Microstructure and mineral composition of dystrophic calcification associated with the idiopathic inflammatory myopathies

Introduction  

Calcified deposits (CDs) in skin and muscles are common in juvenile dermatomyositis (DM), and less frequent in adult DM. Limited information exists about the microstructure and composition of these deposits, and no information is available on their elemental composition and contents, mineral density (MD) and stiffness. We determined the microstructure, chemical composition, MD and stiffness of CDs obtained from DM patients.     

Epigenetic Segregation of Microbial Genomes from Complex Samples Using Restriction Endonucleases HpaII and McrB

We describe continuing work to develop restriction endonucleases as tools to enrich targeted genomes of interest from diverse populations. Two approaches were developed in parallel to segregate genomic DNA based on cytosine methylation. First, the methyl-sensitive endonuclease HpaII was used to bind non-CG methylated DNA. Second, a truncated fragment of McrB was used to bind CpG methylated DNA. Enrichment levels of microbial genomes can exceed 100-fold with HpaII allowing improved genomic detection and coverage of otherwise trace microbial genomes from sputum. Additionally, we observe interesting enrichment results that correlate with the methylation states not only of bacteria, but of fungi, viruses, a protist and plants. The methods presented here offer promise for testing biological samples for pathogens and global analysis of population methylomes.     

Comparative studies on the determination of the A-hel blood group factor in the pig by use of various lectins]

Comparable investigations of the A-hel-receptor with Anti-AHP and 6 different phytagglutinins are reported which have been tested in 305 samples of pig blood. Anti-ADb disposing of a higher specificity is recommended for determining the Hel-factor in pigs instead of Anti-AHP.     

Ecological Restoration Treatments Increase Butterfly Richness and Abundance: Mechanisms of Response

Few ecosystem restoration studies evaluate whether arthropods are important components of ecosystem recovery. We tested the hypothesis that ponderosa pine restoration treatments would increase adult butterfly species richness and abundance as a direct result of increased understory diversity and abundance. To examine mechanisms that potentially affect adult butterfly distribution, we quantified host plant frequency, nectar plant abundance, and insolation (light intensity) in restoration treatment and control forests. This study is unique, because this is the first invertebrate monitoring in ponderosa pine forest restoration treatments in the U.S. Southwest and also because these treatments are the first replicated ponderosa pine restoration treatments at a landscape scale. Three patterns emerged: (1) butterfly species richness and abundance were 2 and 3 times greater, respectively, in restoration treatment units than in paired control forests 1 year after treatment, and 1.5 and 3.5 times greater, respectively, 2 years after treatment, ordination of control and treatment sampling units using butterfly assemblages showed significant separation of control and restoration treatment units after restoration treatment; (2) host plant and nectar plant species richness showed little difference between treated and control forests even 2 years after treatment; and (3) insolation (light intensity) was significantly greater in treated forests after restoration. We suggest that changes in the butterfly assemblage may occur due to light intensity effects before plant community changes occur or can be detected. Butterfly assemblage differences will have additional cascading effects on the ecosystem as prey for higher trophic levels and through plant interactions including herbivory and pollination.     

A home-made solid-phase sequencer operating at the nanomole level

The bulding and functioning of a fully automated solid-phase sequencer is described. The peptide is coupled via its -carbonyl end to activated glass beads and successively reacted with Chang's and Edman's reagents. All operations are electronically controlled by the automated programmer. All components necessary to build the machine are commercially available. This sequencer has been used at a nanomole level in the final phase of a protein sequence determination. The overall cost as well as the sensitivity and efficiency of the final product compare favourably to those of commercial machines.