Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Eimeriida”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 307 records · Page 17Linked to original sources
PubMed1995

Differentiating between Besnoitia besnoiti from cattle and Sarcocystis hoarensis from rodents.

To provide a biological basis for studies designed to establish the mode of transmission of the veterinary pathogen Besnoitia besnoiti, we compared salient features of this pathogen in cattle with those of Sarcocystis hoarensis in rodents. The cysts and cystozoites of these organisms can readily be distinguished morphologically. In contrast to S. hoarensis, which is well adapted to rodents, B. besnoiti fails to mature in jirds or mice and generally is lethal in jirds. Serological reagents discriminately detect these pathogens. B. besnoiti, therefore, can unambiguously be differentiated from S. hoarensis either by morphological or serological methods or on the basis of experimental comparisons of virulence in laboratory rodents.

Animals↗
PubMed1993

Preliminary findings from an experimental study of caprine besnoitiosis in Kenya.

Inoculation of cystozoites obtained from natural, chronic cases of caprine besnoitiosis produced clinical disease in goats but not in rabbits, mice, guinea pigs, hamsters, rats or cattle. Histological examination of tissue sections from the experimental animals showed Besnoitia cysts only in goats. This, together with field observations that cattle reared together with goats having besnoitiosis do not contract the disease, suggests that the Besnoitia species that infects goats in Kenya is host-specific and is not Besnoitia besnoiti. We suggest that the name Besnoitia caprae be adopted for the caprine pathogen.

Animals↗
PubMed1995

Comparative ultrastructural studies on Besnoitia besnoiti and Besnoitia caprae.

Comparative transmission electron microscopy on Besnoitia besnoiti and on a strain of Besnoitia derived from goats in Kenya revealed that the two organisms differ in their pellicle, micropore, microtubules, nucleus, wall-forming body 1 (W1), amount of lipids and amylopectin. Thus the caprine besnoitia is probably a different organism and the term Besnoitia caprae should continue to be used.

Animals↗
PubMed2000

Neospora caninum: its oocysts and its identity: an opinion.

A recently published opinion that Hammondia heydorni, Neospora caninum, and N. hughesi are a single species is not supported by genetic comparisons. Furthermore, the suggestion that oocysts shed by dogs after experimental infection with N. caninum might have been of another organism is not consistent with the finding that these oocysts induced N. caninum infections in mice.

Animals↗
PubMed2000

The taxonomic importance of obligate heteroxeny: distinction of Hammondia hammondi from Toxoplasma gondii--another opinion.

We enumerate identical and divergent findings concerning the obligate heteroxenous Hammondia hammondi and the facultatively homoxenous or heteroxenous Toxoplasma gondii. Differences exist in life-cycles, transmission, and host range, especially transmissibility to birds and mammals other than rodents, in ultrastructural morphology, immunity and serology in cats and to lesser degree in rodents, in DNA sequences and in isoenzymes. Because the recognition of obligate heteroxeny is essential to study these organisms and to recognize them as taxa, it is advantageous to give heteroxeny a generic rather than a specific value. Characterization of organisms with the life-cycle patterns of Hammondia, Sarcocystis, Frenkelia, and Toxoplasma is best achieved by means of the genera presently used.

Animals↗
PubMed2000

Neospora caninum: is it really different from Hammondia heydorni or is it a strain of Toxoplasma gondii? An opinion.

The published data concerning Toxoplasma gondii, Hammondia hammondi, H. heydorni and Neospora caninum on one side and between T. gondii on the other were neglected by most authors. As conclusion we are convinced that there are only two valid species: Isospora (Toxoplasma) gondii and Hammondia heydorni. The first includes as a strain H. hammondi and the latter N. caninum. In any case there is absolutely no reason (with respect to general Zoological nomenclature) to create new genera!

Animals↗
PubMed1991

Besnoitia besnoiti: quantitative in vitro studies.

Experimental parameters for optimization of the growth conditions of Besnoitia besnoiti endozoites in vitro are presented. A combination of Hepes-buffered McCoy and Leibovitz (ML) medium with 10% bovine serum was preferable to Eagle's Minimum Essential Medium (MEM) based on either Hank's or Earle's salts. The ML medium and a CO2 balanced gas phase significantly increased the growth rate of the parasite. Infection of Vero cells at 1 h after subcultivation resulted in higher yields of endozoites than infection of 24- or 48-h-old cells. Increased numbers of parasites (6 x 10(7) and 9 x 10(7)) in the infection inoculum per Roux bottle containing Vero cells produced poor yields, while infection with 2 x 10(7) parasites resulted in a 250 to 300-fold increase after 6 days of cultivation with one medium change.

Animals↗
PubMed1992

Camel (Camelus dromedarius) and sheep (Ovis aries) meat as a source of dog infection with some coccidian parasites.

Experimental infection of dogs with camel (Camelus dromedarius) meat resulted in infection of the dogs with Isospora canis, Hammondia heydorni and Sarcocystis cameli. The dogs fed sheep (Ovis aries) meat passed oocysts of Isospora canis, Isospora ohioensis and sporocyts of Sarcocystis spp. Extraintestinal stages were detected in the intestinal lymph node of a rabbit killed 4 days following inoculation with Isospora ohioensis oocysts. Dogs fed the rabbit (killed 4 days after inoculation with I. ohioensis) passed I. ohioensis oocysts in their faeces 8 days post-infection.

Animals↗
PubMed1992

Specificity of the carbon immunoassay (CIA) test for the diagnosis of Toxoplasma infections.

A rapid and low cost procedure, the carbon immunoassay (CIA) test, was evaluated for the diagnosis of Toxoplasma gondii infections. Using a closely related parasite (Besnoitia jellisoni) as antigen, and homologous or heterologous immune sera, it was demonstrated by light and electron microscopy that CIA is a very reliable and specific test. As it is neither expensive nor time-consuming, it can be recommended for general and routine laboratory use.

Animals↗
PubMed1993

Natural besnoitiosis in a rabbit.

An adult female rabbit was submitted for necropsy after sudden death. Pneumonia and nephritis were diagnosed by gross examination. On histological examination. Besnoitia cysts were seen in the pulmonary interalveolar tissue. The Besnoitia cysts were morphologically normal in appearance, measured 127 to 185 microns in diameter and provoked mild mononuclear inflammatory reaction. To the best of our knowledge there has been no previous report of natural besnoitiosis in rabbits.

Animals↗
PubMed1993

The route of immunization of gerbils with live Besnoitia besnoiti as a factor in protection against lethal challenge.

Gerbils (Meriones tristrami) were infected subcutaneously or intraperitoneally with live culture-grown Besnoitia besnoiti at doses ranging from 10(1) to 10(7) endozoites. All animals injected subcutaneously survived the infection and were refractory to a lethal challenge dose of 10(7) endozoites given intraperitoneally 6 weeks later. By contrast, gerbils surviving primary intraperitoneal inoculation with 10(2) to 10(6) endozoites showed a variable survival rate to challenge. All gerbils developed antibodies to B. besnoiti regardless of the route of inoculation, except for those given 10(1) endozoites intraperitoneally. There was no statistical difference between the immunofluorescent antibody titres developed in groups vaccinated subcutaneously or intraperitoneally (P = 0.556).

Animals↗
PubMed1994

Isolation of Besnoitia wallacei in Kenya.

The development of Besnoitia wallacei was studied in 13 cats fed on tissues of mice and rats previously infected with B. wallacei. The cats were serially killed between Day 1 and Day 16 of infection, and histological sections from the liver and intestines were examined. Asexual stages were seen in both the small intestines and the liver between Day 6 and Day 16 post-infection. Mature microschizonts in intestinal epithelial cells measured 22.6 microns x 14.7 microns (n = 15). Macroschizonts in intestinal lamina propria measured 66.6 microns x 50.3 microns (n = 25). Those in the liver measured 70.9 microns x 55.0 microns (n = 5). Sexual stages were seen in epithelial cells of the small intestines only.

Animals↗
PubMed1994

Caprine besnoitiosis: studies on the experimental intermediate hosts and the role of the domestic cat in transmission.

A study was conducted to test the infectivity of bradyzoites of a Besnoitia species infecting goats in Kenya to rats, mice, rabbits, sheep and goats. Only goats developed infection resulting in tissue cyst formation. Eighteen cats were tested for their role in transmission of this Besnoitia species. Ten of the cats were fed on goat tissues with numerous Besnoitia cysts; four cats were orally inoculated with bradyzoites and four others fed on mice and rat carcasses previously inoculated with bradyzoites. None of these cats produced Besnoitia oocysts in their faeces for 30 days.

Animals↗
PubMed2006

Anticoccidial kinase inhibitors: identification of protein kinase targets secondary to cGMP-dependent protein kinase.

Trisubstituted pyrrole inhibitors of the essential coccidian parasite cGMP dependent protein kinase (PKG) block parasite invasion and show in vivo efficacy against Eimeria in chickens and Toxoplasma in mice. An imidazopyridine inhibitor of PKG activity with greater potency in both parasite invasion assays and in vivo activity has recently been identified. Susceptibility experiments with a Toxoplasma knock-out strain expressing a complementing compound-refractory PKG allele ('T761Q-KO'), suggest a role for additional secondary protein kinase targets. Using extracts from this engineered T. gondii strain and a radiolabeled imidazopyridine ligand, a single peak of binding activity associated with calmodulin-like domain protein kinase (CDPK1) has been identified. Like PKG, CDPK1 has been implicated in host cell invasion and exhibits sub-nanomolar sensitivity to the compound. Amino acid sequence comparisons of coccidian CDPKs and a mutational analysis reveal that the binding of the ligand to PKG and CDPK1 (but not other CDPK isoforms) is mediated by similar contacts in a catalytic site hydrophobic binding pocket, and can be blocked by analogous amino acid substitutions. Transgenic strains over-expressing a biochemically active but compound-refractory CDPK1 mutant ('G128Q') fail to show reduced susceptibility to the compound in vivo, suggesting that selective inhibition of this enzyme is not responsible for the enhanced anti-parasitic potency of the imidazopyridine analog. An alternative secondary target candidate, the alpha-isoform of casein kinase 1 (CK1alpha), shows sensitivity to the compound in the low nanomolar range. These results provide an example of the utility of the Toxoplasma model system for investigating the mechanism of action of novel anticoccidial agents.

Amino Acid Sequence↗
PubMed2006

Dynamics of transcription of immunomodulatory genes in endothelial cells infected with different coccidian parasites.

Sporozoites of Eimeria bovis and tachyzoites of Neospora caninum and Toxoplasma gondii are able to invade and to replicate in endothelial cells. Here we report on responses of bovine umbilical vein endothelial cells (BUVEC) in vitro to these coccidial infections by determining mRNA levels of the CXC chemokines GRO-alpha, IL-8 and IP-10, the CC chemokines MCP-1 and RANTES and of GM-CSF, COX-2 and iNOS relative to the level of housekeeping gene (GAPDH) transcription. T. gondii and N. caninum tachyzoites caused profound transcriptional upregulation of all genes in question. In general, upregulation started 2-4 h p.i. and maximum transcript levels were observed 4 h p.i. GRO-alpha and IL-8 gene transcription had decreased to almost control levels by 12 h p.i.; in the case of the other chemokines enhanced transcript levels persisted longer or showed a biphasic time-course. A similar time-course to CC chemokines was observed for GM-CSF mRNA, whilst COX-2 gene transcript peaks were detected at 2-4 h p.i. and 48-72 h p.i. iNOS mRNA levels increased from 4 to 48 h p.i. In contrast, E. bovis sporozoites failed to induce the transcription of CXC chemokine genes and of COX-2, and only caused moderate transcription upregulation of the other genes considered. In conclusion, infections of BUVEC with these coccidian parasites result in host cell activation associated with enhanced transcription of genes encoding for proinflammatory and immunomodulatory molecules, which are important for innate immune reactions and the transition to adaptive immunity. Differences between E. bovis versus T. gondii and N. caninum may illustrate a particular evasion strategy of E. bovis sporozoites, which is related to their need to persist in the host cell for a long period of time and to the avoidance of inflammatory process-induction.

Animals↗
PubMed1997

Pathogenicity of experimental caryosporosis.

Pathogenicity of the coccidia C. bigenetica and C. simplex was studied in experimentally inoculated pigs, goat kids (untreated and immunosuppressed) and severe combined immunodeficient (SCID) mice. The major pathological changes of caryosporosis were similar in all inoculated animals. In pigs and goat kids, caryosporosis was self-limiting, with clinical responses that included focal swelling and erythema of the muzzle, snout, jaws, cheeks, eyelids, bases of the ears, backs of the necks, scrotum, external genitalia of females, legs and footpads. Histopathological changes were characterized by involvement of the cutaneous mononuclear phagocyte system with an inflammatory exudate containing numerous macrophages, especially around the root sheaths, sensory nervous corpuscles of the hair follicles and surrounding dermal free nerve endings. The tactile hair follicles in the muzzle, snout and upper jaw were most severely changed. In SCID mice, inoculation with C. bigenetica or C. simplex caused a severe, fatal, systemic disease characterized by dissemination of numerous caryosporan developmental stages into the host mononuclear phagocyte system. This study presents evidence that both caryosporan species tested caused similar clinical signs and lesions of dermal coccidiosis in the mammalian secondary hosts.

Animals↗
PubMed1999

Phylogenetic analysis based on full-length large subunit ribosomal RNA gene sequence comparison reveals that Neospora caninum is more closely related to Hammondia heydorni than to Toxoplasma gondii.

Since its first description in the late 1980s, Neospora caninum has been recognised as a prominent tissue cyst-forming parasite due to its ability to induce congenital disease and abortion in animals, especially cattle. It is found worldwide and is a cause of significant economic losses for the livestock industry. However, its place within the family Sarcocystidae, like that of several other taxa, remains unresolved. Neospora caninum shares several morphological and life cycle characters with Hammondia heydorni, although it is most commonly thought of as being a close relative of Toxoplasma gondii. This study presents information regarding the phylogenetic relationship of N. caninum to species currently classified into the genus Hammondia, as well as to two strains (RH and ME49) of T. gondii based on the full-length large subunit ribosomal RNA gene. Phylogenetic analyses using two alignment strategies and three different tree-building methods showed that the two species in the genus Hammondia are paraphyletic. Neospora caninum was shown to form a monophyletic clade with H. heydorni instead of T. gondii, which in turn was shown to be most closely related to H. hammondi. The finding that N. caninum and H. heydorni are closely related phylogenetically may aid the elucidation of currently unknown aspects of their biology and epidemiology, and suggests that H. heydorni should be considered in the differential diagnosis of N. caninum from other apicomplexan parasites.

Animals↗