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Biomedical subjects

G Bieth

Publications and source records attributed to G Bieth.

14 recordsLinked to original sources
PubMed1984

Translocation of antibiotic resistance markers of a plasmid-free Streptococcus pyogenes (group A) strain into different streptococcal hemolysin plasmids.

Wild-type strain A454 (Streptococcus pyogenes) transferred en bloc its erythromycin (Em) and tetracycline (Tc) resistance markers into several plasmid-free streptococcal recipients. No plasmid DNA was detected in either the wild-type or the transconjugant strains. Crosses were performed between A454 and S. faecalis Rec+ or Rec- recipients carrying hemolysin-bacteriocin plasmids, pIP964 or pAD1 . The Em Tc-resistant transconjugants obtained harbored either the parental plasmid or an Em Tc resistance plasmid derived from pIP964 or pAD1 . The restriction endonuclease analysis of 12 derivative plasmids showed insertions of various sizes into different fragments of pIP964 or pAD1 . A454 and the Em Tc-resistant plasmid-free transconjugants were found to contain two EcoRI DNA fragments, that shared homology with 32P-labeled pIP1077 , one of the Em Tc resistance derivative plasmids, but not with 32P-labeled pIP964 . No homology was detected between pIP1077 and the cellular DNA of the antibiotic-susceptible recipients.

Conjugation, Genetic↗
PubMed1984

Broad host range of streptococcal macrolide resistance plasmids.

Four macrolide-lincosamide-streptogramin B resistance plasmids transferred into 13 recipients belonging to Streptococcus, Staphylococcus, and Listeria genera. The plasmids were stably maintained in all new hosts except Streptococcus sanguis, Streptococcus pneumoniae, Staphylococcus aureus, and Listeria innocua and were identical to those found in the corresponding donor strains.

Anti-Bacterial Agents↗
PubMed1982

High-level aminoglycoside resistance in group A, B, G, D (Streptococcus bovis), and viridans streptococci.

Of 20 clinical isolates of group A, B, G, D (Streptococcus bovis), and viridans streptococci, 5 transferred their antibiotic resistance markers into streptococcal recipients at a low frequency (10(-4) to 10(-8)) in the apparent absence of extrachromosomal elements. All strains carried genetic markers for high-level resistance to streptomycin, kanamycin, neomycin, lividomycin A, and ribostamycin, as well as resistance to macrolides and related drugs, tetracycline, and chloramphenicol.

Aminoglycosides↗
PubMed1982

[Antibiotic resistance genetic basis of human origin streptococci (author's transl)].

One hundred strains of group A, B, C, D (S faecalis, S. faecium, S. bovis) F, G, S. pneumoniae and viridans streptococci were studied. All these strains were clinical isolates from infective endocarditis and fron upper respiratory, skin, genital and urinary tract infections. These stains were resistant to one or several antibiotics : tetracycline, macrolide and related drugs, chloramphenicol, aminoglycosides (high-level resistance to streptomycin, kanamycin, gentamicin), and penicillin. Conjugative transfer of antibiotic resistance markers (except penicillin) into streptococcal recipients was obtained at a high frequency (10(-1) to 10(-4)) for 12 strains and at a low frequency (10(-5) to 10(-8)) for 29 strains. R plasmids carrying various groups of resistance markers were isolated with different molecular weights. Enzyme restriction analysis showed the existence of different molecular species of streptococcal plasmids. All attempts to detect extrachromosomal DNA in 17 wild-type strains and in the corresponding transconjugants were unsuccessful.

Anti-Bacterial Agents↗
PubMed1981

Conjugative R plasmids in group C and G streptococci.

Two streptococcal isolates of groups C and G harbored conjugative R plasmids with molecular weights of 17 X 10(6) (pIP646) and 20 X 10(6) (pIP920). These plasmids carried genetic markers for resistance to macrolides and related drugs, as well as to chloramphenicol (pIP920), and have very similar HindIII restriction enzyme patterns.

Conjugation, Genetic↗
PubMed1979

High-level, plasmid-borne resistance to gentamicin in Streptococcus faecalis subsp. zymogenes.

Each of three isolates of Streptococcus faecalis subsp. zymogenes harbored three R plasmids and a hemolysin-bacteriocin plasmid. The plasmids carried by one of these strains were physically characterized after their conjugative transfer. In each strain one of the plasmids carried genetic markers for resistance to gentamicin, kanamycin, sisomicin, netilmicin, and tobramycin.

Anti-Bacterial Agents↗
PubMed1976

R plasmids in Streptococcus agalactiae (group B).

Two plasmids determining resistance to tetracycline (RIP500) and to chloramphenicol, erythromycin, lincomycin, and pristinamycin I (RIP501) were isolated from a strain of Streptococcus agalactiae. The frequency-of-resistance loss is very low for RIP500 (<3 x 10(4)) but higher for RIP501 (the efficiency was dependent upon the curing agents and incubation temperature and varied between 0.5 and 96%). Derivatives susceptible to all drugs were also obtained. RIP500 and RIP501 have similar molecular weights (17.9 x 10(6) and 20 x 10(6), respectively) and represent different percentages of total deoxyribonucleic acid (0.4 and 4%, respectively). The number of copies of RIP500 and RIP501 per cell is different, and these plasmids are likely replicated under different kinds of control (stringent and/or relaxed). No plasmid deoxyribonucleic acid was found in a derivative of strain B96 susceptible to all drugs.

Centrifugation, Density Gradient↗
PubMed1976

[Identification of two plasmids isolated from a bacteriocinogenic strain of Clostridium perfringens].

Two plasmids were found and studied in the bacteriocinogenic strain N5 of Clostridium perfringens: one is a bacteriocinogenic factor (MW=5.7 X 10(6)) and the other a cryptic plasmid (MW 32.4 X 10(6)). Simultaneous loss of the ability to produce bacteriocin and of the bacteriocin resistance in a "cured" variant corresponds to the loss of the bacteriocinogenic plasmid DNA. The syntheses of haemolysin 0 and phospholipase C do not seem to be coded for by the cryptic plasmid.

Acriflavine↗
PubMed1975

Physical studies of a plasmid mediating tetracycline resistance and hydrogen sulfide production in Escherichia coli.

Tetracycline resistance and hydrogen sulfide production have been previously found to be plasmid-mediated in a naturally-occurring strain of Escherichia coli; both functions are specified by a single conjugative plasmid called pIP231(Te-H2S); pIP231DNA was isolated as covalently closed molecules in dye-buoyant density gradients. The base ratio of the DNA was found to be 50% GC by density gradient analysis. Electron micrographs of plasmid molecules showed a contour length of 20 +/- 2 mum (40 +/- 4 X 10(6) daltons). Between one and two copies of pIP231 molecules per host chromosome were found in E. coli K12.

Base Sequence↗
PubMed1975

[Plasmids controlling the resistance to several antibiotics in C. perfringens type A, strain 659].

A strain of C. perfringens type A, isolated from a patient, was found to be resistant to four antibiotics: tetracycline (Tet), chloramphénicol (Chl), erythromycin (Ero) and clindamycin (Cli). Clones resistant to only two drugs (Tet-Chl or Ero-Cli), or sensitive to all drugs were found in cultures of the wild-type strain treated by acridine dyes or ethidium bromide. DNA analysis by equilibrium centrifugation confirmed that the original strain contains two resistance plasmids, one called Rip 401 (Tet-Chl) and the other Rip 402 (Ero-Cli), which represent respectively 1.8 +/- 0.2% and 2.3 +/- 0.2% of the total amount of DNA in this strain of Cl. perfrigens.

Centrifugation, Isopycnic↗
PubMed1975

[Tetracycline resistance in Haemophilus influenzae is plasmid-linked].

A strain of Haemophilus influenzae resistant to tetracycline (MIC 16-32 mug/ml) was "cured" of tetracycline resistance by ethidium bromide. DNA centrifugation in cesium chloride + ethidium bromide density gradients showed the existence of a band of non-chromosomal DNA molecules in the original resistant strain. This band was not found in lysates of a strain "cured" of tetracycline resistance by ethidium bromide. These facts support the hypothesis that in this strain of Haemohpilus influenzae, tetracycline resistance is plasmid mediated.

Centrifugation, Density Gradient↗
PubMedDate not supplied

Physical studies of a Staphylococcus aureus plasmid mediating resistance to streptogramins, lincosamins and aminoglycosides.

Previous studies have demonstrated that resistance to three groups of drugs (streptogramins, lincosamins and aminoglycosides) was plasmid borne in a clinical isolate of Staphylococcus aureus. This plasmid, referred to as pIP524, was transferred in mixed culture or transduced into a plasmid-free host and analyzed for size, molecular weight and replication control. Plasmid pIP524 is a new member of the class of "large" plasmids (8.5 micrometer) isolated from S. aureus and represents up to 7% of total DNA. Some evidence indicates that the number of copies of pIP524 and of plasmids of the same size--penicillinase plasmids--are similar (up to 10 per cell).

Anti-Bacterial Agents↗