Note: 25K microcephaly cases in the US, why? Brazil has less than 300 confirmed cases out of the dubious 4000 claimed cases.
Will W.H.O. declare the US an affected pandemic region in relation to microcephaly of unknown cause?
Hint to CDC and WHO: Vaccine induced damage, GMO crop consumption, glyphosates, pesticides
WHO director general, Margaret Chan called Zika an “extraordinary event” that needed a coordinated response.
“I am now declaring that the recent cluster of microcephaly and other neurological abnormalities reported in Latin America following a similar cluster in French Polynesia in 2014 constitutes a public health emergency of international concern.”
Note: We have several opposing views concerning the cause of microcephaly in Brazil.
1) Zika virus or some other viral fragment carried by Aedes Egypti mosquitoes
2) Pollutants like glyphosate and other pesticides
3) Mandated vaccines during pregnancy, in Brazil TDAP.
WHO Director-general, Margaret Chan has decided on the zika virus as the causal agent in the cases of microcephaly in Brazil.
Their solution? Expedite GMO vaccine and diagnostics research.
27 January 2016
Prof Scott Weaver
Director Institute for Human Infections and Immunity
Dr Shannan Rossie
Uni of Texas Medical Branch
Prof Nikos Vasilakis
Centre for Biodefence and Emerging Infectious Disease
Reporter: James Cook
Scott Weaver: Last Year when it reached Brazil, it really exploded when it reached the Americas, infecting probably a couple of million people at this point
James Cook: and should people we be frightened, especially pregnant women?
Scott Weaver: Absolutely, if you know, if I had a daughter of child bearing age, she was planning a spring break vacation to the carribean, next few months I would strongly urge her not to go there at this point
Note: Prof Scott Weaver is emphatic that Zika is a threat to pregnant women however he said child bearing age was a concern if he had a daughter. Scott Weaver is either a liar or has information on the link between Zika and microcephaly.
Zika is in Africa and the Pacific, so would he be concerned about travelling to those areas? Why not? Is the strain of Zika in Brazil different to those in Africa and Asia-pacific? Oh, the carrier is different possibly, the strain of Aedes egypti, does that have any bearing on the transmission of Zika?
Prof Scott Weaver has no problems with his hypothetical daughter travelling to Zika infested Africa but is concernied with the strain of zika and the strain of mosquito in the carribean?
I was inclined to write off both Prof Scott Weaver and his Galvaston colleague Prof Nikos Vasilakis as liars for not providing the evidence for their assertions. Show us the causal link that gives you the certainty that Zika is linked to microcephaly.
This blogger and others could not understand why they rushed to assert a link without entertaining other possiblities namely vaccines given during pregnancy, pollutants, the impact of malnoutrition or the GM Aedes Egypti mosquitoes themselves.
Then it dawned on me, an unpalatable possibility, they both know that zika passes the placental barrier and impacts fetal brain development. These virologists are amongt a few people that deal with viruses routinely. They would know what type of arbovirus could defeat the placental barrier, they would know what strain of mosquito would be a carrier. Prof Weavers adamant refusal to let his hypohetical daughter visit the carribean starts to make sense. It is also evidence that cannot be shared wihout further questions arising. It also explains why Vasilakis and Rossie were interested in placental fluids on their visit in Dec 2015.
I hope I am wrong. That these f@#king psycopaths would collect viruses, engineer and release them to see the effects is difficult to accept.
Have a look at psycopath Scott C. Weaver’s “encephalitis papers on PubMed. Scotty has been on this topic for 10 years at least. Straight from the horses mouth:
Direct broad-range detection of alphaviruses in mosquito extracts.
“Members of the genus Alphavirus are a diverse group of principally mosquito-borne RNA viruses. There are at least 29 species and many more subtypes of alphaviruses and some are considered potential bioweapons“
Senegalese researchers who helped contain the Ebola epidemic in West Africa are training Brazilians on how to tackle the Zika virus. They have brought along a mobile lab which quickly detects the virus.
Senegalese researcher Amadou Alpha Sall brought with him to Brazil a small team and a lab which fits into a bag. He wants to help Brazilians defeat the current epidemic of mosquito-borne Zika
The head of the Senegalese team believes that the most efficient way to control the epidemic is to quickly identify and isolate infected patients. Zanotto agrees: “People think controlling a vector means killing the mosquito. But controlling a vector means controlling a person in the viremic stage, because it is the patient who infects the mosquito. Once infected, the patient himself turns into a repository for the virus.”
Zika originated in Africa (note: it was extracted from a monkey). But until 2007, it infected only monkeys and didn’t harm humans. Scientists believe that the virus adapted (note: synthetic virologists tinkered) as it spread throughout the continents, becoming more dangerous for humans.
Speculative potential strains/variants:
- Zika virus (original 1947)
- Zika virus (cases 2007)
- Zika virus (French Polynesia 2013)
- Zika virus (Brazil 2015)
Note: Thanks to a post on WRH, posting this for archival purposes. Of interest is the depositor, Rockefeller Foundation. Interesting, Bill and Melinda Gates Foundation (BMGF) share the same interest in viruses and their manipulation. An interest in continuing the rockefeller allopathic eugenicists policies.
Zika virus search link on ATCC Site
Zika virus (ATCC® VR-84™)
ATCC® Number: VR-84™
Classification: Flaviviridae, Flavivirus
Strain: MR 766 (Original)
Product Format: freeze-dried
Biosafety Level: 2
Source: Blood from experimental forest sentinel rhesus monkey, Uganda, 1947
Effect on Host: Paralysis and death
If a small nation state engineers an insect common to a target (enemy) state and releases it within the boundaries of its target country, is that an act of war?
If a DIY synthetic biologists, tinkers with midges, mosquitoes or any biting insect which then inflicts harm on fellow citizens, is he directly culpable?
If a corporation engineers an insect and releases it within a town, is it liable for any resultant harm or injury?
If a nation state in partnership with a corporation releases a “synthetic” mosquito into your neighbourhood that causes harm, are they both liable?
Oxitec/Intrexon are at the forefront of what is a very cheap means of biowarfare or eugenics. The technology is within the reach of time rich and well funded individuals.
Nation states, corporations, individuals creating synthetic insects to design and the consequent mistakes or deliberate actions that will ensure is a reality.
How will the statists or corporate pirates hide their mistakes? If the mistake occurs in the target country, its a release 1.0 build, let us try release 1.1. It will be better.
It is now openly stated and documented by the existence of the field of synthetic virologists and biologists that bacteria, viruses and insects can be made to order.
Acknowledging this fact, what is a community not inclined to use this technology offensively to do? Reactive biological surveillance and analysis?
How do you deal with funded foundations linked to vaccines, gene editing Editas, Glyphosate Monsanto and now GM mosquitoes Oxitec?
A supranational body like WHO is beholden to its sponsers, so in the case of a “pandemic”, what objectives will WHO and linked supra-national bodies achieve? Objectives compliant with their sponsors, no?
What will be the solution? More DNA engineering with viruses and insects. Vaccines and GM research will be the corporate cry.
A country finds itself in the midst of a strange, new, “emerging” disease. It does not have the capability to sequence the offending virus, bacteria or insect, so accepts whatever assistance supra-national and external governments provide. That naivete and lack of independent analysis means even an overt attack will not be seen as an act of war or subjugation, merely a pandemic requiring external assistance.
Synthetic insects, synthetic viruses are a fact. Like any weapon it can be used offensively or defensively but here is the huge problem with the synthetic life technocrats – can you really use synthetic insects in a defensive way? Once released you relinquish control. You have no way to predict the outcome. Even offensively, it is a short term tactic with unknown long term effects for the initiator or its target.
The technology is now routine, its offensive impact has yet to sink in…its defensive usefulness is questionable.
ADVISE TO STATISTS: Start spending some of your public health budget on DNA monitoring/sequencing of your local ecology, pronto! You can then prove an “emerging” pandemic as a foreign introduction.
Here’s the Company That’s the Closest to developing a Zika Vaccine
by Laura Lorenzetti January 28, 2016, 5:37 PM E
[Full article copied for archival purposes, is informational and non-commercial]
The Zika virus has spread rapidly across the Americas, arriving in Brazil last May and creeping into 22 other countries and territories around the region. The virus’ spread has been accompanied by a steep increase in babies born with abnormally small heads and in cases of Guillain-Barre syndrome, an uncommon nervous system disease. This has raised the alarm among public health officials around the world—and launched the quest for a vaccine that could stop its spread.
The U.S. and international governments are pushing forward with programs for Zika vaccines, and at least three pharmaceutical companies are either considering or actively pursing programs, including giants GlaxoSmithKlineGSK, and Sanofi SNY. But the company that appears to be the farthest along is a relatively small $500 million market cap biotech named Inovio Pharmacuetucals INO. Wall Street has shown interest in the company. Inovio’s stock was up about 8% today on news that it is entering clinical trials with its MERS vaccine, which could also hold promise for a future Zika vaccine.
Nonetheless, even Inovio is likely a ways off from developing a human Zika vaccine.
“It is important to understand that we will not have a widely available, safe, and effective Zika vaccine this year, and probably not even in the next few years,” Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases (NIAID), said in a press conference.
The advantage of Zika vaccine programs is that they can use similar mosquito-based diseases, part of a family called flaviviruses, like dengue, West Nile virus, and chikungunya as a “jumping off” point. While researchers are currently trying to learn more about the basics of the Zika virus and its effects on the human body given how new the disease is, they can already use past vaccine development platforms from other flaviviruses as a foundation since they spread in similar ways.
NIAID is already working on two approaches: a DNA-based vaccine, similar to a strategy used for West Nile virus, which has been found safe and effective in a phase one trial. It is also working on a more traditional killed virus-vaccine, similar to those already developed to prevent dengue.
Traditional killed-virus(?) vaccines, also called live-attenuated vaccines, are what most of us are used to. They are grown in eggs using live viruses, and then made inactive by a chemical process, and are the basis for the vast majority of vaccines we take as children and annually to prevent the flu. They are time intensive to develop, typically requiring between 10 and 15 years before they are approved, according to GlaxoSmithKline.
DNA-based vaccines, on the other hand, can reduce that development time by creating a synthetic DNA sequence in a lab that can trigger the human body to create the same antigens as from a killed virus. This cuts development time since it doesn’t need to grow a live virus, which can have unpredictable development pathways.
Inovio Pharmaceuticals has also been working on a DNA-based vaccine for Zika since December. In that time, Inovio has created a DNA strand that can potentially prevent the virus, using its knowledge from its dengue virus program. It is now testing the vaccine in mice and plans to move into testing primates “in the next few weeks,” said Inovio CEO J. Joseph Kim. Once its safety is confirmed, the vaccine will move into phase one testing in humans—as soon as the end of 2016.
“The beauty of this technological platform is that the vaccine is simply a DNA sequence developed in water,” said Kim. “It cuts through all the difficult handling and complex development times of traditional vaccine approaches.”
Inovio has taken this same approach with an Ebola vaccine, going from “bench to clinic”—researcher terms, meaning from initial creation to human testing—in just over 18 months. That program attracted the interest of the U.S. Defense Advanced Research Projects Agency (DARPA), which gave the company $45 million to support the program’s ongoing development. The biotech is also working on a DNA-based vaccine for MERS, which has gone from its creation in a lab to a phase one trial at Walter Reed Army Institute of Research in just over a year.
Still, while animal applications of these preventatives have been approved in animals, DNA-based vaccines are one of the latest medical advancements, and one has yet to be approved for use in humans in the U.S. Even though Inovio has attracted fans on Wall Street, it still has a lot to prove.
Note: Open declaration that the synthetic virologists can and will create viruses or virus fragments to pollute, contaminate your sovereign earthly vehicle for profit!
Don’t forget in the US they are indemnified against lawsuits. They are protected from any harm or damage that their synthetic DNA vaccines cause. A BIG MORAL HAZARD.
THERE IS AN ERROR IN THE VACCINE/SHRUNKEN BABY BRAIN REPORT THAT MUST BE FIXED
They are now fronting brain damage caused by a newly formulated Tdap vaccine as a “Zika virus outbreak”. Problem: The Zika virus, which has been known about for 70 years, has never done anything to babies while the mother was pregnant. Zika results in a mild cold and is all over the world now doing nothing to anyone with a mortality rate of ZERO.
QUESTION: why did it suddenly blow the brains out of thousands of babies in ONE LOCATION – Brazil in the past two months alone when ZERO reported cases of this outcome have ever been recorded prior?
ANSWER: Because a new Tdap vaccine, which was spawned to destroy babies before they were born rather than after birth (due to the new awareness that autism is caused by intentionally destructive vaccines) was launched in Brazil in May of 2015. Gates&Cohorts now need a scapegoat to pin the damage on, and “ZIKA” sounded spooky enough.
In late 2014, the Ministry of Health of Brazil announced the introduction of the Tdap (Tetanus, diphtheria, and acellular pertussis) vaccine for all pregnant women in that country as part of its routine vaccination program. The move was aimed at trying to contain the resurgence of pertussis in Brazil
“Unsurprisingly, the Brazilian government announced on January 15, 2016 it will direct funds to a biomedical research center (Sao Paulo-based Butantan Institute) to help develop a vaccine against Zika. Development of the vaccine is expected to take 3-5 years. Again, no consideration to the irony that you may be developing a vaccine to address a problem that may have been CAUSED by a vaccine, and that that new vaccine may COMPOUND the problem No consideration to the possibility that the answer to the problem may not be to do MORE, but rather to do LESS (simply STOP giving Tdcap to pregnant women).”
Note: We have two things worth noting, GM mosquito trials and the use of a new TDAP vaccine in Brazil. The medical records of the affected babies and their mothers will show directly the causal link between TDAP vaccines and microcephaly. If all the mothers of the affected babies had the new TDAP vaccine, we have a direct causal link and can discount “Zika” virus.
Zika is being used to justify further research by the synthetic biologists – Oxitec/Brazil – and birth control – do NOT get pregant during the “Zika pandemic”.
“Biology is largely about the manipulation, maintenance and transport of DNA.
Oligonucleotide synthesis is too complex and tiresome to make genomes by hand
Technical feasability has been proven by already existing commercial technologies, as well as next-generation platforms from academia.
Material costs of these devices – under $5,000. Traditional synthesizers could be built cheaper.
Mail-order DNA synthesis companies have constructed a shared “harmful sequences” database.”
The Applied Biosystems 3400 DNA Synthesizer is a versatile, four-column,
benchtop instrument designed for 40-nmol, 200-nmol, and 1-μmol synthesis
scales. Simultaneous synthesis and cleavage of four oligonucleotides (25-
mer at 40- or 200-nmol scales) requires approximately four hours
DNA Purity and Quality Established phosphoramidite chemistry
produces DNA that is pure and chemically authentic. The instrument routinely
synthesizes oligonucleotides with average coupling yields > 98% as measured by
HPLC analysis. A simple desalting of crude deprotected oligonucleotides is adequate for most applications
Applied Biosystems 394 DNA/RNA Synthesizer
The Applied BioSystems 394 DNA/RNA Synthesizer, automates all steps of single stranded oligonucleotide synthesis. When used as a system including Applied Biosystems reagents and columns, these instruments produce the highest quality synthetic DNA currently attainable while minimizing synthesis time and cost.
Applied Biosystems 394 DNA/RNA Synthesizer
ABI 3400 DNA/ RNA Synthesizer
Applied Biosystems 3400 DNA / RNA Synthesizer
The Applied Biosystems 3400 DNA Synthesizer is a fully programmable instrument that provides four-column simultaneous synthesis, and features automatic base dilution and analysis of coupling efficiency. Fast cycle times, online cleavage, and proven phosphoramidite chemistry result in exceptionally pure oligonucleotides. Versatile, dependable, and easy to use, the 3400 synthesizer is a compact, bench-top instrument designed for 40 nmol, 200 nmol, and 1 µmol synthesis scales. Simultaneous synthesis and cleavage of four oligonucleotides (25- mer at 40- or 200-nmol scales) requires approximately four hours.
Note: The technology is very CHEAP for a nation state or corporation. The above models can be bought for under $50K. There are DIY efforts to make this even cheaper, think along the lines of 3D-printing. This clearly shows the routine competency regarding DNA/RNA synthesis and tinkering.