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F Meisel-Mikołajczyk

Publications and source records attributed to F Meisel-Mikołajczyk.

At least 37 records · Page 2Linked to original sources

[Toxins of Bacteroides fragilis and Bacteroides thetaiotaomicron rods as stimulators of adhesion molecule expression on the surface of vascular endothelial cells].

Lipopolysaccharides from four Bacteroides fragilis strains: one nonenterotoxigenic (NTBF) and three enterotoxigenic (ETBF), and from three B. thetaiotaomicron strains were extracted by hot phenol-water method and purified. B. fragilis enterotoxin was prepared according to the procedure of van Tassell et al. (1992). The influence of the examined toxins on the expression of adhesion molecules: ICAM-1, VCAM-1 and E-selectin on HMEC-1 (human dermal microvascular endothelial cells) was assayed in ELISA test with monoclonal antibodies. Four concentrations of toxins were applied: 0.01, 0.1, 1.0 and 10.0 (micrograms/ml). Endothelial cells were activated for 24 hours (ICAM-1 and VCAM-1 expression) and for 4 hours (E-selectin expression). The coloured product of immunoenzymatic reaction was measured by reading the absorbance at wavelength 492 nm. Two controls were performed in each experiment: with resting HMEC-1 and E. coli O55:B5 LPS (Sigma, USA). Bacteroides fragilis and B. thetaiotaomicron lipopolysaccharides stimulated three adhesion molecules under investigation. Their activity was comparable, but weaker than the activity of E. coli O55:B5 LPS. ICAM-1 was the most stimulated molecule. B. fragilis enterotoxin induced two adhesion molecules: VCAM-1 and E-selectin demonstrating weaker stimulatory activity than E. coli LPS. Stimulation of adhesion molecules on vascular endothelial cells should be considered to be a biological activity of B. fragilis and B. thetaiotaomicron endotoxins and B. fragilis enterotoxin.

Bacteroides↗

[Effect of suprainhibitory (supra-MIC) concentration of clindamycin on endotoxin release from Bacteroides fragilis].

The aim of this work was to determine the influence of clindamycin at concentration 100 x MIC on the growth of culture and the induction of endotoxin release from the cells of standard B. fragilis IPL E 323 strain. The antibiotic was added to 24-hour culture of the strain in BHI medium (time 0), its final concentration was 12.5 mg/l. The samples for further examinations were collected at time 0 and after 1, 2, 3 and 24 hours of continued incubation. At the same time the strain was cultured in a medium without the antibiotic. The optical density (OD 420 nm) of each sample was determined, they were centrifuged (2000 x g, 10 min), the supernatants were filtered (0.45 micron filters) and concentrated three times (5000 D ultrafilters). Two serological methods were applied to detect the presence of endotoxin in filtrates of culture medium: immunoelectroprecipitation (IEP) and immunoenzymatic assay (dot-ELISA) with rabbit anti-IPL E 323 immune serum. The results of experiments performed with filtrates of culture without the antibiotic indicate that standard B. fragilis IPL E 323 strain liberates endotoxin spontaneously to the culture medium. Single suprainhibitory dose of clindamycin at concentration 100 x MIC inhibits the growth of examined strain and does not cause augmented release of endotoxin from B. fragilis cells in vitro.

Anti-Bacterial Agents↗

Immunochemical characterization of Bacteroides vulgatus cell-surface antigens.

Capsular polysaccharide (CPS) and lipopolysaccharide (LPS) antigens extracted from three Bacteroides vulgatus strains (serotype specific strain, and two others isolated from normal gut flora and gut of a diabetic patient) were studied. Chemical analysis of CPS and purified LPS antigens was performed. The compositions of sugars, amino acids and fatty acids were shown to be different for each antigen. Rabbit antisera against whole bacterial cells were prepared. All antigens proved to be active in immunoelectrophoresis, SDS-PAGE and immunoblot tests. Several cross reactions in these assays were observed.

Animals↗

Dioctahedral smectite neutralization activity of Clostridium difficile and Bacteroides fragilis toxins in vitro.

The neutralization activity of dioctahedral smectite for ten toxigenic Clostridium difficile and eight enterotoxigenic Bacteroides fragilis strains was studied using McCoy and HT 29/C1 cell lines, respectively. Minimalization of the cytopathic effect of C. difficile toxin B on McCoy cell lines by dioctahedral smectite dissolved in PBS was observed. After incubation with dioctahedral smectite the toxic effects of B. fragilis enterotoxins on HT/29C1 (human colon adenocarcinoma cell line) were eliminated. Best neutralization of B. fragilis toxin was achieved using dioctahedral smectite dissolved in BHI.

Animals↗

[Drug resistance in nosocomial strains of staphylococci to methicillin].

The aim of the present study was the analysis of drug susceptibility of MRSA and MRCNS strains isolated from patients hospitalized in 14 wards of the State Clinical Hospital No 1 in Warsaw. The strains were identified (ID 32 STAPH), and their susceptibility to antimicrobial agents (ATB STAPH) was determined in ATB system (bioMérieux, France). Four methods were applied to confirm the resistance to methicillin: ATB-plus system, disc-diffusion method (Oxa 1 microgram, Oxoid, U.K.), Crystal MRSA ID (Becton Dickinson-BBL, USA) and agar screen test in TSA medium (Difco, USA) with methicillin (25 mg/l, Sigma, USA). 108 Staphylococcus spp. strains were found in 300 clinical specimens. 56 strains were methicillin-resistant (52%). Among methicillin-resistant strains 13 MRSA, 28 MRSE and 15 of other species were found. All MRSA strains were susceptible to vancomycin, teicoplanin and fusidic acid. MRCNS were susceptible first of all to vancomycin (43/43), minocycline (42/43) and pristinamycin (42/43). On the basis of the obtained results it can be stated that methicillin-resistant staphylococci occur in hospital wards. The greatest number of methicillin-resistant strains was cultured from patients hospitalized in surgery wards (32), methicillin-resistant strains much more frequently occur among coagulase-negative staphylococci, especially in Staphylococcus epidermis. Glycopeptide antibiotics are most active against isolated MRSA strains. The most active therapeutic agent against MRCNS is vancomycin.

Cross Infection↗

[Detection of toxin producing strains of Clostridium difficile using rapid diagnostic methods].

Feces of 53 patients from different hospital wards suffering from long term post-antibiotic therapy diarrhea were tested. For direct detection of C. difficile toxin A, in samples TCD (Becton-Dickinson), and C. difficile Toxin A Test (Oxoid) tests were used. Toxin A was detected in 16 samples (29.6% tested). C. difficile strains were isolated from 40% of the fecal samples. Toxin A was detected in 25 Clostridium difficile strains with commercial tests and toxin B was detected using McCoy cell line. Toxin A was not produced by 3 C. difficile strains in vitro, but toxin B was produced by all strains. The polymerase chain reaction (PCR) test showed that all isolated strains possess genes of toxins A and B.

Adolescent↗

[Comparison of several methods for detection of methicillin resistance in clinical strains of Staphylococcus sp].

108 Staphylococcus spp. strains from 300 clinical specimens from hospitalized patients were isolated. Identification and drug resistance were determined using automated ATB system. 37 S. aureus strains, 44 S. epidermides strains and 27 strains of other coagulase-negative staphylococci were cultured. Sensitivity to methicillin of S. aureus was determined with four methods: ATB system, disc-diffusion (Oxa 1 microgram), Crystal MRSA ID System and agar screen test in TSA medium with methicillin (25 micrograms/ml). 13 S. aureus strains (about 1/3 of strains) were methicillin-resistant (MRSA). Complete conformity of the results was obtained with Crystal MRSA ID, disc-diffusion and agar screen tests. In the case of three S. aureus strains the results of determination in ATB system were not consistent with the results obtained with the use of the methods mentioned above. Susceptibility to methicillin of 71 coagulase-negative strains (CNS) was determined using two methods at first: ATB and disc-diffusion. In the case of 25 methicillin-resistant strains identical results were obtained. For 20 coagulase-negative strains non-conformity with the results of these two methods was observed. As the decisive method, the agar screen test (TSA-MET) was applied. 18 of these 20 CNS strains were categorized as methicillin-resistant. Finally, 43 MRCNS (i.e. 60%) were detected among 71 coagulase-negative strains. The results of methicillin resistance determination of staphylococci in an automated system should be confirmed with a second test such as agar screen, disc-diffusion or Crystal MRSA ID System (in the case of S. aureus).

Methicillin↗

[Detection of endotoxins and enterotoxins of Bacteroides fragilis in culture media].

Four B. fragilis strains were studied one nonenterotoxigenic (NTBF) and three enterotoxigenic (ETBF). Endotoxin and enterotoxin which are released into the culture medium during the growth of strains were detected. Cultures in BHI broth were incubated for 48 hours at 37 degrees C. After 4, 8, 16, 24 and 48 hours of cultivation, samples of bacterial culture were collected and the optical density was measured. Then the samples were centrifuged, supernatants were filtered through 0.45 micron filters and concentrated three times with 5000 D ultrafilters. Prepared samples were kept frozen at 70 degrees C until use. The presence of endotoxin in samples was revealed by means of immunoelectroprecipitation (IEP) and immunoenzymatic test (dot-ELISA). The assays were performed with antibacterial rabbit immune sera. The activity of enterotoxin was detected on a human colon adenocarcinoma cell line HT 29/C1. The results of the study indicate that endotoxin is released spontaneously by nonenterotoxigenic IPL E 323 strain into the culture medium at the early stages of cultivation. The presence of endotoxin is not demonstrated by means of immunoelectroprecipitation in culture filtrated of ETBF strains. Trace amounts of endotoxin are revealed with dot-ELISA. The activity of enterotoxin is detected after 16 hours of incubation of ETBF strains.

Adenocarcinoma↗

[Microflora of periodontal pockets in advanced periodontitis].

The aim of study was the evaluation of periodontal pockets microflora in patients with advanced periodontitis. From each subject 16-20 samples were taken using paper points. Pooled sample after 60 s. mixing was serially diluted in reduced BHI. For total cell counts and for the isolation of black pigmented anaerobes Brucella agar supplemented with 5% sheep blood, hemin, menadione, with and without Kanamycin-Vancomycin mixture and BM agar plates were used. For isolation of A. actinomycetemcomitans TSBV agar plates were used. Cultures were incubated in anaerobic chamber at 37 degrees C for 7 days and TSBV agar plates in an atmosphere of 95% air-5% CO2 at 37 degrees C for 5 days. Microorganisms were identified by Gram staining, colony morphology, fluorescence in UV-light, haemagglutination of 3% sheep erythrocytes, fermentation of sugars, production of indole, urease (API 20A), specific enzymes (Rapid ID 32A). Twenty seven subjects with clinically recognized periodontitis were examined. Microorganisms important in periodontitis were isolated from periodontal pockets of almost all examined subjects. The number of bacteria obtained from the sample of one patient ranged from 1 x 10(4) CFU/ml to 3,6 x 10(6) CFU/ml. Porphyromonas gingivalis was identified in the samples taken from 17 patients, Prevotella intermedia-19, Actinobacillus actinomycetemcomitans -11, Fusobacterium nucleatum-9, Peptostreptococcus spp.-22.

Adult↗

[Production of enterotoxins by Bacteroids fragilis strains--effect of clindamycin].

Four B. fragilis strains were examined: one nonenterotoxigenic (NTBF) and three producing enterotoxin (ETBF). The growth of cultures was determined and enterotoxin, which is released to the culture medium during growth of strains, was detected. BHI broth and BHI broth with addition of subinhibitory doses (sub-MIC) of clindamycin were applied. Bacterial cultures were incubated at 37 degrees C for 48 hours. After 4, 8, 16, 24, 48 hours of cultivation, samples of bacterial cultures were collected and the optical density was measured. Then the samples were centrifuged, supernatants were filtered through 0.45 micron filters and concentrated three times with 5000 D ultrafilters. Prepared samples were kept frozen at -70 degrees C until used. The titre of enterotoxin in samples was determined on human colon adenocarcinoma cell line HT 29/C1. Neutralization assay was performed with culture filtrates, which were enterotoxin-positive and with rabbit anti-enterotoxin serum. The results of the experiments indicate that enterotoxin is detected after 16 hours of incubation of ETBF strains. Clindamycin at subinhibitory concentrations (sub-MIC) inhibits the growth of B. fragilis cultures. The antibiotic causes also delay and decrease in enterotoxin production by ETBF strains.

Adenocarcinoma↗

[Use of the LAL test for quantitative determination of Bacteroids fragilis endotoxin].

The aim of this study was the evaluation of LAL test with chromogenic substrate usefulness for the quantitative detection of B. fragilis endotoxin and the determination of the amount of endotoxin in culture filtrates of the strains of this species. Also, the trial was undertaken to determine the influence of clindamycin on endotoxin release from B. fragilis rods to the culture medium. Four B. fragilis strains were examined: one nonenterotoxigenic (NTBF) and three enterotoxigenic (ETBF). The growth of cultures was determined and endotoxin liberated to the culture medium during growth of strains was detected. BHI broth and BHI broth with addition of sub inhibitory doses (sub-MIC) of clindamycin were applied. Bacterial cultures were incubated for 48 hours at 37 degrees C. Samples of bacterial cultures were collected after 4, 8, 16, 24 and 48 hours of cultivation, and the optical density was measured. Then the samples were centrifuged, supernatants were filtered through 0.45 micron filters and concentrated three times with 5000 D ultrafilters. Prepared samples were kept frozen at -70 degrees C until used. The amount of endotoxin in samples was determined using quantitative LAL test with chromogenic substrate S-2423. The results of the experiments indicate that LAL test is the useful method for determination of B. fragilis endotoxin concentration. This endotoxin activates the enzymatic system present in Limulus polyphemus amebocyte lysate. Endotoxin is shed spontaneously by B. fragilis rods to the culture medium during growth. Clindamycin at subinhibitory concentrations (sub-MIC) inhibits the growth of cultures of examined strains. The antibiotic caused increase in endotoxin amount in culture medium.

Bacteroides fragilis↗

Tumor necrosis factor-alpha in response to endotoxin administration in the pregnant guinea pig.

OBJECTIVE: Our purpose was to test the hypothesis that an intramuscular endotoxin challenge induces production of tumor necrosis factor-alpha in the pregnant guinea pig and to investigate some of the metabolic effects. STUDY DESIGN: Twelve randomly selected guinea pigs at 33 days' gestation with a sampling catheter in the carotid artery received an intramuscular injection of a solution of endotoxin isolated from Bacteroides fragilis (n = 6) or of solvent alone (n = 6). Plasma values of tumor necrosis factor-alpha, hematocrit, and 6-keto-prostaglandin F1 alpha were determined before and several hours after injection. RESULTS: Tumor necrosis factor-alpha was detected in five of six guinea pigs, but it could not be demonstrated in five of six placebo animals. The hematocrit was significantly decreased, and prostaglandin F1 alpha significantly increased 24 to 48 hours after endotoxin injection. CONCLUSION: In pregnant guinea pigs an intramuscular endotoxin challenge induces the release of tumor necrosis factor-alpha, followed by a reduced hematocrit and an increased prostacyclin concentration. These effects could be involved in the pathogenesis of endotoxin-induced fetal growth retardation.

Animals↗

Enterotoxigenic Bacteroides fragilis isolated from nondiarrheic adults.

From 220 fecal samples of nondiarrheic adults, 29 strains of Bacteroides fragilis were isolated. Nine percent of them were enterotoxigenic Bacteroides fragilis (ETBF) strains. That is the first isolation of ETBF strains from nondiarrheic adults in Poland. Isolated ETBT strains could not be distinguished from non-enterotoxigenic Bacteroides fragilis (NTBF) strains by means of agglutination test. The sensitivity to antimicrobial agents does not differentiate enterotoxigenic from nonenterotoxigenic B. fragilis strains.

Adult↗

Detection of enterotoxigenic Bacteroides fragilis (ETBF), among strains isolated between 1976 and 1995 in Poland.

Thirty five Bacteroides fragilis strains isolated from different, clinical specimens in 1976-1985 and in 1995, preserved in strains collection of Department of Clinical Bacteriology were studied. The cytotoxicity of 35 bacterial culture supernatants, were tested on the human carcinoma cell line HT29/C1. Two strains proved to be enterotoxigenic. One of those strains was isolated in 1985 from the human, before the existence of enterotoxin producing strain was reported. All 35 strains were metronidazol sensitive showing lack of correlation between enterotoxigenicity and metronidazol resistance.

Anti-Bacterial Agents↗

[Fecal flora in infants at the beginning and the end of hospitalization].

The feces of 52 children without diarrhea, aged from 5 days to 22 months, treated in the Department for various causes was investigated for the presence of that might be the cause of infectious diarrhea. Samples were taken at the beginning and the end of hospitalization. The results were analyzed with reference to 5 age subgroups (1 month, 2-3 months, 4-6 months, 7-12 months, 12-22 months) and duration of hospitalization (3-42 days). The presence of potentially pathogenic bacteria in the feces was found in 87% of children without diarrhea, especially at the beginning of hospitalization, which suggests the possible existence of a "transient carrier state". Because of the immaturity of a number of intra-organism mechanisms, the presence of pathogenic bacteria in the alimentary tract in the youngest children, may be a potential danger of developing serious, even generalized disease processes and may constitute an important source of nosocomial infections.

Clostridioides difficile↗

Toxigenicity of Clostridium difficile strains isolated in the surgical ward.

We report the use of the polymerase chain reaction (PCR) for the detection of toxigenic Clostridium difficile strains. PCR was performed as described (McMillin et al., 1991). The results obtained by PCR were compared with those of cytotoxicity assays and of the latex agglutination test. Twenty seven strains cultured from stool specimens of patients and five strains isolated from hospital environment in a surgical ward were investigated. Twenty five of 32 strains produced cytotoxin as shown on the McCoy cell-line (CA). Positive reaction in the latex test was observed in 20 strains supernatants. In 24 strains PCR revealed toxin B gene fragments (1.0 kb). In the 5 strains PCR did not detect toxin B fragments, and these strains were not cytotoxic on McCoy cells. We observed 2 strains toxin B gene fragment negative, which had a low cytotoxic activity on McCoy cells, and were toxin A gene fragment positive.

Base Sequence↗

[Occurrence of Bacteroides fragilis strains in full term and post term pregnancies].

Bacteroides fragilis (B.f.) is an aetiological agent of gynecological and obstetrical infections. The aim of this study was to determine occurrence of B.f. in women genital tract. A total number of 118 women in labor between 38 and 43 gestation age and not demonstrating clinical symptoms of infection was examined. B.f. strains were isolated from 9 women (15.9%). More often B.f. strains were isolated from women delivering post-term and staying previously in Pregnancy Pathology Ward. It was observed that infant mean weight on the 3rd day of life was higher in the vagina. The following features of isolates were compared: presence of the capsule and agglutination of sheet erythrocytes. Differences in haemagglutination and susceptibility to antibiotics were observed.

Bacteroides fragilis↗