Two species of Myxobolus Bütschli, 1882 were found in yellow catfish Tachysurus fulvidraco (Richardson). A species of Myxobolus infecting the gills was morphologically identified as Myxobolus voremkhai (Akhmerov, 1960) and it was characterised here with additional morphological and molecular data. The other species of Myxobolus infecting the host's skin did not conform to any known myxosporean species. It is characterised by the presence of round, black or milky white plasmodia with black spots. Myxospores are pyriform in frontal view and lemon-shaped in lateral view, measuring 12.9-16.2 μm (14.6 ± 0.7 μm) in length, 8.1-10.8 μm (9.4 ± 0.5 μm) in width, and 6.1-8.1 μm (7.0 ± 0.4 μm) in thickness. Two ampullaceous polar capsules are slightly unequal in size, larger polar capsule 7.2-9.5 μm (7.9 ± 0.4 μm) long by 3.0-3.9 μm (3.5 ± 0.2 μm) wide, smaller capsule 6.9-8.0 μm (7.4 ± 0.3 μm) long by 2.9-3.9 μm (3.4 ± 0.2 μm) wide. Polar filaments are coiled with seven to nine turns. Histologically, the plasmodia develop in the stratum spongiosum of skin dermis, resulting in epithelial cell shedding and immunological cell infiltration. Given the morphological and molecular differences between this species and other species of Myxobolus, we proposed the name of Myxobolus pseudowulii sp. n. for this parasite from the skin of yellow catfish. Interestingly, some spores of the new species possess Henneguya-like caudal appendages. Phylogenetically, M. pseudowulii sp. n. and M. voremkhai infecting yellow catfish group together in one clade with other parasites of Siluriformes, indicating that parasites clustering according to the fish host order may be an important factor affecting the evolution of species within the Myxobolus clade., Bo Zhang, Yanhua Zhai, Yang Liu, Zemao Gu., and Obsahuje bibliografii
A list of myxozoan genera is presented in the current taxonomical scheme. These genera are defined; their type species and most important pathogens along with their hosts are listed. Simultaneously, definitions of actinospore stages representing sexual stages of the myxosporean life cycle are given; altogether, 17 actinospore collective groups with 180 types have been described. Life cycles of the two classes of the phylum Myxozoa, Malacosporea and Myxosporea, are briefly outlined with specification of the appropriate terms. Up to now, 4 malacosporean and 2,180 myxosporean species assigned to a total of 62 genera, have been established. The surviving classification of myxosporeans, based on spore morphology, is discussed in the context of the still fragmentary data resulting from SSU rDNA sequence analyses. The main task for the future is a rigorous, detailed morphological description combined with molecular techniques in establishment of new species and in revision of the existing ones. Establishment of a classification acceptable from morphological, biological and phylogenetical viewpoints is necessary.
Myxobolus pseudodispar Gorbunova, 1936 (Myxozoa) was originally described as a parasite of common roach, Rutilus rutilus (Linnaeus), with developing stages in muscles and spores disseminated in macrophage centres of different organs and tissues. Later, this parasite was described from several other cyprinids, but with relatively large intraspecific differences based on SSU rDNA gene sequences. Within our long-term study on myxozoan biodiversity, we performed a broad microscopic and molecular screening of various freshwater fish species (over 450 specimens, 36 species) from different localities. We investigated the cryptic species status of M. pseudodispar. Our analysis revealed four new unique SSU rDNA sequences of M. pseudodispar as well as an infection in new fish host species. Myxobolus pseudodispar sequence analysis showed clear phylogenetic grouping according to fish host criterion forming 13 well-recognised clades. Using 1% SSU rDNA-based genetic distance criterion, at least ten new species of Myxobolus Bütschli, 1882 may be recognised in the group of M. pseudodispar sequences. Our analysis showed the paraphyletic character of M. pseudodispar sequences and the statistical tests rejected hypothetical tree topology with the monophyletic status of the M. pseudodispar group. Myxobolus pseudodispar represents a species complex and it is a typical example of myxozoan hidden diversity phenomenon confirming myxozoans as an evolutionary very successful group of parasites with a great ability to adapt to a new hosts with subsequent speciation events.
As a part of ongoing cytogenetic studies on the bug family Nabidae (Heteroptera), the karyotypes and meiotic patterns of male Nabis (Aspilaspis) viridulus Spinola, 1837, N. (A.) indicus (Stål, 1873) (subfamily Nabinae) and Prostemma guttula (Fabricius, 1787) (subfamily Prostemmatinae) are described.
N. viridulus and N. indicus differ from P. guttula in their chromosome numbers, which are 2n = 32 + XY and 2n = 26 + XY, respectively, and behaviour of the sex chromosomes in male meiosis, which, respectively, show "distance pairing" and "touch-and-go pairing" in spermatocyte metaphase II. The karyotype of 2n = 34 and "touch-and-go pairing" are considered to be plesiomorphic characters in Nabidae. The evolutionary mechanisms that might underlie different chromosome numbers, the taxonomic significance of karyotype variation and the distribution of meiotic patterns in the family, are discussed.
Cryptosporidium fragile sp. n. (Apicomplexa) is described from black-spined toads, Duttaphrynus melanostictus (Schneider) (Amphibia, Anura, Bufonidae) from the Malay Peninsula. The parasitized animals were directly imported from Malaysia and harboured C. fragile at the time of arrival. Oocysts were subspherical to elliptical with irregular contour in optical section, measuring 6.2 (5.5-7.0) × 5.5 (5.0-6.5) µm. Oocyst wall was smooth and colourless in light microscopy. The endogenous development of C. fragile in the stomach of black-spined toad was analysed in detail using light and electron microscopy. Cryptosporidian developmental stages were confined to the surface of gastric epithelial cells. In transmission experiments, C. fragile has not been infective for one fish species, four amphibian species, one species of reptile and SCID mice. Full length small subunit rRNA gene sequence was obtained. Phylogenetic reconstruction revealed distinct status of C. fragile within the clade of species with gastric localisation including Cryptosporidium muris Tyzzer, 1907, Cryptosporidium serpentis Levine, 1980 and Cryptosporidium andersoni Lindsay, Upton, Owens, Morgan, Mead et Blagburn, 2000. Described characteristics differentiate C. fragile from the currently recognized Cryptosporidium species. Our experience with the description of C. fragile has led us to revise the recommended criteria for an introduction of a new Cryptosporidium species name. C. fragile is the first species described and named from an amphibian host. Its prevalence of 83% (15/18) in black-spined toads within the 3 months after importation calls for strict quarantine measures and import regulation for lower vertebrates.
The viviparous gyrodactylid genus Macrogyrodactylus Malmberg, 1957 is endemic to Africa, composed of nine species from hosts of four freshwater fish families, including catfishes (Siluriformes: Clariidae). Three species, Macrogyrodactylus clarii Gussev, 1961; M. congolensis (Prudhoe, 1957) and M. karibae Douëllou et Chishawa, 1995, are primarily known to parasitise the African sharptooth catfish Clarias gariepinus (Burchell) in various African countries. From November 2017 to September 2019, a total of 184 individuals of C. gariepinus were collected from selected localities in southern Africa and their skin, fins and gills were surveyed for monogeneans. Three species of Macrogyrodactylus (M. clarii, M. congolensis and M. karibae) were found parasitising C. gariepinus from five localities in South Africa and Zambia. Overall prevalence was 50% to 100% with intensities of up to 109 parasites per host individual. New locality records in southern Africa, morphological observations and additional molecular data on the complete Internal Transcriber Spacer (ITS-1-5.8S-ITS-2) regions of the rDNA gene for the three gyrodactylid species are presented in this study.
Larvae of three genera representing the staphylinid subfamily Pseudopsinae are described for the first time and illustrated with 33 morphological drawings: Pseudopsis Newman, Zalobius LeConte and Nanobius Herman. Thirty-six characters (mainly of larval morphology) were scored for representatives of six staphylinid subfamilies and a phylogenetic analysis was carried out. The monophyly of the subfamily Pseudopsinae is supported by the presence of a short oblique ridge on ventral side of larval head capsule laterad of maxillary foramina. The monophyly of each of the subfamilies Paederinae and Staphylininae is discussed based on the characters of the immature stages. The subfamily Pseudopsinae is confirmed to be a sister-group of the subfamilies Paederinae + Staphylininae on the basis of six larval synapomorphies. The latter clade is confirmed to be monophyletic on the basis of five larval synapomorphies. A larval identification key to the studied Pseudopsinae genera is provided.
Phylogenetic relationships within the diving-beetle subfamily Hydroporinae are not well understood. Some authors include the genus Pachydrus Sharp, 1882 in the tribe Hyphydrini, whereas others are in favour of excluding Pachydrus from the Hyphydrini and placing it in its own tribe, Pachydrini. Larval characters have been underutilised in phylogenetic studies, mainly because the larvae of many taxa within the family are unknown. In this study, the phylogenetic relationships of Pachydrus are studied based on a cladistic analysis of 34 taxa and 122 morphological larval characters. For this purpose, larvae of P. obesus Sharp, 1882 are described and illustrated in detail for the first time, with particular emphasis on morphometry and chaetotaxy. First and second instars for the genus were unknown. The results support a monophyletic origin of the tribe Hyphydrini excluding Pachydrus, based on four unique character states. On the other hand, Pachydrus is resolved as the sister group of the Hydrovatini. These results suggest Pachydrus should not be placed in the Hyphydrini. Given that the Hyphydrini minus Pachydrus is a distinctive clade, based on this study, it seems useful to recognise this group as Hyphydrini. Including Pachydrus in Hyphydrini would leave the tribe with a single larval apomorphy, as most characters present in the Hyphydrini and Pachydrus are also present in the Hydrovatini. However, in the absence of larvae of Heterhydrus Fairmaire, 1869 and of a more comprehensive and inclusive analysis, we do not propose a formal exclusion of Pachydrus from Hyphydrini at this stage. Pachydrus is a highly distinctive genus within the Hydroporinae and is characterised by several larval apomorphies.
Previous studies have recorded Spironucleus torosus Poynton et Morrison, 1990 from several species of gadoid fishes, including the only freshwater gadoid, the burbot Lota lota (L.). Two morphologically different isolates of S. torosus have been described (elongate and pyriform). Both have been found in saltwater, while only the elongate has been found in freshwater. To address the conspecificity of the two morphs of S. torosus, and to identify the source of S. torosus in burbot in Norway, we have sequenced the small subunit ribosomal RNA (SSU rRNA) gene from 43 isolates of S. torosus from six species of gadoid fishes sampled at 15 localities in Norway, Sweden and the Baltic Sea. Phylogenetic analyses of the SSU rRNA gene sequence data recovered two major clades, one containing mainly isolates from burbot, while the other contained isolates from marine gadoid fishes only. The genetic distance (based on 25 nucleotide substitutions in 789 base pairs) separating the two assemblages was not large enough to consider the two groups separate species. Spironucleus torosus isolated from burbot displayed limited genetic variation in the small subunit ribosomal RNA (SSU rRNA) gene along the post-Pleistocene migration route of its host. The present study is the first report of S. torosus in tusk Brosme brosme (Ascanius), whiting Merlangius merlangus (L.), and fourbeard rockling Enchelyopus cimbrius (L.).
The sterrhine loopers Timandra griseata and T. comae have been treated as distinct species since 1994. However, morphological differences between the taxa are minor and therefore their status has often been disputed. Here, we present a molecular phylogenetic study, which separates T. griseata and T. comae into different clades. Altogether, 43 Timandra specimens from eight European countries were studied. The phylogeny is based on a comparative sequence analysis of mitochondrial genes coding for the cytochrome C oxidase subunit I (COI) and NADH dehydrogenase subunit 1 (ND1). Nevertheless, a single individual of both species was assigned to the "wrong" clade. The symplesiomorphy of T. griseata and T. comae is considered to be a result of introgressive hybridization. Conditions that could lead to the hybridization of T. griseata and T. comae are discussed, as well as the likely distribution history of these taxa in Northern Europe. Results of the current analysis are in favour of retaining the species status of T. griseata and T. comae.