Echinostoma revolutum can be found in the snail Lymnaea elodes in North America (Serensen et al., 1997) and in other lymnaeid species across Eurasia. It has been reported from Germany, Austria, Poland, Bulgaria, England, Russia, Malaysia, Thailand, India, and Vietnam (Kanev, 1994). (Kanev, 1994; Sorensen, et al., 1997)
Eggs of Echinostoma revolutum are found in fresh water habitats (Kanev, 1994) where waterfowl occur. The subsequent life stages are all found in intermediate or definitive hosts, all of which are found in the same still or slow-moving freshwater habitats. As a miracidium, E. revolutum can be found in the ovotestis or digestive gland of the intermediate host (Kanev, 1994). Studies have shown that Lymnaea stagnalis is a widespread spread and common intermediate host for E. revolutum (Kanev, 1994). (Kanev, et al., 1995; Kanev, 1994)
E. revolutum is the nominal member of the 37-collar-spined E. revolutum group (Kanev, 1994; Kanev et al., 1995). The group consists of the closely related species: E. revolutum (Froelich, 1802), E. echinatum (Zeder, 1803), E. trivolvis (Cort, 1914), E. jurini (Skvortzov, 1924), E. caproni (Richard, 1964), and E. paraensei (Lie and Basch, 1967). All miracidia in this group have eighteen epidermal plates, showing a common pattern of 6:6:4:2 (anterior to posterior), six body papillae, two eyespots, and two excretory pores (Dimitrov et al., 1999).
At time of initial infection, metacercariae average 240 micrometers long and 0.02 square mm in body area. By day 14 post infection, worms reach an average of 3.5 mm in length and 2.0 square mm in body area (Humphries et al., 1997). (Dimitrov, et al., 1999; Humphries, et al., 1997)
Adult E. revolutum use avian species, primarily waterfowl as their definitive hosts. Adults are hermaphrodites and live four to eight weeks, occupying the digestive tract of infected birds (Sorensen and Minchella, 1998). Adults begin to produce and release many self-fertilized eggs ten days after infecting the definitive host (Kanev, 1994).
Eggs: The eggs hatch in fresh water in nine to twelve days. Exposure to light stimulates hatching. Eggs hatch into miracidia (Kanev, 1994).
Miracidium: The swimming larval stage can survive six to eight hours before it finds a primary intermediate host, which must be a snail in the family Lymnaeidae (Kanev, 1994). Once a miracidium successfully infects the ovotestis/digestive gland area of the host, it asexually produces three distinct asexual stages, a mother sporocyst and two subsequent redial stages over the course of a month (Sorensen and Minchella, 1998). The final redial produces infective free living cercaria for 25 to 28 days (Kanev, 1994). The cercaria exits the primary intermediate host and infects a secondary intermediate host.
Cercariae: The initialy free-living form infects an aquatic secondary intermediate host within three to six hours. This host can be various pulmonate and prosobranch snails, freshwater mussels (Unionidae), frogs, and freshwater turtles (Testundines) (Kanev, 1994). In the host, cercaria asexually produce metacercariae (Sorensen and Minchella, 1998).
Metacercariae: This stage becomes infective within one to two days (Kanev, 1994). It remains in this stage until the secondary intermediate host has been eaten by the definitive vertebrate host, usually a bird. Once ingested, metacercariae develop into hermaphroditic adults (Sorensen and Minchella, 1998). (Kanev, 1994; Sorensen and Minchella, 1998)
Adult Echinostoma revolutum are hermaphrodites, and produce both self-fertilized and cross-fertilized eggs once in the definitive host. We have no information on mating behavior or mating systems in this species. (Kanev, 1994; Sorensen and Minchella, 1998)
This species reproduces asexually at two stages in its life cycle. Sporocysts and rediae, both produce large numbers of offspring asexually, resulting in hundreds or thousands of cercarie generated from a single parent miracidium infecting a snail. Adults worms are hermaphroditic and self- and cross-fertilize.
'Echinostome Echinostoma parasitism peaks in the late summer and wanes throughout the winter (Sorensen and Minchella, 1998).
The trematode, E. revolutum, has a complex three-host life cycle. Adult E. revolutum use avian species, primarily waterfowl as the definitive host (Sorensen and Minchella, 1998). Adults are hermaphrodites and live four to eight weeks. Adults begin to produce and release many self fertilized eggs ten days after infecting the definitive host (Kanev, 1994). Adults after 14 days contain at least 50 eggs (Humphries et at., 1997). Eggs are passed by feces of the definitive host (Sorensen and Minchella, 1998). (Humphries, et al., 1997; Kanev, 1994; Sorensen and Minchella, 1998)
There is no parental investment beyond the limited provisioning of eggs.
Miracidia and cercariae are active host-seeking larvae that swim. The other stages of this species can move within their hosts, but do not leave them. (Baudoin, 1975; Brown, et al., 1988; Sorensen and Minchella, 1998)
Miracidium are are positively phototactic. Cercariae are negatively phototactic (Kanev, 1994). (Kanev, 1994)
Sporocysts lack ambulatory musculature and absorb primary intermediate host nutrients via their tegument. Rediae have a muscular pharynx and primitive gut. Rediae actively consume and digest primary intermediate host tissues while moving throughout the infected host (Sorensen and Minchella, 1998). (Sorensen and Minchella, 1998)
We have no information on particular predators of this species. It is likely that the host-seeking stages (miracidia, cercariae) are consumed by predators that eat zooplankton. This species depends on predation of its intermediate host to enter its definitive avian hosts.
Infection of Lymnaea elodes by E. revolutum significantly affects growth, fecundity, and survival rates (Sorensen and Minchella, 1998). Snail mortality between zero and four weeks post infection can be attributed to an increase in energetic demands and starvation, while snails four to seven weeks post infection die from tissue degredation (Sorensen and Minchella, 1998).
At five weeks post infection E. revolutum pathology involves destruction of the digestive gland and ovotestis (Sorensen and Minchella, 1998). This type of parasitic castration along with reduced nutrients results in a reduction in snail egg production. It is proposed by Sousa (1983) that gigantism will occur in trematode infected mollusc species because excess host energy reserves are made available via parasitic castration.
Brown et al. (1988) and Sorensen and Minchella (1998) both demonstrate a correlation between increased snail size and trematode infection. E. revolutum infection tends to cause gigantism in lymnaea species. In 1975, Baudoin presented hypotheses to explain the correlation between host size and prevalence of infection. These hypotheses included three basic mechanisms including increased host growth rates, host mortality rates, and host size-specific preferences of parasites. It is proposed that a combination of multiple hypotheses will result in gigantism of the host (Sorensen and Minchella, 1998). (Baudoin, 1975; Brown, et al., 1988; Sorensen and Minchella, 1998)
In Indonesia, Suhardono et al. (2006) have shown that E. revolutum will act competitively to infect Lymnaea rubiginosa. L. rubiginosa is more commonly infected by Fasciola gigantica. L. rubiginosa infected with F. gigantica causes fasciolosis in cattle stocks feeding on harvested rice crop infested with the snails. E. revolutum will compete with F. gigantica, and when successful, prevents F. gigantica from infecting L. rubiginosa (a necessary stage in its life cycle). Inhibition of F. gigantica prevents further life stages and consequently prevents parasitic infection of cattle. E. revolutum will occupy the intermediate host (L. rubiginosa) but will not infect the cattle feeding on the rice crop. (Suhardono, et al., 2006)
Worms in the genus Echinostoma have been known to infect humans who have eaten raw snails or other molluscs.
The world-wide population size of this species is unknown. It has not been considered for conservation status by any agency.
Michael Kortbawi (author), Rutgers University, Rosiane Lesperence (author), Rutgers University, Natasha Lloyd (author), Rutgers University, Alexa Martinez (author), Rutgers University, David V. Howe (editor), Rutgers University, George Hammond (editor), Animal Diversity Web Staff.
living in the Nearctic biogeographic province, the northern part of the New World. This includes Greenland, the Canadian Arctic islands, and all of the North American as far south as the highlands of central Mexico.
living in the northern part of the Old World. In otherwords, Europe and Asia and northern Africa.
reproduction that is not sexual; that is, reproduction that does not include recombining the genotypes of two parents
having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.
an animal which directly causes disease in humans. For example, diseases caused by infection of filarial nematodes (elephantiasis and river blindness).
uses smells or other chemicals to communicate
a period of time when growth or development is suspended in insects and other invertebrates, it can usually only be ended the appropriate environmental stimulus.
animals which must use heat acquired from the environment and behavioral adaptations to regulate body temperature
union of egg and spermatozoan
mainly lives in water that is not salty.
having a body temperature that fluctuates with that of the immediate environment; having no mechanism or a poorly developed mechanism for regulating internal body temperature.
fertilization takes place within the female's body
offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).
marshes are wetland areas often dominated by grasses and reeds.
A large change in the shape or structure of an animal that happens as the animal grows. In insects, "incomplete metamorphosis" is when young animals are similar to adults and change gradually into the adult form, and "complete metamorphosis" is when there is a profound change between larval and adult forms. Butterflies have complete metamorphosis, grasshoppers have incomplete metamorphosis.
having the capacity to move from one place to another.
specialized for swimming
the area in which the animal is naturally found, the region in which it is endemic.
found in the oriental region of the world. In other words, India and southeast Asia.
reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.
an organism that obtains nutrients from other organisms in a harmful way that doesn't cause immediate death
breeding is confined to a particular season
remains in the same area
reproduction that includes combining the genetic contribution of two individuals, a male and a female
a wetland area that may be permanently or intermittently covered in water, often dominated by woody vegetation.
that region of the Earth between 23.5 degrees North and 60 degrees North (between the Tropic of Cancer and the Arctic Circle) and between 23.5 degrees South and 60 degrees South (between the Tropic of Capricorn and the Antarctic Circle).
the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.
uses sight to communicate
Baudoin, M. 1975. Host castration as a parasitic strategy. Evolution, 29: 335-352.
Brown, K., B. Leathers, D. Minchella. 1988. Trematode prevalence and the population dynamics of freshwater pond snails. American Midland Naturalist, 120: 289-301.
Dimitrov, V., I. Kanev, R. Sorensen, M. Alxexiev, M. Nestorov, V. Radev. 1999. Studies on the argentophilic structures of two populations of Echinostoma revolutum (Frolich, 1802) (Trematoda:Echinostomatidae) miracidia. Experimental Pathology and Parasitology, 3: 3-6.
Humphries, J., A. Reddy, B. Fried. 1997. Infectivity and Growth of Echinostoma revolutum (Froelich, 1802) in the Domestic Chick. International Journal for Parasitology, 27/1: 129-130.
Kanev, I., B. Fried, V. Dimitrov, V. Radev. 1995. Redescription of Echinostoma trivolvis (Cort, 1914) with a discussion on its identity. Systematic Parasitology, 32: 61-71.
Kanev, I. 1994. Life-cycle, delimitation and redescription of Echinostoma revolutum (Froelich, 1802) (Trematoda: Echinostomatidae). Systematic Parasitology, 28: 125-144.
Sorensen, R., I. Kanev, B. Fried, D. Minchella. 1997. The occurrence and identification of Echinostoma revolutum from North American Lymnaea elodes snails. Journal of Parasitology, 83(1): 169-170.
Sorensen, R., D. Minchella. 1998. Parasite influences on host life history: Echinostoma revolutum parasitism of Lymnaea elodes snails. Oecologia, 115: 188-195.