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Ribeiroia (//) is a group of trematode parasites (or flatworms) that sequentially infect freshwater snails in the family Planorbidae (ramshorn snails) as first intermediate hosts, fish and larval amphibians as second intermediate hosts, and birds and mammals as definitive hosts (see § Life history). In North America, infection by Ribeiroia has been linked to amphibians with limb malformations. The connection between parasitic infection and limb malformations has generated questions about (a) whether parasite-induced malformations in amphibians are increasing (see § Evidence for emergence), and (b) the consequences of such abnormalities for amphibian population conservation (see § Parasite-induced malformations and amphibian conservation).
- 1 Ribeiroia taxonomy
- 2 Life cycle
- 3 Infection and amphibian malformations
- 4 Geographic distribution
- 5 Evidence for emergence
- 6 Factors influencing infection
- 7 Parasite-induced malformations and amphibian conservation
- 8 See also
- 9 References
- 10 Notes
- 11 External links
Ribeiroia is a genus of parasites in the class Trematoda, phylum Platyhelminthes. Currently three species and one subspecies of Ribeiroia are recognized: R. ondatrae in North America, R. marini in the Caribbean, R. m. guadeloupensis on the Caribbean island of Guadeloupe, and R. congolensis in Africa (Johnson et al. 2004). The trematode Cercaria lileta is also closely related to Ribeiroia, and molecular sequence data indicates that it may be a species of Ribeiroia (Johnson et al. 2004). All species of Ribeiroia share the distinctive morphological characteristic of esophageal diverticula (i.e., two short dead-end branches that extend laterally from the esophagus). Other genera closely related to Ribeiroia include Cladocystis trifolium, Cathemasia, and Echinostoma (Johnson et al. 2004). See Johnson et al. (2004) for more details on morphological and ecological differences as well as phylogenetic relationships between these species.
Ribeiroia ondatrae has an indirect complex life cycle. The adult worms live inside predatory birds or mammals (the definitive hosts), wherein they reproduce sexually if other worms are present. Mature adults release eggs into the host’s intestinal tract, which are passed with the feces of the host, and to develop need to end up in water. The eggs typically develop in 2–3 weeks, but the time varies depending on water temperature. Eggs hatch into miracidia, a ciliated free-living parasite stage, which infect the first intermediate host, ram’s horn snails in the family Planorbidae, colonizing the snail’s reproductive tissue and eventually forming rediae, a slow-moving worm-like parasite stage. The rediae reproduce asexually, castrating the snail as they feed on its reproductive tissue. The infection becomes mature in about six weeks, when the rediae within the snail begin to release a second free-swimming stage called cercariae. The key identifying characteristic of Ribeiroia ondatrae cercariae is the bifurcated esophagus (although this trait can occur in some closely related genera such as Cladocystis trifolium). Cercariae infect amphibians or fish (the second intermediate hosts) wherein they encyst in (with amphibians) the limb buds or (with fish) along the lateral line and scales of the head, body and gills. Encysted cercariae become metacercariae, a dormant parasite stage with a thin outer membrane. Metacercariae resemble cercariae without their tails and do not reproduce. The definitive hosts (birds and mammals) become infected when they consume an amphibian or fish that has encysted metacercariae. The life cycle is completed when the metacercariae emerge from their cyst and attach to the definitive host’s intestinal tract and develop into adults, typically in the proventriculus of birds and the stomach of mammals.
Infection and amphibian malformations
Experimental exposure to Ribeiroia ondatrae cercariae has been shown to cause limb malformations in various frog, toad and salamander species, including Pseudacris regilla, Anaxyrus boreas, Lithobates pipiens, A. americanus, Ambystoma macrodactylum, L. clamitans and L. sylvatica. Cercariae appear to prefer to infect in and around the developing limb buds of larval amphibians, which can alter or inhibit limb development. The risk of malformation and mortality varies as a function of parasite exposure level, host development stage, and the amphibian species involved. As expected for macroparasitic infections, a dose-dependent relationship exists between cercariae exposure and pathology, particularly among larval amphibians at pre- or early-limb development stage. Cercarial penetration of host tissue involves proteolytic enzymes. The exact mechanism which alters limb development is unknown, but potential pathways include mechanical disturbance by invading parasites, release of a teratogenic chemical by parasites, or a combination of the two.
Susceptibility to infection and the subsequent pathology differs among amphibian species. For example, gray tree frogs (Hyla versicolor) are largely resistant to infection, but toads (e.g. A. americanus) exhibit high frequencies of mortality and malformations following parasite exposure (Johnson and Hartson 2009). The types of limb malformations also vary among species and developmental stage of exposure. The most common errors in development associated with Ribeiroia exposure are skin webbings (cutaneous fusion), missing limbs and limb elements (ectromelia and hemimelia), supernumerary limbs and digits (polymelia and polydactyly), and bony triangles. The factors determining variation in susceptibility among species remain poorly understood, but these observations suggest that the type of malformation alone is unlikely to be diagnostic of Ribeiroia exposure.
Ribeiroia infection has been linked to malformations in naturally occurring amphibian populations, especially in the western and midwestern US. In a large-scale study in the western US, both the presence and abundance of Ribeiroia infection predicted higher-than-baseline (e.g., >5%) frequencies of abnormalities in one or more amphibian species. Limb malformations were observed in 9 species and ranged in frequency from <5% to nearly 90%. The role of Ribeiroia in explaining accounts of amphibian malformations in other regions is varied; Ribeiroia has been associated with malformation ‘hotspots’ in the midwestern and northeastern US, but it was not detected in malformation surveys from Vermont, Alaska, Bermuda, and Michigan.
Ribeiroia ondatrae is widely distributed across the US, including records from 22 species in 37 states (Johnson and McKenzie 2008). Most records of Ribeiroia-associated malformations have been reported from California, Oregon, Washington, Montana, Minnesota, Wisconsin, New Jersey and Pennsylvania. Less is known about the distribution of Ribeiroia in Canada and Central America. In amphibians, both the abundance of the parasite and the number of observations appear to correlate positively with major bird migratory flyways, with concentrations along the Pacific, Mississippi, and Atlantic flyways (Johnson et al. 2010). This observation suggests definitive (bird) host activity is an important determinant of parasite distribution at the continental scale, but this hypothesis has yet to be rigorously tested. Ribeiroia ondatrae is most often recovered from amphibians in lentic habitats, such as ponds, lakes, and wetlands, which support planorbid snails. Other species of Ribeiroia occur in the Caribbean and South America (R. marini and R. marini guadeloupensis) and in Africa (R. congolensis). However, whether these species infect amphibians or cause limb malformations has not been explored.
Evidence for emergence
Dating back over 200 years, there have been reports of amphibian malformations suggesting that the general phenomenon is not a new occurrence in amphibian populations (Ouellet 2000). Despite the historical occurrence of amphibian malformations, the real question is whether such malformations are increasing in prevalence and severity in wild amphibian populations. Limited historical data on malformations and the absence of baseline malformation data has complicated attempts to assess whether malformations are emerging. However, research over the past decade has shown that malformations are emerging in some amphibian populations. For example, the background rate of malformations of northern leopard frogs in Minnesota increased from 0.4% in 1958-1963 to 2.5% in 1996-1997 (Hoppe 2000), with recently observed malformations more severe and more diverse. Similarly, Johnson and Lunde (2005), in a comparison of recent (1990–2000) and historical (1899–1989) publications, found that recent reports document:
- a wider range of more severe malformations,
- a greater number of affected amphibian species,
- a larger number of affected sites, and
- a higher frequency range of affected individuals at reported sites.
For both of these studies, however, the mechanisms driving the apparent increase in malformations were not identified (see Factors influencing emergence). In a more rigorous study, Johnson et al. (2003) confirmed that historical malformations at six of eight sites (1947–1990) were associated with Ribeiroia infection. Moreover, three of these sites continued to support limb malformations at frequencies of 7-50% in one or more species. One pond in particular (Jette Pond in western Montana) showed increased prevalence of malformations in Pseudacris regila from 20% in 1960 to 46% in 2000, which was correlated with an increased intensity of Ribeiroia infection. Although more research is necessary, these studies provide evidence that malformations, especially those linked to Ribeiroia infection, are emerging in some amphibian populations.
Factors influencing infection
Nutrients - Nitrogen and phosphorus enrichment are widespread forms of anthropogenic environmental change that may influence parasite infection (Johnson and Carpenter 2008). Nutrient enrichment leads to eutrophication, which has been linked with emergence of Ribeiroia ondatrae through direct and indirect effects on aquatic food webs (Johnson and Chase 2004). The underlying mechanism through which eutrophication can increase infection involves increasing the density of infected first-intermediate snail hosts and by increasing the production of parasites by infected snails (Johnson et al. 2007).
Pesticides - Pesticides are still considered a potential factor influencing amphibian malformations (Johnson et al. 2010). However, recent investigations have focused on the interaction of pesticides with parasite infection (Kiesecker 2002; Rohr et al. 2008). Field experiments indicated a link between agricultural run-off and increased infection (Kiesecker 2002). Laboratory studies further demonstrated that pesticide exposure reduced host immunocompetence against parasites as the biological mechanism (Kiesecker 2002). Furthermore, there may be a link between nutrient addition and pesticide contamination jointly leading to increased infections by simultaneously increasing exposure and suppressing host immune systems (Rohr et al. 2008a, b).
Biodiversity - Host species diversity and community structure have been suggested to influence disease dynamics through a hypothesis termed the ‘dilution effect’ (Ostfeld and Keesing 2000). For Ribeiroia ondatrae, host species differences in susceptibility can influence infection patterns in multi-species communities (Johnson et al. 2008, Johnson and Hartson 2009). As a result, more diverse larval amphibian communities that include species with differing susceptibilities can alter parasite infection success and the resulting pathology in sensitive host species. For instance, larval toads (a sensitive species) raised experimentally alongside larval gray treefrogs (a resistant species) exhibited 37% less infection and fewer malformations (Johnson et al. 2008).
Parasite-induced malformations and amphibian conservation
Perhaps the most unexplored, complex and vital aspects of trematode-caused amphibian malformations are the population-level consequences. Do these parasites and the malformations they induce pose a conservation risk? While no direct evidence linking trematode deformities and amphibian population declines exists, there are legitimate reasons for concern (Johnson and McKenzie 2008). For instance, in multiple species of frogs and toads, laboratory studies show that even low levels of Ribeiroia infection can induce 30-95% mortality (see Johnson et al. 2010). Correspondingly, multi-year field studies show that in localities of high infection and malformations in metamorphosing frogs, <2% of amphibians returning to breed exhibit malformations, suggesting Ribeiroia infection and malformations have deleterious consequences for individual survival and fecundity (Johnson et al. 2001). In specific wetlands that have historically exhibited a high prevalence of infection and malformations, several amphibian species have notably declined or disappeared (see Johnson and McKenzie 2008 for review). In light of these data, and the increasing evidence that Ribeiroia infections are on the rise (Johnson and McKenzie 2008), it is prudent to treat Ribeiroia ondatrae as a threat to amphibian populations and diversity, particularly in combination with other stressors.
- Bacon, J.P., Gray J.A. and L. Kitson (2006). Status and conservation of the reptiles and amphibians of the Bermuda islands. Applied Herpetology 3: 323-344.
- Basch, P.F., and R.F. Sturrock. 1969. Life history of Ribeiroia marini (Faust and Hoffman, 1934) comb. N. (Trematoda: Cathaemasiidae). Journal of Parasitology 55: 1180-1184.
- Beaver, P.C. (1939). The morphology and life history of Psilostomum ondatrae Price 1931 (Trematoda: Psilostomatidae). Journal of Parasitology 25: 383-393.
- Daszak P, Cunningham AA and Hyatt AD (2000). Wildlife ecology - Emerging infectious diseases of wildlife: threats to biodiversity and human health. Science 287: 443-449.
- Dobson, A. and J. Foufopoulos (2001). Emerging infectious pathogens of wildlife. Philosophical Transactions of The Royal Society of London Series B-Biological Sciences 356: 1001-1012.
- Gilliland, M.G. and P.M. Muzzall (2002). Amphibians, trematodes, and deformities: an overview from southern Michigan. Comparative Parasitology 69: 81-85.
- Hoppe DM (2000). History of Minnesota frog abnormalities: do recent findings represent a new phenomenon? - In: Kaiser, H. and Casper, G. S. (eds.), Investigating amphibian declines: proceedings of the 1998 Midwest conference on declining amphibians. University of Iowa Press, pp. 86–89.
- Johnson, P. T. J. and S. R. Carpenter (2008). Influence of eutrophication on disease in aquatic ecosystems: patterns, processes, and predictions. Chapter 4 (pp. 71–99) in R. Ostfeld, F. Keesing and V. Eviner (eds.),Infectious disease ecology: effects of ecosystems on disease and of disease on ecosystems. Princeton University Press.
- Johnson, P. T. J. and J. M. Chase (2004). Parasites in the food web: linking amphibian malformations and aquatic eutrophication. Ecology Letters 7: 521-526.
- Johnson, P. T. J. and R. B. Hartson (2009). All hosts are not equal: explaining differential patterns of malformations in an amphibian community. Journal of Animal Ecology 78: 191-201.
- Johnson, P. T. J., Hartson, R. B., Larson, D. J. and D. R. Sutherland (2008). Linking biodiversity loss and disease emergence: amphibian community structure determines parasite transmission and pathology. Ecology Letters 11: 1017-1026.
- Johnson, P.T.J., Preu, E.R., Sutherland, D.R., Romansic, J., Han, B., and A.R. Blaustein (2006). Adding infection to injury: Synergistic effects of predation and parasitism on salamander limb malformations. Ecology 87: 2227-2235.
- Johnson, P.T.J., Lunde, K.B., Ritchie, E.G., and A.E. Launer (1999). The effect of trematode infection on amphibian limb development and survivorship. Science 284: 802-804.
- Johnson, P.T.J., Lunde, K.B., Zelmer, D.A. and J.K. Werner (2003). Limb deformities as an emerging parasitic disease in amphibians: Evidence from museum specimens and resurvey data. Conservation Biology 17: 1724-1737.
- Johnson P.T.J. and K.B. Lunde (2005). Parasite infection and limb malformations: A growing problem in amphibian conservation. - In: Lannoo, M. (ed.) Amphibian declines: the conservation status of United States species. University of California Press, pp. 124–138.
- Johnson, P. T. J., Lunde, K. B., Ritchie, E. G., Reaser, J. K., and A. E. Launer (2001). Morphological abnormality patterns in a California amphibian community. Herpetologica 57: 336–352.
- Johnson, P.T.J., Lunde, K.B., Thurman, E.M, Ritchie, E.G., Wray, S.N., Sutherland, D.R., et al. (2002). Parasite (Ribeiroia ondatrae) infection linked to amphibian malformations in the western United States. Ecological Monographs 72: 151-168.
- Johnson, P. T. J. and V. J. McKenzie (2008). Effects of environmental change on helminth infections in amphibians: exploring the emergence of "Ribeiroia" and "Echinostoma" infections in North America. Chapter 11 in Fried, B. and R. Toledo, The Biology of Echinostomes, Springer.
- Johnson, P. T. J., Reeves, M. K., Krest, S. K. and A. E. Pinkney (2010). A decade of deformities: advances in our understanding of amphibian malformations and their implications. In Sparling, Linder, Bishop, Krest (eds), Ecotoxicology of Amphibians and Reptiles, 2nd edition. SETAC Press, Pensacola FL
- Johnson P.T.J., Sutherland, D.R., Kinsella, J.M., and K.B. Lunde (2004). Review of the Trematode Genus Ribeiroia (Psilostomidae): Ecology, Life History and Pathogenesis with Species Emphasis on the Amphibian Malformation Problem. Advances in Parasitology: 57: 191-253.
- Kiesecker, J.M. 2002. Synergism between trematode infection and pesticide exposure: A link to amphibian limb deformities in nature? Proceedings of the National Academy of Sciences USA 99: 9900-9904.
- Lannoo, M.J., Sutherland, D.R., Jones, P., Rosenberry, D., Klaver, R.W., Hoppe, D.M. et al. (2003). Multiple causes for the malformed frog phenomenon. In: Multiple Stressor Effects in Relation to Declining Amphibian Populations (eds Linder, G., Little, E., Krest, S. & Sparling, D.). ASTM STP 1443. American Society for Testing and Materials, West Conshoshocken, PA, pp. 233–262.
- Ouellet, M. (2000). Amphibian deformities: current state of knowledge. - In: Sparling, D. W., Bishop, C. and Linder, G. (eds.), Ecotoxicology of amphibians and reptiles. Society for Environmental Toxicology and Chemistry, pp. 617–661.
- Reeves, M.K., Dolph, C.L., Zimmer, H., Tjeerdema, R.S. and A.T. Kimberly (2008). Road Proximity increases risk of skeletal abnormalities in wood frogs from National Wildlife refuges in Alaska. Environmental Health Perspectives 116: 1008-1014.
- Rohr, J. R., Schotthoefer, A. M., Raffel, T. R., Carrick, H. J., Halstead, N., Hoverman, J. T., Johnson, C. M., Johnson, L. B., Lieske, C., Piwoni, M. D., Schoff, P. K. and Beasley, V. R. (2008a). Agrochemicals increase trematode infections in a declining amphibian species. Nature 455: 1235–1239.
- Rohr, J.R., Raffle, T.R., Sessions, S.K., and P.J. Hudson (2008b.). Understanding the net effects of pesticides on amphibian trematode infections. Ecological Applications 18: 1743-1753.
- Skelly, S.R. Bolden, L.K. Freidenburg, N.A. Freidenfelds and R. Levey (2007). Ribeiroia infection is not responsible for Vermont amphibian deformities. EcoHealth 4: 156-163.
- Schotthoefer, A.M., Cole, R.A., and V.R. Beasley (2003). Relationship of tadpole stage to location of echinostoma cercariae encystment and the consequences for tadpole survival. Journal of Parasitology 89: 475-482.
- Stopper, G.F., Hecker, L., Franssen, R.A. and S.K. Sessions (2002). How trematodes cause limb deformities in amphibians. Journal of Experimental Zoology 294: 252-263.
- Sutherland, D.R. (2005) Parasites of North American Frogs. Amphibian Declines: The Conservation Status of United States Species (ed. M.J.Lannoo), pp. 109–123. University of California Press, Berkeley, California.
- Beaver 1939; Basch and Sturrock 1969; Johnson et al. 2004
- Beaver 1939; Basch and Sturrock 1969; Johnson et al. 2004
- Johnson et al. 2004
- Johnson et al. 1999; 2001; 2006; Stopper et al. 2002; Schotthoefer et al. 2003; Johnson and Hartson 2009
- Schotthoefer et al. 2003
- Johnson et al. 1999; Stopper et al. 2002
- reviewed in Johnson et al. 2010
- Johnson et al. 2002
- Kiesecker 2002; Lannoo et al. 2003; Sutherland 2005; Johnson and Hartson 2009
- Gilliland and Muzzall 2002; Bacon et al. 2006; Skelly et al. 2007; Reeves et al. 2008