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26 results for “parasite tolerance”

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dryad40/100

Resistance and tolerance to imperfectly specialized parasites: Milkweed butterflies and their protozoan parasites

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publicMar 2025View details →
dryad36/100

Data from: Elevated atmospheric concentrations of carbon dioxide reduce monarch tolerance and increase parasite virulence by altering the medicinal properties of milkweeds

Hosts combat their parasites using mechanisms of resistance and tolerance, which together determine parasite virulence. Environmental factors, including diet, mediate the impact of parasites on hosts, with diet providing nutritional and medicinal properties. Here, we present the first evidence that ongoing environmental change decreases host tolerance and increases parasite virulence through a loss of dietary medicinal quality. Monarch butterflies use dietary toxins (cardenolides) to reduce the deleterious impacts of a protozoan parasite. We fed monarch larvae foliage from four milkweed species grown under either elevated or ambient CO2, and measured changes in resistance, tolerance, and virulence. The most high-cardenolide milkweed species lost its medicinal properties under elevated CO2; monarch tolerance to infection decreased, and parasite virulence increased. Declines in medicinal quality were associated with declines in foliar concentrations of lipophilic cardenolides. Our results emphasize that global environmental change may influence parasite-host interactions through changes in the medicinal properties of plants.

opencc-zeroDec 2017View details →
dryad36/100

Parasite resistance and parasite tolerance: insights into transgenerational immune priming in an invertebrate host

<p>Parasites impose different selection regimes on their hosts, which respond by increasing their resistance and/or tolerance. Parental challenge with parasites can enhance the immune response of their offspring, a phenomenon documented in invertebrates and termed transgenerational immune priming. We exposed two parental generations of the model organism <em>Daphnia magna</em> to the horizontally-transmitted parasitic yeast <em>Metschnikowia bicuspidata</em>, and recorded resistance- and tolerance-related traits in the offspring generation. We hypothesized that parentally-primed offspring will increase either their resistance or their tolerance to the parasite. Our susceptibility assays revealed no impact of parental exposure on offspring resistance. Nonetheless, different fitness-related traits, which are indicative of tolerance, were altered. Specifically, maternal priming increased offspring production and decreased survival. Grandmaternal priming positively affected age at first reproduction and negatively affected brood size at first reproduction. Interestingly, both maternal and grandmaternal priming significantly reduced within-host parasite proliferation. Nevertheless, <em>Daphnia </em>primed for two consecutive generations had no competitive advantage in comparison to unprimed ones, implying additive maternal and grandmaternal effects. Our findings do not support evidence of transgenerational immune priming from bacterial infections in the same host species, thus emphasizing that transgenerational immune responses may not be consistent even within the same host species.</p>

opencc-zeroMar 2022View details →
dryad36/100

No evidence of adaptive tolerance of parasitism in a cavity-nesting brood parasite host

<p>Acceptance of avian brood parasitism by hosts is one of the most enigmatic aspects of brood parasite-host coevolution. The most common explanation for acceptance of parasitism by hosts of the brown-headed cowbird (<em>Molothrus ater</em>) is evolutionary lag, which suggests that hosts have not had enough time to evolve defenses against parasitism. Alternatively, acceptance may be the optimal strategy when the costs of rejecting parasitism exceed the benefits. The lack of nest site hypothesis applies to secondary cavity-nesting birds that cannot excavate their own nests and predicts that hosts accept parasitism instead of deserting a parasitized nest when there are no vacant nest sites available in which to renest. I tested this hypothesis using the prothonotary warbler (<em>Pronotaria citrea</em>), a commonly parasitized, cavity-nesting cowbird host. I used a paired nest box design and predicted that if hosts accept parasitism because of a lack of alternative nest sites, they should desert parasitized nests and renest in the vacant nest box on their territory. I recorded 37 cases where a nest was parasitized and warblers only deserted 2 parasitized nest boxes for a vacant nest box. Both desertions were attributable to factors other than parasitism and the rate of desertion did not differ from controls that only had a single nest box. Moreover, seven of the warblers initiated clutches in nest boxes that already contained cowbird egg despite having vacant nest boxes available on their territories. These results indicate that warblers do not accept parasitism because of tolerance, but likely due to evolutionary lag.</p>

opencc-zeroJul 2024View details →
dryad36/100

No evidence of adaptive tolerance of parasitism in a cavity-nesting brood parasite host

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publicJul 2024View details →
dryad36/100

Parasite resistance and parasite tolerance: insights into transgenerational immune priming in an invertebrate host

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publicMar 2022View details →
dryad36/100

Data from: Elevated atmospheric concentrations of carbon dioxide reduce monarch tolerance and increase parasite virulence by altering the medicinal properties of milkweeds

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publicMay 2019View details →
dryad36/100

Negative associations between parasite avoidance, resistance and tolerance predict host health in salmonid fish populations

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publicApr 2020View details →
dryad36/100

Migration and tolerance shape host behavior and response to parasites infection

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publicMay 2021View details →
dryad32/100

Data from: Intra- and intersexual differences in parasite resistance and female fitness tolerance in a polymorphic insect

To understand host–parasite interactions, it is necessary to quantify variation and covariation in defence traits. We quantified parasite resistance and fitness tolerance of a polymorphic damselfly (Ischnura elegans), an insect with three discrete female colour morphs but with monomorphic males. We quantified sex and morph differences in parasite resistance (prevalence and intensity of water mite infections) and morph-specific fitness tolerance in the females in natural populations for over a decade. There was no evidence for higher parasite susceptibility in males as a cost of sexual selection, whereas differences in defence mechanisms between female morphs are consistent with correlational selection operating on combinations of parasite resistance and tolerance. We suggest that tolerance differences between female morphs interact with frequency-dependent sexual conflict, which maintains the polymorphism locally. Host–parasite interactions can therefore shape intra- and intersexual phenotypic divergence and interfere with sexual selection and sexual conflict.

opencc-zeroDec 2016View details →
dryad32/100

Data from: The association of feeding behavior with the resistance and tolerance to parasites in recently diverged sticklebacks

Divergent natural selection regimes can contribute to adaptive population divergence, but can be sensitive to human-mediated environmental change. Nutrient loading of aquatic ecosystems, for example, might modify selection pressures by altering the abundance and distribution of resources and the prevalence and infectivity of parasites. Here, we used a mesocosm experiment to test for interactive effects of nutrient loading and parasitism on host condition and feeding ecology. Specifically, we investigated whether the common fish parasite Gyrodactylus sp. differentially affected recently diverged lake and stream ecotypes of three-spined stickleback (Gasterosteus aculeatus). We found that the stream ecotype had a higher resistance to Gyrodactylus sp. infections than the lake ecotype, and that both ecotypes experienced a cost of parasitism, indicated by negative relationships between parasite load and both stomach fullness and body condition. Overall, our results suggest that in the early stages of adaptive population divergence of hosts, parasites can affect host resistance, body condition, and diet.

opencc-zeroDec 2015View details →
dryad32/100

Data from: Annual environmental variation influences host tolerance to parasites

When confronted with a parasite or pathogen, hosts can defend themselves by resisting or tolerating the attack. While resistance can be diminished when resources are limited, it is unclear how robust tolerance is to changes in environmental conditions. Here we investigate the sensitivity of tolerance in a single host population living in a highly variable environment. We manipulated the abundance of an invasive parasitic fly, Philornis downsi, in nests of Galápagos mockingbirds (Mimus parvulus) over four field seasons and measured host fitness in response to parasitism. Mockingbird tolerance to P. downsi varied significantly among years and decreased when rainfall was limited. Video observations indicate that parental provisioning of nestlings appears key to tolerance: in drought years, mockingbirds likely do not have sufficient resources to compensate for the effects of P. downsi. These results indicate that host tolerance is a labile trait and suggest that environmental variation plays a major role in mediating the consequences of host-parasite interactions.

opencc-zeroDec 2018View details →
dryad32/100

Data from: Host developmental stage effects on parasite resistance and tolerance

<p><span>Hosts can defend themselves against parasites by either preventing or limiting infections (resistance), or limiting parasite-induced damage (tolerance). However, it remains underexplored how these defense types vary over host development with shifting patterns of resource allocation priorities. Here, we studied the role of developmental stage on resistance and tolerance in Atlantic salmon (<em>Salmo salar</em>). This anadromous fish has distinct life stages related to living in fresh and sea water. We experimentally exposed one-year old salmon, either at the freshwater stage or at the stage transitioning to the marine phase, to the trematode <em>Diplostomum pseudospathaceum</em>. Using 56 pedigreed families and multivariate animal models, we show that developmental transition is associated with reduced resistance, but does not affect tolerance. Furthermore, by comparing tolerance slopes (host fitness against parasite load) based on additive genetic effects among infected and unexposed control relatives, we observed that the slopes can be largely independent of the infection, that is they may not reflect tolerance. Together, our results suggest that the relative importance of different defense types may vary with host development and emphasize the importance of including control treatments for more confident interpretations of tolerance estimates.</span></p>

opencc-zeroMay 2022View details →
dryad32/100

Data from: Host developmental stage effects on parasite resistance and tolerance

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publicMay 2022View details →
dryad32/100

Data from: Pace of life, predators and parasites: predator-induced life history evolution in Trinidadian guppies predicts decrease in parasite tolerance

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publicOct 2015View details →
dryad32/100

Data from: Parasite infection and decreased thermal tolerance: impact of proliferative kidney disease (PKD) on a wild salmonid fish in the context of climate change

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publicJun 2016View details →
dryad32/100

Data from: Intra- and intersexual differences in parasite resistance and female fitness tolerance in a polymorphic insect

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publicJan 2017View details →
dryad32/100

Data from: The association of feeding behavior with the resistance and tolerance to parasites in recently diverged sticklebacks

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publicJun 2016View details →
dryad32/100

Data from: Host life-history and host-parasite syntopy predict behavioral resistance and tolerance of parasites

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publicDec 2015View details →
dryad32/100

Data from: Annual environmental variation influences host tolerance to parasites

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publicFeb 2019View details →

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International Brain Laboratory public data

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