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1.
Parasitology ; 151(5): 468-477, 2024 Apr.
Article in English | MEDLINE | ID: mdl-38629122

ABSTRACT

Haemogregarine (Apicomplexa: Adeleorina) parasites are considered to be the most common and widespread haemoparasites in reptiles. The genus Hepatozoon (Apicomplexa: Adeleorina: Hepatozoidae) can be found parasitizing a broad range of species and, in reptiles, they infect mainly peripheral blood erythrocytes. The present study detected and characterized a haemogregarine isolated from the lizard species, Ameiva ameiva, collected from the municipality of Capanema, Pará state, north Brazil. Blood smears and imprints from lungs, brain, heart, kidney, liver, bone marrow and spleen were observed using light microscopy and the parasite was genetically identified by molecular analysis. Morphological, morphometric and molecular data were obtained. Parasite gamonts were found in 49.5% (55/111) of the blood smears from A. ameiva, and were characterized as oval, averaging 12.0 ± 0.8 × 5.9 ± 0.6 µm2 in size, which displaced the nuclei of parasitized monocytes laterally. Parasite forms resembling immature gamonts were observed in the spleen and bone marrow of the lizards. Furthermore, phylogenetic analyses of 18S rRNA sequences did not reveal gene similarity with other Hepatozoon spp. sequences from reptiles. Thus, morphological and molecular analyses have identified a new species of Hepatozoon parasite, Hepatozoon lainsoni sp. nov., which infects monocytes of the A. ameiva lizard.


Subject(s)
Coccidiosis , Lizards , Phylogeny , Animals , Lizards/parasitology , Brazil , Coccidiosis/veterinary , Coccidiosis/parasitology , Eucoccidiida/genetics , Eucoccidiida/isolation & purification , Eucoccidiida/classification , RNA, Ribosomal, 18S/analysis , RNA, Ribosomal, 18S/genetics , Apicomplexa/genetics , Apicomplexa/isolation & purification , Apicomplexa/classification , Erythrocytes/parasitology , DNA, Protozoan
2.
An. acad. bras. ciênc ; 89(4): 3111-3121, Oct.-Dec. 2017. tab, graf
Article in English | LILACS | ID: biblio-886824

ABSTRACT

ABSTRACT With the aim of introducing permanent prostheses with main properties equivalent to cortical human bone, Ti-diamond composites were processed through powder metallurgy. Grade 1 titanium and mixtures of Ti powder with 2%, 5% and 10 wt% diamond were compacted at 100MPa, and then sintered at 1250°C/2hr/10-6mbar. Sintered samples were studied in the point of view of their microstructures, structures, yield strength and elastic modulus. The results showed that the best addition of diamonds was 2 wt%, which led to a uniform porosity, yield strength of 370MPa and elastic modulus of 13.9 GPa. Samples of Ti and Ti-2% diamond were subjected to in vitro cytotoxicity test, using cultures of VERO cells, and it resulted in a biocompatible and nontoxic composite material.


Subject(s)
Humans , Animals , Titanium/analysis , Biocompatible Materials/analysis , Materials Testing/methods , Diamond/analysis , Surface Properties , Tensile Strength , Vero Cells , Chlorocebus aethiops , Porosity
3.
Mem. Inst. Oswaldo Cruz ; 104(2): 149-154, Mar. 2009. ilus
Article in English | LILACS | ID: lil-533500

ABSTRACT

Historically, scientists in Brazil has significantly contributed to the biology, cultivation and structural organization of the pathogenic protozoan Toxoplasma gondiiand its interaction with host cells, starting with the description of the protozoan by Splendore in 1908. The intracellular and extracellular corpuscoli observed in rabbits, corresponded to what we now as tachyzoites. Later on, a pioneering method to grow T. gondii in tissue cultures was developed by Guimarães and Meyer, 1942. They also observed for the first time T. gondii by transmission electron microscopy and made the initial description of the cytoskeleton of T. gondii by observing negatively stained cells. In the 1980's, the relation of the cytoskeleton with the sub-pellicular microtubules was reveled by freeze-fracture. More recently, several Brazilian groups have analyzed in detail basic aspects of the early interaction of the protozoan with the host cell, such as the role of protein phosphorylation, transfer of host cell surface components to the protozoan and genesis and organization of the parasitophorous vacuole. Tachyzoites strategically inhibit nitric oxide production during active invasion of activated macrophages. In vitro studies on the sexual cycle of T. gondii using primary cultures of cat enterocytes and the egress from host cells are being carried out. Perspectives are that the contribution of Brazilian science to the knowledge on T. gondii biology will continue to flourish in years to come.


Subject(s)
Animals , Cats , Humans , Rabbits , Toxoplasma/physiology , Brazil , Host-Parasite Interactions
4.
Mem. Inst. Oswaldo Cruz ; 100(1): 33-38, Feb. 2005. ilus, graf
Article in English | LILACS | ID: lil-398112

ABSTRACT

Cells die through a programmed process or accidental death, know as apoptosis or necrosis, respectively. Bothrops jararaca is a snake whose venom inhibits the growth of Trypanosoma cruzi epimastigote forms causing mitochondrion swelling and cell death. The aim of the present work was to determine the type of death induced in epimastigotes of T. cruzi by this venom. Parasite growth was inhibited after venom treatment, and 50 percent growth inhibition was obtained with 10 æg/ml. Ultrastructural observations confirmed mitochondrion swelling and kinetoplast disorganization. Furthermore, cytoplasmic condensation, loss of mitochondrion membrane potential, time-dependent increase in phosphatidylserine exposure at the outer leaflet plasma membrane followed by permeabilization, activation of caspase like protein and DNA fragmentation were observed in epimastigotes throughout a 24 h period of venom treatment. Taken together, these results indicate that the stress induced in epimastigote by this venom, triggers a programmed cell death process, similar to metazoan apoptosis, which leads to parasite death.


Subject(s)
Animals , Antiprotozoal Agents/pharmacology , Apoptosis/drug effects , Bothrops , Crotalid Venoms/pharmacology , Mitochondria/drug effects , Trypanosoma cruzi/drug effects , Cell Membrane/drug effects , Cell Membrane/ultrastructure , Flow Cytometry , Microscopy, Electron, Transmission , Mitochondria/ultrastructure , Time Factors , Trypanosoma cruzi/ultrastructure
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