Coitocaecum parvum | |
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Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Platyhelminthes |
Class: | Trematoda |
Order: | Plagiorchiida |
Family: | Opecoelidae |
Genus: | Coitocaecum |
Species: | C. parvum |
Binomial name | |
Coitocaecum parvum Crowcroft, 1945 | |
Coitocaecum parvum is a digeneic trematode or flatworm (Platyhelminthes) that is parasitic to the intestine of the common bully ( Gobiomorphus cotidianus ) or upland bully (G. breviceps). The common and upland bully are freshwater fish of New Zealand that C. parvum uses as its definitive host. C. parvum is a hermaphroditic freshwater trematode that can omit its definitive host and produce eggs by selfing or progenesis inside its amphipod second intermediate host. [1]
The life cycle of C. parvum begins when eggs are released into the water and hatch into free-swimming miracidia. The miracidia then penetrate the first intermediate host, Potamopyrgus antipodarum (the New Zealand mud snail), where they multiply and develop into sporocysts. Next, free-living cercariae are asexually produced from the sporocysts and shed by the snails. These shed cercarial larvae then penetrate the hemocoel of the second intermediate host, Paracalliope fluviatilis (amphipod) and encyst as metacercariae. [2] At this stage, the metacercariae have two options: 1) to wait for the bully (the definitive host) to eat the amphipod or 2) to undergo selfing (progenesis).
C. parvum will take up residence in the bully intestine where it will mature and reproduce eggs sexually (if it finds a partner) or via self-fertilization (since trematodes are hermaphroditic). However, if the amphipod is not eaten, the C. parvum metacercariae mature within the amphipod where they produce viable eggs within the cyst in the hemocoel (body cavity). [3] Eggs produced in this fashion remain enclosed in the cyst until the amphipod dies. After amphipod death, the eggs are released into the water where they hatch into miracidia and are infective to the snail. [2] The process of maturing within the intermediate host and eliminating the need for the definitive host is known as progenesis. [1]
The progenetic life cycle choice is dependent upon opportunities for transmission and the risk of dead-end transmission. The worm can use cues from the amphipod caused by the presence of the predatory definitive host to interrupt its growth cycle in wait to be eaten. However, under low amounts of stress cues from the amphipod, the worm responds by adopting the progenetic lifecycle. [4]
Another factor involved in the choice of progenesis is the competition with other interspecies and intraspecies competition. In the case of interspecies coinfection, competition with Microphallus sp. (avian definitive host) favors progenesis in order to ensure C. parvum egg production. Intraspecies coinfection is when more than one C. parvum larvae infects the amphipod, and whoever reproduces faster is going to ensure passage of its genetic information. [5]
The progenetic ability of C. parvum is evolutionarily advantageous for this trematode. While inbreeding or selfing is evolutionarily disadvantageous, because it decreases the ability for genetic diversity to adapt to new hosts, this worm utilizes progenesis for reproductive insurance. Since progenesis does not preclude future generations of cross-fertilization in the fish host, it is merely a means of avoiding dead-end hosts.
Trematoda is a class of flatworms known as flukes or trematodes. They are obligate internal parasites with a complex life cycle requiring at least two hosts. The intermediate host, in which asexual reproduction occurs, is usually a snail. The definitive host, where the flukes sexually reproduce, is a vertebrate. Infection by trematodes can cause disease in all five traditional vertebrate classes: mammals, birds, amphibians, reptiles, and fish.
Clonorchiasis is an infectious disease caused by the Chinese liver fluke and two related species. Clonorchiasis is a known risk factor for the development of cholangiocarcinoma, a neoplasm of the biliary system.
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Trematodes are parasitic flatworms of the class Trematoda, specifically parasitic flukes with two suckers: one ventral and the other oral. Trematodes are covered by a tegument, that protects the organism from the environment by providing secretory and absorptive functions.
Paragonimus westermani is the most common species of lung fluke that infects humans, causing paragonimiasis. Human infections are most common in eastern Asia and in South America. Paragonimiasis may present as a sub-acute to chronic inflammatory disease of the lung. It was discovered by Coenraad Kerbert (1849–1927) in 1878.
Echinostoma is a genus of trematodes (flukes), which can infect both humans and other animals. These intestinal flukes have a three-host life cycle with snails or other aquatic organisms as intermediate hosts, and a variety of animals, including humans, as their definitive hosts.
Paragonimiasis is a food-borne parasitic disease caused by several species of lung flukes belonging to genus Paragonimus. Infection is acquired by eating crustaceans such as crabs and crayfishes which host the infective forms called metacercariae, or by eating raw or undercooked meat of mammals harboring the metacercariae from crustaceans.
Brachylaima is a genus of trematodes that can infect the gastrointestinal tract of human beings.
Leucochloridium paradoxum, the green-banded broodsac, is a parasitic flatworm. Its intermediate hosts are land snails, usually of the genus Succinea. The pulsating, green broodsacs fill the eye stalks of the snail, thereby attracting predation by birds, the primary host. These broodsacs visually imitate caterpillars, a prey of birds. The adult parasite lives in the bird's cloaca, releasing its eggs into the faeces.
Metagonimoides oregonensis is a trematode, or fluke worm, in the family Heterophyidae. This North American parasite is found primarily in the intestines of raccoons, American minks, frogs in the genus Rana, and freshwater snails in the genus Goniobasis. It was first described in 1931 by E. W. Price. The parasite has a large distribution, from Oregon to North Carolina. Adult flukes vary in host range and morphology dependent on the geographical location. This results in different life cycles, as well as intermediate hosts, across the United States. On the west coast, the intermediate host is freshwater snails (Goniobasis), while on the east coast the intermediate host is salamanders (Desmognathus). The parasites on the west coast are generally much larger than on the east coast. For example, the pharynx as well as the body of the parasite are distinctly larger in Oregon than in North Carolina. The reverse pattern is observed on the east coast for uterine eggs, which are larger on the west coast. In snails, there is also a higher rate of infection in female snails than in males. Research on the life history traits of the parasites have been performed with hamsters and frogs as model species.
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