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Sökning: WFRF:(Leth F)

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11.
  • Eiland, F, et al. (författare)
  • Influence of initial C/N ratio on chemical and microbial composition during long term composting of straw
  • 2001
  • Ingår i: Microbial Ecology. - : Springer Science and Business Media LLC. - 1432-184X .- 0095-3628. ; 41:3, s. 272-280
  • Tidskriftsartikel (refereegranskat)abstract
    • Shredded straw of Miscanthus was composted in 800-L boxes with different amounts of pig slurry added as nitrogen source. The impact of the different initial CIN ratios (11, 35, 47, 50, and 54) on the composting process and the end product was evaluated by examining chemical and microbiological parameters during 12 months of composting. Low initial C/N ratios caused a fast degradation of fibers during the first three months of composting (hemicellulose: 50-80%, cellulose: 40-60%), while high initial C/N ratios resulted in 10-20% degradation of both hemicellulose and cellulose. These differences were reflected in the microbial biomass and respiration, which initially were higher in low C/N treatments than in high C/N treatments. After 12 months of composting, this situation was reversed. Composts with high initial CIN ratios had high microbial biomass (15-20 mug ATP g(-1) OM) and respiration rates (200 mug CO, h(-1) g(-1) OM) compared to treatments with low initial C/N ratios (less than 10 mug ATP g(-1) OM and 25 mug CO2 h(-1) g(-1) OM). This could be explained by the microorganisms being nitrogen limited in the high C/N ratio treatments. In the low C/N ratio treatments, without nitrogen limitation, the high activity in the beginning decreased with time because of exhaustion of easily available carbon. Different nitrogen availability was also seen in the nitrification patterns, since nitrate was only measured in significant amounts in the treatments with initial C/N ratios of 11 and 35. The microbial community structure (measured as phospholipid fatty acid, PLFA, profile) was also affected by the initial C/N ratios, with lower fungal/bacterial ratios in the low compared to the high C/N treatments after 12 months of composting. However, in the low C/N treatments higher levels of PLFAs indicative of thermophilic gram-positive bacteria were found compared to the high C/N treatments. This was caused by the initial heating phase being longer in the low than in the high C/N treatments. The different fungal/bacterial ratios could also be explained by the initial heating phase, since a significant correlation between this ratio and heat generated during the initial composting phase was found.
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13.
  • Gunther, G, et al. (författare)
  • Availability, price and affordability of anti-tuberculosis drugs in Europe: a TBNET survey
  • 2015
  • Ingår i: The European respiratory journal. - : European Respiratory Society (ERS). - 1399-3003 .- 0903-1936. ; 45:4, s. 1081-1088
  • Tidskriftsartikel (refereegranskat)abstract
    • Data on availability and cost of anti-tuberculosis (TB) drugs in relation to affordability at national level are scarce.We performed a cross-sectional study on availability and cost of anti-TB drugs at major TB-reference centres in 37 European countries. Costs of standardised treatment regimens used for pan-sensitive TB, multidrug-resistant (MDR) TB, pre-extensively drug-resistant (XDR) TB, and XDR-TB were compared using a purchasing power analysis. Affordability was evaluated in relation to monthly national gross domestic products per capita (GDP).At least one second-line injectable and either moxifloxacin or levofloxacin were available in all countries. Linezolid and clofazimine were available in 79% and 46% of the countries, respectively. Drug cost for XDR-TB was three-times more expensive than those for MDR-TB. The average price of treatment for pan-sensitive TB represented a maximum of 8.5% of the monthly GDP across countries, while for standard MDR-TB treatment this was <30% in only six countries and more than 100% in four countries. Treatment of XDR-TB represented more than 100% of a month's GDP in all countries where the regimen was available.High cost and limited availability of drugs for treatment of drug-resistant TB, particularly beyond resistance to first-line drugs, are a major impediment to successful TB control in Europe.
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14.
  • Gunther, G, et al. (författare)
  • Beyond multidrug-resistant tuberculosis in Europe: a TBNET study
  • 2015
  • Ingår i: The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease. - : International Union Against Tuberculosis and Lung Disease. - 1815-7920. ; 19:12, s. 1524-1527
  • Tidskriftsartikel (refereegranskat)
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15.
  • Gunther, G, et al. (författare)
  • Multidrug-resistant tuberculosis in Europe, 2010-2011
  • 2015
  • Ingår i: Emerging infectious diseases. - : Centers for Disease Control and Prevention (CDC). - 1080-6059 .- 1080-6040. ; 21:3, s. 409-416
  • Tidskriftsartikel (refereegranskat)
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17.
  • Heyckendorf, J, et al. (författare)
  • Prediction of anti-tuberculosis treatment duration based on a 22-gene transcriptomic model
  • 2021
  • Ingår i: The European respiratory journal. - : European Respiratory Society (ERS). - 1399-3003 .- 0903-1936. ; 58:3
  • Tidskriftsartikel (refereegranskat)abstract
    • The World Health Organization recommends standardised treatment durations for patients with tuberculosis (TB). We identified and validated a host-RNA signature as a biomarker for individualised therapy durations for patients with drug-susceptible (DS)- and multidrug-resistant (MDR)-TB.MethodsAdult patients with pulmonary TB were prospectively enrolled into five independent cohorts in Germany and Romania. Clinical and microbiological data and whole blood for RNA transcriptomic analysis were collected at pre-defined time points throughout therapy. Treatment outcomes were ascertained by TBnet criteria (6-month culture status/1-year follow-up). A whole-blood RNA therapy-end model was developed in a multistep process involving a machine-learning algorithm to identify hypothetical individual end-of-treatment time points.Results50 patients with DS-TB and 30 patients with MDR-TB were recruited in the German identification cohorts (DS-GIC and MDR-GIC, respectively); 28 patients with DS-TB and 32 patients with MDR-TB in the German validation cohorts (DS-GVC and MDR-GVC, respectively); and 52 patients with MDR-TB in the Romanian validation cohort (MDR-RVC). A 22-gene RNA model (TB22) that defined cure-associated end-of-therapy time points was derived from the DS- and MDR-GIC data. The TB22 model was superior to other published signatures to accurately predict clinical outcomes for patients in the DS-GVC (area under the curve 0.94, 95% CI 0.9–0.98) and suggests that cure may be achieved with shorter treatment durations for TB patients in the MDR-GIC (mean reduction 218.0 days, 34.2%; p<0.001), the MDR-GVC (mean reduction 211.0 days, 32.9%; p<0.001) and the MDR-RVC (mean reduction of 161.0 days, 23.4%; p=0.001).ConclusionBiomarker-guided management may substantially shorten the duration of therapy for many patients with MDR-TB.
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19.
  • Heyckendorf, J, et al. (författare)
  • Treatment responses in multidrug-resistant tuberculosis in Germany
  • 2018
  • Ingår i: The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease. - : International Union Against Tuberculosis and Lung Disease. - 1815-7920. ; 22:4, s. 399-
  • Tidskriftsartikel (refereegranskat)
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20.
  • Klamer, M, et al. (författare)
  • Changes in chemical composition and microbial biomass during composting of straw and pig slurry
  • 2000
  • Ingår i: PROCEEDINGS OF THE INTERNATIONAL COMPOSTING SYMPOSIUM (ICS'99). ; 1-2, s. 322-334
  • Konferensbidrag (övrigt vetenskapligt/konstnärligt)abstract
    • Composting was performed in an 800-L box and a 500-L, reactor system. The material used was shredded straw of Miscanthus with pig slurry added as a nitrogen source. Chemical and microbial parameters were measured at five degree temperature intervals until the end of the heating phase and then with increasing intervals during the remaining experiment. In both systems, major losses of carbon occurred during and after the thermophilic phase as a result of degradation of hemicellulose, followed by degradation of cellulose. Total amounts of phospholipid fatty acid (totPLFA) and adenosine triphosphate (ATP) were used as indirect estimates of microbial biomass. These methods correlated well over time, when the limitations of the method for the determination of ATP were taken into account. Microbial biomass in the two systems showed similar values when measured by totPLFA. In contrast, microbial biomass measured by ATP content was higher in the box system than in the reactor system. In spite of the differences in chemical and physical properties in the two systems, the distribution of taxonomic groups of microorganisms, indicated by marker PLFAs, showed similar patterns in the two systems, emphasising that in composting systems temperature is the major parameter controlling the composition of the microbial community.
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