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STUDENT IJMR
Year : 2013  |  Volume : 137  |  Issue : 5  |  Page : 981-985

Drug resistance & virulence determinants in clinical isolatesof Enterococcus species


1 M.B.B.S. Third year student, Kasturba Medical College, Manipal University, Mangalore, India
2 Department of Microbiology, Kasturba Medical College, Manipal University, Mangalore, India

Date of Submission19-Jul-2012
Date of Web Publication5-Jun-2013

Correspondence Address:
B Dhanashree
Associate Professor, Department of Microbiology, Kasturba Medical College, Manipal University, Mangalore 575 001
India
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Source of Support: None, Conflict of Interest: None


PMID: 23760387

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   Abstract 

Background & objectives: Enterococci are the leading cause of nosocomial infections, and are thus a persisting clinical problem globally. We undertook this study to determine the virulence factors and the antibiotic resistance in Enterococcus clinical isolates.
Methods: One hundred and fifty Enterococcus isolates obtained from various clinical specimens were speciated biochemically and subjected to antibiotic susceptibility testing using Kirby-Bauer disk diffusion method. Resistance to vancomycin was determined by using agar screen method. Haemolysin and gelatinase productions were detected using 5 per cent sheep blood agar and 12 per cent gelatin agar, respectively.
Results: Among the 150 Enterococcus isolates, 84 (56%) were E. faecalis. 51(34%) E. faecium, and 15 (10%) were other Enterococcus spp. Haemolysin production was seen among 123 (82%) isolates while 61 (40.6%) isolates produced gelatinase. Nearly 50 per cent of the isolates showed high level aminoglycoside resistance (HLAR). A total of 13 (8.6%) isolates showed vancomycin resistance, of which 11(7.3%) had an MIC >8 ΅g/ml.
Interpretation & conclusions: Presence of VRE was found to be low among the isolates studied. However, occurrence of VRE along with HLAR calls for regular detection of vancomycin resistance promptly and accurately to recognize VRE colonization and infection. Early detection of VRE and HLAR along with their virulence trait will help in preventing the establishment and spread of multidrug resistant Enterococcus species.

Keywords: Gelatinase - haemolysin - HLAR - vancomycin resistant enterococci


How to cite this article:
Fernandes SC, Dhanashree B. Drug resistance & virulence determinants in clinical isolatesof Enterococcus species. Indian J Med Res 2013;137:981-5

How to cite this URL:
Fernandes SC, Dhanashree B. Drug resistance & virulence determinants in clinical isolatesof Enterococcus species. Indian J Med Res [serial online] 2013 [cited 2019 Sep 20];137:981-5. Available from: http://www.ijmr.org.in/text.asp?2013/137/5/981/112989

Enterococci, recognized as opportunistic pathogens, are natural inhabitants of the oral cavity, gut and the female genital tract in both humans and animals [1],[2] . These are an important global cause of nosocomial infections [3] . Of the two most common Enterococcus species, E. faecalis has been found to be responsible for 80-90 per cent [4] and E. faecium for the remaining human enterococcal infections [5] . The most frequent infections caused by these organisms include urinary tract infections followed by intra-abdominal or intra-pelvic abscesses. Blood stream infections are the third most common infections caused by these organisms [6] . Enterococci with high level aminoglycoside resistance (HLAR), β-lactamase production and glycopeptides resistance including vancomycin resistant enterococci (VRE) have emerged, thus posing a therapeutic challenge to physicians[7],[8] . Epidemiological data also suggest that enterococci are important reservoirs for transmission of antibiotic resistance genes among different species of bacteria [9] . Thus, the occurrence of antimicrobial resistant enterococci, especially VRE is a persisting clinical problem in health care facilities in all geographical areas. This study was undertaken to know about the antimicrobial susceptibility patterns and virulence factors in clinical isolates of enterococci.


   Material & Methods Top


A total of 150 enterococcal isolates obtained from clinical samples (urine, pus, sputum, blood, vaginal swabs) sent to the Department of Microbiology, Kasturba Medical College, Mangalore, India, for routine culture and sensitivity, during July-September 2011, were included in the study by following convenient sampling method. The power of the study was 80 per cent. Ethical clearance of the study protocol was taken from the institutional Ethics Committee prior to the commencement of the study.

All the culture media, antibiotics discs and standard strains of bacteria used in study was procured from Himedia Laboratories Pvt. Ltd., Mumbai, India.

Urine samples were cultured by semiquantitative method on Cysteine Lactose Electrolyte Deficient (CLED) medium and blood agar. Blood samples were processed by BacT/ALERT 3D (BioMerieux Inc. USA) automated system. All other samples were inoculated on blood agar and MacConkey's agar. All culture plates were incubated at 37°C for 24-48 h and examined for growth. Identification of genus Enterococcus was done using colony morphology, Gram staining, bile esculin test and salt tolerance test. Speciation was done according to Manero and Blanch [10] using biochemical tests like tellurite resistance and fermentation of mannitol and sorbitol.

Haemolysin and gelatinase production were studied using the method adopted by Upadhyaya et al[11] . Briefly, a single colony of biochemically identified Enterococcus spp. was inoculated on 5 per cent sheep blood agar and 12 per cent gelatinase agar. The presence of a clear zone of β-haemolysis around the colonies indicated the production of haemolysin while a clear halo around the colonies on gelatinase agar indicated gelatinase activity. Serratia mercenses ATCC 13880 (Himedia Laboratories Pvt. Ltd., Mumbai, India) was used as positive control for gelatinase activity.

Antibiotic susceptibility testing for ampicillin, chloramphenicol, erythromycin, co-trimoxazole and teicoplanin was done by Kirby-Bauer disk diffusion method [12] on Mueller- Hinton agar and the results were interpreted as per Clinical and Laboratory Standards Institute (CLSI) guidelines [13] . E. faecalis ATCC 29212 (Himedia Laboratories Pvt. Ltd., Mumbai, India) was used as a quality control strain. HLAR was determined by disk diffusion method using high level gentamicin (120 μg) and streptomycin (300 μg) disks (Himedia Laboratories Pvt. Ltd., Mumbai, India). A diameter of the zone of inhibition <6 mm indicated resistance, 7-9 mm indicated that the test was inconclusive and ≥10 mm indicated susceptibility [14] .

Vancomycin agar screen test was performed using Brain Heart infusion (BHI) agar with 6μg/ml vancomycin to look for resistance to vancomycin. One or more colony or a film of growth indicated resistance to vancomycin. Vancomycin sensitive strain E. faecalis ATCC 29212 was used as negative control and vancomycin resistant strain E. faecalis ATCC 51299 was used as positive control [14] .

Determination of minimum inhibitory concentration (MIC) of vancomycin for enterococcal isolates which grew on vancomycin agar screen was done by agar dilution method [13] . Brain-heart infusion agar (Hi Media, Mumbai) was supplemented with different concentrations of vancomycin. Ten microliter of bacterial culture was spot inoculated after adjusting the turbidity with McFarland 0.5 standard. The plates were incubated at 37 o C for 24 h and examined for growth. The minimum concentration of vancomycin which inhibited bacterial growth was considered MIC. Enterococci which had MIC >32 μg/ml were considered resistant; 8-16 μg/ml as intermediately resistant and MIC of 4 μg/ml as susceptible to vancomycin as per CLSI guidelines [13] .


   Results Top


E. faecalis was the commonest (56%) species isolated followed by E. faecium (34%) [Table 1]. Haemolysin was produced by 82 per cent and gelatinase by 40.6 per cent of the isolates. Haemolytic activity was seen in all the species studied whereas gelatinase production was not demonstrated in E. durans and E. avium. The production of haemolysin was seen in more number of isolates in each species; 43.9 per cent of E. faecalis and 29.5 per cent of E. faecium produced both the virulence factors tested.
Table 1. Distribution of Enterococcus spp. in various clinical specimens


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Resistance of E. faecium isolates was higher than E. faecalis to all antibiotics except chloramphenicol. HLSR was higher in E. faecium (58.8%) than E. faecalis (48.8%) whereas HLGR was almost similar in both [Table 2]. HLGR was detected in 51.3 per cent and HLSR in 49.3 per cent of the total isolates. Fifty one isolates (34%) showed both HLGR and HLSR which included 35.7 per cent (n=30) of the E. faecalis and 35.3 per cent (n=18) of the E. faecium isolates. Thirteen isolates were found to be vancomycin resistant, of which 11 had an MIC> 8 μg/ml and <16 μg/ml which can be considered as vancomycin intermediately resistant. The VRE included four E. faecalis, six E. faecium, two E. dispar isolates and one E. avium isolate. Among the VRE, three E. faecium isolates (two from urine and one from blood) and one isolate each of E. faecalis and E. avium were found to be resistant to teicoplanin.
Table 2. Antibiotic resistance (%) among the enterococcal isolates


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   Discussion Top


The isolation rate of E. faecalis in our study was more than that of E. faecium. Similar results have been reported from central and south India [15],[16] . However, studies carried out in north India have shown  E.faecium Scientific Name Search  to be responsible for a larger number of enterococcal infections than E. faecalis[17] . In our study 82 per cent of the isolates were tested positive for haemolysin and 40.6 per cent for gelatinase. Haemolysin producing strains were also found to be more than those producing gelatinase by Klibi et al[18] .

It was also observed that, nearly 44 per cent of the E. faecalis isolates possessed both haemolysin and gelatinase enzymes while production of both the factors was substantially lesser in the case of E. faecium isolates. This may possibly be one of the reasons why the species of E. faecalis is responsible for a greater number of infections than E. faecium. The ability to produce haemolysin and gelatinase helps these organisms to acquire adequate nutrition in the host tissues as well as further the spread of infection in the host body, thus increasing the severity of infection [11] . Gelatinase production alone was considerably higher (50%) among the E.faecalis isolates than in E.faecium isolates (34%). Majority of the wound infections in the present study was found to be caused by E. faecium isolates.

Antibiotic resistance among enterococci is a global problem. In our study, the highest resistance was seen against erythromycin, which is in agreement with other studies carried out in India [19],[20] . Forty two per cent of the enterococcal isolates were resistant to ampicillin. This was in concurrence with the findings of Karmarkar et al[21] . However, other studieds [17],[20] have reported higher rates of ampicillin resistance. Overall, E. faecium isolates were more resistant than E.faecalis in our study, as has been reported earlier [15],[16] .

The occurrence of HLGR among the enterococcal isolates in our study was seen to be 53 per cent with no significant difference seen between E. faecalis and E. faecium isolates. Mendiratta et al[15] have reported greater resistance to HLG among E. faecium as compared to E. faecalis isolates. Studies conducted in New Delhi and Mumbai have reported HLGR prevalence to be as high as 70 and 100 per cent, respectively [21],[22] .

High level streptomycin resistance was found in 49.3 per cent of the isolates in our study, with E. faecium (59%) showing greater resistance as compared to E. faecalis (49%). HLSR in our study was observed to be higher than that reported from other Indian studies [17],[19],[22] , thus reflecting greater usage of streptomycin in this region.

In India, the prevalence of VRE has been reported to be between 0- 30 per cent [17],[19],[20],[21],[22],[23] . In our study, 13 isolates were found to be resistant to vancomycin with E. faecium (11.7%) showing higher resistance than E. faecalis (4.7%). Karmarkar et al[21] had also reported greater resistance among E. faecium isolates though Agarwal et al[19] found vancomycin resistance to be greater among E. faecalis isolates.

Resistance to teicoplanin among the VREs was seen to be much lesser in our study than reported by Karmarkar et al[21] . Of the thirteen VRE isolates, five showed resistance to teicoplanin. Seven VREs were found to be susceptible to either high level streptomycin or gentamicin. Hence, these infections could be treated with a combination of a high level aminoglycoside and a β lactam antibiotic. However, the other six isolates showed both HLGR and HLSR, thus making the treatment in such cases extremely difficult.

Vancomycin resistant enterococci can be expected to be a major problem in the coming years and hence it is essential that adequate measures be taken in all health care settings to contain the dissemination of the resistant strains. Routine testing of all enterococcal isolates for vancomycin resistance at least by vancomycin agar screen test, judicious use of vancomycin, rapid isolation of patients suspected to have VRE infections and effective surveillance mechanisms will go a long way in limiting the spread of VRE. Further studies are necessary to characterize the virulence factors and the drug resistance genes of enterococcal isolates by molecular methods to know their role in the pathogenesis of nosocomial infections.


   Acknowledgment Top


The first author (SF) acknowledges the Indian Council of Medical Research (ICMR), New Delhi, for the award of Short-term Research Studentship (STS) for this study of two months.

 
   References Top

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