research probably took place in Madison.

The most telling evidence to date is the UW-Madison Institutional Biosafety Committee minutes from November 2, and December 7, 2005. On November 2, the committee reviewed Dr. Kawaoka's planned experiments, which are succinctly described: "Virulence and pathogenicity of the 1918 and reassortant strains will be tested in mice, ferrets, and NHP [nonhuman primates]."

(The minutes cited here are from the Sunshine Project's large archive of biosafety committee minutes from a large number of institutions engaged in research that could be associated with biological weapons.)

The committee minutes of December 7, 2005, indicate that the experiments were approved but stipulated that the lab should pour disinfectant down the floor drains.

Apparently, leading up to his experiments in Canada, Kawaoka was experimenting with various genetically engineered influenza viruses containing various combinations of genes from the reconstituted 1918 original. Along the way, he demonstrated that one of his designer versions was deadly to mice (Nature 2004, above.) He also uses ferrets and monkeys in his lab, as the biosafety committee minutes make clear, yet he published nothing regarding the effect of these genetic constructs on mice, ferrets or monkeys between 2004 and 2007 [Kawaoka Y. et al. Aberrant innate immune response in lethal infection of macaques with the 1918 influenza virus. Nature. 2007 Jan 18;445(7125):319-23.] The Kawaoka lab is incredibly prolific. In the same period, they published at least 45 other virology papers.

At some point between October 2004 and January 2007, he reconstituted the entire virus. It seems unlikely that Kawaoka was working in the Canadian lab for the intervening two years. The probability that much of the research was done somewhere other than in his Wisconsin lab seems low, given the committee’s approval. The anxious desire to build him a new high security lab, explained in the alumni magazine, where he can “safely” continue his research, is cause for serious concern about what is and has been going on in his present lab.

Tracy says that Kawaoka’s work with the 1918 Spanish flu was conducted in Canada because no similarly secure lab exists in Wisconsin. There is no such lab in Wisconsin, but such a lab does exist at the Wisconsin primate center’s sister facility in San Antonio (Southwest) and there are a few others scattered throughout the country.

There is also the problem associated with the university's oversight of research on animals. Tracy was not present at the November 2, or the December 7, 2005 committee meetings. Given the failure of university oversight in the Terasawa affair, there isn't much reason to believe that he is or was fully cognizant of the research taking place on campus.

Tracy makes an outlandish claim at the end of his letter when he says: “Sharing the important work done by Dr. Kawaoka and his colleagues with 300,000 of our closest friends [subscribers to On Wisconsin] seems like a good way to make this a part of public conversation.”

Public conversation about the reconstitution of the 1918 Spanish flu should have occurred prior to Kawaoka being given the go-ahead to do so. (See here, too. And here.) Public conversation should have occurred prior to the university promising to build him a new more secure lab. Telling the public what was done and decided after the fact is just more gross arrogance by university officials who seem to believe that their neighbors are too stupid to notice the spin.

The university is generally loath to entertain much public conversation about matters having to do with its animal experimentation. It is also uninterested in much discussion regarding its research into highly infectious diseases, if the NBAF meetings were a fair measure. In this instance, these two controversies -- hurting animals and conducting controversial and suspect highly dangerous infectious disease experiments -- combine to create a situation that they understandably don't want to address in depth.

Monday, May 14, 2007

Cutting Close to the Bone

Thursday, May 10, 2007

His Holiness the Dalai Lama is a Callous Prick

How else to characterize a guy who proclaims his compassion yet endorses years of repeated cruelty? Turd?

During the lama’s visit to Madison in May 2007, sitting front and center at one of his $100-$150 per person talks was none other than Richard Davidson, closet Buddhist and monkey vivisector.

In spite of years of correspondence and copies of Davidson’s papers being sent to the lama’s office explaining that Davidson injects acid into the emotion centers of monkeys’ brains and then frightens them in various ways, and then kills them and examines their brains to check his various hypotheses, the lama remains steadfast in his support. What a prick.

See too: Does He or Doesn't He?
Group Asks the Dalai Lama to Renounce Support for Animal Cruelty
Richard Davidson
My Enlightening Meeting with Lama Lhundub Sopa
Could You Recognize Evil if It Stared You in the Face? (Will the anti-Christ come wearing a t-shirt saying I'm the anti-Christ?)

NBAF Fiasco Reveals Idiocy of UW Decision-Makers

According to many sources, UW Madison made a colossal blunder when it invited Homeland Security to build the proposed National Bio-and Agro-Defense Facility (NBAF) in the Town of Dunn, Wisconsin. The UW's arrogance is likely to mean the loss of an initial $451 million in development costs, 1000 construction jobs over five years, and 200 to 400 highly paid permanent jobs. According to a study by the University of Georgia’s Carl Vinson Institute of Government, the NBAF would have brought in between $3.5 billion and $6 billion over 20 years. The report says that salaries alone would have reached up to $2.5 billion over the same period.

Though I consider this turn of events a good thing for the health and safety of the region's residents, and am pleased that the massive suffering to animals that the lab will cause will not be happening right down the road, from the perspective of the university and the local economy, the loss is very large and suggests that the university's decision-making abilities are not commensurate with the seriousness of the issues with which it is involved.

On Thursday, April 3, 2007, the Dane County Board of Supervisors voted 19-7 in support of a resolution opposing the University of Wisconsin, Madison’s bid to host the Department of Homeland Security’s proposed gigantic BSL-4 infectious disease lab, the National Bio-and Agro-Defense Facility (NBAF).

The UW had offered Homeland Security a 40 acre site it owns in the Town of Dunn to construct its 500,000 square foot monstrosity.

The Town of Dunn is known locally and nationally for its progressive land-use ethic.

UW’s decision to name the Town of Dunn as the single location in Wisconsin suitable for the lab was pointed out by many supervisors as a major mistake. One of them commented that the Town of Dunn, with its deserved reputation as a leader in agricultural land conservation, was the absolute worse possible location in the state for such a facility, and that the university couldn’t have made a bigger mistaken than choosing the Town of Dunn as its proposed location. Even worse, from statements made by officials from the Town of Dunn, it is crystal clear that the university was told from the very beginning that the town would resist the university’s plans.

So, from the university’s perspective and all the other development-at-any-cost proponents, the UW’s all-the-eggs-in-one-unwilling-basket approach can only be seen at one of the biggest most costly mistakes ever made.

The reasons this matters go well beyond the state’s very large economic loss caused by the UW’s colossal blunder. The mistake should be cause for grave concern. In spite of being told that there was a problem with the Dunn site, the university refused to change course. Even with $6 billion at stake. This should cause one to wonder about the university’s decision-making skills generally.

The decisions of people making a mistake this big should be regarded with suspicion whenever they make claims about the wisdom of the decisions they make or will make. Unfortunately, these same individuals – those who have repeatedly acted as university spokes persons on the matter of the NBAF – also tell the public that their decisions should be trusted when it comes to ways of safeguarding the public from accidental infections from the university’s ongoing research into deadly highly virulent diseases. See When Spin Turns Deadly.

Every month, university oversight committees and officials make decisions about how many animals a researcher can kill, about how much suffering they should allow, about the safeguards needed to protect the public from possible infectious disease escapes, about providing or destroying public records requested by the public, about the level of research oversight needed. None of these cases come with a potential $6 billion loss; it is unlikely that the daily decision-making is considered as important as in the NBAF case.

Is there any reason to doubt that these day-to-day decisions are any wiser than the NBAF blunder?

Tuesday, May 1, 2007

Blinkered anti-science fanaticism

Early this morning, approximately 700 agents of the British government-pharmaceutical complex were involved in the late-night arrests of 30 animal rights activists suspected of having ties to the campaign to close Huntington Life Sciences, sometimes referred to as Stop Huntington Animal Cruelty (SHAC).

Undercover investigations have repeatedly demonstrated severe neglect and cruelty in the Huntington labs. Much information is available on the Internet.

As of May 1, at 10:00 am central time, there were already more than 125 news items available on line. One was the Guardian Unlimited report titled: Animal rights militants losing the war

The part that caught my eye was the comment:
Much of it has been down to the shared resolve of the government and city investors involved in medical research to fight back against what they perceive as blinkered anti-science fanaticism.
Well, I don’t want to be a blinkered anti-science fanatic, so I’ve decided to set morality aside and embrace all things science. And since you dear reader probably don’t want to be a blinkered anti-science fanatic either, let me warn you of a few cases that those despicable blinkered fanatics use to sow doubt about Science:

1. The Nazi doctors.
2. The Tuskegee syphilis experiments.
3. Dr. J. Marion Sims.
4. Unit 731.
5. Project MKULTRA.
6. And all of these important scientific projects.

Repeat after me, all you free-thinkers:

I pledge allegiance to scientists and Science, and to the power and wealth for which they stand, one mind-set, indivisible, with faith and confidence in all.

Sunday, April 29, 2007

One Monkey's Miserable Life

From the Primate Freedom Project website:

rhao45's life remembered by Amy Christenson, his Tag wearer

rhao45 was a male rhesus macaque born August 1, 1988 at the University of Wisconsin.

According to the 60+ pages I received concerning rhao45's life, the first study he was used in was "Early Maternal Separations and Vunerability to later Peer Separation." This lasted from March of 1990 to December 1993.

From April of 1994 to February of 1995, he was involved in a few different studies: these included "Effects of Early Rearing Conditions," "Caloric Restriction and Aging," and "Sweet Taste in Primates." He was used in the breeding colony from 1995 until 1997.

rhao45 then began a lengthy study titled "Skeletal Effects of Therapeutic Anti-Coagulation Administration (Warfarin)." This included daily doses of Warfarin (from January of 1998 to October of 2000), doses of vitamin K to reverse some of the Warfarin's effects, and two separate rib and hip biopsies.

On October 3, 2000, the day after the second surgery, he suffered some trauma to one of the wounds: "area above biopsy site over right hip is missing skin; area does not appear inflamed and no purulent discharge is present; monitor healing process."

October 10, 2000: "open wound over right hip; full skin necrosis; adjacent to but not confluent with bone biopsy site; cleaned with nolvasan and bandaged; cbc tentative diagnosis etiology unknown; inquinal hernia right; plan: repeat nolvasan flush and bandage or indicate healing by secondary intention."

Also, on October 10, he was assigned to the project, "Regulation of Food Intake in Rhesus Monkeys."

October 12, 2000: "area on right hip appears to have produced some purulent discharge; flushed area and applied ointment."

October 17, 2000: "hip wound open...minimal healing progress; old open wound should be cleaned and flushed daily."

October 30, 2000: "hip biospy site resolving without incident; reation near site may have been draining tract, hypersensitivity response to foreign material or chemical burn; no further treatment indicated."

On February 8, 2001 he was subjected to major surgery and had a cannula implanted in the third ventricle of his brain and a headcap affixed to his skull.

A March 14, remark in his records notes: "self-biting left forearm - wounds are dry and appear OK."

On March 21, 2002 he was treated for a draining abscess of his upper right canine tooth, it was noted taht his upper left canine tooth was fractured and that his inguinal hernia should be monitired.

The headcap, and presumably the canula, were removed in April 2002, after 14 months. A remark states that his was the "removal of headcap," but it is coded in his records as procedure "pl-05513 (removal of therapeutic device)."

From April to May of 2003, rhao45 was used in the project "Metabolic Dysfunction in Prenatally Androgenized Male Rhesus." At Wisconsin, an "a" in a monkey's serial number usually means that his or her mother was treated with sex hormones when she was pregnant. Usually, this is testosterone. In female monkeys it can cause severe genital deformities and hormonal disruptions. He was probably one of the monkeys used in this study.

On October 31, 2003, a test was made to see whether he would get along with another monkey, r97088. On November 3rd, a 30 minute test took place, and on the 4th, a 60 minute test. The remark says there was no agression and they they would be placed together ("pair-caged") the next day.

On November 10, 2003, he was involved in a fight with his cage mate and required stitches to his head. It took nearly a month and daily antibiotics to heal.

On May 5, 2004, his life with a companion came to an end. At Wisconsin, all SIV infected monkeys are kept in solitary cages. rhao45 had 100 times the common tissue infective dose of the simian immunodeficiency virus (SIVmac239) injected into his rectum. This was repeated on June 6, and November 21.

His weight declined, he lost his appetite, he developed non-regenerative anemia. Occasional reports noted that he was vomiting.

The remaining record is one of rhao45's decline. Oddly, the veterinary staff continued trying to treat his many illnesses, all to no effect, all the while knowing exactly why he was dying.

On January 19, 2006, it was noted that he was pulling the hair out of his arms and lower back.

He had a recurring intractable bloody nose until he was killed on October 20, 2006. The notes say that the room he was kept in had exceptionally low humidity that may have exacerbated his raw nasal passages.

Comments before his necropy included, "Elevated CK and AST likely from traumatic blood draw. Leukopenia occasional sign in this animal, may be related to SIV infection."

My heart breaks when I think of the life he didn't get to live. I can only hope he's in a better place now.

Amy Christenson
April, 2007
P.S. I am planning to get a tattoo of his ID# next to a rhesus monkey profile.

Wednesday, April 25, 2007

Group Asks the Dalai Lama to Renounce Support for Animal Cruelty

April 23, 2007

Contacts: Rick Bogle 608 222 2348; Jean Barnes, Executive Director, 770 719 5348.

In observance of the 21 st annual World Week for Animals in Laboratories (April 22-28), the Primate Freedom Project has sent an open letter to Tenzin Gyatso, the 14th Dalai Lama for the third time to reconsider his support of invasive experimentation on living animals' brains. See http://www.madisonmonkeys.com/letter_to_dalai_lama.pdf

“We have urged His Holiness to reaffirm his vow of compassion for all sentient beings. He seems to have stepped off Buddhism's Nobel Eightfold Path to enlightenment and is now wandering aimlessly, attracted to the glitter of honorary university degrees. He seems to be more attracted to titles and prestige than to kindness; it's a loss to the entire world,” says Rick Bogle, spokesperson for the group.

Largely unwritten about has been the Tibetan leader's transformation from an icon of kindness into an admirer of scientists like Richard Davidson and Ned Kalin at the University of Wisconsin who burn monkeys' brains with acid and then frighten them with snakes, scientists, and bigger monkeys.

His Holiness the 14th Dalai Lama, Tenzin Gyatso, is both the head of state in exile and the spiritual leader of Tibet.

Buddhism is based on a set of profound teachings that urge us to harm no sentient being, to dispel all the misery in the world, and to recognize that all beings are as precious as our mothers.

-----

Background:

Dalai Lama at UW-Madison: http://www.news.wisc.edu/6205.html

Kalin NH, Shelton SE, Davidson RJ. The role of the central nucleus of the amygdala in mediating fear and anxiety in the primate. J Neurosci. 2004 http://www.jneurosci.org/cgi/content/full/24/24/5506

Kalin NH, Shelton SE, Davidson RJ, Kelley AE. The primate amygdala mediates acute fear but not the behavioral and physiological components of anxious temperament. J Neurosci. 2001 http://www.jneurosci.org/cgi/content/full/21/6/2067

---end---

When Spin Turns Deadly

Local journalists and media have a responsibility to local citizens. They have a responsibilty to investigate and report fairly on issues that could or do affect the community. Issues involving potential risk to members of the community require particular attention, and as the potential increases, so too does their responsibility to investigate and report.

Recently, it has come to light that a scientist at UW, Madison has been involved with research on the most deadly disease yet encountered by humankind, the 1918 Spanish flu. Both daily newspapers in Madison were alerted to a possible significant risk to the community, and yet neither one seems to have followed up.

An unpublished letter to the Wisconsin State Journal regarding the 1918 Spanish flu research on the UW campus:

April 6, 2007

To the editor:

I have read conflicting reports concerning research at the University of Wisconsin, Madison with the Ebola virus and the most deadly disease yet encountered by humanity, the 1918 Spanish flu.

I’ve read that the extinct Spanish flu was revived by Dr. Yoshihiro Kawaoka at the university and subsequently tested on monkeys at a high security biosafety lab in Canada. The reconstituted virus proved to be as deadly as the original. The UW-Madison magazine On Wisconsin’s Winter 2006 cover story says that the university is building Dr. Kawaoka the most expensive lab in the world, per-square-foot, so he doesn’t have to rely on other labs.

But, I’ve also read the UW-Madison’s biosafety committee minutes that gave him permission to test these deadly viruses on monkeys and ferrets here in his current lab about eighteen months ago. Something seems amiss.

Rick Bogle

Note to editor: see http://www.madisonmonkeys.com/biosafety/11-2-05.pdf and http://www.madisonmonkeys.com/biosafety/12-7-05.pdf
A friend wrote a similar letter to the editors of On Wisconsin and recieved a letter in reply from James W. Tracy, PhD, Responsible Official, Select Agent Program, Professor and Associate Dean.

By his title, he is the UW's official overseeing all uses of agents designated by the CDC as requiring high levels of biosecurity. So, he should know what's going on at the university.

But in his letter, he states:
Your impression that Dr. Kawaoka is now or in the past has conducted experiments with the 1918 flu virus on the Madison campus is incorrect. Dr. Kawaoka has indeed worked on campus with genetic constructs, the genes critical to the pathogenic nature of the 1918 virus. These are not live, infectious agents, and therefore cannot cause influenza.
Leaving aside the issue of whether viruses are indeed ever alive, there does seem to be clear evidence that Dr. Tracy is wrong. Consider the abstract from Dr. Kawaoka's 2004 Nature article: “Enhanced virulence of influenza A viruses with the haemagglutinin of the 1918 pandemic virus”:
The 'Spanish' influenza pandemic of 1918-19 was the most devastating outbreak of infectious disease in recorded history. At least 20 million people died from their illness, which was characterized by an unusually severe and rapid clinical course. The complete sequencing of several genes of the 1918 influenza virus has made it possible to study the functions of the proteins encoded by these genes in viruses generated by reverse genetics, a technique that permits the generation of infectious viruses entirely from cloned complementary DNA. Thus, to identify properties of the 1918 pandemic influenza A strain that might be related to its extraordinary virulence, viruses were produced containing the viral haemagglutinin (HA) and neuraminidase (NA) genes of the 1918 strain. The HA of this strain supports the pathogenicity of a mouse-adapted virus in this animal. Here we demonstrate that the HA of the 1918 virus confers enhanced pathogenicity in mice to recent human viruses that are otherwise non-pathogenic in this host. Moreover, these highly virulent recombinant viruses expressing the 1918 viral HA could infect the entire lung and induce high levels of macrophage-derived chemokines and cytokines, which resulted in infiltration of inflammatory cells and severe haemorrhage, hallmarks of the illness produced during the original pandemic.[emphasis added]
Consider too, the minutes of the biosaftey committee in my original letter to the Wisconsin State Journal:

November 2, 2005: http://www.madisonmonkeys.com/biosafety/11-2-05.pdf

"This amendment seeks approval to generate all eight 1918-like genes from published sequence and to reconstruct recombinate viruses containing some or all segments from this strain, and to test these strains in animals.... Virulence and pathogenicity of the 1918 strain and reassortant strains will be tested in mice, ferrets, and monkeys.... Reconstructed 1918 influenza virus is regulated as a select agent and an amendment needs to be submitted and approved by CDC before viable virus may be used here."

A decision on the protocol was tabled pending additional information from Dr. Kawaoka. The committe met again on December 7, 2005: http://www.madisonmonkeys.com/biosafety/12-7-05.pdf

"Personnel receive the annual influenza virus vaccine, which should provide some protection from the 1918 virus.... The protocol was approved."

So what did Dr. Tracy mean when he said: "These are not live, infectious agents"?

Moreover, why wouldn't local media be interested in this story given that this virus killed an estimated 20 to 50 million people in just over a year?

The extra safety precations discussed in the committee minutes seem pretty weak and suggest that disease agents have been regularly washed down the drain without prior treatment.

I'm reminded of media's sleepy acceptance of the promise that Saddam had weapons of mass destruction. It might just come down to the fact that the UW is a major advertising client.

See too: Courting Cash-Tajima-ushi Risks Deadly Return to 1918.

Friday, April 20, 2007

Do Not Put Dead Monkeys in the Freezer



Martín Espada

Monkeys at the laboratory,
monkeys doing countless somersaults
in every cage on the row,
monkeys gobbling Purina Monkey Chow
or Fruit Loops with nervous greedy paws,
monkeys pressing faces
through a grille of steel,
monkeys beating the bars
and showing fang,
monkeys and pink skin
where fur once was,
monkeys with numbers and letters
on bare stomachs,
monkeys clamped and injected, monkeys.

I was a lab coat and rubber gloves
hulking between the cages.
I sprayed down the batter of monkeyshit
coating the bars, fed infant formula in a bottle
to creatures with real fingers,
tested digital thermometers greased
in their asses, and carried boxes of monkeys
to the next experiment.
We gathered the Fear Data, keeping score
as a mechanical head
with blinking red bulbs for eyes
and a siren for a voice
scared monkeys who spun in circles,
chattering instructions
from bewildered brains.

I did not ask for explanations,
even when I saw the sign
taped to the refrigerator that read:
Do Not Put dead Monkeys in the Freezer.
I imagined the doctor who ordered the sign,
the moment when the freezer door
swung open on that face,
and his heart muscle chattered like a monkey.

So I understood
when a monkey leapt from the cage
and bit my thumb through the rubber glove,
leaving a dollop of blood that gleamed
like icing on a cookie.
And I understood when one day, the doctors gone,
a monkey outside the bell curve of the Fear Data
shrieked in revolt, charging
the red-eyed mechanical head
as all the lab coats cheered.



From: Imagine the Angels of Bread. W.W. Norton. 1996.
Reprinted here with the author's permission.

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Martín Espada teaches English at the University of Massachusetts Amherst. He has been called the Pablo Neruda of North American authors. He was a lab worker in the UW monkey labs in 1979-80 or 1980-81.

Thursday, April 19, 2007

Madison Chambers

12 April 2007 - An aerosol chamber mishap at Texas A&M University in February 2006 caused a researcher to be infected with the bioweapons agent brucella. Texas A&M University then violated federal law by not reporting the brucellosis case to the Centers for Disease Control (CDC) and now faces severe penalties. This information has only come to light as a result of persistent Texas Public Information Act requests by the Sunshine Project.
Texas A&M Unversity (Go Aggies!) kept secret this accidental infection of a student worker at a BSL-3 lab for over a year. It wasn't until the watchdog Sunshine Project kept hammering on them that the situation came to light.
What caught my eye was that the accident stemmed from a mishap with something called a Madison Chamber. This faulty product is built and sold by the University of Wisconsin. It goes without saying that it is probably used in labs at the UW like Dr. Yoshihiro Kawaoka's. This news won't help anyone get a good night's sleep. Of course, who in Madison will even hear about this?

The Sunshine Project
News Release
18 April 2005

Faulty Aerosol Chamber Infects Three

NIAID Encourages Use of Leaky Device in Biodefense
Chambers are Located in Nine US States, India, New Zealand, and Northern Ireland

(Austin, 18 April 2005) - A leaky aerosol chamber manufactured by the University of Wisconsin at Madison was responsible for three laboratory-acquired tuberculosis infections in a Seattle BSL-3 lab last year.... The Sunshine Project
Government oversight is such a joke.