Diagnostic relevance of simultaneous testing for Chlamydia trachomatis and Neisseria gonorrhoeae.

Background: The prevalence of Chlamydia trachomatis (CT) and Neisseria gonorrhoeae (NG) infection in a Swiss cohort among individuals consulting for screening or symptomatic reasons is not very well known.

Methods: Between January 2009 and January 2010, diagnostic samples referred to us to test for either CT or NG or both were simultaneously analysed for both infections. Testing was performed using the commercial m2000sp and m2000rt devices from Abbott Diagnostics involving automated DNA extraction and semi-quantitative real-time polymerase chain reaction (PCR), respectively.

Comparison of MALDI TOF with conventional identification of clinically relevant bacteria.

Background: A completely new approach to diagnose microbial agents at least one day earlier based on mass spectrometric analysis becomes possible in the microbiology laboratory: MALDI TOF: matrix-assisted laser desorption/ionisation time-of-flight. Comparison between results of the new procedure with those obtained by conventional testing is mandatory.

Methods: 204 clinical isolates grown on agar plates were analysed both, by the MALDI TOF Bruker microflex apparatus and by conventional identification using the VITEK II and API systems, both from bioMérieux.

Differential cytotoxic, growth-inhibiting and lipid-peroxidative activities of four different asbestos fibres in vitro.

An attempt was made to characterize the carcinogenic hazard of asbestos fibres by using a set of in vitro screening tests. The fibres tested were the serpentine chrysotile and the three amphiboles anthophyllite, crocidolite and amosite. Their cytotoxic and cytostatic activities in rat primary fibroblast-like cells were assessed along with their effects on enzymic lipid peroxidation by liver homogenates.

Morphological aspects of interactions between asbestos fibers and human mesothelial cell cytoskeleton.

The interaction of chrysotile and amphibole asbestos fibers with the cytoskeleton of cultured human mesothelial cells from nontumoral pleural effusions was studied using scanning electron and immunofluorescence microscopy. Asbestos-exposed mesothelial cells show a massive annular condensation of cytokeratin filaments, forming a concentric ring enveloping the nucleus and the phagocytosed asbestos fibers. By detergent extraction of the cells it could be shown that the asbestos fibers are in close contact with the nuclear membrane and associated with the cytoskeletal framework of the cells.