Oocyst size Dotaz Zobrazit nápovědu
A series of experiments have been undertaken to determine the effect of water extracts from pine bark (Pinus radiata) on the inhibition of the sporulation of oocysts of three species of avian coccidia. Tubes containing coccidian oocysts isolated from droppings of coccidia-infected chickens were randomly assigned to 0, 250, 500 and 1000 microg/ml pine bark extract (PBE). The tubes were incubated at 25-29 degrees C for 48 h depending on the species of Eimeria. Sporulation inhibition bioassay was used to evaluate the activity of PBE on the sporulation of coccidian oocysts. The oocysts were gently aerated with an air pump away from sun light. The results show for the first time that water-soluble extracts from pine bark containing 35% condensed tannins have anticoccidial activity as evidenced by their ability to decrease significantly the sporulation of the oocysts of three species of Eimeria, namely Eimeria tenella (Railliet et Lucet, 1891), E. maxima Tyzzer, 1929 and E. acervulina Tyzzer, 1929, under laboratory conditions. Incubation of unsporulated oocysts of these parasites in water containing 500 microg PBE per ml resulted in inhibition of sporulation of these oocysts by about 28-84% relative to the oocysts in the control incubations. In addition, up to 12% of E. maxima oocysts exposed to 500-1000 microg pine bark/ml were containing abnormal sporocysts in terms of size, number and shape.
Oocysts of coccidia of the genes Cryptosporidium were detected for the first time in the faeces of naturally infected calves using centrifugation floatation method with saturated solution of ZnSo4 and Breza's floatation solution. Since the detection of oocysts in the faeces is very difficult, a new method has been prepared. The oocysts recovered from the faeces were sporulated, spherical or slightly elliptical, with a smooth, colourless and thin wall. In the fresh preparation after floatation the oocysts measured 5.4 X 4.6 micrometer on the average, whereas in the smears stained after Giemsa, their average size was 4.8 X 4.3 micrometer. A typical feature of the oocysts is a residual body appearing as a dark point at one pole of the oocyst when observed by optical microscope. The oocyst contains four sporozoites forming a C-shaped rim around the residual body. No sporocysts were recorded. The residual body stains blue and the nucleus dark red by Giemsa's method.
- MeSH
- Coccidia cytologie izolace a purifikace MeSH
- feces parazitologie MeSH
- kokcidióza parazitologie veterinární MeSH
- metody MeSH
- nemoci skotu parazitologie MeSH
- skot MeSH
- zvířata MeSH
- Check Tag
- skot MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Using a combination of morphological and molecular data, we describe a new apicomplexan parasite, Isospora svecica sp. n., from the white-spotted bluethroat, Luscinia svecica cyanecula, from the Czech Republic. Oocysts were found in its intestinal tract. Sporulation was exogenous and took 1-3 days. The oocysts were slightly ellipsoidal, of average size 26.17 × 20.33 μm, with a smooth bilayered wall. Micropyle, oocyst residuum, and polar granules were absent. Sporocysts were bottle-shaped, of an average size of 18.82 × 8.82 μm, with a thin, colourless wall. A conspicuous knob-like Stieda body was present. Substieda body was barely visible. Sporocyst residuum was present in the form of granules of various sizes. Sporozoites were banana-shaped and contained large anterior and small posterior refractile bodies. Partial DNA sequences of three genes were obtained from oocysts of Isospora svecica sp. n., being most closely related to other isosporans described from passerines. Little is known about the parasites of the avian family Muscicapidae, including coccidia, a highly prevalent parasitic protist group in all vertebrate classes. Only six species of the genus Isospora have so far been described in Muscicapidae, together with several "Isospora sp." that in fact most likely represent Isospora lacazei. The newly described Isospora svecica sp. n. differs morphologically from other coccidia reported from muscicapid birds, and represents the first coccidian species described from Luscinia svecica.
- MeSH
- Isospora klasifikace cytologie genetika růst a vývoj MeSH
- izosporóza parazitologie veterinární MeSH
- oocysty klasifikace cytologie genetika růst a vývoj MeSH
- Passeriformes parazitologie MeSH
- protozoální geny genetika MeSH
- sporozoiti klasifikace cytologie genetika růst a vývoj MeSH
- střeva parazitologie MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Geografické názvy
- Česká republika MeSH
Oocyst morphology and endogenous developmental stages are described for Choleoeimeria salaselensis sp. n. from the gall bladder of 10 horned vipers, Cerastes gasperettii Leviton and Anderson, in Saudi Arabia. Sporulated oocysts are ellipsoidal, 23 x 15 (22-25 x 14-17) microm, length/width ratio (L/W) 1.5 (1.4-1.6), each with 4 sporocysts (Eimeria-like), but lack a micropyle, polar granules and oocysts residuum. Sporocysts are ellipsoidal, 8 x 5 (7-9 x 5-) microm, L/W 1.5 (1.4-1.6), and Stieda, substieda and parasubstieda bodies are all absent, but a longitudinal suture, which divided the sporocysts into 2 plates, is present. Endogenous development is confined to epithelial cells in the bile duct and gall bladder; mature meronts were 11 x 7 microm, each with 10-16 merozoites, microgamonts were -12 microm wide, and macrogamonts were -16 microm wide with a prominent nucleus and wall-forming bodies. Given these two diagnostic features, sporocysts with a suture and composed of two plates and endogenous development limited to the biliary epithelium, we believe this coccidium is best classified as a member of Choleoeimeria Paperna et Landsberg, 1989. There are 5 known Eimeria species from vipers that have sporocysts somewhat similar in size to those of our new form, but all of them have much larger oocysts and larger sporocysts, some of which differ significantly in shape; there are not yet any Choleoeimeria species known from the Viperidae.
- MeSH
- druhová specificita MeSH
- Eimeriidae klasifikace cytologie izolace a purifikace MeSH
- kokcidióza epidemiologie parazitologie veterinární MeSH
- oocysty MeSH
- Viperidae parazitologie MeSH
- žlučník parazitologie MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Saudská Arábie MeSH
The Javan ferret-badger Melogale orientalis (Carnivora: Mustelidae: Helictidinae) is a small carnivore endemic to Indonesia. In the family Mustelidae, 10 Eimeria, 12 Cystoisopora, one Isospora, and one Hammondia species are known, but no eimeriid coccidia has been yet described in the subfamily Helictinidae (ferret badgers). Coproscopic examination of Javan ferret-badgers imported into the Czech Republic revealed the presence of coccidian oocysts. Sporulated oocysts differ from other Eimeria known in the family Mustelidae by their small size (12.4-16.1 × 10.4-13.4 μm) and ovoidal shape. Morphological data and phylogenetic analyses of 18S rRNA and COI genes indicated a new species of Eimeria found in faecal samples of Javan ferret badgers. The species is described as E. melogale n. sp.
- MeSH
- druhová specificita MeSH
- Eimeria klasifikace cytologie genetika MeSH
- feces parazitologie MeSH
- fylogeneze * MeSH
- Mustelidae parazitologie MeSH
- oocysty cytologie MeSH
- RNA ribozomální 18S genetika MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Geografické názvy
- Česká republika MeSH
This study focuses on mapping the life cycle of Cryptosporidium muris in two laboratory rodents; BALB/c mice and the southern multimammate rat Mastomys coucha, differing in their prepatent and patent periods. Both rodents were simultaneously experimentally inoculated with viable oocysts of C. muris (strain TS03). Animals were dissected and screened for the presence of the parasite using a combined morphological approach and nested PCR (SSU rRNA) at different times after inoculation. The occurrence of first developmental stages of C. muris in stomach was detected at 2.5 days post-infection (dpi). The presence of Type II merogony, appearing 36 h later than Type I merogony, was confirmed in both rodents. Oocysts exhibiting different size and thickness of their wall were observed from 5 dpi onwards in stomachs of both host models. The early phase of parasitization in BALB/c mice progressed rapidly, with a prepatent period of 7.5-10 days; whereas in M. coucha, the developmental stages of C. muris were first observed 12 h later in comparison with BALB/c mice and prepatent period was longer (18-21 days). Similarly, the patent periods of BALB/c mice and M. coucha differed considerably, i.e. 10-15 days vs chronic infection throughout the life of the host, respectively.
- MeSH
- Cryptosporidium růst a vývoj fyziologie MeSH
- druhová specificita MeSH
- feces parazitologie MeSH
- kryptosporidióza parazitologie patologie MeSH
- modely nemocí na zvířatech MeSH
- Murinae MeSH
- myši inbrední BALB C MeSH
- myši MeSH
- oocysty MeSH
- stadia vývoje * MeSH
- trofozoiti MeSH
- žaludeční sliznice patologie MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
A new haemogregarine species Hepatozoon affluomaloti sp. n. is described from erythrocytes in the peripheral blood of crag lizards Pseudocordylus melanotus (Smith) and Pseudocordylus subviridis (Smith) (Sauria: Cordylidae) from mountainous regions in the Eastern Free State, South Africa. This species can be distinguished from all other congeners based on its large size, staining properties and life cycle development in its vector, Culex (Afroculex) lineata (Theobald) (Diptera: Culicidae). Mature gamonts stain mostly uniformly pinkish-purple with Giemsa, sometimes containing darker azurophilic granules anterior and posterior to the nucleus. The reflexed posterior extremity of the gamont stage sometimes stains slightly deeper purple and the nucleus is dense and placed in the posterior third of the parasite body. Merogonic stages of this haemogregarine occur in the liver tissues of P. melanotus with dizoic meronts. Macromeronts contains 2-7 macromerozoites and micromeronts contains 9-24 micromerozoites. Sporogonic developmental stages found in the proposed final host and vector, C. lineata, include large oocysts, measuring 54 × 48 µm on average. Sporulating oocysts with 8 nuclei are present in mosquitoes 6-7 days post-feeding on infected lizards. Sporocysts with mature sporozoites measure 31.0 × 21.8 µm on average and each contains 2-8 large sporozoites. It is suggested that transmission of infective sporozoites is achieved through predation of lizards on mosquitoes.
- MeSH
- Apicomplexa * cytologie růst a vývoj ultrastruktura MeSH
- Culicidae parazitologie MeSH
- erytrocyty parazitologie MeSH
- hostitelská specificita MeSH
- játra parazitologie MeSH
- ještěři * parazitologie MeSH
- oocysty cytologie růst a vývoj ultrastruktura MeSH
- parazitární nemoci u zvířat krev přenos MeSH
- sporozoiti cytologie růst a vývoj ultrastruktura MeSH
- stadia vývoje MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- jižní Afrika MeSH
Maturation of trematode larval stages is expected to be temporally and spatially adapted to maximise the encounter with the adequate downstream host, i.e. the host, which will be infected by this parasite stage. Since studies on intramolluscan parasite maturation are scarce but important in the context of parasite transmission, the larval development inside sporocysts was monitored during upshore residency of the snail host Gibbula adansonii (Trochidae), i.e., from March to May (2011 and 2013), when these snails temporarily reside in the intertidal habitat of a Western Mediterranean lagoon (40° 37' 35″ N, 0° 44' 31″ E, Spain). Data on the relative quantity of different maturation stages of Cainocreadium labracis and Macvicaria obovata (Opecoelidae) parasitising the G. adansonii as well as on snail and sporocyst size were explored using linear models and linear mixed models. The effect of the trematodes on snail growth was shown to be species-specific, with snail and sporocyst size acting as proxies of the reproductive capacity of M. obovata but not that of C. labracis. The number of cercarial embryos and germinal balls did not show monthly variation in either parasite species, but a higher number of mature stages and the highest maturity index was found in April. Hence, during the snail's limited spawning-related presence in the upshore waters of the lagoon, continuous production and output of infectious cercariae was observed, which indicates a link between larval maturation and snail migration. The synchronization of snails, mature parasite transmission stages and downstream hosts in time and space guarantees a successful completion of the life cycle.
- MeSH
- cerkárie růst a vývoj MeSH
- druhová specificita MeSH
- ekosystém MeSH
- hlemýždi parazitologie MeSH
- interakce hostitele a parazita MeSH
- larva růst a vývoj MeSH
- lineární modely MeSH
- migrace zvířat MeSH
- mořská voda MeSH
- oocysty MeSH
- roční období MeSH
- rozmnožování MeSH
- stadia vývoje MeSH
- Trematoda růst a vývoj MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Španělsko MeSH
Stomatocystis goerresi sp. n., a gregarine (phylum Apicomplexa, Monocystidae) parasite of an important invasive earthworm in North America, Amynthas tokioensis (Beddard), is described. This is the second species placed into the genus, and details of its morphology and life cycle support Stomatocystis Bandyopadhyay, Mitra et Göçmen, 2006 as a valid taxon. The new species is described using standard nomenclature, measurements, shape descriptors, and photographs of living cells. The parasite was found only in A. tokioensis, and absent in sympatric earthworm species, suggesting it arrived when the earthworms were introduced from their origin from Japan. The species is distinctive from the type species in the genus, S. indica Bandyopadhyay, Mitra et Göçmen, 2006, in being substantially larger in all stages, found in only the host's seminal vesicles, and found in a different host species from East Asia. The distinctive trophozoites/gamonts develop a large funnel structure ringed with a collar of pronounced ridges, and the funnel appears even in the smallest cells. This funnel varies greatly in relative size (to the cell body) and shape, sometimes forming a large fan. The life cycle of S. goerresi is described including distinctive syzygy in which the funnels fuse and then produce a large cell with local centres of isogamete production (thus sex without gender). Gametes are large ( ~5 μm) spheres with complex tips. Oocyst production is large, > 1,000 per mature gametocyst. The genus Stomatocystis is placed into the Monocystidae, but the life cycle of the new species differs from those of other monocystid taxa, which may mean the Monocystidae are not monophyletic or life cycles are variable within the family. Prevalence of S. goerresi at the type locality was high (~ 90%). The parasites destroy the earthworm's organ of sperm self-storage thus eliminating the male function in the hermaphroditic host which may influence the ability of the earthworm to invade and be successful at new sites.
- MeSH
- Apicomplexa klasifikace genetika růst a vývoj izolace a purifikace MeSH
- Oligochaeta parazitologie MeSH
- stadia vývoje MeSH
- zavlečené druhy MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Geografické názvy
- Japonsko MeSH
BACKGROUND: Avian cryptosporidiosis is a common parasitic disease that is caused by five species, which are well characterised at the molecular and biological level, and more than 18 genotypes for which we have limited information. In this study, we determined the occurrence and molecular characteristics of Cryptosporidium spp. in farmed ostriches in the Czech Republic. METHODS: The occurrence and genetic identity of Cryptosporidium spp. were analysed by microscopy and PCR/sequencing of the small subunit rRNA, actin, HSP70 and gp60 genes. Cryptosporidium avian genotype II was examined from naturally and experimentally infected hosts and measured using differential interference contrast. The localisation of the life-cycle stages was studied by electron microscopy and histologically. Infectivity of Cryptosporidium avian genotype II for cockatiels (Nymphicus hollandicus (Kerr)), chickens (Gallus gallus f. domestica (L.)), geese (Anser anser f. domestica (L.)), SCID and BALB/c mice (Mus musculus L.) was verified. RESULTS: A total of 204 individual faecal samples were examined for Cryptosporidium spp. using differential staining and PCR/sequencing. Phylogenetic analysis of small subunit rRNA, actin, HSP70 and gp60 gene sequences showed the presence of Cryptosporidium avian genotype II (n = 7) and C. ubiquitum Fayer, Santín & Macarisin, 2010 IXa (n = 5). Only ostriches infected with Cryptosporidium avian genotype II shed oocysts that were detectable by microscopy. Oocysts were purified from a pooled sample of four birds, characterised morphometrically and used in experimental infections to determine biological characteristics. Oocysts of Cryptosporidium avian genotype II measure on average 6.13 × 5.15 μm, and are indistinguishable by size from C. baileyi Current, Upton & Haynes, 1986 and C. avium Holubová, Sak, Horčičková, Hlásková, Květoňová, Menchaca, McEvoy & Kváč, 2016. Cryptosporidium avian genotype II was experimentally infectious for geese, chickens and cockatiels, with a prepatent period of four, seven and eight days post-infection, respectively. The infection intensity ranged from 1000 to 16,000 oocysts per gram. None of the naturally or experimentally infected birds developed clinical signs in the present study. CONCLUSIONS: The molecular and biological characteristics of Cryptosporidium avian genotype II, described here, support the establishment of a new species, Cryptosporidium ornithophilus n. sp.
- MeSH
- Cryptosporidium klasifikace genetika ultrastruktura MeSH
- fylogeneze MeSH
- hospodářská zvířata parazitologie MeSH
- hostitelská specificita MeSH
- klasifikace MeSH
- kryptosporidióza parazitologie MeSH
- nemoci ptáků parazitologie MeSH
- protozoální geny genetika MeSH
- ptáci parazitologie MeSH
- stadia vývoje MeSH
- Struthioniformes parazitologie MeSH
- taxonomické DNA čárové kódování veterinární MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH