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1.
Ter Arkh ; 72(6): 30-5, 2000.
Article in Russian | MEDLINE | ID: mdl-10900645

ABSTRACT

AIM: To investigate the spectrum of gram-negative agents causing acute and recurrent cystitis in outpatients and sensitivity of uropathogenic E. coli to antibacterial drugs; to compare drug resistance of uropathogenic E. coli isolated in Russia and other countries. MATERIAL AND METHODS: The spectrum of gram-negative bacteria was identified in 299 cases of acute and recurrent cystitis in Moscow, Smolensk and Novosibirsk. 271 E. coli uropathogenic strains were examined according to CA-SFM and NCCLS criteria for sensitivity to ampicilline, gentamycin, trimetoprim, co-trimoxasol, nitrofurantoine, nalidixic acid, pipemidine acid, norfloxacine, ciprofloxacine, nitroxoline. RESULTS: E. coli, K. pneumoniae, K. oxytoca, P. mirabilis, P. vulgaris caused acute and recurrent cystitis in 90.6, 6.4, 1, 1.7, 0.3% of the examinees, respectively. For Moscow relative agents were: E. coli (80.8%), K. pneumoniae (13.1%), K. oxytoca (2.3%), P. mirabilis (3.1%), P. vulgaris (0.7%). In Smolensk E. coli, K. pneumoniae, P. mirabilis were isolated in 96.3, 2.5 and 1.2%, respectively. E. coli occurred in 100% of Novosibirsk cases. Mean Russian values of the resistance to ampicilline, gentamycin, trimetoprim, co-trimoxasol, nitrofurantoin, nalidixic acid, pipemidine acid, norfloxacine, ciprofloxacine, nitroxoline were the following: 33.3, 5.9, 20.3, 18.4, 2.9, 5.5, 4.4, 2.6, 2.6 and 94.1%, respectively. Resistance to 2 and more drugs was registered in 18.4% of E. coli strains. CONCLUSION: Cystitis in women was in most cases caused by E. coli. The highest resistance among uropathogenic strains E. coli was observed to nitroxoline, ampicilline, trimetoprim and co-trimoxasole; maximal antibacterial activity against uropathogenic E. coli was shown by fluoroquinolones (norfloxacin and ciprofloxacin).


Subject(s)
Drug Resistance, Microbial , Gram-Negative Bacteria/drug effects , Gram-Negative Bacterial Infections/microbiology , Outpatients , Urinary Tract Infections/microbiology , Anti-Bacterial Agents , Drug Therapy, Combination/therapeutic use , Female , Gram-Negative Bacteria/isolation & purification , Gram-Negative Bacterial Infections/drug therapy , Gram-Negative Bacterial Infections/epidemiology , Humans , Incidence , Microbial Sensitivity Tests , Outpatients/statistics & numerical data , Russia/epidemiology , Urinary Tract Infections/drug therapy , Urinary Tract Infections/epidemiology , Urine/microbiology
2.
FEMS Microbiol Lett ; 184(2): 215-8, 2000 Mar 15.
Article in English | MEDLINE | ID: mdl-10713423

ABSTRACT

A simple technique providing a means for rapid genetic differentiation of chlamydial strains is described. The technique is based on a single-step sequence-specific separation of PCR-amplified DNA fragments by electrophoresis in an agarose gel containing a DNA ligand - bisbenzimide-PEG. A hypervariable region at the 5' end of the omp2 gene of Chlamydiaceae species encoding the 60-kDa cysteine-rich outer membrane protein was selected as a target for PCR. The appropriate fragments were amplified from strains of Chlamydia trachomatis, Chlamydophila pneumoniae, and Chlamydophila psittaci, and the PCR products originating from different species were electrophoretically separated in the presence of the DNA ligand. We therefore demonstrated that PCR with a single pair of primers followed by simple agarose gel electrophoresis with bisbenzimide-PEG can be applied to the differentiation of three members of the family Chlamydiaceae which are commonly recognized as human pathogens.


Subject(s)
Bacterial Outer Membrane Proteins/genetics , Chlamydiaceae/classification , Chlamydiaceae/genetics , Electrophoresis, Agar Gel/methods , Polymerase Chain Reaction/methods , Animals , Bisbenzimidazole/analogs & derivatives , Chlamydia trachomatis/classification , Chlamydia trachomatis/genetics , Chlamydophila pneumoniae/classification , Chlamydophila pneumoniae/genetics , Chlamydophila psittaci/classification , Chlamydophila psittaci/genetics , DNA, Bacterial/analysis , Genetic Variation , Humans , Polyethylene Glycols , Polymorphism, Restriction Fragment Length , Species Specificity
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