Publication:
Detection of outer membrane porin protein, an imipenem influx channel, in Pseudomonas aeruginosa clinical isolates

dc.contributor.authorPenphun Naennaen_US
dc.contributor.authorPirom Noisumdaengen_US
dc.contributor.authorPintip Pongpechen_US
dc.contributor.authorChanwit Tribuddharaten_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-09-24T09:29:24Z
dc.date.available2018-09-24T09:29:24Z
dc.date.issued2010-05-01en_US
dc.description.abstractDecreased permeability to imipenem is the most frequent mechanism of imipenem resistance in Pseudomonas aeruginosa. We have determined the presence of OprD porin protein, an imipenem influx channel, in 70 carbapenem-resistant P. aeruginosa clinical isolates by Western blot analysis using rabbit anti-OprD polyclonal antibody. Ninety-eight percent (54 of 55 isolates) of imipenem-and meropenem-resistant P. aeruginosa clinical isolates were negative for OprD porin production. A small group of isolates resistant to imipenem but susceptible to meropenem (2 isolates) produced OprD protein but at a level 3-5 times lower than the wild type P. aeruginosa ATCC27853 strains. This study indicates that the loss of OprD porin protein was the main mechanism for imipenem resistance in P. aeruginosa clinical isolates. Determination of the status of OprD level in P. aeruginosa may help in the better selection of appropriate carbapenem antibiotics.en_US
dc.identifier.citationSoutheast Asian Journal of Tropical Medicine and Public Health. Vol.41, No.3 (2010), 614-624en_US
dc.identifier.issn01251562en_US
dc.identifier.other2-s2.0-77954698649en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/29690
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77954698649&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleDetection of outer membrane porin protein, an imipenem influx channel, in Pseudomonas aeruginosa clinical isolatesen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=77954698649&origin=inwarden_US

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