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Query: UMLS:C0519030 (Klebsiella)
 21,988 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The populations of Pseudomonas sp. B4, Escherichia coli, Klebsiella pneumoniae, Micrococcus flavus, and Rhizobium leguminosarum biovar phaseoli declined rapidly in lake water. The initially rapid decline of the two pseudomonads and R. phaseoli was followed by a period of slow loss of viability, but viable cells of the other species were not found after 10 days. The rapid initial phase of decline was not a result of Bdellovibrio spp., bacteriophages, or toxins in the water since Bdellovibrio spp. were not present and passage of the lake water through filters that should not have removed bacteriophages or soluble toxins led to the elimination of the rapid phase of decline. The addition of 250 micrograms of cycloheximide and 30 micrograms of nystatin per ml eliminated viable protozoa form the lake water, and the population of Pseudomonas sp. B4 did not fall and the decline of E. coli and K. pneumoniae was delayed or slowed under these conditions. Pseudomonas sp. L2 proliferated rapidly in lake water amended with glucose, phosphate, and NH4NO3, but its numbers subsequently fell abruptly; however, in water amended with cycloheximide and nystatin, which killed indigenous protozoa, the population density was higher and the fall in numbers was delayed. Of the nutrients, the chief response was to carbon, but when glucose was added, phosphorus and nitrogen stimulated growth further. Removing other bacteria by filtering the lake water before inoculation with Pseudomonas sp. L2 suggested that competition reduced the extent of response of the pseudomonad to added nutrients.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Factors affecting the survival and growth of bacteria introduced into lake water. 306 35

Gentamicin resistance coliforms detected continuously in raw and purified waste water samples of a sewage treatment plant made up less than 0.1% of all coliforms. 43.9%; 31.4%; 13.3% and 11.3% of gentamicin-resistant coliforms were identified as Enterobacter, E. coli, Klebsiella and Citrobacter, respectively. R plasmids encoding a gentamicin resistance phenotype were isolated and characterized. They range between 55 and 60 MD in size and belong to 3 incompatibility groups (IncOF, IncM, IncK). Using restriction endonucleolytic digestion of plasmids, they could be further characterized and subtyped. In contrast to moderate molecular alterations observed among the IncM plasmids, the IncOF plasmids reveal a high stability of restriction pattern. This IncOF plasmid was predominantly found in E. coli wild strains and detected continuously.
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PMID:[Isolation and characterization of gentamicin resistance plasmids of coliform bacteria from the waste water of a water treatment plant]. 306 59

The contamination of semiclosed disposable circuits of Healthdyne and Bourns ventilators was studied in a newborn intensive care unit over a 2-year period. A total of 379 fluid samples was obtained from inspiratory and expiratory tubing condensates and traps and from thermal humidifier columns fed with prefilled containers of sterile water. In addition, 100 tryptic soy agar plates were exposed to the exhalation mist of the circuits sampled. With 24-h changes of circuits a 2.5% contamination rate was observed (phase I). In an effort to contain costs, circuits were changed every 48 h (phase II); the concentration of potential pathogens increased to greater than 10(5) CFU/ml with this extension of changing time. Two long-term (15- and 9-month) infants were colonized and intermittently infected, one with Klebsiella pneumoniae and Staphylococcus aureus and the other with Pseudomonas aeruginosa. When the protocol was readjusted from 48- to 24-h circuit changes (phase II), the contamination rate decreased; for the two colonized infants (35 circuits, 123 samples) the contamination rate decreased from 19 to 6% (P less than 0.01; chi-square test), and for seven noncolonized infants (59 circuits, 217 samples) the contamination rate decreased from 5 to 0.5% P less than 0.001; (chi-square test). These data suggest that frequent changing of the circuits reduces colonization and cross-infection.
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PMID:Microbiological assessment of 24- and 48-h changes and management of semiclosed circuits from ventilators in a neonatal intensive care unit. 308 50

During the period of May 1982 to January 1983 and March 1986 to May 1986, 164 water-specimens had been collected along the river Rhine and its affluxes in the overcrowded Rhine-Neckar-Region from 34 collecting-sites on 8 different days. The specimens were tested for the total-germ-count and the titers of different Enterobacteriaceae-species. The total-germ-count examined concentrations of several hundreds up to 1.8 million germ in 1 ml river-water. Extremely high concentrations were found along the waste-water-influxes (purification-plants) and the overloaded Rhine-affluences (Leimbach, Kraichbach, Speyerbach, Rehbach, Neckar). The waste-water-samples from the central flow of the Rhine-river showed germ-concentrations of less than 10.000/ml, due to the mix-up of the waste water with the Rhine-water. Enterobacteriaceae--549 isolates together--could be found mainly in specimens from all collected sites in low titers. E. coli, Klebsiella pneumoniae, Enterobacter cloacae, Serratia liquefaciens and Citrobacter freundii had been the highest recovery rate. The isolation of Salmonellae was examined because of specific methods in a separate study (2. Communication). Based on these data, it has to be concluded, that the water of the Rhine-river and its affluxes in the Rhine-Neckar-Region is an uncontrolled germ-reservoir. The use of this water for bathing, unprocessed drinking-water or for agriculture purpose has to be refused from the hygienic point of view.
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PMID:[Bacteriologic quality of water from the Rhine and its tributaries in the Rhine-Neckar region. I. Bacterial count and Enterobacteriaceae of the current status of pollution]. 311 8

The enzyme that catalyzes the ADP-ribosylation and concomitant inactivation of dinitrogenase reductase in Rhodospirillum rubrum has been purified greater than 19,000-fold to near homogeneity. We propose dinitrogenase reductase ADP-ribosyltransferase (DRAT) as the working name for the enzyme. DRAT activity is stabilized by NaCl and ADP. The enzyme is a monomer with a molecular mass of 30 kDa and is a different polypeptide than dinitrogenase reductase activating glycohydrolase. NAD (Km = 2 mM), etheno-NAD, nicotinamide hypoxanthine dinucleotide, and nicotinamide guanine dinucleotide will serve as donor molecules in DRAT-catalyzed ADP-ribosylation reaction, and dinitrogenase reductases from R. rubrum, Azotobacter vinelandii, Klebsiella pneumoniae, and Clostridium pasteurianium will serve as acceptors. No other proteins or small molecules, including water, have been found to be effective as acceptors. Nicotinamide is released stoichiometrically with formation of the ADP-ribosylated product. DRAT is inhibited by NaCl and has maximal activity at a pH of 7.0.
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PMID:Purification and properties of dinitrogenase reductase ADP-ribosyltransferase from the photosynthetic bacterium Rhodospirillum rubrum. 314 11

Following their addition to lake water, the populations of Escherichia coli and of antibiotic-resistant strains of Pseudomonas fluorescens, Agrobacterium tumefaciens, Micrococcus flavus, Rhizobium meliloti, and Klebsiella pneumoniae declined rapidly, as determined by counting on media containing antibacterial compounds. The estimates of population sizes were occasionally higher if procedures were used that permitted possible resuscitation of injured cells. No resuscitation procedure yielded consistently higher estimates of populations of surviving cells than the use of selective media alone. The patterns of survival of the test bacteria in lake water amended with eucaryotic inhibitors were essentially the same whether a resuscitation procedure was used or not, and the patterns of survival in sterile lake water or buffer were the same whether counts were made on selective media or on media without antibacterial agents. On the basis of the methods used to show sublethal injury caused by stress, we suggest that such injury to the test bacteria is not a significant factor involved in their decline in lake water.
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PMID:Role of sublethal injury in decline of bacterial populations in lake water. 314 14

The susceptibility of coliform bacteria and bacterial pathogens to free chlorine residuals was determined before and after incubation with amoebae and ciliate protozoa. Viability of bacteria was quantified to determine their resistance to free chlorine residuals when ingested by laboratory strains of Acanthamoeba castellanii and Tetrahymena pyriformis. Cocultures of bacteria and protozoa were incubated to facilitate ingestion of the bacteria and then were chlorinated, neutralized, and sonicated to release intracellular bacteria. Qualitative susceptibility of protozoan strains to free chlorine was also assessed. Protozoa were shown to survive and grow after exposure to levels of free chlorine residuals that killed free-living bacteria. Ingested coliforms Escherichia coli, Citrobacter freundii, Enterobacter agglomerans, Enterobacter cloacae, Klebsiella pneumoniae, and Klebsiella oxytoca and bacterial pathogens Salmonella typhimurium, Yersinia enterocolitica, Shigella sonnei, Legionella gormanii, and Campylobacter jejuni had increased resistance to free chlorine residuals. Bacteria could be cultured from within treated protozoans well after the time required for 99% inactivation of free-living cells. All bacterial pathogens were greater than 50-fold more resistant to free chlorine when ingested by T. pyriformis. Escherichia coli ingested by a Cyclidium sp., a ciliate isolated from a drinking water reservoir, were also shown to be more resistant to free chlorine. The mechanism that increased resistance appeared to be survival within protozoan cells. This study indicates that bacteria can survive ingestion by protozoa. This bacterium-protozoan association provides bacteria with increased resistance to free chlorine residuals which can lead to persistence of bacteria in chlorine-treated water. We propose that resistance to digestion by predatory protozoa was an evolutionary precursor of pathogenicity in bacteria and that today it is a mechanism for survival of fastidious bacteria in dilute and inhospitable aquatic environments.
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PMID:Survival of coliforms and bacterial pathogens within protozoa during chlorination. 322 66

Diarrheal stools from infants from which Klebsiella pneumoniae, Serratia liquefaciens, and Proteus mirabilis were isolated as possible causative agents of diarrhea were studied. These stools, along with control stool specimens which were collected from infants in the same village of Tamooh (near Cairo, Egypt), were analyzed by frequency-pulsed electron-capture gas chromatography (FPEC-GC). Watery stools and formed stools, to which distilled water was added, were centrifuged, and the supernatant was extracted with organic solvents and derivatized with specific functional group reagents to form electron-absorbing derivatives of carboxylic acids, hydroxy acids, alcohols, and amines. Results from the study showed distinct differences in FPEC-GC profiles of stools positive for K. pneumoniae, S. liquefaciens, and P. mirabilis. The major differences found were that diarrheal stools from which K. pneumoniae was isolated contained acetoin, a hydroxy acid-labeled peak F, and an unidentified amine, peak A. S. liquefaciens diarrheal stools had FPEC-GC profiles like the controls with the exception that an amine, peak A, was detected. The diarrhel stools containing P. mirabilis produced a distinct amine profile.
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PMID:Studies of metabolites in diarrheal stool specimens positive for Klebsiella, Serratia, and Proteus spp. by frequency-pulsed electron-capture gas chromatography. 323 97

Sixty-one strains of Enterobacteriaceae were tested for purine assimilation, including twenty-five Klebsiella pneumoniae, seventeen K. oxytoca and nineteen others. Only K. pneumoniae and K. oxytoca were able to use guanosine triphosphate, xanthine, hypoxanthine, or uric acid as sole sources of carbon and nitrogen. When guanosine triphosphate was used as sole source of nitrogen and carbon, the lag phase was prolonged. The addition of glucose did not affect the maximum number of viable cells for K. pneumoniae ATCC 29665, but produced an increase for strain K. oxytoca ATCC 13030. In the case of uric acid, ATCC 29665 had a more distinct lag phase of growth than ATCC 13030. Apart from this, they appeared to be very similar. On solid chemically defined GTP medium, some strains of Klebsiella were able to produce a water-soluble brown pigment.
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PMID:The use of purine compounds as sole sources of carbon and nitrogen by Klebsiella species. 323 19

The R-form lipopolysaccharide (LPS) from Escherichia coli K-12, from which cationic material had been removed by electrodialysis and the pH of which had fallen to 3.6, formed a rough hexagonal lattice structure with the lattice constant of about 19 nm. The rough hexagonal structure was maintained in buffers at pH 5 or lower but disintegrated into the ribbon-like structures in buffers at pH 6 or higher. However, in the presence of 10 mM Mg2+, the hexagonal lattice structure was not disintegrated even at alkaline pH levels but conversely it became more dense. At pH 8.3 to 8.9, the hexagonal lattice structure with the shortest lattice constant (15 nm) was formed. The same optimal pH levels were obtained for formation of the dense hexagonal lattice structure (lattice constant, 14 to 15 nm) by the electrodialyzed LPS from Klebsiella pneumoniae strain LEN-111 (O3-:K1-). The ability of Mg2+ to induce formation of the dense hexagonal lattice structure of the K-12 LPS depends upon the presence of buffers showing the optimal pH levels, since a very high concentration of Mg2+ such as 500 mM was required for the lattice formation in distilled water. The amount of the magnesium bound to the K-12 LPS did not significantly differ throughout the pH range of 3 to 9. Therefore, the optimal pH range is another essential factor for formation of the dense hexagonal lattice structure of the LPS in addition to binding of the magnesium to the LPS.
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PMID:In vitro hexagonal assembly of R-form lipopolysaccharides: effect of pH on the Mg+2-mediated hexagonal assembly. 328 6


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