Author/Authors :
Malekan, Mohammadali Microbiology Research Center - Pasteur Institute of Iran, Tehran, Iran , Tabaraie, Bahman Kousha Faravar Giti - Industrial Research Institute of Biotechnology, Tehran, Iran , Akhoundtabar, Ladan Department of Microbiology - Azad University of Jahrom, Jahrom, Iran , Behrouzi, Ava Department of Mycobacteriology and Pulmonary Research - Pasteur Institute, Tehran, Iran
Abstract :
Background: Stenotrophomonas maltophilia (S. maltophilia) is a multiple-antibioticresistant
opportunistic pathogen that is being isolated with increasing frequency from
patients with health-care-associated infections. S. maltophilia is inherently resistant to
most of the available antimicrobial agents. Spread of resistant strains has been attributed,
in part, to class I integrons. In vitro susceptibility studies have shown trimethoprim-
sulfamethoxazole and new floroquinolones as two important agents with activity
against these organisms.
Methods: 150 isolates of S. maltophilia were isolated from clinical samples such as respiratory
discharges, sputum, and catheter and hospital environments. These isolates
were also subjected to susceptibility testing and polymerase chain reaction for four
groups of genes including int encoding integron elements, sulI and sulII encoding trimethoprim-
sulfamethoxazole resistance and smqnr encoding quinolone resistance.
Results: The rate of resistance to trimethoprim-sulfamethoxazole was up to 27 (18%)
and the highest resistance to quinolone family belonged to ofloxacin (20%) and the
lowest rate was for gatifloxacin (16%). The results showed that 14% of isolates contained
integron elements concomitantly with sulI and sulII genes.
Conclusion: Resistance rate of S. maltophilia to co-trimoxazole and fluoroquinolones
and detection of integron elements between isolates in this study showed that this
rate corresponded to other data obtained from other studies.