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Based on the experimental research the impact of temperature of the source on energetic parameters of a heat pump with an electrically driven compressor such as: thermal rate, power input, rate of the accurateness of real thermodynamic cycle, coefficient of performance. The raise of the source temperature from 3°C to 30°C enables the enhancement of the condenser thermal rate from 9 kW to 15 kW, however, the coefficient of performance relatively increases only by approx. 12%. This is the effect of the indicated drop of the accurateness of the real thermodynamic cycle.
Global climate change is a common phenomenon today. It is mainly caused by increasing greenhouse gas emissions. It has been proven that global climate change affect the emergence and spread of infectious diseases. This applies to both climate change as a whole, as well as individual factors such as temperature, rainfall, humidity, etc. These changes may directly impact the pathogen, and indirectly the vectors of these pathogens. They can also affect the resistance of humans and animals. The association between the emergence of infectious disease outbreaks and global climate change was also shown. This problem should be taken seriously when considering the development of effective prevention programs.
Antimicrobial peptides (AMPs), also called peptide antibiotics, have been discovered in the early 1980s in frogs They were antimicrobial substances called magainins. AMPs are among the oldest defense mechanisms in plants, humans and animals. The major peptides include i.a. defensins, cathelicidins and protegrins. The mechanisms of action of antimicrobial peptides rely on the permeabilization of the microbial membrane, destabilization of the lipid bilayer structure, creation of micelles or channels within the membrane, binding lipopolysaccharide (LPS), preventing DNA replication, inhibiting protein expression, releasing ATP, as well as binding free iron and removing it from the microbial growth environment. At present, intensive research is being conducted on the use of AMPs in human and veterinary medicine, including treatment of infections such as acne, skin infections, sepsis, and bacterial infections of the diabetic foot. Among others, the following preparations are being tested: Ambicin, for the treatment of infections caused by Mycobacterium, and Iseganan, protegrin for the treatment of mouth inflammation, CF and chronic lung infections. P. aeruginosa-infected animals treated with the D2A21 preparation showed 100% survival. Some of the AMPs show biocidal activity against Bacillus anthracis. Defensins isolated from the mucus and tissues of many fish species have the ability to protect fish from infections by Aeromonas hydrophila, Pseudomonas fluorescens, and Vibrio anguillarum. Beneficial effects of using defensins in the treatment of Borrelia burgdorferi infections in dogs have been described. Synthetic peptides are used for the production of a vaccine against parvovirosis. Peptides obtained from lactic acid bacteria (LAB) reduce the contamination and increase the stability of food products. AMPs are also useful for decontaminating the environment and medical equipment, as well as for sterilizing catheters. They have also been used to develop biocidal self-disinfecting surfaces (BSOs). Moreover, AMPs can be used in hospital hygiene and veterinary medicine, e.g., for the treatment of protective clothing, wipes, filters, ventilation, etc.
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Q fever - selected issues

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Q fever is an infectious disease of humans and animals caused by Gram-negative coccobacillus Coxiella burnetii, belonging to the Legionellales order, Coxiellaceae family. The presented study compares selected features of the bacteria genome, including chromosome and plasmids QpH1, QpRS, QpDG and QpDV. The pathomechanism of infection – starting from internalization of the bacteria to its release from infected cell are thoroughly described. The drugs of choice for the treatment of acute Q fever are tetracyclines, macrolides and quinolones. Some other antimicrobials are also active against C. burnetii, namely, telitromycines and tigecyclines (glicylcycline). Q-VAX vaccine induces strong and long-term immunity in humans. Coxevac vaccine for goat and sheep can reduce the number of infections and abortions, as well as decrease the environmental transmission of the pathogen. Using the microarrays technique, about 50 proteins has been identified which could be used in the future for the production of vaccine against Q fever. The routine method of C. burnetii culture is proliferation within cell lines; however, an artificial culture medium has recently been developed. The growth of bacteria in a reduced oxygen (2.5%) atmosphere was obtained after just 6 days. In serology, using the IF method as positive titers, the IgM antibody level >1:64 and IgG antibody level >1:256 (against II phase antigens) has been considered. In molecular diagnostics of C. burnetii infection, the most frequently used method is PCR and its modifications; namely, nested PCR and real time PCR which detect target sequences, such as htpAB and IS1111, chromosome genes (com1), genes specific for different types of plasmids and transposase genes. Although Q fever was diagnosed in Poland in 1956, the data about the occurrence of the disease are incomplete. Comprehensive studies on the current status of Q fever in Poland, with special focus on pathogen reservoirs and vectors, the sources of infection and molecular characteristics of bacteria should be conducted.
Vibrio cholerae is the etiological agent of epidemic cholera. Symptoms include stomach ache, bloody diarrhea, and vomiting, which lead to severe dehydration and even death. Environmental monitoring as well as rapid and accurate identification of this pathogen are important for public health protection. In this study, a real-time PCR method for the detection of toxigenic V. cholerae was developed. In total, 63 environmental and clinical strains were tested for the presence of seven targets, namely ompW, ompU, tcpA, ctxA, zot, rfbO1, and rfbO139. The proposed method is specific, simple, and fast, and can be used for detection of toxigenic and non-toxigenic V. cholerae strains. The minimum detection limit of this assay for V. cholerae in environmental water samples was 1.4 CFU/ml.
Triplex real time PCR method for detection of enterohaemorrhagic strains of Escherichia coli in meat samples was described. Total of 36 strains belonging to different serogroups were used. All strains were cultured in brain heart infusion broth and sorbitol MacConkey agar plates under aerobic conditions. Sets of primers and TaqMan probes were prepared using GenBank resources. Using the designed method we were able to detect bacteria in meat samples and determine genotypes for stx1, stx2, and eaeA genes in tested strains, simultaneously. The described method provides a rapid detection of single colonies of this pathogen in minced meat samples.
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