Isolation, identification and antimicrobial susceptibility pattern of uropathogens isolated at a tertiary care centre

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International Journal of Current Microbiology and Applied Sciences ISSN: 2319-7706 Volume 4 Number 10 (2015) pp. 951-955 http://www.ijcmas.com Original Research Article Isolation, identification and antimicrobial susceptibility pattern of uropathogens isolated at a tertiary care centre Preeti B. Mindolli 1 *, Manjunath P. Salmani 2 and Yasmeen Kausar 1 1 Department of Microbiology, Al Ameen Medical College, H&RC, Athani Road, Vijaypur-586108, Karnataka, India 2 Department of Microbiology, Shri B.M. Patil Medical College, H&RC, Solapur Road, Vijaypur-586103, Karnataka, India *Corresponding author A B S T R A C T K eywo rd s UTI; Animicrobial susceptibility; Kirby-Bauer disc diffusion method; Uropathogens Urinary tract infection (UTI) is one of the most common infections occurring in the hospital. The organisms causing UTI vary from place to place and time to time. The aim of present study was to analyse the prevalence and antimicrobial sensitivity pattern of various pathogens causing UTI. It is a retrospective study carried out from January June 2015 at Al-Ameen Medical College, Vijaypur, Karnataka, a tertiary health care centre. A total of 564 urine samples from clinically suspected UTI cases were examined by semiquantitative culture method. The antimicrobial sensitivity pattern of these urinary isolates was studied by Kirby- Bauer disc diffusion method. Out of 574 urine samples, 220 were culture positive and 354 showed insignificant or no growth. Isolation rate was 39.7% with Escherichia coli 85 (38.6%) being most common followed by Klebsiella pneumoniae 54 (24.6%) Pseudomonas aeruginosa 34 (15.5%) and Staphylococcus aureus 28 (12.7%). Incidence as well as culture positivity was more in females 132 (60.0%) compared to males 88 (40.0%). Isolation rate was more in the age group of 21-30 years in females. The antimicrobial sensitivity pattern showed maximum sensitivity to Imipenem (80.1%) followed by Piperacillin+tazobactum (60.3%), Gentamicin (40.5%), Cefuroxime (38.7%), Netilmicin sulfate (38.2%), Nitrofurantoin (34.2%) and cefotaxime (32.8%). Maximum resistance was seen to Ampicillin followed by Nalidixic acid. Gram negative organisms are most commonly isolated organisms in urine samples of suspected cases of urinary tract infections. Culture and sensitivity of the isolates from urinary samples should be done as a routine before advocating therapy for better therapeutic outcome. Introduction Urinary tract infections (UTI s) are among the most common bacterial infection that lead patients to seek medical care. They are the most common bacterial acquired infections accounting for 35% of nosocomial infections. UTI s are important complications of diabetes, renal diseases, renal transplantations and structural and 951

neurological abnormalities that interfere with urine output. Despite widespread availability of antibiotics, treatment of UTI is still difficult due to antibiotic resistance in uropathogens. Antibiotic resistance in uropathogens is due to frequent misuse of antibiotics. Antibiotics are prescribed even before results of urine culture are available. Since pattern of antibiotic resistance among uropathogens vary even over a short periods and depend on site of isolation in different environments, periodic evaluation of antimicrobial susceptibility pattern of uropathogens is needed to update the information. The present study aim to know most common bacterial cause for UTI and their antimicrobial susceptibility pattern. Materials and Methods It is a retrospective study undertaken from January June 2015 in Al Ameen Medical College, H&RC, Vijaypur, Karnataka. The study protocol was approved by Institutional Ethical Committee of Al-Ameen Medical College, H&RC. A total of 222 culture proven urine isolates were studied. Samples were collected from both in-patient as well as outpatient departments. Majority of samples were clean catch midstream urine specimens, others included catheterized urine specimen and suprapubic aspirates. Culture was done by calibrated loop technique. A calibrated loop which delivers 0.01 ml of specimen was used to detect lower number of organisms in certain specimens. It was plated on Cysteine Lactose Electrolyte Deficient (CLED) agar. The plates were incubated at 37 0 C overnight. For Gram negative bacilli more than 10 5 colonies per ml of urine, for Gram positive 10 3-10 5 colonies per ml was considered significant. Isolates were identified by colony morphology, Gram 952 reaction and various biochemical tests. Reincubation of negative cultures for another 24 hours was done and reported at the end of 48 hours of incubation. Kirby-Bauer disc diffusion method was used to assess antimicrobial sensitivity of isolated pathogens. Different antibiotics included ampicillin (10 µg), nalidixic acid (30 µg), norfloxacin(10 µg), ciprofloxacin(5 µg), nitrofurantoin, (300 µg), gentamicin (10 µg), netilmicin sulfate (30 µg), cefuroxime(30 µg), cefotaxime(30 µg), chloramphenicol(30 µg) piperacillin+tazobactum (100/10 µg), imipenem (10 µg) were used to test sensitivity. Results and Discussion Out of 574 urine samples, 220 were culture positive and 354 showed insignificant or no growth. Isolation rate was 39.7% with Escherichia coli 85 (38.6%) being most common followed by Klebsiella pneumoniae 54 (24.6%) Pseudomonas aeruginosa 34 (15.5%) and Staphylococcus aureus 28 (12.7%) as shown in Table 1 below: Incidence as well as culture positivity was more in females 132 (60.0%) compared to males 88 (40.0%). Isolation rate was more in the age group of 21-30 years in females as shown in Figure 1 below: The antimicrobial sensitivity pattern showed maximum sensitivity to Imipenem (80.1%) followed by Piperacillin+tazobactum (60.3%), Gentamicin (40.5%), Cefuroxime (38.7%), Netilmicin sulfate (38.2%), Nitrofurantoin (34.2%) and cefotaxime (32.8%). Maximum resistance was seen to Ampicillin followed by Nalidixic acid as shown in Table 2 below: The urinary infection can involve any part of the genital tract from urethra to renal parenchyma. The underlying cause of this infection is the retrograde ascent of perineal

flora through the urethra. It especially affects the females because of the shorter and wider urethra. Regional monitoring of the causative bacteria and their susceptibility patterns provides the clinician with data that determines the selection of empirical treatment. Table.1 Bacteria isolated from UTI cases Organisms Total isolates (N=220) Eshcherichia coli 85 (38.6%) Klebsiella pneumoniae 54 (24.6%) Pseudomonas aeruginosa 34 (15.5%) Staphylococcus aureus 28 (12.7%) Table.2 Antibiotic sensitivity pattern of uropathogens Antibiotics Isolates tested Sensitive Intermediate Resistant Imipenem 220 216 (98.2%) 02 (0.9%) 02 (0.9%) Piperacillin+tazobactum 220 208 (94.5%) 03 (1.4%) 09 (4.1%) Gentamicin 220 182 (82.7%) 04 (1.8%) 14 (6.4%) Cefuroxime 220 173 (78.6%) 07 (3.2%) 40 (18.2%) Netilmicin sulfate 220 187 (85.0%) 03 (1.4%) 30 (13.6%) Nitrofurantoin 220 166 (75.5%) 04 (1.8%) 50 (22.7%) cefotaxime 220 192 (87.3%) 06 (2.7%) 22 (10.0%) Ampicillin 220 02 (0.9%) Nil 218 (99.1%) Nalidixic acid 220 02 (0.9%) 01 (0.5%) 217 (98.6%) Fig.1 Age distribution among the growth positive cases 953

Mostly UTIs are bacterial in nature and require broad spectrum antibiotic treatment. The Choice of antibiotics are Floroquinolones, cephalosporins and aminoglycosides. Cephalosporins including cephradine, cefaclor, cefotaxime and ceftazidime act as inhibitor of cell wall and are used frequently for treatment for gram negative infection. The mechanism of action of Floroquinolones including ciprofloxacin, ofloxacin, enoxacin and sparfloxacin is to inhibit the activity of essential enzymes (DNA gyrase and topoisomerase) for the DNA replication. The aminoglycosides act by inhibiting the bacterial protein synthesis. The selection of antimicrobials for treatment should not be arbitary but on knowledge of regional data on microbial isolates and their sensitivity to antibiotic. Based on these data regional empirical therapy is recommended for effective control of infection. We found that E. coli showed maximum resistance to Ampicillin (99.1%) and nalidixic acid (98.6%). Other uropathogens isolated also showed high resistance to ampicillin and nalidixic acid. All the uropathogens isolated in our study showed high sensitivity to imipenem, piperacillin+ tazobactum, cefotaxime, netilmicin sulfate, gentamicin, cefuroxime and nitrofurantoin. These findings are similar to previous studies. The best response against these bacteria was observed with cefotaxime, nitrofurantoin and gentamicin, that corresponds to regional and international findings. Resistance to ampicillin, and nalidixic acid has increased significantly all over the world11. At the same time susceptibility to cefotaxime, piperacillin+tazobactum and imipenem is seen in our region and so are the most effective treatment in UTI. The reason for the low resistance in these antibiotics may be due to their relative expense and because they are not easily available. Thus, these drugs could be considered as alternative options in empirical treatment of UTIs. Since E. coli is the most commonly cultured isolate, its susceptibility should be considered foremost. The most effective antibiotic against E. coli is nitrofurantoin in comparison to other commonly used antibiotics such as ampicillin. Therefore nitrofurantoin should be the first line of treatment in UTI. It is imperative that indiscriminate use of these and all other antibiotics is stopped at all levels so that resistance does not increase and the choice of available and effective antibiotics is not limited. In conclusion, Gram negative organisms are most commonly isolated organisms in urine samples of suspected cases of urinary tract infections. Culture and sensitivity of the isolates from urinary samples should be done as a routine before advocating therapv for better therapeutic outcome. Reference Acharya, A., R Gautam and L Subedee. 2011. Uropathogens and their antimicrobial susceptibility pattern in Bharatpur, Nepal Nepal Med Coll J. 13(1): 30-33. Amin M, Mehdinejad M, Pourdangchi Z. 2011. Study of bacteria isolated from urinary tract infections and determination of their susceptibility to antibiotics. Jundishapur J Microbiol. 2(3): 118-23. Beyene G, Tsegaye W. 2011. Bacterial uropathogens in urinary tract infection and antibiotic susceptibility pattern in Jimma University Specialized Hospital, South-west Ethiopia. Ethiop J Health Sci. 21(2): 141-16. Daza R, Gutierrez J, Piedrola G. 2001. Antibiotic susceptibility of bacterial strains isolated from patients with community-acquired urinary tract 954

infections. Int J Antimicrob Agents. 18(3): 211-15. Gupta, V., A Yadav, RM Joshi. 2002. Antibiotic resistance pattern in uropathogens. 20 (2): 96-8. Hryniewicz K, Szczypa K, Sulikowska A, Jankowski K, Betlejewska K, Hryniewicz W. 2001. Antibiotic susceptibility of bacterial strains isolated from urinary tract infections in Poland. J Antimicrob Chemother. 47(6): 773-80. Khorshidi A, Moniri R, Shajari G. 2003. Antimicrobial Resistance in Gramnegative BacilliIsolated from Urinary Tracts Infections. Arch Razi Ins. 55. Naeem M, Khan M, Qazi S M. 2010. Antibiotic susceptibility pattern of bacterial pathogens causing urinary tract infection in a tertiary care hospital. Ann. Pak. Inst. Med. Sci. 6: 214-18. Rai, GK., HC Upreti, SK Rai, KP Shah 1and RM Shrestha1. 2008. Causative agents of urinary tract infections in children and their antibiotic sensitivity pattern: a hospital based study Nepal Med Coll J. 10(2): 86-90. Sheikholeslami Z, Hassanshahi G. 2010. The frequency of coagulase negative staphylococci urinary infections with antimicrobial resistance pattern in Rafsanjan. Pak J Med Sci. 26(1): 107-10. Tambekar, D.H., D.V. Dhanorkar, S.R. Gulhane, V.K. Khandelwal, M.N.Dudhane. 2006. African Journal of Biotechnology. 5 (17): 1562-1565. 955