47 research outputs found

    Nowhere to go: How stigma limits the options of female drug users after release from jail

    Get PDF
    <p>Abstract</p> <p>Background</p> <p>Drug and alcohol using women leaving prison or jail face many challenges to successful re-integration in the community and are severely hampered in their efforts by the stigma of drug or alcohol use compounded by the stigma of incarceration.</p> <p>Methods</p> <p>This qualitative study is based on individual semi-structured interviews and focus groups with 17 women who had recently left jail about the challenges they faced on reentry.</p> <p>Results</p> <p>Our analysis identified three major themes, which are related by the overarching influence of stigma: survival (jobs and housing), access to treatment services, and family and community reintegration.</p> <p>Conclusion</p> <p>Stigma based on drug use and incarceration works to increase the needs of women for health and social services and at the same time, restricts their access to these services. These specific forms of stigma may amplify gender and race-based stigma. Punitive drug and social policies related to employment, housing, education, welfare, and mental health and substance abuse treatment make it extremely difficult for women to succeed.</p

    HacA-Independent Functions of the ER Stress Sensor IreA Synergize with the Canonical UPR to Influence Virulence Traits in Aspergillus fumigatus

    Get PDF
    Endoplasmic reticulum (ER) stress is a condition in which the protein folding capacity of the ER becomes overwhelmed by an increased demand for secretion or by exposure to compounds that disrupt ER homeostasis. In yeast and other fungi, the accumulation of unfolded proteins is detected by the ER-transmembrane sensor IreA/Ire1, which responds by cleaving an intron from the downstream cytoplasmic mRNA HacA/Hac1, allowing for the translation of a transcription factor that coordinates a series of adaptive responses that are collectively known as the unfolded protein response (UPR). Here, we examined the contribution of IreA to growth and virulence in the human fungal pathogen Aspergillus fumigatus. Gene expression profiling revealed that A. fumigatus IreA signals predominantly through the canonical IreA-HacA pathway under conditions of severe ER stress. However, in the absence of ER stress IreA controls dual signaling circuits that are both HacA-dependent and HacA-independent. We found that a ΔireA mutant was avirulent in a mouse model of invasive aspergillosis, which contrasts the partial virulence of a ΔhacA mutant, suggesting that IreA contributes to pathogenesis independently of HacA. In support of this conclusion, we found that the ΔireA mutant had more severe defects in the expression of multiple virulence-related traits relative to ΔhacA, including reduced thermotolerance, decreased nutritional versatility, impaired growth under hypoxia, altered cell wall and membrane composition, and increased susceptibility to azole antifungals. In addition, full or partial virulence could be restored to the ΔireA mutant by complementation with either the induced form of the hacA mRNA, hacAi, or an ireA deletion mutant that was incapable of processing the hacA mRNA, ireAΔ10. Together, these findings demonstrate that IreA has both HacA-dependent and HacA-independent functions that contribute to the expression of traits that are essential for virulence in A. fumigatus

    A simple and fast method for determination of phosphorus in fish diets and faeces used in animal nutritional studies

    No full text
    The optimization and validation of a simple and fast analytical method for the determination of phosphorus in fish diets and faeces used in animal nutrition studies are shown in this paper, starting with the validation of a preoptimized digestion procedure for biological samples, choice of the best chemical modifier and the minimal sample amounts. The digestion procedure consisted of an acid dissolution of a minimal of 100 mg of dry sample in a domestic microwave system using Parr Teflon bombs at high pressure. The P levels were determined by atomic absorption spectrometry with electrothermal atomisation, using an absorbance of 213.6 nm, a slit width of 1.0 nm, a current lamp of 20 mA and a deuterium lamp for background correction. Different furnace temperature programmes were used, and a final temperature programme was optimized. The optimization stages suggested the use of a 1,000 μg/ml La solution as chemical modifier and 1,600 and 2,700 °C as, respectively, the best pyrolysis and atomisation temperatures. The optimized analytical method was applied to different types of fish diets and faeces, and the percentages of recovery of P in spiked samples were, respectively, 94±11% (n=3) and 100±12% (n=3). The detection limit was 0.15 mg P/g of dry sample. The optimized methodology is simpler, faster and has less sample mass consumption than normally used colorimetric methods.publishe
    corecore