Molecular characterization and phylogenetic analyses of Tripartiella macrosoma Basson and Van As, 1987 and Tripartiella obtusa Ergens and Lom, 1970 based on 18S rRNA gene sequence data.

In the present study, we provided the first 18S rRNA gene sequence data of two Tripartiella species, Tripartiella macrosoma Basson and Van As, 1987 and Tripartiella obtusa Ergens and Lom, 1970, which were isolated from Tachysurus fulvidraco (Richardson, 1846) and Hemibarbus maculatus Bleeker, 1871 in Chongqing, China, respectively. Morphologically, both species fall within the morphometry range of the original descriptions and are very similar to the original populations in the overall appearance of the adhesive disc. Tripartiella macrosoma can be easily distinguished from the other Tripartiella species by possessing the denticle with a long strip and conspicuously inclined backward blade and a robust and short ray. Tripartiella obtusa is mainly characterized by a broad blade and a relatively long ray. Phylogenetically, T. macrosoma clustered with Trichodinella myakkae (Mueller, 1937) Raabe, 1950 and further with Trichodinella sp., which was sister to a group that includes four populations of Trichodinella epizootica (Raabe, 1950) Srámek-Husek, 1953; finally, they formed a small clade with T. obtusa. This result suggested that T. macrosoma had a closer relationship with Trichodinella spp. than with T. obtusa and T. obtusa diverged earlier than T. macrosoma and Trichodinella spp. By combining morphological and molecular data, the polyphyletic characteristics of Tripartiella and Trichodinella were further analyzed, and the results revealed that the validity of the genus Tripartiella is doubtful.

Morphological and Molecular Identification of the New Species, Trichodina pseudoheterodentata sp. n. (Ciliophora, Mobilida, Trichodinidae) from the Channel Catfish, Ictalurus punctatus, in Chongqing China.

It is difficult to differentiate similar trichodinids solely based on morphological examination, thus other identification methods, such as molecular identification, are necessary for identification. One mobilid ciliate named Trichodina pseudoheterodentata sp. n. was isolated from the gills of channel catfish, Ictalurus punctatus, in Chongqing, China. In the present study, its SSU rDNA was sequenced for the first time. Based on the results from both morphological identification and SSU rDNA sequencing, the new species was identified and compared with similar species. The morphological analysis revealed that T. pseudoheterodentata is a large Trichodina species (cell diameter 73.0-82.5 µm) and possesses robust denticles with broad blades and well-developed blade connections. Characterization of its primary and secondary SSU rDNA structures indicated that T. pseudoheterodentata was distinctly different from congeneric species in H12, H15, E10_1, and V4 regions. Phylogenetic analysis revealed that the genetic distances among the new species and similar species reached interspecific levels, furthermore, the phylogenetic study also validated the identification of T. pseudoheterodentata and its placement in the genus Trichodina.

Molecular characterization and phylogenetic analysis of Paratrichodina africana Kazubski and El-Tantawy, 1986 based on 18S rRNA gene data with the evolutionary hypothesis of trichodinids.

In this study, we provided the morphological data and the first 18S rRNA gene data of Paratrichodina africana Kazubski and El-Tantawy, 1986, isolated from hybrids of Oreochromis niloticus × Oreochromis mossambicus in Chongqing, China. Morphologically, P. africana is mainly characterized by the triangular blade and prominent anterior projection. The present population is consistent with the original populations in the overall appearance of the adhesive disc, and falls within the morphometry range of the original descriptions. Phylogenetically, P. africana was clustered into one large clade with Trichodinella and Tripartiella species, which was nested within Trichodina ones with strong support. By combining morphological and molecular data, our results revealed that the validity of the genus Paratrichodina was doubtful, and suggested that the three genera Trichodinella, Tripartiella, and Paratrichodina should be incorporated into one independent genus. In addition, we provided morphological and molecular data of additional eight trichodinids, and further performed the phylogenetic analysis and traced the evolution history of trichodinids' five morphological and bionomical characters for the first time by taking advantage of the current GenBank data. According to the present results, one evolutionary hypothesis of trichodinids was proposed as follows. The most recent common ancestor of trichodinids inhabiting the freshwater environment as a symbiont of vertebrates should evolve from the ancestor with a long-spiral adoral ciliary turn. The first differentiated Trichodina species should be parasitic on one vertebrate distributed in the freshwater environment. During their evolution, some trichodinids expanded to the marine environment, and some switched to invertebrates in the freshwater environment. The denticle of some freshwater Trichodina species became narrower, and the adoral ciliary spiral turn got shorter, forming the ancestor-oid organism with a short-spiral adoral ciliary turn. Then, those Trichodinella, Tripartiella, and Paratrichodina species might evolve from those ancestor-oid organisms with short-spiral adoral ciliary turn.

Trichodinid ectoparasites (Ciliophora: Peritricha) from Misgurnus anguillicaudatus (Cantor) and Anodonta woodiana (Lea) in China, with descriptions of two new species of Trichodina Ehrenberg, 1838.

During parasitological surveys in Chongqing, China, three trichodinids infecting a freshwater fish, Misgurnus anguillicaudatus (Cantor), and a mollusc, Anodonta woodiana (Lea), were investigated. Two of these species were found to be new. Trichodina lechriodentata n. sp., from the fish, was identified by its small-sized body and irregularly rectangular blade, while T. rara n. sp., from the mollusc, is characterised by its overall dimensions, denticle morphology and the presence of a white speckle in some specimens. T. modesta Lom, 1979 is also described from the fish. Photomicrographs and morphometric data are presented for all of the species.