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Evidence for strong host clone-parasite species interactions in the Daphnia microparasite system.

Organisms are often confronted with multiple enemy species. Defenses against different parasite species may be traded off against each other. However, if resistance is based on (potentially costly) general defense mechanisms, it may be positively correlated among parasites. In an experimental study, we confronted 19 clones from one Daphnia magna population with two bacterial and three microsporidian parasite species. All parasites were isolated from the same pond as the hosts. Host clones were specific in their susceptibility towards different parasite species, and parasite species were host-clone specific in their infectivity, spore production, and virulence, resulting in highly significant host-parasite interactions. Since the Daphnia's resistance to different parasite species showed no obvious correlation, neither general defense mechanisms nor trade-offs in resistance explain our findings. None of the Daphnia clones were resistant to all parasite species, and the average level of resistance was quite similar among clones. This may reflect a cost of defense, so that the cumulative cost of being resistant to all parasite species might be too high.

Analysis of Variance↗

Community ecology of the metazoan parasites of Atlantic moonfish, Selene setapinnis (Osteichthyes: Carangidae) from the coastal zone of the State of Rio de Janeiro, Brazil.

Eighty-nine specimens of Selene setapinnis (Mitchill, 1815) collected from the coastal zone of the State of Rio de Janeiro (21-23 degrees S, 41-45 degrees W and 23 degrees 05'S, 44 degrees 30'W), Brazil, from August 2001 to May 2002, were necropsied to study their metazoan parasites. Eighty-one (91%) specimens of S. setapinnis were parasitized by one or more metazoan species. Twenty-one species of parasites were collected: 8 digeneans, 3 monogeneans, 2 cestodes, 5 nematodes, and 3 copepods. The endoparasites (digeneans, cestodes, and nematodes) were 74.1% of total number of parasite specimens collected. The monogenean Pseudomazocraes selene (Hargis, 1957) was the most dominant species with the highest prevalence in the parasite community of S. setapinnis. The metazoan parasites of this host species showed the typical aggregated pattern of distribution. Only one parasite species (Acanthocolpoides pauloi Travassos, Freitas & Buhrnheim, 1955) showed positive correlation between the host total length and parasite abundance in S. setapinnis. Caligus robustus Bassett-Smith, 1898, P. selene, and Terranova sp. demonstrated positive correlation between the host total length and prevalence. Larvae of Terranova sp. showed influence of the host sex on its prevalence. A pair of ectoparasite species, P. selene-C. robustus, exhibited positive covariation between their abundances. Two pairs of endoparasite species, L. microstomum-P. merus and A. pauloi-P. merus showed significant covariation among their abundances; and the pair Terranova sp.-Raphidascaris sp. had positive co-ocorrence and covariation in the infracommunities of S. setapinnis. Like the parasite communities of the other carangid fishes from Rio de Janeiro, the parasite community of S. setapinnis is apparently only a slightly ordered species complex, characterized by dominance of endoparasite species.

Animals↗

Variations in the parasite fauna of the Patagonian toothfish (Dissostichus eleginoides Smitt, 1898), with length, season, and depth of habitat around the Falkland Islands.

The parasite fauna of Dissostichus eleginoides was examined from locations around the Falkland Islands. In total, of 11,362 individual parasites of 27 taxa were recovered from 105 fish. Two species, Ceratomyxa dissostichi and Sphaerospora dissostichi, represent new host records. The nematode Ascarophis nototheniae and the larval acanothocephalan Corynosoma bullosum were found to be new locality records and add to the knowledge of the biogeography and host specificity of parasites on the Patagonian Shelf. There were no significant differences in the mean abundance and prevalence of parasites recovered between sexes. Therefore, sex was not considered in further analysis and the data were pooled. Cysts of unknown etiology (CUE), the monogenean Neopavlovskioides georgianus, the larval acanthocephalan Corynosoma bullosum, and the digenean Neolepidapedon magnatestis had significant positive correlations with increasing host length. The larval Trypanorhynch cestode Grillotia erinaceus and the digenean Elytrophalloides oatesi showed significant negative correlations with increasing host length. CUEs, N. georgianus, the digenean Gonocerca physidis and E. oatesi showed statistically significant prevalence between summer, winter, and spring. The effect of depth on parasite communities was also examined, initially using a linear discriminant function analysis. The prevalence of individual parasites was then compared between depth strata using the chi-square test. The parasite communities on the shelf and deep water (> 1,000 m) were found to be different, whereas those caught at intermediate depths on the shelf slope were found to have parasite communities that were intermediate, containing a mixture of shelf and deeper-water parasites. The causes of the variations in parasite faunas in association with these intrinsic and extrinsic factors are discussed.

Animals↗

Damage due to parasites in Mediterranean teleosts.

Evaluation of damages by parasites in teleosts, even if underextimated in the past, is today one of the most used methods to understand the effective impact of a parasite on a certain ichtyc species. The damage caused by a parasite on the host could be classified into direct, with tissue changes, or indirect, with a decrease of the productive performances. Based on this, a preliminary difference could be traced distinguishing parasites that show a coevolution with their host species, characterized by a low damage, and those parasites that can occasionally infect new host species, showing a high degree of damage. In consideration of the damage, parasites can have different actions on the host: subtractive, irritative, mechanical, traumatic, toxic, dismetabolic, antigenic and foretic. Those parasites able to cause tissue changes must be furtherly classified considering the type of inflammation they evoke on tissues: ulcerous, catarral, haemorrhagic, necrotic and granulomatous. Some parasites are encysted in tissues without any host reaction. The fish response against parasite can be inflammatory, the most frequent, but also hyperplastic, metaplastic, neoplastic and immunitary. The paper goes through different tissue changes due to the main parasites of Mediterranean teleosts.

Animals↗

[The new generations of vaccines against parasites].

The protection of humans and domestic animals against parasitic infections remains a major goal, especially in light of developing of drug resistant strains in many parasite species. "Classic" vaccines are based on attenuated infective stages of protozoan and helminth parasites. Although such vaccines are effective in confering host immunity against several protozoan (coccidiosis, giardiosis, toxoplasmosis) diseases and one helminth (dictyocaulosis) they are very unstable and expensive. Recombinant techniques enable to obtain protective antigens quickly and in considerable quantities, cultivating of the bacteria and purification of the recombinant protein is less expensive than the maintenance of host animals and isolation of the protective antigens from harvested parasites. Moreover, the cloned protective antigens may be deprived of epitopes responsible for immunopathology. However, at present only one anti-parasite recombinant protein vaccine is commercially available (TickGARD). Such a situation may result from that many protective parasitic antigens cannot be expressed in bacteria or yeast in anative from. DNA vaccines present many advantages over protein ones. Firstly, the antigenic proteins synthesised within the host cell possess an appropriate molecular structure and undergo a post-translational modifications specific for a native protein. The next advantage of DNA vaccines is that DNA is easier to handle and more resistant than proteins to temperature changes. DNA vaccines are likely to induce novel mechanisms of immune response, which may be beneficial in case of parasitic invasions. Costs of DNA vaccines are comparable, and may be even lower, in comparison to recombinant protein vaccines. The main obstacle preventing the use of DNA vaccines is still lack of the complete knowledge concerning mechanisms of their action. Vaccines based on transgenic plants (=edible vaccines), expressing the protective parasitic antigens, present another promising approach in research on anti-parasitic vaccines. Such vaccines may be of special importance in prevention of infections with gastrointestinal parasites.

Animals↗

The art of parasite survival.

Parasites develop and survive in an environment which is often hostile to them. When facing aggressive conditions parasites are able to use various and complex strategies. Echinococcus granulosus, Toxocara canis, Pneumocystis carinii, Entamoeba or Toxoplasma gondii are able to seclude from the environment when stressed by surrounding (immunologic or non-immunologic) aggressive factors. Specific antigens which exert a functional activity during a short period of time appear to be concealed from the immune attack at this crucial moment. This is the case for rhoptry or dense granule antigens of Plasmodium or Toxoplasma sporozoa involved in the formation of the parasitophorous vacuole which are released in a space perfectly isolated from the outside and therefore from antibodies. Some parasites like Schistosoma mansoni or Trypanosoma brucei reveal an amazing opportunistic behavior when they use cytokines of host origin induced by the infectious process for their own development. Leishmania, Toxoplasma and Trypanosoma cruzi are able to invade immunologically competent macrophages and to avoid the triggering of killing mechanisms of these cells. Parasites also take advantage of the genetic restriction of the immune response and it has been observed for Plasmodia that some high molecular weight antigens are unable to induce an immune response in particular strains of mice. Parasite receptors involved in the invasion of host cells by parasites can function in the presence of antibodies which can explain the failure of vaccination attempts targeting this type of molecules. Among the mechanisms developed by parasites to resist to drugs it appears that transmembrane transporters described in many protozoa or helminth parasites could play a role. Moreover, the description of parasite-specific enzymes able to protect them against the damaging effects of oxygen radicals suggests that parasites are potentially able to develop a resistance phenomenon against drugs acting via an oxidative burst.

Adaptation, Physiological↗

Immunization against parasitic diseases of fish.

Parasitologists have not, in the past, exploited the immune system to protect fish against parasitic diseases. In the past few years, however, there has been an increased interest in adopting this strategy, and we have made steady and promising progress against a few parasites which are of economic importance. Amyloodinium ocellatum is an ectoparasitic dinoflagellate on brackish and marine fishes, which may also cause problems to aquarium fishes. Antiserum from fish inoculated intraperitoneally (i.p.) with living dinospores of the parasite immobilizes and agglutinates living dinospores; it also reduces parasite infectivity in cell culture. Cryptobia salmositica is a pathogenic haemoflagellate of salmonids on the Pacific coast of North America, causing mortality in semi-natural and intensive salmon culture facilities. A live attenuated vaccine inoculated i.p. protects susceptible juvenile and adult fish for at least 24 months. The protection involves production of complement fixing antibodies, phagocytosis, and antibody-dependent and antibody-independent T-cell cytotoxicity. A monoclonal antibody against a surface membrane glycoprotein (199-200 kDa is therapeutic in that it significantly reduces parasitaemias when inoculated into fish with acute disease. Ichthyophthirius multifiliis is an ectoparasitic ciliate of freshwater fishes with world wide distribution, usually causing disease when fish are stressed and/or when environmental conditions are favourable for parasite multiplication. Live theronts injected into the body cavity protect fish, and monoclonal antibodies with immobilizing activity upon parasites have been developed. There is some evidence of passive transfer of protective immunity from immune to naive fish, and to eggs. Diplostomum spathaceum is an intestinal parasite of gulls; the metacercaria stage of the parasite encyst and causes disease and mortality in numerous species of freshwater fish in Europe and in North America. Fish injected i.p. with sonicated/killed cercariae or metacercariae have fewer metacercariae in the eyes and survives longer. Lepeophtheirus salmonis and Caligus elongatus are parasitic copepods (sea lice), and they are important parasites of Atlantic salmon in cage cultures. A vaccine against fish lice is plausible, and the efficacy of about 20 candidate antigens in protecting fish is being tested.

Animals↗

Trypanosoma musculi: tracking parasites and circulating lymphoid cells in host mice.

Two aspects of host-parasite relationships that seem worthy of more attention are: (a) the distribution of parasites among host organs in the early course of infection, and (b) the dynamics of host lymphocyte tissue localization and recirculation during the course of infection. We have employed the derivatized aminostyrylpyridinium dye, [125I] I 2P-Di-6-ASP, to provide a relatively stable tag on both a parasite, Trypanosoma musculi, and on host mouse splenocytes, enriched B and T lymphocytes, and natural killer cells. The organ distribution of the parasites, splenocytes, and lymphocytes in recipient, host mice was tracked. Radiolabeled T. musculi localized primarily in the liver with lesser numbers in spleen, lungs, and kidneys. Per unit wet weight, the spleen accumulated parasites most efficiently. When T. musculi were inoculated intraperitoneally, most of them remained in the peritoneal space and the numbers that gained access to liver, lungs, and spleen were significantly smaller than in mice inoculated intravenously. The acquisition of parasites by the spleen (and lungs) of mice with an existing T. musculi infection was markedly inhibited. This was true also of syngeneic splenocytes and lymphocytes. In addition, lymphocytes from infected mice were significantly less likely to take residence in the spleens of normal recipient mice and were especially unlikely to localize in the spleens of infected recipients. These and other findings suggested that the inability of circulating lymphocytes to gain access to lymphoid tissues in infected mice, coupled with the poor ability of those tissues to sequester parasite antigens, could account for the known prolonged delay in the development of curative antibody response characteristic of T. musculi-infected mice. It is likely that the marked disruption of lymphoid tissue histoarchitecture that is typical of T. musculi infection contributes significantly to the failure of the tissues to sequester parasites and lymphocytes. Because lymphoid tissue disruption is seen in many parasitic infections, the findings reported here may have fairly broad relevance. In any case, the procedure described here for labeling parasites and lymphocytes should be of general utility for tracking their disposition in vivo.

Aminopyridines↗

Knowing your enemies: seasonal dynamics of host-social parasite recognition.

Despite its evolutionary significance, behavioural flexibility of social response has rarely been investigated in insects. We studied a host-social parasite system: the slave-making ant Polyergus rufescens and its host Formica rufibarbis. Free-living host workers from parasitized and from unparasitized areas were compared in their level of aggression against the parasite and alien conspecifics. We expected that a seasonal change would occur in the acceptance threshold of F. rufibarbis workers from a parasitized area towards the parasite, whereas F. rufibarbis workers from an unparasitized area would not show substantial changes connected with the parasite's peak in activity (raiding and colony-founding season). The results showed a significant adaptive behavioural flexibility of host species workers and are consistent with the acceptance threshold model's (Reeve 1989) prediction that recognition systems are not fixed but context-dependent. In particular, host workers from the unparasitized area were highly aggressive towards the parasite regardless of the season, whereas host workers from the parasitized area significantly increased their aggression towards the parasite during its raiding and colony-founding season. Being able to detect and possibly kill a Polyergus scout searching for host nests can be an effective strategy for a Formica colony to avoid being raided or usurped by a parasite queen.

Aggression↗

Carotenoid-dependent coloration of male American kestrels predicts ability to reduce parasitic infections.

The signaling function of sexually selected traits, such as carotenoid-dependent avian plumage coloration, has received a great deal of recent attention especially with respect to parasitism and immunocompetence. We argue that parasite-mediated models of sexual selection may have an implicit temporal component that many researchers have ignored. For example, previous studies have demonstrated that carotenoid-dependent traits can signal past parasite exposure, current levels of parasitism, or the ability of individuals to manage parasitic infections in the future. We examined repeated measures of carotenoid-dependent skin color and blood parasitism in American kestrels (Falco sparverius) to distinguish whether coloration might signal current parasitism or the potential to deal with infections in the future. We found no evidence that coloration was related to current levels of parasitism in either sex. However, coloration of males significantly predicted their response to parasitism; males with bright orange coloration during prelaying, when mate choice is occurring, were more likely than dull yellow males to reduce their levels of infection by the time incubation began. Coloration during prelaying may advertise a male's health later in the breeding season. For kestrels, the ability to predict future health would be highly beneficial given the male's role in providing food to his mate and offspring. Coloration of females was not a significant predictor of parasitism in the future, and we provide several possible explanations for this result.

Animals↗

Four-year monitoring of parasite communities in gobiid fishes of the south-western BalticII. Infracommunity.

The parasite infracommunity of five goby species (Pomatoschistus minutus, P. pictus, P.microps, Gobiusculus flavescens, Gobius niger) from the south-western Baltic was investigated during spring, summer and autumn of the years 1997-2000. The mean parasite species number in single hosts was high, ranging between 1.1 (P. minutus), 2.1 (P. pictus) to even 3.3 (P. microps). Gobius niger is the only host which lives longer than a year and is infested by almost identical parasites for longer times, i.e. the parasite species composition has greater homogeneity. Most intensity of infestation values peaked in summer and were lowest in autumn; only a few exceptions were found in spring or autumn. Only the Digenea Podocotyle atomon and Cryptocotyle concavum were abundant enough to show a clear seasonal fluctuation in Pomatoschistus minutus, P. pictus and Gobiusculus flavescens. Aphalloides timmi and Apatemon gracilis (Digenea) also attained high intensities in P. microps. These four parasite species and, additionally, Cryptocotyle lingua (Digenea), and Hysterothylacium sp. (Nematoda) can be strongly accumulated from either prey or free-swimming larvae and, thus, decisively influence the structure of the infracommunities. Due to selection by filter mechanisms, rare parasites settle rather by chance after competition with other species. The number of parasite species usually increased significantly with host growth. As many as four parasite species were found at the same time in the intestinal tract microhabitat of Gobius niger and P. minutus; at most three parasite species were present on the skin and fins or in the body cavity. The level of infection is due to the respective life history patterns and the kinds of prey, which harbour different parasites as intermediate hosts. Additionally, it depends on the time of appearance of goby offspring in the course of the year.

Animals↗

Spatial heterogeneity of daphniid parasitism within lakes.

Spatially explicit models show that local interactions of hosts and parasites can strongly influence invasion and persistence of parasites and can create lasting spatial patchiness of parasite distributions. These predictions have been supported by experiments conducted in two-dimensional landscapes. Yet, three-dimensional systems, such as lakes, ponds, and oceans, have received comparatively little attention from epidemiologists. Freshwater zooplankton hosts often aggregate horizontally and vertically in lakes, potentially leading to local host-parasite interactions in one-, two-, or three-dimensions. To evaluate the potential spatial component of daphniid parasitism driven by these local interactions (patchiness), we surveyed vertical and horizontal heterogeneity of pelagic Daphnia infected with multiple microparasites in several north temperate lakes. These surveys uncovered little evidence for persistent vertical patchiness of parasitism, since the prevalence of two parasites showed little consistent trend with depth in four lakes (but more heterogeneity during day than at night). On a horizontal scale of tens of meters, we found little systematic evidence of strong aggregation and spatial patterning of daphniid hosts and parasites. Yet, we observed broad-scale, basin-wide patterns of parasite prevalence. These patterns suggest that nearshore offshore gradients, rather than local-scale interactions, could play a role in governing epidemiology of this open water host-parasite system.

Animals↗

Adaptation, specificity and host-parasite coevolution in mites (Acari).

Parasitism by mites is widespread and involves all the classes of vertebrates, from fishes to mammals. Owing to their small size and their great plasticity, mites are able to adapt to a wide range of habitats. Most of the species are ectoparasites but endoparasitism, especially in the respiratory tract, is common in birds and mammals. The morphological modifications appearing during the process adaptation to parasitic life, especially in Myobiidae, are analysed. Two kinds of characters are particularly important: the constructive specialized characters, consisting of the production of new structures, especially attachment organs allowing the mite to attach to the skin and the hair of the host, and regressive characters. Regression of the external structures is the most important phenomenon appearing in the process of evolution of parasitic mites. The importance of the regression in the parasite is correlated with the degree of evolution of the host. Host and parasite have a parallel evolution, but they go in opposite directions. The author surmises that the regressive evolution is related to the immunological reactions of the host that tend to reject the parasite. To escape from this rejection the parasite tends to select the less antigenic and therefore the most regressed phenotype. Specificity is generally strict in permanent parasites. Coevolution of host and parasite is studied in the family Myobiidae which parasitizes marsupials, insectivores, bats and rodents. The concordance between the radiations of the mites and that of their hosts is very high.

Adaptation, Biological↗

Geographic and within-population structure in variable resistance to parasite species and strains in a vertebrate host.

Host resistance to parasites and parasite infectivity may be subject to significant genetically determined variation within species. However, relatively little is known of how this variability is structured in natural vertebrate populations and their macroparasites. A laboratory experiment on host susceptibility-parasite infectivity variation in a wildlife host-parasite system (subspecies of the anuran X. laevis and their polystome flatworms), including 33 pairwise allopatric and sympatric host-parasite combinations (three parasite geographical isolates x 11 host full-sibling families, n=600), revealed a complex pattern of infection success. Results amongst host sibships from different localities suggested that infection success was subject to a highly significant locality x parasite isolate interaction. Within localities, a highly significant sibship x isolate interaction also occurred in one of two groups of sibships examined. The existence of such interactions suggests a potential for frequency-dependent, Red Queen-like selection. Interaction between locality and isolate was partly due to higher infection levels in sympatric combinations, consistent with a general pattern of host-specific adaptation. However, some allopatric combinations produced unpredictably high infection levels, resulting in very asymmetrical cross-infectivity patterns (where the reciprocal cross-infections produced negligible infection). This phylogeographically structured host-parasite system may, therefore, sometimes generate local parasite strains with high infectivity to allopatric hosts. Secondary contact between populations could thus result in significant, and unequal, transfer of parasites.

Animals↗

Leishmania model for microbial virulence: the relevance of parasite multiplication and pathoantigenicity.

Leishmanial mechanisms of virulence have been proposed previously to involve two different groups of parasite molecules. One group consists of largely surface and secretory products, and the second group includes intracellular molecules, referred to as 'pathoantigens'. In the first group are invasive/evasive determinants, which protect not only parasites themselves, but also infected host cells from premature cytolysis. These determinants help intracellular amastigotes maintain continuous infection by growing at a slow rate in the parasitophorous vacuoles of host macrophages. This is illustrated in closed in vitro systems, e.g. Leishmania amazonensis in macrophage cell lines. Although individual macrophages may become heavily parasitized at times, massive destruction of macrophages has not been observed to result from uncontrolled parasite replication. This is thus unlikely to be the direct cause of virulence manifested as the clinical symptoms seen in human leishmaniasis. Of relevance is likely the second group of immunopathology-causing parasite 'pathoantigens'. These are highly conserved cytoplasmic proteins, which have been found to contain Leishmania-unique epitopes immunologically active in leishmaniasis. How these intracellular parasite antigens become exposed to the host immune system is accounted for by periodic cytolysis of the parasites during natural infection. This event is notable with a small number of parasites, even as they grow in an infected culture. The cytolysis of these parasites to release 'pathoantigens' may be inadvertent or medicated by specific mechanisms. Information on the pathoantigenic epitopes is limited. T-cell epitopes have long been recognized, albeit ill-defined, as important in eliciting CD4+ cell development along either the Th1 or Th2 pathway. Their operational mechanisms in suppressing or exacerbating cutaneous disease are still under intensive investigation. However, immune response to B-cell epitopes of such 'pathoantigens' is clearly futile and counterproductive. Their intracellular location within the parasites renders them inaccessible to the specific antibodies generated. One example is the Leishmania K39 epitope, against which antibodies are produced in exceedingly high titers, especially in Indian kala-azar. Here, we consider the hypothetical emergence of this pathoantigenicity and its potential contributions to the virulent phenotype in the form of immunopathology. Microbial virulence may be similarly explained in other emerging and re-emerging infectious diseases. Attenuation of microbial virulence may be achieved by genetic elimination of pathoantigenicity, thereby providing mutants potentially useful as avirulent live vaccines for immunoprophylasis of infectious diseases.

Animals↗

Patterns of intermediate host use and levels of association between two conflicting manipulative parasites.

For many parasites with complex life cycles, manipulation of intermediate host phenotypes is often regarded as an adaptation to increase the probability of successful transmission. This phenomenon creates opportunities for either synergistic or conflicting interests between different parasite species sharing the same intermediate host. When more than one manipulative parasite infect the same intermediate host, but differ in their definitive host, selection should favour the establishment of a negative association between these manipulators. Both Polymorphus minutus and Pomphorhynchus laevis exploit the amphipod Gammarus pulex as intermediate host but differ markedly in their final host, a fish for P. laevis and a bird for P. minutus. The pattern of host use by these two conflicting manipulative parasites was studied. Their incidence and intensity of infection and their distribution among G. pulex were first examined by analysing three large samples of gammarids collected from the river Tille, Eastern France. Both parasites had low prevalence in the host population. However, temporal fluctuation in the level of parasitic infection was observed. Overall, prevalence of both parasite species was higher in male than in female G. pulex. We then assessed the degree of association between the two parasites among their intermediate hosts, using two different methods: a host-centred measure and a parasite-centred measure. Both measures gave similar results; showing random association between the two acanthocephalan species in their intermediate hosts. We discuss our results in relation to the selective forces and ecological constraints that may determine the pattern of association between conflicting manipulative parasites.

Acanthocephala↗

Interactions between monogenean parasites and their fish hosts.

Parasite factors associated with recognition and selection of the host and the mechanisms in the host responsible for acceptance or rejection of the invading organism were evaluated. Sensory structures in parasites are able to detect differences between different fish species and this ability to discern between fishes may be based on both chemical and mechanical stimuli on the host surface. Complex glycoproteins, proteins, carbohydrates and simple molecules attract parasites or modify their behaviour. Furthermore, attachment of the monogenean parasite to a host is dependent on both mechanical structures and chemical factors in the parasite. These systems comprise anterior pads, posterior haptors, gland secretions, and muscular elements. The parasite needs access to appropriate nutrients which can be absorbed and used for reproduction and in this context signals from the host are needed for an optimal physiological response of the parasite. The innate and adaptive immune systems of the host are important elements in this question. Investigations have indicated that innate host factors (complement, lectins, acute phase reactants, macrophages) can bind to monogeneans and elicit severe damage to the parasites. The targets for these hostile products are not only the monogenean tegument, but may involve the gastrodermis and glands. However, the parasite's ability to avoid and even exploit the wide array of immunological elements of the host may be an important player in the dynamic interactions between host and monogenean determining host specificity. Even fish hosts susceptible to a certain parasite show an ability to mount a protective response at post-infection periods. Elevation of the host's production of adaptive and non-adaptive factors following monogenean infections of a certain duration may explain the acquired response.

Animals↗

Parasite community structure within and across host populations of a marine pelagic fish: how repeatable is it?

The geographical variation in parasite community structure among populations of the same host species remains one of the least understood aspects of parasite community ecology. Why are parasite communities clearly structured in some host populations, and randomly assembled in others? Here, we address this fundamental question using data on the metazoan parasite communities of different host size-classes of four distinct populations of a small pelagic fish, the Argentine anchovy, Engraulis anchoita, from the South West Atlantic. Within each fish sample, fish length was correlated with both the total intensity of parasites and species richness among infracommunities. More importantly, average fish length correlated with mean infracommunity richness and mean total intensity across the fish samples, indicating that the characteristics of parasite assemblages in a fish population are strongly influenced by the size of its fish in relation to those in other populations. Nested subset patterns were observed in about half of the fish samples. This means that the presence or absence of parasite species among fish individuals is often not random; however, no repeatability of nestedness among component communities was observed. Average fish length did not influence directly the likelihood that a parasite assemblage was significantly nested. However, variables influenced by average fish length, namely mean infracommunity richness and mean total intensity, determine the probability that a nested hierarchy will be observed; host size may thus indirectly affect parasite community structure either itself or via its influence on host movement and feeding patterns. To some extent, this apparent link may be due to the sensitivity of nestedness analyses to the proportion of presence in a presence/absence matrix; this in itself is a biological feature of the parasite community, however, which is associated with mean host length.

Animals↗