TEMPORAL DYNAMICS OF OUTCROSSING AND HOST MORTALITY RATES IN HOST–PATHOGEN EXPERIMENTAL COEVOLUTION

Cross‐fertilization is predicted to facilitate the short‐term response and the long‐term persistence of host populations engaged in antagonistic coevolutionary interactions. Consistent with this idea, our previous work has shown that coevolving bacterial pathogens (Serratia marcescens) can drive obligately selfing hosts (Caenorhabditis elegans) to extinction, whereas the obligately outcrossing and partially outcrossing populations persisted. We focused the present study on the partially outcrossing (mixed mating) and obligately outcrossing hosts, and analyzed the changes in the host resistance/avoidance (and pathogen infectivity) over time. We found that host mortality rates increased in the mixed mating populations over the first 10 generations of coevolution when outcrossing rates were initially low. However, mortality rates decreased after elevated outcrossing rates evolved during the experiment. In contrast, host mortality rates decreased in the obligately outcrossing populations during the first 10 generations of coevolution, and remained low throughout the experiment. Therefore, predominant selfing reduced the ability of the hosts to respond to coevolving pathogens compared to outcrossing hosts. Thus, we found that host–pathogen coevolution can generate rapid evolutionary change, and that host mating system can influence the outcome of coevolution at a fine temporal scale.     

Attraction and attachment of zoospores of the parasitic chytridRozella allomycis in response to host-dependent factors

Summary This study examined the behavior of populations of zoospores of the obligately parasitic, endobiotic chytridRozella allomycis towards young, vegetative thalli of various saprophytic fungi, in order to identify host-dependent factors which control the development ofRozella. An inverted microscope was employed for continuous observation of parasite-host interaction in petri dishes of broth or agar medium. Two factors appear to control the initial stages of invasion byRozella of both susceptible and resistant species of the host genus,Allomyces: (i) a soluble exudate which attractsRozella zoospores, (ii) a receptor on the cell-wall surface which causesRozella zoospores to adhere, and to encyst and to germinate immediately thereafter. A related, nonsusceptible species,Blastocladiella emersonii, also attractsRozella zoospores, but supports very limited attachment.Rozella zoospores neither accumulate around, nor adhere to young thalli of non-blastocladialean fungi. This host-specific behavior pattern is compared with that of saprophytic and facultatively parasitic Phycomycetes, whose zoospores show nonspecific chemotactic responses and require no receptor for attachment, encystment and germination.     

DEVELOPMENT OF JANCZEWSKIA MORIMOTOI (CERAMIALES) ON ITS HOST LAURENCIA NIPPONICA (CERAMIALES,RHODOPHYCEAE)1

Janczewskia morimotoi Tokida was successfully cultured from spore to reproductive maturity on its host Laurencia nipponica Yamada. The spore penetrates the host without requirement for wound or abrasion sites, growing between host cortical cells and developing a superficial and an endophytic system simultaneously. During the juvenile period, when the parasite is nonpigmented, it differentiates a cortex and the proliferating endophytic filaments enlarge causing a displacement of layers of host cells into the parasitic tissue. Host cells contacted by cells of the parasite exhibit increased wall thickness, cytoplasmic density and vesicle formation. Pit connections between host and parasite cells were rarely observed whereas penetration of host cell walls was seen commonly. As the parasite increases in size, its cells become pigmented evenly throughout the cortex and host cells show less obvious reactions to the parasite. At this same time, the parasite develops branches and reproductive structures. Host plant segments less than 3 cm long failed to grow when infected with spores of the parasite whereas longer segments were not significantly affected by the parasite. In the absence of the host, the parasite cannot complete its development. Although J. morimotoi is well pigmented at maturity, the absence of pigmentation in the juvenile stage, penetration of host cells, and effect on host growth in culture strongly suggest that it is parasitic during at least its early development.     

Fungal zoospores are induced to encyst by treatments known to degrade cytoplasmic microtubules

Summary Zoospores of the obligately parasitic chytrid Rozella allomycis encyst and germinate after settling on a hypha of the host, the watermold Allomyces arbuscula. Zoospores deprived of a host also encyst after aging, but do not germinate. Hence, means were sought to induce encystment of young zoospores, in order to test whether they would subsequently germinate in the absence of a host.Zoospore suspensions were harvested and exposed to treatments known to degrade cytoplasmic microtubules and to depolymerize fibrillar structures in other organisms: ice temperature, hydrostatic pressure of 2000–10000 psi, cupric ions, and colchicine. These treatments induced rapid encystement—but no germination.The results suggest that the motility, the flagellated state, and the irregular, elongate shape of fungal zoospores depend on the intactness of their fibrillar skeletal structures. The results also support the hypothesis that contact of Rozella with the host surface has two sequential functions: (i) nonspecific (replaceable by other treatments) triggering of encystment, (ii) specific stimulation of germination.     

Cultivation of a vampire: ‘Candidatus Absconditicoccus praedator’

Halorhodospira halophila, one of the most-xerophilic halophiles, inhabits biophysically stressful and energetically expensive, salt-saturated alkaline brines. Here, we report an additional stress factor that is biotic: a diminutive Candidate-Phyla-Radiation bacterium, that we named ‘Ca. Absconditicoccus praedator’ M39-6, which predates H. halophila M39-5, an obligately photosynthetic, anaerobic purple-sulfur bacterium. We cultivated this association (isolated from the hypersaline alkaline Lake Hotontyn Nur, Mongolia) and characterized their biology. ‘Ca. Absconditicoccus praedator’ is the first stably cultivated species from the candidate class-level lineage Gracilibacteria (order-level lineage Absconditabacterales). Its closed-and-curated genome lacks genes for the glycolytic, pentose phosphate- and Entner–Doudoroff pathways which would generate energy/reducing equivalents and produce central carbon currencies. Therefore, ‘Ca. Absconditicoccus praedator’ is dependent on host-derived building blocks for nucleic acid-, protein-, and peptidoglycan synthesis. It shares traits with (the uncultured) ‘Ca. Vampirococcus lugosii’, which is also of the Gracilibacteria lineage. These are obligate parasitic lifestyle, feeding on photosynthetic anoxygenic Gammaproteobacteria, and absorption of host cytoplasm. Commonalities in their genomic composition and structure suggest that the entire Absconditabacterales lineage consists of predatory species which act to cull the populations of their respective host bacteria. Cultivation of vampire : host associations can shed light on unresolved aspects of their metabolism and ecosystem dynamics at life-limiting extremes.     

An ultrastructural study of polyembryonic parasitoid embryo and host embryo cell interactions

The morula‐stage embryo of the polyembryonic egg‐larval parasitoid Copidosoma floridanum forms outside the host embryo and secondarily invades the host body. Electron microscopic analyses of cellular interactions between the extraembryonic syncytium of the parasitic morula and the host embryonic epithelial cells showed that morula penetration into the host embryo did not cause obvious damage to the host cells, except for the abrasion of the embryonic cuticle. Epithelial cells of the host embryo extended microvilli toward the invading C. floridanum morula and also adjacent host cells in the same way. Shortly after settlement of the morula within the host body cavity, gap junctions and adherens junctions with host cells were formed. The morula was then surrounded by a cyst comprised of host cells into which host tracheoles were invaginated. J. Morphol., 2010. © 2010 Wiley‐Liss, Inc.     

Nest desertion cannot be considered an egg‐rejection mechanism in a medium‐sized host: an experimental study with the common blackbird Turdus merula

Two main mechanisms of egg rejection, the main defence of hosts against brood parasites, have been described: ejection and desertion. Desertion of the parasitized nest is much more costly and is usually exhibited by small‐sized host species unable to remove the parasitic egg. However, nest desertion is frequently assumed to be an anti‐parasite strategy even in medium or large‐sized host species. This assumption should be considered with caution because: 1) large‐sized hosts able to eject the parasitic egg should eject it rather than desert the nest, and 2) breeding birds may desert their nests in response to different disturbances other than brood parasitism. This problem is especially important in the common blackbird Turdus merula because this is a medium‐sized species, potential host of the common cuckoo Cuculus canorus, in which desertion has been frequently reported as a response to cuckoo egg models. Here, we seek to determine whether nest desertion can be considered a response unequivocally directed to the parasitic egg in medium‐sized hosts using the blackbird as the study species. In an experimental study in which we have manipulated levels of mimicry and size of experimental eggs, we have found that both colour (mimetic and non‐mimetic; at least for human vision) and size (small, medium, and large) significantly affected ejection rates but not nest desertion rates. In fact, although large eggs disproportionally provoked nest desertion more frequently than did small or medium‐sized eggs, cuckoo‐sized parasitic eggs were not deserted allowing us to conclude that desertion is unlikely to be an adaptive response to brood parasitism at least for this species.     

Concepts of nematode-fungus associations in plant disease complexes: a review

Plant parasitic nematodes interact with fungi in a variety of ways to cause plant disease complexes. Even some nonplant parasitic nematodes are able to carry fungal spores internally which not only increases their mobility, but also protects them from fungicides. Plant parasitic nematodes frequently wound plants in the process of penetration and feeding. These wounds become subject to infection by fungal pathogens that require aid in penetrating their host. Other nematodes modify plant tissue in such a way that it becomes a better substrate for the fungus and thus increases their growth and reproduction to the detriment of the host. Quantitative and qualitative changes in root exudate which are induced by certain nematodes stimulate the germination, growth, and reproduction of fungal propagules in the rhizosphere. These exudates may also indirectly inhibit components of the rhizosphere microflora (e.g., actinomycetes) which are antagonistic to some plant pathogens. Depending on the species of nematode and fungus, concomitant infections may stimulate nematode reproduction (Pratylenchus-Verticillium) or inhibit reproduction (Heterodera-Fusarium).     

Signalling between Pathogenic Rust Fungi and Resistant or Susceptible Host Plants

Rust fungi are obligately biotrophic plant parasites that obtaintheir nutrients from living host cells. The initiation of thetwo parasitic phases of these fungi generally requires topographicsignals from the plant surface followed, for the dikaryoticphase, by a successive sequence of signals to control furtherfungal development within the plant. During the fungal lifecycle, three types of intracellular structures (invasion hyphae,M-, and D-haustoria) are formed and each may differently affectthe host membrane that surrounds it, as well as affecting othercellular components. Each intracellular structure also preventsnon-specific plant defences triggered by fungal activities,possibly by interfering with the signalling system rather thandefence expression. In resistant host cultivars, cellular invasiontriggers a rapid cell death (the hypersensitive response) thatshares some features with developmentally programmed cell deathin animal and plant tissues, and is controlled by parasite-specificresistance genes that resemble those that defend plants againstother types of pathogens. Evidence from one system suggeststhat this response is specifically elicited by a fungal peptideand does not involve the oxidative burst typical of resistanceexpression in other plant-pathogen interactions. However, overall,few of the molecules involved in any of these plant-rust fungiinteractions have been completely characterized and much isleft to be discovered, particularly with respect to how cellularsusceptibility to rust fungi is conditioned.Copyright 1997 Annalsof Botany Company Apoptosis; biotrophy; elicitor; hypersensitive response; oxidative burst; suppressor; Uromyces vignae     

Hyperparasitic Attack of Trichothecium roseum on Conidia of Pestalotiopsis funerea

Trichothecium roseum (Tr) has been shown to be a highly effective hyperparasite on conidia of Pestalotiopsis funerea (Pf) in vivo and in vitro. The stages of this spore parasitism are: positive tropism of Tr towards Pf conidia, contact between Tr and Pf, formation of simple or lobed appressoria of Tr on the host conidial surface, penetration of the attacked host cells from the base of the appressoria, development of host-internal, mostly branching parasitic hyphae by Tr, desintegration, lysis and death of the parasitized host cells, exit of Tr from the destroyed host cells and its intensive sporulation over Pf remnants. Pf did not show any defence reactions against the attack by Tr. In addition to the antagonistic activities of Tr against Pf reported previously, which are due to extracellular toxins released by Tr, direct hyperparasitism is a second mechanism of antagonism, which contributes to the successful competitive ability of Tr in this fungal interaction.     

ADAPTATION BY A PARASITIC TREMATODE TO LOCAL POPULATIONS OF ITS SNAIL HOST

In each of two reciprocal cross-infection experiments, a digenetic trematode (Microphallus sp.) was found to be significantly more infective to snails (Potamopyrgus antipodarum) from its local host populations. This gives strong evidence for local adaptation by the parasite and indicates that there is a genetic basis to the host–parasite interaction. It is suggested that the parasite should be able to track common snail genotypes within populations and, therefore, that it could be at least partially responsible for the persistence of sexual subpopulations of the snail in those populations that have both obligately sexual and obligately parthenogenetic females.     

Immune stress and facultative sex in a parasitic nematode

It has been suggested that sexual reproduction in parasites may be advantageous because it helps evade genotype‐specific host immune responses. Indirect support for this hypothesis has recently come from work on Strongyloides ratti, a parasitic nematode of rats that develops and reproduces sexually or asexually. In this species, host immune responses against S. ratti lead to a higher proportion of individuals reproducing sexually. However, an alternative explanation for these results is that sex is favoured by general environmental stress, including host responses against antigen sources other than S. ratti. Here we test this hypothesis, by determining how host immunity against two other parasitic nematode species (Nippostrongylus brasiliensis & Strongyloides venezuelensis) and commonly used mammalian antigens (sheep red blood cells) affects the likelihood of S. ratti larvae developing sexually. Our results show that increased levels of sex occur in response to immune responses generated against these other species, and not just host immunity elicited by S. ratti. This is consistent with the idea that sex is favoured under stressful conditions, and does not support the immune evasion hypothesis.     

Like herbivores,parasitic plants are limited by host nitrogen content

Herbivores generally benefit from increased plant nitrogen content, because the nitrogen content of animals is much higher than that of plants. Consequently, high plant nitrogen alleviates the profound stoichiometric imbalance that herbivores face in their diets. Parasitic plants provide the opportunity to test this generalization for consumers across kingdoms. We fertilized two microhabitats in a California salt marsh that were dominated by Salicornia virginica or a mixture of S. virginica and Jaumea carnosa. The nitrogen content of both host plants and of the holoparasite Cuscuta salina (dodder) increased in fertilized plots in both microhabitats. Cuscuta preferred to attack Jaumea, although Jaumea had lower nitrogen content than Salicornia. When host nitrogen content was altered by fertilizing plots, however, the percent cover of the parasite doubled. Although parasitic plants and their hosts have similar tissue nitrogen contents, suggesting no stoichiometric imbalance between host and consumer, parasitic plants do not feed on host tissue, but on host xylem and phloem, which are very low in nitrogen. Consequently, parasitic plants face the same dietary stoichiometric constraints as do herbivores, and both herbivores and holoparasitic plants may respond positively to increases in host nitrogen status.     

PARASITIC INTERACTIONS AND VEGETATIVE ULTRASTRUCTURE OF CHOREOAEMA THURETII (CORALLINALES,RHODOPHYTA)1

The monotypic coralline red alga, Choreonema thuretii (Bornet) Schmitz (Choreonematoideae), grows endophytically within three geniculate genera of the Corallinoideae. Although the thallus of Choreonema is reduced, lacks differentiated plastids, and is endophytic except for its conceptacles, its status as a parasite has been questioned because cellular connections to the host had not been ob served. Transmission electron microscopy, however, disclosed a previously undescribed type of parasitic interaction in which Choreonema interacts with its host through specialized cells known as lenticular cells. These small, lens-shaped cells are produced from the single file of host-penetrating vegetative cells. Pit plug morphology between vegetative and lenticular cells is polarized. Plug caps facing the vegetative cell have normal coralline morphology, while those facing the lenticular cell are composed of three layers. Regions of lenticular cells near host cells protrude toward the host cell; upon encountering the host cell wall, the prolrusion produces numerous finger-like fimbriate processes that make cellular connections with the host cell. Lenticular cells may extend several protrusions toward a host cell or penetrate more than one host cell; two or more lenticular cells may also penetrate the same host cell. The lack of secondary pit connections, cell fusions, and passage of parasitic nuclei suggest that this parasitic relationship may be evolutionarily older than previously reported cases of parasitism in red algae.     

Egg Discrimination and Sex-Specific Pecking Behaviour in Parasitic Cowbirds

We studied egg‐pecking behaviour in males and females of three cowbird species: the shiny cowbird (Molothrus bonariensis), a host generalist brood parasite, the screaming cowbird (M. rufoaxillaris), a host specialist brood parasite, and the bay‐winged cowbird (Agelaioides badius), a non‐parasitic species. We conducted three experiments in which we offered each bird an artificial nest with two plaster eggs and recorded whether egg pecking occurred and the number of pecks on each egg. In expt 1, we tested if there were species and sex differences in egg‐pecking behaviour by offering the birds two spotted eggs of similar pattern. Shiny and screaming cowbirds responded in 40.3% and 44% of the trials, respectively, with females and males presenting similar levels of response. In contrast, bay‐winged cowbirds did not show any response. In expt 2, we tested if shiny cowbirds responded differentially when they faced a choice between one host and one shiny cowbird egg, while in expt 3, we tested if screaming cowbirds responded differentially when they faced a choice between one shiny and one screaming cowbird egg. Shiny cowbirds pecked preferentially host eggs while screaming cowbirds pecked more frequently shiny cowbird eggs. Our results show that egg‐pecking behaviour is present in both sexes of parasitic cowbirds, but not in non‐parasitic birds, and that parasitic cowbirds can discriminate between eggs of their own species and the eggs of their hosts or other brood parasites.     

Studies on a species of Monosporascus isolated from triticum

Hyphal parasitic behaviour of Fusarium oxysporum on Rhizoctonia solani and consecutive changes during this phenomenon have been investigated and studied. The hyphal parasitism was very commonly recorded between the test fungi. During the course of parasitism coiling, penetration, lysis and formation of chlamydospores by F. oxysporum on R. solani were observed. R. solani is a new host record for the mycoparasite F. oxysporum.     

Regulation of vole populations by the nematode <Emphasis Type="Italic">Trichuris arvicolae</Emphasis>: insights from modelling

The goal of this study is to determine whether a parasitic nematode may regulate, or destabilise by inducing demographic cycles, its host populations. We explore three host–parasite systems through population dynamic models. The hosts considered are the fossorial water vole, Arvicola terrestris, the common vole Microtus arvalis and the bank vole Myodes (Clethrionomys) glareolus and the parasitic nematode is Trichuris arvicolae. Three differential equation-based mathematical models are developed including host immunity and the existence of trade-off between immunity and host survival. Using parameters estimated from field data and laboratory observations, all these models show that T. arvicolae can induce host population regulation but not demographic cycles. The regulation effect of the nematode is un-ambiguous for the water vole (reduction of 50.2% of the host population size), but less obvious for the common vole (5.9%) and even less for the bank vole (1.4%). Important biological parameters to be taken into account in such models are discussed. Experimental confirmation of the regulatory potential of the nematode and of the costs of mounting an immune response against this nematode are now required. Communicated by W. Lutz     

Evolution of social parasitism in ants

Slave raids of Amazon ants, the beheading of the host colony's queen by a parasitic Bothriomyrmex female, or the protracted throttling of the host queen by an Epimyrma female which has penetrated a Leptothorax nest, are among the most intriguing behaviors to be observed in social parasitic ants. The evolutionary origin of these behaviors, however, is quite obscure, and further work is needed to elucidate how parasitic life cycles could have arisen from the ordinary social organization of ants.     

Colony founding and social parasitism in <Emphasis Type="Italic">Lasius</Emphasis> (<Emphasis Type="Italic">Acanthomyops)</Emphasis>

We investigated colony foundation behavior of three species of the Lasius claviger group, L. latipes, L. interjectus and L. claviger, using field observations and laboratory experiments. Laboratory studies included observing gyne behavior prior to interaction with host colonies (e.g. grouping, overwintering, feeding) and experiments in which gynes were introduced to putative host colonies. Observations of gyne parasitic behavior immediately after mating flights in the field and the discovery of mixed colonies both confirm the parasitic behavior of these species and point toward a wide host species range including two cases of hyperparasitism. L. interjectus and L. latipes enter the host colony immediately after the nuptial flight, while L. claviger may hibernate and enter in the spring. Laboratory experiments showed that L. interjectus gynes prefer to group and suffer lower mortality when in a group, which is consistent with field observations of L. interjectus gynes entering host colonies in large numbers. Details on behavior of L. latipes alpha and beta form gynes are also given.