Название | Parasitology |
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Автор произведения | Alan Gunn |
Жанр | Медицина |
Серия | |
Издательство | Медицина |
Год выпуска | 0 |
isbn | 9781119641223 |
Figure 3.13 Life cycle of Isospora belli. 1: Infection commences following ingestion of a sporulated oocyst. The oocyst releases eight sporozoites when it reaches the small intestine and these invade the gut epithelial cells where they transform into merozoites. The merozoites divide asexually to produce more merozoites. 2: Merozoite forming a multinucleate meront that gives rise to microgametocytes (male). 3: Merozoite giving rise to a macrogametocyte (female). Fusion of a male and a female gamete results in the formation of a zygote, and this develops into an oocyst. 4: Sporulation of the oocyst occurs before it is released in the host’s faeces. Drawings not to scale.
At some point, the merozoites transform into multinucleate meronts and these give rise to microgametes (male) or macrogametes (female). Unless the microgametes and macrogametes occur within the same cell (which is possible), the microgametes leave their host cell to locate a macrogamete and their fusion results in the formation of a zygote that then develops into an oocyst. The death of the host cell releases the oocyst into the gut lumen and leaves the body with the faeces. The oocyst then undergoes sporulation to produce two sporocysts, each of which contains four sporozoites. Transmission is therefore passive by faecal–oral contamination. Environmental conditions probably heavily influence the time taken for sporulation. For example, in some Isospora species, temperatures below 20 °C inhibit sporulation, but it takes less than 16 hours at 30 °C. Nevertheless, transmission is probably through infected food or water rather than direct contact. For example, through not washing one’s hands after defaecation or by contacting an article touched by such a person. This is therefore distinct from Cryptosporidium parvum in which the oocysts are immediately infective after shedding.
3.5.4 Genus Cyclospora
This genus currently contains 13 species that are parasitic in a range of vertebrates (e.g., snakes, rodents), but the most important is Cyclospora cayetanensis that only infects humans.
3.5.4.1 Cyclospora cayetanensis
First described in 1979, this is an emerging parasitic disease with a cosmopolitan distribution (Almeria et al. 2019). There are regular outbreaks in USA and Canada associated with the importation of fresh berries (Dixon et al. 2016). The life cycle begins with the ingestion of oocysts (8–10 μm diameter) containing infective sporozoites. Once the oocysts reach the duodenum and upper small intestine, they release the sporozoites and these invade the gut epithelial cells. They then transform into type I merozoites that then divide to form type II merozoites. The type II merozoites transform into meronts and these give rise to microgametocytes and macrogametocytes. Fusion of a microgametocyte with a macrogametocyte gives rise to zygote, and this develops into an oocyst that is shed with the faeces. The oocyst then undergoes sporulation to produce two sporocysts each containing two sporozoites. Sporulation takes 7–15 days depending upon the environmental conditions and therefore transmission probably occurs through contamination of food and water rather than direct person‐to‐person/contaminated object contact.
The symptoms of infection are non‐specific and resemble those of many other gastrointestinal diseases. Patients suffer from abdominal pain, watery diarrhoea, flatulence, low‐grade fever, anorexia, and weight loss. In endemic regions, the symptoms tend to be worse in young children and in non‐endemic regions most people who become infected express symptoms. Persons who are immunosuppressed and AIDS patients are more seriously affected.
3.5.5 Genus Sarcocystis
Members of this genus are obligate intracellular parasites with a life cycle that involves two hosts – a herbivore intermediate host in which only asexual multiplication occurs and a carnivore definitive host in which sexual reproduction takes place. Most Sarcocystis species are very host‐specific and infect a limited number of closely related intermediate/final hosts (Table 3.3). You will not be surprised to hear that the taxonomy is confused, and one must take care when using the older literature. For example, some animals once thought to harbour just a single Sarcocystis species actually contain several species. In addition, some species are morphologically identical, and others have synonyms (e.g., Sarcocystis cruzi is also known as Sarcocystis bovicanis – a reflection that the intermediate and definitive hosts are cattle and dogs/ other canines respectively).
Table 3.3 Summary of the most important species of Sarcocystis in human and veterinary medicine.
Species of Sarcocystis | Synonym | Intermediate host | Definitive host |
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Sarcocystis bovicanis | Sarcocystis cruzi | Cattle | Dogs and other canines |
Sarcocystis bovihominis | Sarcocystis hominis | Cattle | Humans |
Sarcocystis bovifelis | Sarcocystis hirsuta | Cattle | Cats and other felines |
Sarcocystis Suihominis | Isospora hominis | Pigs | Humans and some primates |
Sarcocystis ovifelis | Sarcocystis tenella | Sheep | Cats and other felines |
Sarcocystis hovathi | Sarcocystis gallinarum | Chicken | Dogs and other canines |
The life cycle of S.