Received 4 August 2016; accepted 14 March 2016; published 17 March 2016
1. Introduction
P. aeruginosa is a gram-negative, aerobic, rod shaped bacterium with unipolar Motility, which is the main cause of prevalent hospital infections [1] [2] . It is recognized as a serious opportunistic pathogen that causes infections in hospitalized patients [3] [4] . The symptoms of these infections are generalized inflammation and sepsis. Particularly in burns patients where the skin host defenses are destroyed [5] [6] , orthopedic related infection, respiratory disease [7] , corneal infections caused by contact lens user [8] , corneal ulceration [8] , patient with impaired immune defense [9] [10] including HIV infection [11] [12] and, also is the most frequent colonizer in medical devices [13] . P. aeruginosa causes clinical problem as a result of its high resistance to a large rang of antibiotics [14] and may demonstrate additional resistance after unsuccessful treatment. Indeed treatment of P. aeruginosa infections in most cases should be conflicted, due to the resistance of these bacterial species and further acquired resistance to extensive range of antibiotics [3] . P. aeruginosa frequently displays resistance to multiple antimicrobial agents [15] [16] . Gentamycine is the only antibacterial agent through which pseudomonas strains are remains sensitive against it. There are different ranges of cross resistance between Carbencilin, Polymaxin, Colistin, Streptomycin, Quinolones, Cephalosporin against it reported [14] [17] . Therefore, antimicrobial resistance is a growing problem worldwide, especially in hospitals. Serious infections due to P. aeruginosa strains that exhibit resistance patterns to most common antibacterial agents are increasingly serious problems [16] . In this regard, the Pseudomonas areuginosa resistance pattern against antibiotics has not been studied in Urmia, Iran. We aimed to determine sensitivity and resistance patterns of P. aeruginosa against various antibiotics among clinical samples of educational Hospitals of Iran, Urmia University of medical science in western of Iran.
2. Material and Methods
2.1. Study Setting
A cross-sectional study during March 2009 to September 2011was performed. This study was conducted in the Internal, surgery, burns and transplantation ward of educational hospitals of Urmia University of medical science, Iran. Indeed we examined 233 clinical samples were collected from different clinical sampling from wound swab, urine samples, blood, trachea samples, eye swabs, ear swabs and pus from their patients then examined. All procedures of this investigation performed with the approval of the scientific and ethical board of this college, and patient consent form signed with each subjects for permission to use of their samples as case of study.
Isolation and identification of Pseudomonas aeroginousa
For these sample processing, in sterill condition, Nutrient agar, Mac Conkey agar and blood agar used for each samples. All plates incubated at 37˚C for 24 h. After incubation periodto obtain pure cultures according to Chessborough (Cheesborough 2002 based protocol), single pure colonies were subcultured. Then pure samples used To isolation and Different identification tests of Pseudomonas aeruginosa strains using macroscopic and microscopic biochemical methods Based on Bergey’s manual of determinative bacteriology that describes Pseudomonas aeruginosa Oxidative and non-fermentative strain, with positive oxidase reaction, citrate utilization test, production of green pigment (Pyocyanin) on Mueller-Hinton agar medium.
2.2. Antibiotic Susceptibility Test
Antibiotics MIC with Agar dilution methods was determined. In this way isolates based on disk diffusion method (using Kirby-baur method) with common and valid Antibiotics on Mueller-Hinton agar (Mueller-Hinton agar Formula/Liter: Beef Extract: 2 g, Acid Hydrolysate of Casein: 17.5 g, Starch: 1.5 g, Agar: 17 g, Final pH 7.3 ± 0.1 at 25˚C) medium, antibiotic susceptibility pattern according to Clinical Laboratory Standard Institute (CLSI) principals (NCCLS 2011) was determined [18] . Paper disk were smeary with antibiotics: Amikacin (30 ug), Gentomycin (10 μg), Imipenem (10 μg), Sparfloxacin (5 μg), Ceftazidime (30 μg), Piperacilin (100μg), Nalidik acid (30 ug), Ceftizoxime (30 μg), Ceftriaxone (30μg), Carpencilin (100 μg) and Trimtoprine (5 μg) Solfametoxasole (23.75 μg) and incubated at 37˚C for 18 hours. We determined the diameter of zone of inhibition as sensitive and semi-sensitive and resistance patterns of P. aeruginosa against different antibioticsbased on CLSI guidelines (NCCLS 2011).
Statistical analysis
Statistical analysis performed with SPSS (ver.18) software, data were reported as mean ± SD for continuous variables.
3. Results
Our study takes almost two years during March 2009 to September 2011.233 samples were isolated from wound swab, urine, trachea, eye swabs, ear swabs and pus of patients.
From Imam Khomeini Hospital, Urmia. Iran, Isolation rates of Pseudomonas aeruginosa according to departments presented in Table 1.
The mean age of the patients was 35.4 ± 14.5 years old and most of the patients were more than 34 years old. 81% were female and the remaining (18.2%) were male. 20.9% patients were illiterate, 20% had studied until the elementary level, 11% attained guidance school, 12% attained high school, 35% had diplomas, and 1.1% patients had an academic degree. Data shown sixty samples were positive to Pseudomonas aeruginosa. Also 25.75% of samples were resistant to all antibiotic, which the majority of them found in Transplantation ward. The resistance pattern against Cefotaxime (94.34%), Ceftazidim (95.68%), Nalidixic acid (95.32%), Gentamycine (79.23%), Carpencilin (81.54%) and Piperacilin (94.37%) was also observed in this study. The maximum antibiotic resistance 99.5% was observed against Trimtoprine Solfametoxole. The most effective antibiotics (sensitive pattern) for P. aeruginosa were Ciprofloxacin (55.33%), Amikacin (61%) and Imipenem (33%). Resistance pattern rate (%) of Pseudomonas aeruginosa against antibiotics presented in Figure 1.
4. Discussion
P. aeruginosa emerged as an important pathogen and was reasonable for nosocomial infections. So, that is one of the important causes of morbidity and mortality among Hospital patients [3] [4] [19] . The current study showed that P. aeruginosa was highly prevalent in clinical samples of urine and pus, was also observed in Arshi, et al. and Murase et al. study [20] [21] . This study shows that P. aeruginosa resistant rate against Gentamycin was 79.23%, while reports of the susceptibility of P. aeruginosa against Gentamycin in different studies have ranged from 49.8%, in Greek to as high as 96.6% in the United Kingdom [22] and in another study, in 1988, from Turkey, it was reported that 54% of gram negative Bacilius were resistant to Gentamycin [23] . This survey shown
Table 1.Isolation rates of Pseudomonas aeruginosa according to departments.
Figure 1. Resistance rate (%) of Pseudomonas aeruginosa against Antibiotics.
in our population study samples analysis revealed resistant patterns to Ceftazidime (95.67%), while, according to different reports, resistance to Ceftazidime was 15% - 22% in the world, also Resistance to Ceftriaxime, Ceftriaxon and Nalidik acid are significant in our study (99.37, 94.37, 95.32 respectively). Previous studies suggested that selective pressure from the use of anti-microbial agents is a major determinant for the emergence of resistant strains [24] - [26] that could be considerable. Our results indicated that the rate of ciprofloxacin resistance pattern against P. aeruginosa was found to be relatively high percent in our population. Other studies show that ciprofloxacin resistance pattern was 23% in Spain [27] , 31.9% in Italy [28] and 26.8% in Latin America [29] . Overall results show that the rate of P. aeruginosa antibiotic resistance was observed in highest rate in case of Trimetoprime Solfametaxasole, while, Ciprofloxacin, Imipenem and Amikacin were identified as the most effective antibiotics in this study against P. aeruginosa. In previous studies it was reported that resistance to Imipenem was 14% in Spain [27] , 19.3% in Italy [28] and 68% in Saudi Arabia [30] that approved with our results. Previous studies show that antibacterial effects of Amikacin against pseudomonal were greater than Gentamycin [23] [31] and only 0.9% resistant reported to Amikacin in Turkey [23] . So, Amikacin is effective antibiotic against P. aeruginosa in their study. In current study, resistance pattern to Piperacillin was also higher, while Piperacillin resistance rate was 10% in Spain [27] , 12% in Italy [28] , 14% in Latin American population [29] . Indeed P. aeruginosa strains Infections, most be treated as soon as possible due to their severe resistance against antibiotics. We have to apply an accurate antibiotic treatment discipline, according to the findings based on antibiogram method in order to prevent its spread. Data showed that this bacterium has developed its resistance pattern against amikacin and Ciprofloxacin in comparison to previous years. So the use of effective infection control practices can go a long way to limiting the development and spread of antimicrobial resistance ensuring that these agents continue to find a place in treatment of P. aeruginosa infections and also, hospital infection monitoring committee needs to force the tasks of more severe monitoring on hospital pathogens and bacterial resistance pattern development studies as important objectives to finding effective antibiotics against P. aeruginosa.
NOTES
*Corresponding author.