122 research outputs found

    Pollination of SliPPer orchidS (cyPriPedioideae): a review

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    AbstRAct. Cypripedioideae (five genera; ca. 176 species) are widespread in temperate and tropical Asia and America. About a quarter (42) of the species have been studied to determine their pollinators and/or breeding systems. All flowers are one-way traps pollinated by insects of particular types and size. Slipper orchids are selfcompatible and pollinated by deceit. Most Cypripedium species are pollinated by bees, whereas some smallerflowered species are pollinated by flies, and a few are pollinated by both. Most bee-pollinated Cypripedium species appear to be generalized food mimics. The fly-pollinated species have evolved diverse pollination systems that utilize a variety of flies as pollen vectors, including fruit flies, dung flies, and a fungal spore-eating hoverfly (Syrphidae). Most species of the tropical Asian Paphiopedilum and tropical American Phragmipedium are pollinated by hoverflies; flowers of many species in both genera have aphid-like spots that attract gravid female hoverflies that normally lay their eggs in aphid colonies. The more brightly colored Paphiopedilum micranthum and Phragmipedium besseae are pollinated by Hymenoptera. Autogamy is limited but occurs most frequently in Phragmipedium species. About two-thirds of the insect-pollinated slipper orchids (25/37) have evolved highly specialized flowers that are pollinated by a single pollinator or several pollinator species in the same genus. Species belonging to the same taxonomic section usually have the same pollination system. The deceit-pollination system of Cypripedioideae appears to have evolved early in diversification of Orchidaceae.

    Tracemaking Activities of Crabs and Their Environmental Significance: The Ichnogenus \u3ci\u3ePsilonichnus\u3c/i\u3e

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    Modem crabs are common inhabitants of shallow subtidal, intertidal, and supratidal environments, and many crabs are capable of producing traces that can be preserved in the rock record. The first crabs, Early Jurassic in age, probably were not fossorial. By Cretaceous time, however, diverse endobenthic lineages were established. Many representatives of these lineages undoubtedly produced domiciles that are preserved in shallow marine to quasimarine sediments and that should be useful in characterizing the depositional environment of the sediments. Nonetheless, most such dwelling structures have been studied little and remain essentially unnamed. The ichnogenus Psilonichnus Fiirsich is amenable to the taxonomic concept of several forms of crab burrows; presently recognized ichnospecies include P. tubiformis Fiirsich and P. upsilon (n. ichnosp.). Future work may reveal the need for further ichnospecific differentiation. The occurrence of Psilonichnus upsilon and related burrow forms should prove to be a useful criterion for the identification of marine-margin facies in the rock record. Certain crabs also produce domiciles referable to Thalassinoides, Gyrolithes, and Skolithos, and possibly Macanopsis and Spongeliomorpha. Except for Skolithos, such structures traditionally have been attributed to shrimp, lobsters, or stomatopods. Ethologic and taxonomic re-evaluation of these burrow forms is needed

    Personalized diagnosis in suspected myocardial infarction

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    Background: In suspected myocardial infarction (MI), guidelines recommend using high-sensitivity cardiac troponin (hscTn)- based approaches. These require fixed assay-specific thresholds and timepoints, without directly integrating clinical information. Using machine-learning techniques including hs-cTn and clinical routine variables, we aimed to build a digital tool to directly estimate the individual probability of MI, allowing for numerous hs-cTn assays. Methods: In 2,575 patients presenting to the emergency department with suspected MI, two ensembles of machine-learning models using single or serial concentrations of six different hs-cTn assays were derived to estimate the individual MI probability ( ARTEMIS model). Discriminative performance of the models was assessed using area under the receiver operating characteristic curve (AUC) and logLoss. Model performance was validated in an external cohort with 1688 patients and tested for global generalizability in 13 international cohorts with 23,411 patients. Results: Eleven routinely available variables including age, sex, cardiovascular risk factors, electrocardiography, and hs-cTn were included in the ARTEMIS models. In the validation and generalization cohorts, excellent discriminative performance was confirmed, superior to hs-cTn only. For the serial hs-cTn measurement model, AUC ranged from 0.92 to 0.98. Good calibration was observed. Using a single hs-cTn measurement, the ARTEMIS model allowed direct rule-out of MI with very high and similar safety but up to tripled efficiency compared to the guideline- recommended strategy. Conclusion We developed and validated diagnostic models to accurately estimate the individual probability of MI, which allow for variable hs-cTn use and flexible timing of resampling. Their digital application may provide rapid, safe and efficient personalized patient care

    Leishmania-Induced Inactivation of the Macrophage Transcription Factor AP-1 Is Mediated by the Parasite Metalloprotease GP63

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    Leishmania parasites have evolved sophisticated mechanisms to subvert macrophage immune responses by altering the host cell signal transduction machinery, including inhibition of JAK/STAT signalling and other transcription factors such as AP-1, CREB and NF-κB. AP-1 regulates pro-inflammatory cytokines, chemokines and nitric oxide production. Herein we show that upon Leishmania infection, AP-1 activity within host cells is abolished and correlates with lower expression of 5 of the 7 AP-1 subunits. Of interest, c-Jun, the central component of AP-1, is cleaved by Leishmania. Furthermore, the cleavage of c-Jun is dependent on the expression and activity of the major Leishmania surface protease GP63. Immunoprecipitation of c-Jun from nuclear extracts showed that GP63 interacts, and cleaves c-Jun at the perinuclear area shortly after infection. Phagocytosis inhibition by cytochalasin D did not block c-Jun down-regulation, suggesting that internalization of the parasite might not be necessary to deliver GP63 molecules inside the host cell. This observation was corroborated by the maintenance of c-Jun cleavage upon incubation with L. mexicana culture supernatant, suggesting that secreted, soluble GP63 could use a phagocytosis-independent mechanism to enter the host cell. In support of this, disruption of macrophage lipid raft microdomains by Methyl β-Cyclodextrin (MβCD) partially inhibits the degradation of full length c-Jun. Together our results indicate a novel role of the surface protease GP63 in the Leishmania-mediated subversion of host AP-1 activity

    Worms take to the slo lane: a perspective on the mode of action of emodepside

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    The cyclo-octapdepsipeptide anthelmintic emodepside exerts a profound paralysis on parasitic and free-living nematodes. The neuromuscular junction is a significant determinant of this effect. Pharmacological and electrophysiological analyses in the parasitic nematode Ascaris suum have resolved that emodepside elicits a hyperpolarisation of body wall muscle, which is dependent on extracellular calcium and the efflux of potassium ions. The molecular basis for emodepside’s action has been investigated in forward genetic screens in the free-living nematode Caenorhabditis elegans. Two screens for emodepside resistance, totalling 20,000 genomes, identified several mutants of slo-1, which encodes a calcium-activated potassium channel homologous to mammalian BK channels. Slo-1 null mutants are more than 1000-fold less sensitive to emodepside than wild-type C. elegans and tissue-specific expression studies show emodepside acts on SLO-1 in neurons regulating feeding and motility as well as acting on SLO-1 in body wall muscle. These genetic data, combined with physiological measurements in C. elegans and the earlier physiological analyses on A. suum, define a pivotal role for SLO-1 in the mode of action of emodepside. Additional signalling pathways have emerged as determinants of emodepside’s mode of action through biochemical and hypothesis-driven approaches. Mutant analyses of these pathways suggest a modulatory role for each of them in emodepside’s mode of action; however, they impart much more modest changes in the sensitivity to emodepside than mutations in slo-1. Taken together these studies identify SLO-1 as the major determinant of emodepside’s anthelmintic activity. Structural information on the BK channels has advanced significantly in the last 2 years. Therefore, we rationalise this possibility by suggesting a model that speculates on the nature of the emodepside pharmacophore within the calcium-activated potassium channels
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