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1.
Parasitology ; 142(6): 839-48, 2015 May.
Article in English | MEDLINE | ID: mdl-25711627

ABSTRACT

Hosts strongly influence parasite fitness. However, it is challenging to disentangle host effects on genetic vs plasticity-driven traits of parasites, since parasites can evolve quickly. It remains especially difficult to determine the causes and magnitude of parasite plasticity. In successive generations, parasites may respond plastically to better infect their current type of host, or hosts may produce generally 'good' or 'bad' quality parasites. Here, we characterized parasite plasticity by taking advantage of a system in which the parasite (the yeast Metschnikowia bicuspidata, which infects Daphnia) has no detectable heritable variation, preventing rapid evolution. In experimental infection assays, we found an effect of rearing host genotype on parasite infectivity, where host genotypes produced overall high or low quality parasite spores. Additionally, these plastically induced differences were gained or lost in just a single host generation. Together, these results demonstrate phenotypic plasticity in infectivity driven by the within-host rearing environment. Such plasticity is rarely investigated in parasites, but could shape epidemiologically important traits.


Subject(s)
Adaptation, Physiological/physiology , Daphnia/microbiology , Genetic Variation , Metschnikowia/genetics , Metschnikowia/physiology , Animals , Host-Pathogen Interactions , Molecular Sequence Data , Polymerase Chain Reaction
2.
J Evol Biol ; 26(11): 2479-86, 2013 Nov.
Article in English | MEDLINE | ID: mdl-24118613

ABSTRACT

Organisms that can resist parasitic infection often have lower fitness in the absence of parasites. These costs of resistance can mediate host evolution during parasite epidemics. For example, large epidemics will select for increased host resistance. In contrast, small epidemics (or no disease) can select for increased host susceptibility when costly resistance allows more susceptible hosts to outcompete their resistant counterparts. Despite their importance for evolution in host populations, costs of resistance (which are also known as resistance trade-offs) have mainly been examined in laboratory-based host-parasite systems. Very few examples come from field-collected hosts. Furthermore, little is known about how resistance trade-offs vary across natural populations. We addressed these gaps using the freshwater crustacean Daphnia dentifera and its natural yeast parasite, Metschnikowia bicuspidata. We found a cost of resistance in two of the five populations we studied - those with the most genetic variation in resistance and the smallest epidemics in the previous year. However, yeast epidemics in the current year did not alter slopes of these trade-offs before and after epidemics. In contrast, the no-cost populations showed little variation in resistance, possibly because large yeast epidemics eroded that variation in the previous year. Consequently, our results demonstrate variation in costs of resistance in wild host populations. This variation has important implications for host evolution during epidemics in nature.


Subject(s)
Biological Evolution , Daphnia/parasitology , Disease Resistance/genetics , Host-Parasite Interactions , Metschnikowia/physiology , Animals , Daphnia/physiology , Fertility , Genetic Variation
3.
Ecology ; 87(6): 1438-44, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16869418

ABSTRACT

Parasites are integral parts of most ecosystems, yet attention has only recently focused on how community structure and abiotic factors impact host-parasite interactions. In lakes, both factors are influenced by habitat morphology. To investigate the role of habitat structure in mediating parasitism in the plankton, we quantified timing and prevalence of a common microparasite (Metschnikowia bicuspidata) in its host, Daphnia dentifera, in 18 lakes that vary in basin size and shape. Over three years, we found substantial spatial and temporal variation in the severity of epidemics. Although infection rates reached as high as 50% in some lakes, they did not occur in most lakes in most years. Host density, often considered to be a key determinant of disease spread, did not explain a significant amount of variation in the occurrence of epidemics. Furthermore, host resistance does not fully explain this parasite's distribution, since we easily infected hosts in the laboratory. Rather, basin shape predicted epidemics well; epidemics occurred only in lakes with steep-sided basins. In these lakes, the magnitude of epidemics varied with year. We suggest that biological (predation) and physical (turbulence) effects of basin shape interact with annual weather patterns to determine the regional distribution of this parasite.


Subject(s)
Ascomycota/physiology , Daphnia/microbiology , Fresh Water/microbiology , Water Microbiology , Animal Diseases/epidemiology , Animal Diseases/microbiology , Animals , Ecosystem , Seasons
4.
Nursingconnections ; 8(1): 45-9, 1995.
Article in English | MEDLINE | ID: mdl-7777075

ABSTRACT

Collaboration between the W.K. Kellogg Foundation and a school of nursing helped to meet health care and environmental needs of the residents in two rural counties burdened with poverty and illiteracy. This endeavor also affords the faculty and students in the school of nursing opportunities to work with underserved populations in rural areas. The project continues its community service through evolving programs.


Subject(s)
Foundations , Interinstitutional Relations , Rural Health , Schools, Nursing , Educational Status , Health Services Needs and Demand , Humans , Poverty
5.
Anal Biochem ; 163(1): 159-64, 1987 May 15.
Article in English | MEDLINE | ID: mdl-3619014

ABSTRACT

Many plant products are biosynthesized and accumulated in epidermal glands. For investigations on the metabolism of these compounds it is most convenient to obtain cell-free preparations enriched in gland contents. Two simple mechanized procedures have been developed for gently abrading the plant surface in order to efficiently extract glandular enzymes in high purity. These methods allow rapid processing of large quantities of plant material and yield extracts largely uncontaminated with materials from underlying tissue. The use of these procedures for isolating several enzymes of terpenoid metabolism is described. These techniques work especially well for microsomal enzymes and may be useful not only for enzymes found in epidermal glands but also for other enzymes localized in or near the epidermis. With simple modification, these procedures can be adapted for use with a variety of different types of plant tissues.


Subject(s)
Plants/enzymology , Cell-Free System , Microsomes/enzymology , Specimen Handling , Surface Properties , Terpenes/biosynthesis
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