A new genus, Laruella n. gen., is proposed for the proteocephalid cestode L. perplexa (La Rue, 1911) n. comb. (syn. Proteocephalus perplexus La Rue, 1911), a parasite of a 'living fossil', the bowfin (Amia calva), in North America. The new genus is differentiated from other proteocephalid genera by having a massive four-lobed scolex without an apical organ and bearing suckers possessing tear-shaped sphincters on their inner rim, vitelline follicles forming L-shaped lateral fields, with the vitellarium turned inwards (medially) ventrally alongside the posterior margin of the ovary, a ring-like vaginal sphincter situated at a considerable distance from the genital atrium, and ellipsoid eggs resembling those of bothriocephalid and diphyllobothriid tapeworms, except for the absence of an operculum. Phylogenetic relationships of the new genus are not resolved, but it belongs to the so-called Neotropical clade of the Proteocephalidae, which is composed mainly of Neotropical tapeworms of siluriforms and other teleosts, but also Nearctic and Palaearctic species of Ophiotaenia La Rue, 1911 from snakes and amphibians. A morphologically similar species, Proteocephalus ambloplitis (Leidy, 1887) from bass (Micropterus spp.) in North America, is provisionally retained in Proteocephalus Weinland, 1858 because its relationships to L. perplexa are not yet clear. The former species differs from L. perplexa by the presence of a large apical organ, large, elongate vaginal sphincter situated near the genital atrium, vitelline follicles limited to lateral longitudinal fields, strongly coiled vas deferens within the cirrus sac, and a convoluted vaginal canal anterior to the ovarian isthmus. Laruella perplexa reportedly has a s broad spectrum of hosts but most are likely postcyclic or accidental hosts. A list of cestode parasites reported from bowfin is provided; it includes eight species and three taxa not identified to the species level. However, only three adult cestodes, L. perplexa and two species of Haplobothrium Cooper, 1914, are typical tapeworm parasites of bowfin, but previous molecular studies indicate possible existence of a putative new species in bowfin.

• Keywords
• Actinopterygii, Morphology, North America, Onchoproteocephalidea, Tapeworms, Taxonomy,
• Publication type
• Journal Article MeSH

Tapeworms (Cestoda) of the Proteocephalus-species aggregate from cyprinoids, pike, eel, smelt and cavefish in the Nearctic region (North America) are reviewed, based on a critical examination of newly collected and museum specimens. For some species neither new nor museum specimens were available and only literature data were used for these taxa. Two species occur in North American cyprinoids: (i) Nearctic Proteocephalus buplanensis Mayes, 1976 in Semotilus atromaculatus (Mitchill) in the upper Mississippi River and Hudson Bay drainage basins, and (ii) Holarctic P. torulosus (Batsch, 1786) (syns. P. ptychocheilus Faust, 1919; P. cobraeformis Haderlie, 1953; and Ophiotaenia critica Mpoame & Landers, 1981, new synonym), which occurs in Ptychocheilus spp. and other leuciscids in the western part of North America. Proteocephalus pinguis La Rue, 1911 is a specific parasite of pike (Esox spp.), which is briefly redescribed here to establish its diagnostic morphological characteristics because the original description was based on a mixture of at least two species. In addition to P. pinguis, pike serve as postyclic hosts of several species of the Proteocephalus-aggregate typical of other fish, such as bass, perch and whitefish, namely P. fluviatilis Bangham, 1925, P. pearsei La Rue, 1919 and P. longicollis (Zeder, 1800). Cavefish (Amblyopsidae) in North America harbour two endemic species, P. chologasteri Whittaker & Hill, 1968 from Chologaster agassizii Putman and P. poulsoni Whittaker & Zober, 1978 from Amblyopsis spelaea DeKay, which have never been found since their original description and their validity should be confirmed based on new collections and molecular data. Two other species of the Proteocephalus-aggregate, P. macrocephalus (Creplin, 1825), a parasite of eels (Anguilla spp.), and P. tetrastomus (Rudolphi, 1810) from smelt (Osmeridae), have circumboreal (Holarctic) distribution. Molecular data are available only for three of the seven species treated herein, but they do not form a monophyletic group.

• MeSH
• Cestoda * classification   genetics   MeSH
• DNA, Helminth genetics   MeSH
• Species Specificity MeSH
• Genetic Variation * MeSH
• Host Specificity * MeSH
• Fish Diseases * parasitology   MeSH
• Rivers MeSH
• Animal Distribution * MeSH
• Fishes * parasitology   MeSH
• Animals MeSH
• Check Tag
• Animals MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH
• Geographicals
• North America MeSH
• Names of Substances
• DNA, Helminth MeSH

An exhaustive literature search supplemented by a critical examination of records made it possible to present an annotated checklist of tapeworms (Cestoda) that, as adults or larvae (metacestodes), parasitize freshwater, brackish water and marine fishes, i.e. cartilaginous and bony fishes, in South America. The current knowledge of their species diversity, host associations and geographical distribution is reviewed. Taxonomic problems are discussed based on a critical evaluation of the literature and information on DNA sequences of individual taxa is provided to facilitate future taxonomic and phylogenetic studies. As expected, the current knowledge is quite uneven regarding the number of taxa and host-associations reported from the principal river basins and marine ecoregions. These differences may not only reflect the actual cestode richness but may also be due to the research effort that has been devoted to unravelling the diversity of these endoparasitic helminths in individual countries. A total of 297 valid species, 61 taxa identified to the generic level, in addition to unidentified cestodes, were recorded from 401 species of fish hosts. Among the recognized cestode orders, 13 have been recorded in South America, with the Onchoproteocephalidea displaying the highest species richness, representing c. 50% of all species diversity. The majority of records include teleost fish hosts (79%) that harbour larval and adult stages of cestodes, whereas stingrays (Myliobatiformes) exhibit the highest proportion of records (39%) among the elasmobranch hosts. Fish cestodes are ubiquitous in South America, being mostly recorded from the Warm Temperate Southeastern Pacific (WTSP; 31%) for marine hosts and the Amazon River basin (45%) for freshwater ones. The following problems were detected during the compilation of literary data: (i) unreliability of many records; (ii) poor taxonomic resolution, i.e. identification made only to the genus or even family level; (iii) doubtful host identification; and (iv) the absence of voucher specimens that would enable us to verify identification. It is thus strongly recommended to always deposit representative specimens in any type of studies, including faunal surveys and ecological studies. An analysis of the proportion of three basic types of studies, i.e. surveys, taxonomic and ecological papers, has shown a considerable increase of ecological studies over the last decade.

• Keywords
• Biodiversity, marine ecoregions, river basins, species richness, tapeworms,
• Publication type
• Journal Article MeSH

Proteocephalidean tapeworms form a diverse group of parasites currently known from 315 valid species. Most of the diversity of adult proteocephalideans can be found in freshwater fishes (predominantly catfishes), a large proportion infects reptiles, but only a few infect amphibians, and a single species has been found to parasitize possums. Although they have a cosmopolitan distribution, a large proportion of taxa are exclusively found in South America. We analyzed the largest proteocephalidean cestode molecular dataset to date comprising more than 100 species (30 new), including representatives from 54 genera (80%) and all subfamilies, thus significantly improving upon previous works to develop a molecular phylogeny for the group. The Old World origin of proteocephalideans is confirmed, with their more recent expansion in South America. The earliest diverging lineages are composed of Acanthotaeniinae and Gangesiinae but most of the presently recognized subfamilies (and genera) appear not to be monophyletic; a deep systematic reorganization of the order is thus needed and the present subfamilial system should be abandoned. The main characters on which the classical systematics of the group has been built, such as scolex morphology or relative position of genital organs in relation to the longitudinal musculature, are of limited value, as demonstrated by the very weak support for morphologically-defined subfamilies. However, new characters, such as the pattern of uterus development, relative ovary size, and egg structure have been identified, which may be useful in defining phylogenetically well-supported subgroups. A strongly supported lineage infecting various snakes from a wide geographical distribution was found. Although several improvements over previous works regarding phylogenetic resolution and taxon coverage were achieved in this study, the major polytomy in our tree, composed largely of siluriform parasites from the Neotropics, remained unresolved and possibly reflects a rapid radiation. The genus Spasskyellina Freze, 1965 is resurrected for three species of Monticellia bearing spinitriches on the margins of their suckers.

• Keywords
• Eucestoda, Proteocephalidae, Spasskyellina, host-parasite associations, molecular phylogeny, systematics,
• Publication type
• Journal Article MeSH

A list and key to the identification of valid species of tapeworms of the Proteocephalus Weinland, 1858 aggregate sensu de Chambrier et al. (2004), i.e. species of the genus occurring in fresh- and brackish-water fishes in the Palaearctic Region, are provided, with data on their hosts and geographical distribution. Instead of 32 taxa listed by Schmidt (1986) and subsequent authors, only the following 14 species are considered to be valid: P. ambiguus (Dujardin, 1845) (type-species); P. cernuae (Gmelin, 1790); P. filicollis (Rudolphi, 1802); P. fluviatilis Bangham, 1925; P. gobiorum Dogiel & Bychowsky, 1939; P. longicollis (Zeder, 1800); P. macrocephalus (Creplin, 1825); P. midoriensis Shimazu, 1990; P. percae (Müller, 1780); P. plecoglossi Yamaguti, 1934; P. sagittus (Grimm, 1872); P. tetrastomus (Rudolphi, 1810); P. thymalli (Annenkova-Chlopina, 1923); and P. torulosus (Batsch, 1786). An analysis of sequences of the nuclear genes (ITS2 and V4 region of 18S rDNA) revealed the following phylogenetic relationships for these taxa: P. torulosus ((P. midoriensis, P. sagittus) (P. fluviatilis (P. filicollis, P. gobiorum, P. macrocephalus)) (P. cernuae, P. plecoglossi, P. tetrastomus ((P. longicollis, P. percae) (P. ambiguus, P. thymalli)))). P. pronini Rusinek, 2001 from grayling Thymallus arcticus nigrescens is synonymised with P. thymalli. P. esocis La Rue, 1911 is apparently invalid but its conspecificity with either P. percae or P. longicollis could not be confirmed due to the absence of the scolex in the holotype and the unavailability of other material for morphological and molecular studies. P. osculatus (Goeze, 1782) has recently been transferred to Glanitaenia de Chambrier, Mariaux, Vaucher & Zehnder, 2004. The validity of the genus is supported by the position of G. osculata within the Proteocephalidea, based on molecular data, as well as its morphology and nature of the definitive host (the European wels Silurus glanis). P. hemispherous Rahemo & Al-Niaeemi, 2001, described from S. glanis in Iraq, is transferred to Postgangesia Akhmerov, 1960 as Postgangesia hemispherous (Rahemo & Al-Niaeemi, 2001) n. comb.

• MeSH
• Cestoda genetics   MeSH
• DNA, Helminth chemistry   genetics   MeSH
• Phylogeny MeSH
• DNA, Ribosomal Spacer chemistry   genetics   MeSH
• Molecular Sequence Data MeSH
• Polymerase Chain Reaction MeSH
• RNA, Ribosomal, 18S chemistry   genetics   MeSH
• RNA, Ribosomal, 5.8S chemistry   genetics   MeSH
• Fishes parasitology   MeSH
• Base Sequence MeSH
• Sequence Alignment MeSH
• Animals MeSH
• Check Tag
• Animals MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH
• Names of Substances
• DNA, Helminth MeSH
• DNA, Ribosomal Spacer MeSH
• RNA, Ribosomal, 18S MeSH
• RNA, Ribosomal, 5.8S MeSH

The fine structure of the mature spermatozoon of the corallobothriine tapeworm Corallobothrium solidum Fritsch, 1886 (Cestoda: Proteocephalidea) from the electric catfish Malapterurus electricus from the Nile River in Egypt was studied by transmission electron microscopy for the first time. The filiform spermatozoon of C. solidum contains two axonemes of unequal length and a typical 9 + "1" trepaxonematan pattern. A single helicoidal crested body (30-200 nm thick) is localized at the anterior extremity of the gamete. The cortical microtubules line the periphery of the cell, largely parallel to the long axis of the spermatozoon and exhibiting signs of twisting at the beginning of region II. The nucleus, in the form of an electron-dense (largely in gametes of testes) and/or fibrous cord (largely in gametes from male reproductive ducts and seminal vesicle), coils in a spiral through the middle part (region III) of the spermatozoon. The cytoplasm contains electron-dense granules in regions II, III and partly in region IV. The cytoplasm of some spermatozoa exhibits an apparently higher electron-density at the end of the nucleated region (III), and continuously toward the middle part of region IV. The anterior and posterior extremities of the spermatozoa have a single axoneme. The ultrastructural features of the mature spermatozoon of C. solidum mostly coincide with those of the spermatozoon of other proteocephalideans, especially the gangesiine Electrotaenia malopteruri parasitizing the same host.

• MeSH
• Cestoda ultrastructure   MeSH
• Cestode Infections parasitology   veterinary   MeSH
• Fish Diseases parasitology   MeSH
• Spermatozoa ultrastructure   MeSH
• Catfishes parasitology   MeSH
• Microscopy, Electron, Transmission MeSH
• Animals MeSH
• Check Tag
• Male MeSH
• Animals MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH