Digenean parasites as novel tracers of predation on jellyfish.

Complex life cycles are a hallmark characteristic of many parasites; however, little is known about the process by which life cycles become more complex through the addition of hosts. Paratenic hosts are present in the life cycles of several phylogenetically distinct groups of helminths; this suggests that they may play a key role during this process. This study examined the development of metacercariae of Halipegus eccentricus within intermediate microcrustacean and odonate paratenic hosts. Then a comparative approach was used to evaluate how life history traits of H. eccentricus within the anuran definitive hosts differ between metacercariae of the same age that developed within an intermediate ostracod host or a paratenic odonate host. The results of this study indicate that metacercariae of H. eccentricus do not grow at the same rate in different intermediate hosts, and significant differences exist in growth within intermediate and paratenic hosts. Individuals from odonate paratenic hosts always had larger bodies and suckers than those of metacercariae of the same age that develop within microcrustacean intermediate hosts. Furthermore, metacercariae from odonates were more successful in establishing and migrating in definitive anuran hosts. Last, individuals from paratenic hosts began reproducing earlier within anuran definitive hosts than age-matched worms that develop within the intermediate hosts. Collectively these results suggest that the variation in body and sucker sizes within odonate and microcrustacean hosts may carry over to the definitive host and in the case of H. eccentricus using the paratenic host increases transmission and alters other life history traits within definitive hosts. These results indicate that using a paratenic host can affect the success of parasites in subsequent hosts, and therefore these hosts may provide benefits other than just increasing transmission by bridging an ecological gap.

Trematode life cycles involve molluscs as first intermediate hosts. The identification of trematodes based on the morphology of cercariae released from molluscs is challenging because the identification relies on adult forms obtained from their definitive hosts. Several studies have recently genetically characterized these larval forms establishing a link with adults sampled from their vertebrate hosts, allowing their identification at species level. In Los Tuxtlas tropical rainforest, in south-eastern Mexico, 57 species of trematodes have been reported from wildlife vertebrates; however, studies evaluating the diversity of trematode cercariae in molluscs are lacking. Here, we studied 11 species of molluscs to assess the diversity of cercariae in two lakes of Los Tuxtlas, Veracruz, Mexico; six of the 11 species were infected. Twelve cercarial morphotypes were collected and characterized morphologically. Sequences of the 28S ribosomal RNA gene were generated to allocate each morphotype into a family using the most recent phylogenetic classification of the Digenea as a framework; molecular work revealed 16 genetic lineages; some cercariae were identified up to genus (Apharyngostrigea, Ascocotyle, Centrocestus, Echinochasmus, Lecithodendrium and Posthodiplostomum), and some to species levels (Gorgoderina rosamondae, Langeronia macrocirra, Oligogonotylus manteri and Phyllodistomum inecoli) based on their phylogenetic position within the tree, and the genetic distance with respect to other sequenced congeners. Therefore, the cercarial morphotypes in the present study represent at least 16 putative species. Our study contributes to a better understanding of the trematode diversity in an area of high vertebrate species diversity, and to the knowledge of trematode life cycles.

Crepidula fornicata is not a first intermediate host for trematodes: who is?

The life cycles of species of Proteocephalus Weinland, 1858 (Cestoda: Proteocephalidea) parasitizing fishes in the Palearctic Region are reviewed on the basis of literary data and personal experimental observations, with special attention being paid to the development within the intermediate and definitive hosts. Planktonic crustaceans, diaptomid or cyclopid copepods (Copepoda), serve as the only intermediate hosts of all Proteocephalus species considered. A metacestode, or procercoid, develops in the body cavity of these planktonic crustaceans and the definitive host, a fish, becomes infected directly after consuming them. No previous reports of the parenteral location of metacestodes within the second intermediate host as it is in the Nearctic species P. ambloplitis have been recorded. Thus, the life cycles of Proteocephalus tapeworms resemble in their general patterns those of some pseudophyllidean cestodes such as Eubothrium or Bothriocephalus, differing from the latter in the presence of a floating eggs instead of possessing an operculate egg from which a ciliated, freely swimming larva, a coracidium, is liberated. The scolex of Proteocephalus is already formed at the stage of the procercoid within the copepod intermediate host; in this feature, proteocephalideans resemble caryophyllidean rather than pseudophyllidean cestodes. The morphology of procercoids of individual species is described with respect to the possibility of their differentiation and data on the spectrum of intermediate hosts are summarized. Procercoids of most taxa have a cercomer, which does not contain embryonic hooks in contrast to most pseudophyllidean cestodes. The role of invertebrates (alder-fly larvae-Megaloptera) and small prey fishes feeding upon plankton in the transmission of Proteocephalus tapeworms still remains unclear but these hosts are likely to occur in the life cycle. Data on the establishment of procercoids in definitive hosts, morphogenesis of tapeworms within fish hosts, and the length of the prepatent period are still scarce and new observations are needed. Whereas extensive information exists on the development of P. longicollis (syns. P. exiguus and P. neglectus), almost no data are available on the ontogeny of other taxa, in particular those occurring in brackish waters (P. gobiorum, P. tetrastomus). The morphology of P. cernuae and P. osculatus procercoids from experimentally infected intermediate hosts is described for the first time.

The complex life cycle of taeniids represents an ideal model of a multi-host system. The complexity of these parasites can therefore cover the epidemiological issues of the interface between wild and domestic animals, especially once spatial overlap between wild and domestic definitive and intermediate hosts occurs. Here we use the occurrence of Taenia ovis krabbei in two model areas as an example of this epidemiological complexity. In two contiguous areas in the Italian northern Apennines, two hunted roe deer (Capreolus capreolus) showed numerous cysticerci in the muscles of their whole body and an adult tapeworm was recorded in a semi-stray dog (Canis lupus familiaris). Through molecular typing of the mitochondrial cytochrome c oxidase I (cox1) gene, cysticerci and the adult tapeworm of T. krabbei were identified. Taenia krabbei cysticercosis was recorded for the first time in Italy. Although the role of dogs in the parasite's life cycle emerges, the overlap between wild and domestic definitive hosts and the increase of wild population densities raise concerns about the temporal (old or new) introduction and the spread of this parasite by one of these canid species (wolf (Canis lupus) or dog). Although T. krabbei is not a public health issue, economic concerns emerged for hunters and meat producers, related to the damage of carcasses by cysticerci. Therefore, there is a need to evaluate the spread of T. krabbei in the intermediate and definitive host populations, and to ensure the relevant sanitary education for hunters in order to avoid practices that could favour the spread and maintenance of its life cycle.

Trematode infection of the second intermediate hosts can lead to changes in their fitness and, as a result, a change in the invasion rate of animal communities. It is especially pronounced during the invasion of parasite species that reduce activity due to the manipulation of hosts through the changes of their morphology and physiology. One of these cases is an anomaly P syndrome hotspot found in some populations of water frogs and toads in Europe caused by the trematode Strigea robusta metacercariae. The occurrence of pathogen and their participation in ecosystems are intrigues questions in the anomaly P phenomenon, as well as the role of planorbid snails that serve as the first intermediate hosts for many trematode species. Herein, we focused on trematodes spectra from planorbid snails and amphibians from the anomaly P hosts with the aim to undetected interactions between the pathways of parasites. Emerging cercariae of 6802 planorbid snails of dominant species (Planorbarius corneus, Planorbis planorbis, and Anisus spp.) were detected by both morphological and molecular methods in seven waterbodies in Privolzhskaya Lesostep Nature Reserve (Russia). A total of 95 sequences of 18 species were received, and 48 sequences were unique and did not present in any genetic databases. The 18 species of trematodes from snails and 14 species of trematodes from amphibian hosts (Pelophylax ridibundus; Ranidae; Anura) were detected. Three species (Echinostoma nasincovae, Tylodelphys circibuteonis and Australapatemon burti) was new for the trematode fauna of the Middle Volga River region and Russia as a whole. Eleven species of parasitic flatworms have amphibians in their life cycles and nine species used amphibians as metacercariae hosts: Echinostoma nasincovae, E. miyagawai, Echinoparyphium recurvatum, Tylodelphys circibuteonis, Neodiplostomum spathula, Paralepoderma cloacicola, Macrodera longicollis, Strigea robusta, and Strigea strigis. The occurrence of trematode species from planorbid mollusks and frogs were compared.

The first record of Brachylaima ezohelicis (Trematoda: Brachylaimidae) in the red fox (Vulpes vulpes schrencki)

Of mice and worms: are co-infections with unrelated parasite strains more damaging to definitive hosts?

Links between parasites and food webs are evolutionarily ancient but dynamic: life history theory provides insights into helminth complex life cycle origins. Most adult helminths benefit by sexual reproduction in vertebrates, often high up food chains, but direct infection is commonly constrained by a trophic vacuum between free-living propagules and definitive hosts. Intermediate hosts fill this vacuum, facilitating transmission to definitive hosts. The central question concerns why sexual reproduction, and sometimes even larval growth, is suppressed in intermediate hosts, favouring growth arrest at larval maturity in intermediate hosts and reproductive suppression until transmission to definitive hosts? Increased longevity and higher growth in definitive hosts can generate selection for larger parasite body size and higher fecundity at sexual maturity. Life cycle length is increased by two evolutionary mechanisms, upward and downward incorporation, allowing simple (one-host) cycles to become complex (multihost). In downward incorporation, an intermediate host is added below the definitive host: models suggest that downward incorporation probably evolves only after ecological or evolutionary perturbations create a trophic vacuum. In upward incorporation, a new definitive host is added above the original definitive host, which subsequently becomes an intermediate host, again maintained by the trophic vacuum: theory suggests that this is plausible even under constant ecological/evolutionary conditions. The final cycle is similar irrespective of its origin (upward or downward). Insights about host incorporation are best gained by linking comparative phylogenetic analyses (describing evolutionary history) with evolutionary models (examining selective forces). Ascent of host trophic levels and evolution of optimal host taxa ranges are discussed.

ABSTRACTRoughage constitutes a fundamental component of dairy cow diets; it promotes rumen health and supports optimal animal productivity. This study applied an ANKOM gas production system to assess the in vitro fermentation characteristics of seven widely used dairy roughages (barley hay, corn silage, lucerne hay, oaten hay, ryegrass hay, timothy hay and wheaten hay) classified into relatively high and low nutritive value groups. Roughage samples representing high and low nutritive values were selected based on the upper and lower quartiles of the feed quality database. The results showed that high‐nutritive value oaten hay exhibited higher dry matter (DM) digestibility (0.50 vs. 0.24–0.43 g/g DM, p < 0.05), total gas production (87.5 vs. 15.3–81.0 mL/g DM) and total volatile fatty acid (63.2 vs. 39.3–62.5 mM) than other roughages. High‐nutritive value barley hay and oaten hay both exhibited higher methane production (7.58 and 7.77 mL/g DM, respectively) compared to other roughages (0.44–4.76 mL/g DM). Similarly, high‐nutritive value barley hay (40.23 mg/100 mL) and lucerne hay (40.76 mg/100 mL) exhibited higher ammonia nitrogen (12.16–31.99 mg/mL) than other roughages. High‐nutritive value oaten and barley hay promoted superior fermentation performance but also led to greater methane emissions, while barley and lucerne hay increased nitrogen release. These results underscore the need to balance productivity with environmental impacts when selecting roughages for dairy systems.

In nature, parasites commonly share hosts with other conspecific parasite genotypes. While adult parasites typically show aggregated distribution in their final hosts, aggregation of clonal parasite genotypes in intermediate hosts, such as those of trematodes in molluscs, is not generally known. However, infection of a host by multiple parasite genotypes has significant implications for evolution of virulence and host-parasite coevolution. Aggregated distribution of the clonal stages can increase host mortality and reduce larval output of each infecting genotype through interclonal competition, and therefore have significant implications for parasite epidemiology. The aim of this study was (i) to find out how common multiple genotype infections (MGIs) are in aquatic snails serving as intermediate hosts for different trematode species; (ii) to find out whether the prevalence of infection could be used to predict MGI frequencies and (iii) to use the relationship to infer whether MGIs aggregate in molluscan hosts. We determined the prevalence of trematode (Diplostomum pseudospathaceum) infections and the frequency of MGIs in snail (Lymnaea stagnalis) host populations as well as compiled corresponding literature data from a range of snail-trematode systems. We used Bayesian simulations to explore the relationship between prevalence of infection and MGI frequency in these data, and tested whether genotypes aggregate in snails by comparing the simulated relations with null model (Poisson and demographic Poisson) expectations. Our results show that MGIs are common in aquatic snails with up to 90% of the infected snails carrying MGIs. Parasite prevalence is a good predictor of MGI frequencies at a range of prevailing natural prevalences of infection (0-50%). The frequency of MGIs was higher than expected by both null models, indicating parasite aggregation at genotype level. These findings are in sharp contrast with the absence of multiple infections in snails at level of trematode species, suggesting that co-infections by multiple species and multiple genotypes of one species are controlled by different biological processes. Aggregation of MGIs in snail hosts appears to be widespread across different snail-trematode systems.

In most parts of the world helminth infestations are responsible for such a heavy wastage of sheep that their control has undoubtedly become one of the most important charges that devolve upon the flock-owner. It might be thought that in tropical regions suited to the raising of sheep the problem of helminth control would cease to be urgent; and that climatic conditions, the general aridity of land chosen in such countries for sheep-rearing, and its consequently smaller carrying capacity, would contribute to form an environment distinctly unfavourable both to the survival of the free-living stages of parasitic worms and to their chances of reaching a suitable intermediary or definitive host. Such areas are not usually well watered, and it certainly does result from the paucity of permanent streams and standing water that few species of trematodes are represented. Those species that do occur, e.g. Fasciola hepatica, F. gigantica, are restricted to particular localities and are easily subjected to control.

BackgroundFlavonoids, despite having low nutritional value, have numerous biological activities and extremely beneficial health effects. This study investigated the anticancer activity of rutin in human glioma CHME cells.MethodsCytotoxicity was determined through the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Protein expression was determined through Western blotting. Apoptosis was detected using annexin V/propidium iodide (PI) and fluorescence microscopy.ResultsRutin induced maximum cytotoxicity in CHME cells, as revealed through MTT assays. Cell death induced by rutin was due to apoptosis via P53 up-regulation. Rutin induced nuclear condensation, fragmentation, and membrane blebbing, as determined through 4',6-diamidino-2-phenylindole (DAPI) staining. Furthermore, rutin increased reactive oxygen species (ROS) levels and caused a loss of mitochondrial membrane potential, activating the intrinsic apoptotic pathway in CHME cells. The induction of apoptosis by rutin was further confirmed by the release of cytochrome c, up-regulation of BAX, and down-regulation of BCL, activated caspase 9, and caspase 3. The knockdown of P53 reversed rutin-induced apoptosis in a concentration-dependent manner.ConclusionsRutin plays an important role in the induction of apoptosis in CHME cells. Based on these data, rutin should be further investigated as an anticancer agent in human glioma CHME cells.

SUMMARYThere are two ways in which trematodes can be used in the control of other trematodes which transmit diseases of medical or veterinary importance. Either they can interfere with the reproductive capacity of the host species of snails, or they can exert an antagonistic effect against the larval stages of the target trematode species inside the snail. Often the two effects act together.There are six essential criteria for the selection of a suitable species of snail for control: (1) complete and permanent sterilizing effect; (2) clear dominance over target trematodes; (3) strong infectivity to molluscs of all ages; (4) high egg productivity in the definitive host; (5) lack of pathogenicity towards man and domestic animals; (6) ease and low cost of maintenance of the life-cycle.Various field trials are discussed and it is considered that trematode species producing rediae are usually dominant over those producing only sporocysts (such as the schistosomes). Most species used in control trials to date have belonged to the family Echinostomatidae as they have rediae, and eggs that can be produced in large numbers in a laboratory host such as the rat.The mathematical basis and feasibility of control schemes are discussed and it is concluded that much more information is necessary before their potential can be evaluated.

Dicrocoelium dendriticum, commonly known as the Lancet liver fluke, is endemic in the Old World since prehistoric times (Le Bailly and Bouchet, 2010).