Title of article :
Clinical Isolates of Acinetobacter baumannii From Tehran
Hospitals: Pulsed-field Gel Electrophoresis Characterization, Clonal Lineages,
Antibiotic Susceptibility, and Biofilm-forming Ability
Author/Authors :
Behmanesh Mehrdad نويسنده , Najar-Peerayeh Shahin نويسنده Department of Bacteriology, Tarbiat Modares University, Tehran, IR Iran , Taherikalani Morovat نويسنده Clinical Microbiology Research Center, Ilam University of Medical Sciences, Ilam, IR Iran , Akbari Dehbalaei Mahdi نويسنده Department of Bacteriology, Faculty of Medical Sciences,
Tarbiat Modares University, Tehran, Iran
Abstract :
Background Acinetobacter baumannii is known as
a potential pathogen in hospitals and is responsible for the dramatic
increase in carbapenem resistance in Iran in the recent years.
Objectives The current study aimed at determining the genetic
association of the isolates by the pulsed-field gel electrophoresis
(PFGE) technique, identify international clones, evaluate biofilm
formation ability and its relationship with antibiotic resistance.
Methods In the current study, a total of 48 A.
baumannii isolates were collected from 2 hospitals in Tehran,
Iran, from 2010 to 2012. Isolates were subjected to antimicrobial
susceptibility testing, determination of carbapenemase encoding genes,
biofilm formation, and genetic relationships analysis. Results The
obtained results demonstrated that the rate of resistance to carbapenem,
meropenem, imipenem, and doripenem was 76%. The carbapenemase-encoding
gene
blaOXA-23-like
was found in 32 isolates, while
blaOXA-40-like
(blaOXA-24-like),
blaOXA-58-like,
blaVIM-type
and
blaIMP-type
were found in 11, 1, 19. and 5 isolates, respectively. When the lineage
of the isolates was evaluated by the multiplex polymerase chain reaction
(PCR), it was found that 28 isolates belonged to group 1 and 8 isolates
to group 2. None of the isolates belonged to group 3. Twelve isolates
could not be typed by this method. The study findings interestingly
demonstrated that 13 isolates showed no biofilm formation. Data of
biofilm formation also demonstrated that 28, 4, and 3 remaining isolates
had weak, moderate, and strong biofilm formation, respectively. The
pulsed field gel electrophoresis result revealed 11 unique clones.
Conclusions International clone 1 was the most commonly identified clone
in the current study. This clone was mostly associated with
blaOXA-23-like
gene; therefore, 64% of the isolates in this clone possessed
blaOXA-23-like
gene.