Coitocaecum Parvum
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''Coitocaecum parvum'' is a digeneic
trematode Trematoda is a class of flatworms known as flukes. 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 ...
or flatworm (
Platyhelminthes The flatworms, flat worms, Platyhelminthes, or platyhelminths (from the Greek language, Greek πλατύ, ''platy'', meaning "flat" and ἕλμινς (root: ἑλμινθ-), ''helminth-'', meaning "worm") are a Phylum (biology), phylum of relati ...
) 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 (Lagrue et al., 2001)


Life cycle

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 (''Potamopyrgus antipodarum'') is a species of very small freshwater snail with a gill and an operculum. This aquatic gastropod mollusk is in the family Tateidae. It is native to New Zealand, where it is found through ...
'' (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 A larva (; plural larvae ) is a distinct juvenile form many animals undergo before metamorphosis into adults. Animals with indirect development such as insects, amphibians, or cnidarians typically have a larval phase of their life cycle. The ...
then penetrate the
hemocoel The blood circulatory system is a organ system, system of organs that includes the heart, blood vessels, and blood which is circulated throughout the entire body of a human or other vertebrate. It includes the cardiovascular system, or vascula ...
of the second intermediate host, '' Paracalliope fluviatilis'' (amphipod) and encyst as metacercariae (Kelly, 2009). 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) (Lefebvre, 2005). 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 (Kelly, 2009). The process of maturing within the intermediate host and eliminating the need for the definitive host is known as progenesis (Lagrue, 2001)


Life cycle choice

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 (Lagrue & Poulin, 2007). 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 (Lagrue and Poulin, 2008)


Progenesis

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.


References

*Kelly, D. W., R. A. Paterson, C. R. Townsend, R. Poulin and D. M. Tompkins. 2009. Has the introduction of brown trout altered disease patterns in native New Zealand fish? ''Freshwater Biology'' 54:1805-1818 *Lagrue, C., J. M. Waters, R. Poulin and D. B. Keeney. 2001. Microsaterllite loci for the progenetic trematode, ''Coitocaecum parvum'' (Opecoelidae). ''Molecular Ecology Notes'' 7:694-696 *Lagrue, C. and R. Poulin. 2007. Life cycle abbreviation in the trematode ''Coitocaecum parvum'': can parasites adjust to variable conditions? ''Journal of Evolutionary Biology'' 20:1189-1195 *Lagrue, C., and R. Poulin. 2008. Intra- and interspecific competition among helminth parasites: Effects on Coitocaecum parvum life history strategy, size and fecundity. International Journal for Parasitology 38:1435-1444 *Lefebvre, B. Fredensborg, A. Armstrong, E. Hansen and R. Poulin. 2005. Assortative pairing in the amphipod ''Paracalliope fluviatilis'': a role for parasites? ''Hydrobiologia'' 545:65-73 {{Taxonbar, from=Q5141665 Animals described in 1945 Opecoelidae