Original article: Nonfermentative gram negative bacilli- characterisation and antibiotic resistant pattern study from a tertiary care hospital

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Original article: Nonfermentative gram negative bacilli- characterisation and antibiotic resistant pattern study from a tertiary care hospital 1Jayapriya Sukumaran, 2 Lata Sriram, 3 Sumathi.G 1Department of Microbiology, Chettinad Hospital & Research Institute,Kancheepuram, India 2Department of Microbiology, Madras Medical College,Chennai, India 3Department of Microbiology, Muthukumaran Medical College, Chennai Corresponding author: Jayapriya Sukumaran Date of submission: 28 July 2014; Date of Publication: 15 September 2014 ABSTRACT Introduction: Non-fermentative gram negative bacilli (NFGNB), frequently considered as contaminants, have emerged as important nosocomial pathogens causing opportunistic infections. The rise in incidence of these infections and resistance to a wide range of commonly used antibiotics necessitates their characterization up to species level. Also, multidrug resistance exhibited by NFGNBs poses a major clinical problem. The objective was to study the species characterization and drug resistance patterns of non-fermenters in various clinical specimens and to estimate the incidence of multidrug resistance of NFGNBs. Materials & methods: Various clinical specimens like pus, urine, blood, broncho-alveolar lavage, endotracheal aspirations, drain tip and cerebrospinal fluids collected from hospital patients were studied. The non-fermenters were identified using a standard protocol that included tests for motility, oxidase production, oxidation-fermentation test for various sugars, and gelatin liquefaction. Antimicrobial sensitivity was determined using Kirby Bauer disc diffusion method. Multidrug resistant (MDR) isolates of the non-fermenters were estimated. Descriptive statistics were used using Microsoft Excel Spreadsheet. Results & conclusion: Incidence of multidrug resistant nonfermenters was 75.6%. 7.7% of nonfermenters were pan-drug resistant showing resistance to all commonly used antibiotics. Combination therapy of Piperacillin-Tazobactum, Quinolones- Aminoglycosides and Imipenam Aminoglycosides were recommended for treatment of infections by nonfermenters. Potentially toxic agents like Colistin and Polymixin B were the only options available for treating the multi-resistant isolates. Keywords: non-fermenters, clinical samples, antibiotic resistance, multidrug resistance INTRODUCTION Humidifiers, ventilator machines, dialysate fluids and Non-fermentative gram negative bacilli (NFGNB) are catheter devices in the hospital environment have a ubiquitous group of aerobic, non-spore forming provided opportunities for these organisms to organisms. Although frequently considered as establish infection [1]. The infections caused by them contaminants, most of them have emerged as include urinary tract infections, wound infections, important nosocomial pathogens causing septicemia, pneumonia, osteomyelitis, meningitis etc. opportunistic infections in immmuno-compromised Chronic infection, longer duration of hospitalization hosts. Longer duration of hospitalization and and prolonged antibiotic therapy has increased the prolonged antibiotic therapy are the predisposing incidence of these infections necessitating their factors for infection with non-fermenters. characterization up to species level. Multidrug 227

resistance exhibited by them pose a major clinical problem in treating them. Therefore early identification and institution of appropriate treatment is necessary to reduce the morbidity and mortality due to these organisms in hospitalized patients [2,3,4, 5]. MATERIALS & METHODS: This cross sectional study included 156 clinical specimens like pus, urine, blood, broncho-alveolar lavage, endotracheal aspiration, drain tip and cerebrospinal fluid collected from patients of a tertiary care hospital. Antimicrobial sensitivity was determined using Kirby Bauer disc diffusion method. Multidrug resistant (MDR) isolates of the nonfermenters were estimated. MDR isolate was defined as resistant to three or more drugs of therapeutic relevance. RESULTS A total of 156 strains of NFGNB from various clinical samples were studied for their role in hospital infections. Higher incidence of non-fermentative isolates was observed in the age group of 21-40 years (51.3%) with a preponderance of males (70.5%). Pus (40.4%) and urine (30.8%) among the various clinical samples showed the highest incidence of nonfermenters and the predominant source of these infections were from surgical wards (25.5%). Infections by NFGNB were frequently associated with risk factors and Intensive Care Units formed a significant source of infections by these organisms (16.9%). Pseudomonas aeruginosa was the predominant isolate (58.9%) among the non-fermenting gram negative bacilli, followed by Acenetobacter baumanii fluorescens (100%) were predominantly isolated from pus; A.baumanii (41.3%), W.virosa (100%) and A.fecalis (100%) from urine; S. maltophilia (57.2%) from tracheal aspirates and B. cepacia (50%) from pus and sputum. The distribution of nonfermeners in various clinical specimens is shown in Table 1. Non-fermenters were most sensitive to Imipenam and Meropenam (87.8%), followed by Piperacillin- Tazobactum(83%), Ceftazidime(59.6%), Amikacin (62.8%) and Quinolones (53.2%). Resistance was observed for Cefotaxime (80.8%) and Gentamicin (72.5%). Incidence of multi-drug resistant nonfermenters was 75.6%. 7.7% of nonfermenters were pan-drug resistant showing resistance to all the commonly used antibiotics. Antibiotic sensitivity pattern of non-fermenters is shown in Table 2. DISCUSSION: In pus samples, Ps. Aeruginosa was the most frequently isolated (65%), followed by A.baumanii (22%), Ps. fluorescens (6.3%), S.maltophilia (5%), and B.cepacia (1.5%). Vijaya D et al reported 78.9% incidence of Ps.aeruginosa and 6.1% incidence of Acinetobacter sp. in a study of 133 NFGNB in clinical specimens. Ashutosh S et al reported an incidence of 63% and 9% in a similar study in UP [6,7]. Among urine samples, 50% had Ps. aeruginosa and 40% had A.baumanii. This is in concordance with other Indian authors - Meharwal et al, Taneja et al and Patel PH et al. [8,9, 10]. A.fecalis (3/3) and W.virosa (2/2) were exclusively isolated from urine samples only. In respiratory specimens (sputum, (29.5%), Stenotrophomonas maltophilia (4.5%), tracheal aspirates and BAL), Ps.aeroginosa and Pseudomonas fluorescens (2.6%), Alcaligenes fecalis (1.9%), Burkholderia cepacia (1.3%) and Weeksella virosa (1.3%). Ps. aeruginosa (44.6%) and Ps. A.baumanii were most frequently isolated. The predisposing factors in the respiratory tract observed in the present study were COPD, Chronic bronchitis 228

and underlying chronic diseases. Studies by Hseuh PR et al, Italy, Mastoraki A et al, Veenu et al, Ferrara et al, Arora et al, have reported Ps. aeruginosa as the most frequent isolate from respiratory tract across the world, however, with a varying incidence rates [11,12,13,14,15]. 8 of 10 blood specimens grew Ps.aeroginosa and the other 2 A.baumanii. One CSF sample and one drain fluid sample showed Ps.aeroginosa. A. baumanii, a major species of Acinetobacter, was the second most frequent NFGNB isolated from 46 of 156 samples (30%). Acinetobacter baumannii has emerged as a highly troublesome pathogen for many institutions globally. As a consequence of its immense ability to acquire or upregulate antibiotic drug resistance determinants, it has justifiably been propelled to the forefront of scientific attention [16]. S.maltophilia is an emerging nococomial pathogen in hospital settings. The significance of this organism lies in its intrinsic multidrug resistance [17]. Seven out of 156 (4.5%) nonfermenting gram negative bacilli were S.maltophilia in this study. This is less compared to the reports in China (9.2%) [18,19] but comparable to other Indian reports - 3.35% (Vijaya et al [6] ) and 1% ( Meharwal, Taneja, and Veenu et al [14,20,21]. Four isolates of S.maltophilia were from endotracheal aspirates in this study. A study by Wu CL et al., [19] had reported S.maltophilia as the third most common organism isolated from endotracheal aspirates. Kollef et al [22] reported that isolation of this high risk pathogen is an important predictor of mortality in Ventilator Associated Pneumonia. In the present study, the other 3 isolates were obtained from pus (2 from diabetic foot ulcer & 1 from postoperative wound swab) similar to the studies by Veenu et al. S.maltophilia has been frequently isolated from wounds and other skin lesions. [14] P.fluorescens is also a common isolate in various clinical specimens mentioned in the literature. In the present study, 4/156 NFGNBs (2.6%) were P.fluorescens. All of them were isolated from pus. A study by Sheretz et al., reported 2.38% incidence in pus. [21] B.cepacia has emerged as a significant respiratory pathogen and especially from sputum of cystic fibrosis patients. Study done in Chandigarh [11] showed that majority of these isolates were from blood. In the present study, one was isolated from sputum and the other from diabetic foot ulcer. A. fecalis is a pathogen in hospital acquired infections especially in persons with underlying diseases. In the present study 3/156 strains were isolated from urinary tract infections. Vijaya et al [6] and Veenu [14] et al isolated 3 and 1 isolates from urine respectively. In the present study 2 W. virosa isolates were obtained from urine. Meharwal et al [20] isolated one strain of W.virosa from urine. Multidrug resistance is a major problem with non fermenting gram negative bacilli and so the infections caused by them are very difficult to be treated. In the present study, 75.6% of NFGNB were resistant to 2 or more drugs of relevance and Ps aeruginosa (77%), A. baumanii (78%) & S.maltophilia (100%) were the most common multidrug resistant strains. This is higher than the studies in India reported previously in the year 1998 (Vijaya et al) and 2000 (Veenu et al) at 31% & 62% respectively but comparable to the study by Patwardhan et el in 2008.[6,14,24] While S.maltophilia is intrinsically resistant to antibiotics, Ps aeruginosa & A.baumanii acquire resistance by many different mechanism like Extended spectrum of betalactamases (ESBL) and Metallobetalactamases(MBL). This is of concern as 228 229

efficacious antimicrobial options are limited. Acinetobacter was found more multidrug resistant than Pseudomonas in our study and this finding correlated with the studies by Tanya et al (53% and 49%) and Homer et al (62% and 58%). [25] Multidrug resistant organisms were susceptible to Piperacillin tazobactum (62.3%), and Carbapenams (82.7%). Maximum resistance was seen with Gentamicin (94.9%) and Cefotaxime (95.9%). The present study observed highest resistance of NFGNB against Cefotaxime & Gentamicin antibiotics which are commonly used drugs. This necessitates the judicious use of these antibiotics in empirical therapy. Maximum sensitivity was observed with newer agents like Carbapenams and Pipercillin-Tazobactum. Moderate sensitivity was seen with Aminoglycosides and Fluroquinolones. Major risk of using monotherapy is the emergence of antibiotic resistant bacteria as observed in the present study which showed high rate of multidrug resistance and ESBL producers. Carbapenamase resistance, though not high was still observed as an emerging drug resistant mechanisms in the NFGNB from this hospital. Antibiotic therapy either empiric or documented is based upon antibiotic combination supplemented by knowledge of local epidemiology of resistance and susceptibilities in choosing a suitable combination.[26,27,28,29,30]therefore combination antibiotic therapy like Piperacillin-Tazobactum, Quinolones-Amikacin, Imipenam-Amikacin would be an ideal choice of therapy on the basis of antibiotic susceptibility testing as observed in this study along with an adequate infection control measures especially in the surgical and ICU units [31,32,33] CONCLUSION Observations from the present study showed the aerobic NFGNB which are usually considered as contaminants are now emerging as important nosocomial pathogens. The various clinical specimens from whom they were isolated proved their existence in all sites leading to a range of diseases. Different sensitivity pattern and multidrug resistance exhibited by non-fermenters pose a great problem in treating these infections. ESBL and MBL production by these organisms lead to high morbidity and mortality as we are left with the only option of treating them by potentially toxic agents like Colistin and Polymyxin B. Awareness of their entry into a hospital environment is the first step that Clinical Microbiologists can take to address this problem. Care in detection, evaluation of effective antibiotic options, and judicious use of antibiotics by instituting antibiotic policy of combination therapy and rigorous infection control measures will help to fight against these multidrug resistant non-fermenters in the effective management of patients. REFERENCES 1. Hill EB, Henry DA, Speert DP. Pseudomonas. In: Murray PR, Baron EJ, Jorgensen JH, Landry ML, Pfaller MA, editors. Manual of Clinical Microbiology. 9th ed. Vol. 1. Washington, D.C: American Society for Microbiology; 2007. pp. 734 48. 2. Quinn JP. Clinical problems posed by multiresistant nonfermenting gram negative pathogens. Clin Infect Dis. 1998;27:S117 24. 3. Aprameya IV. Non-fermenters other than Pseudomonas species. J Acad Clin Microbiol 2013;15:62-5 229 230

4. Meharwal S K, Taneja N, Sharma S K, Sharma M. Complicated nosocomial UTI caused by nonfermenters. Indian J Urol 2002;18:123-8 5. Gales AC, Jones RN, Forward KR, Linares J, Sader HS, Verhoef J. Emerging importance of multidrug-resistant Acinetobacter species and Stenotrophomonas maltophilia as pathogens in seriously ill patients: Geographic patterns, Epidemiological features, and trends in the SENTRY antimicrobial surveillance program (1997-1999) Clin Infect Dis. 2001;32:104 13. 6. Vijaya D, Kamala, Bavani S, Veena M. Prevalence of nonfermenters in clinical specimens. Indian J Med Sci 2000;54:87-91 7. Ashutosh, S, Mastan S, Singh KP, Kumar Ram TP, Gopa B. Identification, Characterization and Antibiotic Susceptibility Pattern of Non Fermenters from Clinical Specimens in Lucknow, Uttar Pradesh. Journal of Communicable Diseases 42.3 (2010): 171. 8. Arora N, Daga MK, Mahajan K, Prakash SK,Gupta N. Microbial Pattern of Acute Infective Exacerbation of Chronic Obstructive Airway Disease in a Hospital Based Study Indian J Chest Dis Allied Sci 2001; 43 : 157-162 9. Hsueh PR, Teng LJ, Chen CY, Chen WH, Ho SW, Luh KT. Pandrug-Resistant Acinetobacter baumannii Causing Nosocomial Infections in a University Hospital, Taiwan Emerg Infect Dis. Aug 2002; 8(8): 827 832. 10. Patel PH, Pethani JD, Rathod SD, Chauhan B, Shah PD. Prevalence of nonfermenting Gram negative bacilli infection in tertiary care hospital in Ahmedabad, Gujarat. Indian Journal of Basic & Applied Medical Research; 2013 (6), Vol.-2, p. 608-613 11. Gautam V, Ray P, Vandamme. P, Sharma M et al, Identification of lysine positive non-fermenting gram negative bacilli (Stenotrophomonas maltophilia and Burkholderia cepacia complex Indian J Med Microbiol 2009: 27(2): 128-3 12. Mastoraki A, Douka E, Kriaras I, Stravopodis G, Manoli H, Geroulanos S. Pseudomonas aeruginosa susceptible only to Colistin in intensive care unit patients Surgical Infections 2008: 9(2): 153-160 13. Hsueh, P. R., Tseng, S. P., Teng, L. J. and Ho, S. W. (2005), Pan-drug-resistant Pseudomonas aeruginosa causing nosocomial infection at a university hospital in Taiwan. Clinical Microbiology and Infection, 11: 670 673. 14. Veenu, Rama S, Arora DR. Isolation and susceptibility pattern of non fermenting Gram negative bacilli from clinical samples. Indian J Med Microbiol; 1999 17(1):14-7 15. Ferrara AM, Potentially multidrug resistant non fermenting Gram negative pathogens causing nosocomial pneumonia. Int.J. Antimicrob Agents 2006: 27(3):183-95 16. Peleg AY, Seifert H,Paterson DL, Acinetobacter baumannii: Emergence of a Successful Pathogen. Clin. Microbiol. Rev. 2008 vol. 21 no. 3: 538-582 17. Denton M, Kerr KG. Microbiological and Clinical Aspects of Infection Associated with Stenotrophomonas maltophilia Clin. Microbiol. Rev. 1998(11-1): 57-80 18. Wang H, Chen MJ, Changes of antimicrobial resistance among nonfermenting gram-negative bacilli isolated from intensive care units from 1994 to 2001 in China. Zhonghua Yi Xue Za Zhi. 2003: 10;83(5):385-90 19. Wu CL, Yang DI, Wang NY, Kuo HT, Chen PZ. Quantitative culture of endotracheal aspirates in the diagnosis of ventilator-associated pneumonia in patients with treatment failure. Chest. 2002 Aug;122(2):662-8. 228 231

20. Meharwal SK, Taneja N, Sharma SK, Sharma M. Complicated nosocomial UTI caused by nonfermenters. Indian J Urol 2002: 18:123-8 21. Taneja N, Maharwal S, Sharma M. Imipenem resistance in nonfermenters causing nosocomial urinary tract infections. Indian J Med Sci 2003;57:294 22. Kollef MH. Ventilator-associated pneumonia: A multivariate analysis. JAMA. 1993; 270:1965 70. 23. Elizabeth TS, Houang YW, Chu CM. et al, Epidemiology and Infection Control Implications Of Acinetbacter spp in Hong Kong Journal Of Clinical Microbiology, 2001: p228-234 24. Sherertz RJ, Sarubbi FA. A three-year study of nosocomial infections associated with Pseudomonas aeruginosa. J Clin Microbiol. 1983; 18(1): 160 164. 25. Patwardhan RB, Dhakephalkar PK, Niphadkar KB, Chopade BA. A study on nosocomial pathogens in ICU with special reference to multiresistant Acinetobacter baumannii harbouring multiple plasmids Indian J Med Res 128, August 2008, pp 178-187 26. Zavascki AP, Carvalhaes CG, Picao RC, Gales AC. Multidrug-resistant Pseudomonas aeruginosa and Acinetobacter baumannii: resistance mechanisms and implications for therapy 2010, (8);1 p 71-93 27. Lee CY1, Chen PY, Huang FL, Lin CF.Microbiologic spectrum and susceptibility pattern of clinical isolates from the pediatric intensive care unit in a single medical center - 6 years' experience.j Microbiol Immunol Infect. 2009: 42(2):160-5. 28. Mc Gowen JE Jr, Resistance in nonfementing gram-negative bacteria: Multidrug resitance to the maximum. American Journal Of Infection Control 2006 Jun;119 (6 Suppl 1):S29-36; S62-70. 29. Hancock RE. Resistance mechanisms in Pseudomonas aeruginosa and other nonfermentative gram-negative bacteria. Clin Infect Dis. 1998 Aug;27 (Suppl 1):S93 S99. 30. Malacarne P, Corini M, Maremmani P, et al, Diagnostic characteristics of routine surveillance cultures of endotracheal aspirate samples in cases of late-onset ventilator-associated pneumonia due to Acinetobacter baumannii. Infect Control Hosp Epidemiol. 2007: Jul 28(7):867-9. 31. Tien HC, Battad A, Bryce EA. Multi-drug resistant Acinetobacter infections in critically injured Canadian forces soldiers. BMC Infectious Diseases, 2007: vol. 7, p. 95. 32. Anupurba S, Bhattacharjee A, Garg A, et al, Antimicrobial susceptibility of Pseudomonas aeruginosa isolated from wound infections. Indian J Dermatol; 2006: 51:286-8 33. Fitzroy A, Orrett MD. Antimicrobial susceptibility survey of P.aeruginosa strains isolated from clinical sources. J Nat Med Assoc; 2004: 96:1065-9. 229 232

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