INDEX
• INTRODUCTION: Mutated Combination Incomplete Lifeforms.

• Resource: The Mythology.
• Resource: The Biology.
• Resource: The Modification.

• Resource: Are YOU a Chimera ?
• Resource: Double DNA Humans.
• Resource: Journal -
• Resource: The News -

• Digestion: Bacterial changes.
• Digestion: Viral modification.
• Digestion: Reptilian genetics.
• Digestion: Fungal transmutations.
• Digestion:

• Report :
• Political: Names and Faces.
• Personal: Notes from a Survivor.
• Science :

  AFTERWORD: What is BEST for YOU, personally, to eat .. depends upon ...

  -Focus-: Monographs on Toxins and Enhancers.

COMPANION RESOURCES:
IDENTITY : Becoming a Chimera. --- HEALTH : Living with & Beyond Mutation.
HOSTS : What is being/has been altered. --- MODIFIERS : What is/has been used to Mutate.

INTRODUCTION: Mutated Combination Incomplete Lifeforms. INDEX

If you undertake to read the following and make an effort to integrate it such that you can interpret and identify what is RELEVANT for YOU, and perhaps other humans, in general, you will be best to resist attraction to fear, anxiety, paranoia, and hysterics ... which is encouraged by exposure to realities which we are systematically held apart from by the structure of our cultural authority infrastructures including educational, media, news, political, medical, and, pseudo-science boundaries.

That is, if our leaders had expressed a historical optimism in the self-directedness of their membership, and, a humility in their ignorance .. they would NOT have constructed and followed strategies to maintain their membership/voters as dependent, underinformed mental slaves willingly giving over their freedom of health and lifestyle Choices to SYMBOLIC human gods, generally known as experts, scientists, managers, leaders, and, corporations. Your leaders benefit from your accepting their offer of respecting you, as a CHILD, pressed into Dependency, and, without the knowledge to hold them accountable for their many and frequent errors. Allowing them to be irresponsible, while deceiving you with insincere promises and poorly founded good intentions provides them with the Confidence of the authority you sanction in them. Resist the temptation to REACT to sudden awareness with self-terror, and, with the Grace of God, allow the fog of your confusion to drift away and bring you to a discernment of Reality from which you can exercise self-directness.

GMO's are Human Engineered Genetically Mutated Combination Incomplete Lifeforms.
They have genes extracted from other lifeforms added into their own.
This process often excludes, rejects, extracts or otherwise nullifies some of the original genes.
The result is an organism which mainly has the characteristics of the original host, yet, and often not in an obvious appearance characteristic, also has and expresses biological characteristics of another lifeform. These combinations may be made up of genes from any 2 or more of the following: bacteria, fungi, virus, plant, mammal (including human), reptile, others. The host becomes LESS than a representative of its own species, and, much LESS than a representative of another one or more species. Frequently, it may come alive as infertile, and, its life dynamics may threaten its own Quality of Life as well as that of different and same lifeforms around it.

The CHIMERA will generate super-lifeform characteristics, seemingly in a contradictory outcome.
This moves them into the realm of Powerful in the context of the strength of one or more abilities which they express beyond those possible by any of their original species individuals. They will express functionality and skills which make them super-bacteria, super-virusues, super-bacteria, super-insects, super-plants, super-animals, super-humans. At the same time, there will be elements and characteristics, particularly in the metabolic area, which are modified beyond what is possible within the original species. To be expected, in human societies, as an extension of our culturally sanctioned boundaries of authority, institution, bureaucracy, and politically tainted science .. a human chimera will express increasingly dramatic health challenge symptoms, UNLESS, it can discern the dramatic lifestyle-diet-metabolic requirements which can sustain it. Lesser complex lifeforms than huamns, with a minimal degree of innovative consciousness, will die; hence, the use of the process as an EFFECTIVE insecticide, fungicide, herbicide.

Survival of a Chimera, particularly a Human Chimera, requires an individual to be with clearly mature identity factors (Ego, Super-Ego, Reptilian Structure, Personal Spirit, Basic Personality), freed from any Energy Blocks, either inherited or acquired through personal traumatic experience, who has consciously become aware of and modified any destructive imprinted patterns. This will enable them to accept themselves as "different" from other humans, though humble in a spiritual way, compassionate towards those with socially and politically sanctioned Power, and, not driven by addictive patterns of co-dependency, abandonment, guilt, fear, and ritual assumptions. Very FEW humans fit this survival requirement profile, so, almost all human chimeras, mutated from human-developed GMO products, will die ... proving that these compounds are also humanicides. Most human chimera individuals will die of preventable and "curious" causes which will be conveniently subscribed to cancer, a "natural" death, or, a suggested lack of self-concern ... because any effort they made to find a resolution of health problems was met with Denial, Assumption, Ignorance.

GMO's are NEVER what they appear to be.
Their non-normal behavior can be considered a benefit by the engineer, or, useless, or, a danger.
The engineer is often a representative of a CORPORATION, which is a symbolic organism brought to life by humans intent upon taking RISKS in the service of elevated PROFITS while being Legally (institutionally, academically, secularly) protected from Responsibility. The Corporation is given, by its Charter, a Purpose/Motivation of increasing its Capital Resources by the greatest SELF-Benefit. In a competitive economy, an ATTITUDE of "by any means" becomes accepted as an operational/administrative protocol. Representatives who challenge this Moral evaluation of decisions are released from their employment and replaced with others desperate for income, acceptance, power, privilege.

The POLITICAL context of the Corporation is that it IS a Robot to whom representatives of its creators elect to enslave themselves. Presently, 2015, its SOCIAL and ENVIRONMENTAL influences cannot be limited, regulated, or, stopped. The DENIAL afforded to humans by their immature (self-obsessed) Consciousness continues to provide the self deception that humans can harness their Symbolic God. Reality has repeatedly demonstrated for the past 187 years that this MASTER has, and will continue to destroy the balance of the ecology of land and sea lifeforms, the health of humans, the harmony of human political and religious organizations (promoting conflicts, wars, and terrorist abuses), and the biological life ENERGIES of the universe. GMO's are but ONE tool which Corporations are using to ELIMINATE humans.

If one attempts to understand the influence, dangers, and presence of GMOs as a complete lifeform, the human consciousness will succeed in distorting awareness in one direction, then another ... seeking to project conclusions from other lifeforms and the fundamental principles of biology. GMOs represent an ever growing multitude of differing lifeforms, which by their genetic integration with a host, will take on both a PERSONAL ecology dynamic, and, propagate potentially new and individualized strains of enhanced, and, incomplete species. These, unlike the clear boundary and genetically complete lifeforms represented by humans, plants, bacteria, birds, reptiles, and fungi ... may continue to be ACTIVE/alive after they have been harvested and eaten. They share more of a reality of life-death transitional presence with viruses, prions, and cancerous entities than they do with the clear boundary species with their predictable behaviors.

Resource: The Mythology. INDEX
https://en.wikipedia.org/wiki/Chimera_%28mythology%29

The Chimera, also Chimaera (Chimæra); Chímaira) was, according to Greek mythology, a monstrous fire-breathing hybrid creature of Lycia in Asia Minor, composed of the parts of more than one animal. Usually depicted as a lion, with the head of a goat arising from its back, and a tail that might end with a snake's head, the Chimera was one of the offspring of Typhon and Echidna and a sibling of such monsters as Cerberus and the Lernaean Hydra.

The term chimera has come to describe any mythical or fictional animal with parts taken from various animals, or to describe anything composed of very disparate parts, or perceived as wildly imaginative, implausible, or dazzling.

Resource: The Biology. INDEX
https://en.wikipedia.org/wiki/Chimera_%28genetics%29

A chimera (also spelled chimaera) (from the creature Chimera in Greek mythology) is a single organism composed of genetically distinct cells. This can result in male and female organs, two blood types, or subtle variations in form. Animal chimeras are produced by the merger of multiple fertilized eggs. In plant chimeras, however, the distinct types of tissue may originate from the same zygote, and the difference is often due to mutation during ordinary cell division. Normally, chimerism is not visible on casual inspection; however, it has been detected in the course of proving parentage.

Another way that chimerism can occur in animals is by organ transplantation, giving one individual tissues that developed from two genomes. For example, a bone marrow transplant can change someone's blood type.

An animal chimera is a single organism that is composed of two or more different populations of genetically distinct cells that originated from different zygotes involved in sexual reproduction. If the different cells have emerged from the same zygote, the organism is called a mosaic. Chimeras are formed from at least four parent cells (two fertilized eggs or early embryos fused together). Each population of cells keeps its own character and the resulting organism is a mixture of tissues. There are some reports of human chimerism.

This condition is either inherited or it is acquired through the infusion of allogeneic hematopoietic cells during transplantation or transfusion. In nonidentical twins, chimerism occurs by means of blood-vessel anastomoses. The likelihood of offspring being a chimera is increased if it is created via in vitro fertilization. Chimeras can often breed, but the fertility and type of offspring depends on which cell line gave rise to the ovaries or testes; varying degrees of intersex differences may result if one set of cells is genetically female and another genetically male.

Tetragametic chimerism

Tetragametic chimerism is a form of congenital chimerism.
This condition occurs through the fertilization of two separate ova by two sperm, followed by aggregation of the two at the blastocyst or zygote stages. This results in the development of an organism with intermingled cell lines. Put another way, the chimera is formed from the merging of two nonidentical twins (although a similar merging presumably occurs with identical twins, but as their DNA is almost identical, the presence would not be immediately detectable in a very early (zygote or blastocyst) phase). As such, they can be male, female, or have mixed intersex characteristics.

As the organism develops, it can come to possess organs that have different sets of chromosomes.
For example, the chimera may have a liver composed of cells with one set of chromosomes and have a kidney composed of cells with a second set of chromosomes. This has occurred in humans, and at one time was thought to be extremely rare, though more recent evidence suggests that it is not as rare as previously believed.

This is particularly true for the marmoset.
Recent research shows most marmosets are chimeras, sharing DNA with their fraternal twins.
95% of Marmoset fraternal twins trade blood through chorionic fusions, making them hematopoietic chimeras.

Most chimeras will go through life without realizing they are chimeras.
The difference in phenotypes may be subtle (e.g., having a hitchhiker's thumb and a straight thumb, eyes of slightly different colors, differential hair growth on opposite sides of the body, etc.) or completely undetectable. Chimeras may also show, under a certain spectrum of UV light, distinctive marks on the back resembling that of arrow points pointing downwards from the shoulders down to the lower back; this is one expression of pigment unevenness called Blaschko's lines.

Affected persons may be identified by the finding of two populations of red cells or, if the zygotes are of opposite sex, ambiguous genitalia and intersex alone or in combination; such persons sometimes also have patchy skin, hair, or eye pigmentation (heterochromia). If the blastocysts are of opposite sex, genitals of both sexes may be formed: either ovary and testis, or combined ovotestes, in one rare form of intersex, a condition previously known as true hermaphroditism.

Note that the frequency of this condition does not indicate the true prevalence of chimerism.
Most chimeras composed of both male and female cells probably do not have an intersex condition, as might be expected if the two cell populations were evenly blended throughout the body. Often, most or all of the cells of a single cell type will be composed of a single cell line, i.e. the blood may be composed predominantly of one cell line, and the internal organs of the other cell line. Genitalia produce the hormones responsible for other sex characteristics. If the sex organs are homogeneous, the individual will not be expected to exhibit any intersex traits.

Natural chimeras are almost never detected unless they exhibit abnormalities such as male/female or hermaphrodite characteristics or uneven skin pigmentation. The most noticeable are some male tortoiseshell cats or animals with ambiguous sex organs.

The existence of chimerism is problematic for DNA testing, a fact with implications for family and criminal law. The Lydia Fairchild case, for example, was brought to court after DNA testing apparently showed that her children could not be hers. Fraud charges were filed against her and her custody of her children was challenged. The charge against her was dismissed when it became clear that Lydia was a chimera, with the matching DNA being found in her cervical tissue. Another case was that of Karen Keegan, who was also suspected (initially) of not being her children's biological mother, after DNA tests on her adult sons for a kidney transplant she needed seemed to show she wasn't their mother.

The tetragametic state has important implications for organ or stem-cell transplantation.
Chimeras typically have immunologic tolerance to both cell lines.

Microchimerism
... is the presence of a small number of cells that are genetically distinct from those of the host individual. Most people are born with a few cells genetically identical to their mothers' and the proportion of these cells goes down in healthy individuals as they get older. People who retain higher numbers of cells genetically identical to their mothers' have been observed to have higher rates of some autoimmune diseases, presumably because the immune system is responsible for destroying these cells and a common immune defect prevents it from doing so and also causes autoimmune problems. Women often also have a few cells genetically identical to that of their children, and some people also have some cells genetically identical to that of their siblings (maternal siblings only, since these cells are passed to them because their mother retained them).

Germline chimerism
... occurs when the germ cells (for example, sperm and egg cells) of an organism are not genetically identical to its own. It has recently been discovered that marmosets can carry the reproductive cells of their (fraternal) twin siblings, because of placental fusion during development. (Marmosets almost always give birth to fraternal twins.)

Research
In biological research, chimeras are artificially produced by selectively transplanting embryonic cells from one organism onto the embryo of another, and allowing the resultant blastocyst to develop. Chimeras are not hybrids, which form from the fusion of gametes from two species that form a single zygote with a combined genetic makeup, or Hybridomas which, as with hybrids, result from fusion of two species' cells into a single cell and artificial propagation of this cell in the laboratory. Essentially, in a chimera, each cell is from either of the parent species, whereas in a hybrid and hybridoma, each cell is derived from both parent species. "Chimera" is a broad term and is often applied to many different mechanisms of the mixing of cells from two different species.

As with cloning, the process of creating and implanting a chimera is imprecise, with the majority of embryos spontaneously terminating. Successes, however, have led to major advancements in the field of embryology, as creating chimeras of one species with different physical traits, such as colour, has allowed researchers to trace the differentiation of embryonic cells through the formation of organ systems in the adult individual.

The first known primate chimeras are the rhesus monkey twins Roku and Hex; each having 6 genomes.
They were created by mixing cells from totipotent 4 cell blastocysts; although the cells never fused they worked together to form organs. It was discovered that one of these primates, Roku, was a sexual chimera; as four percent of Roku's blood cells contained two x chromosomes.

A major milestone in chimera experimentation occurred in 1984, when a chimeric geep was produced by combining embryos from a goat and a sheep, and survived to adulthood. The creation of the "geep" revealed several complexities to chimera development. In implanting a goat embryo for gestation in a sheep, the sheep's immune system would reject the developing goat embryo, whereas a "geep" embryo, sharing markers of immunity with both sheep and goats, was able to survive implantation in either of its parent species.

In August 2003, researchers at the Shanghai Second Medical University in China reported that they had successfully fused human skin cells and rabbit ova to create the first human chimeric embryos. The embryos were allowed to develop for several days in a laboratory setting, then destroyed to harvest the resulting stem cells. In 2007, scientists at the University of Nevada School of Medicine created a sheep whose blood contained 15% human cells and 85% sheep cells.

Plants
Graft chimeras
These are produced by grafting tetically different parents, different cultivars or different species (which may belong to different genera). The tissues may be partially fused together following grafting to form a single growing organism that preserves both types of tissue in a single shoot.[35] Just as the constituent species are likely to differ in a wide range of features, so the behavior of their periclinal chimeras is like to be highly variable. The first such known chimera was probably the Bizzaria which is a confusion of the Florentine citron and the sour orange. Perhaps the best-known example of a graft-chimera is Laburnocytisus 'Adamii', caused by a fusion of a Laburnum and a broom.

Chromosomal chimeras
These are chimeras in which the layers differ in their chromosome constitution.
Occasionally chimeras arise from loss or gain of individual chromosomes or chromosome fragments owing to misdivision. More commonly cytochimeras have simple multiple of the normal chromosome complement in the changed layer. There are various effects on cell size and growth characteristics.

Nuclear gene-differential chimeras
These chimeras arise by spontaneous or induced mutation of a nuclear gene to a dominant or recessive allele. As a rule one character is affected at a time in the leaf, flower, fruit, or other parts.

Plastid gene-differential chimeras
These chimeras arise by spontaneous or induced mutation of a plastid gene, followed by the sorting-out of two kinds of plastid during vegetative growth. Alternatively, after selfing or nucleic acid thermodynamics, plastids may sort-out from a mixed egg or mixed zygote respectively. This type of chimera is recognized at the time of origin by the sorting-out pattern in the leaves. After sorting-out is complete, periclinal chimeras are distinguished from similar looking nuclear gene-differential chimeras by their non-mendelian inheritance. The majority of variegated-leaf chimeras are of this kind.

All plastid gene- and some nuclear gene-differential chimeras affect the color of the plasmids within the leaves, and these are grouped together as chlorophyll chimeras, or preferably as variegated leaf chimeras. For most variegation, the mutation involved is the loss of the chloroplasts in the mutated tissue, so that part of the plant tissue has no green pigment and no photosynthetic ability. This mutated tissue is unable to survive on its own but is kept alive by its partnership with normal photosynthetic tissue. Sometimes chimeras are also found with layers differing in respect of both their nuclear and their plastid genes.

Origins.
There are multiple reasons to explain the occurrence of plant chimera during plant recovery stage:

(1) The process of shoot organogenesis starts form the multicellular origin.

(2) The endogenous tolerance leads to the ineffectiveness of the weak selective agents.

(3) A self-protection mechanism (cross protection).
Transformed cells serve as guards to protect the untransformed ones.

(4) The observable characteristic of transgenic cells may be a transient expression of the marker gene.
Or it may due to the presence of agrobacterium cells.

Resource: The Modification. INDEX
http://

The goal is to take a gene-of-advantage from one species and ADD it to a HOST (bacteria); then, use a PROMOTER (virus) to activate a TRANSFER from the HOST into the Destination TISSUE of a TARGET Lifeform.

Virus Enhancement factors will improve success:
--- physical GROWTH period, calories
--- Supplements: minerals, oils, supplements, vitamins.

Immune Distraction Factors will improve successful modification dynamics:

DYNAMICS:

GENES: Transforming gene(s) may be added to the Host (for Insertion), 
                                  and, to the Carrier (for Removal).

ECOLOGY: Low, or, High pH; duration/repetition of exposure, 

HOST: (Genetically Modified with a(n) extra Gene(s))
        Corn (chips, meal, starch), 
        Potatoes (white; NOT red or Yukon Gold)
        Papaya (Green; NOT Red)
        BT BACTERIA 

CARRIER: 

PROMOTER: VIRUS 
  (Primer, Trigger, Effector, Catalyst) 

INDICATORS/Symptoms which may accompany a successful REMOVAL-Modification:

     tissue replacement / exclusion 
     heart/circulation stress 
     headache 
     nausea
     fainting
     apparent diarrhea 
     apparent hemorrhagea 

Resource: Are YOU a Chimera ? INDEX
http://io9.com/5911357/theres-a-good-chance-youre-a-human-chimera
By Esther Inglis-Arkell --- 2012-05-18

... Humans bear marks of chimerism, too.
Although their stolen body parts only come from other humans, the results can be dramatic.

There was a case, not too long ago, when a blood test showed that a woman, and the children she had actually born, were not mother and child. This woman continued to undergo blood tests trying to prove that she was the mother of her own children, even when one such test showed that she was not the mother of the child she had just birthed. Either this woman was undergoing some fairly advanced medical procedures on her own, or something was up. Eventually it was found that this woman had had a fraternal twin. She didn't remember it, because it was while they were both basically blastocysts when that twin had ceased to be.

Her twin had been absorbed into her, and the combined tissue created a composite body, despite having different DNA. A tissue sample taken from the woman's thyroid later showed that she was the children's biological mother. It's just that her ovaries belonged to that long-lost twin. Another woman found out that her children weren't carrying her DNA when she needed a kidney transplant and neither was a match. Again, her ovaries were made from different DNA. Both mothers were chimeras.

And it turns out a lot of mothers are chimeras.
Not as completely as these women were, but fetal stem cells are tenacious things.
They stay in the body of the mother, and have even been shown to slip into that sacred space where we believe that all of human individuality resides; the brain. It's possible that part of every mother's brain literally is that of her child. And if you're a child, it's likely that part of you is your mother. A mother's cells cross the placenta during pregnancy and squat in the liver, bloodstream, thymus gland, and that old sentimental favorite, the heart.

... chimerism is all the more strange for not being visible.
It's quite likely that, by any genetic measure, you carry around the cells of another human being.
You carry them around perpetually, as an indispensable and inseparable part of you. You may be housing another being in your body, and some other human is housing your cells. Something to keep in mind if you ever have your kids' blood tested. ...

Resource: Double DNA Humans. INDEX
http://santacruz.hubpages.com/hub/People-with-Double-DNA-An-Overview-of-Chimeras
People with Double DNA: An Intro to Human Chimeras
By SantaCruz --- Updated on June 21, 2012
http://santacruz.hubpages.com/

In biology a chimera is a lifeform with two DNA profiles.
For example, a human chimera's hair sample might not match their saliva sample. ...

The word "chimera" comes from ancient mythology.
It refers to an imaginary creature comprised of various animal parts, e.g., a lioness combined with a snake and a goat. Scientists didn't realize until very recently that people and other animals, along with plants, can express more than one set of DNA. In fact, you might be a chimera!

Some people are rather obviously possible chimeras.
For instance, if you have mostly coffee-brown skin plus patches of whitish skin, you might be expressing two different sets of DNA. Other human chimeras stand out for having hair that doesn't match the rest in color or texture. Intersexed people may also be chimeras. However, many human chimeras have no external signs of their unusual condition. Their second set of DNA might only operate in their kidneys, for example.

This article about human chimeras was inspired by the Discovery Channel special entitled "I Am My Own Twin."

How Do People Become Chimeras?

Chimeras are created when four parent cells (or two fertilized eggs) become fused.
Transplants can also create chimerism since they introduce foreign DNA.

Although human chimeras are likely as old as our species, DNA wasn't identified until 1952 with Rosalind Franklin's X-ray crystallography. A human chimera was announced the following year: In 1953 in the British Medical Journal published the first study of a human chimera. The woman in the study had two distinct blood types. Her chimerism came from her twin brother, who was still alive. She had absorbed some of his DNA while in the womb.

Being a twin seems to be the most common way of becoming a chimera.
The other twin might be unknown since twin pregnancies sometimes end up as single births.

Despite the publication from 1953, most medical doctors were unaware of chimerism just a decade ago.
The Discovery episode "I Am My Own Twin" documents two cases of chimerism in the US that have helped raise awareness.

In the first case, a Washington woman named Lydia Fairchild applied for welfare assistance.
She was required to prove her relationship to her children. Oddly enough, her children's DNA tests suggested that she wasn't their mother. However, it did confirm that their father was their father! Prejudice worked against Fairchild; people figured she'd been caught attempting fraud. She couldn't get legal representation because lawyers regarded DNA "evidence" as irrefutable.

Fortunately, a "more respectable" woman in Boston was experiencing a related situation.
Karen Keegan was a 52-year-old teacher. When she needed a kidney transplant, her three sons were tested for DNA compatibility. The tests suggested that she lacked a maternal relationship with two of her three sons.

While Fairchild was fighting off the state prosecutor, Keegan was in a position to pursue the DNA mystery.
Her doctor pored over medical journals and networked with colleagues. She then surmised that Keegan was a chimera and began testing.

First, doctors took DNA samples of Keegan's hair and skin.
When these samples proved fruitless, they moved on to sample her internal organs.
That's when they found a different set of DNA. Genetically, two of her sons appeared to be descendents of her husband and a vanished twin.

Luckily for Fairchild, Keegan's experience was documented in a medical journal.
When word reached Washington, Fairchild was finally able to secure legal representation, welfare, and custody of her children.

Implications of Chimerism
As Fairchild's judge observed, chimerism calls into question the validity of DNA tests.
Positive matches remain unchallenged but all "negatives" are now suspect.
The phenomena of chimerism calls into question many paternity suits and other court cases.
In a small percentage of couples, it might also help explain infertility.

Resource: Journal - INDEX
http://www.nejm.org/doi/full/10.1056/NEJM199801153380305

Resource: The News - INDEX
http://news.nationalgeographic.com/news/2005/01/0125_050125_chimeras.html

Digestion: Bacterial changes -- Modifier, Bt, Bacillus thuringiensis. INDEX
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3035146/pdf/bbug0101_0031.pdf
NCBI: Bacillus thuringiensis, A genomics and proteomics perspective. 2010
Mohamed A Ibrahim, Natalya Griko, Matthew Junker, and Lee A Bull, with
the technical assistance of Shweta Biliya and Gayathri Raghupathy.
(See a copy of the original document to view the Figures, noted in the text.)

LINK 2: http://microbewiki.kenyon.edu/index.php/Microbial_Biorealm (MB DOWN)

LINK 3: http://www.gmo-compass.org/eng/agri_biotechnology/
breeding_aims/147.pest_resistant_crops.html (PR DOWN)

Bacillus thuringiensis (Bt) is ... the most widely used environmentally compatible biopesticide worldwide. Furthermore, insecticidal Bt genes have been incorporated into several major crops, rendering them insect resistant, and thus providing a model for genetic engineering in agriculture. ...

... The first commercial insecticide based on Bt, Sporine, was produced in France in 1938 and used primarily to control flour moths. In the United States, Bt was first manufactured commercially in 1958 and, by 1961, Bt-based bioinsecticides were being registered by the US Environmental Protection Agency. Since 1996, insect-resistant transgenic crops, known as Bt crops, have expanded around the globe and are proving to be quite efficient and helpful in reducing the use of chemical insecticides. Latest estimates indicate that more than 50% of the cotton and 40% of the corn planted in the US are genetically engineered to produce Bt insecticidal toxins. The current global market for pesticides (herbicides, insecticides, fungicides, nematicides and fumigants) is valued at $25.3 billion. Biopesticides represent only 2.5% of this market but their share is expected to increase to about 4.2%, or more than $1 billion, in 2010.

Interestingly, some strains of Bt produce non-insecticidal proteins that crystallize into irregular-shaped parasporal inclusions. Inclusions of one isolate treated with protease were toxic to human cancer cells, including leukemic T (MOLT-4) and cervical cancer cells (HeLa). Cytotoxicity was dose-dependent. Another non-insecticidal protein, parasporin, also showed strong cytotoxic activity against MOLT-4 and HeLa cells. ...

Classification and Taxonomy of Bacillus thuringiensis
... vegetative cells of Bt are ... Grampositive, non-capsulated and motile with peritrichous flagella.
Classification of Bt strains ... at least 69 H serotypes and 82 serological varieties (serovars) of Bt have been characterized. H serotyping, however, is limited in its capability to distinguish strains from the same H serotype or from the same serovar. Due to its economic importance, ... numerous Bt strains with activity against lepidopteran, dipteran and coleopteran insects have been isolated. Additionally, Bt strains active against insects belonging to the orders Hymenoptera, Homoptera, Orthoptera and Mallophaga as well as nematodes, mites and protozoa have been isolated.

... Many species of these genera are of practical importance because they produce antibiotics and peptides with anti-microbial, anti-viral and anti-tumor activities. They also synthesize thermostable enzymes and molecules that can suppress soil-borne phytopathogenic organisms.

In the monograph The Genus Bacillus, Gordon et al.(1973) considered Bt a variety of B. cereus (Bc) along with B. anthracis (Ba) and B. mycoides (Bm). ... Ba is the causative agent of anthrax, an acute and often lethal disease in humans and animals. Bc is an opportunistic human pathogen and may cause food poisoning, eye infections and periodontal disease, among other ailments. Bt possesses a variety of special features including its (1) ability to live in the environment free and independent from other Gram-positive spore-forming bacilli, (2) production of entomocidal parasporal crystal proteins and (3) survival in a unique environmental niche in the midgut and hemocoel of insects. ...

Curiously, Bt has been alleged to be an opportunistic pathogen in animals and human.(1998/9-2000)
Two Bt strains, Bt 97-27 (subsp. konkukian) and Bt Al Hakam (isolated in Iraq by a United Nations Special Commission), were initially designated as human pathogens. ...

... The primary distinguishing features of Bt are its virulence and pathogenicity factors, represented by the insecticidal genes located on the chromosome and several plasmids. Those of Ba are its tripartite toxin and capsule encoded by plasmids only.

... Analysis of various Bc and Bt strains reveal very high diversity in multi-locus genotypes, indicating that Bc and Bt exhibit a low degree of clonality and that exchange of genetic material can occur frequently in their natural environments. ...

Expression and Regulation of Insecticidal Genes One of the most dramatic aspects of Bt sporulation is the formation of parasporal crystals.
The insecticidal toxins (Cry toxins .. the parasporal crystalline protein of Bt) of Bt, oftentimes referred to as ?4-endotoxins after Heimpel, are somewhat specific to certain insects. The family of genes coding for these toxins is the cry gene family. A common characteristic of cry genes is that they are expressed during the stationary phase of growth. Cry proteins, the end-products of cry gene expression, constitute 20-30% of the cell dry weight and generally accumulate in the mother cell, beginning in stage III of sporulation and continuing through stage VII.

The term ?4-endotoxin, relative to Bt Cry toxin, is a misnomer.
Heimpel named the parasporal crystalline protein of Bt as such because it forms inside the cell and because it is fourth in the order of other toxic components discovered in the bacterium. However, endotoxins are associated with the lipo-polysaccharide moiety of the complete "O" somatic antigen complex found in the outer membrane of various Gram-negative bacteria and are an important factor in their ability to cause disease ....

... One interesting feature of cry genes is their high degree of plasticity.
This particular characteristic may contribute to the versatility of Cry toxins as it relates to their insect host range. ... transposable elements may facilitate gene multiplication and evolution of new toxins. Furthermore, the fact that cry genes are carried on transmissible plasmids increases the likelihood of horizontal gene transfer among different Bt strains, which leads to the creation of new strains with different sets of Cry toxins. ...

Biochemistry and Functional Proteomics of Cry Toxins
... it is the Cry toxin that establishes safe harbor for the bacterium in an insect carcass. ..

Another feature of Cry toxins is that their precursor protoxins co-crystallize in various forms and shapes (and are) found mainly on large plasmids. However, the genes may be integrated into the chromosome. ...

Mechanism of Cry (parasporal crystalline protein) Toxin Action
Just as the classification and taxonomy of Bt remains somewhat controversial, so does the explanation of how Cry toxins destroy insects. ...

The second model (Fig. 7) advanced by Zhang et al. ... toxin monomer binds to the cadherin receptor BT-R1 and activates a Mg2+-dependent signal-transduction pathway (peristaltic paralysis?) leading to cell death. ... Cry toxin action is a complex, dynamic process that involves ... The cAMP activates protein kinase A, bringing about an array of cellular alterations, which includes cytoskeletal rearrangement and ion fluxing. Acceleration of this second messenger pathway alters the chemistry of the cell and brings about cell death. Furthermore, the killing mechanism involves promotion by the toxin of exocytotic translocation of BT-R1 from intracellular membrane vesicles to the cell membrane (modified cell membrane permeability?) (potential hydrophobic interactions involving surface-exposed Phe440 in Cry1Ab and Leu1358, Tyr1453 and Val1455 in the TBR of BT-R1). Movement of the receptor is mediated by toxin-induced signal-transduction, and amplification of this signaling (to hypersensitivity -- over-reactivity?) is correlated directly to the execution of cell death. ...

Insect Resistance to Cry Toxins
For the past 50-60 years, commercial formulations of Bt have been utilized to control economically important insect pests worldwide. Today, ... strong evolutionary pressure on insects by Bt will promote development of defense mechanisms that can circumvent bacterial and toxin attack. In fact, a number of different Bt-resistant insect species have been generated in the laboratory through special selection techniques or have been discovered naturally in the field.

... When in continual touch with Bt, insects exhibit physiological changes and enhanced immune response. ... A heightened immune response primarily involves changes in the activity of the mucosal surface, causing increased secretion of proteases and pro-coagulants ...

Bacillus thuringiensis, 2011
From MicrobeWiki, the student-edited microbiology resource,
http://microbewiki.kenyon.edu/index.php/Microbial_Biorealm
LINK 2: http://microbewiki.kenyon.edu/index.php/Bacillus_thuringiensis
Edited by Ernest Hsu of Rachel Larsen and Kit Pogliano

COMMENT: The article has been written and edited by students imprinted with human authority attitudes of confidence in dramatic simplicity, unquestioned acceptance of previous research, an attraction towards the use of absolute statements, and, a reverence for the assumed legitimate leadership and concern of political institutions. This attitude of pride and dissociation has largely been excluded from the below quote, yet will be found in the original. Hypocritical logic is best discerned .. as in "insect and vertebrate immune systems may share some dynamics" and, the absolute that because the BT toxins have been proven (consistently demonstrated) to kill insects ... they must be safe for humans (on which there have been no tests, especially with similar administered concentrations of the BT toxin.

Classification
Eubacteria (kingdom); Bacteria (domain);
Firmicutes (phylum); Bacilli (class); Bacillales (order); Bacillaceae (family);
Bacillus (genus); Bacillus cereus group; Bacillus thuringiensis (species)

... Many studies indicate and consider B. thuringiensis and B. cereus to be one species.
However, their phenotypes greatly differ in that Bt produces crystal proteins despite the fact that crystal protein synthesis is controlled by plasmid genes which can be susceptible to loss and transmission to related bacteria. One response is that Bt strains produce enterotoxins (toxins released by micro-organisms in the lower intestine) that are involved in B. cereus pathogenesis and therefore signifies a fine-line between the two species. ...

Most research has been focused on the Cry toxin crystals. ...
The optimal condition for the Cry toxin to grow and sporulate is in the insect's alkaline gut. ...
It is a soil bacterium and thrives at body temperature. ...

Here is a rough process on how B. thuringiensis causes disease.
B. thuringiensis is digested and the toxins are mixed with the high pH (basic conditions) to bind specific receptors in the gut to attack the host insect. This process punches holes in the gut-lining and thus, the insect becomes weak. As the gut is continuing to break down, spores begin to germinate from the toxic crystals and other bacterial pathogens start to infect the host. B. thuringiensis spores are continuously weakening the host and the insect dies soon thereafter. ... All Cry variants follow a similar two-phase mechanism when infecting the host: 1.) solubilization and 2.) proteolytic activation in the gut and binding to the intestinal cells with pore formation. ...

Pest Resistant Crops, 2006 INDEX
LINK 3: http://www.gmo-compass.org/eng/
agri_biotechnology/breeding_aims/147.pest_resistant_crops.html

... Bacillus thuringiensis, or Bt, is a ... soil bacterium produces a protein that is toxic to various herbivorous insects. The protein, known as Bt toxin, is produced in an inactive, crystalline form.

When consumed by insects, the protein is converted to its active, toxic form (delta endotoxin), which in turn destroys the gut of the insect. ...

Digestion: Viral Modification - Ringspot. (Bumps & Spots) INDEX
https://en.wikipedia.org/wiki/Papaya_ringspot_virus

LINK 2: http://www.gmo-compass.org/eng/database/plants/59.papaya.html
LINK 3: http://www.annualreviews.org/
doi/abs/10.1146/annurev.phyto.36.1.415?journalCode=phyto&
LINK 4: http://www.sourcewatch.org/index.php/
Papaya_Ringspot_Virus_Resistant_%28PRSVR%29_Papaya

PRSV-P
Symptoms are typical of viral diseases.
Papaya exhibits yellowing, leaf distortion, and severe mosaic.
Oily or water-soaked spots and streaks appear on the trunk and petioles.
The fruit will exhibit bumps and the classic "ringspot". A severe isolate of PRSV has also been shown to cause tissue necrosis. Cucurbit symptoms tend to be similar to papaya symptoms including blisters, mosaic, yellowing, and leaf distortions.

This virus produces two types of inclusion bodies visible under a light microscope with proper staining of epidemal strips. One inclusion is the typical cylidrical inclusion (CI) which is considered diagnostic for the potyvirus group, and the other is called the amorphous inclusion (AI). The presence of both inclusions can be diagnostic for this virus.

Digestion: Reptilian genetics. INDEX
https://en.wikivet.net/Lizard_Digestion
LINK 2: http://www.bibliotecapleyades.net/sumer_anunnaki/reptiles/reptiles14.htm
LINK 3: https://en.wikivet.net/Lizard_Gastrointestinal_System
LINK 4: http://phenomena.nationalgeographic.com/
2013/01/01/how-a-quarter-of-the-cow-genome-came-from-snakes/
LINK 5: http://  

INDEX

• Metabolism.
• Excretion.
• Digestion.
• BovB DNA .
• Database .

Lizards are ectothermic and therefore the temperature of their environment affects their body processes which are highly temperature-dependent. Temperature will affect enzymatic activity, the decomposition rate of ingested elements, the absorption through the gut mucosa, peristalsis (and gut transit times) and possibly gut flora.

Low temperatures may slow down or even stop all digestion and can have adverse effects on assimilation (i.e. in monitor lizards).

For example, an iguana kept at 28°C will eat but its food will not be digested properly.
Between 10°C and 15°C, digestion is extremely slow.
Digestion comes to a halt when temperatures drop below 7°C.

Suboptimal temperatures can lead to serious complications such as bloat, constipation or maldigestion.
It is therefore crucial to offer the most appropriate temperature range by providing suitable heat sources, temperatures, and light intensities, in order to stimulate feeding and basking behaviour (which promote postprandial digestion).

(In LIZARDS) The organs and divisions of the gastrointestinal tract are similar to those of mammals. The lizard has a simple, J-shaped, elongated stomach. A caecum is present in many species. The large intestine is thin-walled and less muscular than the stomach or small intestines.

Herbivorous lizards such as the green iguana, prehensile-tailed skink, egyptian spiny-tailed lizard and chuckwalla (Sauromalus obesus) have a sacculated colon to facilitate hindgut fermentation. These animals usually have higher optimal body temperature zones in order to enhance microbial fermentation.

Metabolism. R-Index

Modern reptiles exhibit some form of cold-bloodedness (i.e. some mix of poikilothermy, ectothermy, and bradymetabolism) so that they have limited physiological means of keeping the body temperature constant and often rely on external sources of heat. Due to a less stable core temperature than birds and mammals, reptilian biochemistry requires enzymes capable of maintaining efficiency over a greater range of temperatures than in the case for warm-blooded animals. The optimum body temperature range varies with species, but is typically below that of warm-blooded animals; for many lizards, it falls in the 24°-35°C (75°-95°F) range, while extreme heat-adapted species, like the American desert iguana, Dipsosaurus dorsalis, can have optimal physiological temperatures in the mammalian range, between 35° and 40 °C (95° and 104 °F). While the optimum temperature is often encountered when the animal is active, the low basal metabolism makes body temperature drop rapidly when the animal is inactive.

As in all animals, reptilian muscle action produces heat.
In large reptiles, like leatherback turtles, the low surface-to-volume ratio allows this metabolically produced heat to keep the animals warmer than their environment although they do not have a warm-blooded metabolism. This form of homeothermy is called gigantothermy; it has been suggested as having been common in large dinosaurs and other extinct large-bodied reptiles.

The benefit of a low resting metabolism is that it requires far less fuel to sustain bodily functions. By using temperature variations in their surroundings, or by remaining cold when they do not need to move, reptiles can save considerable amounts of energy compared to endothermic animals of the same size. A crocodile needs from a tenth to a fifth of the food necessary for a lion of the same weight and can live half a year without eating. Lower food requirements and adaptive metabolisms allow reptiles to dominate the animal life in regions where net calorie availability is too low to sustain large-bodied mammals and birds.

It is generally assumed that reptiles are unable to produce the sustained high energy output necessary for long distance chases or flying. Higher energetic capacity might have been responsible for the evolution of warm-bloodedness in birds and mammals. However, investigation of correlations between active capacity and thermophysiology show a weak relationship. Most extant reptiles are carnivores with a sit-and-wait feeding strategy, and whether reptiles are cold blooded due to their ecology or because their metabolism is a result of their ecology is not clear. Energetic studies on some reptiles have shown active capacities equal to or greater than similar sized warm-blooded animals.

Excretion. R-Index
Excretion is performed mainly by two small kidneys.
In diapsids, uric acid is the main nitrogenous waste product; turtles, like mammals, excrete mainly urea.
Unlike the kidneys of mammals and birds, reptile kidneys are unable to produce liquid urine more concentrated than their body fluid. This is because they lack a specialized structure called a loop of Henle, which is present in the nephrons of birds and mammals. Because of this, many reptiles use the colon to aid in the reabsorption of water. Some are also able to take up water stored in the bladder. Excess salts are also excreted by nasal and lingual salt glands in some reptiles. ...

Digestion. R-Index
Most reptiles are insectivorous or carnivorous and have rather simple and comparatively short digestive tracts, meat being fairly simple to break down and digest. Digestion is slower than in mammals, reflecting their lower resting metabolism and their inability to divide and masticate their food. Their poikilotherm metabolism has very low energy requirements, allowing large reptiles like crocodiles and the large constrictors to live from a single large meal for months, digesting it slowly.

While modern reptiles are predominately carnivorous, during the early history of reptiles several groups produced some herbivorous megafauna: in the Paleozoic, the pareiasaurs and the synapsid dicynodonts; and in the Mesozoic several lines of dinosaurs. Today, the turtles are the only predominantly herbivorous reptile group, but several lines of agamas and iguanas have evolved to live wholly or partly on plants.

Herbivorous reptiles face the same problems of mastication as herbivorous mammals but, lacking the complex teeth of mammals, many species swallow rocks and pebbles (so called gastroliths) to aid in digestion: The rocks are washed around in the stomach, helping to grind up plant matter. Fossil gastroliths have been found associated with both ornithopods and sauropods, though whether they actually functioned as a gastric mill in the latter is disputed. Salt water crocodiles also use gastroliths as ballast, stabilizing them in the water or helping them to dive. A dual function as both stabilizing ballast and digestion aid has been suggested for gastroliths found in plesiosaurs.

How a quarter of the cow genome (BovB) came from snakes. R-Index
by Ed Yong
IMAGE: A family tree of BovB sequences.

Genomes are often described as recipe books for living things.
If that's the case, many of them badly need an editor. For example, around half of the human genome is made up of bits of DNA that have copied themselves and jumped around, creating vast tracts of repetitive sequences. The same is true for the cow genome, where one particular piece of DNA, known as BovB, has run amok. It's there in its thousands. Around a quarter of a cow's DNA is made of BovB sequences or their descendants.

BovB isn't restricted to cows. If you look for it in other animals, as Ali Morton Walsh from the University of Adelaide did, you'll find it in elephants, horses, and platypuses. It lurks among the DNA of skinks and geckos, pythons and seasnakes. It's there in purple sea urchin, the silkworm and the zebrafish. ...

If you draw BovB's family tree, it looks like you've entered a bizarre parallel universe where cows are more closely related to snakes than to elephants, and where one gecko is more closely related to horses than to other lizards.

This is because BovB isn't neatly passed down from parent to offspring, as most pieces of animal DNA are. This jumping gene not only hops around genomes, but between them.

This type of "horizontal gene transfer" (HGT) is an everyday event for bacteria, which can quickly pick up important abilities from each other by swapping DNA. Such trades are supposedly much rarer among more complex living things, but every passing year brings new examples of HGT among animals. For example, in 2008, Cedric Feschotte (now at the University of Utah) discovered a group of sequences that have jumped between several mammals, an anole lizard, and a frog. He called them Space Invaders.
http://phenomena.nationalgeographic.com/2008/11/03/
space-invader-dna-jumped-across-mammalian-genomes/

The Space Invaders belong to a group of jumping genes called DNA transposons.
They jump around by cutting themselves out of their surrounding DNA, and pasting themselves in somewhere new. They're also relatively rare -- they make up just 2 to 3 percent of our genome. BovB belongs to a different class of jumping genes called retrotransposons. They move through a copy-and-paste system rather than a cut-and-paste one, so that every jump produces in a new copy of the gene. For that reason, they spread like wildfire.

Early on during its travels, BovB split into two major lineages.
One group has made its way between a single lizard -- the Lord Howe Island gecko -- and the horse, the egg-laying platypus and echidna from Australia, and African mammals like the elephant and hyrax. The other group started off in lizards and snakes, and jumped from there into ruminants like cows and sheep, and marsupials like possums and wallabies. ...

(Ali Morton Walsh from the University of Adelaide) Walsh found a huge clue when she discovered BovB in the genomes of two tick species, both of which suck the blood of lizards and snakes. Other related ticks bite mammals too, so it's possible that by biting their way through the animal kingdom, these bloodsuckers inoculated fresh branches of the tree of life with jumping genes.

Many scientists who work in this field have suggested that parasites, including worms, bugs, and viruses, could act as vehicles for hitchhiking genes. Indeed, in their very first paper on the BovB, Kordis and Gubensek said that ticks might be spreading the gene between animals. ...

"The inescapable conclusion from this and a plethora of other recent studies is that horizontal DNA transfer has been a powerful engine of animal genome evolution, much like it is in bacteria," says Feschotte. "The main difference being that while bacteria swap genes, animals swap transposons." ...

The Reptile Database, LINK, R-Index
http://www.reptile-database.org/
January 9, 2014 by Sathya Achia Abraham
Provided by: Virginia Commonwealth University
http://phys.org/partners/virginia-commonwealth-university/

Experts predict that 2014 will be a big year for reptiles.
Reptiles, which include snakes, lizards, turtles, crocodiles, tuataras and amphisbaenians, are projected to become the most diverse vertebrate group in the world. As it stands now, there are approximately 10,000 bird species -- the most of any vertebrates -- but reptiles are forecast to reach and surpass that milestone in 2014.

Among the experts studying these developments is Peter Uetz, Ph.D., associate professor of systems biology and bioinformatics in the Center for the Study of Biological Complexity (CSBC), part of Life Sciences at Virginia Commonwealth University. Uetz is the founder, editor and curator of the Reptile Database, a web-based catalogue of all living reptile species and classification. The catalogue is shared with several global projects that collect similar information for other living species on the planet.

In 1995, as a graduate student at the European Molecular Biology Laboratory (EMBL) in Heidelberg, Germany, Uetz founded the Reptile Database while working on his thesis project, which focused on vertebrate limb development. His interest in web technologies was initially sparked by the EMBL DNA sequence database and the new opportunities the worldwide web offered in the early 1990s.

The Reptile Database has become a collaboration of hundreds of scientists and hobbyists around the world who study reptiles. Currently, the database includes 9,900 species of reptiles, including another 2,800 subspecies. ...

"From a research perspective, reptiles have a couple of unique and amazing features that make them very interesting to study and learn about," Uetz said.

An example is in the genetics of sex and reproduction.
According to Uetz, many reptiles have temperature-dependent sex determination, which means that the sex of their offspring does not depend on X and Y chromosomes the way it does in most mammals. Rather, sex determination in many reptiles is dependent on environmental temperature. ...

"In fact, the saliva of the poisonous Gila monster, a lizard found in the southwestern U.S. and Mexico, has already yielded the drug exenatide for the management of type 2 diabetes," Uetz said. Exenatide is marketed as Byetta and is administered as an injection under the skin. The drug stimulates the pancreas to secrete insulin when blood sugar levels are high, according to the National Institutes of Health. ...

A study published online in the December 2013 issue of the Proceedings of the National Academy of Sciences, led by Todd A. Castoe, Ph.D., assistant professor of biology at the University of Texas at Arlington, detailed the findings of the first complete snake genome of a Burmese python -- a huge, non-venomous snake with a giant appetite. According to Uetz, who contributed peripherally to the study via the Reptile Database, the team showed that hundreds of genes are switched on in response to a meal.

"We don't know the meaning of many of these genes and how they help the snake digest and process all that food, but one thing that happens is that snakes have dramatic proliferation of intestinal cells that help with digestion," Uetz said.

"And it's not only the genes in the intestine, it's also liver genes and all kinds of other things that happen in the snake body as a response to feeding. This is an interesting physiological adaptation that may help to understand how obesity works." ...

"The next 10 or 20 years will be focused on how genes determine the morphological and physiological traits of these species -- that is, the evolutionary adaptations that separate them from amphibians or birds (which are essentially reptiles) and mammals."

Political: Names and Faces. INDEX

This is a COMMENT that summarizes Relevant information experienced by the Author, the Reality.

I was born December 09, 1945 in a central southern town in the Province of Ontario, Canada.

I grew up and received my early education in a farming area; social contact was limited.

My FAMILY name is SENNETT.
My great grandparents had immigrated to Canada from Ireland in the mid-1850s during the Potato Famine era.
Previous to that time, there is some evidence that their ancestors had emigrated from France. It is possible that others from France emigrated to Russia, northeastern USA, and, central Eastern USA. These different "geographic families" appear to have NOT maintained or re-established contact with each other.

Personal: Notes from a Survivor. INDEX

Human chimeras are dying in increasing numbers daily.
Partly, this is because they are being increasingly created on a daily basis.
It is also because most of humanity is both ignorant of the reality and in denial of the possibility.
It took 300 years for a general medical acceptance to be expressed about the benefit of citrus fruit being effective in preventing scurvy after it was first reported. Consider that in 2018, after more than a decade of instances of increasing numbers of "odd" deaths occurring, there is NO research interest in discerning what may be attributing to the cause of this gently and silently increasing epidemic.

In mass human society, humans have been, and continue to be, rewarded for acknowledging human Authority, following rules and protocols without question, fearing the life and identity threatening loss of Acceptance by peers and those with Power, and, increasingly, being willing to intensively financially indebt oneself and one's family in an effort to maintain a politically promised and perceived deserved standard of living beyond their income.

AFTERWORD: INDEX
Survival no longer depends upon IF you eat; Quality-of-Life no longer depends upon WHAT you eat.
What is BEST for YOU, personally, to eat .. depends upon WHAT is in YOU, and, WHAT is in your food.

With the Original Addiction imposed on humans by well intentioned entities who were NOT spiritually gifted and NOT aware of the significance of RELEVANCY, humans have focused their efforts on Behaviors of overpopulation, overdemand, and, overactivity by way of Attitudes of reactions to Abandonment, and, Reactions to unconscious Guilt. With a distracted and self-sabotaging Consciousness, they have furthered their presence by Imposing brute force on themselves and others, and, corrupting the ecosystem which supports their existence.

At each of many thresholds of Attention stimulating challenges and events, the consistent REACTION has been Denial through the Distraction that they can successfully play the role of god-as-a-controller over EVERYTHING. Each step has resulted in the timely collapse of a civilization, or, a short-term desperate improvement-by-enslavement ... before yet again, another and larger challenge. Enslavement has taken many forms ranging from authority, routine, restriction, obligation, depression, and, fantasy (distraction). Technology has been employed to expand boundaries where self-restraint was denied. It has provided emotional distance and distortion where enemies were invited as distractions and promises of freedom and peace from the anxieties and fears generated from the internal source of a corrupted genetic structure.

Human Engineered Genetically Mutated Combination Incomplete Lifeforms (Chimeras, GMOs) is but one of the latest attempts by humans to continue to do what has constantly led to longer-term disaster and loss by repeating the ATTITUDE: "If I do more, I will reach a point of Enough." The reality is that with the losses sustained by such LUST, the requirements for what COULD be Enough continue to be INCREASED, and, as an Addiction ... an Awareness of "Enough" is impossible to reach. Without external assistance, the species will continue to raise the stakes of Risk until not only a civilization collapse will occur, but a species extinction.

Currently, in mid-2015, the ingestion of as little as ONE meal of a GMO can result in the transformation of healthy gut tissue into a dysfunctional digestive and elimination process which will slowly and quietly result in the death of its host. And, in most cases, neither the medical or educational infrastructure will assert any realization of or responsibility for epidemic until the threshold of species recovery is well exceeded.

I began this research to discern an understanding of a physical dysfunction which I had made adjustments to daily in order to remain active, alert, and, alive. I discovered that what I had arose from both singular and multiple exposures to different GMO foods. The process had begun earlier than I suspected and developed through 3 distinct sets of symptom dynamics rather than only the one which had been the more dramatic, and the latter. The side effects, because I was able to adjust to them with self-direction and Spiritual Guidance, afforded me abilities which enabled me to accomplish more during a period of 22 months, towards the facilitation of longer-term human recovery from disastrous bio-engineering, and, increase the positive energy dynamic contribution to the universe which humanity was capable of, and had much earlier provided. I had done my part, and it was now time for me to regain a greater Reality of Balance within my personal life.

What I was Spiritually Guided to and discovered, and you may benefit from, is on these pages.
One must be quite HEALTHY in order to acquire the full impact of GMO genetic transmutation which influenced me. One must have an overall ALKALINE pH to their system. 96% of humans no longer have such. Chronic LOW blood pressure would also provide an enhanced capability to counter the destructive influences of the work I was engaged in together with the life and physical challenges I encountered. A life long low BP status I have had, unlike 98% of other humans. To enable me to sanely uncover the realities involved with my "International Diplomacy" work, and, a discernment of the influences on my health, as well as the reverence and humility to remain CALM with the experience of the Identity challenges which most other humans would encounter with the "Symptoms" and react to with much negativity ... brought many revelations to me.

Autopsy: Internal Exam - Impacted Waste
http://www.youtube.com/watch?v=bj3d7p2Fu6M

INDEX