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Human-Animal Chimeras

New Developments and Ethical
          Issues
Chimeras

It is a reference to ancient
Greek mythology

 A combination of goat, lion
and snake …
Chimeras are not Hybrids

-Chimeras are organisms comprised of
-cells from two or more individuals of
the same or different species .


-Hybrids : crossbreeding of two
-different species .

-- Human- animal hybrids is a wrong term .

-- Because the chimera contains cells from
two different genetic individuals , and
each of these arose by mating , it has four
parents , a hybrid has only two parents
.
The Importance of Animal Research

  Every medical breakthrough
in the 20th century come
about as a result of research
with animals .
Chimeras , Transgenics , and
            Xenotransplantation

• Chimeras : DNA is not mixed



• Transgenics : Human DNA is mixed with animal
  or plant DNA

• Xenotransplantation : Human DNA might be mixed
  with animal DNA
Transgenic Animals

• Started with the purpose of producing
  better breed lines of farm animals .

• Moved forward in attempting to produce
  important biopharmaceuticals , to that of
  producing organs for humans .
Transgenic Animals

A transgenic animal is one
which has been genetically
altered to have a specific
characteristics it otherwise
would not have. In
animals transgenesis
either means transferring
DNA into the animal or
altering DNA already in
the animal .
Animal-Animal Chimeras

  In the last 25 years , researchers especially
from University of Cornell , have worked with
these half-half creatures , like :
     rabbit-tiger
      goat-sheep
      quail-chick
      mouse-horse
Sheep-Goat Chimera
-First developed by Dr. R.S.White , Australia in
1978.

-- Researches fused a sheep embryo with a
goat embryo , the resulting creature was a
mosaic of goat and sheep tissue . The parts
that grew from the sheep embryo were wooly ,
those from the goat embryo were hairy .

-- This chimera may be fertile , but it passes on
either sheep or goat genes , depending on
whether its reproductive organs were formed
from the goat or sheep embryos .
Quail-Chick Chimera

-Nicole Le Douarin , Institute of Embryology ,France.

--By inserting quail cells of early stages into a chicken
egg.

-- The quail cells act as markers , to be easily identified
when they differentiate and form the chick.

-- By comparing the final product with where the cells
are originally implanted , researchers were able to
track how each muscle develops and where that tissue
originated . The goal was to shed light on the
development of higher animal nervous and immune
systems .

-She showed that procursor cells within the neural crest
were multipotent.
The Vacanti Mouse
-By Dr Charles Vacanti , University of
Massachusetts in 1995.

-- Like a human ear . Was an ear-shaped
cartilage structure grown by seeding cow
cartilage cells – no human tissue used .

-- Created to demonstrate a method of
fabricating cartilage structures for
transplantation into human patients , a
resonable polyester fabric was infiltrated
with bovine cartilage cells and implanted
under the skin of hairless mouse .

-- The picture still provoke controversy .
Human Pluripotent Stem Cells

• hPSCs capable of turning into any kind of tissue
  and stem cells .

• hPSCs , theoretically provide an indefinitely
  renewable source of any kind of human tissue,
  thus offering tremendous potential for basic
  research , drug development and regenerative
  medicine .

• The first sources of hPSCs were human embryos .
How To Examine hPSCs

• The standard method to test that hPSCs are
  truly pluripotent is to inject them into postnatal
  immune-deficient mice , and see whether they
  give rise to teratomas ( tumors that consist of
  disorganized tissue gowth of the three embryonic
  germ layers : endoderm , mesoderm , and
  ectoderm )
Human-sheep
chimera
-By Dr. Esmail Zanjani
university of Nevada.

-This research is going for
the last 2 years and still.

-- Sheep contain 15%
human genes ,body of
sheep but organs that are
partly human.

-Goal is to have partly
human liver , lungs, heart
and brain for human
transplants.
Human-monkey chimera
- Dr Eugene Redmond , Yale University .

-Implanting several millions of human neural cells
(from stem cells )into the brain of an African green
monkey .

-- When the human cell mature they function as
living partners with the billions of monkey brain cells
that are already there.

-- Researchers putting 8-10 million human cells in a
monkey brain that may has 20-40 billion cells.

-- The goal is that will help supply a chemical called
dopamine , which is missing from the brains of
people who have Parkinson’s disease.
Human-Animal Chimeras for Vaccines
• - The field of vaccines for diseases such as
• (HIV) has faced major failures in recent years .

• - Diseases like malaria ,HIV , hepatitis C and dengue
  cause high morbidity and mortality in the
  developing world as compared to the developed
  world .
diseases
• - Viral infections caused by hepatitis B virus ,
  hepatitis C and HIV , affect more than 500 million
  people resulting in more than 3.5 million
  deaths/year .

• - Bacterial and parasitic diseases have a similarity
  high impact . Endemic and epidemic malaria result
  in severe disease in about half-a-billion people each
  year , and causes 1.5 million deaths annually ,
  mostly in developing countries .
Humanized Mice
• - Have recently emerged as powerful tools in the
  investigation of human diseases .
• - Models transplanted with human cells or tissues
  and/or human transgenes that are suited for direct
  investigation of human infections agents .
• - Recent researches focus on HBV, HCV, HIV, TB, and
  malaria , with mice carrying the target tissues of
  human pathogens , as well as bearing human
  immune components to react against them.
Examples of Humanized Mice
                  HIS Mice
• - (HIS) human immune system mice .
• - Are generated by grafting immune-deficient
  animals with suspensions of hematopoietic cells
  and/or human peripheral blood cells with
  supplemental human tissues supporting the
  generation of human immune cells.
• - HIS mice are already showing potential as the
  only available small animal model for HIV infection
  ,for testing the efficacy of antiviral compounds.
Ethical Issues
Chimeras Debate
• There are legitimate ethical questions
  related to chimeras

• At the same time The main health
  benefits of chimeras may occur in the
  developing world .
In The Developed Countries
• There is a strong vocal political opposition
  against chimeras in the west .

• Xenotransplantation and transgenic
  animals for drugs and disease models
  have not faced such opposition .
Rotavirus Vaccine Case
• In general ,there is a precedence of delays in the
  development of life-saving technologies when
  the perspective of communities in developing
  countries is not taken into account .

• Example : An earlier version of the rotavirus
  vaccine was removed from the market in the US
  in 1999, when few children developed negative
  symptoms which postponed research and
  subsequent introduction of rotavirus vaccine in
  developing countries ,where hundreds of
  thousands of children die every year from
  rotavirus associated diarrhea.
Risk and Benefits
Some health officials in the developing
 countries argue , that even though there
 was a small risk of negative effects in
 some children getting the vaccine , the
 benefits of testing the vaccine in
 developing countries , given the disease
 burden , far outweighed the risk .
Public Controversy
 Examples Of Public Media Headlines
* Scientists create animals that are part-human .
* the biological co-mingling of animal and human.
* What if a human mind somehow got trapped
   inside a sheep’s head .
* Harvesting human organs from sheep .
* Combining monkeys and people .
* Researches were attempting to play god ?
* Human born to mice parents ! ( national geog.)
* Mice with human brains .
The latest legislations in some developed
                 countries
• May 2008 : The UK House of Commons , decided
  that embryos would allowed to be made in
  laboratories only if guarantees of destroying them
  within the first 14 days were given.
• Jun2008 : Government of UK approved and granted
  a Newcastle University a permit to use cow eggs
  filled with human DNA to develop therapies for
  Parkinson’s disease and stroke victims ( all cow
  DNA would be removed before the human DNA
  would be inserted )
Legislation
• 2009 : Canada bans all chimera research .
• 2009 : The human-animal hybrid prohibition Act.
  Failed to pass the US Congress.
• June 2010 : In US , some States banned chimera
  research – Ohio-Oklahoma-Louisiana and Arizona.

• Feburary 2009 : US (FDA) ,announced approval of
  Atryn , an anticoagulant protein derived from the
  milk of transgenic goats , (first time) , it was
  approved in Europe before that .
Chimeras Ethical Issues
Summary



 The main concern is : will
chimeras eventually be developed
to be too human .
Chimeras Ethical Issues
 Bioethics , researchers , animal rights
activists ,and others interested in chimeras
can be divided in two broad categories :
1- Complete opposition to research of
    chimeras .
2- Concerns about particular research
    methods to be used , and outcomes
     that may result .
The group who are convinced
that human-animal chimera
should not performed at all .
Because :
• It involves research on human embryos
combining human and animal genetic material.

• Because it disregards the welfare of animals
and animal species involved , especially the
higher primates (Chimpanzees) .
The other group , not
completely opposed to the
research , their concerns :
•Could chimeras have human brains ?

•What is the potential for humanized
chimeras

•How will human-animal primate
chimeras be treated .
What are the scientists
opinions on human-animal
chimeras
•A concern must given to studies in which human
neurons or gametes might be incorporated into the
brain or gonads of a closely related primate.

*The permeability of the boundary between species

• Proposed research for chimeras must have
scientific merit ,be directed to increase the
knowledge and potential public benefit in
appropriate facilities with properly trained and
supported scientists and stuff.
Scientists opinions …….
• Chimeras are designed to have an immune system
  through the use of hESCs, which may allow for
  transgression of species boundaries .

• What would happen if human cells migrated to the
  central nervous system of a chimera and make
  connections with the animal’s neurons?

• The possibility of breeding generations of human-
  animal chimeras and the uncertainty of the nature
  of the offspring .
•
What researchers and research institutes
  working on human-animal chimeras say:
• Having only a few non-human cells in the final
  individual would not suffice since a human with a
  porcine heart valve is still a human being . But
  where to draw the line is unclear ,even for
  researchers .
• The moral confusion argument has been alleged to
  be at the heart of the public controversy ,but this
  allegation is not supported by the extensive social
  science research on public understanding and
  attitudes toward modern biotechnology.
Thank
you
Biosafety in Food and
     Agriculture




                  Tarek
                 Alfallah
Between the 60’s & 90’s

 Milk yield in most dairy cow breeds
 have been more than doubled

 Time needed to produce a slaughter-
 weight broiler fell from 40 to 80 days.
These achievements derive, and
        still increasing
1. improved management practices:
      Record keeping
      Breed societies
      Facilities & equipments
      Computer skills
2.   measurements of the genetic potential
      Heritability's of different traits
      Selection
      Advanced biometric models
Status of Genetically Modified
       GM crop Tech in Africa


Commercial production : Burkina Faso , Egypt and S.F

Confined field testing : Burkina Faso , Egypt , South
     Africa , Kenya , Uganda , Nigeria .

Contained research : at least 14 countries .
Genetic Progress For
         Quantitative Traits

 Made by selection on phenotype or on
  estimated breeding values (EBV)
 Without knowledge of the number of
  genes that affect the trait or the effects
  of each gene.
 Hundreds of genes may affect one
  quantitative trait .
      Molecular genetics
    allows for the study
    the genetic make-up of
    individuals at the DNA
    level .
TWO BIG DIFFERENCES
    Traditional                Genetic
Breeding Methods              Modification
 Require several          Progress can be
  generations to            achieved
  produce beneficial         in one generation .
  traits .
                           More precise ,
 Transfers all the         transfer only
  animal’s genes ( good     desirable genes .
  and bad ) to the next
  generation .
Molecular genetics either by



 Direct selection on genes that affect
  traits of interest , major genes or
  quantitative trait loci ( QTL ) .
 Selection on genetic markers linked
  to QTL .
Why molecular genetic information can
 result in greater gain than phenotypic
              information ?
 Not affected by environmental effects        and ,therefore,
  has heritability equal to 1.
 Can be available at an early age in principle at the
  embryo stage , thereby allowing early selection and
  reduction of generation interval .
 Can be obtained on all selection traits especially :
          - sex-linked traits
          - Expensive or difficult to record
          - Traits that require slaughter of the
             animal ( carcass traits )
One good reason to use new
       biotechnologies

 It ‘s been estimated that the supply
 of food required to adequately meet
 human nutritional needs over the
 next 40 years is equal to the
 amount of food previously produced
 throughout the entire history of
 humankind .
Reproductive
              technology         Genetic
                                modification

                                transgenics




                      Cloning

                                Pharmaceut-
                                 ical farm
Selection &
                                  Animals
  culling

                       Mating
BIOSAFETY

Protecting human and animal health and
Environment from the possible adverse
Effects of products of modern biotechnology
Four main events in the last
           40 years

The United Nations conference on the human
 environment and development .( 1972)

The Rio Earth Summit ( 1992)

Convention on Biodiversity (CBD) 1992

Cartagena Protocol on Biosafety (CPB) 1993
Biosafety issues of transgenic
 crops ( genetic pollution)


1- Laboratory green house stage
2- Confined trial stage

                   New genotypes



  gene flow or spreading by pollen grains or
  Other ways ; means genetically polluted the wild
  Type plant in the area ……
Risks of genetic pollution

 GMO’s enter the food chain


 The risk of loosing the wild type relatives of
  the transgenics ( the natural reserve of
  plant)

 Global warming and genotype –environment
  interaction
CONCL. & RECOM……….

 Biotechnology in food and agriculture already
  put its prints on the industry .

 Biotechnology is needed to the developing
  countries for their food security and health
  now and in the future .

 Modern biotechnology has been identified as
  the most potent technology for rescuing
  Africa from the effects of food shortages .
World focused on issues such as poverty and food
Security , as well as species loss and ecosystem
 destruction ; these quistions are among the most
 important and the most difficult in any society .


Scientific controversies regarding genetic science
cannot be resolved or decided on the basis of a
simple restatment of the scientific issues .
Developing country should establish a strategy
Put in place a legislation for promoting and
facilitating public awareness and education
concerning the new technologies .


Developing country should establish a
mechanism to ensure public access to
information on GM plants or animals that
might be imorted or experimented .
Thank you for your attention .

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Biotechnology in Food and Agriculture; the Biosafety Issues [Tarek Alfalah, University of Tripoli, Libya]

  • 2. Chimeras It is a reference to ancient Greek mythology A combination of goat, lion and snake …
  • 3. Chimeras are not Hybrids -Chimeras are organisms comprised of -cells from two or more individuals of the same or different species . -Hybrids : crossbreeding of two -different species . -- Human- animal hybrids is a wrong term . -- Because the chimera contains cells from two different genetic individuals , and each of these arose by mating , it has four parents , a hybrid has only two parents .
  • 4. The Importance of Animal Research Every medical breakthrough in the 20th century come about as a result of research with animals .
  • 5. Chimeras , Transgenics , and Xenotransplantation • Chimeras : DNA is not mixed • Transgenics : Human DNA is mixed with animal or plant DNA • Xenotransplantation : Human DNA might be mixed with animal DNA
  • 6. Transgenic Animals • Started with the purpose of producing better breed lines of farm animals . • Moved forward in attempting to produce important biopharmaceuticals , to that of producing organs for humans .
  • 7. Transgenic Animals A transgenic animal is one which has been genetically altered to have a specific characteristics it otherwise would not have. In animals transgenesis either means transferring DNA into the animal or altering DNA already in the animal .
  • 8.
  • 9.
  • 10. Animal-Animal Chimeras In the last 25 years , researchers especially from University of Cornell , have worked with these half-half creatures , like : rabbit-tiger goat-sheep quail-chick mouse-horse
  • 11. Sheep-Goat Chimera -First developed by Dr. R.S.White , Australia in 1978. -- Researches fused a sheep embryo with a goat embryo , the resulting creature was a mosaic of goat and sheep tissue . The parts that grew from the sheep embryo were wooly , those from the goat embryo were hairy . -- This chimera may be fertile , but it passes on either sheep or goat genes , depending on whether its reproductive organs were formed from the goat or sheep embryos .
  • 12. Quail-Chick Chimera -Nicole Le Douarin , Institute of Embryology ,France. --By inserting quail cells of early stages into a chicken egg. -- The quail cells act as markers , to be easily identified when they differentiate and form the chick. -- By comparing the final product with where the cells are originally implanted , researchers were able to track how each muscle develops and where that tissue originated . The goal was to shed light on the development of higher animal nervous and immune systems . -She showed that procursor cells within the neural crest were multipotent.
  • 13. The Vacanti Mouse -By Dr Charles Vacanti , University of Massachusetts in 1995. -- Like a human ear . Was an ear-shaped cartilage structure grown by seeding cow cartilage cells – no human tissue used . -- Created to demonstrate a method of fabricating cartilage structures for transplantation into human patients , a resonable polyester fabric was infiltrated with bovine cartilage cells and implanted under the skin of hairless mouse . -- The picture still provoke controversy .
  • 14.
  • 15. Human Pluripotent Stem Cells • hPSCs capable of turning into any kind of tissue and stem cells . • hPSCs , theoretically provide an indefinitely renewable source of any kind of human tissue, thus offering tremendous potential for basic research , drug development and regenerative medicine . • The first sources of hPSCs were human embryos .
  • 16. How To Examine hPSCs • The standard method to test that hPSCs are truly pluripotent is to inject them into postnatal immune-deficient mice , and see whether they give rise to teratomas ( tumors that consist of disorganized tissue gowth of the three embryonic germ layers : endoderm , mesoderm , and ectoderm )
  • 17. Human-sheep chimera -By Dr. Esmail Zanjani university of Nevada. -This research is going for the last 2 years and still. -- Sheep contain 15% human genes ,body of sheep but organs that are partly human. -Goal is to have partly human liver , lungs, heart and brain for human transplants.
  • 18. Human-monkey chimera - Dr Eugene Redmond , Yale University . -Implanting several millions of human neural cells (from stem cells )into the brain of an African green monkey . -- When the human cell mature they function as living partners with the billions of monkey brain cells that are already there. -- Researchers putting 8-10 million human cells in a monkey brain that may has 20-40 billion cells. -- The goal is that will help supply a chemical called dopamine , which is missing from the brains of people who have Parkinson’s disease.
  • 19. Human-Animal Chimeras for Vaccines • - The field of vaccines for diseases such as • (HIV) has faced major failures in recent years . • - Diseases like malaria ,HIV , hepatitis C and dengue cause high morbidity and mortality in the developing world as compared to the developed world .
  • 20. diseases • - Viral infections caused by hepatitis B virus , hepatitis C and HIV , affect more than 500 million people resulting in more than 3.5 million deaths/year . • - Bacterial and parasitic diseases have a similarity high impact . Endemic and epidemic malaria result in severe disease in about half-a-billion people each year , and causes 1.5 million deaths annually , mostly in developing countries .
  • 21. Humanized Mice • - Have recently emerged as powerful tools in the investigation of human diseases . • - Models transplanted with human cells or tissues and/or human transgenes that are suited for direct investigation of human infections agents . • - Recent researches focus on HBV, HCV, HIV, TB, and malaria , with mice carrying the target tissues of human pathogens , as well as bearing human immune components to react against them.
  • 22.
  • 23. Examples of Humanized Mice HIS Mice • - (HIS) human immune system mice . • - Are generated by grafting immune-deficient animals with suspensions of hematopoietic cells and/or human peripheral blood cells with supplemental human tissues supporting the generation of human immune cells. • - HIS mice are already showing potential as the only available small animal model for HIV infection ,for testing the efficacy of antiviral compounds.
  • 24.
  • 26. Chimeras Debate • There are legitimate ethical questions related to chimeras • At the same time The main health benefits of chimeras may occur in the developing world .
  • 27. In The Developed Countries • There is a strong vocal political opposition against chimeras in the west . • Xenotransplantation and transgenic animals for drugs and disease models have not faced such opposition .
  • 28. Rotavirus Vaccine Case • In general ,there is a precedence of delays in the development of life-saving technologies when the perspective of communities in developing countries is not taken into account . • Example : An earlier version of the rotavirus vaccine was removed from the market in the US in 1999, when few children developed negative symptoms which postponed research and subsequent introduction of rotavirus vaccine in developing countries ,where hundreds of thousands of children die every year from rotavirus associated diarrhea.
  • 29. Risk and Benefits Some health officials in the developing countries argue , that even though there was a small risk of negative effects in some children getting the vaccine , the benefits of testing the vaccine in developing countries , given the disease burden , far outweighed the risk .
  • 30. Public Controversy Examples Of Public Media Headlines * Scientists create animals that are part-human . * the biological co-mingling of animal and human. * What if a human mind somehow got trapped inside a sheep’s head . * Harvesting human organs from sheep . * Combining monkeys and people . * Researches were attempting to play god ? * Human born to mice parents ! ( national geog.) * Mice with human brains .
  • 31. The latest legislations in some developed countries • May 2008 : The UK House of Commons , decided that embryos would allowed to be made in laboratories only if guarantees of destroying them within the first 14 days were given. • Jun2008 : Government of UK approved and granted a Newcastle University a permit to use cow eggs filled with human DNA to develop therapies for Parkinson’s disease and stroke victims ( all cow DNA would be removed before the human DNA would be inserted )
  • 32. Legislation • 2009 : Canada bans all chimera research . • 2009 : The human-animal hybrid prohibition Act. Failed to pass the US Congress. • June 2010 : In US , some States banned chimera research – Ohio-Oklahoma-Louisiana and Arizona. • Feburary 2009 : US (FDA) ,announced approval of Atryn , an anticoagulant protein derived from the milk of transgenic goats , (first time) , it was approved in Europe before that .
  • 33. Chimeras Ethical Issues Summary The main concern is : will chimeras eventually be developed to be too human .
  • 34. Chimeras Ethical Issues Bioethics , researchers , animal rights activists ,and others interested in chimeras can be divided in two broad categories : 1- Complete opposition to research of chimeras . 2- Concerns about particular research methods to be used , and outcomes that may result .
  • 35. The group who are convinced that human-animal chimera should not performed at all . Because : • It involves research on human embryos combining human and animal genetic material. • Because it disregards the welfare of animals and animal species involved , especially the higher primates (Chimpanzees) .
  • 36. The other group , not completely opposed to the research , their concerns : •Could chimeras have human brains ? •What is the potential for humanized chimeras •How will human-animal primate chimeras be treated .
  • 37. What are the scientists opinions on human-animal chimeras •A concern must given to studies in which human neurons or gametes might be incorporated into the brain or gonads of a closely related primate. *The permeability of the boundary between species • Proposed research for chimeras must have scientific merit ,be directed to increase the knowledge and potential public benefit in appropriate facilities with properly trained and supported scientists and stuff.
  • 38. Scientists opinions ……. • Chimeras are designed to have an immune system through the use of hESCs, which may allow for transgression of species boundaries . • What would happen if human cells migrated to the central nervous system of a chimera and make connections with the animal’s neurons? • The possibility of breeding generations of human- animal chimeras and the uncertainty of the nature of the offspring . •
  • 39. What researchers and research institutes working on human-animal chimeras say: • Having only a few non-human cells in the final individual would not suffice since a human with a porcine heart valve is still a human being . But where to draw the line is unclear ,even for researchers . • The moral confusion argument has been alleged to be at the heart of the public controversy ,but this allegation is not supported by the extensive social science research on public understanding and attitudes toward modern biotechnology.
  • 41. Biosafety in Food and Agriculture Tarek Alfallah
  • 42. Between the 60’s & 90’s  Milk yield in most dairy cow breeds have been more than doubled  Time needed to produce a slaughter- weight broiler fell from 40 to 80 days.
  • 43. These achievements derive, and still increasing 1. improved management practices:  Record keeping  Breed societies  Facilities & equipments  Computer skills 2. measurements of the genetic potential  Heritability's of different traits  Selection  Advanced biometric models
  • 44. Status of Genetically Modified GM crop Tech in Africa Commercial production : Burkina Faso , Egypt and S.F Confined field testing : Burkina Faso , Egypt , South Africa , Kenya , Uganda , Nigeria . Contained research : at least 14 countries .
  • 45. Genetic Progress For Quantitative Traits  Made by selection on phenotype or on estimated breeding values (EBV)  Without knowledge of the number of genes that affect the trait or the effects of each gene.  Hundreds of genes may affect one quantitative trait .
  • 46. Molecular genetics allows for the study the genetic make-up of individuals at the DNA level .
  • 47. TWO BIG DIFFERENCES Traditional Genetic Breeding Methods Modification  Require several  Progress can be generations to achieved produce beneficial in one generation . traits .  More precise ,  Transfers all the transfer only animal’s genes ( good desirable genes . and bad ) to the next generation .
  • 48. Molecular genetics either by  Direct selection on genes that affect traits of interest , major genes or quantitative trait loci ( QTL ) .  Selection on genetic markers linked to QTL .
  • 49. Why molecular genetic information can result in greater gain than phenotypic information ?  Not affected by environmental effects and ,therefore, has heritability equal to 1.  Can be available at an early age in principle at the embryo stage , thereby allowing early selection and reduction of generation interval .  Can be obtained on all selection traits especially : - sex-linked traits - Expensive or difficult to record - Traits that require slaughter of the animal ( carcass traits )
  • 50. One good reason to use new biotechnologies  It ‘s been estimated that the supply of food required to adequately meet human nutritional needs over the next 40 years is equal to the amount of food previously produced throughout the entire history of humankind .
  • 51. Reproductive technology Genetic modification transgenics Cloning Pharmaceut- ical farm Selection & Animals culling Mating
  • 52. BIOSAFETY Protecting human and animal health and Environment from the possible adverse Effects of products of modern biotechnology
  • 53. Four main events in the last 40 years The United Nations conference on the human environment and development .( 1972) The Rio Earth Summit ( 1992) Convention on Biodiversity (CBD) 1992 Cartagena Protocol on Biosafety (CPB) 1993
  • 54. Biosafety issues of transgenic crops ( genetic pollution) 1- Laboratory green house stage 2- Confined trial stage New genotypes gene flow or spreading by pollen grains or Other ways ; means genetically polluted the wild Type plant in the area ……
  • 55. Risks of genetic pollution  GMO’s enter the food chain  The risk of loosing the wild type relatives of the transgenics ( the natural reserve of plant)  Global warming and genotype –environment interaction
  • 56. CONCL. & RECOM……….  Biotechnology in food and agriculture already put its prints on the industry .  Biotechnology is needed to the developing countries for their food security and health now and in the future .  Modern biotechnology has been identified as the most potent technology for rescuing Africa from the effects of food shortages .
  • 57. World focused on issues such as poverty and food Security , as well as species loss and ecosystem destruction ; these quistions are among the most important and the most difficult in any society . Scientific controversies regarding genetic science cannot be resolved or decided on the basis of a simple restatment of the scientific issues .
  • 58. Developing country should establish a strategy Put in place a legislation for promoting and facilitating public awareness and education concerning the new technologies . Developing country should establish a mechanism to ensure public access to information on GM plants or animals that might be imorted or experimented .
  • 59. Thank you for your attention .