Gastrointestinal Helminths of Magpies (Pica pica), Rooks (Corvus frugilegus) and Carrion Crows (Corvus corone) in Mazandaran Province, North of Iran.

BACKGROUND: Corvidae is a cosmopolitan family of oscine birds including crows, rooks, magpies, jays, chough, and ravens. These birds are migratory species, especially in the shortage of foods, so they can act like vectors for a wide range of microorganisms. They live generally in temperate climates and in a very close contact with human residential areas as well as poultry farms. There is no available information in the literature concerning the parasitic infections of these three species of corvidae in Mazandaran Province, northern Iran, so this study was conducted to clarify this. METHODS: As there are three species of corvid birds in Mazandaran Province, 106 birds including 79 magpies, 11 rooks, and 16 carrion crows were examined between winter 2007 and spring 2008 at post mortem for gastrointestinal helminths. The helminths were drawn and identified morphologically in the Laboratory of Parasitology, Islamic Azad University, Science and Research Branch, Tehran and also partly in the School of Public Health, Tehran University of Medical Sciences, based on the reference books and identification keys like Soulsby, Khalil et al. and Anderson et al. RESULTS: Four species of nematodes, 2 species of cestodes, 1 species of trematodes and 1 species of acanthocephalans were identified in these three corvid species. CONCLUSION: Five species of the helminths are identified for the first time in Iran, and the acanthocephalan species is new host record for rooks. It is clear that these corvid birds have diverse range of helminths and can act as carriers for infecting the domestic fowls.

Interrelationships and evolution of the tapeworms (Platyhelminthes: Cestoda).

Interrelationships of the tapeworms (Platyhelminthes: Cestoda) were examined by use of small (SSU) and large (LSU) subunit ribosomal DNA sequences and morphological characters. Fifty new complete SSU sequences were added to 21 sequences previously determined, and 71 new LSU (D1-D3) sequences were determined for the complementary set of taxa representing each of the major lineages of cestodes as currently understood. New sequences were determined for three amphilinidean taxa, but were removed from both alignments due to their excessively high degree of divergence from other cestode sequences. A morphological character matrix coded for supraspecific taxa was constructed by the modification of matrices from recently published studies. Maximum-parsimony (MP) analyses were performed on the LSU, SSU, LSU+SSU, and morphological data partitions, and minimum-evolution (ME) analyses utilizing a general time reversible model of nucleotide substitution including estimates of among-site rate heterogeneity were performed on the molecular data partitions. Resulting topologies were rooted at the node separating the Gyrocotylidea from the Eucestoda. The LSU data were found to be more informative than the SSU data and were more consistent with inferences from morphology, although nodal support was generally weak for most basal nodes. One class of transitions was found to be saturated for comparisons between the most distantly related taxa (gyrocotylideans vs cyclophyllideans and tetrabothriideans). Differences in the topologies resulting from MP and ME analyses were not statistically significant. Nonstrobilate orders formed the basal lineages of trees resulting from analysis of LSU data and morphology. Difossate orders were basal to tetrafossate orders, the latter of which formed a strongly supported clade. A clade including the orders Cyclophyllidea, Nippotaeniidea, and Tetrabothriidea was supported by all data partitions and methods of analysis. Paraphyly of the orders Pseudophyllidea, Tetraphyllidea, and Trypanorhyncha was consistent among the molecular data partitions. Inferences are made regarding a monozoic (nonsegmented) origin of the Eucestoda as represented by the Caryophyllidea and for the evolution of the strobilate and acetabulate/tetrafossate conditions having evolved in a stepwise pattern.

Origin and evolution of African Polystoma (Monogenea: Polystomatidae) assessed by molecular methods.

Among Polystomatidae (Monogenea), the genus Polystoma, which mainly infests neobatrachian hosts, is the most diverse and occurs principally in Africa, from where half the species have been reported. Previous molecular phylogenetic studies have shown that this genus originated in South America, and later colonised Eurasia and Africa. No mention was made on dispersal corridors between Europe and Africa or of the origin of the African Polystoma radiation. Therefore, a molecular phylogeny was inferred from ITS1 sequences of 21 taxa comprising two species from America, seven representatives from Europe and 12 from Africa. The topology of the phylogenetic tree reveals that a single event of colonisation took place from Europe to Africa and that the putative host carrying along the ancestral polystome is to be found among ancestral pelobatids. Percentage divergences estimates suggest that some presumably distinct vesicular species in unrelated South African anurans and some neotenic forms found in several distinct hosts in Ivory Coast, could, in fact, belong to two single polystome species parasitising divergent hosts. Two main factors are identified that may explain the diversity of African polystomes: (i), we propose that following some degree of generalism, at least during the juvenile stages of both hosts and parasites, distinctive larval behaviour of polystomes engenders isolation between parasite populations that precludes sympatric speciations; (ii), cospeciation events between Ptychadena hosts and their parasites are another factor of diversification of Polystoma on the African continent. Finally, we discuss the systematic status of the Madagascan parasite Metapolystoma, as well as the colonisation of Madagascar by the host Ptychadena mascareniensis.

Nomimoscolex suspectus n. sp. (Eucestoda: Proteocephalidea: Zygobothriinae) with morphological and molecular phylogenetic analyses of the genus.

We describe a new species of Nomimoscolex from the Amazon siluriform fishes Brachyplatystoma filamentosum, B. flavicans and B. vaillanti. It differs from N. piraeeba in a lower mean number of testes, the paramuscular position of the vitelline follicles, the ovarian width/proglottis width ratio and the cirrus-pouch length/proglottis width ratio. Protein electrophoresis assays performed for 25 enzymatic systems showed that specimens of N. suspectus n. sp. from the three host species form a homogenous population which was genetically isolated from N. piraeeba and N. dorad. Moreover, the latter two species, synonymised by Rego (1991) because of their close morphological similarity, could be separated at eight loci. We thus restore N. dorad as a valid species. We finally examined the composition of the genus Nomimoscolex using DNA sequences from the 5.8S rRNA, ITS-2 and 28S rRNA nuclear ribosomal genes and a matrix of 24 morphological characters. Phylogenetic relationships were inferred for nine species of the genus, five members of other monticelliid genera and two outgroup species. The results of the phylogenetic analyses performed on morphological and molecular characters converged with those from allozyme studies and showed that N. suspectus, N. piraeeba and N. dorad clustered in a distinct clade that excluded other members of the genus. We therefore recognised them as an aggregate of species to reflect an isolation supported by both morphological and genetic data. Because relationships among the remaining Nomimoscolex representatives and other genera were generally poorly resolved, regardless of the database analysed, no action was taken to reorganise them into alternative groupings.

Molecular systematics of Mesocestoides sPP (cestoda: mesocestoididae) from domestic dogs (Canis familiaris) and coyotes (Canis latrans).

The genus Mesocestoides Vaillant, 1863 includes tapeworms of uncertain phylogenetic affinities and with poorly defined life histories. We previously documented 11 cases of peritoneal cestodiasis in dogs (Canis familiaris L.) in western North America caused by metacestodes of Mesocestoides spp. In the current study, DNA sequences were obtained from metacestodes collected from these dogs (n = 10), as well as proglottids from dogs (n = 3) and coyotes (Canis latrans Say, 1823 [n = 2]), and tetrathyridia representing laboratory isolates of M. corti (n = 3), and these data were analyzed phylogenetically. Two nuclear genetic markers, 18S ribosomal DNA and the second internal-transcribed spacer (ITS 2), were sequenced. Phylogenetic analysis of the 18S rDNA data recovered a monophyletic group composed of all samples of Mesocestoides spp., distinct from closely related outgroup taxa (Amurotaenia Akhmerov, 1941 and Tetrabothrius Rudolphi, 1819). Initial analysis of the ITS 2 data resolved 3 clades within Mesocestoides. Two proglottids from dogs formed a basal clade, a second clade was represented by tetrathyridial isolates, and a third clade included all other samples. Interpretation of these data from an apomorphy-based perspective identified 6 evolutionary lineages. We also assessed whether metacestodes from dogs (n = 4) are capable of asexual proliferation in laboratory mice. One tetrathyridial and 2 acephalic isolates from dogs proliferated asexually. Further investigation is warranted to determine which of the lineages represent distinct species and to determine the life history strategies of Mesocestoides spp.

Phylogenetic analysis of the suborder plagiorchiata (Platyhelminthes, Digenea) based on partial lsrDNA sequences.

The phylogenetic relationships and systematic position of the members of the suborder Plagiorchiata, one of the derived and most diverse groups of Digenea, have always been controversial. Here, we present a phylogeny of this group based on the analysis of partial sequences of the lsrDNA in 28 species representing 13 families of Plagiorchiata, as well as four outgroups. Our results show that the Plagiorchiata, as considered by most authors, is not monophyletic, and that the superfamilies Opecoeloidea, and most probably Dicrocoelioidea and Gorgoderoidea, may have to be removed from this suborder. According to our results, the Plagiorchiata includes only parasites of terrestrial vertebrates. We find the Plagiorchiata to be composed of two well-supported clades which can be ranked as superfamilies: (1) Plagiorchioidea, including the Plagiorchiidae, Haematoloechidae, Telorchiidae, Brachycoeliidae and Leptophallidae; and (2) Microphalloidea containing the Microphallidae, Prosthogonimidae, Lecithodendriidae and Pleurogenidae. The genetic analysis also allowed revision of the position of several taxa of Plagiorchiata, including: (1) a confirmation of the position of the Brachycoeliidae within the Plagiorchiata; (2) a close phylogenetic relationships of Macrodera with Paralepoderma, Leptophallus and Metaleptophallus; (3) the grouping of Opisthioglyphe and Telorchis within a distinct and strongly supported clade; and (4) the placement of Allassogonoporus amphoraeformis within the Pleurogenidae, and not close to Lecithodendriidae. Some systematic changes, corresponding to these results, are proposed.

Molecular systematic analysis of the order Proteocephalidea (Eucestoda) based on mitochondrial and nuclear rDNA sequences.

Two ribosomal DNA sequences were used to infer phylogenetic relationships among the Eucestoda order Proteocephalidea. A 437 bp portion of the 16S mitochondrial and a 1149 bp 5' portion of the nuclear large sub-unit rRNA molecule were sequenced for 53 proteocephalidean cestodes (representing nine subfamilies and 22 genera) and for one outgroup species. Parsimony and distance-based analyses of the two databases, alone and combined, failed to support the monophyly of the two traditionally accepted families, of numerous subfamilies (with the exception of the Rudolphielliinae and Othinoscolescinae which were validated in our analysis) and of various genera, including the genus Nomimoscolex (Woodland), Ophiotaenia (La Rue) as well as the type genus Proteocephalus (Weinland). Palaearctic Proteocephalus species nevertheless constituted a well-defined clade. The two genes globally yielded compatible results; however, the nuclear ribosomal gene provided a better resolution of relations among Proteocephalidea.

Desiccation- and abscisic acid-responsive genes encoding major intrinsic proteins (MIPs) from the resurrection plant Craterostigma plantagineum.

Major intrinsic proteins (MIPs) are a family of channel proteins that are mainly represented by aquaporins in plants. These are divided into TIPs (tonoplast intrinsic proteins) and PIPs (plasma membrane intrinsic proteins) according to their subcellular localization. Homologues to PIPs and TIPs were isolated from the desiccation-tolerant resurrection plant Craterostigma plantagineum by two approaches: firstly, a cDNA library constructed from RNA of dehydrated C. plantagineum leaves was screened with an Arabidopsis thaliana Ath-PIP1b cDNA probe and, secondly, a cDNA library was screened differentially to isolate early drought-induced transcripts. According to sequence homologies the isolated cDNA clones were grouped as follows: Cp-PIPa, Cp-PIPb, Cp-PIPc and Cp-TIP. Cp-PIPa, Cp-PIPc and Cp-TIP transcript accumulation was regulated by dehydration and abscisic acid (ABA). Within the Cp-PIPa group transcripts were regulated either by drought only or by drought and ABA, indicating that ABA-dependent and -independent signal transduction pathways lead to Cp-PIPa expression. Comparison of Cp-PIPa expression in detached leaves and in whole plants suggested the involvement of a signal transmitted in the whole plant in response to drought. Cp-PIPb transcript levels were constitutive in all organs tested. Antibodies raised against a Cp-PIPA protein recognized a polypeptide with an apparent molecular mass of 28 kDa. Using these antibodies it was shown that both Cp-PIPA and Cp-PIPB proteins were localized to the plasma membrane. The role of different members of the MIP group in the dehydration response is discussed.

A molecular phylogeny of the Eucestoda.

Evolutionary relationships among the orders of the Eucestoda were examined based on data derived from partial sequences of genes encoding 18S rRNA. Considered in this study were 47 species-level taxa, including 1 from Monogenea, 1 from Amphilinidea, both of which were used as outgroups, and 45 from 10 orders of Eucestoda. Parsimony analysis of 1.1 kbp of aligned fragments yielded 480 shortest trees (length 704; consistency index 0.41) the strict consensus of which shows the following relationships: (Monogenea, (Amphilinidea, (Caryophyllidea, (Spathebothriidea, (Trypanorhyncha, (Pseudophyllidea, (Tetraphyllidea, ((Diphyllidea, Proteocephalidea), ((Cyclophyllidea, Tetrabothriidea), Nippotaeniidea))))))))). The Tetraphyllidea, Pseudophyllidea (because of the Diphyllobothriidae), and Cyclophyllidea (because of the Mesocestoididae) were found to be paraphyletic. This tree is almost completely congruent with the most recent hypotheses based on characters derived from comparative morphology, ontogeny, and ultrastructural studies. The only discrepancies between these separate analyses were in the position of the Trypanorhyncha and Diphyllidea. Among the main conclusions corroborated here are the following: (1) the basal position of the Caryophyllidea (and Spathebothriidea), and hence the plesiomorphic condition of monozoism; (2) the monophyly of the "higher tetrafossates" provided the nippotaeniids and tetrabothriids are included; (3) the close relationship between the Tetrabothriidea and Cyclophyllidea; and (4) the paraphyly of the Tetraphyllidea. At lower taxonomic levels, structure could not be defined within Proteocephalidea; within the Cyclophyllidea, all families represented by several taxa (Hymenolepididae, Davaineidae, and Dilepididae) were found to be monophyletic, and Taeniidae may be the most basal family. Furthermore, the validity of the Gryporhynchidae is confirmed. and it is suggested that the Mesocestoididae should be excluded from the Cyclophyllidea.

Phylogeny of the orders of the Eucestoda (Cercomeromorphae) based on comparative morphology: historical perspectives and a new working hypothesis.

The phylogeny of the Eucestoda was evaluated based on a suite of 49 binary and multistate characters derived from comparative morphological and ontogenetic studies; attributes of adult and larval tapeworms were considered. A single most parsimonious tree (MPT) (consistency index = 0.872; retention index = 0.838; and homoplasy index = 0.527) was fully resolved and is specified by the following: (Gyrocotylidea, (Amphilinidea, ((Spathebothriidea, (Pseudophyllidea, ((Diphyllidea, (Trypanorhyncha, (Tetraphyllidea, (Lecanicephalidea, ((Nippotaeniidea, (Tetrabothriidea, Cyclophyllidea)), Proteocephalidea))))), Haplobothriidea))), Caryophyllidea))). Monophyly for the Eucestoda was firmly corroborated. Trees derived from the primary and bootstrap analyses were congruent, but low values, particularly for relationships among the tetrafossate tapeworms, indicated additional examination is warranted. The MPT was found to be the most efficient hypothesis for describing character evolution and in specifying relationships among the orders when compared to those concepts that had been developed for the tapeworms over the past century. Areas of congruence were shared among the current hypothesis and one or more of the prior hypotheses. Major conclusions include: (1) Caryophyllidea are basal and monozooy is ancestral; (2) difossate forms are primitive, and the Pseudophyllidea are the sister group of the strongly polyzoic tapeworms; (3) Nippotaeniidea are highly derived; (4) the higher tapeworms (Tetraphyllidea, Lecanicephalidea, Proteocephalidea, Nippotaeniidea, Tetrabothriidea, and Cyclophyllidea) are closely related or potentially coordinate groups: (5) Tetrabothriidea and the Cyclophyllidea are sister groups; and (6) Tetraphyllidea is paraphyletic, with the Onchobothriidae basal to the Phyllobothriidae. Character support for placement of the Tetrabothriidea continues to be contradictory, and this order may represent a key to understanding the phylogeny of the higher cestodes. The current study constitutes a complete historical review and poses a new and robust hypothesis for the phylogeny of the Eucestoda.

A molecular phylogenetic survey of the nightjars and allies (Caprimulgiformes) with special emphasis on the potoos (Nyctibiidae).

A 656-pb fragment of the mitochondrial cytochrome b gene was sequenced for six species of Central and South American potoos (genus Nyctibius, Nyctibiidae) as well as for selected representatives of all other caprimulgiform families. Sequence divergence among potoos was much higher (11.1-16.2%) than has typically been observed among congeneric species of birds, suggesting that the species of Nyctibius are quite old. Divergence among families was also quite high (13.7-21.8%), confirming recent DNA-DNA hybridization studies. Such high genetic divergences in a functionally constrained gene like cyt b indicate that many of those sites which are free to vary will have experienced multiple substitutions. We therefore performed phylogenetic analysis using parsimony under a variety of weighting schemes intended to reduce the effect of multiple substitutions. The monophyly of all the traditional caprimulgiform families was confirmed and a number of new hypotheses of relationship emerged. From our analysis, it appears that the oilbird (Steatornis) is an ancient member of the order, and it is not closely related to the potoos. We also note the close link between Aegothelidae and Caprimulgidae, and the basal position of the Podargidae/Batrachostomidae clade in the phylogeny. These results are in accordance with several classical works of the first half of the century. The relationships of the various Nyctibius species to each other have not been fully resolved; however, a close link between N. leucopterus and N. maculosus appears to be highly probable from our data.

Cestode systematics: any progress?

In this short review, I summarize the recent advances, the present state and future for research in the field of cestode systematics. First, within an historical context, I briefly outline why our understanding of relationships within the Eucestoda has been problematic and contentious. On this foundation, I then summarize and discuss recent progress at various supraspecific levels, and at the specific level. Of particular interest in this respect is the discrepancy between the methods applied to understand the evolution of a few well-studied taxa, for instance the complex of Echinococcus species, contrasted with our relative ignorance about the systematic status of the vast majority of species. This leads to a review of the diversity of classical and new methodologies currently applied in the field of cestode systematics. Applications of morphoanatomical investigations as well as more recent molecular tools are examined, and some less common approaches are also reviewed. Finally, several practical and theoretical difficulties that are specific to the domain are discussed. These include problems in accessibility of material and adequate consideration of host-specificity. Our current state of knowledge represents an apparent paradox in that significant progress has indeed been achieved during the last 15 years, but appears limited to very specific cases, principally among medically important taxa. Conversely, more general works whose utility has been long recognized have not been addressed despite their conceptual simplicity. Consequently the development of new techniques, especially molecular ones, to allow access to new classes of characters is encouraged. However the need for continuous effort using more traditional approaches, including continued field collection, excellent and detailed descriptions and redescriptions, as well as critical revisions of classical monographs is also emphasized. A synergism linking morphological and molecular characters and phylogenetic approaches to analysis provides a firm foundation for rapid and seminal advances in the elucidation of relationships among the Eucestoda.

A new genus of Metadilepididae (Cestoda: Cyclophyllidea) parasitic in Terpsiphone rufiventer (Aves: Muscicapidae) from the Ivory Coast.

Pseudadelphoscolex eburnensis, a new genus and species of metadilepidid Cyclophyllidea parasitic in the red-bellied paradise flycatcher, Terpsiphone rufiventer, from the Ivory Coast, is described. The new species is characterized by davaineidlike rostellar hooks, absence of a rostellar pouch, a huge cirrus pouch in gravid proglottids, a bilobed uterus that becomes progressively reticular, absence of a paruterine organ, and eggs with an internal coat forming a crescentic protuberance outside the embryophore. The presence of a single row of rostellar hooks together with the lack of spines on the sucker and the structure and position of the uterus exclude this new material from Davaineidae. It cannot be placed in Dilepididae due to the lack of a rostellar pouch or in Paruterinidae because of the lack of a paruterine organ. The position of the excretory ducts in relation to the genital pores and the alternance of these pores are the main characters used to exclude this new species from the known genera of Metadilepididae. The diversity of forms of Metadilepididae in intertropical terrestrial birds is increased, and the validity of this taxon is strengthened.

A new genus of Dilepididae (Cestoda) of the yellowbill Ceuthmochares aereus (Cuculidae) from the Ivory Coast.

Bonaia africana n. gen., n. sp. (Cestoda: Dilepididae) has been found in Ceuthmochares aereus (Aves: Cuculidae) in the Ivory Coast (West Africa). This new tapeworm is mainly characterized by its unusual rostellar hooks that are implanted irregularly and which present a variable form and length in the same rostellum. The differential diagnosis, particularly in comparison with the closely related genera Liga and Amoebotaenia, is presented: Liga possesses an atrial bundle of setae and Amoebotaenia 1 row of well built hooks with a typical blade. It is assumed that the unusual disposition of the rostellar hooks described here could be a transitional form between the 1- and 2-row patterns or a degenerate derivative of a regular arrangement.