Camallanus cotti (Nematoda: Camallanidae), an introduced parasite of fishes 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.     

Some camallanid nematodes from marine perciform fishes off New Caledonia

Two new, one known and three unidentified species of the nematode family Camallanidae are reported and described from the intestines of marine perciform fishes off the southwestern coast of New Caledonia, South Pacific: Camallanus carangis Olsen, 1952 from the forked-tailed threadfin bream Nemipterus furcosus (Nemipteridae), the yellowstriped goatfish Upeneus vittatus and the whitesaddle goatfish Parupeneus ciliatus (both Mullidae) (new host records); Procamallanus (Spirocamallanus) variolae sp. n. from the white-edged lyretail Variola albimarginata (type host) and the blacktip grouper Epinephelus fasciatus (both Serranidae); Procamallanus (Spirocamallanus) longus sp. n. from the twotone tang Zebrasoma scopas (Acanthuridae); Procamallanus (Spirocamallanus) sp. 1 (female tail with 2 terminal spikes on a digit-like projection) from the speckled sand-perch Parapercis hexophtalma (Pinguipedidae); Procamallanus (Spirocamallanus) sp. 2 (female tail with 1 spike on a digit-like projection) from the drab emperor Lethrinus ravus (Lethrinidae) and Procamallanus (Spirocamallanus) sp. 3 (female tail with a smooth digit-like protrusion) from the two-lined monocle bream Scolopsis bilineata (Nemipteridae). Camallanus paracarangis Velasquez, 1980 is synonymized with C. carangis. Several additional species of Camallanus from marine fish of the Indo-Pacific region may be synonymous with C. carangis as it has a poorly sclerotized left spicule and 3 small caudal projections on the tail of young (i.e., non-gravid) females. The fourth-stage larva of C. carangis is described for the first time. P. (S.) variolae differs from most similar species of this region mainly in the position (i.e., at level or posterior to the nerve ring) and shape of deirids. P. (S.) longus differs from the similar P. (S.) chaimha mainly in a different arrangement of postanal papillae, shape of the female tail, much longer right spicule (429 microm) and longer body of gravid females (38-55 mm). All Camallanus and Procamallanus (Spirocamallanus) spp. reported here represent the first records of camallanids from marine fishes in New Caledonian waters.     

Structure of the female cephalic end and cuticular ornamentations of Paraphilometroides nemipteri (Nematoda:Philometridae), as revealed by SEM

Scanning electron microscopy (SEM) examination of a paratype specimen (gravid female) of the philometrid nematode Paraphilometroides nemipteri Moravec et Shaharom-Harrison, 1989, the type species of Paraphilometroides Moravec et Shaharom-Harrison, 1989, made it possible to recognise the true structure of the cephalic end and the shape of cuticular ornamentations on the body. In contrast to other philometrid genera, the cephalic end is angular in lateral view and rounded in dorsoventral view; large external cephalic papillae are fused together to form a marked dorsal and a ventral ala, each bent into a curve; six minute internal papillae, including a pair of previously not reported lateral papillae, were found; amphids were indistinct. Cuticular ornamentations (inflations) were found to be transversely elongated. These features, especially the unique cephalic structure, clearly distinguish Paraphilometroides from other philometrids and confirm the validity of this genus. Moravec and Shaharom-Harrison (1989) erected the hitherto monotypic philometrid genus Paraphilometroides Moravec et Shaharom-Harrison, 1989 with the type species P. Nemipteri Moravec et Shaharom-Harrison, 1989, described from females found in the fins and operculum of the marine fish (notchedfin threadfin bream) Nemipterusperonii (Valenciennes) from off the South China Sea coast, Malaysia. The male of P. nemipteri remains unknown. The authors distinguished Paraphilometroides from the related genus Philometroides Yamaguti, 1935 mainly by the unusual structure of the female cephalic end, which is unique within the family Philometridae (see Moravec 2006). However, P. nemipteri was studied only by light microscopy (LM), whereas some details of the cephalic structure, especially the cephalic papillae of gravid philometrid females are usually difficult to observe by LM due to a various degree of their reduction and atrophy (Moravec 2004); in the past, some philometrid species were even reported to have no cephalic papillae. Consequently, the only reliable method to study the cephalic structures in philometrids is the use of scanning electron microscopy (SEM). Therefore, one of the ethanol-preserved paratype specimens (gravid female) of P. nemipteri, deposited in the Helminthologi-cal Collection of the Institute of Parasitology, Biology Centre     

Age-dependent changes of proinflammatory cytokine production by porcine peripheral blood phagocytes

The aim of the present study was to determine postnatal ontogeny of proinflammatory cytokines IL-1beta, IL-8 and TNF-alpha production by in vitro stimulated porcine blood leukocytes. Four age categories of pigs were chosen. Cytokine production was determined using intracellular flow cytometry. It was found that IL-8 and TNF-alpha production by blood monocytes significantly increased during the postnatal period while production of IL-1beta remained unchanged. In blood neutrophils, the IL-8 production increased only during the postnatal period, while the levels of TNF-alpha and IL-1beta were undetectable during the whole postnatal period. Generally, the most intensive changes in cytokine production occurred before weaning. The production of low levels of cytokines by monocytes and neutrophils from young pigs was not caused by a delayed cytokine response because the cytokine production after 8-h stimulation was lower than that after 4-h stimulation in all age categories. The ontogenetical changes showed the same trends when two different stimulators (LPS, heat-inactivated E. coli) were used, suggesting that the ontogenetical changes are not caused by a simple defect in one signalling pathway, but it is probably a more complex process. No differences in cytokine production between the whole blood and the isolated cells supplemented with newborn or adult serum were found. Thus the ability of newborn monocytes and neutrophils to produce proinflammatory cytokines was not decreased due to the influence of composition of the microenvironment, where the cells were present. In conclusion, the ability of porcine blood leukocytes to produce cytokines develops during postnatal life.     

New data on the morphology and systematic status of Spinitectus petrowi and Spinitectus gigi (Nematoda: Cystidicolidae) parasitic in catfishes in central China

Two little-known nematode species of the genus Spinitectus Fourment, 1883, S. petrowi Belous, 1965 (prevalence 25%, intensity 1-8) and S. gigi Fujita, 1927 (prevalence 10%, intensity 2-3), were collected from the gastrointestinal tract of the yellow catfish, Pelteobagrus fulvidraco (Richardson), from Liangzihu Lake, Hubei Province, central China, in September of 2002. The light and scanning electron microscopical examination of this material, supplemented by a few museum specimens of S. gigi collected from the catfish Clariasfuscus (Lacépède) in southern China, made it possible to study in detail the morphology of these parasite species and to redescribe them. The first species, whose correct name is S. petrowi Belous, 1965, exhibits some morphological features (e.g., unusually short vestibule, shape of pseudolabia and of the left spicule) not found in most other congeners; a unique feature is the presence of peculiar pairs of transversely oriented peg-like cuticular spines with rounded ends on the ventral surface of the female tail. Spinitectus gigi was found to have 28-31 cuticular spines in the first ring, relatively long distances between the 2nd-7th rings of spines, and anterior rings divided into 2 sectors; the excretory pore is located at the level of the 4th ring of cuticular spines; males posses 4 pairs of preanal- and 6 pairs of postanal caudal papillae and a pair of small phasmids. Spinitectus bagri Wang, Wu et Yu, 1993 and S. wulingensis Yu et Wang, 1997 are considered junior synonyms of S. petrowi, whereas S. clariasi Ky, 1971, S. ophicephali Ky, 1971 and S. yuanjiangensis Wang, Wu et Yu, 1997 are regarded to be junior synonyms of S. gigi. Spinitectus petrowi was not previously reported from China.     

Phylogenetic relationships of some spirurine nematodes (Nematoda: Chromadorea: Rhabditida: Spirurina) parasitic in fishes inferred from SSU rRNA gene sequences

Abstract: 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 ofphylogenetic 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 ofAlinema, 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.     

Some aspects of the taxonomy and biology of adult spirurine nematodes parasitic in fishes: a review

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. Consequently, further detailed studies on fish spirurines are significant not only from the theoretical viewpoint, but they may also have practical implications.