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A set of well characterized strains, collected in Polish hospitals, including Gram-negative (n = 93) and Gram-positive (n = 90) isolates was used in the study. The VITEK 2 AST-cards were used in the analysis according to the manufacturer's recommendations. Comparison of the susceptibility data obtained by the standard method and by VITEK 2 cards proved concordant in 99% of cases. Clinically important mechanisms were revealed by the VITEK 2 AES with > 95% agreement with reference data including methicillin resistance in staphylococci (98%), high-level aminoglycoside resistance in enterococci (100%), VanA and VanB phenotypes in enterococci (100%), and ESBLs in Enterobacteriaccae (93.8%). The VITEK 2 AES System appears a reliable tool for the detection and interpretive reading of clinically important mechanisms of resistance and can be recommended for routine work.
Metallo-beta-lactamases (MBLs) produced by Pseudomonas aeruginosa are a serious threat due to their ability to be transmitted between the same as well as different bacterial species. Different methods are applied in the clinical laboratory to detect MBLs. The aim of this study was to compare 4 phenotypic methods and a PCR assay for their ability to detect MBLs in clinical isolates of carbapenem-resistant P. aeruginosa strains. The study embraced a total of 70 carbapenem-resistant P. aeruginosa strains isolated in The Department of Microbiology of Dr A. Jurasz University Hospital in Bydgoszcz. The highest percentage (42.9%) of the strains were isolated from Intensive Care Unit patients, mainly from urine samples (31.4%). Methods used in this study were: double-disc synergy tests in two combinations: using ceftazidime with 2-mercaptopropionic acid and imipenem with EDTA, differences in inhibition zone diameters between discs with imipenem/ EDTA and imipenem, Etest MBL (AB Biodisk) and molecular amplification of blaIMP and blaVIM blaym genes responsible for producing MBLs, using PCR assay. The lowest percentage (1.4%) of positive results in detection of MBLs was obtained using PCR assay, the highest (72.9%) by double-disc synergy tests with imipenem and EDTA, but the specificity of this method may be low.
The interplay of plant resistance mechanisms and bacterial pathogenicity is very complex. This applies also to the interaction that takes place between the pathogen Pseudomonas syringae pv. lachrymans (Smith et Bryan) and the cucumber (Cucumis sativus L.) as its host plant. Research on P. syringae pv. lachrymans has led to the discovery of specific factors produced during pathogenesis, i.e. toxins or enzymes. Similarly, studies on cucumber have identified the specific types of plant resistance expressed, namely Systemic Acquired Resistance (SAR) or Induced Systemic Resistance (ISR). This paper presents a summary of the current state of knowledge about this particular host-pathogen interaction, with reference to general information about interactions of P. syringae pathovars with host plants.
An efficient system of crop plant fertilization is a prerequisite for fulfilling backgrounds of the concept known as sustainable agriculture. A well developed, i.e., adjusted to any site specific conditions of plant production, system of plant crop fertilization should allow to reach by the cultivated plant a state of nutritional homeostasis, as a base to full expression of its resistance mechanisms to pressure of pathogenic organisms. Growth and development of crop plants is under permanent, but variable in the course of vegetation, pressure of pathogens. Plant crop response to their attack is generally a result of its genetic natural backgrounds and/or breeding progress (resistance). Plant crop variety susceptibility to disease is modified by the growth environment, affecting both i) its nutritional status and ii) pathogen’s activity. Mechanisms of plant resistance to pathogens in the course of the growing season results from development of its i) structural and ii) biochemical barriers. Protection functions of nutrients reveal at each stage of both primary and secondary barriers build-up. Plant crop growth under conditions of imbalanced nitrogen economy results in release to the external environment (rhizosphere, fyllosphere) low-molecular compounds, attracting pathogens. The main way to decrease this process is to take nitrogen metabolism under control through its balancing with potassium as the main element, following by sulfur and micronutrients. Accumulation of lignin in the cell wall as physical barrier to penetrating fungal hyphae depends on plant crop nutritional status with respect to copper, sulfur and also on silicon. A highly specific protective functions are related to calcium activity in plants body. On the one hand calcium content in the cell wall controls direct pathogen activity and on the other hand its content in the cell cytoplasm is essential for plant response to stresses, including pathogen’s attack. In the protection cascade a specific, even primary function is attributed to potassium, which controls activity of the plasma membrane located NADPH oxidizes. Increasing activity of these enzymes is a prerequisite for a rapid reactive oxygen forms (ROS) synthesis in the site of pathogen attack. It is necessary to keep in mind, that increased synthesis of primary and secondary metabolites in response to pathogen’s attack depends on availability of sulfur and micronutrients such as manganese, copper, zinc and others. However, the nutrient-induced mechanisms of plant protection can reach their full state, provide that plants are well supplied with macro- and micronutrients.
Winter survival of cereals and grasses depends mainly on plant resistance to low temperature and to snow mould fungi. To persist winter plants have to be tolerant to different kind of stresses: abiotic such as low temperature, long-term snow and ice cover, freeze-induced plant desiccation or frequent freezing and thawing, and biotic - many species of snow mould fungi. During the cold acclimation, cereals and grasses become more resistant to both stresses: cold and snow mould. Earlier seeded plants with a greater number of crowns are more resistant to snow mould. Infection caused by snow mould induces a complex plant response, including such processes as the synthesis of PR (pathogenesis-related) proteins (chitinase and β-1,3-glucanas), production of active oxygen species (AOS), synthesis of phenolics, phyotalexins, accumulation of callosis and soluble carbohydrates, and a decrease of water potential. In the paper the most common defence mechanisms against snow mould pathogens are discussed.
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