A new nematode species, Atractis vidali sp. n., is described from the intestine of cichlid fishes, Vieja intermedia (Günther) (type host) and Cichlasoma pearsei (Hubbs), from specimens collected in three localities in the Mexican states of Campeche (Santa Gertrudis Creek) and Chiapas (Cedros and Lacanjá Rivers). It differs from the only other atractid species reported in fishes of Mexico, Atractis bravoae, mainly in possessing two very unequal spicules. In contrast to the 10 species parasitising amphibians and reptiles in America, the new species has a longer body, spicules and a gubernaculum, and a different distribution of the caudal papillae. This is the second species of the genus Atractis recorded from freshwater fishes.
A new nematode species, Spirophilometra pacifica sp. n. (Philometridae), is described from gravid female specimens collected from the mouth cavity (the upper palate) of the fish (yellow snook) Centropomus robalito (Centropomidae, Perciformes) from the Chantuto-Panzacola system, Chiapas, in the Pacific coast of Mexico. Its morphology is very similar to that of the species originally described as Philometra centropomi Caballero, 1974, but the gravid females of S. pacifica are about three times longer (body length 11.63-18.17 mm); host species and the geographical distribution of both these forms also differ. Scanning electron microscope (SEM) examination of S. pacifica, used for the first time for a Spirophilometra species, confirmed the presence of numerous minute cuticular spines on the body surface, 14 cephalic papillae arranged in two circlets, and two small lateral papilla-like caudal projections. It is evident that some features of P. centropomi were incorrectly described (its types are not available) and this species is now transferred to Spirophilometra as S. centropomi (Caballero, 1974) comb. n.
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.
A pathogenic Asian nematode species of Camallanus, C. cotti Fujita, 1927, was found in New Caledonia, South Pacific, for the first time; it was recorded from two native fishes, Awaous guamensis (Valenciennes) (Gobiidae) (prevalence 51%, intensity 1-25) and Kuhlia marginata (Cuvier) (Kuhliidae) (a single specimen found), of the La Foa River, about 100 km north of Nouméa; the latter represents a new host record. Morphological data on C. cotti based on New Caledonian specimens and those previously collected from aquarium-kept Misgurnus anguillicaudatus (Cantor) in Canada have been provided. The SEM examination of C. cotti, applied for the first time in this species, made it possible to study some of its morphological details; first-stage larvae from the female's uterus were found to possess several digit-like processes on the tail tip, not previously reported for any species of the Camallanidae. Camallanus moraveci Petter, Cassone et France, 1974 is considered a junior synonym of C. cotti. A list of hitherto recorded hosts of C. cotti is provided. Camallanus cotti is assumed to be introduced into New Caledonia along with the introduction of the exotic poeciliid fishes, which are known to be among the most common hosts of C. cotti in aquarium cultures worldwide.
A new species of parasitic nematode, Cucullanus oceaniensis sp. n., is described from the intestine of the giant mottled eel Anguilla marmorata (type host) from Futuna Island (Wallis and Futuna Islands, Polynesia) and from A. marmorata and Anguilla sp. (cf. obscura) from Fiji Islands (Melanesia, South Pacific). The main distinguishing characteristics are the length of spicules (668-1,020 µm), situation of deirids (slightly anterior to the oesophago-intestinal junction) and the excretory pore (some distance posterior to the end of oesophagus), and the arrangement of caudal papillae in the male. It is the third known species of Cucullanus from Oceania and the first one reported from freshwater eels in the region of South Pacific. Cucullanus faliexae Morand et Rigby, 1998 is considered a junior synonym of Cucullanus australiensis Baylis, 1927.
Examinations of nematodes collected from some marine fishes off the southwestern coast of Java, Indonesia in 2000 and 2001 revealed the presence of the following six species: ascaridoids Ichthyascaris grandis sp. n. from the intestine of Lophiomus setigerus (Vahl), I. cf. longispicula Li, Liu, Liu et Zhang, 2012 from the intestine of Conger cinereus Rüppel, Ichthyascaris sp. from the body cavity of Lobotes surinamensis (Bloch), and Raphidascaroides halieutaeae Yin, 1983 from the intestine of Halieutaea stellata (Vahl), and philometrids Philometra ivaschkini Parukhin, 1976 from the stomach wall of Trichiurus lepturus Linnaeus and P. psettoditis Moravec, Walter et Yuniar, 2012 from the body cavity (liver) of Psettodes erumei (Bloch et Schneider). Descriptions of these nematodes based on light and scanning electron microscopical studies are provided. The new species I. grandis sp. n. is mainly characterised by large body measurements (males and females up to 41.8 mm and 73.6 mm long, respectively), the length of spicules (0.99-1.05 mm), the tail tip usually without rudimentary spines and by the presence of 44-53 pairs of caudal papillae, eight to twelve of which being postanals. In addition to new data on the morphology of R. halieutaeae and other nematodes recorded, the 11 species of Raphidascaroides Yamaguti, 1941 poorly described from marine fishes in South Asia and reviewed in the monograph of Sood (2017) are considered species inquirendae and incertae sedis.
A new nematode species, Rhabdochona (Globochona) rasborae sp. n. (Rhabdochonidae), is described from the intestine of the freshwater cyprinid fish (sidestripe rasbora) Rasbora paviana Tirant in the Bangbaimai Subdistrict, Muang District, Surat Thani Province, southern Thailand. It differs from other representatives of the subgenus Globochona Moravec, 1972 which possess eggs provided with lateral swellings in having a spinose formation at the tail tip of both sexes and in some other morphological features, such as the body length of gravid female (8.6-23.7 mm), presence of two-three swellings on the egg, eight anterior prostomal teeth, length ratio of spicules (1 : 5.3-6.7) and arrangement of male genital papillae. This is the third nominal species of Rhabdochona Railliet, 1916 and the second species of the subgenus Globochona reported from fishes in Thailand. The three species of Rhabdochona recently described from fishes in Pakistan, viz. R. annai Kakar, Bilqees et Khan, 2012, R. bifurcatum [sic] Kakar et Bilqees, 2012, and R. pakistanica Kakar, Bilqees et Khan, 2012, are considered to be species inquirendae.
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.
Based on light and electron microscopical studies, a new nematode parasite, Echinocephalus inserratus sp. n. (Spirurida: Gnathostomatidae), is described from the spiral valve of the broad cowtail stingray Pastinachus ater (Macleay) (Dasyatidae, Myliobatiformes) from off New Caledonia. The new species is morphologically and biometrically most similar to Echinocephalus overstreeti Deardorff et Ko, 1983, differing from it mainly in the absence of serrations on the posterior parts of pseudolabia and on interlabia, and in having a longer gubernaculum (150-299 µm long). Morphologically unidentifiable, mostly encapsulated larvae of Echinocephalus spp. were recorded from the following six species of teleost fishes collected in New Caledonian waters, serving as paratenic hosts: Perciformes: Acanthopagrus berda (Forsskål) (Sparidae) and Nemipterus furcosus (Valenciennes) (Nemipteridae); Tetraodontiformes: Abalistes stellatus (Anonymous), Pseudobalistes fuscus (Bloch et Schneider) (both Balistidae), Lagocephalus sceleratus (Gmelin) (Tetraodontidae) and Aluterus monoceros (Linnaeus) (Monacanthidae). Co-parasitising larvae of Ascarophis sp. and Hysterothylacium sp. were also collected from P. fuscus. All these findings represent new host and geographical records. A key to valid species of Echinocephalus Molin, 1858 is provided.
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.
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.
Scanning electron microscopy examinations of trematode specimens belonging to Crepidostomum farionis (O.F. Müller, 1784) and C. metoecus Braun, 1900, collected from brown trout, Salmo trutta fario L., in the Czech Republic, made it possible to study their surface morphology including details not described previously. The tegument of both species bears numerous characteristic papillae around the oral sucker (in C. metoecus also around the ventral sucker) and the ventral and dorsal surfaces of the forebody, exhibiting a high degree of variability in numbers and arrangement, with tegumental bosses forming lateral fields on the forebody and minute sensory receptors with submerged cilia scattered on the surface of the dorsal part of the oral sucker. In addition to marked differences in the size, shape and position of the oral muscular lobes, both species distinctly differ in the number of genital pores: two separate pores in C. farionis and a single pore in C. metoecus.
The nematode Philometra rubra (Leidy, 1856) (Philometridae) is redescribed from subgravid females found in the abdominal cavity of the fish Morone saxatilis (Walbaum) from South Carolina, USA in November 2008. The species is characterized by the presence of 14 cephalic papillae arranged in two circles, a relatively long oesophagus with a distinct anterior inflation, and well-developed papilla-like caudal projections. Cephalic papillae of the external circle differ from those in other congeners in that the dorso-lateral and ventro-lateral papillae are large, dome-shaped, whereas the dorso-dorsal and ventro-ventral papillae are small.
The male of the gonad-infecting nematode Philometra filiformis (Stossich, 1896) (Philometridae) is for the first time described, based on specimens from the ovary of the marine fish Pagellus erythrinus (Linnaeus) from the Tyrrhenian Sea off Sicily, Italy. It is mainly characterized by the testis extending anteriorly nearly to the anterior end of body, the oesophagus without a usual anterior inflation, the absence of a dorsal barb or distinct transverse lamellae on the tip of the gubernaculum, the measurements of the spicules and the gubernaculum, and a fairly long body.
Two species of mayfly nymphs, Habroleptoides modesta (Hagen) and Habrophlebia lauta (Eaton) (Ephemeroptera: Leptophlebiidae), were found as suitable experimental intermediate hosts of the fish nematode Rhabdochona denudata (Dujardin, 1845) (Rhabdochonidae), an intestinal parasite of Palaearctic cyprinids. The parasite's eggs were obtained from nematode gravid females parasitizing the European chub, Leuciscus cephalus (L.), of the Rokytná River, Czech Republic. At the water temperature of 9°C, the eggs of R. denudata were ingested by the intermediate host and the hatched, toothed (with a minute cephalic boring tooth) first-stage larvae about 200 µm long penetrated into the body cavity of the mayfly. There the larvae grew and moulted twice (on 16-18 and 30-35 days p.i.) before attaining the third stage, which is already infective for the fish definitive host. Infective larvae of this stage were about 1.5 mm long and their morphology resembled that of adults except for the vestibule structure; they became encapsulated as in those of other congeneric species.
Based on light and scanning electron microscopical studies, the following five species of the Philometridae (Nematoda: Dracunculoidea) are described from female specimens collected from marine fishes off the southwestern coast of Java, Indonesia: Philometra lobotidis sp. n. from the abdominal cavity of the Atlantic tripletail Lobotes surinamensis (Bloch) (Lobotidae, Perciformes); Philometra javaensis sp. n. from the abdominal cavity of the immaculate puffer Arothron immaculatus (Bloch et Schneider) (Tetraodontidae, Tetraodontiformes); Philometra psettoditis sp. n. from the musculature of the Indian spiny turbot Psettodes erumei (Bloch et Schneider) (Psettodidae, Pleuronectiformes); Philometroides indonesiensis sp. n. from the musculature of the hound needlefish Tylosurus crocodilus crocodilus (Péron et Lesueur) (Belonidae, Beloniformes); and Philometroides trichiuri sp. n. from the dorsal fin of the largehead hairtail Trichiurus lepturus Linnaeus (type host) and the savalai hairtail Lepturacanthus savala (Cuvier) (both Trichiuridae, Perciformes). All these new species are distinguished from their congeners parasitizing marine fishes by morphological (mainly the shape and structure of the cephalic and caudal ends and of the oesophagus) and biometrical features. Besides previously known Philometra pellucida (Jägerskiöld, 1893) and Philometra ocularis Moravec, Ogawa, Suzuki, Miyazaki et Donai, 2002, they are the only nominal philometrid species recorded from Indonesian waters.
Recent examinations of some marine fishes from off the southern coast of Iraq revealed the presence of five species of Philometra Costa, 1845 (Nematoda: Philometridae): Philometra arabiensis sp. n. (males and females) from the ovary of the shrimp scad Alepes djedaba (Forsskål) (Carangidae, Carangiformes), Philometra psettoditis Moravec, Walter et Yuniar, 2012 (females) from the body cavity of the Indian halibut Psettodes erumei (Bloch et Schneider) (Psettodidae, Pleuronectiformes), Philometra terapontis Moravec, Gopalakrishnan, Rajkumar, Saravanakumar et Kaliyamoorthy, 2011 (female) from the ovary of the jarbua terapon Terapon jarbua (Forsskål) (Terapontidae, Centrarchiformes), Philometra sp. (females) from the ovary of the Arabian blackspot threadfin Polydactylus mullani (Hora) (Polynemidae, Carangariformes) and Philometra sp. 2 of Moravec et al. (2016a) (females) from the ovary and body cavity of the bartail flathead Platycephalus indicus (Linnaeus) (Platycephalidae, Perciformes). Philometra arabiensis sp. n. is mainly characterised by the length of spicules (198-243 µm) and gubernaculum (75-99 µm), the gubernaculum/spicule length ratio (1 : 2.33-2.79), the structure of the gubernaculum distal portion and the male caudal end, and the body length of males (1.86-2.73 mm). The present findings of P. psettoditis and P. terapontis in fishes of the Arabian Gulf represent new geographical records for these parasites.