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Infective endocarditis due to unusual or fastidious microorganisms.

Infective endocarditis due to fastidious microorganisms is commonly encountered in clinical practice. Some organisms such as fungi account for up to 15% of cases of prosthetic valve infective endocarditis, whereas organisms of the HACEK group (Haemophilus parainfluenzae, H. aphrophilus, and H. paraphrophilus, Actinobacillus actinomycetemcomitans, Cardiobacterium hominis, Eikenella corrodens, and Kingella kingae) cause 3% of community-acquired cases of infective endocarditis. Special techniques are necessary to identify these microorganisms. A history of contact with mammals or birds may suggest infection caused by Coxiella burnetii (Q fever), Brucella species, or Chlamydia psittaci. A nosocomial cluster of postsurgical infective endocarditis may be caused by Legionella species or Mycobacterium species. If risk factors that are commonly associated with fungal infections (cardiac surgical treatment, prolonged hospitalization, indwelling central venous catheters, and long-term antibiotic use) are present, fungal endocarditis is possible. Patients with endocarditis and a history of periodontal disease or dental work in whom routine blood cultures are negative might have infection due to nutritionally variant streptococci or bacteria of the HACEK group. Communication between the microbiologist and the clinician is of crucial importance for identification of these microorganisms early during the course of the infection before complications such as embolization or valvular failure occur. In this article, we review the microbiologic and clinical features of these organisms and provide recommendations for diagnosis and treatment.

Anti-Bacterial Agents↗

Relationship between the contamination of the nurse's caps and their period of use in terms of microorganism numbers.

Nosocomial infections are a great problem in the health care facilities. The white uniforms of nurses are often washed to keep them clean, but the nurse's caps are not washed as frequently in comparison. It could be that the importance of these caps is being overlooked. If these caps are providing a residence for microorganisms causing nosocomial infection in the health care facility, then they should be washed as frequently as the uniforms. So far, the relationship between the contamination of the nurse's caps and nosocomial infection has not yet been studied. Therefore, this study was conducted to confirm if relationships exist among factors regarding the number of microorganisms on the nurse's caps, the period in which caps were used without being washed, and the individual characteristics of nurse wearing the caps. Results showed that the degree of contamination of the nurse's caps depended on individual characteristics and the period of use. Finally, results led to the conclusion that the nurse's caps should not be worn if their only purpose is to symbolize female workers in the health care facilities because, in actually, they provide a resistance for microorganisms causing nosocomial infections.

Bacteria↗

Inactivation of microorganisms with microwaves at reduced temperatures.

We developed a pilot-plant nonthermal flow process using microwave energy to inactivate microorganisms. The process consists of multiple passes through the microwave generator. Each passed material goes to a receiving tank for subsequent passes. The flow rate was 0.96 to 1.26 kg/min and the dwell time per pass was 1.1 to 1.5 min. Five passes were used. The microwave energy is instantaneously and simultaneously applied to the system, and thermal energy is removed by a cooling tube within the process line in the microwave generator. The cooling tube maintains the temperature below 40 degrees C. There was significant reduction in microorganisms in water, 10% glucose solution, and apple juice, and in yeast in beer. There was a slight decrease in microorganisms in tomato juice, pineapple juice, apple cider, and beer; and no effect in skim milk.

Beer↗

Evaluation of the petrifilm plate method for the enumeration of aerobic microorganisms and coliforms in retailed meat samples.

This study was designed to compare the effectiveness and applicability of the Petrifilm plate method with the Association of Official Analytical Chemists' (AOAC) standard aerobic count method and violet red bile agar method for meat products. The comparison was carried out using 303 meat samples collected from various retailers: 110 pork samples, 87 chicken samples, and 107 beef samples. In the comparison of the correlation coefficient (R) between the conventional method and the Petrifilm plate method by a linear regression analysis, the correlation coefficient in total microorganisms was 0.99, 0.95, and 0.94 in pork, beef, and chicken samples, respectively. The correlation coefficient in coliform count was 0.83, 0.96, and 0.81 in pork, beef, and chicken samples, respectively. Based on the high correlation in the total microorganism count, it might be possible to replace the conventional methods with the Petrifilm plate method. For coliform counts, the Petrifilm plate method also showed a generally high correlation coefficient, except for pork samples, which are more subject to contamination. The Petrifilm plate method was simpler and less time-consuming in sample preparation and, in procedures, faster than the conventional method. These results suggested that the 3M Petrifilm plate method could replace the conventional methods in the analysis of microorganism contamination measurement in meat products.

Agar↗

Reduction of spoilage microorganisms in fresh beef using hydrodynamic pressure processing.

Hydrodynamic pressure processing (HDP) was investigated as a technology to reduce spoilage microorganisms found in fresh beef. In two separate studies (studies 1 and 2), retail ground beef and beef roasts were purchased (day 0). The roasts were divided into stew pieces (30 to 40 g). All meat samples, including control samples, were stored at 5 degrees C for 20 h in a plastic film. After storage, designated samples were treated with HDP In study 3, ground beef was treated with HDP (day 0) and stored aerobically (5 degrees C) for 14 days with control samples. Each meat type was vacuum-packaged for HDP (100 g binary explosive, steel shock wave container). The pHs and the aerobic plate counts (log10 CFU/g) were measured on day 0 (studies I and 2) and on days 0, 7, and 14 (study 3) for control samples and for HDP-treated samples. There was no pH difference between control and HDP-treated meat types (studies 1 and 2); HDP reduced bacteria in both meat types in study 1 (2 log) and study 2 (1.5 log) on day 0. In study 3, there was a significant difference (P < 0.05) in pH between control meat (8.2) and HDP-treated meat (5.6) after storage. There was an immediate reduction (1.5 log) of microorganisms following HDP (day 0) and a 4.5-log difference between control samples (9 log) and HDP-treated samples (4.5) after 14 days of storage. With HDP, it is possible to reduce spoilage microorganisms found in or on different meat types (ground beef versus stew pieces), which could extend the shelf life of meat products.

Animals↗

Antimicrobial activity of potassium hydroxide and lauric acid against microorganisms associated with poultry processing.

The antimicrobial activity of solutions of potassium hydroxide (KOH) and mixtures of KOH and lauric acid against microorganisms associated with poultry processing was determined. In vitro tests were performed by enumerating viable microorganisms recovered from bacterial cultures suspended in peptone water (control) and in solutions of 0.1% KOH or mixtures of 0.1% KOH and 0.25 or 0.50% lauric acid. Additional studies were conducted to identify changes in the native microbial flora of poultry skin washed in distilled water, KOH, or KOH-lauric acid. Although results of in vitro studies indicated that significantly fewer bacteria (P < or = 0.05) were recovered from cultures suspended in KOH than from cultures suspended in peptone water, there were also significantly fewer bacteria recovered from cultures suspended in KOH-lauric acid than from cultures suspended in KOH. Results of experiments with broiler skin indicated that although rinsates of skin washed in 1.0% KOH solutions contained significantly fewer total aerobic bacteria and enterococci than did skin washed in water, significantly fewer of these microorganisms were generally recovered from rinsates of skin washed in mixtures of 1.0% KOH and 0.5, 1.0, 1.5, or 2.0% lauric acid than from skin washed in KOH alone. Washing of broiler skin in solutions of 0.25 to 1.00% KOH or mixtures containing these concentrations of KOH and two parts lauric acid (wt/vol) also significantly reduced the populations of bacteria and yeasts in the native flora of broiler skin. Enterococci, lactic acid bacteria, and staphylococci in the native flora of the skin had the highest level of resistance to the bactericidal activity of KOH-lauric acid. These findings indicate that the antimicrobial activity of KOH-lauric acid is significantly greater than that of KOH alone in vitro and on poultry skin. Thus, KOH-lauric acid may be useful for reducing the level of microbial contamination associated with poultry processing.

Animals↗

Hybrid biosynthesis of derivatives of protylonolide and M-4365 by macrolide-producing microorganisms.

Biotransformation of a macrolide antibiotic and a related compound was studied using various macrolide-producing microorganisms grown in the presence of cerulenin, an inhibitor of de novo synthesis of the aglycone moiety. Protylonolide (1) was transformed into 5-O-(4'-O-propionylmycarosyl)protylonolide (2) by a leucomycin-producing strain, Streptoverticillium kitasatoensis KA-429. M-4365 G2 (3) was bioconverted into M-4365 G3 (4), 9-dihydro M-4365 G3 (5), 3-O-acetyl M-4365 G3 (6) and 3-O-acetyl-9-dihydro M-4365 G3 (7) by a spiramycin-producing strain, Streptomyces ambofaciens KA-1028. Forosaminylated derivatives of M-4365 G2 were not obtained using this microorganism. M-4365 G2 was converted into 3-O-acetyl M-4365 G2 (8) by Stv. kitasatoensis strain KA-429 and a carbomycin-producing strain, S. thermotolerans KA-442. These results suggest that the substrate specificity of mycaminose- and forosamine-binding enzymes is high in Stv. kitasatoensis and S. ambofaciens, respectively, while that of the 3-hydroxyl acylating enzyme and mycarose-binding enzyme is low in these microorganisms. The bioconversion products showed lower antibacterial and antimycoplasmal activities than those of M-4365 G2.

Anti-Bacterial Agents↗

[The taxonomic position, ecological aspects and physiological-biochemical characteristics of microorganisms having industrial importance].

The paper presents fundamental results of the investigations obtained in the Department of Physiology of Industrial Microorganisms at the Institute of Microbiology and Virology of the National Academy of Sciences of Ukraine for the recent 15-20 years, as well as the Department developments directed to creation of biotechnological preparations, products and processes, most of which have been put into practice of the national economy and health protection. Data have been presented concerning the study of systematics, biology and ecology of nocardioform and coryneform bacteria, lactic acid bacteria and yeasts. When studying physiological-biochemical peculiarities and biological effect of the studied microorganisms, considerable attention has been paid to growth physiology of lactic acid bacteria, yeasts, lectin-forming bacteria, to processes of shaping of fungal mycelium under the conditions of batch cultivation as well as to microorganisms which take part in sewage treatment for heavy metals and oil products. The work also deals with the problems of creation and application in the economy of preparations intended for treatment and prophylaxis of gastro-intestinal diseases of cattle, poultry and swine, for siloing fodder, of new lactic acid preparations of functional direction, technological grounds of sewage treatment for oil products and six-valent toxic chrome.

Bacteria↗

Effect of gamma radiation on native endolithic microorganisms from a radioactive waste deposit site.

A time-course experiment was conducted to evaluate the effects of gamma radiation on the indigenous microbiota present in rock obtained from Yucca Mountain, Nevada Test Site. Microcosms were constructed by placing pulverized Yucca Mountain rock in polystyrene cylinders. Continuous exposure (96 h) at a dose rate of 1.63 Gy/min was used to mimic the near-field environment surrounding waste canisters. The expected maximum surface dose rate from one unbreached canister designed to contain spent nuclear fuels is 0.06 Gy/min. Considering the current repository packing design, multiple canisters within one vault, the cumulative dose rate may well approach that used in this experiment. The microbial communities were characterized after receiving cumulative doses of 0, 0.098, 0. 58, 2.33, 4.67, 7.01 and 9.34 kGy. Radiation-resistant microorganisms in the pulverized rock became viable but nonculturable (VBNC) after a cumulative dose of 2.33 kGy. VBNC microorganisms lose the ability to grow on media on which they have routinely been cultured in response to the environmental stress imposed (i.e. radiation) but can be detected throughout the time course using direct fluorescence microscopy techniques. Two representative exopolysaccharide-producing isolates from Yucca Mountain were exposed to the same radiation regimen in sand microcosms. One isolate was much more radiation-resistant than the other, but both had greater resistance than the general microbial community based on culturable counts. However, when respiring cell counts (VBNC) were compared after irradiation, the results would indicate much more radiation resistance of the individual isolates and the microbial community in general. These results have significant implications for underground storage of nuclear waste as they indicate that indigenous microorganisms are capable of surviving gamma irradiation in a VBNC state.

Bacteria↗

Comparative investigations of airborne culturable microorganisms in selected waste treatment facilities and in neighbouring residential areas.

The evaluation of airborne microorganisms in waste treatment facilities is complicated by different measuring systems, a lack of measuring standards and large variations between individual counts. In the present study, different sectors of the waste management industry were compared by determining median values of airborne culturable microorganisms from numerous parallel counts over a prolonged time period. The samples were taken during the warm season using the six-stage Andersen volumetric sampler in a large composting plant and its immediate vicinity, in an agricultural composting plant, a waste disposal site, and a sorting facility for recyclable materials. Control samples were taken at a site not influenced by the waste management industry in an open and largely uninhabited area. The highest median values for culturable bacteria (37 degrees C) found were 1.1 x 10(5) CFU/m3, for moulds (25 degrees C) 1.4 x 10(5) CFU/m3, and for A. fumigatus (37 degrees C) 1.7 x 10(4) CFU/m3 in the sorting cabins of the sorting facility (p < 0.001). The highest median values for thermophilic bacteria (actinomycetes and bacillaceae, 50 degrees C) were 7.3 x 10(3) CFU/m3 in the large composting facility. In all other facilities as well as in the neighbouring residential areas of all facilities investigated, all median values were significantly lower and corresponded to the naturally occurring levels: approx. 10(2) CFU/m3 for bacteria, approx. 10(3) CFU/m3 for moulds and approx. 10(1) CFU/m3 for A. fumigatus and thermophilic bacteria. Only in the neighbouring residential area of the large composting plant, the median values for thermophilic bacteria were approx. 10(2) CFU/m3, but an additional impact from farms cannot be excluded in this case. These results show permanent increased loads of the investigated microorganisms inside large composting facilities and especially in the sorting cabins for recyclable materials. The increasing number of reports on potential health hazards in these areas require adequate measures on the part of occupational medicine in order to limit the health risk to a minimum. The most important task is the automatization of the sorting process for recyclable materials.

Air Microbiology↗

Enumeration of total viable microorganisms in an antibiotic raw material using ChemScan solid phase cytometer.

A preliminary study was performed for the enumeration of microorganism contamination of the macrolide antibiotic, Spiramycin, using epifluorescence with the ChemScan solid phase cytometer. The artificial spiking of Spiramycin powder antibiotic with pure culture of four microorganisms led to complete recovery of the tested organisms, whatever their sensitivity to the bacteriostatic activity of the drug. With the conventional plate method run in parallel, complete recovery was only obtained for Spiramycin resistant organisms. The spiked microorganisms that were sensitive to the antibiotic remained inhibited or stressed by the action of the Spiramycin and did not grow on the plate.

Anti-Bacterial Agents↗

Alternative microbial testing: a novel DNA-based detection system for specified microorganisms in pharmaceutical preparations.

Fluorescence-coupled PCR technology was employed to quantify DNA segments specific for Staphylococcus aureus, Pseudomonas aeruginosa, and Enterobacteriaceae. The PCR procedure is put forward as an alternative method for detecting microbial contaminations in pharmaceutical preparations and is compared to the tests for specified microorganisms described in European Pharmacopoeia (EP) 2, 2.6.13 and the USP, chapter 61. Data presented here describe the validation of this analytical method when used for proof of absence of specified microorganisms. The detection systems were specific for the microorganisms analyzed, and led to linear results over a wide range (more than 6-7 log intervals). The correlation coefficients lay above 0.99. The precision of replicate determinations within a single test was observed to be high, the relative standard deviation being between 0.39% and 1.53%. The precision between different tests was also high, with a relative standard deviation between 0.76% and 1.91%. The sensitivity without pre-enrichment amounted to 1-10 CFU. Since determination of the specified bacteria was performed following pre-enrichment, the limit of detection amounted to 1 CFU. Equivalent results were obtained in a study on nine batches of a milky hydrophilic cream (SH-No. M 440 A) with the conventional test for microbial contamination and the PCR procedure. The data presented here strongly indicate that the use of fluorescence-coupled PCR techniques can prove the absence of specified bacteria faster and more efficiently than conventional methods.

DNA, Bacterial↗

[Development of biological methods of combating steel corrosion, induced by aerobic microorganisms].

Cocultivation of degrading microorganisms and their antagonists decreases the corrosion loss of carbon steel by 20 to 80%. It was found that a microorganism can either accelerate or inhibit corrosion, depending on the nutrient. The magnitude of the effect on corrosion depends on the ability of the microorganism to respond to changes in the nutrient-medium composition by releasing acidic or alkaline metabolites.

Bacteria, Aerobic↗

[The effect of the microwave energy on the water, contaminated by vegetative forms of microorganisms].

The paper presents a technology and a device for super-high sterilization, and results of investigation on the effect of microwave energy on water contaminated by vegetative forms of microorganisms. Temperatures bringing death to microorganisms in water flow were determined. In addition to the thermal effect of microwave energy, a non-thermal "specific" effect of super-high frequencies on various microorganisms (staphylococci, E. coli and Pseudomonas aeruginosa) was also studied.

Bacteria↗

Kinetics of polychlorinated biphenyl dechlorination and growth of dechlorinating microorganisms.

The present study has investigated a correlation between the kinetics of polychlorinated biphenyl (PCB) dechlorination and the growth of dechlorinating microbial populations. Microorganisms were eluted from Aroclor 1248-contaminated St. Lawrence River (NY, USA) sediments and inoculated into clean sediments spiked with Aroclor 1248 at 10 concentrations ranging from 0 to 3.12 micromol/g sediment (0-900 ppm). The time course of PCB dechlorination and population growth were concurrently determined by congener-specific analysis and the most probable number technique, respectively. The specific growth rate was a saturation function of PCB concentrations above the threshold concentration (0.14 micromol/g sediment, or 40 ppm), below which no dechlorination or growth of dechlorinations were observed. The maximum growth rate was 0.20/d with a half-saturation constant of 1.23 micromol/g sediment. The yield of dechlorinating microorganisms showed a peak at 0.70 micromol/g sediment (200 ppm), with a value of 10.3 x 10(12) cells/mol Cl removed, and decreased below and above this concentration. The dechlorination rate (micromol Cl removed/g sediment/d) was a linear function of Aroclor concentration. Both the log of this rate and the maximum level of dechlorination were significantly correlated with growth rate. The biomass-normalized dechlorination rate (micromol Cl removed/g sediment/cell/d) was first order because of the exponential manner of the population growth. The first-order rate constant was a saturation function of Aroclor concentrations, with a maximum of 0.24/d (a half-life of 2.9 d) and a half-saturation constant of 1.18 micromol/g sediment, which are similar to the constants for growth. These results indicate that the dechlorination rate is tightly linked to the population growth of dechlorinating microorganisms.

Aroclors↗

[Invasion of microorganisms in bronchial mucosa of liquidators of the Chernobyl accident consequences].

Bronchial bioptates of 97 liquidators of the Chernobyl accident consequences with chronic bronchitis and 23 patients of control nosological group as well as sputum (174 persons) and BAL (22 persons) of liquidators with chronic obstructive lung disease (COLD) were studied to define pathogenic role of automicroflora in the development of lung diseases. Such methods as electron microscopy, immunohistochemistry and microbiology were used. The revealed invasion of microorganisms occurred against the background of pathology of superficial bronchial epithelium with a decrease of HLA-DR and CD23 lymphocytes and increase of CD1c lymphocytes in lamina propria of bronchial mucosa of the liquidators. Verification of microorganisms characteristic of the upper respiratory tracts and atypical presence of Escherichia coli were found in the contents of the lower parts of broncho-pulmonary system of the liquidators. The obtained results testify to the activation of automicroflora and appearance of pathogenic microorganisms were caused by deterioration of specific and non-specific immune protection in liquidators with COLD.

Bronchi↗

[Discovery of the relationship between carbohydrate determinants of mollicute glycocalyx and affinity of microorganisms, and conditions for their existence].

As a result of comparative analysis of interaction intensity of plant lectins, specific to certain monosaccharides with surface glycopolymers of philogenetically close groups of microorganisms--mollicutes and representatives of group Bacillus--Lactobacillus--Streptococcus the authors have established common features: availability of alpha- and beta-D-galactose, sialic acids, L-fucose, N-acetylglucosamine, alpha-N-acetyl-D-galactosamine and alpha-D-mannose in their glycocalyx, that is a phenotypical manifestation of genetic relations between these microorganisms. The dependence between the availability of sialic acids and L-fucose in the composition of terminal structures of microorganisms glycocalyx and their capacity to occupy certain ecological niches have been found out.

Bacillus↗

The effects of high intensity visible and ultraviolet light on the death of microorganisms.

The expectation that microorganisms would be exposed to very high visible light intensity in a space environment led to the investigation of the killing of microorganisms by visible light. The carotenoid-containing yeast Rhodotorula glutinis was one of the several organisms investigated. It was found that despite the carotenoid content of the organism it can be killed by endogenous photosensitized oxidation. While the effects of various parameters such as culture age, temperature, etc., were studied, particular emphasis was placed upon the development of action spectrum, determination of sites of action and the mechanism by which cells are killed. The portion of the spectrum responsible for lethality lies between 300 and 400 nm with an apparent maximum response around 390 nm. The nucleus appeared to be damaged, as evidenced by a mutagenic effect when cells were radiated with light above 300 nm. Previously the only reported mutagenic responses from light of these wavelengths have been noted when cells have been irradiated in the presence of added sensitizing dyes. Increased leakage of irradiated cells indicated permeability membranes have undergone damage. Overall respiration of the cells is also decreased at a rate corresponding to the loss in viability. Such random damage to cells indicates that whatever the damaging species is, it must be quite non-specific. The sensitizing agent could be a free radical and evidence has been developed to support such a proposal. The sulfhydryl-containing compounds cysteine and gluthathione are capable of protecting the cells from death. Since these compounds are known to protect the organisms from ionizing radiation by the trapping of free radicals, it is logical to presume that the damaging species is a free radical. Little or no protection is offered to the microorganism by fat-soluble antioxidants such as tocopherol and related species. This would indicate that the primary lethal site must be in the water phase. It is likely that dehydration of the cells such as could be expected in a spacial environment would initially increase their susceptibility to irradiation, but upon intense dehydration could also result in their increased resistance.

Carotenoids↗