Silver nanoparticles possess antibacterial effect for various bacteria; however mechanisms of the interaction between Ag-NPs and bacterial cells remain unclear. The aim of our study was to obtain direct evidence of Ag-NPs penetration into cells of Gram-negative bacterium S. typhimurium and Gram-positive bacterium S. aureus, and to study cell responses to Ag-NPs. The Ag-NPs (most 8-10 nm) were obtained by gas-jet method. S. typhimurium (7.81 × 10⁷ CFU), or S. aureus (8.96 × 10⁷ CFU) were treated by Ag-NPs (0.05 mg/l of silver) in orbital shaker at 190 rpm, 37 °C. Bacteria were sampled at 0.5, 1, 1.5, 2, 5 and 23 h of the incubation for transmission electron microscopy of ultrathin sections. The Ag-NPs adsorbed on outer membrane of S. typhimurium and cell wall of S. auereus; penetrated and accumulated in cells without aggregation and damaging of neighboring cytoplasm. In cells of S. aureus Ag-NPs bound with DNA fibers. Cell responses to Ag-NPs differed morphologically in S. typhimurium and S. aureus, and mainly were presented by damage of cell structures. The cytoplasm of S. aureus became amorphous, while S. typhimurium showed lumping and lysis of cytoplasm which led to formation of "empty" cells. Other difference was fast change of cell shape in S. typhimurium, and late deformation of S. aureus cells. The obtained results showed how different could be responses induced by the same NPs in relatively simple prokaryotic cells. Evidently, Ag-NPs directly interact with macromolecular structures of living cells and are exert an active influence on their metabolism.

Multi-year monitoring of atmospheric bioaerosol in Southwestern Siberia revealed the presence of a large number of various culturable microorganisms. It is known that viable microorganisms can cause directly or provoke different human diseases. It's very difficult to evaluate the danger represented by each microorganism to man directly. Therefore, a relatively simple method is required for evaluation of potential danger represented to man by the whole assembly of culturable microorganisms in an atmospheric aerosol sample. For bacteria, the method can be based on a number of individual characteristics of each microorganism determined in the course of biochemical and other test required for identification of the detected bacterium, and a number of other tests. It is proposed to classify the measured individual characteristics of bacteria under four groups of indices responsible for: (i) potential pathogenicity for man; (ii) the numbers of bacteria in the sample; (iii) resistance to unfavorable environmental factors; (iv) drug resistance of bacteria. Each of four groups of indices is numerically evaluated by a certain integral index, which quantitatively reflects the contribution of experimentally determined characteristics of bacteria. Expert evaluation of the contribution of each characteristic of microorganisms to the corresponding group of indices is performed. The generalized index of potential danger of culturable bacteria in atmospheric aerosols for human health is presented as the product of four integral indices summarizing the normalized individual integral indices for all bacteria detected in the sample. The work presents the results of measuring the variations of all the above indices for atmospheric air samples collected during one year.

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