215 research outputs found

    Emotionalization in the Media Coverage of Honey Bee Colony Losses

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    Emotionalization is increasingly used in the daily news. However, communication scholars have only just begun to explore how journalists use emotionalization in coverage of scientific and environmental topics. This study contributes to filling this research gap by investigating emotionalization in reporting on honey bee colony losses. The aim of the study is to analyze the amount of emotionalization that took place, as well as to observe changes over time. Emotionalization is assessed in two ways; by analyzing to what extent journalists (1) explicitly mentioned discrete emotions in news stories (joy, hope, fear, anger, etc.) and/or (2) used rhetorical devices to evoke emotions (affective vocabulary, metaphors, colloquial language, superlatives, etc.). Results from a quantitative content analysis of four Austrian newspapers in 2010/2011, 2013/2014, and 2017/2018 show that the coverage is highly emotionalized across all three time periods studied. Emotionalization occurs far more often by using rhetorical devices than by explicitly mentioning positive or negative emotions. Interestingly, the incorporation of emotional elements and scientific expertise in the news items do not exclude one another. Hence, there seems to be no strict dichotomy between rational/objective and emotional reporting

    The use of vancomycin-loaded poly-l-lactic acid and poly-ethylene oxide microspheres for bone repair: an in vivo study

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    OBJECTIVE: The aim of this study was to investigate bone repair after the implantation of vancomycin-loaded poly-L-lactic acid/poly-ethylene oxide microspheres compared with vancomycin-unloaded poly-L-lactic acid/poly-ethylene oxide microspheres. METHODS: Poly-L-lactic acid/poly-ethylene oxide microspheres were implanted in rat tibiae and evaluated for periods of 2, 4, 8, and 12 days and 4, 8, 16, and 32 weeks. The groups implanted with vancomycin-loaded and vancomycin-unloaded microspheres were compared. Histopathologic (semi-quantitative) and histomorphometric analyses were performed to evaluate the bone formation process. RESULTS: During the first period (second day), fibrin and hemorrhaging areas were observed to be replaced by granulation tissue around the microspheres. Woven bone formation with progressive maturation was observed. All of the histopathological findings, evaluated by a semi-quantitative assay and a quantitative analysis (percentage of bone formation), were similar between the two groups. CONCLUSION: Vancomycin-loaded poly-L-lactic acid/poly-ethylene oxide microspheres are a good bone substitute candidate for bone repair. Local antibiotic therapy using vancomycin-loaded poly-L-lactic acid/poly-ethylene oxide microspheres should be considered after the microbiological evaluation of its efficacy

    A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis

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    Epidermolytic hyperkeratosis (EHK) is a blistering skin disease inherited as an autosomal-dominant trait. The disease is caused by genetic defects of the epidermal keratin K1 or K10, leading to an impaired tonofilament network of differentiating epidermal cells. Here, we describe for the first time a kindred with recessive inheritance of EHK. Sequence analysis revealed a homozygous nonsense mutation of the KRT10 gene in the affected family members, leading to a premature termination codon (p.Q434X), whereas the clinically unaffected consanguineous parents were both heterozygous carriers of the mutation. Semi-quantitative RT-PCR and western blot analysis demonstrated degradation of the KRT10 transcript, resulting in complete absence of keratin K10 protein in the epidermis and cultured keratinocytes of homozygous patients. This K10 null mutation leads to a severe phenotype, clinically resembling autosomal-dominant EHK, but differing in form and distribution of keratin aggregates on ultrastructural analysis. Strong induction of the wound-healing keratins K6, K16 and K17 was found in the suprabasal epidermis, which are not able to compensate for the lack of keratin 10. We demonstrate that a recessive mutation in KRT10 leading to a complete human K10 knockout can cause EHK. Identification of the heterogeneity of this disorder has a major impact for the accurate genetic counseling of patients and their families and also has implications for gene-therapy approache

    LA SEGURIDAD ALIMENTARIA EN NIÑOS DEL BARRIO SANTA ROSA DEL DISTRITO DE CHACHAPOYAS EN TIEMPOS DE LA COVID 19 – 2020

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    El estudio tuvo como objetivo determinar el proceso de la alimentación en niños del barrio Santa Rosa del distrito de Chachapoyas durante la Covid 19 en el año 2020. La investigación fue de nivel descriptivo, de enfoque cualitativo fenomenológico cuya categoría es hermenéutica, la muestra estuvo constituida por 10 familias, las cuales fueron seleccionadas por muestreo no probabilístico por conveniencia. El instrumento utilizado para la recolección de información constó de cuatro preguntas abiertas. Los resultados muestran que del 100% de familias encuestadas, el 70% experimentaron una disminución del acceso hacia alimentos, mientras que un 30% no manifestaron haber tenido inconvenientes para acceder a los alimentos, un 80% experimentó cambios en la disponibilidad de alimentos. De acuerdo a la información obtenida se afirma que todas las familias antes de dar utilidad a los alimentos mantuvieron medidas de higiene adecuadas con los insumos que estaban a su alcance; un 70% de las familias afirmaron que las autoridades si tuvieron control sobre los alimentos, por lo que dificulto su distribución. Se concluye que, la mayoría de las familias pertenecientes al asentamiento humano Santa Rosa del distrito de Chachapoyas presentaron disminución en la seguridad alimentaria para con sus menores hijos

    Leptospira spp. strain identification by MALDI TOF MS is an equivalent tool to 16S rRNA gene sequencing and multi locus sequence typing (MLST)

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    Background: In this study mass spectrometry was used for evaluating extracted leptospiral protein samples and results were compared with molecular typing methods. For this, an extraction protocol for Leptospira spp. was independently established in two separate laboratories. Reference spectra were created with 28 leptospiral strains, including pathogenic, non-pathogenic and intermediate strains. This set of spectra was then evaluated on the basis of measurements with well-defined, cultured leptospiral strains and with 16 field isolates of veterinary or human origin. To verify discriminating peaks for the applied pathogenic strains, statistical analysis of the protein spectra was performed using the software tool ClinProTools. In addition, a dendrogram of the reference spectra was compared with phylogenetic trees of the 16S rRNA gene sequences and multi locus sequence typing (MLST) analysis. Results: Defined and reproducible protein spectra using MALDI-TOF MS were obtained for all leptospiral strains. Evaluation of the newly-built reference spectra database allowed reproducible identification at the species level for the defined leptospiral strains and the field isolates. Statistical analysis of three pathogenic genomospecies revealed peak differences at the species level and for certain serovars analyzed in this study. Specific peak patterns were reproducibly detected for the serovars Tarassovi, Saxkoebing, Pomona, Copenhageni, Australis, Icterohaemorrhagiae and Grippotyphosa. Analysis of the dendrograms of the MLST data, the 16S rRNA sequencing, and the MALDI-TOF MS reference spectra showed comparable clustering. Conclusions: MALDI-TOF MS analysis is a fast and reliable method for species identification, although Leptospira organisms need to be produced in a time-consuming culture process. All leptospiral strains were identified, at least at the species level, using our described extraction protocol. Statistical analysis of the three genomospecies L. borgpetersenii, L. interrogans and L. kirschneri revealed distinctive, reproducible differentiating peaks for seven leptospiral strains which represent seven serovars. Results obtained by MALDI-TOF MS were confirmed by MLST and 16S rRNA gene sequencing
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