October 20, 2003 an article
by Prof. Joe Cummins ( his unedited personal opinion )
e-mail: jcummins@ uwo.ca
" Biosafety
standards for Molecular Farming "
Molecular Farming is primarily focused on the production of biopharmaceutical
proteins in crop plants. Field testing of genetically modified (GM) corn,
canola , tobacco, alfalfa, safflower, rice and tobacco mosaic virus. Seventy-seven
such tests have been undertaken in the United States and a large number
in other countries. These tests have been undertaken , for the most part,
with extreme secrecy regarding location, nature of the product being tested
and the safety considerations of the tests. The few published reviews
of the environmental and human safety evaluations of the tests focused
mainly on the possibility of pollen flow to nearby crops and weeds and
ignored the real hazards of seed transfer by farm machinery and on vehicles
of all types along with browsing animals. The likely pollution of surface
and groundwater by crop leaves and roots debris and breakdown has been
almost entirely ignored event though the pharmaceutical products were
active in minute quantity.
Considering acceptable safety standards for undertaking field tests and
production of biopharmaceutical crops the following recommendations should
be considered:
1. Field tests and production facilities should be fully disclosed to
the public in a timely way. Both the location and the nature of the product
being grown should be made available to the public and any known deleterious
side effects of the product should be disclosed. Public health authorities
should be provided methods of detecting the product in environmental samples
and in human blood and urine.
2. Production and testing of high potency biopharmaceutical products should
be limited to fully isolated green house facilities. The facility should
have restricted human contact ans to prevent access by insects and birds.
Contact with the soil and groundwater should be controlled and only treated
wastewater released from the facility. Most of the biopharmaceutical products
are high value items that can be produced economically in a fully isolated
facility. Organic waste from the facility should be incinerated on site.
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3. All molecular farming production should undertake full studies on the
spread of pollen and seeds from the production sites. Adequate methods
for high sensitivity detection of pollutants in surface and groundwater
should be made available and studies should be undertaken, if possible
, by neutral third parties
Implementation of the standards described above should go a long ways
towards making Molecular Farming acceptable by farmers and the public.
Biographical Sketch:
I am Professor Emeritus of Genetics , University of Western Ontario, London,
Ontario. I was born in Whitefish , Montana Feb. 5, 1933. I obtained a
BS degree in Horticulture, Washington State University 1955 and a PhD
degree in Cellular Biology from University of Wisconsin 1962. My postdoctoral
work was at Edinburgh , Palermo, Stockholm (Karolinska) and the Macardle
Laboratory for Cancer Research University of Wisconsin. I taught genetics
at Rutgers and the University of Washington, Seattle before joining The
University of Western Ontario in 1972. My involvement in environmental
issues arose in 1968 and I have been involved in a range of issues involving
mercury, asbestos and PCB pollution and pesticide pollution along with
waste sites and incinerators. My criticism of genetic modification by
genetic engineering beginning in 1988 when I encountered the power of
multinational corporations over the federal government and their refusal
to face serious risk evaluations.
I have published over 200 scientific and popular articles, my most recent
papers appeared in Nature Biotechnology, The Ecologist, and Biotechnology
and Development Review. I have a number of reviews and comments listed
on the website of The Institute of Science in Society, PO Box 32097, London
NW1 OXR UK http://www.i-sis.org.uk/
© molecularfarming.com 2003
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