Parasitology. Alan GunnЧитать онлайн книгу.
href="#ulink_cb502faa-3c40-55c6-b0f4-33c44843d94b">4.4.1 Phylum Microspora
4.1 Introduction
In this chapter, we will introduce just a few of the kinetoplastid parasites that are important in human and veterinary medicine. This is a remarkable group of protozoa that includes parasites of plants, invertebrates, and vertebrates. Their transmission strategies range from contamination to vector assisted and sexually transmitted. We do not usually think of algae as parasitic organisms but there are a few that have adopted this lifestyle and some even parasitise us. This should not come as a surprise as several notorious protozoan parasites, such as Plasmodium, probably evolved from algal ancestors. The fungi have a Kingdom of their own and are normally considered the preserve of mycologists. However, the microsporidia are something of a special case. Originally classed as protozoa, they fell within the remit of parasitologists. Now, their subsequent reclassification as fungi presents parasitologists with a bit of dilemma. Namely, do they still belong within parasitology textbooks when yeast infections etc. are firmly excluded? At the time of writing, the classification of the Microsporidia is being called into question again, and therefore, we feel justified in including them here.
4.2 Phylum Kinetoplastida
The Kinetoplastida is a large diverse group of protozoa that includes both plant and animal parasites (Table 4.1). Some authors consider the Kinetoplastida to be a phylum, while others refer to it as a class or an order. They are commonly known as the trypanosomes from the genus Trypanosoma that includes the causative agents of Human African Trypanosomiasis (HAT) and several other parasites of medical and veterinary importance. The genus name Trypanosoma derives from the Greek words trypano ( τρύπανο ) = an auger [a device for boring holes in wood] and soma ( σώμα ) = body that refer to their corkscrew‐like locomotion. Magez and Radwanska (2014) provide a comprehensive review of all aspects of trypanosome biology and their transmission.
Table 4.1 Examples of kinetoplastid parasites of medical, veterinary, and agricultural importance and the diseases they cause.
| Genus | Example | Host | Vector/transmission | Disease |
|---|---|---|---|---|
| Leishmania | Leishmania donovani | Humans, dogs, rats | Phlebotomus sandflies | Kala‐azar (visceral leishmaniasis) |
| Leishmania major | Humans, monkeys, dogs, rodents | Phlebotomus sandflies | Cutaneous leishmaniasis | |
| Leishmania tropica | Humans, monkeys, dogs, rodents | Phlebotomus sandflies | Cutaneous leishmaniasis | |
| Leishmania braziliensis | Humans, sloths, monkeys, opossums, and many others | Lutzomyia sandflies | Cutaneous/mucocutaneous leishmaniasis | |
| Trypanosoma | Trypanosoma brucei gambesiense | Humans | Tsetse flies (Glossina spp.) | African trypanosomiasis (sleeping sickness) |
| Trypanosoma congolense | Cattle | Tsetse flies (Glossina spp.) | African trypanosomiasis (nagana) | |
| Trypanosoma equiperdum | Horses | venereal | Dourine | |
| Trypanosoma cruzi | Humans, dogs, cats, rats, and many others | Triatomid bugs | Chagas disease | |
| Phytomonas | Phytomonas staheli | Coconut palms | Lincus lobuliger (Pentatomid bug) | Hartroot |
The Kinetoplastida are characterised by their possession of a flagellum and a unique intracellular structure called a kinetoplast (Figure 4.1). The kinetoplast is a disk of interlocking DNA circles (kDNA) located within a large mitochondrion. The structure of kinetoplast DNA is unlike that found in any other organism and its complex replication involves special proteins (da Silva et al. 2017). It may therefore be possible to design drugs to interfere with the replication of kinetoplast DNA. The position of the mitochondrion is such that the kinetoplast is just underneath the kinetosome that is itself situated underneath the base of the flagellum. The kinetosome (sometimes called the basal body), is a structure found in many organisms and is homologous with the centriole; it is involved in the formation of the flagellum. The Kinetoplastida always have a flagellum that may be long and free, incorporated into the cell surface to form an undulating membrane, or small and enclosed within a pocket. The inner core of the flagellum is the axoneme. Alongside this, and connecting to it, is the paraxial rod that consists of a lattice‐like crystalline array of structural proteins. In the promastigote, epimastigote, and trypomastigote stages, the flagellum emerges at the anterior end of the cell and therefore acts as a propeller that pulls the cell along rather than pushing it from behind (Figure 4.2).
Figure 4.1 Diagram of a typical trypanosome. Kp: kinetoplast; Ks: kinetosome; F: flagellum; Mit: mitochondrion; Gly: glycosome; N: nucleus; Lys: lysosome; Um: undulating membrane.
Figure 4.2 Morphological forms of trypanosomes. (a) Trypomastigote. (b) Epimastigote. (c) Promastigote. (d) Amastigote. The flagellum pulls the cell forwards rather than pushes it from behind. Arrows: direction of movement.
The Kinetoplastida have a unique organelle called the glycosome. This may be related to the peroxisomes (which they do not have) found in other organisms. The glycosomes are about 0.25 μm in diameter and contain glycolytic enzymes that are normally present in the cytoplasm of other organisms. The bloodstream forms of trypanosomes are extremely metabolically