226 research outputs found
Tauberian Results for Densities with Gaussian Tails
We study a class of probability densities with very thin upper tails. These densities generate exponential families which are asymptotically normal. Furthermore the class is closed under convolution. In this paper we shall be concerned with Abelian and strong Tauberian theorems for moment generating functions and Laplace transforms with respect to these densities. We obtain a duality relation between this class of densities and the associated class of moment generating functions which is closely related to the duality relation for convex function
Densities with Gaussian Tails
Consider densities fi(t), for i = 1, ..., d, on the real line which have thin tails in the sense that, for each i, fi(t) ∼ γi(t)e−ψi(t), where γi behaves roughly like a constant and ψi is convex, C2, with ψ′ → ∞ and ψ″ > 0 and l/√ψ″ is self-neglecting. (The latter is an asymptotic variation condition.) Then the convolution is of the same form ft * ... *fd(t) ∼ γ(t)e − ψ(t) Formulae for γ, ψ are given in terms of the factor densities and involve the conjugate transform and infimal convolution of convexity theory. The derivations require embedding densities in exponential families and showing that the assumed form of the densities implies asymptotic normality of the exponential familie
Variability in disease phenotypes within a single PRNP genotype suggests the existence of multiple natural sheep scarpie strains within Europe
Variability of pathological phenotypes within classical sheep scrapie cases has been reported for some time, but in many instances it has been attributed to differences in the PRNP genotype of the host. To address this issue we have examined by immunohistochemistry (IHC) and Western blotting (WB) for the disease-associated form of the prion protein (PrPd), the brains of 23 sheep from five European countries, all of which were of the same ARQ/ARQ genotype. As a result of IHC examinations, sheep were distributed into five groups with different phenotypes and the groups were the same regardless of the scoring method used, ‘long’ or ‘short’ PrPd profiling. The groups made did not respond to the geographical origin of the cases and did not correlate with the vacuolar lesion profiles, which showed a high individual variability. Discriminatory IHC and WB methods coincided to detect a ‘CH1641-like’ case but otherwise correlated poorly in the classification of disease phenotypes. No other polymorphisms of the PRNP gene were found that could account for the pathological differences, except perhaps for a sheep from Spain with a mutation at codon 103 and a unique pathological phenotype. Preliminary evidence indicates that those different IHC phenotypes correlate with distinct biological properties on bioassay, suggesting that they are indicative of strain diversity. We therefore conclude that natural scrapie strains exist and that they can be revealed by detailed pathological examinations, which can be harmonized between laboratories to produce comparable results
Compellingly high SARS-CoV-2 susceptibility of Golden Syrian hamsters suggests multiple zoonotic infections of pet hamsters during the COVID-19 pandemic
Golden Syrian hamsters (Mesocricetus auratus) are used as a research model for severe acute respiratory syndrome coronavirus type 2 (SARS-CoV-2). Millions of Golden Syrian hamsters are also kept as pets in close contact to humans. To determine the minimum infective dose (MID) for assessing the zoonotic transmission risk, and to define the optimal infection dose for experimental studies, we orotracheally inoculated hamsters with SARS-CoV-2 doses from 1 * 105 to 1 * 10-4 tissue culture infectious dose 50 (TCID50). Body weight and virus shedding were monitored daily. 1 * 10-3 TCID50 was defined as the MID, and this was still sufficient to induce virus shedding at levels up to 102.75 TCID50/ml, equaling the estimated MID for humans. Virological and histological data revealed 1 * 102 TCID50 as the optimal dose for experimental infections. This compelling high susceptibility leading to productive infections in Golden Syrian hamsters must be considered as a potential source of SARS-CoV-2 infection for humans that come into close contact with pet hamsters
On the modelling of the excesses of galaxy clusters over high-mass thresholds
In this work we present for the first time an application of the Pareto
approach to the modelling of the excesses of galaxy clusters over high-mass
thresholds. The distribution of those excesses can be described by the
generalized Pareto distribution (GPD), which is closely related to the
generalized extreme value (GEV) distribution. After introducing the formalism,
we study the impact of different thresholds and redshift ranges on the
distributions, as well as the influence of the survey area on the mean excess
above a given mass threshold. We also show that both the GPD and the GEV
approach lead to identical results for rare, thus high-mass and high-redshift,
clusters. As an example, we apply the Pareto approach to ACT-CL J0102-4915 and
SPT-CL J2106-5844 and derive the respective cumulative distribution functions
of the exceedance over different mass thresholds. We also study the possibility
to use the GPD as a cosmological probe. Since in the maximum likelihood
estimation of the distribution parameters all the information from clusters
above the mass threshold is used, the GPD might offer an interesting
alternative to GEV-based methods that use only the maxima in patches. When
comparing the accuracy with which the parameters can be estimated, it turns out
that the patch-based modelling of maxima is superior to the Pareto approach. In
an ideal case, the GEV approach is capable to estimate the location parameter
with a percent level precision for less than 100 patches. This result makes the
GEV based approach potentially also interesting for cluster surveys with a
smaller area.Comment: 10 pages, 8 figures, MNRAS accepted, minor modifications to match the
accepted versio
Prion Infectivity and PrPBSE in the Peripheral and Central Nervous System of Cattle 8 Months Post Oral BSE Challenge
After oral exposure of cattle with classical bovine spongiform encephalopathy (C-BSE),
the infectious agent ascends from the gut to the central nervous system (CNS) primarily via the
autonomic nervous system. However, the timeline of this progression has thus far remained widely
undetermined. Previous studies were focused on later time points after oral exposure of animals
that were already 4 to 6 months old when challenged. In contrast, in this present study, we have
orally inoculated 4 to 6 weeks old unweaned calves with high doses of BSE to identify any possible
BSE infectivity and/or PrPBSE in peripheral nervous tissues during the first eight months postinoculation
(mpi). For the detection of BSE infectivity, we used a bovine PrP transgenic mouse
bioassay, while PrPBSE depositions were analyzed by immunohistochemistry (IHC) and by protein
misfolding cyclic amplification (PMCA). We were able to show that as early as 8 mpi the thoracic
spinal cord as well as the parasympathetic nodal ganglion of these animals contained PrPBSE and
BSE infectivity. This shows that the centripetal prion spread starts early after challenge at least in this
age group, which represents an essential piece of information for the risk assessments for food, feed,
and pharmaceutical products produced from young calves
De bediening van navigatie-ondersteuning voor blinden en slechtzienden - naar een generieke interface
Zelfstandige navigatie en oriëntatie voor blinden en slechtzienden kan worden ondersteund met hiervoor geëigende systemen. Bestaande systemen zijn echter vaak niet toegerust met een bruikbare interface. In het huidige onderzoek zijn drie interfaces voor een routegeleidingssysteem voor blinden en slechtzienden getest. Hoewel één variant een beter algemeen resultaat bood dan de twee anderen was het resultaat zodanig dat een integratie van de positieve aspecten van de verschillende interfacevarianten aan te bevelen is
EU-Approved Rapid Tests for Bovine Spongform Encephalopathy Detect Atypical Forms: A Study for Their Sensitivities
Since 2004 it become clear that atypical bovine spongiform encephalopthies (BSEs) exist in cattle. Whenever their detection has relied on active surveillance plans implemented in Europe since 2001 by rapid tests, the overall and inter-laboratory performance of these diagnostic systems in the detection of the atypical strains has not been studied thoroughly to date. To fill this gap, the present study reports on the analytical sensitivity of the EU-approved rapid tests for atypical L-and H-type and classical BSE in parallel. Each test was challenged with two dilution series, one created from a positive pool of the three BSE forms according to the EURL standard method of homogenate preparation (50% w/v) and the other as per the test kit manufacturer's instructions. Multilevel logistic models and simple logistic models with the rapid test as the only covariate were fitted for each BSE form analyzed as directed by the test manufacturer's dilution protocol. The same schemes, but excluding the BSE type, were then applied to compare test performance under the manufacturer's versus the water protocol. The IDEXX HerdChek (R) BSE-scrapie short protocol test showed the highest sensitivity for all BSE forms. The IDEXX (R) HerdChek BSE-scrapie ultra short protocol, the Prionics (R) - Check WESTERN and the AJ Roboscreen (R) BetaPrion tests showed similar sensitivities, followed by the Roche (R) PrionScreen, the Bio-Rad (R) TeSeE (TM) SAP and the Prionics (R) - Check PrioSTRIP in descending order of analytical sensitivity. Despite these differences, the limit of detection of all seven rapid tests against the different classes of material set within a 2 log(10) range of the best-performing test, thus meeting the European Food Safety Authority requirement for BSE surveillance purposes. These findings indicate that not many atypical cases would have been missed surveillance since 2001 which is important for further epidemiological interpretations of the sporadic character of atypical forms
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