13) Plum Island
as the original outbreak area
(Bosler),
and "contrary to the evidence" (http://www.ncbi.nlm.nih.gov/pubmed?term=20394659[uid]&cmd=DetailsSearch
"Despite the intimate association of B. burgdorferi and I.
scapularis, the population structure, evolutionary history, and
historical biogeography of the pathogen are all contrary to its
arthropod vector")
as "an evolutionary bottleneck."
14)
Staph Enterotoxin Weaponized during WWII
and Cuban Missile Crisis:
http://en.wikipedia.org/wiki/Staphylococcal_Enterotoxin_B
15) John Dunn and/or some other MD at SUNY-SB talking about "the perfect stealth pathogen" (stealth pathogens being a known class of bioweapons):
"It's the perfect stealth
bacteria," says one frustrated
physician. He's talking about Borrelia burgdorferi, the bacterium that causes Lyme disease. This illness, which is often mistaken for diseases ranging from multiple sclerosis to Lupus, can inflict excruciating headaches and muscle pain, affect the brain and nervous system, attack major organs, and inflame joints.
16) Oh, and
Willy Burgdorfer having NIH spooks
show up at his house to monitor the
conversation with the Under Our
Skin team:
"Soon after we turned-off the camera and began packing up our gear, Dr. Burgdorfer told us with a wry smile, 'I didn’t tell you everything.'"
You may
wonder, what is the criminally retarded
CDC hiding-not-very-well?
Dr. Burgdorfer:
"Neurologic manifestations have to be
the next stage of research. Also [Borrelia
burgdorferi’s] antigenicity.
Ecologically,
the diversification of Borrelia
is tremendous. Because of the
spirochete’s ability to change—to change
its physiology, to change its
“antigenic” structure for instance—a
spirochete may be capable of producing
disease or not. And one piece of work
that needs to be done, that has lately
been neglected, is development of the
spirochete—whether it transfers [genes
via] fission, or whether individual
spirochetes have the ability to break
into spheres or particles. We don’t
know yet how they do it but they do.
They go into the lymphocytes, they go
into every tissue. Just because we have
not seen [them], does not mean that they
are not there. Once the immune response
is down, are [they] capable of
re-entering the bloodstream and
producing disease?"
Or be
dessicated and aerosolized, like the
Leptospira that the US Army warns its
soldiers about - "be careful not to
inhale dried animal urine, because it
contains dessicated spirochetes..."
Or, be dessicated and aersolized and
inhaled inhaled like Allen Steere's lab
workers apparently did.
Jus sayin.
Ya'll need to be scared about how
stupid these people are, and
less about the danger of each individual
pathogen.
NIH: "Anthrax is less virulent when
it doesn't behave like like Lyme,
LYMErix, Tuberculosis and MRSA
(immunosuppressive via TLR2-agonism)":
"Lipoprotein biosynthesis by
prolipoprotein diacylglyceryl
transferase is required for efficient
spore germination and full virulence of
Bacillus anthracis." http://www.ncbi.nlm.nih.gov/pubmed/22103323
Needs
lipoproteins like OspA or LYMErix for
efficient spore formation?
Is that
like the US Army reporting that soldiers
should be careful not to inhale
dessicated animal urine because it might
contain leptospira cysts (below snippit)?
Is that like
Allen Steere using the seronegative Lyme
assay to determine that
4/9 of
his lab workers inhaled spirochetes?
Is that like, why Willy Burgdorfer was
emphasizing the granule or cyst form of
the spirochetes in his interview with
the Under Our Skin crew... and an NIH
bioweapons spook from the Rocky Mountain
Bioweapons lab showed up to monitor
the interview?? -
Is that like what was reported about
spirochetes abundantly in the literature
prior (which you can see here, in the
last Chapter of Cryme Disease - because
it should be the first,
The History of
Relapsing Fever) to 1975 when CDC
"officer" Allen Steere bumbled onto the
scene? ...
