Title of article :
Prevalence of AmpC β-lactamase in Clinical Isolates of Escherichia coli,
Klebsiella spp., and Proteus mirabilis in a Tertiary Hospital in Tehran,
Iran
Author/Authors :
Saffar، Hiva نويسنده Department of Pathology, Shariati Hospital, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran , , Asgari Niaraki، Neda نويسنده Department of Microbiology, Islamic Azad University,
Varamin Pishva, IR Iran , , Ghahroudi Tali، Arash نويسنده Department of Pathology and Laboratory Medicine, Tehran
University of Medical Sciences, Tehran, IR Iran , , Baseri، Zohre نويسنده Department of Pathology and Laboratory Medicine, Shariati Hospital, Tehran University of Medical Sciences,Tehran, Iran Baseri, Zohre , Abdollahi، Alireza نويسنده , , Yalfani، Rouzbeh نويسنده Department of Microbiology, Islamic Azad University,
Varamin Pishva, IR Iran ,
Abstract :
AmpC β-lactamase confers resistance to a variety of β-lactam
agents, and all plasmid-mediated AmpC genes are considered clinically
significant. The transfer of the AmpC gene to plasmid has resulted in
dissemination among the Enterobacteriaceae family, including Escherichia
coli, Klebsiella spp., and Proteus mirabilis. The prevalence of
plasmid-mediated AmpC genes was determined in isolates of E. coli,
Klebsiella spp., and P. mirabilis with reduced susceptibility to
cefoxitin or extended-spectrum cephalosporins by the multiplex PCR
method. A total of 310 consecutive non-duplicate isolates of E. coli,
Klebsiella spp., and P. mirabilis were obtained from various clinical
specimens. Isolates with positive screening test results were subjected
to further molecular evaluation. Fifty isolates were positive on the
screening test. Among them, positive PCR reactions were identified in
35/221 and 12/77 isolates of E. coli and Klebsiella spp., respectively,
including 16 (34.0%) for CIT only, 7 (14.8%) for DHA only, and 24
(51.0%) for both DHA and CIT. No isolate was positive for FOX or MOX. No
Proteus organism was positive for AmpC genes. Currently, phenotypic
tests are unable to accurately and reliably recognize plasmid-mediated
AmpC β-lactamase-producing organisms. Although not possible for routine
testing, clinical laboratories, especially in referral centers, should
employ molecular testing for surveillance studies.