Egyszerű nézet

dc.contributor.author Juhász, Emese
dc.contributor.author Pongrácz, Júlia
dc.contributor.author Iván, Miklós
dc.contributor.author Kristóf, Katalin
dc.date.accessioned 2016-09-14T10:58:19Z
dc.date.available 2016-09-14T10:58:19Z
dc.date.issued 2015
dc.identifier.citation pagination=295-305; journalVolume=62; journalIssueNumber=3; journalTitle=ACTA MICROBIOLOGICA ET IMMUNOLOGICA HUNGARICA;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/2246
dc.identifier.uri doi:10.1556/030.62.2015.3.7
dc.description.abstract Sulfamethoxazole-trimethoprim (SXT) is the drug-of-choice in Stenotrophomonas maltophilia caused infections. There has been an increase in resistance to SXT of S. maltophilia over recent years. In this study 30 S. maltophilia clinical isolates resistant to SXT were investigated. Antibiotic susceptibilities for ciprofloxacin, moxifloxacin, levofloxacin, doxycycline, tigecycline, ceftazidime, colistin and chloramphenicol were determined by broth microdilution method. None of the strains were susceptible to ciprofloxacin, tigecycline, ceftazidime or colistin. Only 37% of the isolates were susceptible to levofloxacin or moxifloxacin. Two isolates resistant to all tested antibiotic agents and two others susceptible only to doxycycline were further investigated: susceptibility for combinations of antibiotics was analyzed by checkerboard technique. According to the fractional inhibitory concentration indices calculated, moxifloxacin plus ceftazidime combination was found to be synergistic in each case. Genetic testing revealed the predominance of sul1 gene. Our study concluded that the range of effective antibiotic agents is even more limited in infections caused by SXT-resistant S. maltophilia. In these cases, in vitro synergistic antibiotic combinations could be potential therapeutic options.
dc.relation.ispartof urn:issn:1217-8950
dc.title ANTIBIOTIC SUSCEPTIBILITY OF SULFAMETHOXAZOLE-TRIMETHOPRIM RESISTANT STENOTROPHOMONAS MALTOPHILIA STRAINS ISOLATED AT A TERTIARY CARE CENTRE IN HUNGARY
dc.type Journal Article
dc.date.updated 2015-10-30T11:21:54Z
dc.language.rfc3066 en
dc.identifier.mtmt 2960885
dc.identifier.wos 000361849200007
dc.contributor.department SE/AOK/I/Laboratóriumi Medicina Intézet
dc.contributor.institution Semmelweis Egyetem


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