1,779 research outputs found
Molecular approaches to diagnosing and managing infectious diseases: practicality and costs.
As molecular techniques for identifying and detecting microorganisms in the clinical microbiology laboratory have become routine, questions about the cost of these techniques and their contribution to patient care need to be addressed. Molecular diagnosis is most appropriate for infectious agents that are difficult to detect, identify, or test for susceptibility in a timely fashion with conventional methods
Sub-gap spectroscopy of thermally excited quasiparticles in a Nb contacted carbon nanotube quantum dot
We present electronic transport measurements of a single wall carbon nanotube
quantum dot coupled to Nb superconducting contacts. For temperatures comparable
to the superconducting gap peculiar transport features are observed inside the
Coulomb blockade and superconducting energy gap regions. The observed
temperature dependence can be explained in terms of sequential tunneling
processes involving thermally excited quasiparticles. In particular, these new
channels give rise to two unusual conductance peaks at zero bias in the
vicinity of the charge degeneracy point and allow to determine the degeneracy
of the ground states involved in transport. The measurements are in good
agreement with model calculations.Comment: 5 pages, 4 figure
Amino acid incorporation into mitochondrial ribosomes of Neurospora crassa wild-type and Mi-1 mutant
A homogenized constrained mixture model of cardiac growth and remodeling: Analyzing mechanobiological stability and reversal
Cardiac growth and remodeling (G&R) patterns change ventricular size, shape,
and function both globally and locally. Biomechanical, neurohormonal, and
genetic stimuli drive these patterns through changes in myocyte dimension and
fibrosis. We propose a novel microstructure-motivated model that predicts
organ-scale G&R in the heart based on the homogenized constrained mixture
theory. Previous models, based on the kinematic growth theory, reproduced
consequences of G&R in bulk myocardial tissue by prescribing the direction and
extent of growth but neglected underlying cellular mechanisms. In our model,
the direction and extent of G&R emerge naturally from intra- and extra cellular
turnover processes in myocardial tissue constituents and their preferred
homeostatic stretch state. We additionally propose a method to obtain a
mechanobiologically equilibrated reference configuration. We test our model on
an idealized 3D left ventricular geometry and demonstrate that our model aims
to maintain tensional homeostasis in hypertension conditions. In a stability
map, we identify regions of stable and unstable G&R from an identical parameter
set with varying systolic pressures and growth factors. Furthermore, we show
the extent of G&R reversal after returning the systolic pressure to baseline
following stage 1 and 2 hypertension. A realistic model of organ-scale cardiac
G&R has the potential to identify patients at risk of heart failure, enable
personalized cardiac therapies, and facilitate the optimal design of medical
devices
Automatic Mapping of Atrial Fiber Orientations for Patient-Specific Modeling of Cardiac Electromechanics using Image-Registration
Knowledge of appropriate local fiber architecture is necessary to simulate
patient-specific electromechanics in the human heart. However, it is not yet
possible to reliably measure in-vivo fiber directions, especially in human
atria. Thus, we present a method which defines the fiber architecture in
arbitrarily shaped atria using image registration and reorientation methods
based on atlas atria with fibers predefined from detailed histological
observations. Thereby, it is possible to generate detailed fiber families in
every new patient-specific geometry in an automated, time-efficient process. We
demonstrate the good performance of the image registration and fiber definition
on ten differently shaped human atria. Additionally, we show that
characteristics of the electrophysiological activation pattern which appear in
the atlas atria also appear in the patients' atria. We arrive at analogous
conclusions for coupled electro-mechano-hemodynamical computations
Biogenesis of mitochondrial porin
We review here the present knowledge about the pathway of import and assembly of porin into mitochondria and compare it to those of other mitochondrial proteins. Porin, like all outer mitochondrial membrane proteins studied so far is made as a precursor without a cleavble lsquosignalrsquo sequence; thus targeting information must reside in the mature sequence. At least part of this information appears to be located at the amino-terminal end of the molecule. Transport into mitochondria can occur post-translationally. In a first step, the porin precursor is specifically recognized on the mitochondrial surface by a protease sensitive receptor. In a second step, porin precursor inserts partially into the outer membrane. This step is mediated by a component of the import machinery common to the import pathways of precursor proteins destined for other mitochondrial subcompartments. Finally, porin is assembled to produce the functional oligomeric form of an integral membrane protein wich is characterized by its extreme protease resistance
The role of Isocitrate Lyase (ICL1) in the metabolic adaptation of Candida albicans biofilms
Background
A major characteristic of Candida biofilm cells that differentiates them from free-floating cells is their high tolerance to antifungal drugs. This high resistance is attributed to particular biofilm properties, including the accumulation of extrapolymeric substances, morphogenetic switching, and metabolic flexibility.
Objectives
This study evaluated the roles of metabolic processes (in particular the glyoxylate cycle) on biofilm formation, antifungal drug resistance, morphology, and cell wall components.
Methods
Growth, adhesion, biofilm formation, and cell wall carbohydrate composition were quantified for isogenic Candida albicans ICL1/ICL1, ICL1/icl1, and icl1/icl1 strains. The morphology and topography of these strains were compared by light microscopy and scanning electron microscopy. FKS1 (glucan synthase), ERG11 (14-α-demethylase), and CDR2 (efflux pump) mRNA levels were quantified using qRT-PCR.
Results
The ICL1/icl1 and icl1/icl1 strains formed similar biofilms and exhibited analogous drug-tolerance levels to the control ICL1/ICL1 strains. Furthermore, the drug sequestration ability of β-1, 3-glucan, a major carbohydrate component of the extracellular matrix, was not impaired. However, the inactivation of ICL1 did impair morphogenesis. ICL1 deletion also had a considerable effect on the expression of the FKS1, ERG11, and CDR2 genes. FKS1 and ERG11 were upregulated in ICL1/icl1 and icl1/icl1 cells throughout the biofilm developmental stages, and CDR2 was upregulated at the early phase. However, their expression was downregulated compared to the control ICL1/ICL1 strain.
Conclusions
We conclude that the glyoxylate cycle is not a specific determinant of biofilm drug resistance
Mitochondrial precursor proteins are imported through a hydrophilic membrane environment
We have analyzed how translocation intermediates of imported mitochondrial precursor proteins, which span contact sites, interact with the mitochondrial membranes. F1-ATPase subunit β(F1β) was trapped at contact sites by importing it into Neurospora mitochondria in the presence of low levels of nucleoside triphosphates. This F1β translocation intermediate could be extracted from the membranes by treatment with protein denaturants such as alkaline pH or urea. By performing import at low temperatures, the ADP/ATP carrier was accumulated in contact sites of Neurospora mitochondria and cytochrome b2 in contact sites of yeast mitochondria. These translocation intermediates were also extractable from the membranes at alkaline pH. Thus, translocation of precursor proteins across mitochondrial membranes seems to occur through an environment which is accessible to aqueous perturbants. We propose that proteinaceous structures are essential components of a translocation apparatus present in contact sites
Statistical analyses of correlation between fluconazole MICs for Candida spp. assessed by standard methods set forth by the European Committee on Antimicrobial Susceptibility Testing (E.Dis. 7.1) and CLSI (M27-A2).
The European Committee on Antimicrobial Susceptibility Testing (EUCAST) Subcommittee on Antifungal
Susceptibility Testing recently published a standard for determining the susceptibility of fermentative yeasts
to antifungals. From the beginning, the EUCAST and its North American counterpart, the CLSI, decided to
work together in order to establish common standards. As part of this exercise, the susceptibility of a set of 475
yeast isolates was tested by both standards. The intraclass correlation coefficient and the equations defining
the linear regression between both methods were estimated. Both methods produced very similar results, with
an intraclass correlation coefficient of 0.954 (0.945 to 0.962), although linear regression analysis shows that the
EUCAST standard resulted in slightly lower MICs. There were only eight isolates showing at least four twofold
dilution MIC differences between both standards. After 24 h of incubation, the MICs obtained by the CLSI
method were equivalent to those obtained by the EUCAST standard. In summary, both methods produce very
similar MICs, indicating that methodology does not pose any obstacle to obtaining uniform standards for
antifungal susceptibility testing of yeast
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