New Findings For Bee Colony Collapse Disorder (CCD) To Be Presented at World Vaccine Congress in Washington March 24-26 Increase in Concentration of Newly Identified Replikin Beetoxingene Preceded Current CCD Outbreaks; Beetoxingene Sequences are CCD Blocker and Vaccine Candidates
LONDON, March 21, 2014 /PRNewswire/ -- Bee Colony Collapse Disorder (CCD) is increasing with unknown cause(s). There is no effective treatment or prevention of CCD. Increasing loss of bee colonies since 2005 is resulting in the loss of bee pollination which poses a threat to food production worldwide.
Bioradar UK Ltd. announced today that the principal organisms associated to date with Colony Collapse Disorder (CCD) in bees, all have increased concentrations of a structure in their genes, which the Replikins scientists have named Beetoxingene™. These CCD genes are related to the specific Replikin gene sequence structures previously described in which relate to infectivity and lethality (1-8).
In the present study, Bioradar software was used to analyze annually all the gene sequence data available on PubMed data bases, independently for Replikins in each organism for which there is evidence of involvement in CCD in all pre-outbreak years available and in the years of the current CCD outbreaks 2005-2013. The genes of organisms such as Varroa Destructor mite, Nosema Cerenae fungus, and bee viruses including Sackbrood, Israeli, and Kashmir strains, were each independently found to have increased Replikin Counts, Beetoxingene Counts, at p<0.001 at the same times as the lethal CCD pandemic was occuring. The highest Counts, up to over 10, were found in the genes of the bees themselves.
Most important, the increases in the bees and in each of the associated organisms was found to occur at the same times. Annual mean Beetoxingene Counts (number per 100 amino acids) pre-outbreak, before CCD, in each of the organisms and in the bees were usually approximately 2. Increases and peaks of Counts were observed during the CCD pandemic years both preceding and at the height of CCD attacks (see Figure). The results in the Figure also show a correlation in time between two cycles of independent peak Counts in the two organisms, Varroa Destructor and Sackbrood virus as well as in the bee gene.
The Beetoxingenes may increase independently in each organism and in the bees, and the associated organisms of the CCD simply may be multiple independent hosts and carriers of lethal Beetoxingenes. Alternately, the Beetoxingenes may be transferred from the individual organisms to the genes of the bee. The Beetoxingene Counts in individual organisms may not be sufficient to kill the individual organism, permitting each to function as a carrier to the ultimate host, the bee, where the cumulative Counts reach double or triple that of each individual organism (see Figure), and where the cumulative doses kill the bee.
Increase in Replikin and Beetoxingene Counts has been found to be related to lethality, and Replikins blockers and vaccines have been shown to act effectively against Replikins disorders. However, all of Koch's Postulates for causality have not yet been fulfilled, and increased Beetoxingene Counts do not alone exclude other as yet unidentified CCD pathogens which carry Replikins in their genes.
These findings are the basis of specific solid phase synthetic Anti-Beetoxingene Blockers™ and Vaccines against CCD in bees like those found effective against H5N1 influenza virus in chickens and against Taura Syndrome Virus in shrimp.
The findings will be presented at the World Vaccine Congress at the Marriot Wardman Park Hotel Washington D.C. March 24th to 26th 2014.
Contact: Anne Borsanyi
1. Bogoch S and Bogoch ES.Genome Replikin Count Predicts Increased Infectivity/Lethality of Viruses doi:10.1038/npre.2012.7144.1
2. Bogoch S and Bogoch ES. Genome Replikin Count Predicts Increased Lethality of Cancer. doi:10.1038/npre.2012.7143.1
3. Bogoch S and Bogoch ES. Genomic Replikin Count Predicts Increased Lethality of Malaria doi:10.1038/npre.2012.7142.1
4. Bogoch S and Bogoch ES Genome Replikin Count Predicts Increased Lethality of Resistant Tuberculosis doi:10.1038/npre.2012.7141.1
5. Bogoch S and Bogoch ES Genomic Replikin Counts of Infectious Salmon Anemia Virus (ISAV) in Canada Exceed the Counts in Lethal Outbreaks in Norway, Chile, and Scotland. Real-Time Tracking of the Evolution of the ISAV Genome and the Resultant Replikins Solid Phase ISAV Vaccine Make ISAV Pandemic Prevention Possible. doi:10.1038/npre.2012.6991.1 6. Bogoch S and Bogoch ES Bogoch Replikins Pandemic Prevention: Increase of Strain-Specific Influenza Genomic Replikin Counts, Having Predicted Outbreaks and their Location Seven Times Consecutively, Up to Two Years in Advance, Provides Time for Prevention of Pandemics doi:10.1038/npre.2012.6952.1
7. Bogoch S and Bogoch ES Marked Rise in Replikin Counts in H5N1 Influenza Virus Localized to Lethality Gene p B1. doi:10.1038/npre.2011.6420.1
8. Bogoch S and Bogoch ES Prediction of specific virus outbreaks made from the increased concentration of a new class of virus genomic peptides, replikins. doi:10.1038/npre.2011.6279.1
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SOURCE Bioradar UK, Ltd.