| Apicomplexa | |
|---|---|
| Plasmodium | |
| Scientific classification | |
| Domain: | Eukaryota |
| Kingdom: | Chromalveolata |
| Superphylum: | Alveolata |
| Phylum: | Apicomplexa Levine, 1970 |
| Classes & Subclasses Perkins, 2000 | |
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The Apicomplexa (also referred to as Apicomplexia) are a large group of protists, most of which possess a unique organelle called apicoplast and an apical complex structure involved in penetrating a host's cell. They are unicellular, spore-forming, and exclusively[1] parasites of animals. Motile structures such as flagella or pseudopods are present only in certain gamete stages. This is a diverse group including organisms such as coccidia, gregarines, piroplasms, haemogregarines, and plasmodia. Diseases caused by apicomplexan organisms include, but are not limited to:
The name of the taxon Apicomplexa is derived from two Latin words - apex (top) and complexus (infolds) - and refers to a set of organelles in the sporozoite. The older taxon Sporozoa grouped the Apicomplexa together with the Microsporidia and Myxosporida. This grouping is no longer regarded as biologically valid and its use is discouraged.[2]
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The first apicomplexan protozoan was seen by Antony van Leeuwenhoek who in 1674 saw oocysts of Eimeria stiedae in the gall bladder of a rabbit. The first member of the phylum to be named (by Dufour in 1828) was Gregarina ovata in earwigs. Since then many more have been identified and named. During the quarter century 1826-1850, 41 species and 6 genera of Apicomplexa were named. In the quarter century 1951-1975, 1873 new species and 83 new genera were added.
The field of classifying Apicomplexa is in flux and classification has changed throughout the years.
By 1987 a comprehensive survey of the phylum was completed: in all, 4516 species and 339 genera had been named. They consisted of:
Although there has been considerable revision of this phylum (the order Haemosporidia now has 17 genera rather than 9) it seems likely these numbers are still approximately correct.
Jacques Euzéby in 1988[3] created a new class Haemosporidiasina by merging subclass Piroplasmasina and suborder Haemospororina.
Roberts and Janovy in 1996 divided the phylum into the following subclasses and suborders (omitting classes and orders):[4]
These form the following five taxonomic groups:
This scheme is taken from Perkins et al.[5] It is outdated as the Perkinsidae have since been recognised as a sister group to the dinoflagellates rather that the Apicomplexia. The remainder of the scheme appears to be valid:
All members of this phylum have an infectious stage - the sporozoite - which possess three distinct structures in an apical complex. The apical complex consists of a set of spirally arranged microtubules (the conoid), a secretory body (the rhoptry) and one or more polar rings. Additional slender electron dense secretory bodies (micronemes) surrounded by one or two polar rings may also be present. It is this structure that gives the phylum its name.
A further group of spherical organelles are distributed throughout the cell rather than being localized at the apical complex and are known as the dense granules. These typically have a mean diameter of about 0.7 micrometers. Secretion of the dense-granule content takes place after parasite invasion and localization within the parasitophorous vacuole and persists for several minutes
Other morphological findings that are common to all members of this phylum include:
Replication:
Within this phylum there are four groups - Perkinsus, coccidians, gregarines and haemosporidians. The coccidians and gregarines appear to be relatively closely related and Perkinsus appears to be basal within this phylum, and will not be described here (see class Perkinsasida).
The gregarines are generally parasites of annelids, arthropods and mollusks. They are often found in the guts of their hosts but may invade the other tissues. In the typical gregarine life cycle a trophozoite develops within a host cell into a plasmodium. This then divides into a number of merozoites by schizogony. The merozoites are released by lysing the host cell which in turn invade other cells. At some point in the life cycle gamonts are formed. These are released by lysis of the host cells and group together by syzygy. Each gamont forms multiple gametes. The gametes fuse with another to form oocysts. The oocysts leave the host to be taken up by a new host.
Coccidians are generally parasites of vertebrates. Like gregarines they are commonly parasites of the epithelial cells of the gut but may infect other tissues. The typical coccidial life cycle while similar to that of the gregarines differs in zygote formation. Some trophozoites enlage and become macrogamete while others divide repeatedly to form microgametes. The microgametes are motile and must reach the macrogamete to fertilize it. The fertilized macrogamete forms a zygote which in its turn forms an oocyst which is normally released from the body.
The Haemosporidians have more complex life cycles that alternate between an arthropod and a vertebrate host. The trophozoite parasitises erythrocytes or other tissues in the vertebrate host. Microgametes and macrogametes are always found in the blood. The gametes are taken up by the insect vector during a blood meal. The microgametes migrate within the gut of the insect vector and fuse with the macrogametes. The fertilized macrogamete now becomes an ookinete which penetrates the body of the vector. The ookinete then transforms into an oocyst and divides initially by meiosis and then by mitosis (haplontic life cycle) to give rise to the sporozoites. The sporozoites escape from the oocyst and migrate within the body of the vector to the salivary glands where they are injected into the new vertebrate host when the insect vector feeds again.
Many Coccidiomorpha have an intermediate host as well as a primary host, and the evolution of hosts proceeded in different ways and at different times in these groups. For some coccidiomorphs, the original host has become the intermediate host while in others it has become the definitive host. In the genera Aggregata, Atoxoplasma, Cystoisospora, Schellackia and Toxoplasma the original is now definitive while in Akiba, Babesiosoma, Babesia, Haemogregarina, Haemoproteus, Hepatozoon, Karyolysus, Leucocytozoon, Plasmodium, Sarcocystis and Theileria, the original hosts are now intermediate.
Similar strategies to increase the likelihood of transmission have evolved in multiple genera. Polyenergid oocysts and tissue cysts are found in representatives of the orders Protococcidiida and Eimeriida. Hypnozoites are found in Karyolysus lacerate and most species of Plasmodium; transovarial transmission of parasites occurs in life cycles of Karyolysus and Babesia.
Most members have a complex life-cycle, involving both asexual and sexual reproduction. Typically, a host is infected via an active invasion by the parasites (similar to entosis), which divide to produce sporozoites that enter its cells. Eventually, the cells burst, releasing merozoites which infect new cells. This may occur several times, until gamonts are produced, forming gametes that fuse to create new cysts. There are many variations on this basic pattern, however, and many Apicomplexa have more than one host.
The apical complex includes vesicles called rhoptries and micronemes, which open at the anterior of the cell. These secrete enzymes that allow the parasite to enter other cells. The tip is surrounded by a band of microtubules, called the polar ring, and among the Conoidasida there is also a funnel of tubulin proteins called the conoid.[6] Over the rest of the cell, except for a diminished mouth called the micropore, the membrane is supported by vesicles called alveoli, forming a semi-rigid pellicle.
The presence of alveoli and other traits place the Apicomplexa among a group called the alveolates. Several related flagellates, such as Perkinsus and Colpodella have structures similar to the polar ring and were formerly included here, but most appear to be closer relatives of the dinoflagellates. They are probably similar to the common ancestor of the two groups.
Another similarity is that many apicomplexan cells contain a single plastid, called the apicoplast, surrounded by either 3 or four membranes. Its functions are thought to include tasks such as lipid and heme biosynthesis, and it appears to be necessary for survival. Plastids are generally considered to share a common origin with the chloroplasts of dinoflagellates, and evidence generally points to an origin from red algae rather than green.[7][8]
The Apicomplexa comprise the bulk of what used to be called the Sporozoa, a group for parasitic protozoans without flagella, pseudopods, or cilia. Most of the Apicomplexa are motile however. The other main lines were the Ascetosporea, the Myxozoa (now known to be derived from animals), and the Microsporidia (now known to be derived from fungi). Sometimes the name Sporozoa is taken as a synonym for the Apicomplexa, or occasionally as a subset.
Within the Apicomplexa there are three suborders of parasites.
Within the Adelorina are species that infect invertebrates and others that infect vertebrates.
The Haemosporina includes the malaria parasites and their relatives.
The Eimeriorina - the largest suborder in this phylum - the life cycle involves both sexual and asexual stages. The asexual stages reproduce by schizogony. The male gametocyte produces a large number of gametes and the zygote gives rise to an oocyst which is the infective stage. The majority are monoxenous (infect one host only) but a few are heteroxenous (life cycle involves two or more hosts).
Both the number of families in this later suborder is debated with the number of families being between one and twenty depending on the authority and the number of genera being between nineteen and twenty five. This somewhat unsatisfactory state of affairs awaits resolution with DNA based methods.
As noted above, many of the apicomplexan parasites are important pathogens of human and domestic animals. In contrast to bacterial pathogens, these apicomplexan parasites are eukaryote and share many metabolic pathways with their animal hosts. This fact makes therapeutic target development extremely difficult – a drug that harms an apicomplexan parasite is also likely to harm its human host. Currently there are no effective vaccines available for most diseases caused by these parasites. Biomedical research on these parasites is challenging because it is often difficult, if not impossible, to maintain live parasite cultures in the laboratory and to genetically manipulate these organisms. In the recent years, several of the apicomplexan species have been selected for genome sequencing. The availability of genome sequences provides a new opportunity for scientists to learn more about the evolution and biochemical capacity of these parasite. One prominent source of this genomic information is the EuPathDB family of websites, which currently provide specialised services for Plasmodium species (PlasmoDB),[9][10] coccidians (ToxoDB),[11][12] piroplasms (PiroplasmaDB),[13] and Cryptosporidium species (CryptoDB).[14][15] One possible target for drugs is the plastid, and in fact existing drugs such as tetracyclines which are effective against apicomplexans seem to operate against the plastid.[16]
Most apicomplexans have plastid (also known as apicoplast) and mitochondrial genomes as well as nuclear ones, although Cryptosporidium spp. and possibly gregarines are exceptions as they are thought to have lost their plastids after the diverging last common ancestor of apicomplexans.
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