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- Pfaller, M.A., et al.
(author)
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Twelve years of fluconazole in clinical practice : Global-trends in species distribution and fluconazole susceptibility of bloodstream isolates of Candida
- 2004
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In: Clinical Microbiology and Infection. - : Elsevier BV. - 1198-743X .- 1469-0691. ; 10:SUPPL. 1, s. 11-23
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Journal article (peer-reviewed)abstract
- We determined the species distribution and in-vitro susceptibility of 6082 bloodstream infection (BSI) isolates of Candida spp. collected from 250 medical centres in 32 nations over a 10-year period from 1992 through 2001. The species included 3401 C. albicans, 984 C. glabrata, 796 C. parapsilosis, 585 C. tropicalis, 153 C. krusei, 67 C. lusitaniae, 48 C. guilliermondii, 10 C. famata, 10 C. kefyr, six C. pelliculosa, five C. rugosa, four C. lipolytica, three C. dubliniensis, three C. inconspicua, two C. sake and one isolate each of C. lambica, C. norvegensis and C. zeylanoides. Minimum inhibitory concentration determinations were made using the National Committee for Clinical Laboratory Standards reference broth microdilution method. Variation in the rank order and frequency of the different species of Candida was observed over time and by geographic area. The proportion of BSI due to C. albicans and C. glabrata increased and C. parapsilosis decreased over time in Canada, the USA and Europe. C. glabrata was an infrequent cause of BSI in Latin America and the Asia-Pacific region. Very little variation in fluconazole susceptibility was observed among isolates of C. albicans, C. tropicalis and C. parapsilosis. These species accounted for 78% of all BSI and remained highly susceptible (91-100% susceptible) to fluconazole from 1992 to 2001 irrespective of geographic origin. The prevalence of fluconazole resistance among C. glabrata isolates was variable both over time and among the various countries and regions. Resistance to fluconazole among C. glabrata isolates was greatest in the USA and varied by US census region (range 0-23%). These observations are generally encouraging relative to the sustained usefulness of fluconazole as a systemically active antifungal agent for the treatment of candida BSI. © 2004 Copyright by the European Society of Clinical Microbiology and Infectious Diseases.
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- Davidson, M., et al.
(author)
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Nanotube-vesicle networks with functionalized membranes and interiors
- 2003
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In: Journal of the American Chemical Society. - 0002-7863 .- 1520-5126. ; 125:2, s. 374-8
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Journal article (peer-reviewed)abstract
- We describe nanotube-vesicle networks with reconstituted membrane protein from cells and with interior activity defined by an injection of microparticles or molecular probes. The functionality of a membrane protein after reconstitution was verified by single-channel ion conductance measurements in excised inside-out patches from the vesicle membranes. The distribution of protein, determined by fluorescence detection, in the network membrane was homogeneous and could diffuse via a nanotube connecting two vesicles. We also show how injecting small unilamellar protein-containing vesicles can differentiate the contents of individual containers in a network. The combination of membrane activity and interior activity was demonstrated by ionophore-assisted accumulation, and internal Calcium Green-mediated detection, of Ca2+ within a single network container. This system can model a variety of biological functions and complex biological multicompartment structures and might serve as a platform for constructing complex sensor and computational devices.
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- Johansson, Sveneric, et al.
(author)
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New forbidden and fluorescence Fe III lines identified in HST spectra of eta Carinae
- 2001
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In: Astronomy and Astrophysics. - 1432-0746. ; 361, s. 977-977
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Journal article (peer-reviewed)abstract
- We discuss the origin of eight emission lines in the spectra of gas blobs close to the central star of eta Carinae. The spectra have been obtained with the Goddard High Resolution Spectrograph (GHRS) and the Space Telescope Imaging Spectrograph (STIS) onboard the Hubble Space Telescope. Between 2400 and 2500 Å five narrow lines are identified as new forbidden lines of doubly ionized iron, [Fe III]. We present gA-value data for the corresponding transitions, which combine two different metastable configurations of Fe III. An anomalous intensity of the narrow Fe III line (UV 34) at 1914 Å is explained as fluorescence due to HLyalpha pumping. A level mixing of about 1% increases the f-value of the pumped excitation channel by more than two orders of magnitude, which makes the pumping efficient and the fluorescence significant. We introduce a new designation for fluorescence lines photoexcited by an accidental resonance, eg. < Fe III> in the case of doubly ionized iron. Based on observations with the NASA/ESA Hubble Space Telescope, and supported by grant numbers GO-6501 and GO-7302 from the Space Telescope Science Institute. The STScI is operated by the Association of Universities for Research in Astronomy, Inc., under NASA contract NAS5-26555.
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- Karlsson, M, et al.
(author)
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Electroinjection of colloid particles and biopolymers into single unilamellar liposomes and cells for bioanalytical applications
- 2000
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In: Analytical Chemistry. - Univ Gothenburg, Dept Chem, SE-41296 Gothenburg, Sweden. Univ Gothenburg, Dept Chem Phys, SE-41345 Gothenburg, Sweden. : AMER CHEMICAL SOC. - 0003-2700 .- 1520-6882. ; 72:23, s. 5857-5862
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Journal article (peer-reviewed)abstract
- A combined electroporation and pressure-driven microinjection method for efficient loading of biopolymers and colloidal particles into single-cell-sized unilamellar liposomes was developed. Single liposomes were positioned between a similar to2-mum tip diameter solute-filled glass micropipet, equipped with a Pt electrode, and a 5-mum-diameter carbon fiber electrode. A transient, 1-10 ms, rectangular waveform de voltage pulse (10-40 V/cm) was applied between the electrodes, thus focusing the electric field over the liposome. Dielectric membrane breakdown induced by the applied voltage pulse caused the micropipet tip to enter the liposome and a small volume (typically 50-500 x 10(-15) L) of fluorescein, YOYO-intercalated T7-phage DNA, 100-nm-diameter unilamellar liposomes, or fluorescent latex spheres could be injected into the intraliposomal compartment. We also demonstrate initiation of a chemical intercalation reaction between T2-phage DNA and YOYO-1 by dual injection into a single giant unilamellar liposome. The method was also successfully applied for loading of single cultured cells.
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