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PubMed1983

[Argyrophilic structures of the larval forms of 2 strains of Paramphistomum microbothrium: 1 a parasite of Isidora guernei and Ovis aries, the other a parasite of Isidora truncata and Bos taurus].

The life cycle of a Paramphistome from North Senegal is completed starting from cercariae shed by naturally infected Isidora guernei: a sheep and then uninfected Isidora guernei were successively infected experimentally. Adults obtained were identifiable as P. phillerouxi or as P. microbothrium. Species determination cannot be made on the basis of argentophilic structures in the miracidium. Morphology of sporocysts and rediae differs from that observed in P. phillerouxi but is undistinguishable from that described in P. microbothrium. Cercarial chaetotaxy differs from that of P. phillerouxi. Mollusc host: Isidora guernei belongs to the same genus as Isidora truncata and I. alluaudi, reported hosts to P. microbothrium. Therefore the material is provisionally identified as P. microbothrium. To confirm this, a strain of P. microbothrium from naturally infected Bos taurus in Egypt was studied. Miracidia were used to experimentally infect Isidora truncata; cercariae obtained were identical to those previously described for this species from I. truncata and I. alluaudi. Cercarial chaetotaxy was not significantly different from that of material from North Senegal. They represent therefore two strains of Paramphistomum microbothrium.

Animals↗
PubMedDate not supplied

[Host-parasite interactions between Coccus hesperidum L. (Hom. Coccidae) and its parasite Coccophagus scutellaris Dalman (Hym. Aphelinidae)].

The eggs laid in the host gut will develop normally. The larva resulting from those eggs penetrate the hemocele through the gut wall. The structure of the cells near the entry point is not affected because of the continuous renewal of those cells. On the other hand, development of the ovaries is most seriously affected. In fact, ovogenesis is stopped and vitellogenesis slowed down. But this phenomenon is related to the initial level of ovary development. If the attack takes place when the host is young, the effect on the ovaries is more serious. In extreme cases gonad development is annihilated. Otherwise, the host will still be able to lay eggs, but its reproduction capacity is diminished. Factors reducing development of gonads or maintaining them at a juvenile stage are discussed.

Animals↗
PubMed1998

Skin problems and parasites in children: 2. Parasitic worms.

The skin is an organ which has many important functions for body maintenance and health. Infestation by a wide variety of worms is a worldwide public health problem. Threadworms are believed to infect up to 50% of London school children. Dogs and other pets have much to teach children but regular care of pets should include attention to hygiene. Nurses and midwives can help to educate the public about worms and their advice can help prevent toxocara infections.

Adult↗
PubMed2000

The diversity of parasites.

Parasitism is one of the most successful modes of life displayed by living organisms, as measured by how often it evolved and how many parasitic species are presently in existence. Studying the diversity of parasites is particularly relevant because sympatric diversification may be important in some parasite taxa, and because of the opportunity for independent tests of evolutionary hypotheses in the many separate lineages in which parasitism evolved. Our incomplete knowledge of existing parasite species--the result of a range of phenomena that includes inadequate sampling effort or the lumping of different cryptic species under one name--is not always a major obstacle for the study of parasite diversity. Patterns in the diversity of parasites may be associated with either host or parasite characteristics. The distribution of parasite diversity among host taxa does not simply reflect the species diversity of the host taxa themselves; life history and ecological traits of hosts appear to play important roles. These may determine the likelihood that hosts are colonized by parasite species over evolutionary time. It is not yet clear whether some host traits also favor intrahost speciation and diversification of parasites, and the formation of new parasite species. Certain features of parasites may also be associated with speciation and diversification. Only parasite body size has received much attention; the patterns observed are not greatly different from those of free-living species, with small-bodied parasite taxa being more speciose than related large-bodied taxa. Epidemiological parameters such as the basic reproductive rate of parasites, or R0, can also generate predictions regarding the distribution or evolution of parasite diversity. For instance, parasite taxa characterized by high R0 values may be more speciose than related taxa with lower values of R0; such predictions remain untested. Large-scale biogeographical patterns of diversity have only been well studied for metazoan parasites of marine fish; for these parasites, latitudinal patterns can be explained by effects of temperature on speciation rates and epidemiological variables, though other causes are possible. The emphasis for future research must shift from pattern description to the elucidation of the processes responsible for the structure and diversity of parasite faunas. A better integration of ecological and historical (or phylogenetic) approaches to the study of parasite diversity should make this objective possible.

Animals↗
PubMed2003

Can animals use foraging behaviour to combat parasites?

Host-parasite interactions are often seen as an arms race, with parasites attempting to overcome host resistance to infection. Herbivory is a common route of transmission of parasites that represents the most pervasive challenge to mammalian growth and reproduction. The present paper reviews the foraging skills of mammalian herbivores in relation to their ability to exploit plant properties to combat parasites. The starting point is that foraging behaviour may ameliorate the impact of parasitism in three ways; hosts could: (1) avoid foraging in areas contaminated with parasites; (2) select diets which increase their resistance to parasites; (3) select for foods containing anti-parasitic properties (self-medication). Details are given of the pre-requisite skills needed by herbivores if they are to combat parasitism via behaviour, i.e. herbivores are able to: (a) determine their parasitic state and alter their behaviour in relation to that state (behaviours 1, 2 and 3); (b) determine the environmental distribution of parasites (behaviour 1); (c) distinguish plant species or plant parts that increase their resistance to parasites (behaviour 2) or have anti-parasitic properties (behaviour 3). Mammalian herbivores cannot detect the presence of the parasites themselves and must rely on cues such as faeces. Despite the use of these cues contacting parasites may be inevitable and so mechanisms to combat parasitism are necessary. Mammalian herbivores have the foraging skills needed to exploit the heterogeneous distributions of nutrients and parasites in complex foraging environments in order to avoid, and increase their resistance to, parasites. Current evidence for the use of plant secondary metabolites (PSM) by herbivores for self-medication purposes remains equivocal. PSM have both positive (anti-parasitic) and negative (toxic) effects on herbivores. Here details are given of an experimental approach using tri-trophic (plant-herbivore-parasite) interactions that could be used to demonstrate self-medication in animals. There is strong evidence suggesting that herbivore hosts have developed the foraging skills needed to take advantage of plant properties to combat parasites and thus use behaviour as a weapon in the host-parasite arms race.

Animal Feed↗
PubMedDate not supplied

[Seasonal dynamics of the component community structure of parasites of the minnow Phoxinus phoxinus (L.)].

The material represented by 75 specimens of minnow of the age 2-2(+) was collected according to the standard technique in the Chovju River (tributary of the Vychegda River, a region of the settlement Nizniy Chov, district of Syktyvkar town) during the period June-September 2000. The quantitative estimation of the structure of the component parasite communities was performed by calculating errors of the equation of regression for each species group separately, with subsequent summarizing of means of errors by all parasite groups comprising the community (Dorovskikh, 2001 6; 2002 B). In order to have a possibility to get data complementing each other, the calculation of variety indexes and other indexes have been made for metazoan parasites only and for the whole community, including the protozoan parasites. In both cases, i.e. considering only metazoan parasites and the whole composition of parasite species, three states of the component parasite community have been recognised: the formed community (June), the community in destroying (July and August), the community in the process of formation (September). In the course of working on the total species composition we recorded the beginning of community destroying on 30th of June, and the beginning of community formation in August. Considering only the metazoan parasites, the community is defined (after: Pugachev, 1999) as the mature (balanced) one in June, while in July, August and September, it was unmature (off-balance) by its characteristics. Regarding the protozoan parasites, the community in June, August and September was characterized as the mature one based on indices of parasite biomass, and as unripe one based on the number of parasite individuals; however in July, both groups of indices allowed to refer it to the unripe state. However, these unripe states are essentially different. In July, it is the result of dieing out the parasites of the past generation; in August and September, it is the result of the appearances of new generations. Therefore we recognise three states of parasite community named above. Considering the whole species composition of parasites we noted the greater difference of index values based on the parasite specimen numbers and their conventional biomass, that was in the case of the metazoan parasites only. It is particularly noticeable in the middle of the June, in the period of the formed community. This fact, together with high errors of the equations of regression and the presence of the high number of Apiosoma, points to the disturbance in the structure of component parasite community in the minnow from the Chovju River. This is easily explicable, because the Chovju River is the polluted reservoir, and pollution comes from agricultural fields, Verhny-Chov settlement, pigsties and cow-sheds. The pollution is a seasonal factor here. The most powerful pollution was noted at May-June, and then it decreased along the beginning of rains in the end of August; in September it increased again. It is important to point out that the monitoring of the metazoan parasites only allows to reveal the general dynamics of the community during the period of observation, but does not allow to catch the beginning of its destroying and developing and to notice possible disturbances in the community structure caused by pollution of reservoirs, particularly, if this pollution is a seasonal factor as in the Chovju River. Three named states of the component community of the fish parasites take place in other periods of year than this observed in the intestional parasite communities of fish helminths of the temperate climate zone. The developing of parasite communities of the intestinal helminths of the Anguilla anguilla in England (Kennedy, 1997) and of Leuciscus idus from the Rybinsk reservoir (Zhohov, 2003) starts in the beginning of summer. In May, their species diversity is minimal and in August is maximal. In conditions of the middle stream of the Vychegda River, the species diversity of parasite community associated with the minnow is maximal in June and minimal in August, when it only begins developing.

Animals↗
PubMed2002

Ecology and biogeography of marine parasites.

A review is given of (mainly recent) work on the biodiversity, ecology, biogeography and practical importance of marine parasites. Problems in estimating species numbers have been thoroughly discussed for free-living species, and the main points of these discussions are reviewed here. Even rough estimates of the richness of most parasite groups in the oceans are premature for the following reasons: species numbers of host groups, in particular in the deep sea and the meiofauna, are not known; most host groups have been examined only insufficiently for parasites or not at all; even in some of the best known groups, latitudinal, longitudinal and depth gradients in species richness are only poorly understood or not known at all; effects of hosts on parasite morphology and geographical variation have been studied only in a few cases; there are few studies using techniques of molecular biology to distinguish sibling species. Estimates of species richness in the best known groups, trematodes, monogeneans and copepods of marine fishes, are given. Parasites are found in almost all taxa of eukaryotes, but most parasitic species are concentrated in a few taxa. Important aspects of the ecology of marine parasites are discussed. It is emphasized that host specificity and host ranges should be distinguished, and an index that permits calculation of host specificity is discussed. The same index can be applied to measure site specificity. Central problems in ecology are the importance of interspecific competition and whether equilibrium or non-equilibrium conditions prevail. Marine parasites are among the few groups of organisms that have been extensively examined in this regard. A holistic approach, i.e. application of many methods, has unambiguously shown that metazoan ecto- (and probably endo-) parasites of marine fish live in largely non-saturated niche space under non-equilibrium conditions, i.e. they live in assemblages rather than in communities structured by competition. Nestedness occurs in such assemblages, but it can be explained by characteristics of the species themselves. There is little agreement on which other factors are involved in "structuring" parasite assemblages. Few studies on metapopulations of marine parasites have been made. A new approach, that of fuzzy chaos modelling, is discussed. It is likely that marine parasites are commonly found in metapopulations consisting of many subpopulations, and they are ideally suited to test the predictions of fuzzy chaos. Some recent studies on functional ecology and morphology--especially with regard to host, site and mate finding--are discussed, and attention is drawn to the amazing variety of sensory receptors in some marine parasites. Effects of parasites on hosts, and some studies on the evolution and speciation of marine parasites are discussed as well. A detailed overview of biogeographical studies is given, with respect to latitudinal gradients in species diversity, reproductive strategies and host ranges/specificity. Studies of marine parasites have contributed significantly to giving a non-equilibrium explanation for latitudinal diversity gradients. Recent studies on longitudinal and depth gradients are discussed, as well as parasites in brackish water, parasites as indicators of zoogeographical regions and barriers, and parasites as biological tags. The practical importance of marine parasites in mariculture, as monitors of pollution, agents of human disease, the use of parasites for controlling introduced marine pests, and some related aspects, are also discussed.

Animals↗
PubMedDate not supplied

[Parasite communities and a fish spawn].

High values of dominance index, low values of evenness and Shannon index are characteristic of component parasite communities of prespawning (Prosopium cylindraceum) and spawn migratory fishes (Coregonus autumnalis, Oncorhynchus nerka). Autogenic specialists are dominant in the component parasite communities of C. autumnalis. The component parasite communities of P. cylindraceum and O. nerka are dominant in a content of generalist species. The O. nerka parasite communities are communities "sentenced to death". Low values of dominance index, high values of evenness abd Shannon index are peculiar to component parasite communities of prespawning and spawning cyprinid fishes (Phoxinus phoxinus, Oreoleuciscus humilis). Autogenic specialists are dominant. Increase of dominance index and decrease of two other indexes characterize the postspawning period. The same tendency characterises infracommunities. Thus, the component parasite communities respond differently to the fish spawn of the cyprinid and coregonid/salmonid fishes. Similarity is in the dominance of autogenic specialists in one case only (C. autumnalis). These differences are defined by the mode of fish stock formation for spawn. The cyprinids congregate for spawning and move apart for foraging and vice versa is observed in the coregonids and salmonids. Autogenic specialists dominance seems to be the important adaptation to reduce a negative effect to host during spawning. Bush and Kennedy in 1994 established that "parasites live in patches (host individuals) and fragments (host populations)". They consider the host fragmentation as "hedging your bets against extinction" due to frequency and magnitude anthropogenic factors, which increase fragmenting of host populations. This conclusion was made for a species level. From the other hand the fragmentation is a natural feature for a single host population too. Such fragmentation is a host population structure. The role of fragmentation is obvious from the data on component parasite communities during fish spawn. The fragmentation decreases in the cyprinids and increases in the salmonids that leads to the growing of the cyprinid component parasite communities diversity and to declining the salmonid component parasite communities diversity. Nevertheless the role of host population structure in a component parsite community structure is not obvious, because parasites are able or not able to "recognise" different host subpopulation groups. It is well known from data on parasite species population biology. Such recognizable subpopulation groups or groups can be a "real fragment" for the parasite community. The question is what parameters could be used for this purpose on a component community level. Host population age structure can be used as an example, because the age groups are one of the invariable population characters. Value of Shannon index for component parasite communities of spawn migratory O. nerka (5+) is similar to that of fishes of 1+ age. Difference is statistically insignificant. It is insignificant between the parasite communities of 2+ and 3+ age groups too. Fishes of these two groups could be defined as a real united fragment. It spite of similarity between the fishes of 5+ age group and fish of 1+ age group they are not united fragment. The parasite community of 1+ age fishes is not stabilized yet and one of 5+ age is a community "sentenced to death". Thus the structuring of O. nerka freshwater parasite communities are defined by 3 real host age fragments: 1+ age group, 2 and 3+ age group, 4+ age group. It looks as that Shannon index is suitable parameter to study a parasite communities structure.

Age Factors↗
PubMed2005

Nutrition interacts with parasitism to influence growth and physiology of the insect Manduca sexta L.

The influence and interaction of dietary protein:carbohydrate balance and parasitism by Cotesia congregata on nutrient intake and growth were examined over the last two larval stadia of Manduca sexta. Effects of nutritional status on host blood metabolite concentrations were also determined. Six fat-free chemically defined diets were tested, each having the same total level of casein and sucrose, but with casein to sucrose ratios varying from low protein/high carbohydrate to equal levels of both nutrients through to high protein/no carbohydrate. Nutrient ratio and parasitism each affected nutrient consumption and growth. Feeding responses differed between normal and parasitized larvae, as illustrated by nutrient arrays, two-dimensional plots of protein and carbohydrate consumption on diets having different nutrient ratios. Normal larvae consumed more nutrients and took longer to develop as dietary nutrient ratio was displaced from equal levels of both nutrients. Except on the diet having the same amount of protein and carbohydrate, parasitized larvae consumed less nutrients than normal larvae, although on all diets parasitized larvae took longer to develop. When the contribution of parasite biomass was excluded, parasitized larvae showed lower mass gain than normal larvae on all diets. Total mass gain by normal and parasitized larvae with parasite biomass included, however, was similar on diets having intermediate nutrient ratios. Differences in mass gain between diets relative to nutrient consumption were evident from multi-dimensional representations of mass gain with protein and carbohydrate consumption. Three-dimensional plots and contour maps of normal and parasitized larvae were different. When differences in nutrient consumption between diets were taken into account, protein consumption had a greater effect on growth than carbohydrate consumption and normal larvae generally displayed greater mass gain than parasitized larvae on the same diets. Utilization efficiency, the efficiency of conversion of ingested food to body mass, was, therefore, generally reduced in parasitized insects. Concentrations of blood protein, total free amino acids and trehalose were each influenced by dietary nutrient ratio and parasitism. Concentrations of protein and free amino acids generally increased and trehalose concentration decreased as dietary protein increased and carbohydrate decreased. The opposite was the case as dietary carbohydrate increased and protein decreased. Dietary nutrient ratio, however, affected normal and parasitized larvae differently. Parasitized larvae had higher overall trehalose concentrations while normal larvae had higher protein and total free amino acid concentrations. When differences in nutrient consumption between diets were accounted for, protein consumption had a greater effect on blood protein and free amino acid concentrations than did dietary nutrient ratio or parasitism. Protein consumption, however, did not affect trehalose concentration. Carbohydrate consumption had no effect on the concentration of any of the metabolites after differences in nutrient consumption were taken into account. Effects of nutrient consumption on trehalose concentration, therefore, were due to dietary nutrient ratio and parasitism. The potential relevance of the above findings to the biology of parasitized M. sexta larvae is discussed.

Amino Acids↗