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  • Dr Mercola interviews Dr Huber about GMO

    Dr Huber describes the hazards of using glyphosate herbicide (Roundup by Monsanto) and the “Roundup Ready” glyphosate-resistant genetically modified line of crops.  This is particularly relevant now due to the recent deregulation of glyphosate resistant GMO alfalfa for animal feed.

    He also announces the discovery of a novel pathogenic organism which is associated with GMO-induced infertility in animals and humans.

    Hopefully this will inspire farmers to rethink their use of Round Up and consumers to demand proper labeling of GMO foods.

  • RNA interference (RNAi)

    Biotech breakthru could allow temporary control over gene expression

    Zero Hedge

    .. As the name implies, the technique involves interrupting the function of RNA (ribonucleic acid), one of the key components of all living cells.

    Once genetic mapping became a reality, researchers quickly discovered that it was possible to sabotage wayward mRNA before it ever gets to the ribosome. All you had to do was synthesize the anti-sense form of the undesirable mRNA and inject it into the cell, where it would bond with the sense sequence automatically, effectively “switching off” the message. If the ribosome can’t read it, you’ve achieved RNA interference, and the offending proteins will never be produced at all.

    Read more

  • The Future of Food

  • Fury as EU approves GM potato

    Critics claim plant could spread antibiotic-resistant diseases to humans

    BASF's genetically modified Amflora potato, which has just been approved by the European Commission, contains genes that are resistant to antibiotics By Martin Hickman and Genevieve Roberts
    Thursday, 4 March 2010
    Independent.co.uk

    BASF’s genetically modified Amflora potato, which has just been approved by the European Commission, contains genes that are resistant to antibiotics

    The introduction of a genetically modified potato in Europe risks the development of human diseases that fail to respond to antibiotics, it was claimed last night.

    German chemical giant BASF this week won approval from the European Commission for commercial growing of a starchy potato with a gene that could resist antibiotics – useful in the fight against illnesses such as tuberculosis.

    Farms in Germany, Sweden, the Netherlands and the Czech Republic may plant the potato for industrial use, with part of the tuber fed to cattle, according to BASF, which fought a 13-year battle to win approval for Amflora. But other EU member states, including Italy and Austria and anti-GM campaigners angrily attacked the move, claiming it could result in a health disaster.

    During the regulatory tussle over the potato, the EU’s pharmaceutical regulator had expressed concern about its potential to interfere with the efficacy of antibiotics on infections that develop multiple resistance to other antibiotics, a growing problem in human and veterinary medicine. Amflora contains a gene that produces an enzyme which generally confers resistance to several antibiotics, including kanamycin, neomycin, butirosin, and gentamicin.

    The antibiotics could become “extremely important” to treat otherwise multi-resistant infections and tuberculosis, the European Medicines Authority (EMA) warned. Drug resistance is part of the explanation for the resurgence of TB, which infects eight million people worldwide every year.

    “In the absence of an effective therapy, infectious Multiple Drug Resistant TB patients will continue to spread the disease, producing new infections with MDR-TB strains,” an EMA spokesman said. “Until we introduce a new drug with demonstrated activity against MDR strains, this aspect of the TB epidemic could explode at an exponential level.”

    After member states become deadlocked on the potato’s approval, the European Commission approved it for use in industries such as paper production, saying it would save energy, water and chemicals. Once the starch has been removed, the skins can be fed to animals, whose meat would not have to be labelled as GM.

    The EC, whose decision was backed by the European Food Safety Authority (Efsa), said there was no good reason for withholding approval. Health and consumer policy commissioner John Dalli said: “Responsible innovation will be my guiding principle when dealing with innovative technologies.”

    “Stringent” controls would ensure none of the tubers were left in the ground, ensuring altered genes did not escape into the environment. Opponents fear bacteria inside the guts of animals fed the GM potato – which can cause human diseases – may develop resistance to antibiotics.

    Some member states were furious. “Not only are we against this decision, but we want to underscore that we will not allow the questioning of member states’ sovereignty on this matter,” said Italy’s Agriculture Minister, Luca Zaia. Austria said it would ban cultivation of the potato within its borders, while France said it would ask an expert panel for further research.

    Campaigners accused Brussels of failing to follow the precautionary principle. Friends of the Earth’s Heike Moldenhauer said: “The commissioner whose job is to protect consumers has, in one of his first decisions, ignored public opinion and safety concerns to please the world’s biggest chemical company.”

    Campaigners suspect Brussels is in favour of the widespread planting of GM crops despite opposition by some member states. Yesterday it also announced its intention to allow states more leeway in backing GM organisms.

  • Texas Supplied Newborn Blood Samples to Forensic Database

    by Jennifer Couzin-Frankel on February 22, 2010 3:58 PM | ScienceMag.org

    Dogged investigation by a non-profit online media organization in Texas has revealed that between 2003 and 2007, the state quietly gave hundreds of newborn blood samples to a U.S. Armed Forces laboratory for use in a forensics database. The revelation will likely raise questions about how newborn screening programs are run and how the samples are disseminated, almost always without families knowing where they go.

    In this case, 800 blood samples were to be part of a new, national mitochondrial DNA database intended as a reference databank for the forensic community and for research into mitochondrial DNA variation—DNA we inherit from our mother. California, Minnesota, and Florida have also reportedly supplied infant blood samples to the effort, according to The Texas Tribune investigation.

    Like virtually every state, Texas routinely screens almost all newborns for rare diseases, collecting a few drops of blood at birth. In recent years many states, Texas included, have stored the samples and offered them up for research, mainly in pediatrics. Because the samples are anonymous (though they may come with some demographic information, depending on the study), researchers have argued that they don’t need to seek informed consent to use them.

    That hasn’t gone over well recently; in March of last year, a civil rights group sued the Texas screening program. In December, the state settled the case and agreed to destroy all newborn blood spots collected before May 2009, when legislation passed allowing for sample storage.

    That’s where the story gets interesting. The Texas Tribune describes a drawn-out effort to review records of the newborn blood spots. After a couple requests, the Texas Department of State Health Services released a batch of documents, which included a single e-mail mentioning the mtDNA project at the Armed Forces Institute of Pathology in Washington, D.C. “When the Tribune pressed health officials about the missing research files, they produced them, saying it was an oversight, and that the documents had been overlooked in their initial search,” writes The Tribune’s Emily Ramshaw.

    There’s growing concern among researchers that public wariness about the newborn screening program will create a backlash—with parents declining to screen their kids (who may end up much sicker because their disease wasn’t caught early), and with the spots no longer made available for valuable pediatrics research, such as tracing the origins of childhood leukemia. This new revelation is likely to fan those flame—even if the samples in question are being destroyed.

  • First commercial 3-D bio-printer makes human tissue and organs

    rdmag.com
    Thursday, December 10, 2009

    Invetech, an innovator in new product development and custom automation for the biomedical, industrial and consumer markets, today announced that it has delivered the world’s first production model 3D bio-printer to Organovo, developers of the proprietary NovoGen bioprinting technology. Organovo will supply the units to research institutions investigating human tissue repair and organ replacement.

    Dr. Fred Davis, president of Invetech, which has offices in San Diego and Melbourne, said, “Building human organs cell-by-cell was considered science fiction not that long ago. Through this clever combination of technology and science we have helped Organovo develop an instrument that will improve people’s lives, making the regenerative medicine that Organovo provides accessible to people around the world.”

    First commercial 3-D bio-printer makes human tissue and organs

    Keith Murphy, CEO of Organovo, based in San Diego, said the units represent a breakthrough because they provide for the first time a flexible technology platform for organizations working on many different types of tissue construction and organ replacement.

    ”Scientists and engineers can use the 3-D bio printers to enable placing cells of almost any type into a desired pattern in 3-D,” said Murphy. “Researchers can place liver cells on a preformed scaffold, support kidney cells with a co-printed scaffold, or form adjacent layers of epithelial and stromal soft tissue that grow into a mature tooth. Ultimately the idea would be for surgeons to have tissue on demand for various uses, and the best way to do that is get a number of bio-printers into the hands of researchers and give them the ability to make three dimensional tissues on demand.”

    The 3-D bio-printers include an intuitive software interface that allows engineers to build a model of the tissue construct before the printer commences the physical constructions of the organs cell-by-cell using automated, laser-calibrated print heads.

    To help them develop the 3D bio-printers, Organovo selected Invetech in May 2009 as their technology development partner. “We selected Invetech because of their capabilities for sophisticated engineering and automation, cultural fit as a long term partner and their consideration towards protecting Organovo’s bioprinting IP and maximizing our commercial return on the program. They have good processes for product development and project management, and it was apparent that project execution would be handled very well. Invetech really offered the best overall package.” said Mr. Murphy.

    Invetech was asked to design and develop a highly integrated, extremely reliable and simple to use 3D bio-printer system which could then be transferred to manufacture and commercial sale. Because of its history with precision design, robotics and manufacturing products, Invetech was able to combine prior art with new ideas to come up with a development plan that met Organovo’s budget and design goals. The process advanced smoothly and on schedule with Invetech teams in Melbourne and its San Diego office, not far from the Organovo office.

    The printer, developed by Invetech, fits inside a standard biosafety cabinet for sterile use. It includes two print heads, one for placing human cells, and the other for placing a hydrogel, scaffold, or support matrix. One of the most complex challenges in the development of the printer was being able to repeatedly position the capillary tip, attached to the print head, to within microns. This was essential to ensure that the cells are placed in exactly the right position. Invetech developed a computer controlled, laser-based calibration system to achieve the required repeatability.

    Invetech plan to ship a number of 3D bio-printers to Organovo during 2010 and 2011 as a part of the instrument development program. Organovo will be placing the printers globally with researchers in centers of excellence for medical research

    Invetech

    Organovo

  • closer, now…

  • Just what we needed: DARPA’s radioactive cyborg insects

    Via: IEEE:

    This week at the International Electron Devices Meeting (IEDM), in Baltimore, Md., Cornell University engineers presented research that shows progress in powering cybernetic organisms with a radioactive fuel source.

    Electrical engineering associate professor Amit Lal and graduate student Steven Tin presented a prototype microelectromechanical systems (MEMS) transmitter—an RF-emitting device powered by a radioactive source with a half-life of 12 years, meaning that it could operate autonomously for decades. The researchers think the new RFID transmitter, which produces a 5-milliwatt, 10-microsecond-long, 100-megahertz radio-frequency pulse, could lead to the widespread use of radioisotope power sources.

    The work is funded by the Defense Advanced Research Projects Agency (DARPA), which also funds Lal and Tin’s work on another project, called Hybrid Insect Micro-Electro-Mechanical Systems (HI-MEMS), whose aim is the creation of hybrid cybernetic organisms. In his presentation, Tin said that part of the goal of the radioisotope transmitter work is to power the insects that the group is developing for DARPA. The HI-MEMS program, which is approaching its fourth year, has already grown several kinds of insects—moths and beetles—with implanted control electronics. With such controls, they can be driven by a remote operator for ”stealth applications” and disaster response.

    The insects themselves are powered by their own living tissue, but the onboard electronics (sensors and transmitters) require a separate power source. But the insects are too light to carry batteries, and logistical problems would prevent regular battery changes regardless. Therefore, Lal and his group at Cornell turned to radioactive isotopes to generate the necessary power.