133 resultados para CRITHIDIA FASCICULATA
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Background: Magnetic hyperthermia is currently a clinical therapy approved in the European Union for treatment of tumor cells, and uses magnetic nanoparticles (MNPs) under time-varying magnetic fields (TVMFs). The same basic principle seems promising against trypanosomatids causing Chagas disease and sleeping sickness, given that the therapeutic drugs available have severe side effects and that there are drug-resistant strains. However, no applications of this strategy against protozoan-induced diseases have been reported so far. In the present study, Crithidia fasciculata, a widely used model for therapeutic strategies against pathogenic trypanosomatids, was targeted with Fe3O4 MNPs in order to provoke cell death remotely using TVMFs. Methods: Iron oxide MNPs with average diameters of approximately 30 nm were synthesized by precipitation of FeSO4 in basic medium. The MNPs were added to C. fasciculata choanomastigotes in the exponential phase and incubated overnight, removing excess MNPs using a DEAE-cellulose resin column. The amount of MNPs uploaded per cell was determined by magnetic measurement. The cells bearing MNPs were submitted to TVMFs using a homemade AC field applicator (f = 249 kHz, H = 13 kA/m), and the temperature variation during the experiments was measured. Scanning electron microscopy was used to assess morphological changes after the TVMF experiments. Cell viability was analyzed using an MTT colorimetric assay and flow cytometry. Results: MNPs were incorporated into the cells, with no noticeable cytotoxicity. When a TVMF was applied to cells bearing MNPs, massive cell death was induced via a nonapoptotic mechanism. No effects were observed by applying TVMF to control cells not loaded with MNPs. No macroscopic rise in temperature was observed in the extracellular medium during the experiments. Conclusion: As a proof of principle, these data indicate that intracellular hyperthermia is a suitable technology to induce death of protozoan parasites bearing MNPs. These findings expand the possibilities for new therapeutic strategies combating parasitic infection.
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The Crithidia fasciculata RNH1 gene encodes an RNase H, an enzyme that specifically degrades the RNA strand of RNA–DNA hybrids. The RNH1 gene is contained within an open reading frame (ORF) predicted to encode a protein of 53.7 kDa. Previous work has shown that RNH1 expresses two proteins: a 38 kDa protein and a 45 kDa protein which is enriched in kinetoplast extracts. Epitope tagging of the C-terminus of the RNH1 gene results in localization of the protein to both the kinetoplast and the nucleus. Translation of the ORF beginning at the second in-frame methionine codon predicts a protein of 38 kDa. Insertion of two tandem stop codons between the first ATG codon and the second in-frame ATG codon of the ORF results in expression of only the 38 kDa protein and the protein localizes specifically to the nucleus. Mutation of the second methionine codon to a valine codon prevents expression of the 38 kDa protein and results in exclusive production of the 45 kDa protein and localization of the protein only in the kinetoplast. These results suggest that the kinetoplast enzyme results from processing of the full-length 53.7 kDa protein. The nuclear enzyme appears to result from translation initiation at the second in-frame ATG codon. This is the first example in trypanosomatids of the production of nuclear and mitochondrial isoforms of a protein from a single gene and is the only eukaryotic gene in the RNase HI gene family shown to encode a mitochondrial RNase H.
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Telomerase RNAs (TERs) are highly divergent between species, varying in size and sequence composition. Here, we identify a candidate for the telomerase RNA component of Leishmania genus, which includes species that cause leishmaniasis, a neglected tropical disease. Merging a thorough computational screening combined with RNA-seq evidence, we mapped a non-coding RNA gene localized in a syntenic locus on chromosome 25 of five Leishmania species that shares partial synteny with both Trypanosoma brucei TER locus and a putative TER candidate-containing locus of Crithidia fasciculata. Using target-driven molecular biology approaches, we detected a ∼2,100 nt transcript (LeishTER) that contains a 5' spliced leader (SL) cap, a putative 3' polyA tail and a predicted C/D box snoRNA domain. LeishTER is expressed at similar levels in the logarithmic and stationary growth phases of promastigote forms. A 5'SL capped LeishTER co-immunoprecipitated and co-localized with the telomerase protein component (TERT) in a cell cycle-dependent manner. Prediction of its secondary structure strongly suggests the existence of a bona fide single-stranded template sequence and a conserved C[U/C]GUCA motif-containing helix II, representing the template boundary element. This study paves the way for further investigations on the biogenesis of parasite TERT ribonucleoproteins (RNPs) and its role in parasite telomere biology.
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Two xenic isolates and cloned cultures of Entamoeba dispar were submitted to monoxenization using Crithidia fasciculata as the associated organism. Growth in monoxenic cultivation and ability of xenic and monoxenic trophozoites to destroy VERO cells and produce lesions in hamster livers were compared to those of a virulent E. histolytica. Parental and cloned E. dispar under monoxenic cultivation showed a remarkable lower growth than the monoxenic E. histolytica and were avirulent in both in vivo and in vitro tests. When xenically cultured, trophozoites of E. dispar showed a moderate lytic activity against VERO cells (1.5 to 41.8% of destruction) but caused severe hepatic lesions in hamsters as those caused by the virulent E. histolytica (29 to 100% in prevalence and 0.86 to 4.00 in lesion degree). Although E. dispar has not been associated with invasive disease in men, the ability of xenic trophozoites to produce prominent tissue damage in experimental conditions has indicated that some strains have a considerable pathogenic potential when in presence of bacteria.
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Heteroxenic and monoxenic trypanosomatids were screened for the presence of actin using a mouse polyclonal antibody produced against the entire sequence of the Trypanosoma cruzi actin gene, encoding a 41.9 kDa protein. Western blot analysis showed that this antibody reacted with a polypeptide of approximately 42 kDa in the whole-cell lysates of parasites targeting mammals (T. cruzi, Trypanosoma brucei and Leishmania major), insects (Angomonas deanei, Crithidia fasciculata, Herpetomonas samuelpessoai and Strigomonas culicis) and plants (Phytomonas serpens). A single polypeptide of approximately 42 kDa was detected in the whole-cell lysates of T. cruzi cultured epimastigotes, metacyclic trypomastigotes and amastigotes at similar protein expression levels. Confocal microscopy showed that actin was expressed throughout the cytoplasm of all the tested trypanosomatids. These data demonstrate that actin expression is widespread in trypanosomatids.
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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
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Although trypanosomatids are known to rapidly transaminate exogenous aromatic amino acids in vitro and in vivo, the physiological significance of this reaction is not understood. In postmitochondrial supernatants prepared from Trypanosoma brucei brucei and Crithidia fasciculata, we have found that aromatic amino acids were the preferred amino donors for the transamination of alpha-ketomethiobutyrate to methionine. Intact C. fasciculata grown in the presence of [15N]tyrosine were found to contain detectable [15N]methionine, demonstrating that this reaction occurs in situ in viable cells. This process is the final step in the recycling of methionine from methylthioadenosine, a product of decarboxylated S-adenosylmethionine from the polyamine synthetic pathway. Mammalian liver, in contrast, preferentially used glutamine for this reaction and utilized a narrower range of amino donors than seen with the trypanosomatids. Studies with methylthioadenosine showed that this compound was readily converted to methionine, demonstrating a fully functional methionine-recycling pathway in trypanosomatids.
A single-stranded DNA binding protein binds the origin of replication of the duplex kinetoplast DNA.
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Replication of the kinetoplast DNA (kDNA) minicircle of trypanosomatids initiates at a conserved 12-nt sequence, 5'-GGGGTTGGTGTA-3', termed the universal minicircle sequence (UMS). A sequence-specific single-stranded DNA-binding protein from Crithidia fasciculata binds the heavy strand of the 12-mer UMS. Whereas this UMS-binding protein (UMSBP) does not bind a duplex UMS dodecamer, it binds the double-stranded kDNA minicircle as well as a duplex minicircle fragment containing the origin-associated UMS. Binding of the minicircle origin region by the single-stranded DNA binding protein suggested the local unwinding of the DNA double helix at this site. Modification of thymine residues at this site by KMnO4 revealed that the UMS resides within an unwound or otherwise sharply distorted DNA at the minicircle origin region. Computer analysis predicts the sequence-directed curving of the minicircle origin region. Electrophoresis of a minicircle fragment containing the origin region in polyacrylamide gels revealed a significantly lower electrophoretic mobility than expected from its length. The fragment anomalous electrophoretic mobility is displayed only in its native conformation and is dependent on temperature and gel porosity, indicating the local curving of the DNA double helix. We suggest that binding of UMSBP at the minicircle origin of replication is possible through local unwinding of the DNA double helix at the UMS site. It is hypothesized here that this local melting is initiated through the untwisting of unstacked dinucleotide sequences at the bent origin site.
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A flagellte trypanosomatid was isolated in culture from the digestive tract of the mosquito Culex saltanensis Dyar, 1928. It grows exuberantly in liver infusion in the form of epimastigotes and choanomastigotes typical of the genus Crithidia. The trypanosomatid was compared to C. deanei, C. fasciculata, C. luciliae, C. oncopelti and C. guilhermei. The techniques used for comparison were electron transmission microscopy, isoenzymes and kDNA restriction profiles. No endosymbionts were found at electron microscopy. Results for the biochemical methods employd indicate that the trypanosomatid isolated from C. saltanensis is a new species of Crithidia. The name C. ricardoi sp. n. is proposed for thes new species.
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Este trabalho apresenta 79 espécies de plantas que fornecem néctar e/ou pólen para operárias de Melipona compressipes fasciculata, que é a abelha mais comum do Maranhão. A maioria dessas plantas são também visitadas por Apis mellifera. Sugere-se, com isso, o plantio de algumas espécies em estradas, cercas, ruas, avenidas e praças, a fim de melhorar a pasto apícola.
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Este trabalho relata detalhes da vida reprodutiva de duas espécies de abelhas sem ferrão. Rainhas velhas de Melipona compressipes fasciculata, no Maranhão, morrem e são substituídas com sucesso em todos os meses. Rainhas de Melipona scutellaris, trazidas de Lençóis (BA - nordeste do Brasil) para Uberlândia (MG, centro-sudeste do Brasil) morreram durante todos os meses e não mostraram a existência de trimestre preferencial para as novas rainhas iniciarem postura. Quarenta machos de M. scutellaris, após serem marcados no tórax e libertados em grupos de 10 a 100, 400, 800 e 1000 metros do meliponário, tiveram seus retornos observados. Todos os machos libertados a 100 e 400 metros regressaram ao meliponário, 7 de 10 machos e 2 de 10 machos retornaram de 800 e 1000 metros, respectivamente. Os machos esperam constantemente pela saída de uma rainha virgem, próximos às colônias órfãs, o que indica que a maioria das rainhas é inseminada próximo aos seus ninhos, portanto, a dispersão dos genes depende do vôo dos machos e da distância de enxameagem para ocupação de uma cavidade para o novo ninho.
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O espectro polínico do mel de Melipona fasciculata Smith foi analisado com o objetivo de identificar os recursos nectaríferos utilizados por essa espécie. A identificação das plantas visitadas foi realizada com base na análise dos tipos polínicos encontrados em 12 amostras de mel coletadas, mensalmente, em uma colônia localizada no município de Palmeirândia, na área da Baixada Ocidental Maranhense (02º40'47,6S, 44º52'39,8"W), Brasil. As análises quantitativas e qualitativas foram realizadas com o objetivo de determinar as porcentagens e classes de frequência dos tipos polínicos presentes nas amostras de mel. Foram encontrados 45 tipos polínicos, sendo Pontederia parviflora Alexander (Pontederiaceae), espécie mais frequente em todo o período de amostragem (38,6%), pólen dominante em Outubro (86%), Junho (85%), Julho (76%), Agosto (49%) e Setembro (51%) e pólen acessório em Dezembro, Janeiro e Março. Mimosa caesalpiniifolia Benth (Mimosaceae) foi a segunda espécie mais frequente (22,8%) sendo pólen dominante em Novembro (46%), Abril (74%) e Maio (72%). Myrcia eximia DC (Myrtaceae) foi considerada pólen isolado importante. As famílias mais representativas no espectro polínico das amostras de mel foram Pontederiaceae e Mimosaceae. 50% dos méis foram biflorais, havendo também méis monoflorais (41,7%) e heteroflorais (8,3%).
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Amapá amargo (Parahancornia fasciculata (Poir.) Benoist) produz um látex, que se presume ter propriedades medicinais, pois é usado no tratamento da malária, problemas pulmonares, gastrite, e como um agente de cura. Este estudo teve como objetivo analisar estrutural e histoquimicamente os locais de produção e/ou acumúlo de compostos biologicamente ativos, bem como realizar o doseamento de flavonóides presentes no limbo do amapá amargo. Para a análise estrutural e histoquímica foram utilizados protocolos padrão em anatomia vegetal. Considerando que, para o doseamento de flavonóides utilizou-se a espectrometria de absorção na região ultravioleta-visível. O sistema secretor das folhas de amapá amargo é constituído de idioblastos secretores e laticíferos ramificados. Os testes histoquímicos revelaram diferentes tipos de substâncias químicas nos protoplastos celulares de idioblastos e laticíferos. Propriedades farmacológicas do látex de amapa amargo podem ser atribuídas à dois compostos químicos (flavonoides e alcaloides) encontrados neste estudo, ambos estão presentes em idioblastos e laticíferos.
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La más compleja de las interacciones que plantas e insectos han desarrollado durante el transcurso de su evolución, son las agallas. Las especies de insectos galícolas se encuentran en la mayoría de las regiones biogeográficas, principalmente en ambientes xéricos, de los cuales un ejemplo lo constituye la ecorregión del Espinal, ubicada en la Provincia Biogeográfica de la Pampa, Subregión Chaqueña. Schinus fasciculata (Griseb.) I.M. Johnst. (Anacardiaceae) es una especie arbórea o arbustiva representativa de la ecorregión del Espinal que presenta diversas agallas entomógenas. Los objetivos del presente trabajo son identificar las especies de insectos que producen agallas en hojas y tallos de Schinus fasciculata en un relicto de Espinal de la provincia de Córdoba y caracterizar exomorfológicamente las agallas. Se seleccionaron 18 ejemplares de S. fasciculata distribuidos en cuatro transectas de 100 m2. Se caracterizaron cinco morfotipos de agallas, tres en hojas, inducidas por insectos del orden Hemiptera y dos en tallos, originadas por insectos del orden Lepidoptera. Los insectos productores de las mismas fueron identificados a nivel de especie y los distintos morfotipos de agallas fueron únicos para cada especie de insecto inductor.