Academic literature on the topic 'Zoogonidae'

The Zoogonidae is the only digenean family where known cercariae lack the tail but actively search for the second intermediate host. However, the data on the zoogonid life cycles are scarce. In the present study, we elucidated and verified life cycles of the Zoogonidae from the White Sea. Using rDNA data, we showed that Pseudozoogonoides subaequiporus utilizes gastropods from the family Buccinidae as the first intermediate host and protobranch bivalves as the second one. This life cycle can be facultatively truncated: some cercariae of P. subaequiporus encyst within the daughter sporocysts. Molecular data also confirmed previous hypotheses on Zoogonoides viviapus life cycle with buccinid gastropods acting as the first intermediate hosts, and annelids and bivalves as the second intermediate hosts. We demonstrated the presence of short tail primordium in the developing cercariae of both species. Based on the reviewed and our own data, we hypothesize that the emergence of tailless cercariae in the evolution of the Zoogonidae is linked to the switch to non-arthropod second intermediate hosts, and that it possibly happened only in the subfamily Zoogoninae. Basally branching zoogonids have retained the ancestral second intermediate host and might have also retained the tail.

Anarhichotrema Shimazu, 1973 is a monotypic digenean genus, with the type- and only species, Anarhichotrema ochotense Shimazu, 1973, known to infect North Pacific fishes. This genus was originally described as a member of the Lissorchiidae (Monorchioidea) and later moved to the Zoogonidae (Microphalloidea). Its exact phylogenetic position has remained unresolved due to the lack of molecular data. In this study, we isolated specimens of A. ochotense from the Bering wolffish, Anarhichas orientalis Pallas, 1814 caught in the Sea of Okhotsk, described them morphologically and performed a molecular phylogenetic analysis of their nuclear 18S and 28S rDNA regions. The specimens examined in our study generally corresponded to previous morphological descriptions of A. ochotense but were noticeably smaller, possibly due to the crowding effect. The phylogenetic analysis placed Anarhichotrema within the Lissorchiidae as a sister taxon to the group comprising freshwater lissorchiids. Thus, we restore Anarhichotrema to the Lissorchiidae, as originally assigned.

A checklist of cercariae parasitizing marine molluscs from Patagonian coast, Argentina, based on literature sources and new records here presented.In total, cercariae of 31 species of marine digeneans, including 11 new records here presented, are known to infect 20 species of molluscs (14 in nine gastropods species; 17 in 11 bivalve species). These records include two species of Aporocotylidae, four Bucephalidae, one Fellodistomidae, five Gymnophallidae, one Hemiuroidea, four Lepocreadiidae, two Microphallidae, five Monorchiidae, one Notocotylidae, one Philophthalmidae, two Renicolidae, one Schistosomatidae and two Zoogonidae. For each digenean species, their hosts, habitat type, localities, infection site, prevalence, life cycle advances, and access numbers in helminthological collections and GenBank, when available, are detailed. Regarding the life cycles, eight were completely elucidated and four were partially elucidated. Moreover, there are molecular data for 15 species. The data here presented constitutes an advance in the parasites biodiversity knowledge and their life cycles.

AbstractDiphtherostomum brusinae was first recorded by the present study in the north of Portugal. Sporocysts, containing cercariae and encysted metacercariae, were observed in the gonads and digestive gland of the gastropod Nassarius reticulatus. Metacercariae were also found infecting the foot, mantle border and gills of the cockle Cerastoderma edule. The adult form was lodged in the rectum of the definitive host Diplodus sargus. The morphology of the three parasitic stages was studied by light (LM) and scanning electron microscopy (SEM). Despite the close similarity between cercaria and metacercaria, SEM data provided information that allowed their differentiation, namely the presence of a dense crown of microvilli around the oral cavity of the cercariae, which was absent in the metacercariae. In addition, the metacercariae presented a specific pre-acetabular rectangular band with conspicuous triangular spines. The adult showed characteristics of D. brusinae species, in particular the presence of acetabular lips, compact vitellaria and large elliptical eggs. Sequenced ITS1 data clearly demonstrated that the cercariae and metacercarial cysts from N. reticulatus, the cysts from C. edule and the adult isolated from D. sargus were life cycle stages that belonged to the same species, i.e. D. brusinae. Two transmission strategies in the life cycle of this species were observed: (1) cercariae encyst within the sporocysts of N. reticulatus and await ingestion by the definitive host; and (2) N. reticulatus naturally emits cercariae; they encyst in C. edule or the environment and are ingested by the definitive host.

"The biodiversity and ecology of marine cercariae in Australia is poorly known. Although nassariid gastropods are widely distributed in Australia and are expected to have a diverse parasite fauna similar to that of other nassariids worldwide, their cercariae have not been characterised. Nassarius dorsatus, N. olivaceus and N. pullus were collected at three separate estuarine localities in central Queensland between August 2004 and August 2006 and their emergent cercariae characterised using morphological and molecular methods. Fifteen morphotypes of cercariae from six families that infect fishes and birds as definitive hosts were characterised. The highest richness was within the Acanthocolpidae (nine morphotypes) which comprised three cercariae interpreted as species of Stephanostomum and a complex of six unusual cercariae with a ventral keel. Molecular characterisation of these six cercariae supported their placement in the Acanthocolpidae and indicated that they comprised only three species, two of which displayed marked phenotypic plasticity. Molecular analysis supported the characterisation of the three species of Stephanostomum and suggested that one of the unusual cercariae was a species of Stephanostomoides. Dissection of fish from Sandy Point provided a single match; the sequence for a metacercaria in Valamugil buchanani, the blue-tail mullet, was identical to that of one of the species of Stephanostomum. There were two cercariae from the Echinostomatidae and one from each of the Lepocreadiidae, Microphallidae, Opecoelidae and Zoogonidae. Molecular analyses supported the placement of the cercariae from the Echinostomatidae, Lepocreadiidae, Opecoelidae and Zoogonidae within their respective families. The cercaria from the Lepocreadiidae was identified by comparison to known adult data and putatively corresponds to Prodistomum keyam, a parasite of Monodactylus argenteus, the silver moony or butter bream, common in the study region. Morphological analysis supported the characterisation of both of the Echinostomatidae as species of Himasthla. Although no other cercariae could be characterised to genus level, the opecoelid cercaria was determined to be in the subfamily Opecoelinae. Nassarius olivaceus was infected by three acanthocolpid cercariae and one cercaria from each of the other families. Nassarius dorsatus was infected by five acanthocolpid cercariae and one each from the Echinostomatidae and Lepocreadiidae. Nassarius pullus was infected by a single cercaria from the Echinostomatidae. Most cercariae were specific to a single species of gastropod; only four infected two species and none infected all three. Cercariae that infect fish as a definitive host were found at all three localities; but cercariae that infect birds were restricted to a single locality, Sandy Point at Corio Bay, important for domestic and migratory bird species. These results emphasise the relative significance of Sandy Point as an important bird habitat. In total, 126 infections were diagnosed (115 by cercarial emergence), with both the highest frequency of infection and number of infections in N. olivaceus (frequency 5.3%; n=102; 81% of infections), followed by N. dorsatus (1.1%; 20; 16%) and N. pullus (0.2%; 4; 3%). The highest number of infections occurred at Sandy Point (66; 52% of infections), followed by Cawarral Creek (38; 30%) and then Ross Creek (22; 17%). The highest number of infections was by the Acanthocolpidae (54; 43%). Diagnosis of infection by emergence was suitable for all cercariae except the opecoelid, which was underdiagnosed. Nassarius olivaceus had the longest survival in captivity (~4.5 y), followed by N. dorsatus (~0.8 y) and N. pullus (~0.3 y). Almost all infections remained patent for the life of the gastropod. Families commonly found in nassariids worldwide include Acanthocolpidae, Echinostomatidae, Lepocreadiidae and Zoogonidae. Nassariid gastropods are also the dominant marine first intermediate hosts for the Acanthocolpidae, Lepocreadiidae and Zoogonidae and one of the three most common first intermediate host families for species of marine Himasthla. Molecular relationships also indicate that the Acanthocolpidae and Brachycladiidae may actually be comprised of three discrete groups, the Stephanostomum + Monostephanostomum group, the Brachycladiidae, and a group of non-Stephanostomum species comprising Pleorchis, Tormopsolus and Stephanostomoides. This research adds information about the parasite assemblages of nassariid gastropods in Australia, adding 12 new cercarial species and 16 new host-parasite records. Cercarial reports for the Acanthocolpidae, Echinostomatidae, Lepocreadiidae, Opecoelidae and Zoogonidae have been comprehensively reviewed and patterns of association between nassariids and their common parasite families presented. As well, this research has provided a potential avenue for a review of the Acanthocolpidae, a family which is currently considered a ‘catch-all’ group."