High Level Gentamicin Resistance and Vancomycin Resistance in Enterococcus species at a tertiary care hospital in India

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ISSN: 2347-3215 Volume 3 Number 10 (October-2015) pp. 276-280 www.ijcrar.com High Level Gentamicin Resistance and Vancomycin Resistance in Enterococcus species at a tertiary care hospital in India Sangram Singh Patel 1, Bhawna 2, Ravi Kumar Sharma 3*, Vishakha Srivastava 4, Dilip Kumar Singh Kushawaha 4 and Jitendra Prasad 4 1 Asst. Professor, Hind Institute of Medical Sciences, Safedabad, U.P., India 2 Senior Resident, Hind Institute of Medical Sciences, Safedabad, U.P., India 3 Tutor, Hind Institute of Medical Sciences, Safedabad, U.P., India 4 Junior Resident, Hind Institute of Medical Sciences, Safedabad, U.P., India *Corresponding author KEYWORDS Enterococcus species Sugar fermentation, High Level Gentamicin Resistance, vancomycin resistance Enterococcus, NorthIndia Introduction A B S T R A C T The Enterococcus species has emerged as a major nosocomial pathogen, and common difficulty faced in treatment of such infections are attributed to the presence of high level amino-glycosides resistance in them. Continuous monitoring of the antibiotics susceptibility pattern of Enterococcus species thus became inevitable for control of Hospital Acquired infection. The objective of the study was to isolate speciate and determine the antibiotic sensitivity pattern of Enterococcus species from various clinical samples. Samples collected were processed under aseptic condition and the Enterococcus species were isolated by growth characteristics in culture plate, Gram staining, biochemical testing and speciated accordingly with the sugar fermentation test. Antibiogram of the resultant isolates were done in regards to the CLSI standards. Out of 96 isolates, Enterococcus faecalis accounted for 55, followed by Enterococcus faecium 35, Enterococcus avium 6. Total of 47 isolates showed resistant to high level Gentamicin (HLG) and 10 were resistant to Vancomycin. Enterococcus species are gram positive cocci which cause Nosocomial infection because of their resistance to many antibiotics. Thus, it is necessary for laboratories to provide accurate antimicrobial pattern for Enterococcus species so that effective therapy and infection control measures can be initiated. During past years, Enterococcus species have became increasingly resistant to many antibiotics in terms of both the level of resistance and multiplication of resistance to many particular drugs. 1 The member of this species are natural habitat intestinal flora of humans but now they are also becoming as leading to cause of hospital acquired 276

infection due to higher antibiotics resistance. 2 The most serious Enterococcus species infections are often difficult to treat since the organisms have a tremendous capacity to acquired resistance to vancomycin, penicillin and high concentration aminoglycosides. 3 The most common Enterococcus species responsible for infections are Enterococcus faecalis 80-90% 4 and Enterococcus faecium for the remaining. 5 Urinary tract infection (UTIs) is most frequent infection, which is caused by Enterococci and second most frequent infection is intra pelvic abscesses and intra abdominal or post surgery wound infections 6. Epidemiological data suggested that Enterococcus species are most important reservoir for transmission of antibiotics resistant gene among different bacteria 7. Material and Methods The study was conducted at Hind Institute of Medical Sciences, Safedabad, U.P, India during period of April 2015 to September 2015. Clinical specimens collected like Urine, Blood, Pus, Sputum and CSF were sent to the Microbiology laboratory. Samples were processed aseptically for direct microscopy, gram staining, growth in culture plates like Nutrient agar, MacConkey agar, Blood agar, CLED Agar for 37 C aerobically overnight. Later, the next day biochemical tests were done from the growth obtained and speciated accordingly. Antibiotic sensitivity test was done by Kirby - Bauer disc diffusion method and reporting was done with respective to CLSI standards. Drugs like (ciprofloxacin, norfloxacin, ampicillin, high level gentamicin (120µg), vancomycin, penicillin, tetracycline and erythromycin) were used. After that the identification of genus Enterococcus, specific test like Bile esculin hydrolysis test, growth on 6.5% Nacl, growth on Potassium tellurite agar (PTA) and Sugar fermentation test was done to speciate the obtained sample. E. faecalis ATCC 29212and E. faecium ATCC 19434 were used as quality control strains. Result and Discussion Total 1266 samples were collected in which 718 were reported sterile, 452 were species like E.coli, Pseudomonas, and other than Enterococcus species 96 were isolated to be Enterococcus species. The total no. of sample reported sterile were 718 and positive isolates were 548. Positivity percentage of male was 56.38 and females were 43.61. Out of 96 positive, 33 (34.37%) were males and 63 (65.6%) were females. There are total 96 isolates of Enterococcus species from different clinical specimens like urine 64 (66.7%), Blood 17(17.8%), Pus 9 (9.3%), and others 6 (6.2%). Table no.1 Showing differentiation of Enterococcus species on the basis of sugar fermentation test Acid Produced E.feacalis E.faecium E.avium E.durans Mannitol + + + _ Sorbitol + +/- Arabinose _ + +/- _ Raffinose + +/- +/- _ Pyruvate + _ 277

Table.2 Showing total positive male and female% (gender point) Gender Sterile Sample Percentage Positive Sample Percentage Male 366 50.97 309 56.38 Female 352 49.02 239 43.61 Total 718 100 548 100 Table.3 Showing positive male and female ratio difference in Enterococcal infection Gender Samples positive for Enterococcus species Percentage Male 33 34.37 Female 63 65.6 Total 96 100 Table.4 Showing total number and percentage of different isolated Enterococcus species in different specimen Specimen E.facelis E. faecium E.avium Urine 35(63.63%) 26(72.22%) 3(60%) Blood 10(18.18%) 5(13.88%) 2(40%) Pus 6(10.90%) 3(8.33%) 00(00%) Other 4(7.27%) 2(5.55%) 00(00%) Total 55(100%) 36(100%) 5(100%) Table.5 Showing Antibiotic resistivity pattern in the Enterococcus species Antibiotics E.avium [N=6] E.faecalis [N=55] E.faecium [N=35] Ampicillin(10µg) 3 24 8 Norfloxacin(5µg) 3 29 12 Ciprofloxacin(5µg) 2 26 21 HLG(120µg) 2 32 12 Vancomycin(30µg) 2 5 3 Penicillin(10µg) 4 45 19 Tetracycline(30µg) 0 18 9 Erythromycin(15µg) 3 49 17 In the recent years, there has been a scenario of enhanced Enterococcus species infection due to their ability to cause nocosomial infection as well as increasing resistant to many antimicrobial agent 8-10. This study has the total sample of 1266 in which 452 were positive for other species only 96 were positive for Enterococcus species which 33(34.48%) were male and 63(65.62%) were female. In the present study the ratio of females infected with Enterococcal infection is more than ratio of male. The ratio 278

difference because Enterococcus species are frequently causative agent of the urinary tract infection which is more common in female this feature of ratio difference can be attributed to the factor that, the place where the study was conducted is a rural area hence females are not well educated enough to share their medical condition directly with the physicians. Out of 96 positive isolation of current study, 65 from urine, 17 from blood, 9 from pus, and 6 from other specimens like CSF, swab etc. Findings in present study revealed E.faecalis as predominant species which was 57.29% followed by E. faecium 37.5%, our study results goes similar with study conducted in CSM medical college, lucknow, as their result were, out of 86 samples,42 were E. faecalis,33 were E.faecium, 5 were E. avium 11. 47 (48.95%) of the Enterococcus species showed HLGR in our study, which is lower than the study of Zervous and associates whose shows reported a prevalance of 55% of HLGR in Enterococcus species in US centres 12. This study had HLGR in E.faecalis was 58.18% and E.faecium was 34.28% but in the result (Table No. 2) of prevalence of multidrug resistant Enterococci in tertiary care hospital in India, in which HLGR in E.faecalis was 44.4% and in E.faecium was 53.4% 13. In our study out of 96 isolates 10 (10.41%) showed resistant to vancomycin which was 8.57% in E.faecium, 9% in E.faecalis in contrast to Islamic azad university zanzan branch Iran were the percentage of vancomycin in E. faecalis is 0% and in E. faecium is 10% (47.6%) respectively 14. Conclusion To conclude Enterococcus species are gram positive cocci which are harmless commensals, but cause nosocomial infection because their resistant to many antibiotics. The most frequent infections caused by them are urinary tract infection followed by blood stream infection. Enterococcus family poses therapeutic dilellmas for clinicians, due to their increase activity of resistance Species. Thus, providing accurate antibiogram results and periodic invigilation of hospital infection control program is inevitable to control the emerging infections. References 1. Patterson JE, Zerros MJ. High-Level gentamicin resistance in Enterococcus Microbiology, genatic basis, and epidemiology. Rev Infect Dis 1990; 12:644-52. 2. Shankar, N., Baghdagan, A.S. and Gilmore, M.S. (2002) Modulation of virulence within a pathogenicity Island in vancomycin-resistant Enterococcus faecalis. Nature, 417, 746-750. 3. Mohanty, S., Dhawan, B., Gadepalli, R.S., Lodha, R. and Kapil, A. (2006) Case Report of Vancomycin Resistant Enterococcus faecium VanA phenotype: First Documented Isolation in India. The Southeast Asian Journal of Tropical Medicine and public health, 37, 335-337. 4. Jones ME, Draghi DC, Thornsberry C, Karlowsky JA, Sham DF, Wenzel RP. Emerging resistance among bacterial pathogens in the intensive care unit- a European and North Amaerican Surveillance study (2000-2002). Ann Clin Microbiol Antimicrob 2004; 3: 14-25. 5. Jatt BD, Huycke MM, Gilmore MS. Virulence of Enterococci Clin Microbiol Rev1994; 7: 462-78. 6. Low DE, Keller N, Barth A, Jones RN. Clin prevalence, antimicrobial susceptibility and geographic 279

resistance patterns of Enterococci: results from the SENTRY Antimicrobial surveillance program, 1997-1999. Clin Infect Dis 2001; 32 (supply 2): S133-45. 7. Cetinkaya Y, Falk P, Mayhall CG. Vancomycin- resistant Enterococci. Clin Microbiol Rev 2000; 13: 686-707. 8. Murray BE. The life and times of the Enterococcus. Clin Microbiol Rev 1990; 3:46-65. 9. Jesudason MV, Pratima VL, Pandian R, Abigail S. Characterization of penicillin resistant Enterococci. Indian J Med Microbiol 1998; 16:8-16. 10. Patterson JE, Zervos M. High-level gentamicin resistance in Enterococcus: Microbiology, genetic basis and epidemiology. Rev Infect Dis 1990; 12:644-51. 11. Agarwal J, Kalyan R, Singh M. High Level Aminoglycosides Resistance and - Lactamase Production in Enterococci at a Tertiary Care Hospital in India. Jpn. J. Infect. Dis., 62, 158-159, 2009. 12.Zerovos MJ, Kauffman CA, Therasse PM, Bergman AG, Mikesell TS, Schaberg DR. Nosocomial infection by gentamicin resistant Streptococcus faecalis. Ann Intern Med 1987; 106: 687-91. 13. Gangurde, N., Mane, M. and Phatale, S. (2014) Prevalance of Multidrug Resistant Enterococci in a Tertiary Care Hospital in India: A Growing Threat. Open Journal of Medical Microbiology, 4, 11-15. 14. Dadfarma Narges, Fooladi Abbas Ali imani, Oskoui Mahvash, Hosseini Hamidwh Mahmoodzadeh. HLGR among Enterococcal strain isolated from clinical specimen. Journal of infection and public health (2013),6, 202-208. 280