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1.
Int Microbiol ; 14(1): 51-8, 2011 Mar.
Article in English | MEDLINE | ID: mdl-22015702

ABSTRACT

This study explored the evolutionary mechanism by which the clinical isolate PA110514 yields the imipenemresistant derivative PA116136. Both isolates were examined by PFGE and SDS-PAGE, which led to the identification of a new insertion sequence, ISPa133. This element was shown to have distinct chromosomal locations in each of the original isolates that appeared to explain the differences in imipenem susceptibilty. In strain PA110514, ISPa133 is located 56 nucleotides upstream of the translational start codon, which has no effect on expression of the porin OprD. However, in strain PA116136 ISPa133 it is located in front of nucleotide 696 and, by interrupting the coding region, causes a loss of OprD expression, thus conferring imipenem resistance. In vitro experiments mimicking the natural conditions of selective pressure yielded imipenem-resistant strains in which ISPa133 similarly interrupted oprD. A mechanism is proposed whereby ISPa133 acts as a mobile switch, with its position in oprD depending on the degree of selective pressure exerted by imipenem.


Subject(s)
Anti-Bacterial Agents/pharmacology , Carbapenems/pharmacology , DNA Transposable Elements , Pseudomonas aeruginosa/drug effects , Pseudomonas aeruginosa/genetics , beta-Lactam Resistance , Codon, Initiator , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , Electrophoresis, Gel, Pulsed-Field , Electrophoresis, Polyacrylamide Gel , Gene Expression , Gene Expression Regulation, Bacterial , Gene Knockout Techniques , Humans , Molecular Sequence Data , Mutagenesis, Insertional , Proteome/analysis , Pseudomonas Infections/microbiology , Pseudomonas aeruginosa/isolation & purification , Sequence Analysis, DNA
2.
Int. microbiol ; 14(1): 51-58, mar. 2011. ilus, tab
Article in English | IBECS | ID: ibc-94606

ABSTRACT

This study explored the evolutionary mechanism by which the clinical isolate PA110514 yields the imipenemresistant derivative PA116136. Both isolates were examined by PFGE and SDS-PAGE, which led to the identification of a new insertion sequence, ISPa133. This element was shown to have distinct chromosomal locations in each of the original isolates that appeared to explain the differences in imipenem susceptibilty. In strain PA110514, ISPa133 is located 56 nucleotides upstream of the translational start codon, which has no effect on expression of the porin OprD. However, in strain PA116136 ISPa133 it is located in front of nucleotide 696 and, by interrupting the coding region, causes a loss of OprD expression, thus conferring imipenem resistance. In vitro experiments mimicking the natural conditions of selective pressure yielded imipenem-resistant strains in which ISPa133 similarly interrupted oprD. A mechanism is proposed whereby ISPa133 acts as a mobile switch, with its position in oprD depending on the degree of selective pressure exerted by imipenem (AU)


No disponible


Subject(s)
Humans , Carbapenems/pharmacokinetics , Drug Resistance, Microbial , Pseudomonas aeruginosa/genetics , Microbial Sensitivity Tests/methods , Pseudomonas Infections/microbiology , DNA Transposable Elements
3.
Article in Es | IBECS | ID: ibc-28865

ABSTRACT

En el presente trabajo se valora la eficacia antibacteriana del colutorio Tantum verde® y la de su, presuntamente, único principio activo, la bencidamina clorhidrato. Para ello, se ensayó la actividad in vitro de la bencidamina HCl y del Tantum verde mediante la obtención de las correspondientes CMI (Concentración Mínima Inhibitoria) siguiendo la técnica de la dilución en medio sólido. Inicialmente, se estudiaron ocho cepas de uso común en el laboratorio y, posteriormente, el estudio fue ampliado a cepas de patógenos bucales aisladas de muestras clínicas. Los estudios realizados, demuestran una eficacia bactericida real frente a patógenos bucales pertenecientes a géneros tales como Actinomyces, Bacillus, Actinobacillus, Veillonella o Streptococcus. Además, el Tantum verde como colutorio posee, en general, una mayor actividad antibacteriana que la demostrada por su principal principio activo, la bencidamina HCl, por lo que cabe pensar que la presencia de etanol a baja concentración, en su composición contribuye de forma notable a la acción antibacteriana (AU)


Subject(s)
Humans , Benzydamine/therapeutic use , Anti-Inflammatory Agents/therapeutic use , Anti-Infective Agents/therapeutic use , Gram-Negative Bacteria , Gram-Positive Bacteria , Drug Evaluation , Microbial Sensitivity Tests
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