ASA Newsletter

For the Professional in Government, Industry and Academia with an interest in Nuclear, Biological and Chemical Defense, Disarmament and Verification; Chemical and Biological Terrorism; Emergency and Disaster Medical Planning; Industrial Health and Safety; and Environmental Protection.

ASA 02-1, Issue No. 88, February 29, 2002


CBMTS IV: Selected Abstracts

Anthrax Vaccines: Future Targets
Robert M. DeBell, Ph.D. , Battelle Memorial Institute

          In 1997, a Russian paper in the journal Vaccine described the transfer of the cereolysin AB genes from B. cereus to B. anthracis. This recombinant B. anthracis lysed red blood cells and caused anthrax in Golden hamsters vaccinated with the STI-1 vaccine. These two observations may not be mutually exclusive. A recent report from a group at the Institut Pasteur showed that the insertion of a multicopy plasmid containing the plcR gene into B. anthracis resulted in the expression of several proteins. Similar results were obtained when a single copy of the plcR gene was inserted into the chromosome of B. anthracis. In both cases, the recombinant organisms showed hemolytic activity. Using an E. coli T7 expression system, another research group cloned the cereolysin AB genes (cerA and cerB) and the plcR gene from both B. anthracis and B. cereus. They found that cerA and cerB in B. anthracis are functionally active and similar to those of B. cereus.

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The Chemical and Biological Medical Treatment Symposium (CBMTS) IV
Spiez Laboratory

Spiez, Switzerland
28 April - 3 May 2002

Spiez, Switzerland.
          Many to most of the registration forms have been completed, accommodations are being selected, and many to most of the abstracts have been received. We are still accepting requests for registration but the numbers to be accepted will be limited because of space restraints.
          We are very pleased with the number, exceptional high quality and the pertinence of the papers to today's environment and the CBMTS IV requirements. These papers cover every facet of the problems all face in the convoluted and complex arena of chemical, biological and radiological readiness, whether the problems are war, terrorism or accidents and incidents involving the civil and military infrastructure, public health and the industrial base in every country. These papers not only help surface and define the problems but they provide the knowledge needed to develop those solutions that most adequately fit the requirements of our members as individuals and as representatives of over 25 countries that will be present at CBMTS IV.

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The Anthrax Saga: A Different Scenario
by Reginald Bartholomew

          Although the US position seems to be that the prime suspect in the Anthrax saga is an American, could we consider a different scenario? Could this scenario be wrong - sure.
          Some givens in our position are based on assumptions. The US does not operate in a vacuum and what is available in the US is in all probability available around the world where there is technical expertise and the required funds to carry out whatever program is desired. ASA has previously stated that US organizations, such as American Type Culture and others in that business, have sold feed stock for innumerable pathogens to innumerable bad actors, such as Saddam, over the many years that it took them to understand that academic freedom in a dictatorship is problematic at best. Actually, Congress put the pressure on these organizations to get their act together.

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Due to events following September 11th, the focus of recent ASA Newsletter issues has been predominantly on bio and terrorism. Now, with John Hart's piece on the current treatment of PFIB under the CWC, the Newsletter is able to shift back towards the problems within the chemical arena. PFIB will be familiar to most as a potential CW agent. It is also produced in significant quantities by the fluoropolymer industry as a temporary by-product. The article shows CWC implementation at the working-level and gives readers background information on how the chemical might be captured by the CWC. As always the ASA Newsletter would welcome your comments on this significant area.

The Treatment of Perfluorisobutylene under the Chemical Weapons Convention
by John Hart
SIPRI*

          Introduction Perfluoroisobutylene (PFIB) is produced as a common by-product, in tens of thousands of ton quantities, in the fluoropolymer industry, including the production of 1,1,1,3,3,3-hexafluoro-2-propanol (HFP) and tetrafluoroethylene (TFE) and processes involving the pyrolysis of polytetrafluoroethene (PTFE), more commonly known by its trade name Teflon. As an unwanted by-product with apparently no known commercial uses above 1 metric ton [1], it is generally eliminated through scrubbing or thermal treatment. PFIB can cause pulmonary edema and those affected must then be treated for "polymer fume fever."[2] It can also act as a "mask breaker". Because PFIB is nonpolar it cannot be adsorbed by carbon. [3] PFIB's toxicity and effect are similar to those of phosgene and, like phosgene, no treatment for exposure is currently available with the exception of complete avoidance of physical activity. Based on publicly available literature, it seems impossible to state with certainty whether the compound has ever actually been weaponized and incorporated into an offensive chemical weapon (CW) program.

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For the Professional in Government and Industry with an interest in Nuclear, Biological and Chemical Defense, Disarmament and Verification; Emergency and Disaster Medical Planning; Industrial Health and Safety; and Environmental Protection