Parasite infections often lead to dramatically different outcomes among host species. Although an emerging body of ecoimmunological research proposes that hosts experience a fundamental trade-off between pathogen defences and life-history activities, this line of inquiry has rarely been extended to the most essential outcomes of host-pathogen interactions: namely, infection and disease pathology. Using a comparative experimental approach involving 13 amphibian host species and a virulent parasite, we test the hypothesis that Ôpace-of-lifeÕ predicts parasite infection and host pathology. Trematode exposure increased mortality and malformations in nine host species. After accounting for evolutionary history, species that developed quickly and metamorphosed smaller (Ôfast-speciesÕ) were particularly prone to infection and pathology. This pattern likely resulted from both weaker host defences and greater adaptation by parasites to infect common hosts. Broader integration between life history theory and disease ecology can aid in identifying both reservoir hosts and species at risk of disease-driven declines.
Summary1. An emerging framework in animal disease ecology seeks to 'decompose' a host's response to disease into resistance, or its ability to resist infection following exposure, and tolerance, or its ability to limit the damage associated with infection. How these processes vary over the life history of a host, however, and whether developmental changes in resistance and tolerance account for 'critical windows' of disease vulnerability remain open questions. 2. Critical developmental windows are particularly important for infections that alter host development. Recently, increased observations of amphibians with severe limb malformations have stimulated debate over the causes responsible and whether malformation types can be used to infer the agent responsible. The trematode parasite Ribeiroia ondatrae, for example, is often implicated in accounts of extra-legged frogs, but is believed to be unimportant in explaining missing legged animals. Here, we test the influence of host developmental stage, from eggs to post-metamorphosis, on the risk of mortality and the types of malformations produced in Pacific chorus frogs (Pseudacris regilla) following exposure to trematode infection. 3. Consistent with a critical window of vulnerability, host mortality and malformations were greatest among animals exposed during pre-limb and early limb development (15-90%) and decreased to <5% with progressive development. Early stage animals also exhibited a higher frequency of missing limbs, whereas extra limbs and limb elements developed predominantly among tadpoles exposed after limb development was initiated. Hosts infected later in limb development were normal or exhibited only minor outgrowths and abnormal skin webbings. 4. Increases in host tolerance rather than host resistance largely explained the observed changes in pathology. Prior to host metamorphosis, parasites exhibited comparable success invading host tissue, but the amount of resulting damage differed significantly as a function of host size and developmental stage. Following metamorphosis hosts were significantly more resistant to infections, however. 5. These findings highlight the importance of critical developmental windows for infectious diseases and underscore the role of developmental changes in host tolerance in controlling this process. Forecasted changes in climate, for example, have enormous potential to influence both the timing and intensity of host-parasite interactions in nature.
First information is provided on the parasitation and feeding ecology of the myctophid fish species Myctophum punctatum and Notoscopelus kroyeri from the Mid-Atlantic Ridge (MAR), Central Atlantic. Four different parasite species were found in both fish with a similar high prevalence and intensity of infestation. The digeneans Gonocerca phycidis and Lethadena sp. were isolated as adults from the stomach, larval tetraphyllidean cestodes (Scolex pleuronectis) from the intestine, and genetically identified larval anisakid nematodes of Anisakis simplex (s.s.) from the body cavity. No further Anisakis sibling species could be identified. Both myctophids had small pelagic crustaceans, mainly copepods and hyperiids, within their stomach contents. Ostracods, euphausiids, decapods, and amphipods were minor food components, demonstrating the pelagic environment for both fish. The recorded parasites including the anisakid A. simplex (s.s.) perform pelagic life cycles within the region, benefiting from extensive diurnal vertical migrations of their fish hosts. Comparison of the host range among the anisakis sibling species suggests that the A. simplex complex has low host specificity, infecting toothed and baleen whales on their extensive oceanic migrations. This contrasts the Anisakis physeteris complex that is restricted to toothed whales of the families Kogiidae and Physeteridae. Specificity in the teleost intermediate hosts for both complexes seems to be low, and sympatric occurrence of different siblings within the same intermediate hosts is likely. Myctophid swarm fish as important copepod feeders at the MAR significantly contribute to the oceanic anisakid nematode life cycle, especially considering the 100% prevalence and high intensity of infestation. Further genetic identification of Anisakis nematodes is needed in order to understand the sibling species distribution, along the MAR and within other oceanic environments.
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