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.
Over a 7-year period, parasites have been collected from 28 species of groupers (Serranidae, Epinephelinae) in the waters off New Caledonia. Host-parasite and parasite-host lists are provided, with a total of 337 host-parasite combinations, including 146 parasite identifications at the species level. Results are included for isopods (5 species), copepods (19), monogeneans (56), digeneans (28), cestodes (12), and nematodes (12). When results are restricted to those 14 fish species for which more than five specimens were examined and to parasites identified at the species level, 109 host-parasite combinations were recorded, with 63 different species, of which monogeneans account for half (32 species), and an average of 4.5 parasite species per fish species. Digenean records were compared for 16 fish species shared with the study of Cribb et al. (2002); based on a total of 90 parasite records identified at the species level, New Caledonia has 17 new records and only seven species were already known from other locations. We hypothesize that the present results represent only a small part of the actual biodiversity, and we predict a biodiversity of 10 different parasite species and 30 host-parasite combinations per serranid. A comparison with a study on Heron Island (Queensland, Australia) by Lester and Sewell (1989) was attempted: of the four species of fish in common and in a total of 91 host-parasite combinations, only six parasites identified at the species level were shared. This suggests strongly that insufficient sampling impairs proper biogeographical or ecological comparisons. Probably only 3% of the parasite species of coral reef fish are already known in New Caledonia.
The development of the nematode Spinitectus inermis (Zeder, 1800), a parasite of the stomach of eels, Anguilla anguilla (L.) in Europe, was experimentally studied. Mayfly nymphs Caenis macrura, Ecdyonurus dispar, Heptagenia sulphurea, Potamanthus luteus and Seratella ignita from Portugal and the Czech Republic were found to serve as experimental intermediate hosts. After ingestion of the nematode eggs by the mayfly nymphs, the toothed first-stage larvae were released and penetrated into the body cavity of the intermediate host. There they moulted twice (on day 4 and 6 post infection [p.i.] at water temperatures of 20-25°C), attaining the third infective stage. The definitive host, A. anguilla, undoubtedly acquires infection by feeding on mayfly nymphs harbouring infective-stage larvae. In an experimentally infected eel, the fourth-stage larva undergoing the third moult was observed 28 days p.i. at water temperature of 20ºC. The larval stages, including moulting forms, are described and illustrated. The prepatent period of S. inermis is estimated to be about two months.
The egg shell of Huffmanela huffmani Moravec, 1987 forms three main layers: an outer vitelline layer, a middle chitinous layer, and an inner lipid layer. The vitelline layer, forming the superficial projections of the egg shell, comprises two parts: an outer electron-dense, and an inner electron-lucid part. The chitinous layer is differentiated into three parts: an outer homogenous electron-dense part, a lamellated part, and an inner electron-dense net-like part. The lipid layer comprises an outer net-like electron-lucid part, and an inner homogenous electron-lucid part. The polar plugs are formed by electron-lucid material with fine electron-dense fibrils.
Three hitherto unknown oxyuroid nematode species of the family Pharyngodonidae are described from the intestine of South American freshwater fishes, two of them being established as species new to science: Spinoxyuris annulata sp. n. from Myleus ternetzi (Norman) (Serrasalmidae) from French Guiana (Sinnamary River) and Ichthyouris ovifilamentosa sp. n. from Cichlasoma sp. (Cichlidae) from Amazonas (Negro River, São Gabriel da Cachoeira), Brazil. A third species, recovered from the same host as the latter (Cichlasoma sp.), was identified only as Ichthyouris sp. because of the absence of the male, although it probably also represents a new species. S. annulata differs from the only other congeneric species, S. oxydoras Petter, 1994, mainly in the absence of egg filaments, the location of an unpaired postanal papilla in the male, a distinctly longer spicule, and in an approximately double length of the body. Ichthyouris ovifilamentosa is closest to I. ro Inglis, 1962, differing from it principally in the structure of the cephalic end, the position of the excretory pore, and in the presence of filamented eggs. Ichthyouris sp. females differ from their congeners mainly in a characteristic structure of the cephalic end, the extent of lateral alae and the shape of their posterior ends, and in the character of egg filaments.
A new cucullanid nematode, Dichelyne mexicanus sp. n., is described from the intestine of three species of fishes, Agonostomus monticola (Bancroft) (Mugilidae, Perciformcs) (type host), Ictalurus balsanus (Jordan et Snyder) (Ictaluridac, Siluriformes) and Cichlasoma beani (Jordan) (Cichlidae, Perciformes), from three rivers (la Maquina River, Veracruz; Chontalcoatlán River, Guerrero and Santiago River, Nayaril) in central Mexico. This species is characterised by the absence of a ventral sucker in the male (subgenus Dichelyne) and it differs from its congeners mainly in possessing very unequal and dissimilar spicules (left 0.465-0.768 mm and right 293-548 mm long), an asymmetrical gubernaculum, and two intestinal caeca. Another cucullanid nematode, Cucullanus cabaUeroi Petter, 1977, is reported from Dormitator maculalus (Bloch) (Eleotridae, Perciformes) from the La Palma and La Maquina Rivers and Balzapote stream, Veracruz, being briefly described and illustrated; this represents a new host record. Findings of D. mexicanus and C. cabalteroi represent a new record of cucullanid nematodes from fishes in Mexican fresh waters.
The nematode parasite Huffmanela huffmani Moravec, 1987 (Trichosomoididae) infects swimbladders of fishes in the family Centrarchidae. Only fish collected from the upper San Marcos River (Texas) have been found infected with H. huffmani eggs with a prevalence of 90%. Hundreds of thousands of H. huffmani eggs have been observed in these fish but only a few specimens of adult worms have ever been found. The San Marcos River arises from springs along the Balcones Fault Zone in San Marcos, Hays County, Texas. The restriction of the parasite to the upper San Marcos River and the high prevalence of the parasite eggs in centrarchids would seem to enable one to solve the life cycle of H. huffmani but this has proved false. Here, the insights and experiments used to help define some of the aspects concerning the life cycle of this enigmatic parasite are described. This study of H. huffmani includes a description of the habitat, the known limits of geographic distribution of the parasite, possible dispersal processes, egg characteristics, the testing of a possible intermediate host, Palaemonetes antrorum (Benedict) (Decapoda: Palaemonidae), and the effects of the digestion process on H. huffmani eggs.
Based on light and scanning electron microscopical studies, the following nine species of Philometridae (Nematoda: Dracunculoidea) are described from female worms parasitizing marine perciform fishes belonging to six families off the northern coast Australia (near Darwin): Philometra australiensis sp. n. from the swimbladder of the king threadfin Polydactylus macrochir (Günther) (Polynemidae); P. epinepheli Dewi et Palm, 2013 from the operculum of the orange-spotted grouper Epinephelus coioides (Hamilton) (Serranidae); Philometra johnii Moravec et Ali, 2013 from the gonad of the croaker Johnius sp. (Sciaenidae); P. macrochiri sp. n. from the sensory fin of P. macrochir; P. zabidii sp. n. from the ovary of the ninespine batfish Zabidius novemaculeatus (McCulloch) (Ephippidae); Philometra sp. 1 and Philometra sp. 2 from the ovary of the Spanish flag snapper Lutjanus carponotatus (Richardson) (Lutjanidae) and the silver grunt Pomadasys argenteus (Forsskål) (Haemulidae), respectively; Philometroides eleutheronemae Moravec et Manoharan, 2013 from the ovary of the fourfinger threadfin Eleutheronema tetradactylum (Shaw) (Polynemidae); and Spirophilometra endangae Dewi et Palm, 2013 from the pectoral fins of E. coioides. The new species P. australiensis is characterized mainly by the structure of the cephalic end, 14 minute cephalic papillae, absence of caudal projections and body length of gravid female (67 mm), P. macrochiri by the presence of a conspicuously large anterior oesophageal bulb, 14 very small cephalic papillae and the truncated posterior end of body without any caudal projections, whereas P. zabidii is characterized by the presence of distinct caudal projections, the number (14) and larger size and arrangement of cephalic papillae, a poorly developed anterior oesophageal inflation, the body length (114 mm) and the host family (Ephippidae). All above-mentioned species were recorded from Australian waters for the first time.
Small subunit rRNA sequences were obtained from 38 representatives mainly of the nematode orders Spirurida (Camallanidae, Cystidicolidae, Daniconematidae, Philometridae, Physalopteridae, Rhabdochonidae, Skrjabillanidae) and, in part, Ascaridida (Anisakidae, Cucullanidae, Quimperiidae). The examined nematodes are predominantly parasites of fishes. Their analyses provided well-supported trees allowing the study of phylogenetic relationships among some spirurine nematodes. The present results support the placement of Cucullanidae at the base of the suborder Spirurina and, based on the position of the genus Philonema (subfamily Philoneminae) forming a sister group to Skrjabillanidae (thus Philoneminae should be elevated to Philonemidae), the paraphyly of the Philometridae. Comparison of a large number of sequences of representatives of the latter family supports the paraphyly of the genera Philometra, Philometroides and Dentiphilometra. The validity of the newly included genera Afrophilometra and Caranginema is not supported. These results indicate geographical isolation has not been the cause of speciation in this parasite group and no coevolution with fish hosts is apparent. On the contrary, the group of South-American species of Alinema, Nilonema and Rumai is placed in an independent branch, thus markedly separated from other family members. Molecular data indicate that the skrjabillanid subfamily Esocineminae (represented by Esocinema bohemicum) should be either elevated to the rank of an independent family or Daniconematidae (Mexiconema africanum) should be decreased to Daniconematinae and transferred to the family Skrjabillanidae. Camallanid genera Camallanus and Procamallanus, as well as the subgenera Procamallanus and Spirocamallanus are confirmed to be paraphyletic. Paraphyly has also been found within Filarioidea, Habronematoidea and Thelazioidea and in Cystidicolidae, Physalopteridae and Thelaziidae. The results of the analyses also show that Neoascarophis, Spinitectus and Rhabdochona are monophyletic, in contrast to the paraphyletic genus Ascarophis. They further confirm the independence of two subgenera, Rhabdochona and Globochona, in the genus Rhabdochona. The necessity of further studies of fish-parasitizing representatives of additional nematode families not yet studied by molecular methods, such as Guyanemidae, Lucionematidae or Tetanonematidae, is underscored.
Dracunculus globocephalus Mackin, 1927 (Nematoda: Dracunculoidea) is redescribed from specimens collected from the mesentery of the snapping turtle, Chelydra serpentina (L.), in Louisiana, USA. The use of scanning electron microscopy, applied for the first time in this species, made it possible to study details in the structure of the cephalic end and the arrangement of male caudal papillae that are difficult to observe under the light microscope. This species markedly differs from all other species of Dracunculus in having the spicules greatly unequal in size and shape, in the absence of a gubernaculum, and in the disposition of male caudal papillae. The validity of D. globocephalus is confirmed, but the above mentioned morphological differences are not sufficient for listing it in a separate genus. This is the first record of D. globocephalus in Louisiana.