Antibiotic Therapy for ESBL and NDM producing Escherichia coli and Klebsiella pneumoniae isolates in a Tertiary Care Center

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JMID/ 2018; 8 (4):153-157 Journal of Microbiology and Infectious Diseases doi: 10.5799/jmid.493854 RESEARCH ARTICLE Antibiotic Therapy for ESBL and NDM producing Escherichia coli and Klebsiella pneumoniae isolates in a Tertiary Care Center Vedant Vikrom Borah 1,2, Mrinal Kumar Baishya 2, Kandarpa Kr Saikia 2 1 Department of Microbiology, School of Life Sciences, Assam Don Bosco University, Sonapur, Assam (India) 2 Department of Bioengineering & Technology, Gauhati University, Guwahati, Assam (India) ABSTRACT Objective: Antibiotic resistance is a global phenomenon wherein physicians face the most challenging decision to make for the right kind of drug, and its combinations, to tackle the ever growing ESBL and NDM on pathogens. The aim of the study is to understand outcome of hospitalized patients undergoing antibiotic therapy for bacterial infections. These patients are from Kamrup District of Assam, India. Materials and methods: A total of 185 clinical isolates of Escherichia coli and Klebsiella pneumoniae were collected from hospitalized patients of a tertiary care centre presenting symptoms of infection. Upon biochemical identification, their antibiotic susceptibility were assessed; isolates resistant to 3rd or 4th generation cephalosporins or carbapenem were phenotypically and genotypically determined for the production of extended spectrum β-lactamase (ESBL) and carbapenemase. PCR was carried out for CTX-M, TEM, SHV, OXA-48 and New Delhi Metallo-β-lactamase (NDM). Results: Bacterial infection is ubiquitous among male and female patients, with high isolation rate of Escherichia coli among female patients with urinary infection. The highest resistance against E. coli isolates was nalidixic acid (82.9%; p 0.005) and cefixime (81.4%; p 0.005). The highest resistance against K. pneumoniae was cefotaxime (77.7%; p 0.005) and ceftazidime (73%; p 0.005). Imipenem was the most effective antibiotic while ertapenem was the least. Antibiotic therapy included piperacillin (alone or in combination with tazobactam) for both E. coli and K. pneumoniae infections. Conclusions: Ceftriaxone, amikacin, cefepime, ceftriazone and imipenem were chosen as treatment options; isolates showed intermediate to negligible resistance to these drugs. Tigecycline was administered to patients infected with NDM producing pathogens. J Microbiol Infect Dis 2018; 8(4): 153-157. Keywords: antibacterial agents, drug resistance, ESBL, NDM INTRODUCTION β-lactamase mediated antibiotic resistance is a worldwide health threat [1,2]. The choice of drugs administered to infected patients is primarily based on the knowledge of the antibiotic resistance patterns within the given geographical boundary which is crucial for the initial empirical antibiotic therapy [3]. The antibiotics that are clinically appropriate for any given bacterial infection are ineffective in inhibiting bacterial infection. This result in antibiotic discordance wherein the causative organism demonstrates in vitro non susceptibility to the empiric antibiotic therapy administered. The aim of this article is to report the antibiotic resistance trend in hospitalized patients undergoing antibiotic therapy. The prevalence of β-lactam antibiotic resistance is correlated with patient demographics and status for those presenting Escherichia coli and Klebsiella pneumoniae infection in a tertiary care hospital. METHODS Sample design The clearance certificate was procured from the Institutional Ethical Committee of Gauhati University (GU/ACA/Ethics/2012/3993 dated 10/1/12). A total of 185 non-repetitive E. coli and K. pneumoniae isolates were collected from hospitalized patients presenting symptoms of Correspondence: Dr. Vedant Vikrom Borah, Department of Microbiology, School of Life Sciences, Assam Don Bosco University, Tapesia Gardens, Kamarkuchi, Sonapur, Assam, India Email: monshbrh@gmail.com Received: 16 February 2018 Accepted: 30 August 2018 Copyright JMID / Journal of Microbiology and Infectious Diseases 2018, All rights reserved

154 Borah VV et al., Antibiotic Therapy for drug resistant pathogens bacterial infection. These isolates were then identified by Gram s staining and biochemical tests (IMViC tests) [4]. The specimens collected include urine (n=83), sputum (n=53), pus (n=20), blood (n=11) and others (n=18) comprising of wound swab, high vaginal swab, and throat swab. Patients information in terms of demographics, age, gender, disease condition was collected from the respective departments. Antibiotic susceptibility test and β-lactamase production The antibiotic susceptibility testing was carried out for commonly used antibiotics 3rd and 4th generation cephalosporins, nalidixic acid and carbapenems as per the guidelines by the Clinical and Laboratory Standards Institute, 2011 [5]. Isolates resistant to any 3rd or 4th generation cephalosporin (cefexime, ceftazidime, cefotoxime, cefexime), and any carbapenem (imipenem, ertapenem, doripenem, meropenem) were selected for further analysis. Phenotypic characterization for the production of extended spectrum-β-lactamase (ESBL) and carbapenemases was carried out by Double Disk Synergy Test (DDST) [5] and presence of metallo-β-lactamases by Double Disk Diffusion test employing Ertapenem (5 ug) and Ertapenem + 0.5M EDTA [6]. Molecular detection of β-lactamase genes PCR confirmation was performed for ESBL and carbapenemase genes including Ambler class A (blactx-m, blatem, blashv and blakpc), class B (blavim, blaimp, and blandm), and class D (blaoxa-48). Primers for molecular detection were taken from published literature [1, 7-9]. Positive controls used for the multiplex PCR were K. pneumoniae ATCC 700603 (SHV-18), J53 pmg298 (CTX-M-15) and autoclaved distilled water was used as negative control. PCR positive TEM, OXA-48 and NDM amplicons were sequenced and compared to the Genbank database for confirmation of correct amplification of target gene; these isolates were then used as positive controls. RESULTS Clinical samples were collected from hospitalized patients who are from Kamrup district of Assam. These patients are admitted to various departments namely male medicine unit, female medicine unit, intensive care unit, urology and nephrology department, postoperative care ward, gynecology (septic) ward, paediatric ward, etc. Patients with urinary tract infections, respiratory infection, catheter-based infections, and septicemia in cancer patients, patients with diabetes, ear nose throat infections, pot operative infection, and infection in pregnancy constitute the sampling pool in this study. Of which patient with urinary infections and chronic kidney disease (44.3%) were higher in number followed by infections of the respiratory tract (20.9%) and during pregnancy (15.8%). Further classification of the diagnosis along with patient age and gender is presented in Table- 1, along with the distribution of E. coli and K. pneumoniae isolates. Of a total of 185 clinical bacterial isolates collected, E. coli isolates showed the highest antibiotic resistance to nalidixic acid (30 µg) (87/105, 82.9%; p 0.005) followed by cefixime (5 ug), (85/105, 81.4%; p 0.005), while the most effective antibiotic (least resistance shown) was imipenem (10 µg), (9/105, 8.4%; p 0.005) and nitrofurantoin (30 µg) (33/105, 31.2%; p 0.005). Among K. pneumoniae, highest resistance was documented against cefotaxime (30 µg) (62/80, 77.6%; p 0.005) and ceftazidime (10 µg) (58/80, 73.1%; p 0.005) while the most effective antibiotic (least resistance shown) was imipenem (10 µg) (9/80, 11.2%; p 0.005) and chloramphenicol (30 ug) (12/80, 15.4%; p 0.005). Ertapenem is one antibiotic that showed a high resistance in both groups of bacterial isolates: 93/105 (88.9%; p 0.005) and 63/80 (84.2%; p 0.005), respectively. Amongst ESBL producing E. coli, PCR positive results for CTX-M, TEM and SHV was observed for 43, 37 and 12 isolates, whereas ESBL producing K. pneumoniae showed positive PCR results in 32, 32 and 37 isolates, respectively. Furthermore, it was observed that the percentage of CTX-M (41% vs 39%; p 0.005) and NDM (21.9% vs 12.2%; p 0.005) genes detected was significantly higher among E. coli compared to K. pneumoniae, respectively and TEM (39.1% vs 35.2%; p 0.05) and SHV (45.1% vs 11.4%; p 0.005) genes were detected higher among K. pneumoniae than in E. coli, respectively. PCR detection of OXA-48 was reported for the first time in Assam [10] and upon further screening among all samples reported here, there were 5 isolates carrying this β-lactamase gene with a

155 Borah VV et al., Antibiotic Therapy for drug resistant pathogens Table 1. Characteristics of patients with E. coli and K. pneumoniae infection Escherichia coli Klebsiella pneumoniae Characteristics Non β-lactamase ESBL producer NDM OXA-48 Total Non β-lactamase ESBL producer NDM gene OXA-48 Total producer (n=45) (n=57) (n=23) (n=2) (n=105) producer (n=35) (n=45) producer (n=12) (n=3) (n=80) n (%) n (%) n (%) n (%) n (%) n (%) n (%) n (%) n (%) n (%) Age 18 years 5 (11.1) 11 (19.3) 5 (21.7) 1 (50) 16 (16.2) 4 (11.4) 5 (10.9) 1 (8.3) ND 10 (12.2) 19-45 years 22 (48.8) 27 (47.4) 8 (34.8) ND 49 (46.7) 16 (45.8) 21 (45.6) 6 (50) 1 (33.4) 37 (45.1) 46 years 18 (40) 19 (33.3) 10 (43.5) 1 (50) 37 (36.2) 15 (42.8) 20 (43.3) 5 (41.7) 2 (66.6) 35 (42.7) Sex Male 16 (35.5) 26 (45.6) 11 (47.8) 1 (50) 42 (40.9) 27 (77.14) 31 (67.4) 7 (58.3) 2 (66.6) 59 (72) Female 29 (64.5) 31 (54.4) 12 (52.2) 1 (50) 60 (59.1) 8 (22.85) 15 (32.6) 5 (41.7) 1 (33.4) 23 (28) Diagnosis Urinary Tract infections 7 (15.5) 14 (24.6) 5 (21.7) 1 (50) 21 (20) 1 (2.85) 5 (11.1) 1 (8.3) 2 (66.6) 6 (7.5) Chronic Kidney Disease 5 (11.1) 10 (17.5) 7 (30.4) ND 15 (14.3) 2 (5.71) ND ND ND 2 (2.5) Chronic Liver Disease 2 (4.4) 3 (6.6) 2 (8.6) ND 5 (4.8) ND 4 (8.8) 1 (8.3) ND 5 (6.2) Tuberculosis 4 (8.8) ND ND ND 4 (3.8) 2 (5.71) ND ND ND 2 (2.5) Enteric fever 1 (2.2) 2 (3.5) ND ND 3 (2.8) ND 1 (2.2) ND ND 1 (1.3) Respiratory Infections 1 (2.2) ND ND ND 1 (0.9) 7 (20) 9 (20) 2 ND 16 (20) Pregnancy 4 (8.8) 6 (10.5) 3 (1.3) 1 (50) 10 (9.5) 2 (5.71) 3 (6.6) 1 (8.3) ND 5 (6.2) Tonsilitis ND ND ND ND ND 3 (8.57) 2 (4.4) ND ND 5 (6.2) Chronic Obstructive Pulmonary Disease ND ND ND ND ND 2 (5.71) 2 (4.4) 1 (8.3) ND 4 (5) Pnuemonia ND ND ND ND ND 2 (5.71) 1 (2.2) ND ND 3 (3.8) Fracture/Bone injury 1 (2.2) 1( 1.7) ND ND 2 (1.9) 2 (5.71) 1 (2.2) 1 (8.3) ND 3 (3.8) Brain injury 2 (4.4) 1( 1.7) ND ND 3 (2.8) 2 (5.71) 4 (8.8) ND ND 6 (7.5) HIV positive ND ND ND ND ND ND 2 (4.4) 1 (8.3) ND 2 (2.5) Blood Infections 4 (8.8) ND ND ND 4 (3.8) ND ND ND 1 (33.4) ND Other diseases 10 (2.2) 20 (35.1) 10 (43.5) ND 32 (30.5) 11 (31.42) 9 (20) 1 (8.3) ND 20 (25) ND: Not Detected ESBL: Extended Spectrum β-lactamase NDM: New Delhi Metallo-β-lactamase

156 Borah VV et al., Antibiotic Therapy for drug resistant pathogens total prevalence percentage of 1.9% and 3.6% in E. coli and K. pneumoniae, respectively. Hospitalized patients were treated empirically with pipericillin (alone or in combination with tazobactam), ceftriaxone, amikacin which have been shown to be among the less resistant drugs with improvement in nosocomial K. pneumoniae infection. While, E. coli mediated infections were treated with piperacillintazobactam, imipenem, cefepime, ceftriazone +sulbactam with reduction in infection. Tigecycline was administered to patients infected with NDM producing pathogens. All patients upon antibiotic treatment showed signs of improvement and were discharged to be followed up with routine check-up. However, there were three patient deaths amongst those reported here - a 57-year old male suffering from respiratory tract infection, a 22 year old female with acute respiratory distress syndrome and an 8 years old female with acute membranous tonsillitis who died of cardiac arrest. DISCUSSION This study was conducted to understand the patient recovery outcome based on the antibiotic treatment carried out for bacterial infections among hospitalized patients admitted to a tertiary care hospital in Assam, India. This also allowed for the investigation of antibiotic resistance in two most commonly circulating bacterial pathogen in Assam. It was observed that patients belonging to the age group of 45-90 years are affected by bacterial infections more often than other age groups while 19-30 years age group were more commonly affected by Klebsiella pneumoniae. We suspect it could be attributed to two factors (i) with age people are prone to infections due to compromised immune system and diseases that call for long term hospitalization or infection leading to nosocomial infections, and (ii) the younger generation being more robust, requiring to travel long distances are exposed to the environmental agents leading to more community based infections. The isolation rate of E. coli as a common causative bacterium in urinary infections is high as compared to K. pneumoniae which is consistent with the findings of previous studies in which E. coli was the predominant pathogen isolated from patients with urinary tract infections [11]. E. coli infections, however, are very common in all age groups which could be owing to poor personal hygiene. For the compilation of results, intermediate resistance and resistance were clubbed under resistance group as few types of β-lactamases exhibit low hydrolysis of the antibiotic with a lower MIC value or intermediate range of clearance [12]. NDM-producing isolates are resistant to different number of antibiotics tested whether coprevalence of ESBL genes is present or not. Most of the tested clinical isolates were susceptible to imipenem suggesting possible options, but alternatively are resistant to ertapenem, meropenem and doripenem; ertapenem shows a reduced inhibition against all isolates whether they are carbapenemaseproducing or not. High resistance of ertapenem could be a result of combinations of ESBLs in addition to decreased permeability or increased influx [13]. Presence of KPC gene was not observed in the given bacterial isolates. This study allowed for the realization that administration of antibiotics that the clinical isolate shows intermediate resistance to, when used in combination with another effective antibiotic did provide relief to the patient. Piperacillin with and without tazobactam and ceftriazone with and without sulbactam were the choice of antibiotics for treatment, including imipenem and cefepime in certain cases, and the patients responded to the medication positively; some were discharged from hospitalization while the study was in progress. The MIC values for the tested antibiotics as a means of discriminating between antibiotic resistant and susceptible clinical isolate was not carried out as part of the experiments which could have helped us correlate the extent of hydrolysis of the antibiotic with the gene status of each isolate. The challenge in dealing with resistant gramnegative pathogens is the lack of effective antibiotic agents. Cautious use of antimicrobials is therefore increasingly important as we are faced with a reduced repertoire of effective drugs. It is a not rare for a physician to have a patient die of an overwhelming infection for which there are no therapeutic options. Development of proper antibiotic policies, abstaining from the over-use of antibiotics, channeling proper and correct information among the local and rural communities,

157 Borah VV et al., Antibiotic Therapy for drug resistant pathogens development of infection control strategies remain crucial in curbing the dissemination of antibiotic resistant bacteria. ACKNOWLEDGMENTS Sample and patient details were from Department of Microbiology, Gauhati Medical College and Hospital, Guwahati, Assam, India. Financial Disclosure: Department of Biotechnology, Government of India (Grant no. BT/213/NE/TBP/2011). Declaration of Conflicting Interests: The authors declare that they have no conflict of interest. REFERENCES 1. Nordmann P, Nass T, Poirel L. Global spread of carbapenemase-producing Enterobacteriaceae. Emerg Infect Dis 2011; 17(10):1791-1798. 2. Michael CA, Dominey-Howes D, Labbate M. The antibiotic resistance crisis: causes, consequences, and management. Front Public Health 2014; 2:145. 3. Jerardi KE, Auger KA, Shah SS, et al. Discordant antibiotic therapy and length of stay in children hospitalized for urinary tract infection. J Hosp Med 2012; 7(8):622-627. 4. Levine M, Epstein SS, Vaughn RH. Differential Reactions in the colon group of bacteria. Am J Public Health Nations Health 1934; 24(5):505-510. 5. Clinical and Laboratory Standards Institute. Performance Standards for Antimicrobial Susceptibility Testing; Twenty-first Informational Supplement. CLSI Document 2011; M100-S21:44-51. 6. Hornsey M, Phee L, Wareham DW. A novel variant, NDM-5, of the New Delhi metallo-βlactamase in a multidrug resistant Escherichia coli ST648 isolate recovered from a patient in the United Kingdom. Antimicrob Agents Chemother 2011; 55(12):5952-5954. 7. Amudhan MS, Sekar U, Kamalanathan A, Balaraman S. blaimp and blavim mediated carbapenem resistance in Pseudomonas and Acinetobacter species in India. J Infect Dev Countries 2012; 6(11):757-762. 8. Schechner V, Strauss-Robinson K, Schwartz D, et al. Evaluation of PCR-Based Testing for Surveillance of KPC-Producing Carbapenem- Resistant Members of the Enterobacteriaceae Family. J Clin Microbiol 2009; 47(10):3261 3265. 9. Lal P, Kapil A, Das BK, Sood S. Occurrence of TEM & SHV gene in extended spectrum b- lactamases (ESBLs) producing Klebsiella sp. isolated from a tertiary care hospital. Indian J Med Res 2007; 125(2):173-178. 10. Borah VV, Saikia KK, Hazarika NK. First report on the detection of OXA 48 β lactamase gene in Escherichia coli and Pseudomonas aeruginosa co infection isolated from a patient in a Tertiary Care Hospital in Assam. Indian J Med Microbiol 2016; 34 (2):252-53. 11. Maji SK, Maity C, Halder SK, et al. Studies on drug susceptibility and bacterial prevalence of UTI in tribal population of Paschim Medinipur, West Bengal, India. Jundishapur J Microbiol 2013; 6(1):42-46. 12. Rodloff A, Bauer T, Ewig S, et al. Susceptible, Intermediate, and Resistant The Intensity of Antibiotic Action. Deutsches Ärzteblatt International, 2008;105(39):657 662. 13. Lartigue MF, Poirel L, Poyart C, et al. Ertapenem Resistance of Escherichia coli. Emerging Infectious Diseases 2007; 13(2):315-317.