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.
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.
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.