Members of the Philometridae represent the most important group of dracunculoid nematodes parasitizing fishes. In his monograph treating the Dracunculoidea, Moravec (2006) reported a total of 11 genera and 105 species of philometrids parasitizing freshwater, brackish-water and marine fishes. However, during the last six years (2007-2012), an additional 42 new species of Philometridae have been described, representing a 40% increase of the number of nominal species. Most of these species (30) belong to Philometra Costa, 1845, mainly represented by parasites of marine fishes, a few others (8) to Philometroides Yamaguti, 1935, and a single one to each of the following genera: Caranginema Moravec, Montoya-Mendoza et Salgado-Maldonado, 2008, Dentiphilometra Moravec et Wang, 2002, Dentirumai Quiazon et Moravec, 2013* and Spirophilometra Parukhin, 1971. Moreover, three new genera, Afrophilometra Moravec, Charo-Karisa et Jirků, 2009, Caranginema and Dentirumai, were erected. Representatives of seven genera, Afrophilometra, Buckleyella Rasheed, 1963, Caranginema, Dentiphilometra, Dentirumai, Paraphilometroides Moravec et Shaharom-Harrison, 1989 and Rumai Travassos, 1960, were studied using scanning electron microscopy (SEM) for the first time. Thirteen known but poorly described philometrid species were redescribed and, in some species of Caranginema and Philometra, previously unknown conspecific males were discovered and described. The male surface ultrastructure studied by SEM provided new taxonomically important features for species distinction. Gene sequencing was used in several recent studies and advanced our understanding of phylogenetic interrelationships among representatives of seven genera (Afrophilometra, Alinema Rasheed, 1963, Caranginema, Nilonema Khalil, 1960, Philometra, Philometroides and Rumai) and of the extent of the biodiversity of philometrids. New data were obtained on the biology and pathogenicity of several species of Nilonema, Philometra, Philometroides and Rumai. The need to carry out surveys in order to find males and to use SEM and gene sequencing to identify philometrids is emphasized. Appropriate quantitative methods to determine the impact of philometrids in ovarian tissue on host fecundity are recommended. Further detailed studies on philometrids would be significant not only from the theoretical viewpoint, but also because of their practical implications. A list of philometrid nematode species by continents is provided.
The larval development of the nematode Contracaecum rudolphii (Rudolphi, 1819), a common parasite of the proventriculus of cormorants, was experimentally studied. Within the eggs cultivated in freshwater under laboratory temperatures of 20-22 °C, the developing larva undergoes two moults on days 4-5, attaining the third larval stage. Most of the ensheathed third-stage larvae, 291-457 µm long, hatch spontaneously from egg shells on days 5-6. Experiments have indicated that hatched ensheated third-stage larvae and those still inside egg capsules are already infective to copepods and fishes, which both can be considered paratenic (metaparatenic) hosts. Five copepod species, Acanthocyclops vernalis, Cyclops strenuus, Ectocyclops phaleratus, Eucyclops serrulatus and Megacyclops viridis, the isopod Asellus aquaticus and small carps Cyprinus carpio were infected by feeding them these larvae. In addition, 9 fish species, Alburnoides bipunctatus, Anguilla anguilla, Barbatula barbatula, Cyprinus carpio, Gobio gobio, Perca fluviatilis, Phoxinus phoxinus, Poecilia reticulata and Tinca tinca, were successfully infected by feeding them copepods previously infected with C. rudolphii third-stage larvae. In fishes, larvae from copepods penetrate through the intestinal wall to the body cavity, where, in a few weeks, they become encapsulated; the larvae substantially grow in fish, attaining the body length up to 4.87 mm. In carp fry, the nematode third-stage larvae survived for about 15 months (up to 18 months in fish infected directly, i.e., without copepods). One small cormorant (Phalacrocorax carbo sinensis) was successfully infected by feeding it with copepods harbouring C. rudolphii third-stage larvae.
A new species of trichosomoidid nematode, Huffmanela paronai sp. n., is established on the basis of its egg morphology and biological characters. The dark-shcllcd, cmbryonatcd eggs of this histozoic parasite occur in masses in the epidermis of the swordfish Xiphias gladius L. (Xiphiidae, Perciformes) from the Ligurian Sea in northern Italy. The eggs are concentrated in groups appearing as black spots in the skin of the fish host, being distributed mainly on the lower part of its body (lower jaw, gill covers, pectoral, anal and caudal fins, lower half of body). The parasite’s eggs are characterised mainly by their shape and markedly small size (48-51 x 21-24 pm), an aspinose surface, relatively small polar plugs, and thick egg wall (3 pm). This is the first Huffmanela species reported from fish in Europe.
Two little-known species of Spinitectus (Nematoda: Cystidicolidae) were, for the first time, recorded from fishes of the Lacantún River (Usumacinta River basin) in the Lacandon rain forest, Chiapas, southern Mexico: S. tabascoensis Moravec, García-Magaña et Salgado-Maldonado, 2002 in intestines of Ictalurus furcatus (Valenciennes) (Ictaluridae) (adults and juveniles), Cathorops aguadulce (Meek) and Potamarius nelsoni (Evermann et Goldsborough) (both Ariidae) (in both only juveniles), and S. osorioi Choudhury et Pérez-Ponce de León, 2001 in Atherinella alvarezi (Díaz-Pardo) (Atherinopsidae) (adults in intestine) and Eugerres mexicanus (Steindachner) (Gerreidae) (adults and juveniles in stomach). Eugerres mexicanus, C. aguadulce and P. nelsoni represent new host records. Detailed light and electron microscopical studies of S. tabascoensis revealed some taxonomically important, previously not observed features, such as cuticular spines arranged in four sectors, the cephalic structure, the number (2) of ventral precloacal ridges or the structure of the male caudal end. Therefore, Spinitectus tabascoensis is redescribed. Spinitectus macrospinosus Choudhury et Perryman, 2003, described from ictalurids in Canada and the USA, is considered its junior synonym. Spinitectus tabascoensis seems to be a specific parasite of Ictalurus spp., whereas C. aguadulce and P. nelsoni, as well as some other fishes, serve only as its paratenic hosts. The definitive hosts of S. osorioi are atherinopsid fish (A. alvarezi, Chirostoma spp.), whereas the gerreid E. mexicanus probably serves only as its postcyclic host.
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.
The present paper comprises a systematic survey of nematodes found in 88 specimens of 24 species of freshwater fishes in Venezuela in 1992 and 1994. The following 13 species of nematodes were recorded: Adults: Guyanema longispiculum Moravec, Prouza et Royero, 1996, Guyunema sp., Procamallanus (Spiracamallanus) inupinatus Travassos, Artigas et Pereira, 1928, P. (S.) krameri (Petter, 1974) comb, n., P. (S.) pintoi (Kohn et Fernandes, 1988) comb, n., Procamallanus (Spiracamallanus) sp., Ruphidascaris (Sprentascaris) mahnerti (Petter et Cassone, 1984). Larvae: Anisakidae gen. sp., Brevimullicaecum sp., Ctmtracaecum sp. Type 1, Contracaecum sp. Type 2, Contracaecum sp. Type 3, Eustrongylides sp. All these parasites are reported from Venezuela for the first time and all findings represent new host records. Brevimulticae-cum larvae are reported from fishes for the first time. Almost all parasites are briefly described and illustrated and problems concerning their morphology, taxonomy, hosts and geographical distribution are discussed. A new name, Terranova diazungriai nom. nov. is proposed for T. caballeroi Diaz-Ungrfa, 1968 (a junior homonym of T. caballeroi Baruš et Coy Otero, 1966).
Based on the original description, the nematode genus Piscinema Gambhir et Ng, 2014 and its type species, P. barakensis [sic] Gambhir et Ng, 2014 (probably a misidentified physalopterid larvae), are removed from the Philometridae, where they were allocated; they are considered a genus inquirendum and incertae sedis and a species inquirenda, respectively. The poorly described nematode Rhabdochona carpiae Nimbalkar, Deolalikar et Kamtikar, 2013 (Rhabdochonidae) appears largely fabricated and is regarded a species dubia.
Two new nematodes, Paraseuratoides ophisterni gen. et sp. n. (Seuratoidea: Quimperiidae) and Philometra ophisterni sp. n. (Dracunculoidea: Philometridae) are described based on specimens recovered from the intestine and mesentery, respectively, of the swamp-eel Ophisternon aenigmaticum Rosen et Greenwood (Synbranchiformes: Synbranchidae) from a canal of the Papaloapan River in Tlacotalpan, State of Veracruz, Mexico. The genus Paraseuratoides is most similar to Paraseuratum Johnston et Mawson, 1940, differing from it mainly in the absence of a bulbous inflation on the anterior end of the oesophagus and in the structure of the mouth (presence of 6 spines in addition to 6 oesophageal teeth). Neoquimperia Wang, Zhao, Wang et Zhang, 1979 and Wuinema Yu et Wang, 1992 are synonymised with Ezonema Boyce, 1971 and Paragendria Baylis, 1939, respectively, and Haplonema hamulatum Moulton, 1931 is considered a junior synonym of Ichthyobronema conoura Gnedina et Savina, 1930. Philometra ophisterni (only females) is mainly characterised by minute cephalic papillae, a greatly developed anterior oesophageal bulb separated from the cylindrical part of the oesophagus, anterior extension of the oesophageal gland anterior to the nerve ring, and by the character of large caudal projections. This is the first Philometra species recorded from inland fishes in Mexico.