Parasites reduce host fitness via perturbations to host energy allocation, growth, survival, and reproduction. Here, we investigate the independent effects of parasite exposure and infection on host metabolic rate. Our study focuses on Drosophila hydei and a naturally occurring ectoparasitic mite, Macrocheles muscaedomesticae. We use flow-through respirometry to measure the metabolic rate of flies during the period of exposure (preinfection) and during mite attachment. Flies were exposed to mites either indirectly (through a mesh screen) or directly, allowing for physical contact between the fly and the mite. We predicted that fly metabolic rate would increase with the level of parasite exposure: unexposed flies < flies with indirect exposure to mites < flies with direct contact with mites < flies actively infected with mites. As expected, flies indirectly exposed to but not in direct contact with mites produced 70% more CO than unexposed flies. Flies in direct contact with mites produced 35% more CO than flies with indirect contact, and this was more than double the amount of CO produced by unexposed flies. However, infected flies-those actually carrying mites-did not produce significantly more CO than uninfected flies. Our results show that simply being exposed to mites, either indirectly or directly, was sufficient to elicit a response from the host in terms of elevated CO production. Our results show that the costs of parasitism can potentially extend beyond the physiological costs of infection per se to include the energetic costs associated with parasite avoidance. Although studies have shown energetic costs associate with predator-avoidance behaviors, no study to our knowledge has measured the metabolic cost of parasite avoidance.

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A survey of nematodes associated with terrestrial slugs was conducted in residential gardens, nurseries, greenhouses and agricultural sites located in and around Edmonton, Alberta, Canada. A total of 2406 slugs were collected from 82 sites. Slugs were decapitated and cadavers were incubated for two weeks, with emerging nematodes removed and processed for identification. Nematodes were identified using molecular sequence data for the 18S ribosomal DNA. Nematodes were recovered from 20 of the 82 sites surveyed, with 24.4% of the slugs infected with nematodes. A total of seven nematodes were identified to species level, including Caenorhabditis elegans, Panagrolaimus papillosus, Pellioditis typica, Pelodera pseudoteres, Rhabditella axei, Rhabditoides inermiformis and Phasmarhabditis californica. An additional four specimens were identified to genus level, including Oscheius sp. (9), Pristionchus sp., Rhabditis sp. and Rhabditophanes sp. (1). The two most common nematode species were C. elegans and P. pseudoteres. The facultative parasite, P. californica, was recovered from a single Arion rufus specimen, collected from a seasonal nursery. To our knowledge, this study represents the first survey of slug-associated nematodes in Canada.

Parasites can evolve phenotypically plastic strategies for transmission such that a single genotype can give rise to a range of phenotypes depending on the environmental condition. State-dependent plasticity in particular can arise from individual differences in the parasite's internal state or the condition of the host. Facultative parasites serve as ideal model systems for investigating state-dependent plasticity because individuals can exhibit two life history strategies (free-living or parasitic) depending on the environment. Here, we experimentally show that the ectoparasitic mite Macrocheles subbadius is more likely to parasitize a fruit fly host if the female mite is mated; furthermore, the propensity to infect increased with the level of starvation experienced by the mite. Host condition also played an important role; hosts infected with moderate mite loads were more likely to gain additional infections in pairwise choice tests than uninfected flies. We also found that mites preferentially infected flies subjected to mechanical injury over uninjured flies. These results suggest that a facultative parasite's propensity to infect a host (i.e. switch from a free-living strategy) depends on both the parasite's internal state and host condition. Parasites often live in highly variable and changing environments, an infection strategy that is plastic is likely to be adaptive.

For many organisms, habitat avoidance provides the first line of defence against parasitic infection. Changes in infection status can shift the cost-benefit ratio of remaining in a given habitat vs dispersing. The aim of this study was to test the hypothesis that the propensity to disperse in Drosophila nigrospiracula is mediated by current parasite load and the risk of further infection by an ectoparasitic mite (Macrocheles subbadius). An activity monitor was used to assess dispersal propensity among infected and uninfected flies. The activity level of uninfected females increased threefold upon exposure to a mite, whereas the activity among uninfected males increased by 17-fold in the presence of a questing mite. Among infected flies, the risk of further infection also generated a change in activity, but the magnitude of the response was dependent on host sex. Current infection status influenced the probability of acquiring more parasites due to increased susceptibility to infection with mite load. The probability of acquiring additional mites among males increased more rapidly compared to female flies. Current infection status can potentially determine the risk of further infection, the host propensity and ability to disperse, with consequence for hosts and parasites at the individual, population and species level.

Parasites exert numerous effects upon their hosts, including physiological and metabolic changes that can in turn influence various aspects of host life history. Using flow‐through respirometry, we investigated how infection intensity of an ectoparasitic mite (Macrocheles subbadius) affects the respiratory rate (CO2 production) of its host Drosophila nigrospiracula. Mean fly respiratory rate increased with infection intensity with the strongest effect, a 40% increase relative to uninfected controls, occurring with three mites attached. We also verified the causal relationship between elevated respiration rate and mite attachment by examining changes in host respiration before and after mite exposure. We found that the rate of CO2 production increased by 11% for individual flies following parasite attachment. Fly locomotor activity was not significantly different between infected and uninfected individuals. Metabolic rate of hosts increased as a result of infection in an intensity dependent manner and was not simply due to changes in host activity. These results demonstrate that parasites can have a significant influence on the energy requirements of their host, which may account for the parasite‐mediated loss in host fitness.

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