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Host Exploitation (host + exploitation)
Selected AbstractsVirulence evolution via host exploitation and toxin production in spore-producing pathogensECOLOGY LETTERS, Issue 4 2002Troy Day Many pathogens produce resilient free-living propagules that allow their dissemination in the absence of direct contact between susceptible and infected hosts. One might expect pathogens capable of producing such long-lived propagules to evolve high levels of virulence because their reproductive success is de-coupled from the survival of their host. Despite some comparative data supporting this prediction, theory has questioned its general validity. I present theoretical results that incorporate two transmission routes neglected by previous theory: death-mediated propagule production and direct host-host transmission. This theory predicts that spore-producing pathogens should evolve high levels of virulence under quite broad conditions. Moreover, a novel prediction of this theory is that the production of propagules can generate selection for the evolution of pathogen characteristics such as toxins whose sole function is to kill the host. This latter result reveals an unanticipated mechanism through which virulence is expected to evolve in spore-producing pathogens. [source] Segregation of temporal and spatial distribution between kleptoparasites and parasitoids of the eusocial sweat bee, Lasioglossum malachurum (Hymenoptera: Halictidae, Mutillidae)ENTOMOLOGICAL SCIENCE, Issue 2 2009Carlo POLIDORI Abstract Cuckoo bees and velvet ants use different resources of their shared host bees, the former laying eggs on the host pollen stores and the latter on immature stages. We studied the activity patterns of the cuckoo bee Sphecodes monilicornis and the velvet ant Myrmilla capitata at two nesting sites of their host, the social digger bee Lasioglossum malachurum, over a 3 year period. Due to the difference in host exploitation, we expected different temporal patterns of the two natural enemies as well as a positive spatial association with host nest density for both species. At a daily level, S. monilicornis was more abundant between 10.00 and 15.00 h, while M. capitata was most active in the early morning and late afternoon; both species activities were independent from host provisioning activity. The activity of cuckoo bees was in general positively correlated with the density of open host nests (but not with the total number of nests), while that of velvet ants was rarely correlated with this factor. Sphecodes monilicornis was seen both attacking the guard bees and directly entering into the host nests or digging close to nest entrances, while M. capitata only gained access to host nests through digging. We conclude that the temporal and spatial segregation between the two species may be, at least partially, explained both by the different resources exploited and by the different dynamics of host interactions. [source] Does Host Value Influence Female Aggressiveness, Contest Outcome and Fitness Gain in Parasitoids?ETHOLOGY, Issue 4 2007Marlene Goubault Intraspecific competition for resources is common in animals and may lead to physical contests. Contest outcomes and aggressiveness can be influenced by the resource holding potential of contestants but also by their perception of the resource value (RV). Competitors may assess resource quality directly (real RV) but may also estimate it according to their physiological status and their experience of the habitat quality (subjective RV). In this article, we studied contests between females of the solitary parasitoid Pachycrepoideus vindemmiae Rondani (Hymenoptera: Pteromalidae) when exploiting simultaneously a host, a Delia radicum L. (Diptera: Anthomyiidae) pupa. We tested the effect of factors modifying host value on the occurrence of agonistic behaviours, contest outcomes and host exploitation. The factors tested were: the quality of the previous habitat experienced by females, female egg load, host parasitism status and the stage reached by the owner female in her behavioural oviposition sequence. Females successfully protected their host against intruders during its exploitation, but not after oviposition, and their aggressiveness did not seem to be influenced by their perception of the RV. The fact that the host is subsequently parasitized by the opponent females appears to mainly depend on the host selectiveness of females. [source] THE EVOLUTION OF SPECIFICITY IN EVOLVING AND COEVOLVING ANTAGONISTIC INTERACTIONS BETWEEN A BACTERIA AND ITS PHAGEEVOLUTION, Issue 1 2008Virginie Poullain The evolution of exploitative specificity can be influenced by environmental variability in space and time and the intensity of trade-offs. Coevolution, the process of reciprocal adaptation in two or more species, can produce variability in host exploitation and as such potentially drive patterns in host and parasite specificity. We employed the bacterium Pseudomonas fluorescens SBW25 and its DNA phage ,2 to investigate the role of coevolution in the evolution of phage infectivity range and its relation with phage growth rate. At the phage population level, coevolution led to the evolution of broader infectivity range, but without an associated decrease in phage growth rate relative to the ancestor, whereas phage evolution in the absence of bacterial evolution led to an increased growth rate but no increase in infectivity range. In contrast, both selection regimes led to phage adaptation (in terms of growth rates) to their respective bacterial hosts. At the level of individual phage genotypes, coevolution resulted in within-population diversification in generalist and specialist infectivity range types. This pattern was consistent with a multilocus gene-for-gene interaction, further confirmed by an observed cost of broad infectivity range for individual phage. Moreover, coevolution led to the emergence of bacterial genotype by phage genotype interactions in the reduction of bacterial growth rate by phage. Our study demonstrates that the strong reciprocal selective pressures underlying the process of coevolution lead to the emergence and coexistence of different strategies within populations and to specialization between selective environments. [source] Diversity,stability relationships in multitrophic systems: an empirical explorationJOURNAL OF ANIMAL ECOLOGY, Issue 5 2003Priyanga Amarasekare Summary 1The relationship between diversity and stability is crucial in understanding the dynamics of multitrophic interactions. There are two basic hypotheses about the causal link between diversity and stability. The first is that fluctuations in resource abundance allow consumer coexistence, thus increasing diversity at the consumer trophic level (resource variability hypothesis). The second is that interactions between coexisting consumer species reduce consumer efficiency and dampen population fluctuations, thus increasing consumer,resource stability (consumer efficiency hypothesis). 2The two hypotheses lead to three comparative predictions: (i) fluctuations should be greater (resource variability) or smaller (consumer efficiency) in resource populations with coexisting consumer species, compared to those invaded only by the consumer species superior at resource exploitation; (ii) average resource abundance should be greater (resource variability) or smaller (consumer efficiency) in resource populations with greater fluctuations; and (iii) removal of the consumer species inferior at resource exploitation should increase or not affect resource population fluctuations (resource variability), or always increase them (consumer efficiency). 3I tested these predictions with data from a host,multiparasitoid community: the harlequin bug (Murgantia histrionica) and two specialist parasitoids (Trissolcus murgantiae and Ooencyrtus johnsonii) that attack the bug's eggs. 4Local host populations with coexisting parasitoids exhibited smaller fluctuations and greater average abundance compared to those with just Trissolcus, the species superior at host exploitation. Local populations that lost Ooencyrtus, the species inferior at host exploitation, exhibited an increase in host population fluctuations compared to those that did not. 5The results contradict the expectations of the resource variability hypothesis, suggesting that host population fluctuations are unlikely to be driving parasitoid coexistence. They are consistent with the consumer efficiency hypothesis, that interactions between coexisting parasitoid species dampens host population fluctuations. I discuss the implications of these results as well as possible caveats. [source] | ||||||||||