Neutralization of IL-12 decreases resistance to Listeria in SCID and C.B-17 mice. Reversal by IFN-gamma

Interleukin-12 (IL-12) is necessary for the production of IFN-gamma by NK cells during the generation of innate immunity and by T cells for the development of the Th1 response during specific cell-mediated immunity. Here we demonstrate that the endogenous production of IL-12 is critical to the survival of both immunocompromised SCID mice and normal C.B-17 control mice during a primary infection with Listeria monocytogenes. When IL-12 is neutralized in vivo, both strains of mice die at a normally sublethal dose of Listeria. Anti-IL-12 antibody-treated mice showed a decrease in macrophage I-Ad expression and an increase Listeria burden in the spleen. Furthermore, as has been demonstrated in vitro, these effects of IL-12 in vivo were predominantly regulated through the production of IFN-gamma. Administration of IFN-gamma simultaneously with neutralizing antibodies to IL-12 restored macrophage I-Ad expression, limited the spread of the infection, and resulted in the survival of SCID mice. Thus, IL-12 is critical for resistance to infection with Listeria monocytogenes, and this resistance is mediated through stimulation by IL-12 of IFN-gamma production. Concomitant experiments confirmed that anti-TNF antibodies also resulted in uncontrolled infection and a decrease in macrophage I-Ad expression. However, administration of IFN-gamma restored the levels of I-Ad in macrophages but did not limit Listeria growth.     

Synthesis, FTIR studies and sensor properties of WO3 powders

Several synthetic approaches were used to obtain nano-sized porous and nonporous monoclinic WO₃ (m-WO₃) powders. All of these methods begin with a standard preparative method where H₂WO₄ is first generated by passing a Na₂WO₄ solution through a cation-exchange resin. It is shown that high surface area particles are produced by dripping the H₂WO₄ exiting from the ion-exchange column into a solution containing oxalate and acetate exchange ligands or alternatively, into a water-in-oil (W/O)-based emulsion. Porous materials are produced using surfactant-templating architectures. The surface properties were investigated by IR spectroscopic studies during thermal evacuation and the use of chemical probes. The nature of the surface depends on the initial evacuation temperature of the WO₃ surface as this alters the relative number of the Lewis and Brønsted acid sites along with the amount of adsorbed water. Infrared studies of the adsorption of various molecules on the powders led to a new size-selective approach to improve selectivity in semiconducting metal oxide (SMO) sensors. The key for achieving high selectivity is based on using a dual sensor configuration where the response on a porous WO₃ powder sensor was compared to the response on a nonporous WO₃ powder sensor. Detection selectivity between methanol and dimethyl methylphosphonate (DMMP) is obtained because the access of a gas molecule in the interior pore structure of WO₃ is size-dependent leading to a size-dependent magnitude change in the conductivity of the SMO sensor.     

Ultraviolet Light-Assisted Photocatalytic Disinfection of <Emphasis Type="Italic">Escherichia coli</Emphasis> and Its Effects on the Quality Attributes of White Grape Juice

Ultraviolet (UV) light-assisted titanium dioxide (TiO₂) photocatalysis is an emerging technology in food safety that utilizes TiO₂ photocatalysts to accelerate the generation of reactive oxygen species during UV illumination. In this work, we studied the use of immobilized TiO₂-SiO₂ photocatalysts illuminated with UVA radiation (350 nm; 14.8 mW/cm²) for the inactivation of Escherichia coli ATCC 25922 in white grape juice, and compared the effectiveness of the photocatalytic disinfection with respect to the quality attributes of white grape juice against those of thermal and UVC (254 nm; 19.7 mW/cm²) treated samples. To obtain a 5-log reduction of the target microorganism, treatment durations of UVA in the absence and presence of the photocatalyst were 60 and 40 min, respectively. A 5-log reduction with UVC radiation led to the loss of health-related compounds such as vitamin C, total phenolic content, and total antioxidant capacity at 92.0?±?1.1%, 19.4?±?5.6%, and 54.3?±?10.0%, respectively. However, the same level of reduction with UVA led to a loss of 74.2?±?2.3%, 7.1?±?3.6%, and 39.7?±?2.5%, and with UVA-assisted photocatalytic method resulted in a loss of 75.8?±?6.1%, 13.6?±?5.8%, and 45.6?±?4.4% of vitamin C, total phenolic content, and total anti-oxidant capacity, respectively. Given its efficacy in deactivating E. coli while retaining a relatively higher level of health-related constituents in the fruit juice compared to other common pasteurization techniques, the photocatalyst developed in this study provides a promising technology for food disinfection.     

Validation of procedures for quantitative whole-body autoradiography using digital imaging

The objective of this study was to demonstrate that tissue concentrations of radioactivity derived by digital analysis of autoradiograms were comparable to values derived from direct sampling and analysis of tissues. In addition, we describe the preparation and calibration of standards for use in quantitative whole-body autoradiography. For this study, three male Long-Evans hooded rats were administered 14C radioactivity intravenously. The animals were sectioned for whole-body autoradiography, with concomitant sampling of blood and 16 selected tissues. After 3 weeks of film exposure, the optical densities of the resulting autoradiograms were analyzed with a RAS3000 digital imaging system to estimate tissue concentrations of radioactivity. These concentrations were then compared with those obtained by direct analysis of the tissue samples. The concentrations derived from digital analysis of the autoradiograms were very highly correlated with those determined from direct tissue analysis (r = 0.956). Linear regression analysis yielded a straight line with a slope of 0.97 and a goodness of fit (r2) of 0.913. This analysis suggested that there is an approximate 1:1 correlation between concentration values determined by the two methods. Marked differences between the values derived via the two techniques were observed for only three tissues. However, this subset of the data accounted for only 6% of the total data, and the differences were probably due to contamination from adjacent tissues during excision. Overall, the concentrations of radioactivity derived from digital analysis of the autoradiograms were comparable to those derived from direct analysis of tissue samples. The results indicated that the digital analysis procedure for film can serve as a valuable adjunct to conventional tissue analysis for radioactivity.     

Implementation of a fault tolerant distributed control system

The design aspects of the implementation of a fault tolerant distributed control sytem are reviewed, including specific strategies for processor and input/output redundancy. Actual results of component and system reliability achieved through the fault tolerant design are discussed as well as the implications of these results for the user.     

Forced degradation of Fas inhibits apoptosis in adenovirus-infected cells

DNA viruses have evolved elaborate mechanisms to overcome host antiviral defences. In adenovirus-infected cells, programmed cell death (apoptosis) induced by the cytokine tumour necrosis factor (TNF) is inhibited by several adenovirus-encoded proteins. Occupation of the cell-surface receptor Fas, a member of the TNF-receptor superfamily that is expressed on most cell types, triggers apoptosis of that cell. Here we show that the adenovirus RID (for receptor internalization and degradation) protein complex, which is an inhibitor of TNF-induced apoptosis, mediates internalization of cell-surface Fas and its destruction inside lysosomes within the cell. Fas has not previously been shown to be internalized and then degraded. RID also mediates internalization of the receptor for epidermal growth factor, but it does not affect the transferrin receptor or class I antigens of the major histocompatibility complex. Removal of Fas from the surface of adenovirus-infected cells expressing RID may allow infected cells to resist Fas-mediated cell death and thus promote their survival.     

Physical and fine structure properties of cotton fibers swollen with trimethylbenzylammonium hydroxide

Cotton fiber was treated with aqueous trimethylbenzylammonium hydroxide (Triton B) at concentrations over the range 25%–40%. After complete removal of the swelling agent, the samples were evaluated for the extent of swelling, strength and elongation, birefringence, moisture regain, density, crystallinity, x-ray diffraction patterns, and microfibrillar morphology. Electron-microscopical examination and other evaluation of fine structure properties revealed that the nature of swelling is intercrystalline up to 30% concentration of Triton B, and intracrystalline beyond that. Although the swelling as measured by propanol-2 retention after treatment with 30% Triton B is about twice as much as that of the control, the original structure remains almost unchanged except for some gain in strength and elongation and increase in moisture regain. At 32% Triton B concentration and beyond, rapid decrystallization takes place, accompanied by a fall in birefringence, density, and crystallinity index. X-Ray analysis showed significant loss of lateral order and partial conversion of cellulose I to cellulose II at 35% and 40% Triton B concentrations. The results indicate that, used at the critical concentration of 30%, Triton B can be a useful swelling agent for cotton fibers as it opens up the fine structure of cellulose considerably without impairing any important physical properties.     

Determining subnanomolar iron concentrations in oceanic seawater using a siderophore-modified film analyzed by infrared spectroscopy

Iron is a bioactive trace element in seawater that regulates photosynthetic carbon dioxide drawdown and export from surface waters by phytoplankton in upward of 40% of the world's oceans. While autonomous sensor arrays are beginning to provide high-resolution data on temporal and spatial scales for some key oceanographic parameters, current analytical methods for iron are not amenable to autonomous platforms because of the need for user involvement and wet chemistry-based approaches. As a result, very large gaps remain in our understanding of iron distribution and chemistry in seawater. Here we present a straightforward nanostructure-based method to measure dissolved iron in natural seawater. The device comprises an iron-specific chelating biomolecule, desferrioxamine B (DFB), covalently immobilized on a mesoporous silica film. Changes in infrared spectral signatures of the immobilized DFB upon Fe(III) complexation provide an accurate and precise measure of iron on the surface of a chip exposed to seawater. The current system has a detection limit of approximately 50 pM for a 1-L sample at pH 1.7 and was used to measure dissolved iron in subarctic Pacific waters without interference from other elements in seawater. This technology provides a major step toward obtaining accurate iron measurements on autonomous research platforms.     

Generation and characterization of inorganic and organic nanotubes on bioengineered flagella of mesophilic bacteria

Three types of rationally designed peptide loops were genetically engineered for display on the surface of the FliTrx E. coil flagella scaffold, a type of bacterial bionanotube adapted for the multivalent display of peptide loops. The resulting three types of loop flagella fibers were used to demonstrate the feasibility of templating synthesis of inorganic nanotubes and nanoparticles and organic nanotubes. Purified flagella fibers displaying a cationic arginine-lysine loop peptide with three guanidine and three amine functional groups were used to form silica bionanotubes, using two types of silicate ion precursors. Purified flagella fibers displaying a tyrosine-serine-glycine loop peptide with six phenolic and three aliphatic hydroxyl groups were used to initiate formation of titania bionanotubes. Purified flagella fibers displaying an anionic aspartate-glutamate loop peptide with 18 carboxylate groups were used to initiate formation of polyaniline nanotubes and hydroxyapatite nanoparticles, a key component of bones. The resulting nanomaterials were mainly characterized by transmission electron microscopy and additionally by scanning electron microscopy, in the case of polyaniline nanotubes. The studies demonstrate the versatility of employing bioengineered flagella for the generation of a variety of nanoparticle arrays and nanotubes.