Antibiotic sensitivity of Stenotrophomonas maltophilia in a 5-year

Introduction: Stenotrophomonas maltophilia, which is able to form a biofilm, has mostly been related to catheters when it is the agent in hospital infections; these infections generally present as bacteremia and pneumonia, which may progress with complications and result in death. Methodology: The s...

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Bibliographic Details
Main Authors: Caliskan, A, Cicek, AC, Ejder, NA, Karagoz, A, Kirisci, O, Kilic, S
Format: Article in Journal/Newspaper
Language:English
Published: J INFECTION DEVELOPING COUNTRIES 2019
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Online Access:http://hdl.handle.net/11499/32156
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Summary:Introduction: Stenotrophomonas maltophilia, which is able to form a biofilm, has mostly been related to catheters when it is the agent in hospital infections; these infections generally present as bacteremia and pneumonia, which may progress with complications and result in death. Methodology: The study included 153 S. maltophilia strains isolated from clinical samples sent to our hospital laboratory between 1 January 2014 and 30 June 2018. The bacteria were identified and their antibiotic sensitivity was determined using the VITEK-2 automated system. PFGE (Pulsed Field Gel Electrophoresis): The strains isolated from 34 patient clinical samples and from 1 patient bedcover were taken for PFGE examination. Results: The TMP/SXT and levofloxacin sensitivity of 153 S. maltophilia strains was examined. TMP/SXT resistance was determined to be 39% and levofloxacin resistance at 5%. Among 35 S. maltophilia strains, seven genotypes were identified using the PFGE method. While three strains showed a specific genotype profile, the other 32 were determined to consist of four clusters. The cluster rate was therefore 91.4% (32/35). Conclusions: There was a clonal relationship between the vast majority of the 35 S. maltophilia isolates, which suggests that there was a cross-contamination problem in the hospital. One strain (#4) was identified by dendrogram analysis showed a high rate of similarity to the other strains and was determined to be the common source of the cross-contamination. C1 [Caliskan, Ahmet] Pamukkale Univ, Fac Med, Dept Med Microbiol, Denizli, Turkey. [Cicek, Aysegul Copur; Ejder, Nebahat Aydogan] Recep Tayyip Erdogan Univ, Fac Med, Dept Med Microbiol, Rize, Turkey. [Karagoz, Alper] Usak Univ, Dept Microbiol Mol Biol & Genet, Usak, Turkey. [Kirisci, Ozlem] Necip Fazil City Hosp, Microbiol Lab, Kahramanmaras, Turkey. [Kilic, Selcuk] Publ Hlth Inst Turkey, Microbiol Reference Labs Dept, Ankara, Turkey.