CUBA: THE THREAT
DR.
MANUEL CEREIJO
The
Beginning
In
1982, Dr. Ernesto Bravo, from the Medical School, Universidad de La Habana, a
biochemist, visited Boston University. Dr. Lynn Margulis, then at Boston
University, introduced Dr. Harlyn O. Halvorson to Dr. Bravo. Dr. Bravo's real
mission was to develop interactions between Cuban and United States scientists.
Soon, in summer 1983, Dr. Margulis and Dr. Halvorson visited Cuba. Shortly
thereafter they created an organization called North American/Cuban Scientific
Exchange, known by NACSEX.
NACSEX
organized visits of scientists to Cuba to exchange ideas and information. About
80 individuals were part of this program which continued in the 1980's and still
is going on. These first visits led to a series of training programs. Primarily,
new molecular biology technology from the United States was brought to the
attention of active young Cuban scientists. Courses were given in La Habana.
Advice was provided to a growing program. The Cuban medical and engineering
community built a basic infrastructure in a very short period of
time.
In
1985, NACSEX conducted the Second International Seminar on Biotechnology and
Interferon in Cuba. Dr. Silva Rodriguez, a well known Cuban scientist, spent
then 3 months at University of Massachusetts, Amherst, learning new technology
related to biotechnology and genetic engineering from Dr. Robert Zimmerman, a
prominent United States scientist.
At
this time also, during a visit of Castro to the Soviet Union, in February 1981,
Castro visited a laboratory where E. coli bacteria had been genetically altered
to produce interferon. Castro's interest resulted in obtaining the help of
Brezhnev, and immediately a strain of E. coli was sent to Cuba, along with the
equipment and working technology.
General
Vladimir Lebedinsky, from the Soviet Union, visited Cuba in 1982, at Castro's
personal invitation, with a team of military scientists. They assisted then the
young Cuban scientists who were engaged in the creation of what can be
considered today one of the most sophisticated genetic engineering labs in the
world-capable of the kind of advanced bioweapons research done in Russia, Iraq,
and North Korea.
The
Development
Cuba's
biotechnology sector has come a long way since 1981. It is the world's
second-largest producer, by volume, of Alpha interferon. Cuba is also the only
country, besides highly developed nations, producing a range of human and
recombinant interferon on an industrial scale.
Cuba's
research centers have also produced monoclonal antibodies, as well as chemically
synthesized gene fragments and breakthroughs in virological research. One
center, the most important one, the Center for Genetic Engineering and
Biotechnology, CIGB, handles the research on proteins, hormones, vaccines DNA
probes, modification of enzymes, biomass, and cell
genetics.
The
biotechnology program has focused on the following areas:
·
development
of genetic engineering
·
origination
of vaccines, biological preparations
·
development
of biotechnology for immunochemical applications
·
production
of monoclonal antibodies
·
research
with fetus
·
medical
microbiology and tropical medicine
·
production
of in vitro cultures
·
manipulation
of embryos
Cuba
has had long practice in the art of deceiving outsiders, not to mention its own
people. There is an official version for the general public and the outside
world, one official version for the scientific community, and yet another secret
series of activities known only to a small group of elite scientists and
military personnel working on these centers.
Despite
the country's achievements in research and development, it has made limited
progress in selling its products worldwide. At a 1993 trade fair, Foreign Trade
Minister Ricardo Cabrisas reported that medical products had accounted for 10%
of the value of exports in 1992. But more
than
half of that figure corresponded to sales of a meningitis vaccine to
Brazil.
A
considerable proportion of the rest was sales of interferon to China. It is
estimated that, since 1991, Castro has spent over $3,500 million dollars in the
development of this sector. In 1998, according to Cuba's official figures, the
government spent $95 million dollars in modernizing the
facilities.
A
report submitted by the U.S. Office of Technological Assessment to hearings at
the Senate identified seventeen countries believed to possess biological
weapons- Libya, North Korea, South Korea,Taiwan, Syria, Israel, Iran, China,
Egypt, Vietnam, Laos, Cuba, Bulgaria, India, South Africa, and
Russia.
Main
Centers
Center
for Genetic Engineering and Biotechnology
The
most important institution in Cuba's biotechnology industry is the Center for
Genetic Engineering and Biotechnology, CIGB. It was established in La Habana, in
1986, at a cost of $150 million dollars. Located west of La Habana, 31 Ave,
between 158 and 190 Streets, Cubanacan.
The
CIGB has the most modern and efficient technology for bioscientific research as
well as facilities for manufacturing and continuous work flow. It has a total
area of 60,000 square meters. The Center has state-of-the-art equipment, second
only to the United States in the Americas.
At
the center work outstanding scientists and engineers dedicated to genetic
research, virology, cloning, with the capacity to develop bioweapons, such as
anthrax, smallpox, Ebola, and others.
The
main CIGB buildings cover an area of 43,200 square meters and contain
specialized labs for both general purposes and dedicated research. The CIGB has
a biotherium, barrier zones or white rooms, which allow research with sensitive
and lethal agents. The CIGB's modern and efficient technological equipment
includes mass spectrometers, infrared and ultraviolet, electron and scanning
microscopes, gamma counters, DNA synthesizers. Also, and very important,
downstream fermenters, drying and milling machines, centrifuges, which can,
therefore guarantee research and development of bioweapons, such as bacteria and
virus agents.
In
the CIGB work more than 700 highly skilled researchers, scientists, and
engineers. Russians scientists cooperated with the CIGB several times,
including, according to certain intelligence sources, assisting in the
development of altered strains of bacteria. Major General Yury Kalinin, chief of
the Main Directorate, and Deputy Minister of Russia, was invited to Cuba in 1990
to discuss the creation of a new biotechnology plant ostensibly devoted to
single-cell protein.
To
facilitate the development of biological agents without suspicion, the CIGB has
efficient, flexible, and dynamic organizations. It is structured into several
large sub-directions made up, in turn, by a number of divisions with
specifically oriented work lines.
The
main ones are: research and development in diseases in humans; development of
new vaccines by genetic engineering; recombination of enzymes; analysis, design
and modeling of peptides and proteins.
The
process of weaponizing anthrax, for example, can be done easily at these
facilities. A few grains of freeze- dried bacteria are kept in a stoppered vial.
Then, a small amount of a nutrient medium is put into the vial. A mother culture
is created. With tiny pipettes, a scientist draws the mixture out of the vial
and transfers a small amount into several slightly larger bottles. The bottles
are left to incubate in a thermostatic oven for two days. So far, this process
is very similar to the one to make a vaccine.
A
seed stock in a standard vial will swell to billions of microorganisms after 48
hours, but it will take weeks to of brewing to produce the quantities required
for weaponization. Once the culture emerges from the oven, it is siphoned off
into large flasks. The flasks are taken into a special room where they are
connected to air-bubbling machines, which turn the liquid into a light froth.
The bacteria can grow now more efficiently.
Each
new generation of bacteria is transferred into larger vessels, until is vacuum
pressure into fermenters. These fermenters incubate the substance for two days.
The bacteria continue to multiply until scientists decide they have reached
maximum concentration. At this point, they process it through a centrifuge to be
concentrated as much as thirty times further.
Fermenters,
and centrifuges, are equipment very similar to the ones used in the dairy
industry, in the sugar industry, and liquor industries. These are industries
where Cuba has had experience for years. Therefore, the equipment is now
manufactured in Cuba. Even at this stage, there is not a weapon. The pathogen
has to be mixed with special additives to stabilize it over a long period. A scientist works with recipes. The raw
ingredients are similar, but quantities and combinations of nutrient media,
heat, and time vary. If something fails, the scientist has to start all over
again.
Smallpox,
as mentioned before, requires no concentration. Also, it is a virus, not
bacteria. Tissue cells are obtained from animals or humans. The tissue has to be
kept alive outside its natural habitat in cell lines and stored at precise
temperatures. Cells can be taken from the
kidneys
of green monkeys or from the lungs of human embryos.
The
nutrient media needed to cultivate tissue cultures are different from those used
to grow bacteria. A special complex of amino acids, vitamins, salts, and sera,
distilled with de-ionized water, is crucial to the process that promote tissue
cells and ultimately viruses to grow. The CIGB, in conjunction with other Cuban
biological centers and institutes, like the Finlay Institute, or the Biocen, are
quite capable of weaponizing such agents.
Commercially,
the CIGB has developed a number of preparations, such as:
·
Heberbiovac
HB, a hepatitis B recombinant vaccine, the production of which has now been
switched to a new purpose-built plant
·
Heberkinasa,
a recombinant streptokinase. Applied by intravenous or intra-coronary injection,
it rapidly dissolves life-threatening blood clots. This product is one of 50
types of enzymes obtained in Cuba
·
Hebermin,
a healing and antiseptic cream containing human recombinant epidermal growth
factor.
·
Hebertrans,
which contains human transfer factor obtained from human leukocytes. It is used
to treat herpectic infections
The
CIGB also has a computer network created in 1991 to provide computer
communications, database access, information services and data processing to the
Cuban scientific research community.
View
of CIGB
Other
Bio-Centers
Cuba’s
Main Biological Scientific Pole
Biocen
The
National Bio-preparations center, Biocen, located in Bejucal, south of Habana
province, at Carretera de Beltran km 1 1/2 is engaged in industrial scale
production of human vaccines. Also, culture media, nutritive bases and a wide
range of genetic engineering products, developed at the CIGB and the Finlay
Institute. It was created in 1992, at a cost of $15 million
dollars.
Biocen's
culture media plant has an annual 40 tons capacity. It is equipped to carry out
homogenization, hydrolisis, dehydration, milling, sifting, filtration, and
several other processes required not only for the biotech and pharmaceutical
industries, but for bacteria and virus weaponization. A new department that
manufactures recombinant products went into operation in 1993. The complex also
includes a plant producing immunological reagents and two vivaria
labs.
Innovative
techniques have been developed at Biocen for obtaining culture media,
substituting the traditional expensive nutritive bases, like meat, casein. They
have developed 14 alternative protein sources. The development is vital for the
creation of bioweapons.
Among
Biocen's special products are allergenic extracts, dust mites, insects,
atmospheric fungi. A prominent Cuban scientist, Dr. Mario Estrada has done
extensive research on fish-transgenesis with the assistance of the CIGB. Most of
the more lethal toxins are developed from fish and marine
research.
Biocen
follows the organization and functions of the Soviet Union, now Russia, mos
important center, Biopreparat. Biocen can be considered the brains of the
weapons program, and secrecy is vital. It supplies the scientific and
engineering expertise for the projects commissioned by the
military.
Staff
members do not know what colleagues in other parts of the organization are
doing. Yet, even the most furtive networks are made of human beings. However,
gossip, rivalry, desertion, allows information of secret activities to be
known.
The
Finlay Institute
The
Carlos J. Finlay Medical Research Institute is commercially best known for the
development of the world's first effective vaccine against both meningitis B and
C. It is located in Ave. 27, No. 19805, La Lisa, Habana. The Institute occupies
an area of 23,000 square meters, divided
into
three areas: fermentation, purification, and "clean rooms". Over 950 persons work at the Institute.
Of these, 60% are engineers and scientists.
The
Institute has done extensive work in the research and development of new
vaccines. Among them are vaccines against Leptospirosis, Hepatitis, Cholera, and
Meningitis. The Plant III area is well prepared for the production of
bioweapons.
The
main areas of research and production of the Institute are related to bacteria
and viruses. The Institute has been as important as the CIGB in the research and
production of bioweapons. Commercially, it has worked on research and production
of vaccines.
The
Institute of Tropical Medicine
The
Institute was founded in 1937 by Dr. Flori, a very well known Cuban scientist.
The center's research area is in microbiology. The Institute has the necessary state-of
the-art equipment for research and development of bioweapons related to tropical
bacteria and viruses.
Lately,
the Institute has done extensive work on the strains of viruses and cells
related to parainfluenza 3, adenovirus 3, measles, and influenza type A. Hep2 two cell line was grown in minimum
essential medium, MEM, containing 10% fetal calf serum, 1% glutamine, 100
U/ml
penicillin
and 100 mg/ml streptomycin sulfate.
Clinical
specimens were processed using nasopharyngeal exudates of children who had been
admitted to the William Soler Pediatric Hospital, in La Habana. An extensive
scientific process was followed to evaluate the ability of the RNA-PCR
method.
The
Institute has also conducted extensive research on yellow fever. Yellow fever is
a viral disease that has caused large epidemics in the world. Infection causes a
wide spectrum of disease, from mild symptoms to severe illness and death. The
yellow in the name is explained by the jaundice that affects some patients. The
disease is caused by the yellow fever virus, which belongs to the flavivirus
group.
The
virus remains silent in the body during an incubation period of three to six
days. There are two disease phases. Those patients who enter into the second
phase or toxic phase develop jaundice, bleeding, kidney function deteriorates.
Half of the patients in the toxic phase die within 10
days.
A
weaponized yellow fever virus produces a strong strain of what is known as urban
yellow fever. There is no specific treatment for yellow fever. Prevention is
through vaccination. There are other tropical disease that could be used as
bioweapons, such as: malaria, dracunculiasis, filariasis, leishmaniasis, dengue,
dengue hemorrhagic fever.
Dengue
is caused by the Dengue viruses. The disease is tropical in origin. There is no
specific treatment available. Intravenous fluids and oxygen therapy are often
used for patients who experience shock during their illness. Dengue is
characterized by the rapid development of fever, intense headache, joint and
muscle pain, and a rash.
The
hemorrhagic form of dengue fever is more severe and associated with loss of
appetite, vomiting, and high fever. Untreated hemorrhagic dengue results in
death in up to 30 percent of cases.
The
Institute is probably the best in the world in research and development related
to tropical diseases. The Institute is funded in many activities by UNESCO, OMS,
and the French government.
CIM
The
Center for Molecular Immunology is a 15,000 square meter, two floor facility.,
built at a cost of $20 million dollars. Over 250 employees work at the Center,
of which, 200 are scientists and engineers. The ground floor includes
development, pharmacology, and toxicology. The auxiliary technical services, and
secret research and development are on the second floor. Hollow fiber,
fermenters, and "cleaning in place" units are installed on this
floor.
Their
main research activities are on antibodies-hybridoma, molecular biology,
cellular immunology. CIM has
laboratories equipped for cell culture, immunochemistry, and radiochemistry.
Their work on the immune system is related to the development of stronger
strains of virus and bacteria. The Center has all the pertinent equipment to
produce
bio-weapons.
Conclusions
There
was a slippery interrelation between Soviet support to scientific programs to
Cuba and Cuba's ability to develop biological weapons. For many years, the
Soviet Union organized courses in genetic engineering and molecular biology for
Cuban scientists. Scientists from the United States also organized courses,
seminars, and other similar activities in Cuba since 1981. Many prominent
European scientists have also cooperated in the development of Cuba's
biotechnological industry in the last 20 years.
There
has been a constant exchange of scientific information, visiting scientists,
technology transfer from the Soviet Union and the United States to Cuba. The
Soviet Union sold industrial fermentation equipment vessels to Cuba. The models
were the ones used to develop and manufacture bacterial biological
weapons.
Cuba
also acquired equipment from other European countries under the excuse that the
equipment was intended to grow single-cell protein for cattle feed. However,
even exhaust filtration equipment capable of achieving 99.99 percent air purity
was sold to Cuba. This level is used only in weapons labs.
Cuba
has also acquired the technology and the capacity to manufacture their own
equipment. Some of the equipment required is very similar to equipment related
to diary production, sugar cane processing, and liquor manufacturing, areas
where Cuba has had great experience.
There
is a definitive and important relation with Iran in the field of biotechnology.
Luis Herrera, one of the founders of the CIGB and the biotechnology program in
Cuba is directing the Iran/Cuba activities. Refer to Chapter XIII for further details on Cuba/Iran
cooperation.
Some
analysts maintain that evidence of biological warfare research is not proof that
viable weapons are being produced. However, even the most primitive biological
weapons lab can produce enough of an agent to cripple a major city. Certainly,
Cuba's facilities are recognized as outstanding.
Viruses
and bacteria can be obtained from more than two thousand microbe banks around
the world. The international scientific community depends on this network for
medical research and for exchange of information vital to the fight against
disease. There are very few restrictions on the cross-border trade in
pathogens.
In
the past twenty years Cuba has been working in the research and development of
biotechnological products. Research has proven that viruses and toxins can be
genetically altered to heighten their lethality, paving the way for the
development of pathogens capable of overcoming existing
vaccines.
The
arsenal of Cuba could include weapons based on tularemia, anthrax, epidemic
typhus, smallpox, dengue fever, Marburg, Ebola. It could also extend to
neurological agents, based on chemical substances produced naturally in the
human body. It is easier to make a biological weapon than to create an effective
system of biological defense.
The
United States plan to stockpile and develop vaccines against known agents is the
most comprehensive of its kind in the world. Vaccines work by inducing the
creation of antibodies that fight specific diseases. It is not medically
advisable to combine too many different courses of vaccination. There are
currently no known vaccines for brucellosis, glanders, and melioidosis, or for
many viral diseases, such as Ebola and Marburg.
Vaccines
provide excellent protection against specific diseases, but the characteristics
that makes them so effective is also the source of their limitations. Smallpox
antibodies offer no protection against plague. Combined vaccines are possible,
but most of these go straight to the metabolism of specific organisms. An all
purpose antidote simply does not exist.
Countries
with the capacity and technology to produce sophisticated vaccines can certainly
produce bioweapons. Cuba's biotechnology efforts have been very successful in
the creation of vaccines.
In
1957, European scientists identified the first cytokine, named interferon, which
form a bridge between specific and nonspecific immune systems. They are produced
in response to viruses and bacteria, or to a general stimulus in the blood.
Interferon took years to isolate, but in 1979 an American produced interferon
alpha artificially, called antiviral penicillin, a sophisticated
biotechnological achievement. Cuba is a large producer of
interferon.
Cuba's
biotechnological capacity places it in group four of the World Health
Organization's five national categories. To reach group five, which contains the
seven top industrial economies, Cuba must produce at least 20 percent of the 260
basic materials. It regularly produces 17 percent of these and certainly has the
scientific ability to produce the others with biotech
methods.
Priority
access to research and development funding, 160 distinct research units and over
10,000 researchers give the Cuban scientific establishment an edge over their
counterparts even, in some Western countries.
Research
is ongoing in medicine, genetic engineering, biotechnology, industrial
applications, and bioweapons. Development of hardware and software for the
research effort has been also a priority.
The
range of products, and research and development areas, include: monoclonal
antibodies, vaccines against hepatitis B and bacterial meningitis, a neural
growth factor, a range of interferon, enzymes, streptokinase, culture media with
14 alternative protein sources, several reagents, transgenetic fish, interferon
beta, proteolytic peptides, lipopolysaccharide peptides, LBP-derived synthetic
peptides, human Papillomavirus 16, MT-4 cells, and many
others.
Certainly,
a country with such capacity can produce bioweapons. There is really no
technical solution to the problem of bioweapons in Cuba. It would need an
ethical, human, and moral solution, which is obviously impossible while the
government is in the hands of a sociopath. Ordinary intelligence and
surveillance techniques cannot prove the existence of a biological warfare
program.
Even the highest resolution satellite imagery can't distinguish between a large pharmaceutical plant or center and a weapons complex. The only conclusive evidence comes from first hand information. A site inspection of Cuba's facilities, by an objective international team must be requested.
TABLE
FACTS
Disease or agent |
Lethality,Fatality
rate |
Delivery methods |
Diagnosis |
Incubation |
Vaccine |
Symptoms |
Anthrax |
100% 20% |
Aerosol Direct contact |
Non-specific. May see a wide mediastinum on
CXR |
1-10 days |
Yes. Booster yearly |
Fever, malaise, cough, severe respiratory distress,
shock |
Botulism |
10% |
Ingested Aerosol |
Serology/Culture |
1-5 days |
Pentavalent
anti-toxin |
Ptosis, Weakness, dizziness, blurred
vision,respiratory failure |
Cholera |
50% If noRx |
Drinking Water |
Clinical/Darkfield,
Culture |
4hours-5 days |
Yes. Lasts 6 months |
Vomiting, intestinal
cramps,diarrhea |
Glanders |
90-100% If not Rx |
Aerosol |
Sputum cultureMiliary lesion on
CXR |
10-14 days |
NONE |
Fever, sweats,myalgia,chest pain,diarrhea,
pnemonia |
Plague |
Bubonic60% Pneumonic 98% |
Zoonosis Aerosol |
Nasal, Sputum culture,PCR
immunoassay |
2-3 days |
Yes, Bubonic, not
aerosol |
High fever, chills, headache, toxemia,
cyanosis |
Tularemia |
35% If not Rx |
Aerosol |
Culture serology |
1-10 days |
Yes |
Local ulcer, fever, headache, cough,
prostation |
Ricin |
100% |
Aerosol Ingestion Injection |
Protein toxin |
8hours, death in 36
hours |
None |
Gastrointestinal hemorrhage, necrosis, fever,
cough |
Small Pox |
35% |
Aerosol |
PCR |
7-19 days |
Yes. Not available for mass
use |
Fever, malaise, vomiting,
|
T-2Mycotoxins |
100% |
Aerosol,
contact,ingestion |
Blood Toxicology |
Death in minutes,
hours |
NONE |
Pruritus, necrosis, dyspnea, hemoptysis, bone
marrow collapse |
Viral Hemmorrhagic
Fever |
Ebola, Marburg, Rift
Valley 90% |
Several methods |
Viral isolation |
Varies with type, Few
hours |
Only for Yellow
Fever |
Bleeding, vomiting, microvascular
damage |