Representatives of Ligophorus Euzet et Suriano, 1977 were found on the gills of Mugil liza Valenciennes caught in southern Brazil. They were identified as Ligophorus uruguayense Failla Siquier et Ostrowski de Núñez, 2009 and Ligophorus saladensis Marcotegui et Martorelli, 2009, even though specific identification proved to be difficult due to inconsistencies in some diagnostic features reported for these two species. Therefore, a combined morphological and molecular approach was used to critically review the validity of these species, by means of phase contrast and confocal fluorescence microscopical examination of sclerotised hard parts, and assessing the genetic divergence between L. saladensis, L. uruguayense and their congeners using rDNA sequences. The main morphological differences between the two species relate to the shape of the accessory piece of the penis and the median process of the ventral bar. The accessory piece in L. uruguayense is shorter than in L. saladensis, has a cylindrical, convex upper lobe and straight lower lobe (vs with the distal tip of the lower lobe turning away from the upper lobe in the latter species). The ventral bar has a V-shaped anterior median part in L. uruguayense (vs U-shaped in L. saladensis). The two species are suggested to be part of a species complex together with L. mediterraneus Sarabeev, Balbuena et Euzet, 2005. We recommend to generalise such comparative assessment of species of Ligophorus for a reliable picture of the diversity and diversification mechanisms within the genus, and to make full use of its potential as an additional marker for mullet taxonomy and systematics., Natalia C. Marchiori, Antoine Pariselle, Joaber Pereira Jr., Jean-François Agnèse, Jean-Dominique Durand, Maarten P.M. Vanhove., and Obsahuje bibliografii
Frezella gen. n. is proposed to accommodate Frezella vaucheri sp. n. from poorly known auchenipterid fish, Tocantinsia piresi (Miranda Ribeiro), from the Xingú River, one of the principal tributaries of the lower Amazon River in Brazil. The new genus belongs to the Proteocephalinae because of the medullary position of the testes, ovary (yet some follicles penetrate to the cortex on the dorsal side), vitelline follicles and uterus. It differs from other proteocephaline genera in the morphology of the scolex, which includes a metascolex composed of two distinct zones: anterior, strongly wrinkled part posterior to the suckers, and posterior, sparsely folded zone. Frezella can also be differentiated by having the internal longitudinal musculature hypertrophied laterally on both sides, the presence of some ovarian follicles in the cortex on the dorsal side and the presence of additional pair of tiny, thin-walled osmoregulatory canals situated slightly dorsomedian to ventral canals. Frezella vaucheri is the first helminth parasite reported from T. piresi, which occurs in the lower reaches of the Amazon and Tocantins River basins in Brazil., Philippe Vieira Alves, Alain de Chambrier, Tomáš Scholz, José Luis Luque., and Obsahuje bibliografii
Forticulcita platana sp. n. and Forticulcita apiensis sp. n. are described from Mugil liza Valenciennes in Argentina, and from Mugil cephalus Linnaeus in Salt Springs, Florida, USA, respectively. Supplemental material relating to the hermaphroditic sac of Forticulcita gibsoni Blasco-Costa, Montero, Balbuena, Raga et Kostadinova, 2009 is provided from a specimen isolated from M. cephalus off Crete, Greece.Forticulcita platana can be distinguished from all species of Forticulcita Overstreet, 1982 except F. gibsoni, based on possessing small pads or gland cells along the hermaphroditic duct. It can be differentiated from that species in possessing a hermaphroditic sac that is one and a half to two times longer than wide rather than one that is approximately three times longer than wide, longer eggs (44-52μm rather than 34-44 μm long) and a shorter post-testicular space (<45% of the body length). Forticulcita apiensis can be differentiated from the other species of Forticulcita in possessing a testis that is shorter than or equal to the pharynx rather than one that is longer than the pharynx. Xiha gen. n. is erected for Dicrogaster fastigatus Thatcher et Sparks, 1958 as Xiha fastigata (Thatcher et Sparks,1958) comb. n., and we tentatively consider Dicrogaster fragilis Fernández Bargiela, 1987 to be Xiha fragilis (Fernández Bargiela, 1987) comb.n. The new genus fits within the concept of Forticulcitinae Blasco-Costa, Balbuena, Kostadinova et Olson, 2009 in having a vitellarium comprised of a single elongate to subspherical mass. Xiha can be differentiated from Forticulcita in having spines lining the hermaphroditic duct, or intromittent organ. A Bayesian inference analysis of partial 28S rDNA sequences of the two New World species of Forticulcita, Xiha fastigata and previously published haploporids places Xiha fastigata within the Forticulcitinae and sister to Forticulcita. Amended diagnos for the subfamily and for Dicrogaster Looss, 1902 are provided., Michael J. Andres, Stephen S. Curran, Thomas J. Fayton, Eric E. Pulis, Robin M. Overstreet., and Obsahuje bibliografii
a1_Understanding of the diversity of species of Cryptosporidium Tyzzer, 1910 in tortoises remains incomplete due to the limited number of studies on these hosts. The aim of the present study was to characterise the genetic diversity and biology of cryptosporidia in tortoises of the family Testudinidae Batsch. Faecal samples were individually collected immediately after defecation and were screened for presence of cryptosporidia by microscopy using aniline-carbol-methyl violet staining, and by PCR amplification and sequence analysis targeting the small subunit rRNA (SSU), Cryptosporidium oocyst wall protein (COWP) and actin genes. Out of 387 faecal samples from 16 tortoise species belonging to 11 genera, 10 and 46 were positive for cryptosporidia by microscopy and PCR, respectively. All samples positive by microscopy were also PCR positive. Sequence analysis of amplified genes revealed the presence of the Cryptosporidium tortoise genotype I (n = 22), C. ducismarci Traversa, 2010 (n = 23) and tortoise genotype III (n = 1). Phylogenetic analyses of SSU, COWP and actin gene sequences revealed that Cryptosporidium tortoise genotype I and C. ducismarci are genetically distinct from previously described species of Cryptosporidium. Oocysts of Cryptosporidium tortoise genotype I, measuring 5.8-6.9 µm × 5.3-6.5 µm, are morphologically distinguishable from C. ducismarci, measuring 4.4-5.4 µm × 4.3-5.3 µm. Oocysts of Cryptosporidium tortoise genotype I and C. ducismarci obtained from naturally infected Russian tortoises (Testudo horsfieldii Gray) were infectious for the same tortoise but not for Reeve's turtles (Mauremys reevesii [Gray]), common garter snake (Thamnophis sirtalis [Linnaeus]), zebra finches (Taeniopygia guttata [Vieillot]) and SCID mice (Mus musculus Linnaeus)., a2_The prepatent period was 11 and 6 days post infection (DPI) for Cryptosporidium tortoise genotype I and C. ducismarci, respectively; the patent period was longer than 200 days for both cryptosporidia. Naturally or experimentally infected tortoises showed no clinical signs of disease. Our morphological, genetic, and biological data support the establishment of Cryptosporidium tortoise genotype I as a new species, Cryptosporidium testudinis sp. n., and confirm the validity of C. ducismarci as a separate species of the genus Cryptosporidium., Jana Ježková, Michaela Horčičková, Lenka Hlásková, Bohumil Sak, Dana Květoňová, Jan Novák, Lada Hofmannová, John McEvoy, Martin Kváč., and Obsahuje bibliografii
During an ongoing systematic survey on species diversity of myxozoans parasitising allogynogenetic gibel carp Carassius auratus gibelio (Bloch) in China, plasmodia were detected in the fins, lip, jaw, gill chamber, gill arches, operculum and oral cavity of infected fish. Combining the morphological and molecular data, the present species was identified as Myxobolus turpisrotundus Zhang, Wang, Li et Gong, 2010. Histopathological examination revealed that despite infecting different organs, M. turpisrotundus always occurred in dermis, demonstrating its affinity to this tissue. Histopathological effect of M. turpisrotundus on the host is relatively mild except parasites in the gill arches producing compression of the adipose tissue and heavy adductor muscles deformation with lymphohistiocytic infiltrates. In addition, the plasmodia in different sites were with the same complex structure arrangement: cup-like cells with unknown derivation, a thin collagenous fibril layer, areolar connective tissue, basement membrane and host epithelial cell. Ultrastructural analysis showed that the parasite has monosporic pansporoblast and sporogenesis followed the usual pattern of most of the myxosporeans., Qingxiang Guo, Yanhua Zhai, Zemao Gu, Yang Liu., and Obsahuje bibliografii
During a survey the occurrence of Kudoa quraishii Mansour, Harrath, Abd-Elkader, Alwasel, Abdel-Baki et Al Omar, 2014, recently identified in the muscles of the Indian mackerel, Rastrelliger kanagurta (Cuvier), a species of Kudoa Meglitsch, 1947 infecting oocytes of mature females of the same host fish was found. The new species, for which the name Kudoa saudiensis sp. n. is proposed, infects oocytes that are enlarged with a whitish colour. The parasite develops in vesicular polysporous plasmodia within the oocyte. Infection occurs with a mean prevalence of 20% (7/35) of examined females. Mature spores are quadratic in shape in apical view, having four equal valves and four symmetrical polar capsules. Fresh spores are 2.4-3.6 µm long (mean ± SD 3.1 ± 0.3 µm), 4.3-5.4 µm (4.7 ± 0.3 µm) wide and 3.4-4.3 µm (3.8 ± 0.3 µm) in thickness and long. The smaller size of the new Kudoa species was the distinctive feature that separates it from all previously described species. Molecular analysis based on the SSU rDNA sequences shows that the highest percentage of similarity of 98.5% was observed with K. ovivora Swearer et Robertson, 1999, reported from oocytes of labroid fish from the Caribbean coasts of Panama. The percentage of similarity was 98% with K. azevedoi Mansour, Thabet, Chourabi, Harrath, Gtari, Al Omar et Ben Hassine, 2013 and 89% with K. quraishii. Phylogenetic analysis of the SSU and LSU rDNA data revealed a consistent of the new species with K. azevedoi and K. ovivora. Our findings support the creation of Kudoa saudiensis sp. n. that infects oocytes of the Indian mackerel Rastrelliger kanagurta., Lamjed Mansour, Abdel Halim Harrath, Abdel-Azeem S. Abdel-Baki, Saleh Alwasel, Saleh Al-Quraishy, Suliman Y. Al Omar., and Obsahuje bibliografii
Recently, malaria is remain considered as the most prevalent infectious disease, affecting the human health globally. High morbidity and mortality worldwide is often allied with cerebral malaria (CM) based disorders of the central nervous system, especially across many tropical and sub-tropical regions. These disorders are characterised by the infection of Plasmodium species, which leads to acute or chronic neurological disorders, even after having active/effective antimalarial drugs. Furthermore, even during the treatment, individual remain sensitive for neurological impairments in the form of decrease blood flow and vascular obstruction in brain including many more other changes. This review briefly explains and update on the epidemiology, burden of disease, pathogenesis and role of CM in neurological disorders with behaviour and function in mouse and human models. Moreover, the social stigma, which plays an important role in neurological disorders and a factor for assessing CM, is also discussed in this review., Arif Jamal Siddiqui, Mohd Adnan, Sadaf Jahan, Whitni Redman, Mohd Saeed and Mitesh Patel., and Obsahuje bibliografii
Based on light and scanning electron microscopical studies, two new species of parasitic nematodes are described from marine perciform fishes off New Caledonia: Cucullanus epinepheli sp. n. (Cucullanidae) from the intestine of the brownspotted grouper Epinephelus chlorostigma (Valenciennes) (Serranidae) and Procamallanus (Spirocamallanus) sinespinis sp. n. from the intestine of the silver grunt Pomadasys argenteus (Forsskål) (Haemulidae). Cucullanus epinepheli sp. n. differs from its congeners mainly in possessing a unique structure of the anterior, elevated cloacal lip with a large posterior outgrowth covering the cloacal aperture and in the presence of cervical alae and two small preanal papillae on the median dome-shaped precloacal elevation. This is the second known nominal species of this genus parasitising fishes of the family Serranidae and the second representative of Cucullanus Müller, 1777 recorded from fishes in New Caledonian waters. Procamallanus (Spirocamallanus) sinespinis sp. n. is mainly characterised by 10-12 spiral ridges in the buccal capsule, the presence of wide caudal alae, three pairs of pedunculate preanal papillae, two unequally long spicules (465-525 µm and 218-231 µm) and by the tail tip with a knob-like structure in the male, and the broad, rounded tail with a terminal digit-like protrusion without cuticular spikes in the female. This is the fifth nominal species of the subgenus Spirocamallanus Olsen, 1952 reported from fishes in New Caledonian waters., František Moravec, Jean-Lou Justine., and Obsahuje bibliografii
Two new lung-dwelling nematode species of the genus Rhabdias Stiles et Hassall, 1905 were discovered in Caxiuanã National Forest, Pará state, Brazil. Rhabdias galactonoti sp. n. was found in a dendrobatid frog Adelphobates galactonotus (Steindachner). The species is characterised by the regularly folded inner surface of the anterior part of the buccal capsule seen in apical view, flask-shaped oesophageal bulb and narrow, elongated tail. Rhabdias stenocephala sp. n. from two species of leptodactylid frogs, Leptodactylus pentadactylus (Laurenti) (type host) and L. paraensis (Heyer), is characterised by a narrow anterior end that is separated from the remaining body by a constriction. Both species possess six small but distinct lips, a cuticle that is inflated along the whole body, a doliiform buccal capsule separated into a longer anterior and a shallow, ring-shaped posterior part, lateral pores in the body cuticle and zones of spermatogenesis in the syngonia. Rhabdias galactonoti sp. n. is the first species of the genus found in Dendrobatidae; R. stenocephala sp. n. is the second species described from Leptodactylidae in eastern Amazonia., Yuriy Kuzmin, Francisco Tiago de Vasconcelos Melo, Heriberto Figueira da Silva Filho, Jeannie Nascimento dos Santos., and Obsahuje bibliografii
Using scanning and transmission electron microscopy, ultrastructure of the anterior organ and posterior funnel-shaped canal of Gyrocotyle urna Wagener, 1852 (Cestoda: Gyrocotylidea) from ratfish, Chimaera monstrosa (Holocephali), was studied for the first time. The proper anterior organ is localised at a short distance (about 170 µm) from an apical pore surrounded by a receptor field, whereas its distal end is marked by a muscular sphincter. The tegumental surface of this organ is covered with short filitriches of irregular length; large area of muscle layers traverse beneath the tegumental layer. The funnel-shaped canal of G. urna (2.5-3.0 mm long) is a specialised, muscular part of the posterior attachment organ; it opens on the rounded elevation on the dorsal body surface. The tegumental layer bears conical sclerite-like structures (up to 1.5 µm long). It produces electron-dense bodies that are transported into a canal lumen and surrounded thick muscle area mixed with numerous nerve fibres. The present ultrastructural study of G. urna indicates that gyrocotylideans share some ultrastructural characters of the anterior organ with spathebothriidean cestodes with a single anterior attachment sucker-like organ. In contrast, the unique posterior rosette attachment organ with funnel-shaped canal of the Gyrocotylidea resembles the haptor of polyopisthocotylean monogeneans in its position at the posterior end of the body and presumed origin. The above-mentioned features add more clarity to support the basal position of the Gyrocotylidea Poche, 1926 among cestodes. In addition, they also indicate a possible relationship of gyrocotylidean ancestors with monogeneans., Larisa G. Poddubnaya, Roman Kuchta, Glenn A. Bristow, Tomáš Scholz., and Obsahuje bibliografii