NIH's Anthony Fauci Confirms the Phage-Vectoring Plum Island Method of Bioweapons Production

To: kathleen.sebelius@hhs.gov, francis.collins@nih.hhs.gov, margaret.hamburg@fda.hhs.gov, dwhelan@forbes.com, carol@drcarolgoodheart.com, lPickering@cdc.gov, Durland.fish@yale.edu, Aag1@columbia.edu, gary_wormser@nymc.edu, scientificintegrity@ostp.gov, pkrugman@princeton.edu, Stanley.fish@fiu.edu, margaret.hamburg@hhs.fds.gov, emcsweegan@niaid.nih.gov, afauci@niaid.nih.gov, SpinLyme@yahoogroups.com, kshepard@calea.org, fitzmas@gmail.com, patrick.fitzgerald@usdoj.gov, modelt1918@sbcglobal.net, jdrazen@nejm.org, letters@courant.com, Jgerberding@cdc.gov, michael.cole@ct.gov, conndcj@po.state.ct.us, executive-editor@nytimes.com, managing-editor@nytimes.com, news-tips@nytimes.com, bizday@nytimes.com, foreign@nytimes.com, national@nytimes.com, dvbid@cdc.gov, brigidcallahan@optonline.net, trvl@hotmail.com, illinoislyme@aol.com, jlender@courant.com, tinajgarcia@yahoo.com, jhornberger@fff.org, thomas.carson@usdoj.gov, thomas.ryan@ct.gov, kurtzh@washpost.com, georgewill@washpost.com, pj@allegorypress.com, commissioner.dcf@po.state.ct.us, bransfield@comcast.net, vtsherr@comcast.net, oca@po.state.ct.us, freethinker@charter.net, scott.murphy@po.state.ct.us, governor.rell@po.state.ct.us, attorney.general@ct.gov, randall.samborn@usdoj.gov, Robert.shiller@yale.edu, editor@greenwich-post.com, harold.koh@yale.edu, sedmonds@nswbc.org, rrmcgovern@aol.com, frich@nytimes.com, saint.michael@sbcglobal.net

Cc: francam@ucia.gov, dr-ahmadinejad@president.ir, eugenerobinson@washpost.com, bmiller@newstimes.com, trvl@hotmail.com, rastro18@aol.com, billcurryct@gmail.com, amcguigan@rms-law.com, rjmurzyn@aol.com, paulcraigroberts@yahoo.com, criminal.division@usdoj.gov, karla.dobinski@usdoj.gov, christopher.christie@usdoj.gov, richard.Levin@yale.edu, harold.koh@yale.edu, james.phillips@yale.edu, inquire@aldf.com, lyme@idsociety.org, meganmcardle@theatlantic.com

"Guidelines also forbade certain experiments, including the cloning of recombinant DNA derived from highly pathogenic organisms."

http://www.jsonline.com/features/health/scientists-agree-to-60day-pause-in-controversial-bird-flu-research-gg3snj1-137807753.html

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And that prohibition on Plum Island-like experiments was because of "Lyme Disease," where virulence factors were added to Relapsing Fever to make Lyme the deadliest of all spirochetal diseases.

"Lyme Disease" wasn't first discovered and reported in 1975. That was only the year Dr. Bumble Steere arrived on the scene. Polly Murray had for years tried to get someone in some health department to look into the epidemic she discovered in Lyme, Connecticut.

It was observed prior to 1975 when Mr. Violin-Player who likes to hide in his high-security freezer with his imaginary T cell culprits arrived on the scene:
http://www.actionlyme.org/STEERE_FAIRY_UNSTALKED.htm
(BTW, that ^^ was a deliberately fraudulent article by David
Grann of the New York Times. I met with and spoke with
Grann for at least 20 minutes in the Albany legislative
building in May 2001, which was a few months after I explained
the very same Dearborn crime to the FDA Vaccine Committee in person
that I described to Grann, in person:
http://www.actionlymw.org/DICKSON_FDA_SUBMISSION_FULL.htm )

The mechanisms of addition of virulence factors is within
mini-Frankenstein laboratories (tick guts) within "tick
nurseries" (a term we learned from UNSCOM, which they reported
they were looking for in Iraq in the 1990, a good 2 years before
the 9/11 stunt).

That is, where ticks - being hosts to multiple pathogens
and pathogens with their own pathogens, called bacteriophages,
laterally transfer DNA from one organism to another.

Once transferred and successfully adopted by the recipient
bioweapon, we call them "plasmids."

Here is Willy Burgdorfer on the subject of how the
Relapsing Fever spirochetes acquired the Fungal or
Brucellar OspA antigen on Plum Island:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC217620/?tool=pubmed

"Bacteriophage in the Ixodes dammini spirochete, etiological agent of Lyme disease.
S F Hayes, W Burgdorfer, and A G Barbour
This article has been cited by other articles in PMC.
"AbstractA bacteriophage with a B-3 morphology was detected by electron microscopy in a spirochete isolated from the tick Ixodes dammini. It has a 40- to 50-nm elongated head and a tail 50 to 70 nm in length. It appears devoid of collars or kite-tail structure. The spirochete has been identified as the causative agent of Lyme disease."

Willy wondered, being an expert on Relapsing
Fever spirochetes, How did Relapsing Fever
organisms adapt to HARD BODIED TICKS, when
previously they only lived in soft-bodied
Ornithodorus ticks??

OspA helped :))

You can see on my homepage:
http://www.actionlyme.org
Update 1: CDC says the pandemic swine flu is the Don Wiley H9N5 (Danish scientists say "BS" to American "medicine.")

In other ▲ words, the NIH would like the Danes to be quiet about how to create the swine flu from ferret-pharming, when the CDC already published exactly how it is done (Jan 5, 2012), LOL!!

AND, this seems to be the same H9N5 conformation that the murdered Don Wiley described as the pandemic strain.

So, we believe Don Wiley.

*** What you do to make a pandemic flu is: pharm the virus back and forth between ferrets and pigs.

*** This is the ▲ Plum Island method of "vector-pathogen competence studies" and how Relapsing Fever adapted to the local hard-bodied ticks giving us "Lyme Disease." OspA-added was probably from contaminated ticks - ticks contaminated with spiroplasma or mycoplasma.
http://www.actionlyme.org/PIIB.htm

The DNA was bacteriophage-vectored. Then, the sea birds who traveled by Plum Island brought us the ticks, since the cows and other livestock were kept outside on Plum Island... and the rest was the typical Yale-distorted history.

Update 3, Michael Osterholm: http://www.cidrap.umn.edu/cidrap/content/influenza/avianflu/news/jan1712leader.html ◄ I don't care. I am publishing the method. It's already been published by the CDC, Don Wiley and from what we know goes on at Plum Island.

***To create a pandemic, one should infect the intermediate host animals with several viruses, including the human strains of influenza. This increases the likelihood that the genes will be shared or mutate. Best to add a fungal infection to the flu-infected animals which will allow the greater proliferation of viruses (as is what happens with Lyme/OspA and Epstein-Barr) and varieties of viruses due to LYMErix-Disease (immunosuppression). This was why using ticks was such a great idea. Contaminated ticks add the extra step where the mix of infections get an extra chance to mutate and exchange genetic material (through bacteriophages) before pharming back into the animal hosts.***

Here is an example of DNA-sharing among LYMErix-covered biofilms:

Ability of Candida albicans mutants to induce Staphylococcus aureus vancomycin resistance during polymicrobial biofilm formation

'The fungal infection C. albicans being hidden by/covered in Alan Barbour's and Yale's immunosuppressing fake OspA vaccine, ImmuLyme, and LYMErix which is the TLR2 agonist makeup of the biofilm...

The Candida share the antibiotic-resistance genes with Staph aureus,... how?
http://www.ncbi.nlm.nih.gov/pubmed?term=%28%22bacteriophages%22%5BMeSH%20Terms%5D%20OR%20%22bacteriophages%22%5BAll%20Fields%5D%20OR%20%22bacteriophage%22%5BAll%20Fields%5D%29%20AND%20%28%22drug%20resistance%2C%20microbial%22%5BMeSH%20Terms%5D%20OR%20%28%22drug%22%5BAll%20Fields%5D%20AND%20%22resistance%22%5BAll%20Fields%5D%20AND%20%22microbial%22%5BAll%20Fields%5D%29%20OR%20%22microbial%20drug%20resistance%22%5BAll%20Fields%5D%20OR%20%28%22antibiotic%22%5BAll%20Fields%5D%20AND%20%22resistance%22%5BAll%20Fields%5D%29%20OR%20%22antibiotic%20resistance%22%5BAll%20Fields%5D%29&cmd=DetailsSearch

See? You're learning the Plum Island method of creating out-of-control pandemics!!

OspA is very sticky. It sticks to itself. See the graphics below about the HIV-LYMErix molecule. In that HIV-Pam3Cys-LYMErix report you will see that OspA sticks to itself, which was why the Western Blots in the LYMErix vaccinated people were unreadable. The Western Blots were smudged in the OspA vaccine trials (there were 2 OspA vaccine trials), so the criminal IDSA gang lied about those Western Blot results.

And ▲ there you have the results of Yale torturing Lyme victims instead of treating us. We were forced to look into exactly what else they were lying about, besides persistence. This is how Yale's perverted lying shit boomerangs. Now the whole world knows all their tricks. There are no secrets.

The thing is out and out of control. They shouldn't have tortured their already-sick victims. Payback. There WILL be payback. This is a Guarantee.

=====================================================

120121:

So, we know how to create a pandemic anything, thanks
to what was done on Plum Island. Use ticks, and use
swine flu, and especially, fungally-suppress the human-
analog host.

This is approximately what happened in 1918. It is
alleged that swine and bird flu occured together in pigs.
When you have an immunosuppressed animal, anything can
happen with its coinfections and dormant viral
infections. (Pig tissue is more like human tissue
than any other mammal's.)

In the case of pandemic MRSA, as we have seen, the
vaccine didn't work because TLR2 agonists (lipoproteins)
suppress the immune system. We also learned from the MRSA
vaccine patent, that:

"Several established vaccines consist of live attenuated organisms where ***the risk of reversion to the virulent wild-type strain exists. In particular in immunocompromised hosts this can be a live threatening scenario.*** Alternatively, vaccines are administered as a combination of pathogen-derived antigens together with compounds that induce or enhance immune responses against these antigens (these compounds are commonly termed adjuvant), since these subunit vaccines on their own are generally not effective."
http://patft.uspto.gov/netacgi/nph-Parser?Sect1=PTO1&Sect2=HITOFF&d=PALL&p=1&u=%2Fnetahtml%2FPTO%2Fsrchnum.htm&r=1&f=G&l=50&s1=7,771,728.PN.&OS=PN/7,771,728&RS=PN/7,771,728

We learned that this was the reason for the
pandemic of vaccine brain damaged children:
This is the ^^^ "Mumps without the Lumps, the Measles
without the Spots,"... the Post-natal instead of
Prenatal Rubella-induced "autism" (the reason
for the Rubella vaccine in the first place).

The CDC also previously reported that immunosuppressed
children should not get live attenuated virus vaccines:

Measles, Mumps, and Rubella -- Vaccine Use and Strategies for Elimination of Measles, Rubella, and Congenital Rubella Syndrome and Control of Mumps: Recommendations of the Advisory Committee on Immunization Practices (ACIP) http://www.cdc.gov/mmwr/preview/mmwrhtml/00053391.htm

"Updated information on adverse events and contraindications, particularly for persons with severe HIV infection, persons with a history of egg allergy or gelatin allergy, persons with a history of thrombocytopenia, and persons receiving steroid therapy." [are immunosuppressed- KMD]

And we knew quite a bit about immunosuppression and activated
viruses from "Lyme Disease," where OspA is immunosuppressive
and the disease we ended up with seems to activated Epstein-Barr,
Cytomegalovirus, HHV-6 ... all the herpesviruses, all of which
become stealth due to general immunosuppression and tolerance...

- - -

"Lyme Disease" is a ruse. A misnomer.

It technically is Brucellar-Relapsing Fever.

Or Fungal-Relapsing Fever.

Or Spiroplasma-Relapsing Fever.

Or Epstein-Borreliosis because of OspA's and
http://www.actionlyme.org/101016.htm
Epstein-Barr's independent capacity to
inhibit the autokill kinases and their
combined ability to mess with mitochondrial
membranes and its function.

See:
http://www.actionlyme.org
at the bottom for the reports linked from
within the chart.

===================

So, we learned all about bioweapons thru the
abuse of Lyme victims. As far as the flu
pandemic, we know Don Wiley was bumped off
in the same way as the Plum Island mycoplasma
(infertility in cows) Iraqi scientist was
murdered.
http://www.ncbi.nlm.nih.gov/sites/entrez?Db=pubmed&Cmd=DetailsSearch&Term=Al-Aubaidi+jm[Author

Al-Aubaidi.

Wiley claimed:
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC58807/
In contrast, the H9 swine and H3 human virus HAs recognize the cis conformation of the α2,6 and α2,3 glycosidic linkage, where the linkage carbon atoms of Gal-2 C6 in LSTc and Gal-2 C3 in LSTa and the Gal-2 ring of LSTa make nonpolar contacts with Leu-226 (Fig. (Fig.2 2 e and f and figure 2 in ref. 19) and the glycosidic oxygen points toward solution. *** α2,6 apparently is favored by the H9 swine HA (Fig. (Fig.33f) because only sialic acid and Gal-2 of the oligosaccharide are detected interacting with the HA in the α2,3 pentasaccharide sialoside complex (Fig. (Fig.33e). The width of avian virus-binding sites is narrower than the swine and human HA sites, which appears to optimize contacts with the preferred sialoside linkages. ***The H9 swine HA with Leu-226/Gly-228 may represent an evolutionary intermediate (33), with a binding site not yet as optimal for human cells as the human 1968 H3 site (Fig. (Fig.44).***

==================================

And the CDC claimed, 10 years later, that
they agree with Don Wiley's predicted
pandemic - at least, pandemic swine/human
intermediate:

http://www.ncbi.nlm.nih.gov/pubmed?term=22056389

Virology. 2012 Jan 5;422(1):105-13. Epub 2011 Nov 5.
In vitro evolution of H5N1 avian influenza virus toward human-type receptor specificity.
Chen LM, Blixt O, Stevens J, Lipatov AS, Davis CT, Collins BE, Cox NJ, Paulson JC, Donis RO.
SourceInfluenza Division, Centers for Disease Control and Prevention, Atlanta, GA 30333, United States.

Abstract
Acquisition of α2-6 sialoside receptor specificity by α2-3 specific highly-pathogenic avian influenza viruses (H5N1) is thought to be a prerequisite for efficient transmission in humans. By in vitro selection for binding α2-6 sialosides, we identified four variant viruses with amino acid substitutions in the hemagglutinin (S227N, D187G, E190G, and Q196R) that revealed modestly increased α2-6 and minimally decreased α2-3 binding by glycan array analysis. However, a mutant virus combining Q196R with mutations from previous pandemic viruses (Q226L and G228S) revealed predominantly α2-6 binding. Unlike the wild type H5N1, this mutant virus was transmitted by direct contact in the ferret model although not by airborne respiratory droplets. However, a reassortant virus with the mutant hemagglutinin, a human N2 neuraminidase and internal genes from an H5N1 virus was partially transmitted via respiratory droplets. The complex changes required for airborne transmissibility in ferrets suggest that extensive evolution is needed for H5N1 transmissibility in humans.

Published by Elsevier Inc.

=====================

So, that's how to do it.

Best to have a mini-lab with-in-a-lab like "tick
nurseries."

Then you get whatever.

A Pandora's Box of Trojan Horses.

-- - -

The USA is not a human-rights protecting or defending
nation, so to side with any USA/Globalist Diktats
is to be complicit in genocides and the rampant and
epidemic acts of extreme terrorism.

Think of Lyme activists as the Von Stauffenberg
Committee: We're disabled, but we will still
deploy INFORMATION BOMBS in the form of
unanswered complaints to the powers-that-be
like this one.

Then I repost to an outside news site where
the world can watch Uncle Sam's non-response.

It's great.

The best credibility America lends to an American
scientist is to either kill them or trash their
reputation.

KMKDickson
http://www.actionlyme.org