A myxosporean producing actinospores of the tetractinomyxon type in Hydroides norvegicus Gunnerus (Serpulidae) in Denmark was identified as a member of the family Parvicapsulidae based on small-subunit ribosomal DNA (SSU rDNA) sequences. Myxosporean samples from various Danish and Norwegian marine fishes were examined with primers that detect the novel myxosporean. Sprattus sprattus (Linnaeus) and Clupea harengus Linnaeus (Teleostei, Clupeidae) were found to be infected. The sequences of this parvicapsulid from these hosts were consistently slightly different (0.8% divergence), but both these genotypes were found in H. norvegicus. Disporic trophozoites and minute spores of a novel myxosporean type were observed in the renal tubules of some of the hosts found infected through PCR. The spores appear most similar to those of species of Gadimyxa Køie, Karlsbakk et Nylund, 2007, but are much smaller. The actinospores of the tetractinomyxon type from H. norvegicus have been described previously. In GenBank, the SSU rDNA sequences of Parvicapsulidae gen. sp. show highest identity (82%) with Parvicapsula minibicornis Kent, Whitaker et Dawe, 1997 infecting salmonids (Oncorhynchus spp.) in fresh water in the western North America. A phylogenetic analysis places P. minibicornis and Parvicapsulidae gen. sp. in a sister clade to the other parvicapsulids (Parvicapsula spp. and Gadimyxa spp.).
A total of 22 specimens of whiting Merlangius merlangus (L.) (Teleostei, Gadidae) from the northern Øresund, Denmark were examined for Myxosporea. Zschokkella hildae Auerbach, 1910 (Myxidiidae), Gadimyxa sp. (Parvicapsulidae) and a species of Bipteria occurred in the renal tubules of 9%, 18% and 68% whiting, respectively. Immature spores of the Bipteria species are very similar to spores of Myxoproteus formosus Kovaleva et Gaevskaya, 1979 originally described from the urinary system of whiting from the Celtic Sea. We therefore consider Bipteria sp. from whiting in Denmark conspecific with M. formosus and propose Bipteria formosa (Kovaleva et Gaevskaya, 1979) comb. n. The spore of Bipteria formosa is described in detail and compared with other Bipteria spp. The phylogenetic position of B. formosa, based on partial 18S rDNA sequences, is closest to Leptotheca fugu Tun, Yokoyama, Ogawa et Wakabayashi, 2000 and the Sphaerosporidae.
Nereis diversicolor O.F. Müller and N. succinea Frey et Leuckart (Polychaeta, Nereidae) living in brackish shallow areas in Denmark are naturally infected with tetractinomyxon actinospores. Infected Nereis spp. were experimentally fed to various potential fish hosts, and the actinosporean stages developed into myxosporean stages of Ellipsomyxa gobii Køie, 2003 (Ceratomyxidae) in the gallbladder of the common goby Pomatoschistus microps (Krøyer) (Gobiidae). The European eel Anguilla anguilla (L.), three-spined stickleback Gasterosteus aculeatus L., small sand eel Ammodytes tobianus L., flounder Platichthys flesus (L.), European plaice Pleuronectes platessa L. and common sole Solea solea (L.) did not become experimentally infected. In Danish shallow brackish areas P. microps is naturally infected with E. gobii, in some areas with a prevalence >90%. We compared small subunit ribosomal DNA sequences of the actinosporean with E. gobii from P. microps. Sequences were identical, which further verifies that both forms belong to the same organism. This is the first myxozoan two-host life cycle in the marine environment.
A new myxosporean species Ellipsomyxa gobii gen. et sp. n. is described from the common goby Pomatoschistus microps (Krøyer) (Perciformes, Gobiidae). Plasmodia with long branched pseudopodia in the gallbladder develop to subspherical bisporous plasmodia. The myxospores were found in the gallbladder, and the hepatic and bile ducts. The new genus is characterised by the morphology of the myxospores. The myxospores have smooth thin valves elongated in the direction perpendicular to the plane of the straight central transverse indistinct sutural line. The two spherical polar capsules open some distance from the sutural line on opposite sides. The new genus thereby differs from Leptotheca Thélohan, 1895. Ellipsomyxa gobii is tentatively placed in the Ceratomyxidae.
Mature specimens of the nematode Dichelyne (Cucullanellus) minutus (Rudolphi, 1819) (Ascaridida, Cucullanidae, Seuratoidea) were obtained from the intestine of flounder Platichthys flesus (L.) caught in the Øresund, Denmark. Plaice Pleuronectes platessa L. and common goby Pomatoschistus microps (Kröyer) also harbour this species. The eggs embryonate on the seabottom. Larvae about 440 µm long, and believed to be in their third stage, hatch from the eggs. These larvae are not directly infective to flounders or gobies. The polychaete Nereis diversicolor O.F. Müller acts as obligatory intermediate host. Experimental infections showed that larvae >600 µm long and provided with a chitinous tooth survived in flounder and common goby. The third-stage larvae moult to fourth-stage larvae in the fish gut wall. Mature worms occur in the lumen of the anterior part of the intestine. All developmental stages may be transferred from one flounder to another; thus the flounder may acquire the parasite also by devouring infected gobies.
Sequencing of SSU rDNA showed that actinospores of the tetractinomyxon type, which develop in Chone infundibuliformis Krøyer (Annelida, Polychaeta, Sabellidae) from the northern Øresund, Denmark, are identical with Ceratomyxa auerbachi Kabata, 1962 (Myxozoa, Ceratomyxidae). This myxosporean was found in the gallbladder of the Atlantic herring Clupea harengus L. from the northern Øresund, Denmark, and from the Bergen area, western Norway. The pansporocysts and actinospores of C. auerbachi are described. This is the third elucidated two-host life cycle of a marine myxozoan, and the first involving a marine ceratomyxid.
A new myxosporean species, Trilosporoides platessae gen. et sp. n. (Multivalvulida), is described from the gallbladder of the plaice Pleuronectes platessa L. (Pleuronectidae) from Denmark. The myxospore of T. platessae is conical in side view, with a 24 µm long, pointed posterior projection. In apical view, the myxospore (diameter 9.4 µm) is round, trilobed and with three spherical polar capsules arranged peripherally, equidistant and opening peripherally through protruding tips. The polar capsules are of different sizes, one often larger than the others (diameter 3.3 µm vs. 2.5 µm). Apart from the long posterior projection, the myxospore of T. platessae differs from those of the three known species of Trilospora Noble, 1959 and from all genera within the order Multivalvulida Shulman, 1959 in the arrangement of the polar capsules. Trilosporoides platessae may temporarily be placed in the vicinity of the Trilosporidae.