|LETTERS TO EDITOR
|Year : 2015 | Volume
| Issue : 4 | Page : 272-273
Study of biofilm production and antimicrobial sensitivity pattern of urinary tract infection causing Acinetobacter baumannii and Pseudomonas aeruginosa in a tertiary care hospital
Pragyan Swagatika Panda1, Uma Chaudhary1, Surya Kumar Dube2
1 Department of Microbiology, Pandit B.D. Sharma Post Graduate Institute of Medical Sciences, Rohtak, Haryana, India
2 Department of Neuroanaesthesiology, All Institute of Medical Sciences, New Delhi, India
|Date of Web Publication||20-Oct-2015|
Pragyan Swagatika Panda
Department of Microbiology, Pandit B.D. Sharma Post Graduate Institute of Medical Sciences, Rohtak, Haryana
Source of Support: None, Conflict of Interest: None
|How to cite this article:|
Panda PS, Chaudhary U, Dube SK. Study of biofilm production and antimicrobial sensitivity pattern of urinary tract infection causing Acinetobacter baumannii and Pseudomonas aeruginosa in a tertiary care hospital. Int J Health Allied Sci 2015;4:272-3
|How to cite this URL:|
Panda PS, Chaudhary U, Dube SK. Study of biofilm production and antimicrobial sensitivity pattern of urinary tract infection causing Acinetobacter baumannii and Pseudomonas aeruginosa in a tertiary care hospital. Int J Health Allied Sci [serial online] 2015 [cited 2020 Aug 6];4:272-3. Available from: http://www.ijhas.in/text.asp?2015/4/4/272/167655
Urinary tract infection (UTI) now-a-days is one of the most common nosocomial infections. Both Pseudomonasaeruginosa (PA) and Acinetobacterbaumannii (AB) can cause UTI and they have high potential to form biofilm that is responsible for their high survival potential, antibiotic resistance, and virulence. Contrary to previous belief, AB is an important emerging nosocomial pathogen worldwide and its infections have high mortality rates at present. But, studies on the biofilm production by UTI causing PA and AB are scarce. So we prospectively investigated biofilm production and antimicrobial susceptibility pattern of UTI causing PA and AB.
Total 50 isolates of PA and 10 isolates of AB from the nosocomial urinary samples were investigated for biofilm production by tissue culture plate assay. The antimicrobial susceptibility of the biofilm producing isolates was done by Kirby-Bauer disc diffusion technique. Biofilm production was detected in 58% and 70% isolates of PA and AB, respectively. All the biofilm producing PA and AB isolates were multidrug resistant (MDR). Both PA and AB isolates were highly resistant to ceftazidime, cefepime, gentamicin, and ciprofloxacin. However, in contrast to PA (highest sensitivity to imipenem), AB showed maximum sensitivity to piperacillin-tazobactam and netilimicin [Table 1].
|Table 1: Antibitotic resistance pattern of the biofilm producing Pseudomonas spp. (n = 29) Acinetobacter spp. (n = 7) as detected by TCP method|
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Biofilm production by PA and AB isolates were reported to be 75% and 66.7%, respectively, in previous studies. All (100%) the PA isolates in the study by Nagaveni et al. were resistant to cefepime, ceftazidime, and ciprofloxacin, which is higher than that in our study. The resistance to cefepime, ceftazidime by AB isolates in the study by Rao et al., were 30.9% and 36.3%, respectively, which is lower than that in our study. However, ciprofloxacin resistance in their study was similar to our study (72.7%). Moreover, the resistance of biofilm producing PA to imipenem has been reported to be 20%, which is similar to our study, result (27.5%). The resistance of biofilm producing AB to netilimicin has been reported to be 27.5%, which different from our study result (14.2%).
Gurung et al., reported a study similar to ours. However, the method used for biofilm detection in their study was less accurate (i.e. tube method) leading to detection of biofilm in only 25% of AB and 40% of PA isolates in contrast to our results. Secondly, they have studied biofilm production in various clinical isolates and the urinary sample in their study was only 10 in contrast to 60 isolates in our study. Lastly, among the biofilm producers 57% of PA and 73% of AB were MDR, but in our study all the biofilm producing isolates (100%) were MDR.
Thus, we conclude that biofilm production is very common among UTI causing PA and AB now-a-days and the biofilm producing PA and AB are MDR. The UTI causing MDR PA is sensitive to imipenem whereas, AB is sensitive to netilimicin and piperacillin-tazobactam.
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Conflicts of interest
There are no conflicts of interest.
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