A farm-level study of risk factors associated with the colonization of broiler flocks with <Emphasis Type="Italic">Campylobacter</Emphasis> spp. in Iceland, 2001 – 2004

Background  

Following increased rates of human campylobacteriosis in the late 1990's, and their apparent association with increased consumption of fresh chicken meat, a longitudinal study was conducted in Iceland to identify the means to decrease the frequency of broiler flock colonization with Campylobacter. Our objective in this study was to identify risk factors for flock colonization acting at the broiler farm level.     

Purification of glycogen debranching enzyme from rabbit muscle using omega-aminoalkyl agarose chromatography

Rabbit muscle glycogen debranching enzyme binds to all of a homologous series of ω-aminoalkyl agaroses. The debrancher can be eluted from ω-aminoethyl and ω-aminobutyl agarose with 0.5 m NaCl, and it desorbs more readily and elutes sooner from ω-aminoethyl agarose than from ω-aminobutyl agarose. No activity is eluted from ω-aminohexyl, octyl, or decyl agaroses. An improved purification procedure has been developed which includes chromatography on ω-aminoethyl agarose. This procedure enables the isolation of over 90% yield of the debranching enzyme from muscle within 3 days.     

Production and utilization of growth factors related to fibroblast growth factor by embryonal carcinoma cells and their differentiated cells

Previous studies have established that embryonal carcinoma (EC) cells produce several different growth factors, but express few, if any, receptors for epidermal growth factor, platelet-derived growth factor, or transforming growth factor type-beta. In this study, the production and utilization of fibroblast growth factor (FGF) by EC cells and their differentiated cells were investigated. We have determined that EC cells produce a heat-labile, heparin-binding factor that competes with FGF for binding to membrane receptors and appears to be immunologically related to FGF. The same or a similar factor is produced by three different EC cell lines, including a multipotent human EC cell line. However, production of this factor is apparently reduced when each EC cell line differentiates. Unlike the parental EC cells, the differentiated cells respond to FGF by growth stimulation and the growth responses to FGF correlate with increased binding of FGF. Although the binding data indicate that both the EC cells and their differentiated cells exhibit high affinity receptors for FGF, the differentiated cells express these receptors at levels approximately 10-fold higher. These findings suggest that the FGF-related growth factor could influence the growth of EC cells or their differentiated cells.     

Radiographic estimation of long bone cross-sectional geometric properties

Because of their biomechanical significance, cross-sectional geometric properties of long bone diaphyses (areas, second moments of area) have been increasingly used in a number of form/function studies, e.g., to reconstruct body mass or locomotor mode in fossil primates or to elucidate allometric scaling relationships among extant taxa. In the present study, we test whether these biomechanical section properties can be adequately estimated using biplanar radiographs, as compared to calculations of the same properties from computer digitization of cross-sectional images. We are particularly interested in smaller animals, since the limb bone cortices of these animals may not be resolvable using other alternative noninvasive techniques (computed tomography). The test sample includes limb bones of small (25–5,000 g) relatively generalized quadrupedal mammals—mice, six species of squirrels, and Macaca fascicularis. Results indicate that biplanar radiographs are reasonable substitutes for digitized cross-sectional images for deriving areas and second moments of area of midshaft femora and humeri of mammals in this size range. Potential application to a variety of questions relating to mechanical loading patterns in such animals is diverse. © 1993 Wiley-Liss, Inc.     

Characterization of TsaR, an Oxygen-Sensitive LysR-Type Regulator for the Degradation of p-Toluenesulfonate in Comamonas testosteroni T-2

TsaR is the putative LysR-type regulator of the tsa operon (tsaMBCD) which encodes the first steps in the degradation of p-toluenesulfonate (TSA) in Comamonas testosteroni T-2. Transposon mutagenesis was used to knock out tsaR. The resulting mutant lacked the ability to grow with TSA and p-toluenecarboxylate (TCA). Reintroduction of tsaR in trans on an expression vector reconstituted growth with TSA and TCA. The tsaR gene was cloned into Escherichia coli with a C-terminal His tag and overexpressed as TsaR^His. TsaR^His was subject to reversible inactivation by oxygen, which markedly influenced the experimental approaches used. Gel filtration showed TsaR^His to be a monomer in solution. Overexpressed TsaR^His bound specifically to three regions within the promoter between the divergently transcribed tsaR and tsaMBCD. The dissociation constant (K_D) for the whole promoter region was about 0.9 μM, and the interaction was a function of the concentration of the ligand TSA. A regulatory model for this LysR-type regulator is proposed on the basis of these data.