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The Park: Malaria 1/2
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In this section advise is offered on malaria as it is present in the Kruger
National Park.
Malaria
Malaria,
disease of animals, especially birds, monkeys, and humans,
caused by infection by protozoans of the genus Plasmodium and
characterized by chills and intermittent fever. The causative
organisms of human malaria are transmitted by the bite of about
60 species of mosquitoes in the genus Anopheles. The disease may
occur in subtropical and tropical regions in almost all parts of
the world as well as in other temperature areas. With the advent
of control programs based on the use of residual insecticides,
the distribution of malaria changed rapidly. Since 1950 malaria
has been eliminated from almost all of Europe and from large
areas in Central and South America. It remains a major problem
in parts of Africa and in southeastern Asia. About 100 million
cases of human malaria develop each year; about 1 percent are
fatal.
Malaria in humans
Human malaria occurs in four forms, each caused by a different
species of parasite. In each form, the symptoms usually are
chills, fever, and sweating. In untreated cases, these attacks
recur periodically. The mildest form of malaria is benign
tertian malaria, caused by Plasmodium vivax, in which the fever
may occur about every second day after the initial attack (which
may occur within two weeks after infection). Jungle fever,
malignant tertian malaria, or estivo-autumnal malaria, caused by
Plasmodium falciparum, is responsible for most of the deaths
from malaria. The organisms in this form of the disease often
block the blood vessels of the brain, producing coma, delirium,
and finally death.
Quartan malaria, caused by Plasmodium malariae, has a longer
incubation period than either tertian malaria or jungle fever;
the first attack does not appear until 18 to 40 days after
infection. The attacks recur about every third day. The fourth
and rarest form of the disease, caused by Plasmodium ovale, is
similar to benign tertian malaria. In all forms of the disease,
periodic fevers may be less regularly spaced in some people.
During the incubation period of malaria, the protozoan grows
within cells in the liver; a few days before the first attack,
the organisms invade the red blood cells, which they destroy in
the course of their development, producing the typical febrile
attack.
History
Since 1638 malaria has been treated with an extract from the
bark of the cinchona tree, known as quinine. Quinine, which is
somewhat toxic, suppresses the growth of protozoans within the
bloodstream. In 1930, German chemists synthesized Atabrine,
which is more effective than quinine and less toxic. A new drug,
chloroquine, that became available at the end of World War II in
1945, was found to be capable of preventing and curing jungle
fever completely and to be much more effective in suppressing
the other forms of malaria than Atabrine or quinine. It also had
a much lower toxicity than any of the earlier drugs and was
effective in less frequent doses. Recently, strains of
Plasmodium falciparum, the organism that causes jungle fever,
have shown resistance to chloroquine and other synthetic
anti-malaria drugs. These strains are encountered most
frequently in Vietnam, and also in the Malay Peninsula, Africa,
and South America.
Quinine is still the agent used against Plasmodium falciparum
strains resistant to synthetics. In addition to the occurrence
of strains of drug-resistant parasites, the fact that some
vector mosquitoes (Anophelines) have become resistant to
insecticides such as DDT has led to an upsurge of malaria in
certain tropical countries. As a result, malaria has increased
among American and Western European travellers to Asia and
Central America and among refugees from these areas. Currently,
work is progressing on the development of a malaria vaccine.
Several vaccine candidates are now undergoing clinical trials
for safety and effectiveness in human volunteers, and scientists
look forward to having a vaccine for general distribution.
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