RESUMO
Peroxisomes perform various metabolic processes that are primarily related to the elimination of reactive oxygen species and oxidative lipid metabolism. These organelles are present in all major eukaryotic lineages, nevertheless, information regarding the presence of peroxisomes in opportunistic parasitic protozoa is scarce and in many cases it is still unknown whether these organisms have peroxisomes at all. Here, we performed ultrastructural, cytochemical, and bioinformatic studies to investigate the presence of peroxisomes in three genera of free-living amoebae from two different taxonomic groups that are known to cause fatal infections in humans. By transmission electron microscopy, round structures with a granular content limited by a single membrane were observed in Acanthamoeba castellanii, Acanthamoeba griffini, Acanthamoeba polyphaga, Acanthamoeba royreba, Balamuthia mandrillaris (Amoebozoa), and Naegleria fowleri (Heterolobosea). Further confirmation for the presence of peroxisomes was obtained by treating trophozoites in situ with diaminobenzidine and hydrogen peroxide, which showed positive reaction products for the presence of catalase. We then performed comparative genomic analyses to identify predicted peroxin homologues in these organisms. Our results demonstrate that a complete set of peroxins-which are essential for peroxisome biogenesis, proliferation, and protein import-are present in all of these amoebae. Likewise, our in silico analyses allowed us to identify a complete set of peroxins in Naegleria lovaniensis and three novel peroxin homologues in Naegleria gruberi. Thus, our results indicate that peroxisomes are present in these three genera of free-living amoebae and that they have a similar peroxin complement despite belonging to different evolutionary lineages.
Assuntos
Acanthamoeba castellanii/ultraestrutura , Balamuthia mandrillaris/ultraestrutura , Peroxinas/genética , Peroxissomos/ultraestrutura , Acanthamoeba castellanii/enzimologia , Acanthamoeba castellanii/genética , Balamuthia mandrillaris/enzimologia , Balamuthia mandrillaris/genética , Catalase/metabolismo , Microscopia Eletrônica de Transmissão , Peroxinas/metabolismo , Peroxissomos/enzimologia , Peroxissomos/genética , FilogeniaRESUMO
Several filamentous fungi are known to produce macroscopic pigmented hyphal aggregates named sclerotia. In recent years, some entomopathogenic fungi were reported to produce small sclerotia termed 'microsclerotia', becoming new potential propagules for biocontrol strategies. In this study, we described the production of microsclerotia-like pellets by the entomopathogenic fungus Beauveria bassiana. The carbon: nitrogen ratio equal to or higher than 12.5:1 amended with Fe2+ induced the germination of conidia, producing hyphal aggregate that formed sclerotial structures in submerged liquid cultures. These aggregates were able to tolerate desiccation as they germinated and subsequently produced viable conidia. Conidia derived from microsclerotial aggregates formulated with diatomaceous earth effectively kill Tribolium castaneum larvae. Optical and transmission microscopical imaging, qPCR and spectrophotometric analysis revealed that an oxidative stress scenario is involved in conidial differentiation into microsclerotia-like pellets, inducing fungal antioxidant response with high peroxidase activity - mainly detected in peroxisomes and mitochondria - and progress with active peroxisome proliferation. The results provide clues about B. bassiana microsclerotial differentiation and indicate that these pigmented aggregates are promising propagules for production, formulation and potentially application in the control of soil-inhabiting arthropod pests.
Assuntos
Beauveria/fisiologia , Estresse Oxidativo , Peroxissomos/metabolismo , Animais , Beauveria/crescimento & desenvolvimento , Beauveria/patogenicidade , Beauveria/ultraestrutura , Meios de Cultura , Terra de Diatomáceas/farmacologia , Estruturas Fúngicas/crescimento & desenvolvimento , Estruturas Fúngicas/patogenicidade , Estruturas Fúngicas/fisiologia , Estruturas Fúngicas/ultraestrutura , Larva/microbiologia , Estresse Oxidativo/genética , Peroxidase/metabolismo , Peroxissomos/genética , Peroxissomos/ultraestrutura , Controle Biológico de Vetores , Tribolium/microbiologia , VirulênciaRESUMO
In this work, we have genetically transformed tobacco (Nicotiana tabacum) plants with the peroxisome proliferator-activated receptor cDNA (xPPARalpha) from Xenopus laevis, which is a transcriptional factor involved in the peroxisomal proliferation and induction of fatty acid beta-oxidation in animal cells. Several transgenic lines were generated and one representative line (T) from the R2 generation was selected for further studies. Analysis of free fatty acids revealed that unsaturated fatty acids such as C16:2 and C16:3 were deficient in line T, whereas saturated fatty acids like C16:0, C18:0, and C20:0 were more abundant than in non-transformed plants. Acyl-CoA oxidase (ACOX) activity was assayed as a marker enzyme of beta-oxidation in crude leaf extracts and it was found that in line T there was a threefold increase in enzyme activity. We also found that the peroxisome population was increased and that catalase (CAT) activity was induced by clofibrate, a known activator of xPPARalpha protein, in leaves from line T. Taken together, these findings suggest that xPPARalpha is functional in plants and that its expression in tobacco leads to changes in general lipid metabolism and peroxisomal proliferation as reported in animal cells. Furthermore, it indicates that there is an endogenous ligand in tobacco cells able to activate xPPARalpha.
Assuntos
Nicotiana/genética , PPAR alfa/metabolismo , Plantas Geneticamente Modificadas/metabolismo , Acil Coenzima A/metabolismo , Animais , Biomarcadores , Catalase/metabolismo , Clofibrato/farmacologia , Ácidos Graxos não Esterificados/metabolismo , Hipolipemiantes/farmacologia , Ligantes , PPAR alfa/genética , Peroxissomos/metabolismo , Peroxissomos/fisiologia , Peroxissomos/ultraestrutura , Folhas de Planta/anatomia & histologia , Folhas de Planta/efeitos dos fármacos , Folhas de Planta/metabolismo , Proteínas de Plantas/metabolismo , Plantas Geneticamente Modificadas/anatomia & histologia , Plantas Geneticamente Modificadas/efeitos dos fármacos , Nicotiana/anatomia & histologia , Proteínas de Xenopus/genética , Proteínas de Xenopus/metabolismo , Xenopus laevisRESUMO
Alzheimer disease is a neurodegenerative process that leads to severe cognitive impairment as a consequence of selective death of neuronal populations. The molecular pathogenesis of Alzheimer disease involves the participation of the beta-amyloid peptide (Abeta) and oxidative stress. We report here that peroxisomal proliferation attenuated Abeta-dependent toxicity in hippocampal neurons. Pretreatment with Wy-14.463 (Wy), a peroxisome proliferator, prevent the neuronal cell death and neuritic network loss induced by the Abeta peptide. Moreover, the hippocampal neurons treated with this compound, showed an increase in the number of peroxisomes, with a concomitant increase in catalase activity. Additionally, we evaluate the Wy protective effect on beta-catenin levels, production of intracellular reactive oxygen species, cytoplasmic calcium uptake, and mitochondrial potential in hippocampal neurons exposed to H(2) O(2) and Abeta peptide. Results show that the peroxisomal proliferation prevents beta-catenin degradation, reactive oxygen species production, cytoplasmic calcium increase, and changes in mitochondrial viability. Our data suggest, for the first time, a direct link between peroxisomal proliferation and neuroprotection from Abeta-induced degenerative changes.
Assuntos
Peptídeos beta-Amiloides/farmacologia , Morte Celular/efeitos dos fármacos , Hipocampo/citologia , Neurônios/fisiologia , Proliferadores de Peroxissomos/farmacologia , Peroxissomos/fisiologia , Peptídeos beta-Amiloides/química , Peptídeos beta-Amiloides/metabolismo , Animais , Cálcio/metabolismo , Catalase/genética , Catalase/metabolismo , Expressão Gênica/efeitos dos fármacos , Hipocampo/embriologia , Peróxido de Hidrogênio/farmacologia , Camundongos , Camundongos Transgênicos , Mitocôndrias/fisiologia , Neuritos/fisiologia , Neurônios/efeitos dos fármacos , Neurônios/ultraestrutura , Fármacos Neuroprotetores/farmacologia , Estresse Oxidativo , PPAR alfa/genética , PPAR alfa/fisiologia , Peroxissomos/efeitos dos fármacos , Peroxissomos/ultraestrutura , Pirimidinas/farmacologia , Ratos , Ratos Sprague-Dawley , Espécies Reativas de Oxigênio/antagonistas & inibidores , Espécies Reativas de Oxigênio/metabolismo , Reação em Cadeia da Polimerase Via Transcriptase Reversa , beta Catenina/metabolismoRESUMO
Parasitic protozoa comprise a large number of species, some of which are agents of important diseases. They are also of interest from the point of view of cell biology since they contain special organelles and structures. This review analyses our present knowledge of (1). the glycosomes, found in members of the Kinetoplastida order, (2). the hydrogenosomes found in some anaerobic protozoa, especially in trichomonads, (3). the acidocalcisomes, recently described in several protozoa, and (4). structures and organelles participating in the endocytic pathway in trypanosomatids.
Assuntos
Eucariotos/ultraestrutura , Animais , Cisteína Endopeptidases/metabolismo , Endocitose/fisiologia , Eucariotos/patogenicidade , Técnica de Fratura por Congelamento , Leishmania/citologia , Leishmania/fisiologia , Leishmania/ultraestrutura , Microcorpos/metabolismo , Microcorpos/ultraestrutura , Organelas/classificação , Organelas/metabolismo , Organelas/ultraestrutura , Peroxissomos/metabolismo , Peroxissomos/ultraestrutura , Proteínas de Protozoários , Trichomonas/citologia , Trichomonas/ultraestrutura , Trypanosoma cruzi/citologia , Trypanosoma cruzi/ultraestrutura , Trypanosomatina/citologia , Trypanosomatina/ultraestruturaRESUMO
Hepatocytes from different vertebrates are used increasingly as models of environmentally driven cell structure plasticity and for the investigation of ultrastructural pathological patterns induced by cell injury. The present study was carried out to assess the morphological changes in hamster hepatocytes subjected to chronic infection by amastigote forms of Leishmania donovani. Liver fragments were processed for routine light and transmission electron microscopy. For cytochemical visualization of peroxisomes, liver slices were incubated in alkaline 3,3'-diaminobenzidine (DAB) medium at pH 10.0. The results showed that the presence of Leishmania donovani induced distinct ultrastructural changes in the liver acinus (zone 2). The significant pathological changes in hepatocytes consisted of disruption of the endomembrane system and alterations of both the peroxisomal compartment and the distribution of hepatic glycogen. Particularly, hepatic peroxisomes exhibited different shapes and sizes, with modifications of the peroxisomal matrix, including absence of the catalase reaction. These observations suggest an adaptive response of hepatocytes, with cytological reorganization after parasitic infection. The presence of DAB-negative peroxisomes could be morphological evidence of a metabolic disturbance of this organelle. The parasitic infection, through deregulation of the cytokene network, is probably responsible for those structural alterations, since similar changes have been observed in vivo and in vitro.
Assuntos
Hepatócitos/patologia , Leishmania donovani/patogenicidade , Leishmaniose Visceral/patologia , 3,3'-Diaminobenzidina/química , Animais , Cricetinae , Hepatócitos/parasitologia , Hepatócitos/ultraestrutura , Histocitoquímica , Transmissão Vertical de Doenças Infecciosas , Leishmania donovani/crescimento & desenvolvimento , Leishmania donovani/isolamento & purificação , Leishmaniose Visceral/diagnóstico , Leishmaniose Visceral/parasitologia , Fígado/citologia , Fígado/patologia , Lisossomos/metabolismo , Lisossomos/ultraestrutura , Masculino , Mesocricetus , Peroxissomos/metabolismo , Peroxissomos/ultraestruturaRESUMO
The feeding of high-fat diets rich in polyunsaturated fatty acids (PUFAs) caused a marked increase in the acyl CoA thioesterase activity of the Walker 256 tumour. Diets containing lower levels of PUFAs did not alter the activity of acyl CoA thioesterase and the exposure of LLC-WRC256 tumour cells, in culture, to PUFAs (150 microM) also was ineffective in altering activity. The tumours from n-3 PUFA-rich and control diets were analysed by transmission electron microscopy in order to compare peroxisomal content. The presence of PUFAs led to an almost 10-fold increase in the number of peroxisomes present in the tumour tissue. A common feature of the PUFA-treated tumour was the presence of many cells containing highly condensed heterochromatin at the periphery of the nucleus, indicative of apoptosis. The sparsity of endoplasmic reticulum and the lack of detection of mitochondrial acyl CoA thioesterase, MTE-I, led to the conclusion that the increase in tumour acyl CoA thioesterase activity may be due to an increase in the activity of the peroxisomal enzyme.