22 research outputs found
Натечные карбонатные новообразования набережной реки Туры: особенности строения и процессы формирования
International audienc
Effectiveness of two trapping protocols for studying the demography of common voles
<strong>Efficacia di due metodi di trappolaggio per lo studio della demografia dell&rsquo;arvicola campestre.</strong><br /> Per valutare l'efficacia di due tipi di trappole, trappole &ldquo;killer&rdquo; e trappole &ldquo;a vivo&rdquo; tipo R&ouml;dl, sono stati confrontati i risultati della rimozione completa di una popolazione di arvicola campestre <em>Microtus arvalis</em> in merito a et&agrave;, sesso, status riproduttivo e peso degli individui trappolati tramite ciascun metodo. Le trappole R&ouml;dl hanno catturato, in media, animali di et&agrave; maggiore e pi&ugrave; femmine riproduttive, mentre non sono state rilevate differenze significative in termini sia di rapporto sessi sia di peso medio. I risultati ottenuti suggeriscono di utilizzare almeno due metodi di cattura e che il confronto dei parametri demografici di popolazioni differenti pu&ograve; essere considerato valido solo quando siano stati utilizzati gli stessi metodi di trappolaggio
Outcomes of robotic versus open partial nephrectomy: Results of a single institution series
Povidone iodine skin absorption: An ex-vivo study
Povidone iodine is a water-soluble complex used to disinfect the skin surface and it exerts prolonged germicidal action against a broad spectrum of germs. Indeed, it is often applied on burned skin, large wounds, deep tissues or mucosa. Notably some surgical hand-scrub solutions, which are considered safe antiseptics, contain large amounts of iodine that can be absorbed by skin. The aim of present study was to study the skin absorption of iodine after the application on the skin of povidone-iodine solution, used by health care workers during surgical procedure. We use Franz diffusion static cells with human skin. After 24h from the beginning of our measurement the iodine concentration in the receiving compartment was 11.59\ub16.3\u3bcg/cm(2). The medium flux calculated was 0.73\ub10.33\u3bcg/cm(2)/h with a lag time of 8.9\ub11.5h. These in vitro results confirmed that povidone iodine could pass through the skin in a relevant amount that can explain the clinical findings in burned or surgically treated patients. In professional use the repetitive contact with povidone iodine, also as soap, can cause iodine skin permeation that must be considered when the washing procedures are repeated more than 20 times a day
The Quality of DNA Isolated from Processed Food and Feed via Different Extraction Procedures
The extraction of DNA is a critical step for species identification by PCR analysis in processed food and feed products. In this study, eight DNA extraction procedures were compared—DNeasy Blood and Tissue Kit, DNeasy mericon Food Kit, chemagic DNA Tissue 10 Kit, Food DNA Isolation Kit, UltraPrep Genomic DNA Food Mini Prep Kit, High Pure PCR Template Preparation Kit, phenol—chloroform extraction, and NucleoSpin Food—Using self-prepared samples from both raw and heat-processed and/or mechanically treated muscles and different types of meat products and pet food (pork, beef, and chicken). The yield, purity, and suitability of DNA for PCR amplification was evaluated. Additionally, comparisons between the effectiveness of various extraction methods were made with regard to price, and labor- and time-intensiveness. It was found that the DNeasy mericon Food Kit was the optimal choice for the extraction of DNA from raw muscle, heat-treated muscle, and homemade meat products from multiple and single species.</jats:p
The Quality of DNA Isolated from Processed Food and Feed via Different Extraction Procedures
The extraction of DNA is a critical step for species identification by PCR analysis in processed food and feed products. In this study, eight DNA extraction procedures were compared—DNeasy Blood and Tissue Kit, DNeasy mericon Food Kit, chemagic DNA Tissue 10 Kit, Food DNA Isolation Kit, UltraPrep Genomic DNA Food Mini Prep Kit, High Pure PCR Template Preparation Kit, phenol—chloroform extraction, and NucleoSpin Food—Using self-prepared samples from both raw and heat-processed and/or mechanically treated muscles and different types of meat products and pet food (pork, beef, and chicken). The yield, purity, and suitability of DNA for PCR amplification was evaluated. Additionally, comparisons between the effectiveness of various extraction methods were made with regard to price, and labor- and time-intensiveness. It was found that the DNeasy mericon Food Kit was the optimal choice for the extraction of DNA from raw muscle, heat-treated muscle, and homemade meat products from multiple and single species
An integrated system of four multiplex qPCR assays for the precise and sensitive identification of animal species in food and feed
Brucellosis of the common vole (Microtus arvalis)
A systemic disease occurred in a wild population of the common vole Microtus arvalis in South Moravia (Czech Republic) during the years 1999-2003. Acute infections were characterized by edema of extremities, occasionally with colliquating abscesses, arthritis, lymphadenitis, perforations of the skin resulting from colliquated abscesses, orchitis, and peritoneal granulomas. From the clinical samples, small Gram-negative coccobacilli were isolated and identified as Ochrobactrum intermedium by API 20NE and colistin sensitivity profiles. However, subsequent rrs (16S rRNA) and recA (recombinase A) gene sequencing analysis of two isolates (CCM 4915 = CAPM 6434; CCM 4916 = CAPM 6435) identified them as Brucella sp. with sequence identities of 100% to other Brucella spp. Analysis of the omp2a/b genes confirmed the two isolates as Brucella. In AMOS polymerase chain reaction (PCR), a 2000-bp fragment was generated that was not seen in other brucellae. Experimental infection of outbred ICR mice with these isolates resulted in a mortality rate of 50%. Based on the results of the molecular investigations and the mortality observed in experimentally infected mice we conclude that the epizootic was caused by Brucella sp. and not by Ochrobactrum intermedium. The study demonstrates the limitations of commercial biochemical test systems in accurately differentiating among Ochrobactrum and Brucell
