Estudos citológicos e citoquímicos em Stenophoridae crawley, 1903 (Eugregarinidae, Protozoa): I - microscopia óptica e citoquímica do núcleo

Neste trabalho os autores apresentam uma revisão da morfologia das gregarinas do gênero Stenophora Labbé, 1899, baseada principalmente em S. juli (Frantzius, 1848) Labbé, 1899. Caracterizam citoquìmicamente os elementos da estrutura nuclear, ficando evidenciado que o corpúsculo nuclear referido por muitos como um cariossomo apresenta reações positivas para o RNA, sendo portanto um nucléolo. O suco nuclear apresenta reações para o DNA pouco intensas, devido as granulações de cromatina se apresentarem muito finas. Fazem referências também à estrutura do nucléolo, que varia com as técnicas empregadas e salientam a necessidade de comparação dêstes resultados com aquêles obtidos com o auxílio da microscopia eletrônica e que são tratados no segundo trabalho desta série.

Estudos citológicos e citoquímicos em Stenophoridae Crawley, 1903 (Eugregarinidae, Protozoa) II - ultra-estrutura

1 - Indivíduos de Stenophora juli (Frantzius, 1848) Labbé, 1899, parasitos de um Diplopoda, Rhinochricus padbergi Schubart. 1930 foram examinados em microscópia óptica e eletrônica. 2 - Os resultados do estudo citoquímico confirmam os dados obtidos por outros autores em outras espécies de gregarinas. 3 - Quanto à estrutura fina da morfologia celular foi examinada detalhadamente a película a qual apresenta cristas longitudinais de forma e estrutura complexas. 4 - No sulcos da película, entre as cristas, foram encontrados poros na membrana, por onde é realizada a secreção de muco. 5 - Aderente à película, pròpriamente dita foi encontrada, no deutomerito, uma camada homogênea de natureza desconhecida, abaixo da qual encontra-se o mionema. 6 - O septo que separa o proto do deutomerito é constituído por espêssa camada de mionemas incluindo numerosas mitocôndrias. 7 - O endoplasma é extremamente rico em granulações de paraglicogênio, aparecendo em menor quantidade os lipídeos. Observamos também mitocôndrias, retículo endoplasmático e o complexo de Golgi.

Lankesterella alencari n. sp., a toxoplasma-like organism in the central nervous system of Amphibia (Protozoa, Sporozoa)

Lankesterella alencari n. sp. a Sporozoa that occur in the blood and CNS of the South American frog Leptodactylus acellatus is described. Since the tissue forms of this parasite have been previously reported as belonging to the genus Toxoplasma, we attempted in fection of 2 species of amphibia (Bufo marinus an dLeptodactylus ocellatus) with a Toxoplasma strain of human origen; inoculation was by intraperitoneal injection of parasite-containing ascitic fluid from infected mice. Attempt of experimental inoculation of the parasite found in the CNS of L. ocellatus in a highly susceptible host (mice) was unsuccessful. These results suggest that Toxoplasma does not occur naturally in the amphibia; be related to Toxoplasma is excluded. The following genera of haematozoa found in brazilian amphibia have been considered briedfly: Haemobartonella, Cytamoeba, Dactylosoma, Hepatozoon and Trypanosoma.

Besnoitia (protozoa: toxoplasmatinae) isolado de mucuras Didelphis marsupialis na Região Amazônica, Brasil

Cistos de Besnoitia foram encontrados nos músculos e vísceras de quinze exemplares de Didelphis marsupialis de um total de duzentos e vinte e quatro examinados. É a primeira vez que este protozoário e isolado de animais infectados naturalmente no Brasil. A transmissão experimental foi feita para animais de laboratório pela inoculação de triturados de tecidos e cistos.

Effect of cAMP on macromolecule synthesis in the pathogenic protozoa Trypanosoma cruzi

Macromolecule synthesis of Trypanosoma cruzi in culture was monitored using radioactive tracers. Cells of different days in culture displayed a preferential incorporation of precursors as follows: 1 day for (³H)-thymidine cells; 3 days for (³H)-uridine cells, and 4 days for (³H)-leucine cells. Autoradiographic studies showed that (³H)-thymidine was incorporated in the DNA of both kinetoplast and nucleus in this order. Shifts in the intracellular content of cAMP either by addition of dibutyryl-cAMP or by stimulation of the adenylcyclase by isoproterenol, caused an inhibition in the synthesis of DNA, RNA and proteins. Addition to the T. cruzi cultures of these agents which elevate the intracellular content ofcAMP provoked an interruption of cell proliferation as a result of the impairment of macromolecule synthesis. A discrimination was observed among the stereoisomers of isoproterenol, the L configuration showing to be most active.

Trypanosoma guairaensis sp. n. (Protozoa, Kinetoplastida) parasita de megaloancistrus aculeatus (Perugia, 1891) (Pisces, Loricariidae)

Descreve-se a espécie Trypanosoma guairaensis sp. n. parasita de Megaloancistrus aculeatus do rio Paraná (reservatório de Itaipu). Características morfométricas como comprimento e largura do núcleo e comprimento da parte livre do flagelo, bem como os valores do índice nuclear, diferenciam T. guairaensis de todas as espécies de tripanosomas descritas para peixes de água doce do Brasil.

Trypanosoma nupelianus sp. n. (Protozoa, Kinetoplastida) parasitizing rhinelepis aspera (Osteichthyes, Loricariidae) from Paraná river, Brazil

It is described Trypanosoma nupelianus sp. n. parasitizing Rhinelepis aspera taken from Paraná river (Itaipu reservoir, Brazil). Morphometric characters such as body length, width of the body and nucleus dimensions show that T. nupelianus sp. n. is different from other trypanosomes described for fishes from tropical regions.

Trypanosomatid protozoa in fruit of solanaceae in southeastern Brazil

Fruits of cultivated and indigenous Solanaceae from Southeastern Brazil have been examined for the presence of trypanosomatid flagellates. The 14 species found infected were: Capsicum annum, C. praetermissum, Lycopersicon esculentum, Nicandra physaloides, Physalis angulata, Solanum sp., S. americanum, S. concinnum, S. diflorum, S. erianthum, S. gilo, S. robustum, S. variable and S. viarum. The pentatomid hemipteran Arvelius albopunctatus experimentally transmitted flagellates to fruits of some species. Cultures of flagellates were obtained form fruits of eight species of Salonaceae and from A. albopunctatus.

Cytological Findings Suggesting Sexuality in Phytomonas davidi (Protozoa: Kinetoplastida)

On few occasions, Phytomonas davidi (McGhee & Postell isolate) cultures in LIT (liver infusion-tryptose) medium around 27oC presented, as seen in Giemsa-stained smears, a set of peculiar morphological features, among them being noticeable the pairs of apposed cells attached by their posterior ends, where occurred a stained line and/or a dilatation, usually bulb-like in shape; sometimes this dilatation could occupy one of the cells or hold both together. In some pairs, the nucleus of each parasite seemed migrating towards the other, entering into such dilatation; in others, both nuclei were inside it, sometimes in close proximity or seeming fused; peculiar chromatin arrangements involving both nuclei were occasionally observed. Several mono or binucleate round forms bearing one or two flagella, as well as flagellate slender cells without nucleus were concomitantly seen there. In some instances, an intriguing small stained body occurred beside a single large nucleus, either in pairs presenting the bulb-like structure or in round cells. These cytological findings seemed steps of a dynamic process suggesting sexuality, since in several of them nuclear interactions following fusion of two parasites appeared to occur

Separation and Mapping of Chromosomes of Parasitic Protozoa

Many protozoan parasites represent an important group of human pathogens. Pulsed Field Gradient Gel Electrophoresis (PFGE) analysis has been an important tool for fundamental genetic studies of parasites like Trypanosoma, Leishmania, Giardia or the human malaria parasite Plasmodium falciparum. We present PFGE conditions allowing a high resolution separation of chromosomes ranging from 500 to 4000 kb within a two day electrophoresis run. In addition, we present conditions for separating large chromosomes (2000-6000 kb) within 36 hr. We demontrate that the application of two dimentional PFGE (2D-PFGE) technique to parasite karyotypes is a very useful method for the analysis of dispersed gene families and comparative studies of the intrachomosomal genome organization

Infections by protozoa in immunocompromised hosts

Protozoa are among the most important pathogens that can cause infection in immunocompromised patients. They infect particularly individuals with impaired cell immunity, such as those with hematologic neoplasias, those submitted to transplant of solid organs, those under high-dose corticosteroid therapy, and carriers of the human immunodeficiency virus. Among the protozoa that most commonly cause disease in immunocompromised individuals are Toxoplasma gondii, Trypanosoma cruzi, Cryptosporidium parvum, Isospora belli, Cyclospora cayetanensis and microsporidia; the former two cause severe encephalitis and myocarditis, and the others cause gastrointestinal infections. Early diagnosis and prompt institution of specific therapy for each of these organisms are basic measures to decrease morbidity and mortality associated with these infections.

Leucocytozoon toddi and Haemoproteus tinnunculi (Protozoa: Haemosporina) in the Chimango caracara (Milvago chimango) in southern Chile

Two species of blood protozoans were identified from blood smears collected from 15 specimens of the Chimango caracara (Milvago chimango) on Isla Grande de Chiloé in southern Chile. These included Leucocytozoon toddi in 13 birds, including all 5 of the 4-6 week old nestlings examined, and 8 of the subadults or adults. One of the nestlings also had a dual infection of L. toddi and Haemoproteus tinnunculi. These are the first reports of blood parasites from M. chimango.

Cell fractionation of parasitic protozoa: a review

Cell fractionation, a methodological strategy for obtaining purified organelle preparations, has been applied successfully to parasitic protozoa by a number of investigators. Here we present and discuss the work of several groups that have obtained highly purified subcellular fractions from trypanosomatids, Apicomplexa and trichomonads, and whose work have added substantially to our knowledge of the cell biology of these parasites.