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Malaria
- The Mosquito Connection
V.B. Kamble Deadly fevers - probably malaria - have been recorded since the beginning of the written word, that is, about 6000 - 5500 B.C. There are references to such types of fevers even in the vedic writings some 3500 - 4000 years ago. Even Hippocrates recorded such fevers some 2500 years ago. Malaria existed and still exists in many parts of the world. Malaria was widespread in India during the colonial period, that is, during the 19th and 20th centuries.
Mal Aria About a century ago, of the British Army in India, amounting to about 1,78,000 men, close upon 76,000 men were admitted into hospitals for malarial fever in the year 1897. In this single year, the mortality from fever among the civil population in India, amounted to a total of more than five millions. Today, malaria is considered to be one of the most important parasitic diseases worldwide. 40 per cent of the worlds population lives in malaria endemic areas. 500 million clinical cases and about 3 million deaths are reported each year. In Africa, malaria deaths may account for 10 per cent of the overall annual mortality in children under 14. The worldwide distribution of malaria is shown in Figure 1 based on 1976 statistics. It reveals the presence of malaria in most of the worlds developing regions and its notable absence in arid or mountainous areas where mosquitoes usually do not breed. Malaria parasites causing malaria are prevalent in regions lying roughly between latitudes 60 N and 40 N. It is widespread in tropical and temperate countries.  Fig 1: Malaria, one of the world's most persistent diseases, affects 500 million people - many of whom suffer recurrent attacks - and kills 3 million each year. Almost all of the victims live in moist, tropical regions where disease-bearing mosquitoes breed freely. Attempts to control the spread of malaria by means of pesticides have not been successful, and in the 1970s there was a resurgence of the diseases, carried by mosquitoes immune to the pesticides. This map, based on 1976 statistics, reveals the presence of malaria in most of the world's developing regions-and its notable absence in arid or mountainous areas where mosquitoes usually do not breed. Till over a century ago, the popular view had been that malaria was caused by bad air (mal aria - Italian for bad air) or contaminated water. However, only in 1880, the first true sighting of the malarial parasite was made in Algeria by a French Army physician, Charles - Louis - Alphonse Laveran (1845-1922) while viewing blood slides of infected soldiers under a microscope. He showed that patients with malaria carried a protozoan parasite (called plasmodium), in their blood, and doctors began suspecting that mosquitoes spread the parasite causing the malarial infection. Laverans discovery was, however, rejected by the medical community and it was not until 1886 that his discovery was accepted by Italian scientists, who were the leaders in the field at the time. We may remark here that it was in 1882 that the mosquito transmission hypothesis was first made as a result of the association between the presence of mosquitoes and the occurrence of malaria - a case of guilt by association! By this discovery, the name of Laveran has forever become renowned in the history of malaria. The Mosquito Trail In the early days, research about malaria was chiefly based on Laverans discovery. It helped gain knowledge of the different forms of the malarial parasite in blood. It was found that it differed in the special forms of the disease. The relation between the parasite and the red blood corpuscles, in which it is chiefly to be found, was established. The Italian investigator Camillo Golgi (1843 - 1926) revealed the remarkable fact that the periodicity of the malarial attacks depended on the appearance of new generations of the parasite in the blood. Moreover allied parasites in the blood of several mammals and birds also were found.
The important question, previously mentioned, as to possibility of the malarial parasite living outside the body, and its way of obtaining entrance into the blood remained unanswered. Fore some reasons, among others owing to various facts that were known concerning other parasites of an animal nature, it was supposed that the malarial parasite in some way leaves the blood so as to exist in some form in nature, probably as a parasite of some other being. As nothing indicated that the parasite was to be found in the secretions or excretions, the supposition lay near at hand, that suctorial insects would assist in carrying the parasite to a place, where it had to pass the aforementioned part of its life-cycle. Attention was therefore directed to the mosquito, which was thus supposed to spread the malarial infection. The importance of the mosquito in this respect was proved. In this case, as in several others, tradition anticipated science; it is even said, that Negroes in the East-Africa use the same name for the mosquito and for malaria. The mosquito theory of malaria was introduced to science by A.F.A. King in 1883. The theory, however, remained a conjecture without other evidence than some suggestions given by epidemiological observations. The attempts made in Italy around that time with the view of examining the theory experimentally, and, eventually, proving it to be true, gave results that seemed anything but encouraging; being far more likely to prevent the investigators from following this line. A person of great merit concerning the solution of the problem was the English Investigator, Patrick Manson. It was a change in the appearance of the parasite, which was sometimes observed to occur, as the blood is shed, that Manson especially regarded as the first stage of its life outside the body. This phenomenon was afterwards shown by the American pathologist Mac Callum to imply an act of reproduction of the parasite. Manson was moreover guided by his experience regarding another parasite of the blood, a little worm, filaria, the transference of which from one part of its life-cycle to another he had found effected by the mosquito, and more particularly by special species of the mosquito. By his views set forth on malaria, and by exciting expectation that the solution of the malaria problem was to be found in the direction he indicated, Manson gave an impulse to the further testing of the mosquito-theory and at last to its being established. Manson, who lived in England, had no opportunity of taking up the experimental work of the problem. The solution came from India. Ronald Ross
It was at this juncture that Ronald Ross entered the arena. He was born in Almora, India, on May 13, 1857 - the year of the great Indian uprising - as the son of Sir C.C.G. Ross, a general in the English Army. Ross received an English dame and boarding school education. Subsequently he studied medicine at St. Bartholomews Hospital, London, but with little enthusiasm. Although he had bowed to his fathers wish that he not become an artist, his passionate interest in the arts took up much of his time. Ross published plays, short dramas, romances, fables, and poetry. He was married in 1889 to Rosa Bloxam and had two sons and two daughters. He was elected to the Royal Society in 1901 and knighted in 1911.
Apart from the arts, Ross had an abiding interest in mathematics, much of his self-education in the subject being undertaken while he was serving in the Indian Medical Service (1881-1888). Ross became more and more conscious of medical problems the longer he remained in India. Later he wrote: I was neglecting my duty in the medical profession. I was doing my current work, it was true; but what had I attempted towards bettering mankind by trying to discover the causes of those diseases which are perhaps mankinds chief enemies? In India, Ross succeeded in demonstrating the life cycle of the parasites of malaria in mosquitoes. Ross collected and identified various kinds of mosquitoes, dissected their guts and in August 1897 found his quarry in Anopheles mosquito that had just fed on a malaria patient. December 18, 1897 issue of the British Medical Journal reported that Dr. Ronald Ross discovered malaria cysts containing sporozoites (the same parasite Laveran had seen in the blood of his patients) in the stomach wall of anopheline mosquitoes that fed on a malaria patient. By July 1898, malaria transmission through the mosquito was established. In 1899, Ronald Ross joined the Liverpool School of Tropical Medicine. He was immediately sent to West Africa to continue his investigations, and there he found the species of mosquitoes which convey the deadly African fever. In 1901, Ross was elected a Fellow of the Royal College of Surgeons of England and a Fellow of the Royal Society. In 1926, he assumed the post of Director in Chief of the Ross Institute and Hospital of Tropical Diseases and Hygiene, which had been created by the admirers of his work. During his active career, Ross interest lay mainly in the initiations of the measures for the prevention of malaria in different countries of the world. He carried out surveys, initiated schemes, and established organisations for the prevention of malaria in several countries and places including the planting industries of India and Sri Lanka. Probably his greatest contribution was the development of mathematical models for the study of the epidemiology of malaria - that is, the causes, distribution and control of the diseases. Ronald Ross received the Nobel Prize for Physiology or Medicine in 1902 for his monumental work.Ronald Ross died in London on 16 September 1932 at the age of seventy five. Mosquito Trail Continued Unlike most of his colleagues in the Indian Medical Service, Ross was research-minded. In 1888, during his first furlough in England, he earned the newly established Diploma of Public Health and took a course in bacteriology. On returning to India, he studied malaria, initially believing that it was caused by intestinal auto-intoxication. During Rosss next furlough in England (1894) his successful, far-reaching malarial studies were initiated. This was due in large measure to the influence of Patrick Manson, for three reasons a key figure in Rosss contribution to the unravelling of the life history of the malarial parasite. First, Manson demonstrated convincingly to a skeptical Ross the correctness of Alphonse Laverans pioneering observations of 1880: that the blood of malarial patients contained pigmented bodies of parasites.
The main points in Rosss contributions to the problem during 1895 - 1898 can be summarized as follows: First, Ross demonstrated that volunteers who drank water contaminated with infected mosquitoes (including larvae) failed to contract the disease. This, along with his earlier doubts that aerial and water contamination provided a ready explanation for the epidemiology of malaria, did much to direct his attention to the possibility that transmission might be via mosquito bites ( a point of view expressed by A.F.A.King in 1883). Ross apparently was ignorant of Kings work until 1899; and in fact he met continual problems because of a shortage of scientific literature in India, above all in connection with identifying and classifying mosquitoes. Second, Rosss studies on the parasites in mosquitoes involved learning how to identify mosquitoes and to dissect their internal organs. From the beginning Ross was especially concerned with the motile parasitic filaments found in mosquito stomachs. The question was what happened to them. While he failed to recognize that the filaments were gametes (a point first appreciated by W. G. Mac Callum in 1897), Rosss supposition that they developed into another stage stood him in good stead, for it ensured that he spaced out his examination of individual mosquitoes from groups that had fed on malarial patients.
Rosss discoveries into malaria were immediately followed by a series of important works. The Italian investigator, Grassi, in association with his colleagues, Bignami and Bastianelli, proved that the human malarial parasite not only in its early stage, already detected by Ross, but also in its further development undergoes the same evolution that Ross described for the growth of the avian malarial parasite in the body of the mosquito. Grassi also precisely indicated the species of mosquito that are of import for the malaria of man. Life Cycle of Plasmodium
Schizogony When an infected female Anopheles (Figure 2) bites
man for its blood meal (Figure 3) it inoculates the malarial parasites
into the human blood alongwith the saliva. This infective stage is a minute
sickle shaped sporozoite which enter in thousands and remain in the blood
for about half an hour. After that they enter the parenchymatous cells
of the liver to escape from phagocytic white blood corpuscles and multiply
in number. Basically schizogony is a phase of growth and multiple fission
to form the merozoites. It is subdivided into the following phases:- Sporozoites enter the liver cell, enlarge to
form a schizont which divides to form about 1000 small spindle shaped
merozoites called cryptozoites. They are immune to medicine and
also to the resistance of the host. This is called the pre-erythrocytic
phase. Cryptozoites (merozoites) enter new liver cells,
grow into schizonts which again divide to form metacryptozoites
(merozoites). This phase may continue in fresh liver cells or attack
erythrocytes. Those which attack the erythrocytes are called metacrypto-merozoites.
This is called the exo-erythrocytic phase. On entering the RBC, the merozoites begin to
feed on the corpuscles to form the adult stage or the trophozoite.
The trophozoite grows further at the expense of the corpuscles to
form the signet ring stage, amoeboid stage and schizont respectively.
These are characterized by the presence of haemozoin granules and
Schuffners dots.he schizont ruptures to liberate the schizozoites
(merozoites) and toxins which cause the periodic paroxysms (bouts
of chills and fevers) and other symptoms as the cycle is repeated
every 48 hours in new erythrocytes in case of P. Vivax - a species
of plasmodium. This is called the Erythrocytic phase. Sometimes during the post erythrocytic phase, some
merozoites produced in erythrocytic schizogony reach the liver cells and
undergo schizogonic development in liver cells. Gamogony It is the sexual phase beginning in man but completed
only in the female Anopheles. Some merozoites enlarge and produce pigment
to form the gametocytes. Megagametocyte or female gametocyte is round
with food laden cytoplasm and a small eccentric nucleus. Microgametocyte
or male gametocyte have clear cytoplasm and a large central nucleus. The gametocytes can develop further only in the body
of a mosquito where suitable temperature is available. When mosquito sucks the infected blood, the corpuscles
are dissolved but the gametocytes are not digested. Microgametocytes undergo
exflagellation i.e. the nucleus divides into 4-8 nuclei around which cytoplasm
collects to form long flagellated structures called microgametes which
break and begin to swim in the stomach of the mosquito. In the megagametocyte the nucleus divides into two,
one of which projects out as the polar body. Fertilization takes place
to form zygote. Sexual cycle is completed in any kind of mosquito but
further development is possible only in the female Anopheles. Those zygotes which penetrate the stomach wall undergo
further development or else they elongate and pass out with the faeces
as the ookinese or the dying stage. The zygote comes to lie below the
outer epithelium where it becomes encysted to form the oocyst. The oocyst
absorbs nourishment, grows about 5 times in size. Its nucleus divides
repeatedly to form many nuclei and cytoplasm develops large vacuoles called
zoitoblasts. Nuclei arrange themselves around the margin of vacuoles.
Each nucleus acquires some cytoplasm to form a slender spindle shaped
sporozoite. Later the sporozoites break loose and form a tangled mass
in the oocyst. About 50 wart like oocysts are formed in the stomach
of a single mosquito and each oocyst may have 10,000 sporozoites. The
sexual phase takes about 10-21 days in the mosquito. When oocysts burst,
sporozoites are liberated and reach the salivary glands of the mosquito.
Thus the sporozoite is the infective stage which reaches fresh host when
it bites a man. Four species of Plasmodium cause malaria in man but their
life-histories are very much alike with minor differences (see Box). In the heydays of the war on malaria - especially from
the World War II through 1970s, widespread DDT spraying campaigns were
organised including in India to stifle the annoying blood suckers. Larvicides
and insecticides were used to kill mosquitoes before they could carry
the parasite between the victims. In fact, once upon a time, malaria seemed
destined for the history books, since it was supposedly caught in a pincer
attack. But, DDT played havoc with the environment - it killed the
birds and beneficial insects as well as anopheles mosquitoes. Further,
a cheap, plant derived medicine chloroquine was available to kill parasites
before they gained a foothold in their victims. Then nature took over With a little help from modern ecological disturbances
and tight government budgets: Most important species of malaria vectors (i.e. agents
- mosquitoes in this case) evolved resistance to one or more insecticides. Malaria parasites in particular plasmodium falciparum,
evolved resistance to chloroquine and then to several successor drugs.
Increases in travel and international trade moved drug-resistant
parasites around the globe. As mosquito-control efforts expanded, they grew more
expensive, forcing some governments to abandon them. The unfortunate result was a resurgence of malaria.
There were major programs to control malaria, and they were quite successful.
But the need to use more expensive insecticides over a broader range meant
they were not sustainable. Indeed, World Health Organisation (WHO) had initiated
strategies for the global eradication of malaria in the mid-1950s. But,
in 1960s, chloroquine resistant strains of plasmodium falciparum had arisen.
This was the result of over usage and probably under dosage of chloroquine.
At the time, there were no drugs to treat chloroquine-resistant malaria
except the ancient, quinine. Quinine has now been completely synthesized,
its synthetic analogue is called mefloquin. A new anti-malarial is a
drug called Qinghaosu that is derived from the sweet wormwood (Qinghao)
plant (genus Artemisia). It has been used in China for more than two thousand
years to treat fevers associated with malaria. The drug has been shown
to be effective in the treatment of the most deadly forms of falciparum
malaria and has been effective against strains of plasmodium falciparum
that are solidly resistant to chloroquine. In 1967, WHO realized that the global eradication of
malaria was impossible for a variety of reasons and the focus shifted
to control of the deadly disease. Since the idea of eradicating mosquitoes
was not realistic, the efforts were directed towards the reduction and
management of their population below the threshold that would cause disease.
(It may be remarked that besides malaria and filaria, the deadly dengue
fever is also spread by mosquitoes belonging to a different species, viz.
Aedes Aegyptes). Only a combination of the following measures would
help control the scourge of mosquitoes: 1. Public Education to
explain to the people that some disease carrying mosquitoes breed in puddles
of water, air coolers, tyres and other artificial containers, including
flower pots around the house. 2. Behavioural controls
like sleeping under mosquito nets - preferably soaked in insecticide. 3. Chemical controls
with focussed use of less hazardous insecticides. 4. Biological controls
through introducing organisms that eat or otherwise harm mosquitoes, or
their larvae. We have come a long way since Ronald Ross discovered
malaria parasite in the gut of the female anopheles mosquito. Though the
cause of malaria was discovered nearly a century ago by him, the scourge
of the mosquito still persists. Mosquitoes are back with vengeance, and
its guest plasmodium falciparum has not only developed resistance to quinine,
but continues to develop strains resistant to even newer drugs. This war
is continuing. We know how malaria is caused, but we have yet to develop
strategies and means to control the spread of the disease. It is imperative
that we channelise our efforts in controlling and managing the mosquito
menace, just the way Ross did throughout his life. 1. World Book Medical Encyclopaedia, World Book, Inc.
1998 An up-to-date resource on Medicine, Health and Diseases. 2. The Biographical Dictionary of Scientists Edited
by Roy Porter, Second Edition, Oxford University Press 1994 Gives brief
accounts of lives of scientists and their work. 3. Dictionary of Scientific Biography Vol. IX & XI
Editor-in-chief Charles Coulston Gillispie Charles Scribners Sons, New
York 1975 A wonderful resource in 14 volumes. 4. http://www.nobel.se official website of the Nobel
Foundation A treasure house on Nobel Laureates. 5. Grzimeks Animal Encyclopedia Vol. 2 Insects Van
Nostrand Reinhold Company 1969 Editor-in-Chief Dr. Dr. h.c. Bernhard Grzimek
A great resource in 13 volumes. 6. Health and Disease Rene Dubos and Maya Pines Second
Edition. Time - Life Books, Hong Kong, 1984 Profusely illustrated and
lucidly written with text followed by a picture essay supplementing the
text. 7. Surolia V Malaria - how to remove plaques and parasites
D. Balasubramanian The Hindu, March 1, 2001 Fighting
the War Once Again The National Malaria Health Programme in the
early 1950s was a vigorous national health effort. Combing the
length and the breadth of the country, the health workers sprayed
DDT and other insecticides so as to wipe out mosquitoes that bred
in stagnant pools of water, and also distributed quinine pills house
to house. In the 1960s, the war against malaria appeared to have
been won. But, malaria returned with greater force - not just in
India, but the world over. The war is being fought once again. 40
per cent of the worlds population lives in malaria endemic areas,
500 million clinical cases and about 3 million deaths each year
thanks plasmodium falciparum! Plasmodium has resurfaced in mutant
strains that are resistant to quinine, and its more potent cousins,
chloroquine and mefloquine. Other strains of the parasite, like
plasmodium vivax hit at the brain and the central nervous system.
What
could be the strategy then to wipe out malaria? One could attempt
to attack the parasite by targetting some processes or metabolic
paths crucial for its survival, or make a vaccine that can be inoculated
into us developing immunity against it. Alternatively, spray insecticides
to kill mosquitoes, and take steps not to allow stagnant pools of
water to collect where mosquitoes breed. Thus, these are the broad
strategies to fight malaria - hit at the parasite through drugs
that disable it, develop a vaccine that offers us immunity against
it, and target the mosquito which is the carrier of the parasite,
by insecticide spray and removing its breeding grounds. Let us consider
them briefly. Some
people are trying clever strategies on mosquitoes. These include
genetically engineered mosquitoes in such a manner that they become
unable to carry the parasite within, or shuffle the genes of the
mosquito in such a manner that it would kill the rider within -
called the transposon technology. There are also attempts to make
the mosquitoes sterile by exposing them to raidation, and then unleash
millions of these mosquitoes in the breeding grounds and let them
mate. Over 5-6 generations, the population could be wiped out. There
are attempts to make vaccines against malaria, in our country as
well as in other parts of the world. Each group looks at what it
considers to be an essential component in the assembly of the parasite
or body chemistry, and using this component as the antigen, and
tries to make a vaccine that would produce the desired antibody.
In our country, the work is on at ICGEB, New Delhi, and CDFD, Hyderabad.
Since as of today, there is no malaria vaccine, we await the result
from these labs with much hope. The
third front is the development of drugs against the parasite. In
earlier times, drugs were identified and developed empirically.
Native medical practice and folk tradition were of occasional help.
This is how quinine was found to be useful. However, the malaria
parasite lives on human blood and liver where it runs through its
entire life cycle. It degrades the proteins of our red blood cell
and lives on the digested soup. While doing so, it needs to watch
out for the iron-containing component of the red cell hemoglobin,
called heme, which can puncture holes in the parasites cells and
leak them to death. The parasite packages off the heme as safe garbage
in a lump of a pigment called hemozoin. (It is this pigment that
serves as the tell-tale sign of the presence of the parasite in
our body). The continuous playing out of its life cycle between
the tissues of the body makes the task of containing the parasite
difficult. The drug we use should not be toxic to the liver, should
not cause anemia or blood loss, and should target the parasite alone
and not the surroundings of the zone that it colonizes. As it goes
through its drama of devastation, it changes shape, size, the surface
coat and the biochemical strategies of its survival. The researcher
who wishes to devise an effective antimalarial drug needs to address
this issue of multiple avatar or reincarnation of the pathogen.
As
noted earlier, quinine had lost its effectiveness over the years
in many parts of the world, since the plasmodium parasites have
developed genetic strains or variants resistant to it. Better drugs
of the quinine class have been developed over the last 50 years,
notably chloroquine and mefloquine, by tinkering with the chemical
structure of the parent quinine. Both have been widely effective
and popular. Soon enough, chloroquine resistant strains of the parasite
emerged, and some groups tried to attack this problem by devising
a combination drug called Fansider (also called PM/SD). Strains
resistant to this drug too emerged! Now three other drugs are suggested
- one of them, called holopantrine, is effective against PM/SD resistant
strains. In the meantime, two products coming out of Chinese medicines
have proved useful - artemesinin, a plant product and the other
being pyromaridine, but the action of the latter is unknown as of
now. Parasites
breed fast and prolifically, these alongwith the feature adaptive
mutations, makes the emergence of strains resistant to any newly
introduced dru a frustrating reality. how does one overcome this
difficulty and attempt to conquer disease of this kind? Namita Surolia
of Jawahar Lal Nehru Centre for Advanced Scientific Research, Bangalore,
and Avdesh of Indian Institute of Science, Bangalore (Namitas husband)
argued that no matter what mutations or strains there may be - all
of them must share some inescapable physological or biochemical
features, mutations in which would be lethal and not let the parasites
survive. It is these vital processes that should be identified and
chosen as drug targets. Very recently, the couple has been able
to identify one such target feature. Organisms like plasmodium parasites
are not fully competent and self-sufficient in their fatty acid
production which are important structural materials and energy sources
for them. They rely symbiotically on organelles called apicoplasts
residing in their cellular compartment; for some enzymes needed
for the process. Now, these organelles could be thought of as drug
targets. This is what Namita and Avdesh did in their quest for an
effective anti-malarial drug. They reasoned that parasites cannot
afford to bear any mutation in their apicoplast; it is too vital
an organelle to become inefficient or disabled! Next, having realised
that the apicoplast aids in making fatty acids for use by the parasites,
they started looking for inhibitors of enzymes that catalyse the
synthesis of fats and fatty acids. One such inhibitors is the antibiotic
Triclosan. Incidentally, Triclosan is used as a broad spectrum/antimicrobial
in pastes, mouth wash, shampoo and so forth. Surelias
tested the effect of Triclosan on the growth of P. falciparum and
found that it arrested the growth of the parasite at concentrations
as low as one milligram of the stuff in 3 litres of the medium!
The discovery by the Surolia couple that Triclosan is an antimalarial
drug has been well secured. However, they warn that Triclosan should
be used judiciously, or in combination with other antimalarials,
so as to avoid the problem of resistance currently seen with drugs
like chloroquine. They also found that another antibiotic Cerulenin
acts synergistically with Triclosan. Indeed, this discovery of Surolias
could pave the way for developing more patent analogues of Triclosan
for treating malaria. Malaria: Glossary
Important
terms used in connection with Malaria are given below. The terms given
do not necessarily appear in the present article. Anopheles : A genus of mosquitoes in the family Culicidae; members
are vectors of malaria, dengue, and filariasis. Anopheline : Pertaining to mosquitoes of the genus Anopheles or
a closely related genus. Cinchona : The dried, alkaloid-containing bark of trees of the
genus Cinchona Cinchonine : C19H22N2O. A colourless, crystalline alkaloid that
melts at about 245C; extracted from cinchona bark, it is used as a substitute
for quinine and as a spot reagent for bismuth. Cyst : A normal or pathologic sac with a distinct wall, containing
fluid or other material Cytoplasm : The protoplasm of an animal or plant cell external
to the nucleus. DDT : Common name for an insecticide; melting point 108.5C, insoluble
in water, very soluble in ethanol and acetone, colourless, and odorless;
especially useful against agricultural pests, flies, lice, and mosquitoes.
Also known as dichlorodiphenyltrichloroethane. Dengue : An acute viral disease of man characterized by fever,
rash, prostration, and lymphadenopathy; transmitted by the mosquito Aedes
aegypti. Also known as breakbone fever; dandy fever. Epidemiology : The study of the mass aspects of disease. Filaria : A parasitic filamentous nematode belonging to the order
Filaroidea. Filariasis : A disease due to the presence of hairline nematodes
(filariae) in humans, including Wuchereria bancrofti, W. pacifica, and
Onchocerca volvulus. Flagella : Relatively long, whiplike, centriole-based locomotor
organelles on some motile cells (sing. Flagellum). Flagellate : 1. Having flagella. 2. An organism that propels itself
by means of flagella. 3. Resembling a flagellum. Gamogony : Spore formation by multiple fission in sporozoans.
Sexual reproduction. Inoculation : Introduction of a disease agent into an animal
or plant to produce a mild form of disease and render the individual immune.
Introduction of microorganisms onto or into a culture medium. Lymphadenopathy : Enlargement or disease of lymph-nodes. Malaria : A group of human febrile diseases with a chronic relapsing
course caused by hemosporidian blood parasites of the genus Plasmodium,
transmitted by the bite of the Anopheles mosquito. Malaria pigment : Dark-brown, amorphous, micro-crystalline and
birefringent pigment found in parasitized erythrocytes, especially with
malarial parasites, and in littoral phagocytes of spleen, liver, and bone
marrow. Merozoite : An ameboid trophozoite in some sporozoans produced
from a schizont by schizogony. Motile : Capable of spontaneous movement. Oocyst : The encysted zygote of some sporozoa. Organelle : A specialized subcellular structure, such as a mitochondrion,
having a special function; a condensed system showing a high degree of
internal order and definite limits of size and shape. Parasite : An organism that lives in or on another organism of
different species from which it derives nutrients and shelter. Paroxysm : 1. A sudden attack, or the periodic crisis in the
progress of a disease. 2. A spasm, convulsion, or seizure. Pathogen : A disease-producing agent; usually refers to living
organisms. Pigment : Any colouring matter in plant or animal cells. Plasmodium : A genus of protozoans in the family Plasmodiidae
in which all the true malarial parasites are placed. Protozoa : A diverse phylum of eukaryotic microorganisms; the
structure varies from a simple uninucleate protoplast to colonial forms,
the body is either naked or covered by a test, locomotion is by means
of pseudopodia or cilia or flagella, there is a tendency towards universal
symmetry in floating species and radial symmetry in sessile types, and
nutrition may be phagotrophic or autotrophic or saprozoic. Quinidine : C20H24N2O2. A crystalline alkaloid that melts at 171.5C
and that may be derived from the bark of cinchona; used as the salt in
medicine. Also known as chinidine; -quinine. Quinine : C20H24N2O2. An alkaloid of cinchona, used principally
as an antimalarial drug. Schizogony : A sexual reproduction by multiple fission of a trophozoite;
a characteristic of certain Sporozoa. Schizont : A multinucleate cell in certain members of the Sporozoa
that is produced from a trophozoite in a cell of the host, and that segments
into merozoites. Spore : A uni- or multicellular, asexual, reproductive or resting
body that is resistant to unfavourable environmental conditions and produces
a new vegetative individual when the environment is favourable. Sporogony : Reproduction of means of spores. Propagative reproduction
involving formation, by sexual processes, and subsequent division of a
zygote. Sporozoa : A subphylum of parasitic Protozoa, typically producing
spores during the asexual stages of the life cycle. Sporozoite : A motile, infective stage of certain sporozoans,
which is the result of sexual reproduction and which gives rise to an
asexual cycle in the new host. Trophozoite : A vegetative protozoan; used especially of a parasite.
Zygote : 1. An organism produced by the union of two gametes. 2. The fertilized ovum before cleavage. Malaria is a serious disease caused when a parasitic single celled
organism, called plasmodium, enters the red blood cells. It is transmitted
by several different species of mosquitoes of the genus anopheles
that includes many that are carriers of the malarial parasite (plasmodium).
The most severe form of malaria is caused by the parasite plasmodium
falciparum. Generally, mosquitoes carrying malaria are found in
tropical and sub-tropical climates. Symptoms of malaria After an incubation period of about 2 - 5 weeks, there is a sudden
attack of shivering followed by a high fever of about 1040F. This
is often accompanied by headache and vomiting that lasts for several
hours. These symptoms may occur at interval of 2 - 3 days, depending
on the type of malaria. If the disease is not treated, the symptoms
may recur at irregular intervals and even for many years. How is malaria diagnosed and treated? Though periodic bouts of shivering and high fever are symptomatic
of malaria, only a blood examination can reveal the presence
of malarial parasites. Initial treatment is with the drug
chloroquine. Unfor-tunately, the parasite plasmodium falciparum
is often resistant to chloroquine and many other drugs. In 1890, Manson had set up a practice in London and was appointed
Physician to the Seamens Hospital, where he had access to many
cases of tropical disease. He carried out prolonged observations
on the exflagellation of malaria and, in a paper published in
1894, postulated that the process was a normal part of the life
cycle of the parasite in the stomach of the mosquito. In the same
year he met Ronald Ross, with whom, after showing him the malaria
parasite, he spent long hours discussing the mosquito-malaria theory.
Largely as a result of pressure on the India Office brought to bear
by Manson, Ross was dispatched to India the following year to investigate
the theory. Mansons advice was to follow the flagellum, and Ross
soon succeeded in observing exflagellation in the stomach of the
mosquito. But the problem of following the parasite into the tissues
of the mosquito, of which only one species is suitable for development,
proved to be a Herculean task. Throughout the months of investigation
that followed, Manson maintained a continuous correspondence with
Ross. In August 1897 Ross dissected a new type of mosquito (Anopheles)
that had fed on a malaria patient, and in it he found pigmented
round bodies on the stomach wall. The pigmented bodies were sent
to Manson, who confirmed their significance. Soon afterward Ross
was removed to an area where human malaria was absent, and there
he applied himself to the study of Proteosoma, a malaria parasite
of sparrows. From this study he was able in 1898 to describe its
complete life cycle in the mosquito. The discovery was announced
by Manson at a meeting of the British Medical Association in Edinburgh.
Ross fully acknowledged the part played by Manson; but Manson, with
characteristic modesty, disclaimed any credit save that of having
discovered Ross. Malaria is caused by PLASMODIUM, a Protozoan involving two different
hosts in its life cycle. There are more than hundred species of
Plasmodium, but only four species have human as their natural vertebrate
host. They are : P. vivax: i. Widely distributed. ii. New generation of merozoites formed every 48 hours causing
fever. iii. Incubation period is 10 days. P. ovale : i. Found in West Africa and South America. ii. Fever comes every 48 hours (due to the formation of new generation
of merozoites) iii. Incubation period is 14 days. P. malariae : i. Found in both tropics and temperate zones but not very widespread.
ii. Fever comes after every 72 hours. iii. Incubation period varies from 27 - 37 days. P. falciparum : i. Common in tropics, including India. ii. Most dangerous as it causes almost continuous fever but the
course is shorter and without relapses. iii. Incubation period is 10 days. The arthropod hosts are females of certain species of Anopheles
mosquito. There is no animal reservoir for any of these human parasites
except possibly chimpanzees for P. Malariae. Malaria therefore cannot
be acquired in uninhabited regions, for malaria to thrive there
must be infected human beings and plenty of man-biting Anopheles,
and easy contact between the two. Plasmodium also parasitizes lizards,
birds and mammals but these differ from human malaria parasite.
The life cycle of all Plasmodium species is complex. Infection
in humans begins with the bite of an infected female Anopheline
mosquito. Sporozoites released from the salivary glands of the
mosquito enter the bloodstream during feeding quickly invade liver
cells (hepatocytes). Sporozoites are cleared from the circulation
within 30 minutes. During the next 14 days in the case of P. falciparum,
the liver-stage parasites differentiate and undergo asexual multiplication
resulting in tens of thousands of Merozoites which burst from
the hepatocyte. Individual merozoites invade red blood cells (erythrocytes)
and undergo an additional round of multiplication producing 12-16
merozoites within a schizont. The length of this erythrocytic
stage of the parasite life cycle depends on the parasite species.
The clinical manifestations of malaria, fever and chills, are
associated with the synchronous rupture of the infected erythrocyte.
The released merozoites go on to invade additional erythrocytes. Not all of the
merozoites divide into schizonts, some differentiate into
sexual forms, male and female gametocytes. These gametocytes
are taken up by a female anophylis mosquito during a blood
meal. Within the mosquito midgut, the male gametocyte
undergoes a rapid nuclear division, producing 8 flagellated
microgamtes which fertilize the female macrogamete. The
resulting ookinete traverses the mosquito gut wall and
encysts on the exterior of the gut wall as a oocyst. Soon
the oocyst ruptures, releasing hundreds of sporozoites
into the mosquito body cavity where they eventually migrate
to the mosquito salivary gland.
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