not always form but if they do, they are a reliable indicator of the nature of the disease. The onset of paralysis marks the third stage of the disease. Often this begins in the nose and face. It then spreads to affect the rest of the body and can result in complete paralysis affecting all the limbs. The course of the disease may take as long as 2 years and mortality can be as high as 70%.
The relationship between T. equiperdum, T. evansi, and T. brucei remains uncertain. Molecular evidence indicates that T. equiperdum and T. evansi independently diverged from T. brucei on several occasions. According to Cuypers et al. (2017), T. equiperdum arose from an East African T. brucei ancestor whilst T. evansi derives from a West African T. brucei ancestor.
Trypanosoma equiperdum is primarily a tissue parasite and not usually present in the circulating blood, but it occurs in smears taken from the genitalia or plaques. Diagnosis has traditionally relied on serological complement fixation tests and in some countries where dourine is endemic, they are mandatory. However, such tests will not reliably distinguish T. equiperdum from other trypanosomes such as T. evansi and T. brucei – which is hardly surprising because they are all closely related.
4.2.2.6 Trypanosoma cruzi
Trypanosoma cruzi causes Chagas disease – a potentially fatal infection that afflicts around 11 million people in the New World from Argentina to the southern United States of America. In addition, owing to migration, the disease now occurs in many other parts of the world with important foci in Canada, North America, Europe, and Australia. The name Chagas disease derives from that of Carlos Chagas who first described the parasites in 1910. Chagas initially believed that the parasites underwent schizogony within their mammalian host and hence named them Schizotrypanum cruzi – ‘cruzi’ derives from the famous Oswaldo Cruz Institute in Brazil. Subsequently, it became clear that the parasite’s life cycle does not include schizogony and most workers now refer to it as Trypanosoma cruzi.
In addition to humans, T. cruzi infects many domestic and wild mammals including dogs, cats, bats, rats, and armadillos. This makes disease control difficult because there are numerous potential reservoirs of infection. Trypanosoma cruzi infections are especially common among animals that utilise burrows and hollow trees because these are ideal dwellings for the insect vectors. The parasite is transmitted by blood‐feeding reduviid bugs (Order Hemiptera, Family Reduviidae, Sub‐Family Triatominae) that because of their appearance are sometimes called cone‐nosed bugs. Over 130 species of reduviid bug can act as vectors but only those living near humans are medically important. Although Chagas disease now occurs in many countries, the lack of suitable vectors limits its potential for transmission outside Central and South America. There is therefore concern over the potential for vector species to disperse by air or sea (the bugs can survive for weeks without feeding) to other countries with luggage or farm produce. Trypanosoma cruzi can infect several other blood‐feeding invertebrates. These include the bed bug (Cimex lectularius; Order Hemiptera, Family Cimicidae), the argasid tick Ornithodoros moubata and the medicinal leech Hirudo medicinalis. However, these are probably not important in the transmission of the parasite to humans. Trypanosoma cruzi can also infect vampire bats, but it is uncertain whether they transmit the parasite in their bite. During the acute phase of infection, the parasite occurs within the saliva of dogs, so it is clearly a possibility. However, whether a very ill bat would be capable of flying and feeding is uncertain.
The life cycle of T. cruzi differs from that of the other trypanosome species discussed so far in that it involves stercorarial transmission from the invertebrate vector to the vertebrate host (i.e., via the faeces rather than the saliva/bite). Reduviid bugs often defecate during or immediately after feeding, and they void the infective metacyclic stage trypanosomes with their faeces. The bugs feed at night and they often bite their victims around the face. They have therefore gained the common name of kissing bugs. On waking, the natural reaction is to rub/scratch at the bite site, and this rubs the parasite‐infected faeces into the wound site. However, most infections result from bug faeces contaminating the victim’s fingers and from there transferring to the eyes and mucous membranes where the parasites can penetrate more easily. We can also become infected from organ transplants and the use of contaminated blood during transfusions (Ries et al. 2016). In endemic areas, where the likelihood of acquiring T. cruzi infection from a blood transfusion is high, haematologists sometimes treat donated blood with gentian violet. This kills the parasites, but as the blood infuses through the tissues of the recipient, it also has the unfortunate effect of turning the patient purple temporarily. There are isolated reports of oral transmission of T. cruzi that date back many years. These arise through consuming food contaminated with infected bug faeces. They were considered rare oddities, but this mode of transmission is apparently becoming more common (Robertson et al. 2016). Furthermore, oral transmission tends to result in acute infections that may prove rapidly fatal. Congenital infection via the placenta is possible and can result in spontaneous abortion or serious disease of the infant at birth. Reservoir animals can acquire infections through being bitten, as well as from consuming bugs containing the parasites and from food contaminated with their faeces.
Once T. cruzi enters a suitable mammalian host, the trypomastigotes invade both phagocytic and non‐phagocytic cells. Indeed, they are apparently capable of invading all nucleated cells. However, most of the pathology arises from their invasion of smooth, cardiac, and skeletal muscle cells, nerve cells, and cells comprising organs such as the liver, spleen, and lymphatics. Within a host cell, the parasites develop within a parasitophorous vacuole. The mechanism by which a trypomastigote enters a host cell varies between cell types and may involve active invasion by the parasite and passive internalization through endocytosis/phagocytosis. Within the host cell, a parasitophorous vacuole forms around the parasites and within this, they transform into the amastigote stage (1.5–4 μm in size). The amastigotes multiply by binary fission and once large numbers are present within a cell, it is sometimes referred to as a pseudocyst. Eventually, the parasites kill their host cell and then they transform back to trypomastigotes (Figure 4.10). The trypomastigotes then invade new cells and repeat the process. This distinguishes T. cruzi from Leishmania in which the parasites occur mainly within phagocytic cells and remain in the amastigote stage within the vertebrate host. The trypomastigotes of T. cruzi are unable to reproduce although large numbers of them may occur in the blood stream, especially during the early stages of infection. Broad and slender morphotypes of the trypomastigotes exist. Both forms are small (16.3–21.8 μm in length including the flagellum) compared with those of some other trypanosomes and they have a characteristic curved ‘C’ shape. By contrast, their kinetoplast is exceptionally large and the cell membrane sometimes bulges around it.
Figure 4.10 Trypanosoma cruzi. Note the characteristic C shape often seen in the trypomastigote stage.
A reduviid bug vector acquires an infection when it feeds on blood containing the trypomastigote stage. Reduviid bugs can take in large blood meals several times their own body weight, and this increases their chances of ingesting a trypomastigote. In some bug populations, over half of them carry a T. cruzi infection. In addition to feeding on blood, reduviid bugs will also attack and feed on one another. Therefore, bugs may acquire an infection by ingesting parasites from one of their brethren. However, this is probably not a common means of infection. When the parasites reach the posterior of the insect’s midgut, they transform into short epimastigotes. These then divide by longitudinal fission to form long epimastigotes. Ultimately, the epimastigotes move to rectum where they transform into the infective short metacyclic trypomastigote stage. The gut of infected bugs can contain huge numbers of parasites but unlike some of the other trypanosome species, T. cruzi does not appear to harm its invertebrate host.
The