Indian Journal of Basic and Applied Medical Research; June 2016: Vol.-5, Issue- 3, P

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Original article: Evaluation of antimicrobial sensitivity and resistance pattern of Gram positive and Gram negative bacteria to monitor drug resistance among clinical isolates 1Dr Razia Khatoon, 2 Mahak Jain, 3 Dr Noor Jahan, 4 Mukesh Kumar Singh, 5 Shivendra Dutt, 6Mohd Shahid Khan 1MD Microbiology, Associate Professor, Department of Microbiology, Hind Institute of Medical Sciences, Mau, Ataria, Sitapur-261303, India. 2MSc Medical Microbiology, Tutor, Department of Microbiology, Hind Institute of Medical Sciences, Mau, Ataria, Sitapur-261303, India. 3MD Microbiology, Associate Professor, Department of Microbiology, Integral Institute of Medical Sciences & Research, Integral University, Lucknow-226026, India. 4MSc Medical Microbiology, Tutor, Department of Microbiology, Hind Institute of Medical Sciences, Mau, Ataria, Sitapur-261303, India. 5MSc Medical Microbiology, Tutor, Department of Microbiology, Hind Institute of Medical Sciences, Mau, Ataria, Sitapur-261303, India. 6MSc Medical Microbiology, Tutor, Department of Microbiology, Hind Institute of Medical Sciences, Mau, Ataria, Sitapur-261303, India. Corresponding author : Dr Razia Khatoon Abstract: Introduction: Antibiotic therapy is usually given to protect from infection against various organisms, however, routine use of empirical treatment has resulted in widespread antibiotic resistance and development of antibiotic resistant genes. Objective: To identify the bacterial pathogens isolated from various clinical specimens and to determine their antibiotic sensitivity and resistance pattern against the commonly used standard antibiotics. Materials & Methods: All the clinical specimens submitted to microbiology laboratory were processed as per standard microbiological procedures and antibiotic sensitivity tests were performed on the isolates as per guidelines of clinical and laboratory standards institute (CLSI). Result: A total of 154 organisms were isolated from all clinical specimens, out of which 82 were Gram positive and 72 were Gram negative bacteria. Doxycycline (63.4%) and amikacin (84.4%) showed high degree of sensitivity among Gram positive bacteria. Amikacin (77.8%) showed high degree of sensitivity in Gram negative bacteria. Gram positive bacteria showed highest degree of resistance to penicillin (63.4%), whereas, Gram negative bacteria showed highest degree of resistance to cefazolin (73.6%). Conclusion: High frequency of resistance against commonly used antibiotics such as penicillin and cefazolin as shown in the present study indicates a serious problem in the treatment of infections by gram positive and negative organisms. Therefore continuous surveillance is needed and treatment based on antibiogram report is essential. Keywords:- Gram positive bacteria, Gram negative bacteria, Antibiotic sensitivity pattern, Antibiotic resistance pattern, Mueller Hinton Agar. 72

Introduction Antibiotic therapy is usually given to protect from infection against various organisms and a wide generation of antibiotics are available for treatment. Prophylactic antibiotics play a significant role in the control of infections. However routine use of empirical treatment in both medical and veterinary medicine has resulted in widespread antibiotic resistance and development of antibiotic resistant genes. [1] There is a continuous rise in the problem of antibiotic resistance throughout the world. Antimicrobial (AM) resistance is a serious clinical problem especially in intensive care units (ICUs), including critical care (CCU), neonatal and intensive cardiac care unit. Antimicrobial resistance in both Gram- negative and Gram-positive bacteria is commonly reported in hospital-acquired infections. Such drug resistance compromises the management of acute respiratory infections, sexually transmitted diseases and diseases spread by the fecal oral route, such as typhoid fever, cholera, dysentery and other diarrheal diseases. [2-5] In developed countries constant examination in this field has helped in recognizing antibiotic resistance pattern. Also, it has been reported that the spectrum and resistance of the pathogenic bacteria have constantly changed year after year because of extensive application of antimicrobial drugs. Widespread use of broad-spectrum antibiotics is the most important factor responsible for drug resistance. To overcome this problem and to improve the outcome of serious infections in our institution, monitoring of resistance patterns among clinical isolates in the hospital is needed. Also, it has been found that proper designing and follow up of Antibiotic control policy plays a major role in controlling drug resistance. [2,3,6-11] Therefore, keeping the above mentioned things in mind the present study was done to identify bacterial pathogens isolated from various clinical specimens and determine their antibiotic sensitivity and resistance pattern against the commonly used standard antibiotics. Materials & methods A hospital based prospective study was conducted from August to October 2015, and various clinical specimens, such as, urine, pus, sputum, blood, synovial fluid, bone, high vaginal swab and ear swab, submitted to the department of microbiology were included in the study. All the collected specimens were cultured on blood agar and MacConkey agar and incubated aerobically at 37 o C for 24 48 hours, but in case of urine the culture was done on Cystiene lactose electrolyte deficient agar (CLED) and the plates were incubated for 24 hours at 37 o C aerobically. Growth on culture plates were identified by culture characteristics, gram s staining and standard biochemical test. [12] The antimicrobial susceptibility test was performed on Mueller Hinton agar (Blood agar in case of Streptococcus pyogenes) by Kirby Bauer Disc diffusion method [13], and zone diameters in millimeters were recorded after incubation at 37 o C for 24 hours as per guidelines of clinical and laboratory standards institute (CLSI) using antibiotic discs (HiMedia Laboratories, India) such as, amikacin (30µg), gentamicin (10µg), clindamycin (2 µg), levofloxacin (5 µg), chloramphenicol (30 µg), cefoxitin (30 µg), ofloxacin (5 µg), ciprofloxacin (5 µg), pristinamycin (15 µg), tobramycin (10 µg), erythromycin (15 µg), netilmicin (30 µg), penicillin (10 units), co-trimoxazole (1.25/23.75 µg), ampicillin (10 µg), high strength gentamicin (120 µg), high strength streptomycin (300 µg), vancomycin (30 µg), linezolid (30 µg), piperacillin (100µg), piperacillin/tazobactam (100/10µg), ceftazidime (30µg), cefotaxime (30µg), ceftriaxone 73 72

(30µg), cefepime (30µg), cefaclor (30 µg), cefixime (5 µg),cefuroxime (30 µg), cefazolin (30 isolated were Staphylococcus aureus (40.2%), Staphylococcus epidermidis (1.3%), Streptococcus µg), imipenem (10µg), aztreonam (30 µg), pyogenes (2.6%) and Enterococcus (9.1%), doxycycline (30µg), fosfomycin (200 µg), whereas gram negative bacterial isolates were norfloxacin (10µg), nitrofurantoin (300µg) and Escherichia coli (29.9%), Pseudomonas colistin (10 µg). Staphylococcus aureus ATCC aeruginosa (5.2%), Citrobacter (2.6%), 25923, Escherichia coli ATCC 25922 and Acinetobacter (1.3%) and Klebsiella Pseudomonas aeruginosa ATCC 27853 were used as standard quality control strains. [14] Result A total of 636 samples were included in the study, out of which 154 showed positive bacterial growth and 482 were negative for any bacterial growth. Out of 154 isolated organisms, 82 were gram positive and 72 were gram negative bacteria [Figure 1]. As shown in Figure 2, maximum (7.8%) [Table1, Figure 3]. Antibiotic sensitivity test of all the clinical isolates was performed as per CLSI and sensitivity pattern was noted. Doxycycline (63.4%) and amikacin (84.4%) showed high degree of sensitivity, whereas, penicillin (63.4%) showed high degree of resistance among gram positive bacteria. Amikacin (77.8%) showed high degree of sensitivity, whereas, cefazolin (73.6%) showed high degree of organisms were isolated from pus (58.4%) resistance in gram negative bacteria [Table 2 and followed by urine (29.9%). Gram positive bacteria 3]. Table 1: Distribution pattern of isolated organisms according to specimens SAMPLES TESTED ORGANISMS ISOLATED Urine Pus Sputum Blood Synovial Fluid Bone High Vaginal Swab Ear Swab TOTAL Staphylococcus aureus 4 48 2-2 - 4 2 62 Staphylococcus epidermidis - 2 - - - - - - 2 Streptococcus pyogenes - 2 2 - - - - - 4 Enterococcus 10 4 - - - - - - 14 7473

Escherichia coli 28 16 - - - - 2-46 Pseudomonas aeruginosa - 4-2 - 2 - - 8 Klebsiella 4 8 - - - - - - 12 Citrobacter - 4 - - - - - - 4 Acinetobacter - 2 - - - - - - 2 TOTAL 46 90 4 2 2 2 6 2 154 Table 2: Antibiotic sensitivity pattern of gram positive isolates ORGANISMS (n=82) Staphylococcus Staphylococcus Streptococcus Enterococcus aureus epidermidis pyogenes (n=62) (n=2) (n=4) (n=14) ANTIBIOTICS TESTED S R S R S R S R Amikacin 52 10 2 0 NT NT NT NT Clindamycin 40 22 2 0 4 0 NT NT Doxycycline 42 20 0 2 4 0 6 8 Levofloxacin 34 28 2 0 4 0 NT NT Chloramphenicol 36 26 2 0 NT NT 8 6 Cefoxitin 38 24 2 0 NT NT NT NT Ofloxacin 32 30 2 0 3 1 NT NT 75 73

Ciprofloxacin 32 30 2 0 NT NT NT NT Gentamicin 32 30 0 2 NT NT NT NT Pristinamycin 38 24 2 0 NT NT 4 10 Tobramycin 34 28 2 0 NT NT NT NT Netilmicin 34 28 2 0 NT NT NT NT Erythromycin 22 40 2 0 4 0 8 6 Penicillin 18 44 0 2 2 2 10 4 Co-trimoxazole 24 38 0 2 NT NT NT NT Ampicillin 28 34 0 2 0 4 12 14 High strength Streptomycin NT NT NT NT NT NT 10 4 High strength Gentamicin NT NT NT NT NT NT 11 3 Vancomycin NT NT NT NT 4 0 12 2 Linezolid 62 0 2 0 NT NT 14 0 S= sensitive; R= resistant; n=number of organisms; NT= Not tested. 7476

Table 3: Antibiotic sensitivity pattern of gram negative isolates ORGANISMS (n=72) ANTIBIOTICS TESTED Escherichia coli (n=46) Pseudomonas aeruginosa (n=8) Klebsiella (n=12) Citrobacter (n=4) Acinetobacter (n=2) S R S R S R S R S R Amikacin 32 14 8 0 10 2 4 0 2 0 Doxycycline 14 32 NT NT 2 10 2 2 2 0 Levofloxacin 16 30 8 0 4 8 3 1 2 0 Cefoxitin 26 20 NT NT 1 11 1 3 NT NT Ofloxacin α 8 38 4 4 2 10 3 1 NT NT Ciprofloxacin 10 36 2 6 4 8 2 2 0 2 Gentamicin 16 30 6 2 6 6 2 2 2 0 Ampicillin 18 28 NT NT NT NT 0 4 NT NT Cefotaxime 10 34 NT NT 2 10 3 1 0 2 Ceftazidime 8 38 6 2 3 9 2 2 2 0 Ceftriaxone 10 36 NT NT 2 10 3 1 1 1 Cefepime 16 30 8 0 4 8 2 2 2 0 Cefaclor 12 34 NT NT 1 11 0 4 NT NT Cefixime 14 32 NT NT 3 9 3 1 NT NT Cefuroxime 6 40 NT NT 2 10 2 2 NT NT Cefazolin 8 38 NT NT 1 11 0 4 NT NT 75 77

Piperacillin 20 26 3 5 4 8 2 2 0 2 Piperacillin- 24 22 8 0 6 6 3 1 1 1 Tazobactam Fosfomycin β 28 18 NT NT NT NT NT NT NT NT Nitrofurantoin γ 30 16 NT NT 8 4 4 0 NT NT Norfloxacin α 24 22 4 4 6 6 2 2 NT NT Aztreonam 22 24 6 2 2 10 1 3 NT NT Imipenem 44 2 6 2 11 1 4 0 1 1 Colistin NT NT 4 4 NT NT NT NT NT NT S= sensitive; R= resistant; n=number of organisms. NT = Not tested. α tested for urinary isolates only; β tested for urinary isolates of Escherichia coli only; γ tested for urinary isolates of Enterbacteriaceae only; tested for Pseudomonas aeruginosa only. Figure 1: Distribution of positive and negative growth in all clinical specimens. 76 78

Figure 2: Distribution of various specimens which were showing positive growth. Figure 3: Distribution of various isolated organisms from clinical samples. 77 79

Discussion The discovery of antibiotics revolutionized the management of infectious diseases. However, the overuse and misuse of antibiotics is leading to the emergence of resistance to these life saving drugs. Resistance due to adulteration of the antibiotics has also been reported. The microbial pathogens, as well as their antibiotic sensitivity patterns may change from time to time and place to place. Hospital antibiograms are commonly used to help guide empirical antimicrobial treatment and are an important tool for detecting and monitoring trends in antimicrobial resistance. [15,16] Keeping this in mind the present study was done to evaluate the sensitivity and resistance pattern of various clinical isolates. A total of 636 samples were submitted in the microbiology laboratory, out of which 154 showed positive bacterial growths. In the present study maximum clinical isolates were from pus (58.4%) followed by urine (29.9%). The prevalence of gram positive cocci was higher (53.2%) than the gram negative rods (46.7%). These findings are similar to those of other worker who also reported higher growth of gram positive bacteria (51%) as compared to gram negative bacteria (49%) from clinical samples. [17-20] Amongst the gram negative isolates in our study most of them were found to be sensitive to amikacin (77.8%), piperacillin-tazobactam (58.3%) and imipenem (91.7%) and maximum resistance was shown to cefazolin (73.6%). This finding is similar to another study which also showed maximum sensitivity of gram negative bacteria to amikacin (87.8%), piperacillin-tazobactam (79.7%) and imipenem (78.3%). [20] In the present study, all the Pseudomonas aeruginosa isolates were found to be 100% sensitive to amikacin, piperacillin-tazobactam and cefepime, followed by sensitivity to imipenem (75%), ceftazidime (75%) and colistin (50%). This is similar to another study which showed highest sensitivity of Pseudomonas aeruginosa isolates to amikacin (68.01%) followed by ceftazidime (57.08%), however, in contrast to our study, they reported 100% sensitivity to imipenem. [19] In our study the most prevalent gram positive bacteria was Staphylococcus aureus (40.2 %) followed by Enterococcus (9.1%), which is comparable to another study done previously. [21] In the present study it was found that most of the isolates of Staphylococci were highly sensitive to amikacin (84.4%). Amongst other tested drugs doxycycline (63.4%) showed high sensitivity among gram positive bacteria, whereas, most of them were found to be resistant to penicillin (63.4%). This finding is similar to another study which also reported high susceptibility of Staphylococcus to amikacin. [22] In our study it was seen that the isolates of Enterococcus were highly susceptible to penicillin (71.4%), vancomycin (85.7%) and linezolid (100%). Also, these isolates showed high susceptibility to both high strength gentamicin (78.6%) and high strength streptomycin (71.4%), therefore, combination treatment with penicillin / vancomycin and aminoglycosides can be given to treat infection effectively. Conclusion High frequency of resistance against commonly used antibiotics such as penicillin and cefazolin as reported in the present study indicates a serious problem in the management and treatment of infections caused by gram positive and negative organisms. To overcome this problem of drug resistance, continuous surveillance is needed and treatment based on antibiogram report is essential. 7280 80

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