The development of the nematode Procamallanus saccobranchi Karve, 1952, a parasite in the stomach of the fish Heteropneustes fossilis (Bloch), was studied in Mesocyclops crassus (Fischer) and Mesocyclops leuckarti (Claus). After being ingested by the copepods the nematode first-stage larvae penetrated into the haemocoel of the intermediate host; there they moulted twice (on days 3 and 5 p.i. at 28-30°C) attaining the third, infective stage. The definitive host H. fossilis acquired infection by feeding on copepods harbouring infcclivc-stage larvae; in the stomach of this definitive host, the larvae were observed to undergo two more moults. The third moult occurred on day 13 p.i. and the fourth moult on day 38 p.i. and day 66 p.i. in “male” and “female” larvae, respectively. The larval stages, including the moulting forms are described and illustrated.
Larval development of the nematode Onchocamallanus bagarii (Karve et Naik, 1951), recovered from the intestine of the fish Bagarius bagarius (Hamilton) was studied under laboratory conditions. The cyclopoid copepods Mesocyclops leuckarti (Claus) and M. crassus (Fischer) were infected with first-stage larvae from female uteri and maintained at temperatures 29-30°C. After being swallowed by the copepods, first-stage larvae burrow through the intestinal wall and reach the haemocoel of the copepods and there they grow and moult twice to attain the third and infective-stage. First-stage larvae become ensheathed after 65 hours of infection and second-stage larvae first appeared on day 3 post infection (p.i.). The second moult occurred on day 5 p.i. The larval stages occurring during development are described.
The developmental stages and life cycle of the nematode Camallanus anabantis Pcarse, 1933 an intestinal parasite of Anabas testudineus (Bloch) arc described. The copepod Mesocyclops leuckarti (Claus) was used as experimental intermediate host. After being ingested by the copepods the nematode first-stage larvae enter its haemocoel, where they moult twice, 4 d.p.i. and 11 d.p.i., at 21-26°C, respectively to become the infective third-stage larvae. The definitive fish hosts become infected when feeding on copcpods harbouring infective larvae. In the fish host’s intestine the larvae undergo two more moults, the third on day 15 p.i. The fourth moult of “male” larvae occurred on day 68 p.i. and that of “female” larvae on day 86 pi. at water temperatures 24-36°C- A female with eggs and few larvae in the uteri was first observed on day 187 p.i.
An examination of a sample of European eels, Anguilla anguilla (L.), collected from Lake Bracciano near Rome in 1993, the only known European locality with the occurrence of the introduced swimbladder nematode Anguillicola novaezelandiae Moravec et Taraschewski, 1988, revealed for the first time the presence of two Anguillicola species, A. novaezelandiae and A. crassus. In view of the investigations carried out by current authors in Bracciano Lake in the years 1982-1992, it is apparent that the latter species has been introduced into the lake quite recently, where it quickly became a dominant species. The development of A. novaezelandiae was experimentally studied in the copepod intermediate host, Cyclops strenuus, for the first time. The copepods were infected with nematode second-stage larvae at 21-22°C; fully developed infective third-stage larvae were obtained 13 days p.i. The general morphology of individual larval stages of A. novaezelandiae was similar to that of larvae of the related species Λ. crassus.
The development of the nematode Anguillicola crassus, a swimbladder parasite of eels, was experimentally studied in copepod intermediate hosts Cyclops strenuus and Acanthocyclops vernalis. The copepods, kept at a laboratory temperature of 20-22 °C, were infected with nematode second-stage larvae; the second moult of larvae (the only one in the intermediate host) was observed to start 10 days p,i„ but third-stage larvae liberated from their cuticular sheath were first observed 20 days p.i. These proved to be infective for experimental eels. Free second-stage larvae as well as larvae from copepods were described. The morphology of A. crassus larvae and the mode of their development in the intermediate host were compared with those of other dracunculoid nematodes. From this point of view, Anguillicola members appear to represent an ancient group of dracunculoid nematodes.
A description is given of the life cycle of the nematode Procamallanus (Spirocamallanus) rebecae (Andrade-Salas, Pineda-Lopez et García-Magafia, 1994), an intestinal parasite of cichlids in Mexico. The copepod Mesocyclnps sp. was found to be a suitable experimental intermediate host. After the copepod’s ingestion of free first-stage larvae of the nematode, these enter the haemocoel of the intermediate host; they moult twice (on the 3rd and 5-6th day p.i. at 21-22”C) before they attain the third, infective stage. The third-stage larva already possesses the large buccal capsule without spiral thickenings and its tail tip bears three cuticular spines. The larvae undergo two additional moults (13-14 days and 42 days p.i.) in the definitive host (Cichlasoma urophthalmus) before changing to adults; the prepatent period is about 2-3 months. Experimental infection of guppies, Poecilia reticulata, have shown that these fishes may become paratenic (metaparatenic) hosts of this parasite. The morphology of individual larval stages of this nematode is described.
The development of the nematode Procamalianus (Spirocamallanus) neocaballeroi (Caballero-Deloya, 1977), an intestinal parasite of the characid fish, Astyanax fasciatus (Cuvier) in Mexico, was studied in the experimental copepod intermediate host, Mesocyclops sp. After the copepod’s ingestion of free first-stage larvae of the nematode, these penetrate into the haemocoel of the intermediate host; they moult twice (on the 3rd and 4-5th day p.i. at 21-22”C) before they attain the third, infective stage. The third-stage larva already possesses the large buccal capsule subdivided into an anterior broad portion with eight spiral thickenings (as observed in lateral view) and a narrow posterior portion, and its tail tip bears three conical processes. The definitive host acquires infection by feeding on infected copepods; in the intestine of this fish, the nematode larvae undergo two more moults (on the 10th and 14-15th day p.i. at 25-32°C) before attaining their maturity. The prepatent period is approximately two months.