Antibiotic resistance and biofilm formation among coagulase-negative staphylococci isolated from clinical samples at a tertiary care hospital of eastern Nepal

The study was carried out in the Department of Microbiology, B.P. Koirala Institute of Health Sciences, Dharan, Nepal from July 2013 to June 2014. Consecutive sampling method was used i.e. all the clinically significant CoNS isolates obtained during the study period were enrolled. A total of 52 CoNS isolates were obtained from various clinical specimens (blood, pus, urine, CVC, tracheostomy tube, tissue) were included in the study.

Bacterial isolates obtained were identified by colony morphology, gram staining and biochemical tests (catalase test, slide coagulase, tube coagulase and mannitol test). Once the identity of the isolate as CoNS was confirmed, several biochemical tests and antimicrobial discs were used for their characterization upto species level. All the tests were performed according to standard microbiological methodology [6, 7].

Antimicrobial susceptibility testing of the isolates was performed on Mueller-Hinton Agar by.

Kirby-Bauer disk diffusion method recommended by clinical laboratory standard institution.

(CLSI) guidelines against following antimicrobial discs (HiMedia Laboratories): amikacin, ampicillin, ceftriaxone, ciprofloxacin, azithromycin, cotrimoxazole, vancomycin and linezolid.

Cefoxitin disc was used to detect methicillin resistance. Staphylococcus aureus ATCC 25923 and Escherichia coli ATCC 25922 were used as control strains and tested along with the test strains.

MIC of oxacillin and Vancomycin was determined by agar dilution technique as per CLSI guidelines. Oxacillin powder (815 μg/g) and Vancomycin powder (potency = 930 μg/g) was obtained from HiMedia laboratories India. The concentration at which complete inhibition of growth is achieved is considered the MIC. The results were interpreted according to the CLSI guidelines.

Biofilm production were investigated by the tube adherence test described by Christensen et al. (1982) and Congo red agar method as described by Freeman et al. (1989) and Tissue culture plate method as described by Christensen et al. (1985) [5, 11, 12]. Results were interpreted considering Tissue culture plate method as gold standard [13‐15].

A loopful of bacterial suspension from overnight culture were inoculated into the Trypticase.

Soy Broth with 1% glucose (TSBGlu, 10 mL) and incubated for 24 h at 37 °C. The tubes were gradually poured down and was washed with phosphate buffer solution (pH 7.3). After drying, the tubes were stained with 0.1% crystal violet. Excess stains were removed and tubes were washed away with water multiple times. Tubes were then kept in inverted position and finally observed for biofilm formation.

Congo red agar was prepared by mixing 37 g Brain heart infusion broth (HiMedia), 50 g sucrose (HiMedia), 0.8 g congo red dye and 10 g agar in 1 l distilled water. The solution was then sterilized by autoclave (121 °C, 15 lbs. for 15 min) and dispensed onto 90 mm petri dishes. CoNS isolates were plated and were incubated at 37 °C for 24 h. Biofilm production was detected by culturing the CoNS isolates on congo red agar plates. The biofilm forming strains produced black colonies while non-forming strains developed red colonies.

Trypticase soy broth with 1% glucose (TSBglu) was used as culture media. Isolates from fresh agar plates were inoculated in TSBglu media and incubated for 18–24 h at 37 °C in aerobic condition. After incubation, 0.2 ml of culture was filled onto individual wells of 96 well flat-bottom tissue culture plates. For control to check sterility and non-specific binding of media, only broth without the bacteria was used. The tissue culture plates were incubated aerobically at 37 °C for 18–25 h. The plates were gently tapped for the removal of unbound content. For the removal of free floating bacteria, the individual wells were cleaned four times with 0.2 ml of phosphate buffer saline (PBS pH 7.2). The biofilms formed by adherent organisms in tissue culture plate were fixed with sodium acetate (2%) and stained with 0.1% crystal violet. The plates were washed with water for excess stain and were left for drying. The isolates which formed biofilm were adherent on all side wells and stained uniformly with crystal violet.

Biofilm formation was studied in this study by three methods i.e. Tissue culture plate method,

Congo red agar method and tube adherence method. Among 52 isolates, 34 isolates were biofilm formers; 34 of them were detected by tissue culture plate method, 29 by congo red agar method while 27 isolates were biofilm positive by tube adherence method.

The tissue culture plate method was used as the standard method to evaluate the congo red agar and tube adherence method [13‐15]. Sensitivity, specificity, positive predictive value, negative predictive value, and accuracy were calculated by analysis of 2*2 table (Table 2). The sensitivity of congo red agar was 82.35% which is higher than tube adherence method 76.47%. The specificity of two tests was similar 94%. The accuracy of congo red agar method (86.5%) was also higher than tube adherence method (82.69%) (Table 3).

Biofilm formation was seen most commonly in S. epidermidis followed by S. haemolyticus.

The biofilm producers were resistant to multiple antibiotics in comparison to biofilm non- formers. Resistance to ampicillin and methicillin was seen in 100% and 86% of biofilm producers while only 42% and 30% resistance was seen in biofilm non-producers (Fig. 3).

The biofilm producer isolates were studied on the basis of the origin of the sample. All the isolates obtained from the intensive care unit (ICU) were biofilm former while no isolates obtained from outpatient department produced biofilm.

A total of 52 clinically significant isolates of coagulase-negative staphylococci obtained during the period of 1 year (July 2013–June 2014) were included in our study. Among the isolates, 6 different species of coagulase-negative staphylococci were encountered: S. epidermidis (27, 52%), S. saprophyticus (10, 19%), S. haemolyticus (8, 15%), S. hominis (4, 8%), S. capitis (2, 4%) and S. warneri (1, 2%). The findings of the present study are in agreement with the various studies which shows S. epidermidis as the most common coagulase-negative staphylococci [16, 17]. In contrast to the finding of our study, Jain A et al. isolated S. haemolyticus as (58%) as the most common isolate, followed by S. epidermidis (17%) [18]. S. epidermidis was isolated from various clinical specimens like blood, central venous catheter, pus and urine, while S. saprophyticus was predominantly obtained from urine samples (90%). The result correlates with the other studies which reported the pathogenic role of S. epidermidis in catheter related sepsis and that of S. saprophyticus in UTI [4, 5]. The higher incidence of S. saprophyticus in UTI is due to its colonization of the rectum or urogenital tracts of 5–10% of women [4].

In our study, the antimicrobial susceptibility of isolates was tested against 9 antimicrobials in accordance with the CLSI guidelines [8]. AST pattern of the isolates showed 80% resistance to ampicillin, 55% to ceftriaxone. Fifty-eight percent of the isolates were characterized as methicillin-resistant CoNS. All the 52 isolates were susceptible to vancomycin and linezolid. The susceptibility of vancomycin was confirmed by MIC against the isolates. The result of our study is consistent with other research article [19]. However some studies have suggested that vancomycin resistance does exist and is in increasing trends. Natoli S et al. observed no resistance to vancomycin but 5.4% isolates had reduced susceptibility to vancomycin [20].

Isolates obtained from intensive care unit (ICU + NICU) were more resistant when compared to other wards and outpatient department. A similar pattern of drug resistance was documented by several other studies [19, 21]. The patients hospitalized in intensive care unit are managed with multiple indwelling medical devices for the medication, nutrition and respiration. They are more vulnerable to biofilm formation and subsequent infection [22].

Among the 52 isolates, 34 (65.38%) isolates were biofilm formers. Biofilm formation was detected by tissue culture plate method in 34 isolates, congo red agar in 29 isolates, while 27 isolates showed positive biofilm formation test by tube adherence method. Similar results were obtained in previous studies [23, 24].

Congo red agar detected 85% (29/34) biofilm producer and tube adherence method detected 79% (27/34). Tissue culture plate is used as the standard method for detection of biofilm formation [13‐15] and the results of our study supports the evidence. Similar results were documented in various studies [13, 17].

The sensitivity, specificity, accuracy of the two tests were calculated using tissue culture plate as the reference [13‐15]. The sensitivity (82.35%) and accuracy (86.5%) of congo red agar were higher than tube adherence method (sensitivity = 76.47, accuracy = 82.69%), while no difference was observed in the specificity of these two methods. The positive predictive value of both congo red agar and tube adherence method is good (above 90), and they may therefore be used in clinical decision making. Similar results were documented by Saising et al. [24].

The present study also reveals that 100% of isolates obtained from intensive care units were biofilm formers while only 40% of isolates from surgery ward and none of the isolates obtained from the outpatient departments were biofilm formers. Similarly, the biofilm producers were more resistant to antimicrobial agents as compared to non-producers which agree with the study done in the past [5].