| |||||||||||||||
|
|||||||||||||||
| Copyright © 2009. National Academy of Sciences. All rights reserved. Terms of Use and Privacy Statement |
Below are the first 10 and last 10 pages of uncorrected machine-read text (when available) of this chapter, followed by the top 30 algorithmically extracted key phrases from the chapter as a whole.
Intended to provide our own search engines and external engines with highly rich, chapter-representative searchable text on the opening pages of each chapter.
Because it is UNCORRECTED material, please consider the following text as a useful but insufficient proxy for the authoritative book pages.
Do not use for reproduction, copying, pasting, or reading; exclusively for search engines.
OCR for page 74
F
Australia Group
Chaired by Australia, the "Australia Group" (AG) is an informal forum of states whose goal is to
discourage and impede chemical weapons (COO) proliferation by harmonizing national export controls on
CW precursor chemicals, sharing information on target countries, and seeking other ways to curb the use
of CW.
The Group was formed in 1984 as a result of CW use in the Iran-Iraq war. Members meet annually in
Paris, where the 1925 Geneva Protocol is deposited. The Group's actions are viewed as complementary
measures in support of the 1925 Geneva Protocol, the 1972 Biological and Toxins Weapons Convention
and the 1993 Chemical Weapons Convention.
There are presently 30 members of the Group, including: EC-12, Australia, Argentina, Austria, Czech
Republic, Hungary, Iceland, New Zealand, Japan, Canada, Norway, Finland, Sweden, Switzerland,
Poland, Romania, the Slovak Republic, South Korea, and the United States. Requests by other states to
join the Group are considered on a case-by-case basis.
The Group has no charter or constitution. It operates by consensus. On December 10, 1992, the AG
issued its first joint background paper on the Group's activities.
The Group has established common export controls for chemical and biological weapons
nonproliferation purposes. For CW, members of the AG control a list of 54 chemical precursors and a
list of CW-related production equipment as well. For BW, members have established export controls on
certain microorganisms, toxins, and equipment that could be used in a BW program.
In tandem with export controls, the AG has periodically used warning mechanisms to sensitize its public
to CBW proliferation. The Group has issued an informal "warning list" of dual-use CW precursors and
bulk chemicals, and on CW-related equipment. Members develop and share the warning lists with their
chemical industries and ask industry to report on any suspicious transactions. The AG has also used an
approach to warn industry, the scientific community, and other relevant groups of the risk of
inadvertently aiding BW proliferation.
The Group's meetings focus on sharing information about national export controls, considering proposals
for "harmonization" the adoption of common controls by all members on chemical precursors,
equipment, biological weapons related materials, and considering other measures to address CBW
proliferation and use.
LIST OF DUAL-USE BIOLOGICAL EQUIPMENT
FOR EXPORT CONTROL
Complete containment facilities at P3, P4 containment level
Complete containment facilities that meet the criteria for P3 or P4 (BL3, BL4, L3, L4)
containment as specified in the WHO Laboratory Biosafety manual (Geneva, 1983) are subject to
export control.
OCR for page 75
2. Fermenters*
Fermenters capable of cultivation of pathogenic micro-organisms, or viruses or of toxin
production, without the propagation of aerosols, and having all the following characteristics:
(a) Capacity equal to or greater than ~ 00 litres.
*Sub-groups of fermenters include bioreactors, chemostats and continuous-flow systems.
3. Centrifugal Separators*
Centrifugal separators capable of the continuous separation of pathogenic microorganisms,
without the propagation of aerosols, and having all the following characteristics:
(a) Flow rate greater than 100 litres per hour;
(b) Components of polished stainless steed or titanium;
(c) Double or multiple sealing joints within the steam containment area; and
(d) Capable of in-situ steam sterilization in a closed state.
*Centrifugal separators include decanters.
4. Cross-flow filtration equipment
Cross-flow filtration equipment capable of continuous separation of pathogenic microorganisms
viruses, toxins, and cell cultures without the propagation of aerosols, having all the following
characteristics:
(a) Equal to or greater than 5 square metros;
(b) Capable of in situ sterilization.
a. Freeze-drying equipment
Steam sterilizable freeze-drying equipment with a condenser capacity greater than 50 kg of ice in
24 hours and less than ~ 000 kg of ice in 24 hours.
6. Equipment that incorporates or is contained in P3 or P4 (BL3, BL4, L3, L4) containment
housing, as follows:
(a) Independently ventilated protective full or half suits; and
(b) Class Ill biological safety cabinets or isolators with similar performance standards.
7. Aerosol inhalation chambers
Chambers designed for aerosol challenge testing with microorganisms, viruses, or toxins and
having a capacity of ~ cubic metre or greater.
The experts propose that the following items be included in awareness-raising guidelines to industry:
OCR for page 76
1. Equipment for the microencapsulation of live microorganisms and toxins in the range of ~ -! 0 ,um
particle size, specifically:
(a) Tnterfacial polycondensors; and
(b) Phase separators.
2. Fermenters of less than 100 litre capacity with special emphasis on aggregate orders or designs
for use in combined systems.
3. Conventional or turbulent air-flow clean-air rooms and self-contained fan-HEPA filter units that
may be used for P3 or P4 (BL3, BL4, L3, L4) containment facilities.
LIST OF BIOLOGICAL AGENTS FOR EXPORT
CONTROL CORE LIST
Viruses
V! . Chikungunya virus
V2. Congo-Crimean haemorrhagic fever virus
V3. Dengue fever virus
V4. Eastern equine encephalitis virus
V5. Ebola virus
V6. Hantaan virus
V7. Junin virus
V8. Lassa fever virus
V9. Lymphocytic choriomeningitis virus
VI0. Machupo virus
V! ~ . Marburg virus
VI2. Monkeypox virus
VI3. Rift Valley fever virus
Vl4. Tick-borne encephalitis virus (Russian spring-summer encephalitis virus)
V! 5. Variola virus
VI6. Venezuelan equine encephalitis virus
VI7. Western equine encephalitis virus
Vl 8. White pox
V!9. Yellow fever virus
V20. Japanese encephalitis virus
Rickettsiae
RI. Coxiella burnetii
R2. Bartonelia quintana (Rochalimea quintana, Rickettsia quintana)
R3. Rickettsia prowasecki
R4. Rickettsia rickettsii
Bacteria
Bl. Bacillus anthracis
B2. Brucella abortus
OCR for page 77
B3. Brucelia meliter~sis
B4. Brz~celia suds
B5. Chlamydia psittaci
B6. Clostridium botulinum
B7. Frar~cisella tularensis
B8. Burkholderia mallet (Pseudomonas malleiJ
B9. Burkholderia pseudomallei (Pse?~domonas pseudomallei)
B10. Salmonella typhi
B 1 1. Shigella dysenteriae
Bl2. Vibrio cholerae
B13. Yersiniapestis
GeneticallY modified microorganisms
GI. Genetically modif~ed microorganisms or genetic elements that contain nucleic acid sequences
associated with pathogenicity and are derived from organisms in the core list.
G2. Genetically modif~ed microorganisms or genetic elements that contain nucleic acid sequences
coding for any of the toxins in the core list or their subunits.
l oxins as follows and subunits thereof:2
TI. Botulinum toxins
T2. Clostridium perfringens toxins
T3. Conotoxin
T4. Ricin
T5. Saxitoxin
T6. Shiga toxin
T7. Staphylococcus aureus toxins
T8. Tetrodotoxin
T9. Verotoxin
TI0. Microcystin (Cyanginosin)
T! T. Aflatoxins
.
1. Except where the agent is in the form of a vaccine.
2. Excluding immunotoxins.
WA~ING LIST~
Viruses
WVI. Kyasanur Forest virus
WV2. Louping ill virus
WV3. Murray Valley encephalitis virus
WV4. Omsk haemorrhagic fever virus
WV5. Oropouche virus
WV6. Powassan virus
WV7. Rocio virus
OCR for page 78
WV8. St. Louis encephalitis virus
Bacteria
WE 1. Clostridium perfringens*
WB2. Clostridium tetani*
WB3. Enterohaemorrhagic Escherichia colt, serotype 0157, and other verotoxin-producing serotypes
WB4. Legionella pneumophila
WB5. Yersinia pseudotuberculosis
Genetically modified microorganisms
WGI. Genetically modified microorganisms or genetic elements that contain nucleic acid sequences
associated with pathogenicity and are derived from organisms in the warning list.
WG2. Genetically modified microorganisms or genetic elements that contain nucleic acid sequences
coding for any of the toxins in the warning list or their subunits.
Toxins as follows and subunits thereof:2
WTI. Abrin
WT2. Cholera toxin
WT3. Tetanus toxin
WT4. Trichothecene mycotoxins
WT5. Modeccin
WT6. Volkensin
WT7. Viscum album lectin ~ (Viscumin)
*The Australia Group recognizes that these organisms are ubiquitous, but, as they have been
acquired in the past as part of biological weapons programs, they are worthy of special caution.
~ . Except where the agent is in the form of a vaccine.
2. Excluding immunotoxins.
Viruses
LIST OF ANIMAL PATHOGENS FOR EXPORT CONTROL1
AV! . African swine fever virus
AV2. Avian influenza virus2
AV3. Bluetongue virus
AV4. Foot and mouth disease virus
AV5. Goatpox virus
AV6. Herpesvirus (Aujeszky's disease)
AV7. Hog cholera virus (synonym: swine fever virus)
AV8. Lyssa virus
AV9. Newcastle disease virus
OCR for page 79
AV10. Peste des petite ruminants virus
AV11. Porcine enterovirus type 9 (synonym: swine vesicular disease virus)
AV12. Rinderpest virus
AV13. Sheeppox virus
AVIS. Teschen disease virus
AV! 5. Vesicular stomatitis virus
~ . Except where the agent is in the form of a vaccine.
2. This includes only those avian influenza viruses of high pathogenicity as defined in EC Directive
92/401EC: "Type A viruses with an {VPT (intravenous pathogenicity index) in 6 week old chickens of
greater than I.2, or Type A viruses HS or H7 subtype for which nucleotide sequencing has demonstrated
multiple basic amino acids at the cleavage site of haemagglutinin."
Bacteria
AB3. Mycoplasma mycoicles
Genetically-modified microorganisms
AGI. Genetically modified microorganisms or genetic elements that contain nucleic acid sequences
associated with pathogenicity and are derived from organisms in the list.
CONTROL LIST OF PLANT PATHOGENS FOR EXPORT CONTROL
CORE LIST
Bacteria
PB ~ . Xanthomonas albilineans
PB2. Xanthomonas campestris pv. citri
F.
ung1
PF] . Colletotrichum coffeanum var. virulans (Colletotrichum kanawaeJ
PF2. Cochliobolus miyabeanus (Helminthosporium oryzoeJ
PF3. Microcyclus ulei (synonym Dothidella uleiJ
PF4. Puccinia graminis (synonym Puccinia graminis f. sp. triticiJ
PF5. Puccinia striiformis (synonym PucciniaglumarumJ
PF6. Pyricularia grisea/Pyricularia oryzue
Genetically modif1ed Microorganisms
PGI. Genetically modifed microorganisms or genetic elements that contain nucleic acid sequences
associated with pathogenicity derived from the plant pathogens identifed on the export control list.
OCR for page 80
ITEMS FOR INCLUSION IN AWARENESS-RAISING GUIDELINES
Bacteria
PWB 1. Xanthomonas campestris pv. oryzae
PWB2. Xylella fastidiosa
Fungi
PWF1. Deuterophoma tracheiphila (synonym Phoma tracheiphila)
PWF2. Monilia rorei (synonym Moniliophthora rorei)
Viruses
PWVI. Banana bunchy top virus
Genetically modified microorganisms
PWGI. Genetically modified microorganisms or genetic elements that contain nucleic acid
sequences associated with pathogenicity derived from the plant pathogens identified on the
awareness-raising list.
Source: U.S. Arms Control and Disarmament Agency
Representative terms from entire chapter:
encephalitis virus