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Biomedical subjects

L Edebo

Publications and source records attributed to L Edebo.

At least 37 records · Page 2Linked to original sources

Antimicrobial activity of betaine esters, quaternary ammonium amphiphiles which spontaneously hydrolyze into nontoxic components.

A series of quaternary ammonium compounds that are esters of betaine and fatty alcohols with hydrocarbon chain lengths of 10 to 18 carbon atoms were tested with respect to antimicrobial activities and rates of hydrolysis. When the tetradecyl derivative was tested against some selected microorganisms, the killing effect was comparable to that of the stable quaternary ammonium compound cetyltrimethylammonium bromide. At higher pH values, both the antimicrobial effect and the rate of hydrolysis of the esters increased. However, whereas at pH 6 greater than 99.99% killing of Salmonella typhimurium was achieved with 5 micrograms/ml in 3 min, the rate of hydrolysis was less than 20% in 18 h. At pH 7, a similar killing effect was achieved in 2 min and 50% hydrolysis occurred in ca. 5 h. Thus, it is possible to exploit the rapid microbicidal effect of the compounds before they hydrolyze. The rate of hydrolysis was reduced by the presence of salt. The bactericidal effect of the betaine esters increased with the length of the hydrocarbon chain of the fatty alcohol moiety up to 18 carbon atoms. Since the hydrolysis products are normal human metabolites, the hydrolysis property may extend the use of these quaternary ammonium compounds as disinfectants and antiseptics for food and body surfaces.

Bacteria↗

Selective toxicity of alkanolamines.

The antimicrobial effects of diethanolamine, dimethylamino-methyl-propanol, and butylethanolamine are greatly enhanced at high pH. Their antimicrobial activities are closely correlated with their uncharged forms, indicating that diffusion through cell membrane(s) is rate limiting for the antimicrobial action. Since these compounds are selectively toxic at high pH, they are appropriate antimicrobial agents for use in alkaline metalworking fluids.

Dose-Response Relationship, Drug↗

Microbial growth and accumulation in industrial metal-working fluids.

The dynamics of microbial growth in metal-working fluids (MWF) and the effect of the addition of biocides were studied in large fluid systems, in this case, one central tank which holds 150 m3. In this system, populations of Pseudomonas pseudoalcaligenes (greater than 10(8) CFU/ml) were sustained for a year, although large quantities of biocides were added. Quantitation of 3-OH lauric acid, a marker for many Pseudomonas spp., by gas chromatography indicated that the bacterial biomass exceeded the viable counts by approximately 15 times. Fungi were grown on several occasions, the dominating genera being Fusarium and Candida. Soon after the old MWF was removed and the tank was provided with fresh MWF, which consisted of an emulsion of mineral oil in water, there was a massive growth of P. pseudoalcaligenes that reached levels of greater than 10(8) bacteria per ml. Initially, only low concentrations of other species were found for some weeks. After this period, different enterobacteria and other gram-negative rods often appeared at high concentrations (10(7) and 10(8) bacteria per ml, respectively). Bacteria identified as P. pseudoalcaligenes showed great variation with respect to colony morphology and a certain heterogeneity with respect to biochemical characteristics. Certain bacterial species grew as microcolonies on metal strips immersed in the circulating MWF, but P. pseudoalcaligenes was not recovered from this habitat. The total bacterial count in the air surrounding the machines in the metal-working shop showed an inverse relation to increasing distance from the machine. The concentration of bacteria in the air varied because of the number of machines in use, temperature, and humidity.(ABSTRACT TRUNCATED AT 250 WORDS)

Air Microbiology↗

Serum antibodies to Pseudomonas pseudoalcaligenes in metal workers exposed to infected metal-working fluids.

Metal workers exposed to aerosol from metal-working fluid were examined with respect to serum antibody to the lipopolysaccharide (LPS) of Pseudomonas pseudoalcaligenes. During 1 year of observation this species grew at high concentrations in the fluid (approximately 10(8) CFU/ml), and the air surrounding the metal-working machines sometimes contained more than 10(5) CFU/m3. The levels of antibody belonging to the IgG and IgA classes were significantly higher than in blood donors and in workers newly employed. Comparison with employees not working in the machine hall showed a significantly higher IgG, but not IgA, antibody level. For IgM antibody no such difference was found. Among the exposed workers, non-smokers had significantly higher IgG antibody levels than smokers, whereas no such difference was established for IgA and IgM antibodies. In smokers the IgG antibody level seemed to decline in the long-range time, since there was a negative correlation between the time of employment with exposure to metal-working fluids and IgG antibody level. The antibody data indirectly demonstrate that P. pseudoalcaligenes grown in metal-working fluid penetrated the body surface of metal workers to yield an immune response most probably after inhalation of aerosol containing bacteria. In the metal workers this long-term exposure did not lead to any acute or chronic respiratory discomfort.

Adult↗

Toxic mussels and okadaic acid induce rapid hypersecretion in the rat small intestine.

The diarrheic activity of algal toxins in blue mussels (Mytilus edulis) has been quantitatively determined in ligated intestinal loops of the rat. Hepatopancreas from toxic mussels were disintegrated by freeze-pressing, and the homogenized tissue suspended in an equal amount (w/v) of buffer or in the liquid recovered after steaming. When such suspensions were injected into ligated loops of rat small intestine a rapid fluid secretion was observed. In contrast, the liquid from non-toxic mussel tissue homogenate was absorbed. Toxic tissue homogenates, liquid recovered after steaming of toxic mussels as well as purified okadaic acid produced maximum fluid accumulation in the loops within two hours. The maximum net fluid accumulation observed was ca 300 mg of weight increase per cm length of intestine. Within a range of 50-200 mg/cm the dose-response relationship was close to linear (r = 0.96, 0.99). In duplicate tests the average deviation from the mean was +/- 9 mg/cm (SD = +/- 4.9). Mussels yielding less than 100 mg/cm of weight increase per g hepatopancreas have been allowed for human consumption, a quantity agreeing with the allowed level of okadaic acid. The minimum quantity of okadaic acid which produced significant secretion in the rat intestinal ligated loop test was approx. 0.5 microgram. On a body weight basis, therefore, humans are estimated to be at least four times as sensitive as the rat to enteral challenge with okadaic acid.

Animals↗

Seasonal, geographic and individual variation of okadaic acid content in cultivated mussels in Sweden.

In Western Europe the dinoflagellate toxin, okadaic acid (OA) has been the main cause of diarrheic shellfish poisoning (DSP). Chemical determination of OA in mussels by homogenization of the hepatopancreas, extraction, purification, reaction with 9-anthryldiazomethane (ADAM), HPLC-separation, and fluorometric quantification has been used for weekly monitoring of mussel growing farms and to control harvested mussels. Within a week, substantial rises (from 0.41 to 5.4 micrograms OA/g hepatopancreas) as well as great reductions (from 7.2 to 1.8 micrograms/g hepatopancreas) were recorded. The rapid rise implies that weekly sampling is not sufficient to ensure that mussels are free from toxic levels of OA. The rapid decrease reveals that efficient toxin clearance mechanisms exist in the mussels. Substantial OA clearance occurs also at low temperatures (1.4-3 degrees C). Within a mussel growing site the OA concentrations could differ considerably between adjacent mussels (0.63 and 4.2 micrograms OA/g hepatop.) and even more between mussels grown at different depths along the same rope (0.63 and 10 micrograms OA/g hepatop.). These data emphasize the importance of sampling in studies on DST in mussels. Great differences between the different mussel growing sites were also observed. These data have been discussed with respect to the spread of the toxin by the sea, and the possibilities of reducing the exposure of the mussels to the toxic algae.

Animals↗

Enhancement of hydrophobic interaction, negative charge and phagocytosis by dinitrophenyl ligand coupling to Salmonella typhimurium 395 MS.

Dinitrophenylation of Salmonella typhimurium bacteria increased their hydrophobicity, negative charge, and interaction with PMNL in vitro, effects which are similar to the consequences of S-R mutation in S. typhimurium. The effects are ascribed to the hydrophobicity of the dinitrophenyl (DNP) ligand. Coupling of DNP-groups to the bacteria also enhanced their clearance by the reticuloendothelial system after intravenous injection into mice. Extensive DNP-coupling to the bacteria led to rapid deposition of injected bacteria outside the reticuloendothelial system. The kinetics of DNP-coupling showed saturation at 4-5 X 10(7) DNP groups per bacterium, similar for S and R bacteria, boiled and nonboiled. After 2 h of reaction with fluoro-2,4-dinitrobenzene (FDNB) more than 80% of the total DNP coupling observed after 4 h had occurred. The capacity of MOPC-315 IgA myeloma protein, which possesses anti-DNP activity, to bind to dinitrophenylated bacteria paralleled the number of DNP groups per bacterium, but smaller numbers of IgA molecules were bound. Approximately one IgA molecule bound per thousand DNP ligands. Only when bacteria were boiled prior to DNP coupling was agglutination observed after the addition of anti-DNP-IgA.

Binding Sites, Antibody↗

The effects of binding mouse IgA to dinitrophenylated Salmonella typhimurium on physicochemical properties and interaction with phagocytic cells.

The binding of mouse IgA antibody to DNP-conjugated bacteria enhanced the hydrophobic interaction when measured in dextran-poly(ethyleneglycol) two-phase systems and hydrophobic interaction chromatography. Similarly the interaction with polymorphonuclear leukocytes in vitro increased. In contrast, the rate of clearance of IgA-reacted bacteria from the blood stream of mice, after intravenous injection, was reduced under the conditions tested. Our data showed, with respect to increased hydrophobic interaction and opsonization, that binding of IgA antibody to bacteria produced less pronounced effects than those of IgG antibody binding. In contrast, secretory IgA antibody binding has been shown to reduce hydrophobic interaction and phagocytosis. Thus, serum IgA antibody has properties intermediate to IgG and SIgA with respect to hydrophobicity and opsonization.

Animals↗

Activation of polymorphonuclear leukocytes by salmonella.

The interaction of polymorphonuclear leukocytes (PMN) with salmonella, as studied by chemiluminescence and phagocytosis, was very different for a number of clinical isolates. Particularly bacteria in the serogroups C1 and E4 deviated from other Salmonella. The differences were observed in the rate of activation, peak value, duration of the chemiluminescence, and in the extent of association and ingestion as studied microscopically. Old laboratory S-strains such as Salmonella typhimurium 395 MS and S. minnesota S99 , which did not associate with the PMN, showed little activation of the PMN, whereas their phagocytosis-sensitive R-mutants induced rapid activation, high peak values, and short duration of the chemiluminescence. Certain isolates belonging to the C1/E4 group induced intermediate types of reactions. The kinetics of the activation was related to the physicochemical surface properties of the bacteria. Heating the bacteria at 70 degrees C for 45 min enhanced the activation of PMN by the S-type strains conspicuously but in different ways, whereas that of R-mutants was delayed. Different clinical isolates of salmonella have shown different physico-chemical surfaces, liability to phagocytosis by PMNs and different degrees of eliciting inflammatory mediators from PMNs in vitro. The results indicate that the C1/E4 group of Salmonella has pathogenicity mechanisms different from most salmonellae.

Hot Temperature↗

Carbohydrate exposure on salmonella and E. coli bacteria after reaction with antibody IgG and secretory IgA (SIgA) assessed with fluorescent lectins.

The carbohydrate moieties exposed on enterobacteria before and after antibody binding have been tested with fluorescent lectins. Salmonella typhimurium 395 MS (S-type) and its Rd-mutant MR10 were coated with hyperimmune anti-MS and anti-MR 10 IgG, respectively. MR 10 bacteria and Escherichia coli O86 bacteria were coated with human colostral secretory IgA (SIgA). There was a conspicuous binding of some of the lectins to untreated bacteria not always closely related to the sugar composition of the outer membrane lipopolysaccharide (LPS) or other known sugar residues. Antibody IgG and SIgA binding modified the affinity for the lectins. The binding of some lectins was reduced, presumably by masking the bacterial sugars. Antibody IgG binding to S. typhimurium MS and R 10 enhanced the affinity for RCA-I (Gal) and to a smaller extent for WGA (GlcNAc) which may be explained by exposure of IgG oligosaccharide. Antibody SIgA binding to S. typhimurium R 10 and E. coli O86 enhanced the affinity for the above lectins to a larger extent as well as for Con A (Man, Glc). The corresponding sugars N-acetylglucosamine, mannose and glucose are present in the carbohydrate chain of the secretory component as well as in IgA indicating that when SIgA antibody binds its sugar components are exposed.

Carbohydrates↗

Physicochemical surface properties and phagocytosis by polymorphonuclear leucocytes of different serogroups of Salmonella.

Salmonella isolates belonging to different serogroups have been analysed with respect to physicochemical surface properties and interaction with human polymorphonuclear granulocytes (PMNs). Most (22/34) recent isolates of the different serotypes showed hydrophilic surface properties and little if any negative charge accompanied by resistance to phagocytosis by PMN similar to the old laboratory S strains Salmonella typhimurium 395MS and Salmonella minnesota S99 (main group). However, all isolates belonging to the serogroups C1 (5 isolates), E4 (2), O43 (1), and one out of three E1 isolates (C1/E4 group) differed from the main group. In aqueous biphasic partition in dextran-polyethyleneglycol (PEG) systems the bacteria in the main group accumulated in the PEG-rich phase to 55-97%, those in the C1/E4 group to less than 10%, and R-mutants only to 1-2%. The bacteria in the C1/E4 group displayed a negative surface charge and a susceptibility to phagocytosis by PMNs that were greater than those for strains in the main group but much lower than those shown by the R-mutants. Bacteria belonging to serogroup C1 also displayed a significant susceptibility to hydrophobic interaction. The results are discussed in relation to the pathogenicity of salmonella.

Cell Membrane↗

Physico-chemical surface properties of Shigella sonnei.

In partition in two-phase systems as well as in hydrophobic and ion exchange chromatography a number of Sh. sonnei isolates with different phage patterns showed similar physico-chemical surface properties. All the isolates displayed hydrophobicity and a small negative charge. In this way the shigellae were different from salmonella S-strains and E. coli strains associated with infantile diarrhoea which have shown hydrophilic properties and nearly no charge. They were also different from E. coli strains with typical K-antigen often grown from patients with septicemia and upper urinary tract infection, which have shown hydrophilic properties and a great negative charge. However, the Sh. sonnei isolates were similar to E. coli strains belonging to certain serogroups which have been grown from patients with dysentery-like diseases. The results indicate that physico-chemical surface properties are related among enterobacteria belonging to different genera which have been grown from similar types of infections.

Adhesiveness↗

Physicochemical properties and blood clearance of human serum albumin conjugated to different extents with dinitrophenyl groups.

Human serum albumin (HSA) conjugated to various extents with dinitrophenyl (DNP) groups and labelled with 125I was studied with regard to physicochemical properties and blood clearance after intravenous injection in mice. Increasing the degree of DNP conjugation increased the tendency to hydrophobic interaction, and increased the net negative charge. Heavily DNP-substituted HSA molecules tended to aggregate. The higher the degree of DNP substitution the faster was the conjugate eliminated from the circulation. Blood clearance was independent of serum complement, and was not affected by galactose, N-acetylglucosamine, mannose, alpha-methyl-D-mannoside, or fucose. It is proposed that the differences in blood clearance between the different DNP-HSA conjugates mainly depend upon differences in the tendency to hydrophobic interaction.

Animals↗

Gastrointestinal uptake and blood clearance of antigen in the presence of IgA antibodies.

In selected experiments, IgA antibodies with specificity for dinitrophenyl (DNP) groups appeared to prevent gastrointestinal passage of antigenic fragments of DNP-conjugated protein given orally to mice. The antigen did not, however, pass across the gut as an intact macromolecule even in control animals. IgA was not found to increase the blood clearance of DNP-conjugated protein given intravenously and it is concluded that IgA probably does not have any important role in mediating elimination of macromolecular antigens from the blood.

Administration, Oral↗

Class of serum antibodies towards Salmonella enteritidis in gastro-enteritis, as measured by mixed reverse passive antiglobulin haemagglutination (MRPAH).

Sera taken from a well-mapped epidemic of Salmonella enteritidis gastro-enteritis among school children and teachers have been tested for antibodies of the IgG, IgM and IgA classes by MRPAH (mixed reverse passive antiglobulin haemagglutination) and for IgG and IgM classes by ELISA. When suitable threshold titres were chosen all sera taken up to 10 days after infection were negative by MRPAH, whereas all samples but one taken between day 16 and 48 showed the presence of antibodies of each three immunoglobulin classes. IgG antibody titres often remained elevated one year after infection whereas IgM and particularly IgA antibodies returned to negative. Up to the 28th day the IgG antibody titre showed a logarithmic increase with time, whereas no simple relationship was observed for the IgM and IgA antibody responses. Estimation of the regression equations for the titres measured by ELISA and MRPAH shows agreement between the two methods.

Antibodies, Bacterial↗

Serological and physicochemical reactivity of bovine erythrocytes before and after trypsin treatment.

On partition in aqueous polymer two-phase systems containing dextran, poly(ethyleneglycol) (PEG), and PEG substituted with charged or hydrophobic groups "inagglutinable" ox erythrocytes showed more negative surface charge and less hydrophobicity than "agglutinable" ox erythrocytes. Tryspin treatment of the erythrocytes increased the agglutinability, reduced the negative charge, and seemed to increase the liability to hydrophobic interaction. Haemagglutination of highly negatively charged ox erythrocytes is almost impossible to accomplish by antibody against the ox erythrocytes alone or against IgG antigen linked to the erythrocytes in passive haemagglutination. Likewise, reverse passive (antiglobulin) haemagglutination cannot be accomplished with these cells when immunoglobulin antigens of moderate molecular size (less than or equal to 900,000) are used. However, these cells may be agglutinated when a non-charged carrier such as a bacterium coated with sensitizing antibody (immunoglobulin) is used to bridge the antiglobulin-coupled erythrocytes in a mixed latticer aggllutinate. Such a bridging can also be accomplished by heat aggregation of the immunoglobulin antigen.

Animals↗