The Morgellons, GMO link persists
About the time that Dr. Wymore’s forensic investigation of fibers was completed, a specialist in infectious disease detection, Ahmed Kilani, claimed to have broken down two fiber samples and extracted their DNA. He found that they belonged to a fungus.
Meanwhile, Vitaly Citovsky, Professor of Biochemistry and Cell Biology at Stony Brook University in New York, discovered the fibers contained the substance Agrobacterium Tumafaciens, the bacteria causing crown gall disease in plants (formation of tumors in more than 140 species of dicot plants). It is a genus of gram-negative bacteria capable of genetically transforming not only plants, but also other eukaryotic species, including humans.
Anonymous samples were provided to Professor Citovsky by the Morgellon’s Research Foundation to use in investigating the potential presence of Agrobacterium Tumafaciens in biopsies from Morgellon’s patients. Control reactions included samples provided by healthy donors. Only Morgellons, not healthy subjects, tested positive for the bacterium in these studies.
Professor Citovsky issued a statement saying his observation does not imply that Agrobacterium Tumafaciens causes Morgellons, or that Morgellons is indeed an infectious disease. However, he has called for further study to determine (1) statistical significance of data, (2) whether the bacterium is not only present extracellularly, but also causes genetic transformation of the infected tissues, and (3) whether infection of laboratory animals with the bacterium can recreate symptoms of Morgellons.
Agrobacteerium Tumafaciens is a soil bacterium. Symptoms of grown gall disease are caused by the insertion of a small segment of DNA into the plant cell, which is incorporated at a semi-random location into the plant genome. They are parasitic and detrimental to the plant.
DNA transmission capabilities of Agrobacterium have been extensively exploited by biotechnologists as a means for inserting foreign genes into plants. They discovered the gene transfer mechanism between Agrobacterium and plants, and developed methods to alter Agrobacterium into an efficient delivery system for gene engineering in plants. This is done by cloning the desired gene sequence into the transfer DNA (T-DNA) that will be inserted into the host DNA. Under laboratory conditions the T-DNA has also been transferred to human cells, demonstrating the diversity of insertion application. The mechanism through which Agrobacterium inserts materials into the host cell is very similar to mechanisms used by pathogens to insert materials (usually proteins) into human cells.
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