The nematode Rhabdochona anguillae Spaul, 1927, a specific intestinal parasite of the European eel, Anguilla anguilla (L.), is redescribed and illustrated from specimens collected from eels of the Sousa River, northern Portugal (prevalence 20%, intensity 2-13). The species is characterized by the presence of 14 anterior teeth in the prostom, small non-bifurcate deirids, absence of lateral preanal papillae, by the length (0.460-0.660 and 0.130-0.150 mm) and the shape of spicules, fairly large (0.041-0.054 x 0.025-0.030 mm) mature eggs without filaments, and by the bluntly pointed to rounded tip of the tail. Its morphological features are discussed in relation to other congeneric species. This nematode has hitherto been recorded only from eels in southern Europe (Portugal, Spain, Bulgaria).
Ascaridoid nematodes referable to Brevimulticaecum heterotis (Petter, Vassiliadès et Marchand, 1979) Khalil, 1984 were recorded from the intestine of the African bonytongue, Heterotis niloticus (Cuvier) (Arapaimidae, Osteoglossiformes), from the Mare Simenti in the Niokolo Koba National Park, East Senegal and from Kosti, Sudan. Their examination using light microscopy and for the first time both environmental scanning electron microscopy and scanning electron microscopy revealed some previously unreported morphological features and made possible a detailed redescription of this species. The most important finding is the presence of dentigerous ridges on the inner edges of the lips, which confirms the attribution of this species to Multicaecum Baylis, 1923, where it was originally placed, and not to Brevimulticaecum Mozgovoy in Skryabin, Shikhobalova et Mozgovoy, 1951 where it had subsequently been transferred. A key to Brevimulticaecum and Multicaecum species is provided. Multicaecum heterotis is the first species of the genus to be sequenced. Partial sequences of the small ribosomal subunit (18S) and internal transcribed spacer 2 region (ITS2) of nuclear ribosomal DNA (rDNA) have been analysed and compared with other nematode species.
Rhabdias kongmongthaensis sp. n. is described based on specimens found in the lungs of the tree frog Polypedates leucomystax (Gravenhorst) (Amphibia: Rhacophoridae) from Kanchanaburi Province, western Thailand. The new species is similar to two North-American species, Rhabdias ranae and R. americanus, by presence of two lateral pseudolabia, each with two inner submedian protuberances. R. kongmongthaensis differs from both species by relative length and shape of the tail, and by its distribution and host specificity. Presence of lateral pseudolabia distinguishes the new species from the geographically closest Rhabdias species as well as from those parasitizing other rhacophorid frogs.
A new nematode, Rhabdochona mexicana sp. n., is described based on specimens recovered from the intestine of two species of fishes, Astyanax mexicanus (De Filippi) (type host) and Astyanax J'asciatus (Cuvier) (Characidae: Characiformes) in central Mexico. This species is characterised by the following characters: 10 anteriorly directed teeth in the prostom, a larger (left) spicule which is slender in form with a small bifurcation at its distal tip covered by a culicular membrane, a smaller (right) spicule without a barb at its distal tip, eggs bearing an irregular flock-like coaling, and a conical tail without a cuticular spike (in both sexes).
External morphology of the nematode Pterygodermatites bovieri (Blanchard, 1886), a very rare parasite of bats in the Palaearctic region, was studied by scanning electron microscopy. Special attention was paid to the cephalic end structure and cutieular armament, which are of great systematic importance in this group of nematodes. The mouth opening of P. bovieri is subterminal and oriented dorsally. Numerous sclerotized denticles, arranged in two rows, are situated in the buccal cavity around the mouth opening. They are better developed in its ventral part. In females there are 12-14 ventral denticles. Cephalic papillae are arranged in two rows: internal (six papillae - two dorsal, two lateral and two ventral) and external (four papillae). Amphids are small, situated close to lateral cephalic papillae of the internal row. Males possess 40-41 cutieular combs in each ventro-lat-eral plate row, and, in addition, a short row of four ventral, unpaired precloacal fans. Females in our material possessed 68 cu-ticular elements represented by combs and spines, in each row. Changes of the cutieular elements shape along the nematode body length are described. Results of SEM observations are compared with previous descriptions of P. bovieri based on the light microscopical observations.
The seasonal changes of the nematode Camallanus anabantis Pearse, 1933, in the climbing perch (Anabas testudineus) from the freshwater swamps near Kalyani town, West Bengal, India were studied during the period from February 1988 to August 1989. The nematode exhibited a one-year cycle. Larvated females occurred in the fishes from October to February at a water temperature of 12“-29 °C. New infection of fishes occurred from February to May and occasionally in September. The fourth-stage larvae, the males, and the young females (without eggs), although irregularly, were found present throughout the year. Egg-laden females occurred in the fishes in August, October to February, and March.
About 300 species belonging to four superfamilies (Gnathostomatoidea, Habronematoidea, Physalopteroidea and Thelazioidea) of the nematode suborder Spirurina are known as the adult parasites of freshwater, brackish-water and marine fishes. They are placed in four families, of which the Gnathostomatidae, including Echinocephalus with a few species and the monotypic Metaleptus, are parasites of elasmobranchs, whereas Ancyracanthus contains one species in teleosts; the Physalopteridae is represented in fish by four genera, Bulbocephalus, Heliconema, Paraleptus and Proleptus, each with several species in both elasmobranchs and teleosts. The majority of fish spirurines belongs to the Rhabdochonidae, which includes 10 genera (Beaninema, Fellicola, Hepatinema, Heptochona, Johnstonmawsonia, Megachona, Pancreatonema, Prosungulonema, Rhabdochona and Vasorhabdochona) of species parasitizing mainly teleosts, rarely elasmobranchs, and the Cystidicolidae with about 23 genera (Ascarophis, Caballeronema, Capillospirura, Comephoronema, Crenatobronema, Cristitectus, Ctenascarophis, Cyclozone, Cystidicola, Cystidicoloides, Johnstonmawsonoides, Metabronema, Moravecnema, Neoascarophis, Parascarophis, Prospinitectus, Pseudascarophis, Pseudoproleptus, Salvelinema, Similascarophis, Spinitectoides, Spinitectus, Sterliadochona), with many species parasitic in teleosts only. Because of difficulties in studying fish spirurines, associated with their morphological and biological peculiarities, most species of these parasites are poorly known. It is apparent that their present classification system does not reflect phylogenetic relationships and a taxonomic revision of this nematode group, based on detailed morphological (including SEM and TEM), life history and molecular studies of individual species, is quite necessary. In Cystidicolidae, several genera have been based on details in the cephalic structures visible only with the aid of SEM, but it will be evident whether or not these tiny features are of generic importance only when more cystidicolids are described using SEM and comparative molecular data become available. Data on the biology of fish spirurines are scarce. In known cases, their life cycles involve aquatic arthropods (crustaceans or insects) as intermediate hosts, in which, sometimes, the larvae undergo a precocious development and may even attain adulthood and become gravid in these invertebrates; sometimes, fish paratenic hosts are known to occur in cystidicolids parasitizing as adults piscivorous definitive hosts. Some spirurine species are pathogenic and are known as causative agents of serious fish diseases. and Consequently, further detailed studies on fish spirurines are significant not only from the theoretical viewpoint, but they may also have practical implications.
The nematode superfamily Dracunculoidea includes 166 recognized species, of which 150 (90%) are parasitic in about 300 species of freshwater, brackish-water and marine fishes. Fish dracunculoids are placed in 31 genera (86% of all dracunculoid genera) belonging to eight of the nine dracunculoid families: Anguillicolidae, Daniconematidae, Guyanemidae, Lucionematidae, Micropleuridae, Philometridae, Skrjabillanidae, and Tetanonematidae; the genus Lockenloia is considered incertae sedis. Because of difficulties in studying fish dracunculoids, associated with their morphological and biological peculiarities, most species of these largely histozoic parasites are poorly known and males of the majority of species and of eight genera have not yet been discovered. It is apparent that the present classification system of dracunculoids as a whole does not reflect phylogenetic relationships and a taxonomic revision of this nematode group, based on detailed morphological (including SEM and TEM), life history and molecular studies of individual species, is quite necessary. Data on the biology of fish dracunculoids is scarce. In known cases, their life cycles involve copepods, ostracods or branchiurids as intermediate hosts and, sometimes, fish paratenic hosts are known to occur in dracunculoid species parasitizing as adults piscivorous definitive hosts. However, nothing is known about the life cycles of representatives of 20 genera. Some species of dracunculoids, particularly of philometrids, are highly pathogenic and are known as agents of serious fish diseases. During recent years, especially the importance of Philometra spp. parasitizing the gonads of many species of marine fishes has increased due in particular to the rapid development of marine aquaculture, because they may significantly decrease fish reproduction or even cause full parasitic castration. Therefore, further detailed studies on fish dracunculoids are significant not only from the theoretical viewpoint, but they may also have practical implications.
Three species of planktonie crustaceans, Cyclops strenuus and Macrocyclops alhidus (Copcpoda) and Notodromas monacha (Ostracoda), were experimentally infected with the eggs and second-stage larvae of the swimbladder nematode Anguillicola crassus originating from eels from Neusiedler Lake in Austria. At 20-22°C, third-stage larvae of the parasite developed in all these invertebrate hosts within 16-20 days p.i. Ostracods harbouring the nematode third-stage larvae (33 days p.i.) were fed to small eels (Anguilla anguilla), while infected copepods (20 days p.i.) to seven other fish species. By these experiments, the larvae from ostracods proved to be infective for the definitive host and the ostracod was thus confirmed as a true intermediate host of Anguillicola crassus. Notodromas monacha represents a new experimental intermediate host of A. crassus and the second known invertebrate other than a copepod in which the larval development of this nematode up to the infective stage takes place. Five species of fish, cyprinids Tinca tinea, Alhumus alburnus, Gobio gobio and Albumoides bipunctatus (the latter representing a new host record), and guppy, Poecilia reticulata, were found to serve as experimental paratenic hosts for A. crassus, in which the live nematode infective larvae were recorded 49 days p.i.
The development of the nematode Anguillicola crassus, a swimbladder parasite of eels, was experimentally studied in copepod intermediate hosts Cyclops strenuus and Acanthocyclops vernalis. The copepods, kept at a laboratory temperature of 20-22 °C, were infected with nematode second-stage larvae; the second moult of larvae (the only one in the intermediate host) was observed to start 10 days p,i„ but third-stage larvae liberated from their cuticular sheath were first observed 20 days p.i. These proved to be infective for experimental eels. Free second-stage larvae as well as larvae from copepods were described. The morphology of A. crassus larvae and the mode of their development in the intermediate host were compared with those of other dracunculoid nematodes. From this point of view, Anguillicola members appear to represent an ancient group of dracunculoid nematodes.