187 research outputs found

    On the canonical divisor of smooth toroidal compactifications

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    In this paper, we show that the canonical divisor of a smooth toroidal compactification of a complex hyperbolic manifold must be nef if the dimension is greater or equal to three. Moreover, if n3n\geq 3 we show that the numerical dimension of the canonical divisor of a smooth nn-dimensional compactification is always bigger or equal to n1n-1. We also show that up to a finite \'etale cover all such compactifications have ample canonical class, therefore refining a classical theorem of Mumford and Tai. Finally, we improve in all dimensions n3n\geq 3 the cusp count for finite volume complex hyperbolic manifolds given in [DD15a].Comment: Title shortened to match published versio

    Exceptional collections and the bicanonical map of Keum's fake projective planes

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    On Seshadri constants of varieties with large fundamental group

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    Let XX be a smooth variety and let LL be an ample line bundle on XX. If π1alg(X)\pi^{alg}_{1}(X) is large, we show that the Seshadri constant ϵ(pL)\epsilon(p^{*}L) can be made arbitrarily large by passing to a finite \'etale cover p:XXp:X'\rightarrow X. This result answers affirmatively a conjecture of J.-M. Hwang. Moreover, we prove an analogous result when π1(X)\pi_{1}(X) is large and residually finite. Finally, under the same topological assumptions, we appropriately generalize these results to the case of big and nef line bundles. More precisely, given a big and nef line bundle LL on XX and a positive number N>0N>0, we show that there exists a finite \'etale cover p:XXp: X'\rightarrow X such that the Seshadri constant ϵ(pL;x)N\epsilon(p^{*}L; x)\geq N for any xpB+(L)=B+(pL)x\notin p^{*}\textbf{B}_{+}(L)=\textbf{B}_{+}(p^{*}L), where B+(L)\textbf{B}_{+}(L) is the augmented base locus of LL

    Production of probiotic bovine salami using Lactobacillus plantarum 299v as adjunct

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    BACKGROUND: Five probiotic lactobacilli were tested, alone or in combination with two commercial starters, to select the most suitable strain for a probiotic bovine salami production. Lactobacillus plantarum 299v was used with both starters, to make salami according to a traditional recipe. Salami obtained by using just the starters and by spontaneous fermentation, served as control. Microbial dynamics, as well as the main physico-chemical parameters, were monitored throughout ripening. The survival of probiotic 299v was confirmed by strains' tracking by means of RAPD-PCR coupled to a culture-independent approach PCR-DGGE-based. RESULTS: The results showed a remarkable viability of the probiotic strain even after 60 days of storage. Experimental salami exhibited the same level of sensory acceptance of control salami, were hygienically safe, and characterised by pH, weight loss and microbiological loads within the ranges conventionally advocated for optimal fermented sausages. CONCLUSION: Outcomes indicate the workable possibility of using second-quality beef cuts for probiotic salami production. © 2017 Society of Chemical Industry

    Giardia duodenalis assemblages and Entamoeba species infecting non-human primates in an Italian zoological garden: zoonotic potential and management traits

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    <p>Abstract</p> <p>Background</p> <p><it>Giardia duodenalis </it>and <it>Entamoeba </it>spp. are among the most common intestinal human protozoan parasites worldwide and they are frequently reported in captive non-human primates (NHP). From a public health point of view, infected animals in zoos constitute a risk for animal caretakers and visitors. In this study we carried out the molecular identification of <it>G. duodenalis </it>and <it>Entamoeba </it>spp. from nine species of primates housed in the zoological garden of Rome, to better ascertain their occurrence and zoonotic potential.</p> <p>Results</p> <p><it>G. duodenalis </it>was found only in <it>Lemur catta </it>(47.0%). <it>Entamoeba </it>spp. were detected in all species studied, with the exception of <it>Eulemur macaco </it>and <it>Varecia rubra</it>. The number of positive pools ranged from 5.9% in <it>L. catta </it>to 81.2% in <it>Mandrillus sphinx; </it>in <it>Pan troglodytes </it>the observed prevalence was 53.6%. A mixed <it>Entamoeba</it>-<it>Giardia </it>infection was recorded only in one sample of <it>L. catta</it>. All <it>G. duodenalis </it>isolates belonged to the zoonotic assemblage B, sub assemblage BIV. Three <it>Entamoeba </it>species were identified: <it>E. hartmanni</it>, <it>E. coli </it>and <it>E. dispar</it>.</p> <p>Conclusions</p> <p>Our results highlight the importance of regularly testing animals kept in zoos for the diagnosis of zoonotic parasites, in order to evaluate their pathogenic role in the housed animals and the zoonotic risk linked to their presence. A quick detection of the arrival of pathogens into the enclosures could also be a prerequisite to limit their spread into the structure via the introduction of specific control strategies. The need for molecular identification of some parasite species/genotype in order to better define the zoonotic risk is also highlighted.</p

    Effect of chicken bone extracts on metabolic and mitochondrial functions of K562 cell line

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    Background: Tetracyclines’ use in intensive animal farming has raised some concerns regarding the biosafety for humans. Increasing evidences have revealed the presence of these drugs in processed animal by-products, such as bone, throughout the food chain. A potential off-target of tetracyclines is the bacterial-like mitochondrial translational machinery, thereby causing proteostatic alterations in mitochondrial DNA-encoded components of the oxidative phosphorylation system. Methods: The Seahorse methodology, confocal microscopy imaging of mitochondrial potential and reactive oxygen species, and q-RT-PCR analysis of the expression of genes involved in mitochondrial biogenesis and mitophagy were carried out on human lymphoblast derived K562 cell line challenged with bone powder derived from chicken treated with or without oxytetracycline and pure oxytetracycline. Results: A complex dose-dependent profile was attained with a low dosage of bone powder extracts causing a metabolic adaptation hallmarked by stimulation of the mitochondrial respiration and enhanced expression of mitochondriogenic factors in particular in cells challenged with oxytetracycline-free bone extract. Conversely, a higher dosage of bone powder extracts, regardless of their source, caused a progressive inhibition of mitochondrial respiration and glycolysis, ultimately leading to cell death. No significant effects of the pure oxytetracycline were observed. Conclusion: Bone powder, regardless of chicken treatment, contains and releases factors/chemicals responsible for the observed effects on energy metabolism. Quantitative differential effects appear to depend on biochemical alterations in the bone matrix caused by antibiotics rather than antibiotics themselves

    Understanding the Pathogenesis of Red Mark Syndrome in Rainbow Trout (Oncorhynchus mykiss) through an Integrated Morphological and Molecular Approach

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    Red mark syndrome (RMS) is a widespread skin disorder of rainbow trout in freshwater aquaculture, believed to be caused by a Midichloria-like organism (MLO). Here, we aimed to study the pathologic mechanisms at the origin of RMS by analyzing field samples from a recent outbreak through gene expression, MLO PCR, quantitative PCR, and a histopathological scoring system proposed for RMS lesions. Statistical analyses included a One-Way Analysis of Variance (ANOVA) with a Dunnett’s multiple comparisons test to assess differences among gene expression groups and a nonparametric Spearman correlation between various categories of skin lesions and PCR results. In short, the results confirmed the presence of a high quantity of 16S gene copy numbers of Midichloria-like organisms in diseased skin tissues. However, the number of Midichloria-like organisms detected was not correlated to the degree of severity of skin disease. Midichloria-like organism DNA was found in the spleen and head kidney. The spleen showed pathologic changes mainly of hyperplastic type, reflecting its direct involvement during infection. The most severe skin lesions were characterized by a high level of inflammatory cytokines sustaining and modulating the severe inflammatory process. IL-1 β, IL-6, IL-10, MHC-II, and TCR were upregulated in severe skin lesions, while IL-10 was highly expressed in moderate to severe ones. In the moderate form, the response was driven to produce immunoglobulins, which appeared crucial in controlling the skin disease’s severity. Altogether our results illustrated a complex immune interaction between the host and Midichloria-like organism

    Zoledronic acid induces a significant decrease of circulating endothelial cells and circulating endothelial precursor cells in the early prostate cancer neoadjuvant setting

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    Purpose: Published data demonstrated that zoledronic acid (ZOL) exhibits antiangiogenetic effects. A promising tool for monitoring antiangiogenic therapies is the measurement of circulating endothelial cells (CECs) and circulating endothelial precursor cells (CEPs) in the peripheral blood of patients. Our aim was to investigate the effects of ZOL on levels of CECs and CEPs in localized prostate cancer. Methods: Ten consecutive patients with a histologic diagnosis of low-risk prostate adenocarcinoma were enrolled and received an intravenous infusion of ZOL at baseline (T0), 28 days (T28) and 56 days (T56). Blood samples were collected at the following times: T0 (before the first infusion of ZOL), T3 (72 h after the first dose), T28, T56 (both just before the ZOL infusion) and T84 (28 days after the last infusion of ZOL) and CEC/CEP levels were directly quantified by flow cytometry at all these time points. Results: Our analyses highlighted a significant reduction of mean percentage of CECs and CEPs after initiation of ZOL treatment [p = 0.014 (at day 3) and p = 0.012 (at day 84), respectively]. Conclusion: These preliminary results demonstrate that ZOL could exert an antiangiogenic effect in early prostate cancer through CEP and CEC modulation
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