RESUMEN
Most parasitic flatworms go through different life stages with important physiological and morphological changes. In this work, we used a transcriptomic approach to analyze the main life-stages of the model tapeworm Hymenolepis microstoma (eggs, cysticercoids, and adults). Our results showed massive transcriptomic changes in this life cycle, including key gene families that contribute substantially to the expression load in each stage. In particular, different members of the cestode-specific hydrophobic ligand-binding protein (HLBP) family are among the most highly expressed genes in each life stage. We also found the transcriptomic signature of major metabolic changes during the transition from cysticercoids to adult worms. Thus, this work contributes to uncovering the gene expression changes that accompany the development of this important cestode model species, and to the best of our knowledge represents the first transcriptomic study with robust replicates spanning all of the main life stages of a tapeworm.
Asunto(s)
Hymenolepis/genética , Estadios del Ciclo de Vida , Transcriptoma , Animales , Regulación del Desarrollo de la Expresión Génica , Proteínas del Helminto/genética , Proteínas del Helminto/metabolismo , Hymenolepis/crecimiento & desarrollo , Hymenolepis/metabolismo , Familia de MultigenesRESUMEN
BACKGROUND: Reference genome and transcriptome assemblies of helminths have reached a level of completion whereby secondary analyses that rely on accurate gene estimation or syntenic relationships can be now conducted with a high level of confidence. Recent public release of the v.3 assembly of the mouse bile-duct tapeworm, Hymenolepis microstoma, provides chromosome-level characterisation of the genome and a stabilised set of protein coding gene models underpinned by bioinformatic and empirical data. However, interactome data have not been produced. Conserved protein-protein interactions in other organisms, termed interologs, can be used to transfer interactions between species, allowing systems-level analysis in non-model organisms. RESULTS: Here, we describe a probabilistic, integrated network of interologs for the H. microstoma proteome, based on conserved protein interactions found in eukaryote model species. Almost a third of the 10,139 gene models in the v.3 assembly could be assigned interaction data and assessment of the resulting network indicates that topologically-important proteins are related to essential cellular pathways, and that the network clusters into biologically meaningful components. Moreover, network parameters are similar to those of single-species interaction networks that we constructed in the same way for S. cerevisiae, C. elegans and H. sapiens, demonstrating that information-rich, system-level analyses can be conducted even on species separated by a large phylogenetic distance from the major model organisms from which most protein interaction evidence is based. Using the interolog network, we then focused on sub-networks of interactions assigned to discrete suites of genes of interest, including signalling components and transcription factors, germline multipotency genes, and genes differentially-expressed between larval and adult worms. Results show not only an expected bias toward highly-conserved proteins, such as components of intracellular signal transduction, but in some cases predicted interactions with transcription factors that aid in identifying their target genes. CONCLUSIONS: With key helminth genomes now complete, systems-level analyses can provide an important predictive framework to guide basic and applied research on helminths and will become increasingly informative as new protein-protein interaction data accumulate.
Asunto(s)
Hymenolepis/genética , Mapeo de Interacción de Proteínas , Proteoma/genética , Animales , Bases de Datos Genéticas , Eucariontes/clasificación , Eucariontes/genética , Eucariontes/metabolismo , Redes Reguladoras de Genes , Genoma de los Helmintos/genética , Proteínas del Helminto/genética , Proteínas del Helminto/metabolismo , Hymenolepis/clasificación , Hymenolepis/metabolismo , ProbabilidadRESUMEN
The Wnt/beta-catenin pathway has many key roles in the development of animals, including a conserved and central role in the specification of the primary (antero-posterior) body axis. The posterior expression of Wnt ligands and the anterior expression of secreted Wnt inhibitors are known to be conserved during the larval metamorphosis of tapeworms. However, their downstream signaling components for Wnt/beta-catenin signaling have not been characterized. In this work, we have studied the core components of the beta-catenin destruction complex of the human pathogen Echinococcus multilocularis, the causative agent of alveolar echinococcosis. We focused on two Axin paralogs that are conserved in tapeworms and other flatworm parasites. Despite their divergent sequences, both Axins could robustly interact with one E. multilocularis beta-catenin paralog and limited its accumulation in a heterologous mammalian expression system. Similarly to what has been described in planarians (free-living flatworms), other beta-catenin paralogs showed limited or no interaction with either Axin and are unlikely to function as effectors in Wnt signaling. Additionally, both Axins interacted with three divergent GSK-3 paralogs that are conserved in free-living and parasitic flatworms. Axin paralogs have highly segregated expression patterns along the antero-posterior axis in the tapeworms E. multilocularis and Hymenolepis microstoma, indicating that different beta-catenin destruction complexes may operate in different regions during their larval metamorphosis.
Asunto(s)
Proteína Axina/genética , Complejo de Señalización de la Axina/genética , Echinococcus multilocularis/genética , Glucógeno Sintasa Quinasa 3/genética , Proteínas del Helminto/genética , Hymenolepis/genética , beta Catenina/genética , Secuencia de Aminoácidos , Animales , Proteína Axina/química , Proteína Axina/metabolismo , Complejo de Señalización de la Axina/química , Echinococcus multilocularis/crecimiento & desarrollo , Echinococcus multilocularis/metabolismo , Perfilación de la Expresión Génica , Glucógeno Sintasa Quinasa 3/metabolismo , Proteínas del Helminto/química , Humanos , Hymenolepis/crecimiento & desarrollo , Hymenolepis/metabolismo , Larva/metabolismo , Filogenia , Alineación de Secuencia , beta Catenina/metabolismoRESUMEN
Wnt genes encode secreted glycoproteins that act in cell-cell signalling to regulate a wide array of developmental processes, ranging from cellular differentiation to axial patterning. Discovery that canonical Wnt/ß-catenin signalling is responsible for regulating head/tail specification in planarian regeneration has recently highlighted their importance in flatworm (phylum Platyhelminthes) development, but examination of their roles in the complex development of the diverse parasitic groups has yet to be conducted. Here, we characterise Wnt genes in the model tapeworm Hymenolepis microstoma and mine genomic resources of free-living and parasitic species for the presence of Wnts and downstream signalling components. We identify orthologs through a combination of BLAST and phylogenetic analyses, showing that flatworms have a highly reduced and dispersed complement that includes orthologs of only five subfamilies (Wnt1, Wnt2, Wnt4, Wnt5 and Wnt11) and fewer paralogs in parasitic flatworms (5-6) than in planarians (9). All major signalling components are identified, including antagonists and receptors, and key binding domains are intact, indicating that the canonical (Wnt/ß-catenin) and non-canonical (planar cell polarity and Wnt/Ca(2+)) pathways are functional. RNA-Seq data show expression of all Hymenolepis Wnts and most downstream components in adults and larvae with the notable exceptions of wnt1, expressed only in adults, and wnt2 expressed only in larvae. The distribution of Wnt subfamilies in animals corroborates the idea that the last common ancestor of the Cnidaria and Bilateria possessed all contemporary Wnts and highlights the extent of gene loss in flatworms.
Asunto(s)
Hymenolepis/genética , Hymenolepis/metabolismo , Proteínas Wnt/genética , Proteínas Wnt/metabolismo , Animales , Evolución Biológica , Tipificación del Cuerpo , Expresión Génica , Genoma , Hymenolepis/embriología , Filogenia , Vía de Señalización WntRESUMEN
The oncosphere larvae of tapeworms cyclically extend and retract their hooks during the penetration of the intestine of their intermediate hosts. The mechanisms regulating these movements are essentially unknown, in part due to the biohazardous nature of oncospheres from human pathogens. In this work, we standardized a method for the analysis of motility of hatched oncospheres (hexacanths) of the model tapeworm Hymenolepis microstoma. We used this assay to explore the relevance of protein kinases C (PKC) and A (PKA) in these processes. Pharmacological inhibition of the PKC pathway resulted in impaired larval motility. On the other hand, the PKA inhibitor H-89 potently blocked larval motility, as well as the motility of other life stages, although other inhibitors of the PKA pathway were not effective. This work represents the first study of the mechanisms that regulate the motility of oncospheres, and provides a path for further exploration.
Asunto(s)
Cestodos , Infecciones por Cestodos , Hymenolepis , Animales , Humanos , Hymenolepis/metabolismo , Larva , Proteínas Quinasas/metabolismoRESUMEN
Cestodes are platyhelminth parasites with a wide range of hosts that cause neglected diseases. Neurotransmitter signaling is of critical importance for these parasites which lack circulatory, respiratory and digestive systems. For example, serotonin (5-HT) and serotonergic G-protein coupled receptors (5-HT GPCRs) play major roles in cestode motility, development and reproduction. In previous work, we deorphanized a group of 5-HT7 type GPCRs from cestodes. However, little is known about another type of 5-HT GPCR, the 5-HT1 clade, which has been studied in several invertebrate phyla but not in platyhelminthes. Three putative 5-HT GPCRs from Echinococcus canadensis, Mesocestoides vogae (syn. M. corti) and Hymenolepis microstoma were cloned, sequenced and bioinformatically analyzed. Evidence grouped these new sequences within the 5-HT1 clade of GPCRs but differences in highly conserved GPCR motifs were observed. Transcriptomic analysis, heterologous expression and immunolocalization studies were performed to characterize the E. canadensis receptor, called Eca-5-HT1a. Functional heterologous expression studies showed that Eca-5-HT1a is highly specific for serotonin. 5-Methoxytryptamine and α-methylserotonin, both known 5-HT GPCR agonists, give stimulatory responses whereas methysergide, a known 5-HT GPCR ligand, give an antagonist response in Eca-5-HT1a. Mutants obtained by the substitution of key predicted residues resulted in severe impairment of receptor activity, confirming that indeed, these residues have important roles in receptor function. Immunolocalization studies on the protoscolex stage from E. canadensis, showed that Eca-5-HT1a is localized in branched fibers which correspond to the nervous system of the parasite. The patterns of immunoreactive fibers for Eca-5-HT1a and for serotonin were intimately intertwined but not identical, suggesting that they are two separate groups of fibers. These data provide the first functional, pharmacological and localization report of a serotonergic receptor that putatively belongs to the 5-HT1 type of GPCRs in cestodes. The serotonergic GPCR characterized here may represent a new target for antiparasitic intervention.
Asunto(s)
Cestodos/metabolismo , Proteínas del Helminto/metabolismo , Sistema Nervioso/metabolismo , Receptores de Serotonina 5-HT1/metabolismo , Secuencia de Aminoácidos , Animales , Echinococcus/metabolismo , Regulación de la Expresión Génica/efectos de los fármacos , Proteínas del Helminto/química , Proteínas del Helminto/genética , Humanos , Hymenolepis/metabolismo , Receptores de Serotonina 5-HT1/química , Receptores de Serotonina 5-HT1/genética , Alineación de Secuencia , Antagonistas de la Serotonina/farmacología , Agonistas de Receptores de Serotonina/farmacologíaRESUMEN
Comparative studies of thymidylate synthases, isolated from the tapeworm, Hymenolepis diminuta, and regenerating liver of its host, rat, aimed at a possibility of specific inhibition of the helminthic enzyme, are presented. While similar in structure (dimers with monomer molecular masses of 33.7 kDa and 34.9 kDa, respectively) and parameters describing interactions with substrates and products, the tapeworm and rat enzymes differed in the dependences of reaction velocity on temperature (Arrhenius plots biphasic and linear, respectively). The tapeworm, compared with the host, enzyme was less sensitive to the competitive slow-binding inhibition by 5-fluoro-dUMP and its 2-thio congener, but equally sensitive to inhibition by 4-thio-5-fluoro-dUMP, N4-hydroxy-dCMP and N4-hydroxy-5-fluoro-dCMP, the latter being more potent inhibitor of the parasite enzyme than 5-fluoro-dUMP. alpha-Anomer of 5-fluoro-dUMP behaved as a very weak competitive slow-binding inhibitor of both enzymes. Both enzymes differed markedly in sensitivity to inhibition by 10-propargyl-5,8-dideazafolate and its di- and triglutamates (pddPteGlu1-3), with pddPteGlu1 being stronger inhibitor of the mammalian enzyme, but pddPteGlu3 showing opposite specificity. Sulfonamidobenzoylglutamate analogue of pddPteGlu (pddPteSO2Glu) and 2-desamino-2-methyl derivative of this analogue (CH3pddPteSO2Glu) were weaker inhibitors of both enzymes than the parent compound. Substitution of the glutamyl residue in CH3pddPteSO2Glu with either norvaline or alanine increased inhibition potency, whereas similar substitutions with glycine, valine or phenylglycine were without a distinct effect with the host enzyme but weakened inhibition of the tapeworm enzyme.
Asunto(s)
Hymenolepis/metabolismo , Hígado/enzimología , Timidilato Sintasa/aislamiento & purificación , Animales , Fluorodesoxiuridilato/análogos & derivados , Fluorodesoxiuridilato/farmacología , Cinética , Hígado/parasitología , Regeneración Hepática , Masculino , Peso Molecular , Ratas , Ratas Wistar , Temperatura , Tetrahidrofolatos/farmacología , Timidilato Sintasa/antagonistas & inhibidores , Timidilato Sintasa/químicaRESUMEN
A fraction with enriched colchicine-binding properties prepared from Hymenolepis diminuta was found to possess many of the properties of tubulin isolated from other sources. Colchicine was bound by a simple saturable process with a dissociation constant of 13.2 microM. The binding capability decayed with a half-life of about 5 h. Binding was unaffected by lumicolchicine, was competitively inhibited by podophyllotoxin (inhibition constant of 4.8 microM) and showed an apparent stimulation by vinblastine sulphate. Sodium chloride also appeared to stimulate the binding process. The ligand/receptor complex had a molecular weight of approx. 112 000 as determined by gel filtration. On the basis of this biochemical and pharmacological evidence it was concluded that the colchicine receptor in the supernatant fraction of the H. diminuta homogenate was almost certainly tubulin. Refinement of the preparation should facilitate further studies on the mode of action of certain types of anthelmintic compound.
Asunto(s)
Colchicina/metabolismo , Hymenolepis/metabolismo , Tubulina (Proteína)/metabolismo , Animales , Sitios de Unión , Semivida , Lumicolchicinas/farmacología , Peso Molecular , Podofilotoxina/farmacología , Ratas , Cloruro de Sodio , Vinblastina/farmacologíaRESUMEN
The manner in which the flatworm, Hymenolepis diminuta (Cestoda), regulates the transport of glucose and Na+ across the brush border was examined. While the presence of an unstirred region in the brush border may favor the reabsorption of leaked glucose, some leaked glucose was lost to the ambient medium. This loss was markedly enhanced by preloading the worms with glucose and by removing Na+ from the incubation medium. Since glucose and Na+ influxes are coupled, glucose leakage stimulated the influx of 22Na+. However, this 22Na+ influx was balanced by a simultaneous increased 22Na+ efflux. The presence of phlorizin inhibited both unidirectional fluxes of 22Na+ indicating that efflux of 22Na+ occurred by countertransport; countertransport of [14C] glucose appeared to be negligible. A model has been proposed in which the transport of glucose and compensating transfers of Na+ across the membrane occur via the same carrier.
Asunto(s)
Cestodos/metabolismo , Glucosa/metabolismo , Hymenolepis/metabolismo , Sodio/metabolismo , Animales , Unión Competitiva , Transporte Biológico , Transporte Biológico Activo , Desoxiglucosa/farmacología , Glucosa/farmacología , Hymenolepis/efectos de los fármacos , Cinética , Larva , Modelos Biológicos , Ouabaína/farmacología , Florizina/farmacologíaRESUMEN
Serotoninlike immunoreactivity in the cestode Hymenolepis diminuta was studied at the light microscope level by using an antibody specific to serotonin. The rostellum, the cerebral ganglia and commissure, and the strobila contained numerous process-free, unipolar and multipolar serotoninlike immunoreactive cells. The suckers contained a plexus of branching immunoreactive fibers. In the strobila the multipolar cell bodies were situated laterodorsal and lateroventral to the longitudinal nerve cords, from which neurites were directed to the contralateral and ipsilateral nerve cord to form up to three transverse commissures per proglottid. Secondary varicose branches passed anteriorly, posteriorly, and obliquely along the proglottids at the level of the deep longitudinal muscles. Other varicose multi-branching neurites passed centrifugally from the primary and secondary neurites, forming vertebratelike en passant or terminal varicosities on the deep longitudinal muscles with bulbous or spinose terminals at the level of the superficial longitudinal muscles, or in the cortical parenchyma. Serotoninlike immunoreactivity was seen on the external seminal vesicle, the sphincter and cirrus sac, and the proximal portion of the vagina. Varicose terminals were concentrated at the sphincter. The close association of serotoninlike immunoreactive terminals and varicosities with the longitudinal muscles gives credence to the concept that serotonin functions as a neuromuscular transmitter or modulator in the platyhelminths.
Asunto(s)
Hymenolepis/metabolismo , Sistema Nervioso/metabolismo , Serotonina/metabolismo , Animales , Técnicas para Inmunoenzimas , Masculino , Neuronas/citología , RatasRESUMEN
This review is an account of modern research into the immunology and biochemistry of the rat tapeworm, Hymenolepis diminuta. The first half of the review is devoted to the immunological responses of the host to the parasite. It describes the specific responses that occur when the host is exposed to a primary infection, and the changes that occur when further infections are superimposed on the primary one. The aquisition of immunity to the tapeworm and its persistence in the absence of the infection are also discussed, as well as the non-specific responses of the host to the parasite. The second half of the review is concerned with biochemistry, summarizing the early biochemical work that has been carried out on the tapeworm and describing the metabolic pathways now thought to be characteristic of the parasite. What little information that exists on intermediary metabolism in eggs and larvae is summarized here. Much of this section is concerned with the role of mitochondria in H. diminuta, especially the control of the critical branchpoint (PK/PEPCK), which partitions carbon into either the cytosol or the mitochondrion. The role of 5-hydroxytryptamine in controlling both worm behaviour and metabolism is discussed, followed by a brief look at some other effectors that may prove in the future to have great significance in regulating the parasite. Finally, there is a detailed consideration of strain variation within H. diminuta and of the impact on the tapeworm of components of the immune system, formerly described as the 'crowding effect'. The review concludes with a brief discussion of evolutionary aspects of the rat-tapeworm relationship and a comprehensive bibliography.
Asunto(s)
Himenolepiasis/veterinaria , Hymenolepis/inmunología , Hymenolepis/metabolismo , Enfermedades de los Roedores/inmunología , Animales , Evolución Biológica , Interacciones Huésped-Parásitos , Himenolepiasis/inmunología , Larva/metabolismo , Mitocondrias/metabolismo , Óvulo/metabolismo , RatasRESUMEN
Cestode worms, commonly also known as 'flat' worms or tapeworms, are an important class of endoparasitic organisms. In order to complete their life cycle, they infect intermediate and definitive hosts in succession, through oral ingestion of eggs or larvae, respectively. Serious disease in humans or other mammalian hosts is mostly caused by the larval stages. Echinococcus spp. and Taenia spp. have been extensively investigated in the laboratory due to the fact that they represent important veterinary medical challenges and also cause grave diseases in humans. In contrast, Hymenolepis spp. and Mesocestoides spp. infections are relatively rare in humans, but these parasites have been extensively studied because their life cycle stages can be easily cultured in vitro, and can also be conveniently maintained in laboratory animal hosts. Thus they are more easily experimentally accessible, and represent important models for investigating the various aspects of cestode biology. This review will focus on in vitro and in vivo models which have been developed for studies on the host-parasite relationship during infection with Echinococcus, Taenia, Hymenolepis, Mesocestoides and Spirometra, and will cover the use of these models to investigate the morphology and ultrastructure of respective genera, the immunological relationship with the host and the development of vaccination approaches, as well as applications of these models for studies on parasite metabolism, physiology and gene expression. In addition, the use of these models in the development of chemotherapeutic measures against cestode infections is reviewed.
Asunto(s)
Cestodos/fisiología , Infecciones por Cestodos/parasitología , Animales , Antihelmínticos/metabolismo , Antihelmínticos/uso terapéutico , Gatos , Bovinos , Cestodos/genética , Cestodos/crecimiento & desarrollo , Infecciones por Cestodos/patología , Infecciones por Cestodos/terapia , Perros , Echinococcus/crecimiento & desarrollo , Echinococcus/metabolismo , Regulación de la Expresión Génica , Interacciones Huésped-Parásitos , Humanos , Hymenolepis/crecimiento & desarrollo , Hymenolepis/metabolismo , Estadios del Ciclo de Vida , Mesocestoides/crecimiento & desarrollo , Mesocestoides/metabolismo , Ratones , Modelos Animales , Ratas , Ovinos , Spirometra/crecimiento & desarrollo , Spirometra/metabolismo , Porcinos , Taenia/crecimiento & desarrollo , Taenia/metabolismoRESUMEN
The 31P NMR spectrum of the adult tapeworm, Hymenolepis diminuta, at 37 degrees C during perfusion with physiological saline was composed of 10 peaks. Based on chemical shifts and analysis of worm extracts, the phosphorus components included glucose-6-phosphate, fructose-6-phosphate, phosphorylcholine, glycerophosphoryl choline and -ethanolamine, nucleotide monophosphate-diphosphate and -triphosphate, nicotinamide adenine dinucleotide and uridine diphosphate glucose. The mean level of nucleotide triphosphate was 0.86 nmol (mg fresh weight)-1 and the nucleotide triphosphate/-diphosphate ratio 3.9. Based on the nucleotide triphosphate level, worms were viable for at least 3 h and the intracellular pH was maintained constant at approximately 6.7. Short-term exposure to mebendazole perfused at 11 or 27 microM solubilized in physiological saline containing 0.5% Tween 80 or 0.1% dimethyl sulphoxide had little effect on the nucleotide triphosphate level. Some cytological changes, however, were evident following perfusion of mebendazole. In contrast, exposure to 2,4-dinitrophenol caused a rapid decline in nucleotide triphosphate level. It was concluded that mebendazole does not exert its primary effect on oxidative phosphorylation.
Asunto(s)
Hymenolepis/efectos de los fármacos , Mebendazol/farmacología , Nucleótidos/metabolismo , Animales , Hymenolepis/metabolismo , Hymenolepis/ultraestructura , Espectroscopía de Resonancia Magnética , Microscopía Electrónica , Nucleótidos/análisis , FosforilaciónRESUMEN
Both patent and prepatent adult Hymenolepis diminuta excreted 20-hydroxyecdysone into the culture medium when maintained in vitro. Patent worms also excreted ecdysone and comparatively large quantities of unidentified immunoreactive material of a relatively apolar nature. This latter material was shown to be depleted from the endogenous free ecdysteroids of patent adults during the culture period. Ecdysteroid excretion was affected both qualitatively and quantitatively when culturing conditions were varied.
Asunto(s)
Ecdisterona/metabolismo , Hymenolepis/metabolismo , Animales , Cromatografía Líquida de Alta Presión , Ecdisona/metabolismo , Cromatografía de Gases y Espectrometría de Masas , Técnicas In Vitro , Masculino , Radioinmunoensayo , Ratas , Ratas EndogámicasRESUMEN
Glucose uptake by Hymenolepis diminuta was linear for up to 60 min following in vitro incubation in 10 mM glucose. Following the addition of 1 mM 5-HT, with a 95% O2/5% CO2, gas phase, glucose uptake by H. diminuta was significantly (P less than 0.001) enhanced, remaining linear and parallel to that of control groups between 15 and 60 min incubation. Under air, the rates of glucose uptake were higher, but were only significantly increased by 5-HT during the first 30 min of incubation. In further experiments, in the absence of glucose in the incubation media worm glycogen reserves decreased by over 50% after 60 min. With the addition of 1 mM 5-HT, the reduction in glycogen content was significantly (P less than 0.025) greater, exceeding 65% after 60min. When glucose was added to the incubation media, worm glycogen reserves were not significantly depleted irrespective of the presence or absence of 5-HT. Incubations under a 95% O2/5% CO2 gas phase did not significantly influence glycogen content compared to corresponding groups incubated in air. The results suggest that 5-HT stimulates glycolysis in H. diminuta through increased glucose uptake by the worm or by a reduction in glycogen reserves in the absence of external glucose.
Asunto(s)
Glucosa/metabolismo , Glucógeno/metabolismo , Hymenolepis/metabolismo , Serotonina/farmacología , Animales , Hymenolepis/efectos de los fármacos , Ratas , Ratas Endogámicas , Factores de TiempoRESUMEN
The occurrence of rhodoquinone as a mitochondrial membrane component was demonstrated in adult Hymenolepis diminuta. Chromatographic separation of pentane extracts, from lyophilized mitochondrial membranes, coupled with spectral analyses of separated material demonstrated the presence of rhodoquinone. The presence of ubiquinone was not apparent. Rhodoquinone content of membranes was about 1.2 micrograms (mg protein)-1. The rhodoquinone requirement of the H. diminuta electron transport system was demonstrated both in terms of the less active NADH oxidase and the physiologically required, NADH-dependent fumarate reductase employing lyophilized mitochondrial membranes as the source of activities. Pentane extraction of membranes virtually abolished the oxidase and fumarate reductase systems. Supplementation of pentane-treated membranes with H. diminuta rhodoquinone restored oxidase and fumarate reductase activities to levels simulating those of lyophilized membranes. Ubiquinone did not substitute for rhodoquinone. The rhodoquinone-reconstituted membranes displayed rotenone sensitivity. These findings represent the first direct demonstration of the rhodoquinone requirement of helminth electron transport-coupled oxidase and fumarate reductase.
Asunto(s)
Hymenolepis/metabolismo , Mitocondrias/metabolismo , Oxidorreductasas actuantes sobre Donantes de Grupo CH-CH , Ubiquinona/análogos & derivados , Animales , Transporte de Electrón , Hymenolepis/análisis , Hymenolepis/enzimología , Membranas Intracelulares/análisis , Membranas Intracelulares/enzimología , Membranas Intracelulares/metabolismo , Mitocondrias/análisis , Mitocondrias/enzimología , Complejos Multienzimáticos/metabolismo , NADH NADPH Oxidorreductasas/metabolismo , Oxidorreductasas/metabolismo , Consumo de Oxígeno , Peróxidos/metabolismo , Succinatos/biosíntesis , Ubiquinona/análisis , Ubiquinona/metabolismoRESUMEN
Adult Hymenolepis diminuta incorporated label from L[U-14C]serine, [1-14C]palmitic acid, [1-14C]palmitoyl-CoA and cytidine-5'-diphospho[methyl-14C]choline into the various intermediates of sphingomyelin synthesis (ketosphingosine, dihydrosphingosine, sphingosine, ceramide and sphingomyelin). From the results it was concluded that H. diminuta possessed the five enzymes involved in sphingomyelin synthesis, namely serine palmitoyl-transferase, 3-oxosphinganine reductase, flavoprotein dihydrosphingosine reductase, sphingosine acyltransferase and ceramide choline-phosphotransferase.
Asunto(s)
Hymenolepis/metabolismo , Esfingomielinas/biosíntesis , Aciltransferasas/metabolismo , Oxidorreductasas de Alcohol/metabolismo , Animales , Ceramidas/biosíntesis , Citidina Difosfato Colina/metabolismo , Diacilglicerol Colinafosfotransferasa/metabolismo , Hymenolepis/enzimología , Oxidorreductasas/metabolismo , Ácido Palmítico , Ácidos Palmíticos/metabolismo , Palmitoil Coenzima A/metabolismo , Serina/metabolismo , Serina C-Palmitoiltransferasa , Esfingosina/biosíntesis , Esfingosina N-AciltransferasaRESUMEN
Praziquantel (PZ) at concentrations down to 5 x 10(-8) M induced a rapid contraction of Hymenolepis diminuta musculature. This effect was accompanied by a strong inhibition of 45Ca2+ incorporation which showed some dependence on Ca2+ concentration. Ca2+ efflux experiments showed that PZ markedly stimulated the release of Ca2+ from tapeworms preloaded with 45Ca2+, with the effluxed Ca2+ being derived from a small fast pool and a larger slow pool. This stimulatory effect appeared., like PZ-induced muscle contraction, to be independent of external Ca2+. By carrying out 45Ca2+ exchange experiments under near equilibrium conditions and atomic absorption spectroscopy it could be demonstrated that PZ resulted in a net excretion of endogenous Ca2+. In PZ-induced contracted worms adenylate nucleotide levels and the adenylate energy charge were not significantly different from those of untreated control worms. Also, PZ had no effect on Ca2+-stimulated ATPase activity of the tapeworm's tegumental brush border. Nor did the drug alter the activities of Ca2+-ATPases in whole homogenates of worms or mitochondria, microsomal or soluble fractions. Although the mechanism of PZ-induced changes in Ca2+ transport was not elucidated, it is suggested that the sustained release of endogenous Ca2+ may affect the sequence of excitation-contraction coupling and that such interference may cause the observed massive contraction of the tapeworm's musculature.
Asunto(s)
Calcio/metabolismo , Hymenolepis/efectos de los fármacos , Isoquinolinas/farmacología , Praziquantel/farmacología , Nucleótidos de Adenina/metabolismo , Animales , Transporte Biológico/efectos de los fármacos , ATPasas Transportadoras de Calcio/metabolismo , Hymenolepis/metabolismo , Cinética , Microvellosidades/enzimología , Mitocondrias/enzimología , Contracción Muscular/efectos de los fármacosRESUMEN
The mechanism by which Hymenolepis diminuta (Cestoda) absorbs 3-0-methylglucose (30MG) in vitro was analyzed. Influxes of 0.1 and 0.01 mM-3H-30MG during incubations ranging from 5 s to 60 min were not affected significantly when 10 mM-unlabeled 30MG was present as an inhibitor. After 60 min in 0.1 mM-3H-30MG, the concentration of labeled substrate within tapeworms (0.04 mumol ml-1 worm water = 0.04 mM) was less than that of the bathing medium. Tapeworms incubated for 1 h with either 5 mM-glucose or 5 mM-beta-methylglucose (beta MG) gained 15-20% more water than did tapeworms in saline alone, but addition of 5 mM-30MG to the saline had no significant effect on weight change. When the 3H-30MG concentration was varied from 0.01 to 10 mM, influxes were a linear function of substrate concentrations. These analyses show that H. diminuta absorbs 30MG by simple diffusion alone. Thus, use of this monosaccharide to estimate the internal concentration of actively transported sugars (e.g. glucose or beta MG) in H. diminuta is invalid.
Asunto(s)
Hymenolepis/metabolismo , Metilglucósidos/metabolismo , 3-O-Metilglucosa , Animales , Transporte Biológico ActivoRESUMEN
Individual worms from rats infected with different strains of Hymenolepis diminuta were incubated in vitro and the products lactate, succinate, acetate and ammonia assayed. Variability in excretion was not confined to differences between strains. Two metabolic types were identified. Where succinate was above 20 mumol g-1 h-1, lactate excretion was low. Where succinate was not detected, lactate excretion was high. Acetate excretion was variable. Lactate and ammonia excretion were positively correlated. All worms from one rat were of the same type but could be of either type from different rats. The host strain had no effect. A relationship was shown between lactate excretion and the number of worms from a standard inoculum present at 21 days of infection. The incidence of high lactate excretion was increased in worms from secondary infections. Components of the host immune response may thus exert effects on the metabolism of H. diminuta, manifest as shifts in emphasis on cytosolic and mitochondrial metabolism.