Phagocytosis of Cryptococcus neoformans by,and Nonlytic Exocytosis from,Acanthamoeba castellanii

Cryptococcus neoformans, an encapsulated, pathogenic yeast, is endowed with a variety of virulence factors, including a polysaccharide capsule. During mammalian infection, the outcome of the interaction between C. neoformans and macrophages is central to determining the fate of the host. Previous studies have shown similarities between the interaction of C. neoformans with macrophages and with amoebae, resulting in the proposal that fungal virulence for mammals originated from selection by amoeboid predators. In this study, we investigated the interaction of C. neoformans with the soil amoeba Acanthamoeba castellanii. Comparison of phagocytic efficiency of the wild type, nonencapsulated mutants, and complemented strains showed that the capsule was antiphagocytic for amoebae. Capsular enlargement was associated with a significant reduction in phagocytosis, suggesting that this phenomenon protects against ingestion by phagocytic predators. C. neoformans var. neoformans cells were observed to exit amoebae several hours after ingestion, in a process similar to the recently described nonlytic exocytosis from macrophages. Cryptococcal exocytosis from amoebae was dependent on the strain and on actin and required fungal viability. Additionally, the presence of a capsule was inversely correlated with the likelihood of extrusion in certain strains. In summary, nonlytic exocytosis from amoebae provide another parallel to observations in fungus-macrophage interactions. These results provide additional support for the notion that some mechanisms of virulence observed during mammalian infection originated, and were selected for, by environmental interactions.The encapsulated yeast Cryptococcus neoformans is an environmental organism that is capable of causing human disease. This fungus is a facultative intracellular pathogen with a unique pathogenic strategy, despite no obvious need for replication in an animal host as part of its life cycle (10). C. neoformans is known to interact with protozoa, some of which have been shown to be effective predators for this fungus (6, 26), and amoebae appear to be important for the control of C. neoformans in the environment (28). Previously, we reported that the interaction of C. neoformans with Acanthamoeba castellanii directly paralleled the interaction with human macrophages (33). Similarities between C. neoformans interactions with amoebae and macrophages included intracellular replication in a phagosome and the release of polysaccharide-containing vesicles into the cytoplasm (33). Furthermore, passage of avirulent C. neoformans and Histoplasma capsulatum through slime mold and amoebae was shown to increase virulence in mice (31, 32). On the basis of these observations, it was proposed that the capacity for mammalian virulence emerged from interactions with phagocytic predators, such as amoebae and slime mold, in the environment (7, 17, 30). Consequently, single-cell protists have emerged as important systems for the study of C. neoformans virulence, and subsequent studies have investigated the interaction of this fungus with slime mold and paramecia (9, 31). Additional evidence for this concept comes from studies of insect fungal pathogens, which suggest that the capacity for insect pathogenicity may follow preadaptation from interactions with amoebae in the environment (4). Understanding the mechanisms by which virulence emerges in environmental microbes is important considering that global warming has been hypothesized to bring about new fungal diseases in the coming century (13).Recent work in our laboratory and in that of Robin May simultaneously uncovered a novel strategy of avoiding macrophage killing whereby yeast cells were expulsed without lysis of the host cell (2, 19). The process is remarkable in that extrusion of the C. neoformans-filled phagosome is accompanied by the survival of both the host cells and the yeast cells. Phagosome extrusion or fungal exocytosis appears to be a C. neoformans-dictated event that is dependent on both the presence of the polysaccharide capsule and on the depolymerization of actin. A corollary of the hypothesis that C. neoformans virulence emerged from interactions with environmental predators is that phenomena observed with mammalian cells are likely to have a counterpart in free-living phagocytic cells. Consequently, the observation of an apparently unique event such as phagosomal extrusion from mammalian macrophages suggested a need to search for similar events in C. neoformans interactions with environmental phagocytic predators.In this study, we investigated parallels between the intracellular pathogenic strategy of C. neoformans in both macrophages and A. castellanii, focusing on characterizing the impact of the capsule on protozoan phagocytosis and on ascertaining whether fungal cells could also exit amoebae, including the role of the capsule in that possible mechanism. Using time-lapse microscopy, we observed the exocytosis of C. neoformans from A. castellanii. While there are significant differences in the nonlytic exocytosis process when comparing amoebae and macrophages, the observation of this phenomenon in amoebae provides additional support for the idea that the virulence of C. neoformans was selected for, and is maintained, by interactions in the environment with other soil organisms.(This research was conducted by Cara Chrisman in partial fulfillment of the requirements for a Ph.D. from the Sue Golding Graduate Division of Medical Science, Albert Einstein College of Medicine, Yeshiva University, Bronx, NY [awarded in 2010].)     

Effects of hydromorphological integrity on biodiversity and functioning of river ecosystems

River channels tend to a dynamic equilibrium driven by the dynamics of water and sediment discharge. The resulting fluctuating pattern of channel form is affected by the slope, the substrate erodibility, and the vegetation in the river corridor and in the catchment. Geomorphology is basic to river biodiversity and ecosystem functioning since the channel pattern provides habitat for the biota and physical framework for ecosystem processes. Human activities increasingly change the natural drivers of channel morphology on a global scale (e.g. urbanization increases hydrological extremes, and clearing of forests for agriculture increases sediment yield). In addition, human actions common along world rivers impact channel dynamics directly, e.g. river regulation simplifies and fossilizes channel form. River conservation and restoration must incorporate mechanisms of channel formation and ecological consequences of channel form and dynamics. This article (1) summarizes the role of channel form on biodiversity and functioning of river ecosystems, (2) describes spatial complexity, connectivity and dynamism as three key hydromorphological attributes, (3) identifies prevalent human activities that impact these key components and (4) analyzes gaps in current knowledge and identifies future research topics.     

Synthesis and characterization of copper(I) and silver(I) complexes with heterocyclic bidentate ligands (N, X), X = S, Se

The synthesis and structural characterization of series of copper and silver homoleptic complexes [M(R-pyX)], M = Cu, Ag, X = S, Se; R = H, 3-CF₃, 5-CF₃ (not all combinations), is described. The copper compounds, as well as [Ag(pySe)] and [Ag(3-CF₃-pySe)], were synthesised by electrochemical oxidation of anodic metal in a cell containing an acetonitrile solution of the corresponding proligand. The other homoleptic silver complexes were obtained by direct reaction between AgNO₃ and the salt of the corresponding ligand in methanol. In addition, the reaction of the metal thiolate compounds with bis(diphenylphosphino)ethane (dppe) in acetone allowed the synthesis of heteroleptic compounds [M₂(R-pyX)₂(dppe)₃]. The compounds obtained have been characterized by microanalysis, IR spectroscopy and mass spectrometry and, in cases where the complexes were sufficiently soluble, by ¹H NMR spectroscopy. The proligands (3-CF₃pySe)₂ (1), (5-CF₃-pySe)₂ (2) and (5-CF₃-pySe-DMF) (3) and the complexes [Cu(3-CF₃-pyS)] (4), [Ag(3-CF₃-pyS)] (5) and [Cu₂(5-CF₃-pyS)₂(dppe)₃] (6) were obtained as crystalline products and were studied by X-ray diffraction methods.     

Canopy Herbivory and Insect Herbivore Diversity in a Dry Forest–Savanna Transition in Brazil

This study aimed to compare canopy herbivore diversity and resultant insect damage to vegetation in two distinct and adjacent ecosystems, specifically a dry forest ecosystem and a cerrado (savanna) ecosystem that occur together in an abrupt transition zone in southeastern Brazil. In the dry forest, the canopy was reached using a single rope climbing technique, whereas the shorter canopy of the cerrado was assessed using a 7 m ladder. Insect specimens were collected by beating the foliage, and 20 representative leaves were collected to calculate the specific leaf mass (SLM) and leaf area loss through herbivory. Also, we collected ten soil samples from each habitat to determine soil nutrient content. We sampled 118 herbivorous insects from ten families, mostly in dry forest trees (96 individuals belonging to 31 species). A higher abundance of chewing and sap-sucking insects were observed in dry forest trees than in cerrado trees. The same pattern was observed for the richness of chewers, with a higher degree of diversity of chewers found in dry forest trees than in cerrado trees. Herbivorous insects were not affected by SLM regardless of guild and habitat. However, we observed a negative correlation between the herbivory rate and the specific leaf mass (SLM). The cerrado trees showed a higher SLM and lower herbivory rates than trees occurring in the dry forest. These results suggest that herbivory rates in the transition dry forest–cerrado may be driven by soil nutrient content, which is thought to influence leaf sclerophylly.
Abstract in Portuguese is available at http://www.blackwell-synergy.com/loi/btp .     

Fungal Cell Gigantism during Mammalian Infection

The interaction between fungal pathogens with the host frequently results in morphological changes, such as hyphae formation. The encapsulated pathogenic fungus Cryptococcus neoformans is not considered a dimorphic fungus, and is predominantly found in host tissues as round yeast cells. However, there is a specific morphological change associated with cryptococcal infection that involves an increase in capsule volume. We now report another morphological change whereby gigantic cells are formed in tissue. The paper reports the phenotypic characterization of giant cells isolated from infected mice and the cellular changes associated with giant cell formation. C. neoformans infection in mice resulted in the appearance of giant cells with cell bodies up to 30 µm in diameter and capsules resistant to stripping with γ-radiation and organic solvents. The proportion of giant cells ranged from 10 to 80% of the total lung fungal burden, depending on infection time, individual mice, and correlated with the type of immune response. When placed on agar, giant cells budded to produce small daughter cells that traversed the capsule of the mother cell at the speed of 20–50 m/h. Giant cells with dimensions that approximated those in vivo were observed in vitro after prolonged culture in minimal media, and were the oldest in the culture, suggesting that giant cell formation is an aging-dependent phenomenon. Giant cells recovered from mice displayed polyploidy, suggesting a mechanism by which gigantism results from cell cycle progression without cell fission. Giant cell formation was dependent on cAMP, but not on Ras1. Real-time imaging showed that giant cells were engaged, but not engulfed by phagocytic cells. We describe a remarkable new strategy for C. neoformans to evade the immune response by enlarging cell size, and suggest that gigantism results from replication without fission, a phenomenon that may also occur with other fungal pathogens.     

Rapid determination of 25-hydroxy vitamin D3 in swine tissue using an isotope dilution HPLC-MS assay

A rapid method for quantification of 25-hydroxy vitamin D3 in different swine tissues based on isotope dilution HPLC-MS has been developed and validated. Six times deuterated analyte is used as internal standard. The method is fast and can be performed with only 1 g sample. Sample preparation for kidney, liver, muscle and spleen requires only homogenisation and extraction with methanol. An additional enzymatic digest is required for skin, and clean-up of the extract by solid-phase extraction (SPE) is used for adipose tissue and skin. The lower limit of detection varies from 1 ng/g (muscle) to 5 ng/g (adipose and skin). The method has been successfully applied to various tissue samples of pigs fed for 119 days either 2000 IU of vitamin D3 or 50 μg of 25-hydroxy vitamin D3 per kg feed. For animals ingesting 25-OH-D3 supplements the highest tissue contents were observed in the skin (24.8 ± 3.5 ng/g), followed by kidney (14.2 ± 1.5 ng/g), liver and muscle (5.7 ± 0.6 ng/g). The 25-OH-D3 content in the skin was significantly higher in animals ingesting 2000 IU/kg of vitamin D3 (39.5 ± 13.4 ng/g). Levels in selected tissues of some animals were below the lower limit of quantification. No measurable amounts of 25-OH-D3 were found in spleen, abdominal fat and subcutaneous fat of the animals of both groups as well as in the liver, kidney and muscle of the animals ingesting 2000 IU/kg of vitamin D3.     

Antiangiogenic and Antitumor Effects of Trypanosoma cruzi Calreticulin

Background

In Latin America, 18 million people are infected with Trypanosoma cruzi, the agent of Chagas'' disease, with the greatest economic burden. Vertebrate calreticulins (CRT) are multifunctional, intra- and extracellular proteins. In the endoplasmic reticulum (ER) they bind calcium and act as chaperones. Since human CRT (HuCRT) is antiangiogenic and suppresses tumor growth, the presence of these functions in the parasite orthologue may have consequences in the host/parasite interaction. Previously, we have cloned and expressed T. cruzi calreticulin (TcCRT) and shown that TcCRT, translocated from the ER to the area of trypomastigote flagellum emergence, promotes infectivity, inactivates the complement system and inhibits angiogenesis in the chorioallantoid chicken egg membrane. Most likely, derived from these properties, TcCRT displays in vivo inhibitory effects against an experimental mammary tumor.

Methodology and Principal Findings

TcCRT (or its N-terminal vasostatin-like domain, N-TcCRT) a) Abrogates capillary growth in the ex vivo rat aortic ring assay, b) Inhibits capillary morphogenesis in a human umbilical vein endothelial cell (HUVEC) assay, c) Inhibits migration and proliferation of HUVECs and the human endothelial cell line Eahy926. In these assays TcCRT was more effective, in molar terms, than HuCRT: d) In confocal microscopy, live HUVECs and EAhy926 cells, are recognized by FITC-TcCRT, followed by its internalization and accumulation around the host cell nuclei, a phenomenon that is abrogated by Fucoidin, a specific scavenger receptor ligand and, e) Inhibits in vivo the growth of the murine mammary TA3 MTXR tumor cell line.

Conclusions/Significance

We describe herein antiangiogenic and antitumor properties of a parasite chaperone molecule, specifically TcCRT. Perhaps, by virtue of its capacity to inhibit angiogenesis (and the complement system), TcCRT is anti-inflammatory, thus impairing the antiparasite immune response. The TcCRT antiangiogenic effect could also explain, at least partially, the in vivo antitumor effects reported herein and the reports proposing antitumor properties for T. cruzi infection.     

The Subventricular Zone En-face: Wholemount Staining and Ependymal Flow

The walls of the lateral ventricles contain the largest germinal region in the adult mammalian brain. The subventricular zone (SVZ) in these walls is an extensively studied model system for understanding the behavior of neural stem cells and the regulation of adult neurogenesis. Traditionally, these studies have relied on classical sectioning techniques for histological analysis. Here we present an alternative approach, the wholemount technique, which provides a comprehensive, en-face view of this germinal region. Compared to sections, wholemounts preserve the complete cytoarchitecture and cellular relationships within the SVZ. This approach has recently revealed that the adult neural stem cells, or type B1 cells, are part of a mixed neuroepithelium with differentiated ependymal cells lining the lateral ventricles. In addition, this approach has been used to study the planar polarization of ependymal cells and the cerebrospinal fluid flow they generate in the ventricle. With recent evidence that adult neural stem cells are a heterogeneous population that is regionally specified, the wholemount approach will likely be an essential tool for understanding the organization and parcellation of this stem cell niche.     

AC29: the most abundant protein of Alexandrium catenella and its potential use in encystment/excystment studies

The objective of this research was to characterize specific protein(s) from Alexandrium catenella to evaluate its use as markers for specific physiological functions. To identify such protein(s) we concentrated our efforts on characterizing proteins with a high level of expression in vegetative cells of A. catenella. The electrophoretic analysis of a total protein cell extract showed the presence of a very abundant 29 kDa protein that we have named AC29. Analysis by 2D SDS-PAGE shows that the 29 kDa band contains one abundant protein (AC29) and various less abundant polypeptides, suggesting the presence of either different proteins with similar molecular weight or isoforms of AC29 protein. Ultracytolocalization using antibodies raised against gel purified AC29 indicates that this protein localizes within the chloroplast and that it is associated with thylakoid membranes, as well as with other membranes surrounding the chloroplast. Western blot analysis of cells grown under light starvation shows that the expression of the AC29 protein is down regulated. A similar analysis shows that this protein is not expressed in natural cysts or by isolated intracellular bacterium. The amino terminus of the AC29 protein that was recovered from 2D SDS-PAGE was sequenced. The sequence shows homology to the peridinin-chlorophyll a-protein from the marine organisms Alexandrium cohorticula, Amphidinium carterae and Symbiodinium. Based on these results, we suggest that the AC29 protein has the potential of being used as a marker for A. catenella encystment and excystment processes.     

The role of polyamine architecture on the pharmacological activity of open lactone camptothecin-polyamine conjugates

A series of camptothecin open-ring lactone tripartate conjugates were synthesized, in which polyamine side chains with different architecture (ethane-1,2-diamine, spermidine, homospermidine, spermine, and 4,8,13,17-tetraza-icosane-1,20-diamine) are linked to the 21-carboxylic function through an amidic bond, while the 17-CH(2)OH is acetylated. The rationale for the synthesis of these compounds was to explore the influence of the polyamine architecture on the activity of these CPT conjugates into cells, since the positively charged ammonium cations would favor interaction through electrostatic binding to the negatively charged DNA backbone. Topoisomerase I-mediated DNA cleavage assay was used to investigate the ability of these compounds to stimulate the DNA damage. The cleavage pattern was found to be similar to that of SN38 for all the new CPTs. The CPT tripartates were tested for growth inhibition ability against the human non-small-cell lung cancer carcinoma NCI-H460 cell line. Although these compounds were less potent than topotecan, SN38, and CPT after 1 h of treatment, the antiproliferative effects greatly increased after 72 h of exposure. The growth inhibition potency during long-term exposure is correlated with the number of charges of the 21-amide substituent. Both cleavage assay and in vitro effects support the interpretation that the compounds may have inhibitory activity also in the open-ring form. The architecture of the polyamine moiety is important for antiproliferative activity, and a balance between the hydrophilic and lipophilic properties of the polyamine is critical for CPT potency.