- Research article
- Open Access
Dio-sensimedia: a novel culture medium for rapid detection of extended spectrum β-lactamases
BMC Infectious Diseases volume 3, Article number: 22 (2003)
Resistance to contemporary broad-spectrum β-lactams, mediated by extended-spectrum β-lactamases (ESBL), is an increasing problem worldwide. Many of the emerging antimicrobial resistance problems of this decade have been characterized by difficulty in the recognition of resistance in the laboratory, particularly by rapid susceptibility test methods. The plasmid-encoded ESBL represent such a resistance phenomenon that is difficult to recognize.
We compared Dio-Sensimedia-ES (DSM-ES; Diomed, Istanbul, Turkey) and Mueller-Hinton (MH) agar in the double-disk synergy test (DDST) as a novel rapid system for detecting ESBL directly from bacterial culture.
Sixty ESBL-producing Klebsiella pneumoniae isolates cultured from blood (30), endotracheal aspirates (20), urine (5) and pus (5), as well as 40 Escherichia coli isolates cultured from endotracheal aspirates (15), urine (10), blood (8) and pus (7) were studied. Isolates positive for ESBL by the combined disk tests were tested with the DDST using MH and DSM-ES agar to detect ESBL-mediated resistance in K. pneumoniae and E. coli. DSM-ES agar was also used to determine the susceptibility of Enterobacteriaceae and staphylococci.
Among 60 ESBL-producing K. pneumoniae isolates, 59 (98.3%) were identified as ESBL-positive by the DDST using MH, and 58 (96.6%), using DSM-ES agar. Of 40 ESBL-producing E. coli isolates, 38 (95%) were ESBL-positive by the DDST on MH agar, and 37 (92.5%), on DSM-ES agar. The average incubation period required for ESBL detection by the DDST on DSM-ES agar was 4 hours.
Since the DDST results were available within 4 hours when DSM-ES agar was used, the use of this media may significantly lower the length of hospital stay, the total cost for patient care and even the mortality rate by fascilitating early treatment against ESBL-producing organisms.
Microbial resistance through extended-spectrum β-lactamases (ESBL) was first reported in Europe, and subsequently in the United States. Today this resistance mechanism has been recognized globally [1–6]. Many clinical microbiology laboratories have problems to detect ESBL-mediated resistance. Controversy exists regarding the clinical importance of such resistance, the choice of optimal laboratory methods to detect it, and surveillance of ESBL-producing organisms. Failure to detect ESBL-mediated resistance has contributed to uncontrolled spread of ESBL-producing organisms and related treatment failures.
Among the genera of Enterobacteriaceae, ESBL are most commonly produced by Klebsiella spp. and Escherichia coli . In addition, these enzymes have been isolated from other Gram-negative bacilli including Pseudomonas aeruginosa and Acinetobacter spp. . Most ESBL are mutants of TEM and SHV ß-lactamase types [9, 10]. Unlike these parent enzymes, ESBL hydrolyse penicillins and oxyimino-aminothiazolyl cephalosporins including cefuroxime, ceftriaxone, ceftizoxime, ceftazidime, cefpirome, cefepime, but not cephamycins [10–13].
The ESBL-producing Gram-negative bacilli possess genes encoding more than one type of the ESBL and enzymes that are responsible for resistance to other antibiotics such as aminoglycosides and fluoroquinolones that are active against Gram-negative bacilli [14, 15]. The emergence of multidrug resistance in these virulent pathogens has significantly hampered the efforts to devise effective empiric or directed antibiotic treatment regimens .
ESBL-mediated resistance may be determined by several laboratory methods, including the combined disk methods (Oxoid "Combination disks" and Mast "MAST DD"), the double-disk synergy test (DDST), the three-dimensional agar test, the investigational Vitek ESBL cards (bioMérieux, Hazelwood, Mo., USA), and the ε-test ESBL strip (AB Biodisk, Solna, Sweden; Cambridge Diagnostic Services, Cambridge, UK) [17–19].
In our study, we report a novel rapid system for detecting the presence of ESBL directly from microbiological cultures. DSM (Diomed, Istanbul, Turkey) enables observation of the inhibition zones within 4 hours by changing its color in response to the metabolic activity of growing bacteria, even before the bacterial layer has had an opportunity to grow. DSM is an antibacterial susceptibility testing agar media, which is poured in Petri dishes and used to determine susceptibility to antibacterials by the disk diffusion method. The use of this medium in disk diffusion technique is analogous to an improved, chromogenic version of the Kirby-Bauer disk diffusion method.
Bacterial strains and culture media
Sixty ESBL-producing K. pneumoniae isolates cultured from blood (30), endotracheal aspirates (20), urine (5), and pus (5) as well as 40 E. coli isolates cultured from endotracheal aspirates (15), urine (10), blood (8), and pus (7) were studied. The isolates were non-repetitive. All isolates were cultured from patients hospitalized in an intensive care unit at Istanbul Faculty of Medicine, Istanbul University from January 2000 through December 2001. Identification of the isolates was performed by API 20E (bioMérieux, Hazelwood, Mo., USA). E. coli ATCC 25922 and K. pneumoniae K6 (ATCC 700603) were used as reference strains.
Screening and confirmatory tests to detect ESBL-mediated resistance were performed according to the National Committee for Clinical Laboratory Standards criteria . Modified criteria, i.e., a diameter of <22 mm for ceftazidime; <25 mm, for ceftriaxone; and <27 mm, for cefotaxime or aztreonam were used for interpretation of Kirby-Bauer disk zone diameters. In this study, a combination of ceftazidime (30 μg) and clavulanic acid (10 μg) was used. Zones around K. pneumoniae or E. coli colonies, which were larger than that around the disk containing ceftazidime-clavulanic acid, were deemed to indicate ESBL-positivity.
DMS-ES agar was also used to determine susceptibility of Enterobacteriaceae and staphylococci. This media changes its color from red to yellow as bacteria grow and red circular inhibition zones forms around disks containing the antibacterial agent. All isolates that were positive for ESBL by the combined disk tests were tested with the DDST on Mueller-Hinton (MH) and DSM-ES agar to detect ESBL-mediated resistance. E. coli ATCC 25922 and K. pneumoniae ATCC 13883 were used as negative controls.
Double-disk synergy test
The detection of ESBL-mediated resistance by the DDST was performed according to a published protocol [11, 12]. Bacterial suspensions were prepared from overnight cultures of clinical isolates to produce a turbidity of a 0.5 McFarland standard. These suspensions were then spread on the surface of MH and DSM-ES agar plates as in the Kirby-Bauer disk diffusion technique. Antibiotic susceptibility disks containing amoxicillin (20 μg) plus clavulanate (10 μg) were placed on the centre of Petri dishes containing the two different media. Ceftazidime (30 μg), ceftriaxone (30 μg), cefpodoxime (10 μg), aztreonam (30 μg), cefotaxime (30 μg) disks were placed 25–30 mm apart circularly around the co-amoxiclav disk. The MH agar plates were incubated for 24 hours at 35°C. DSM-ES agar that is originally red, changed its color to yellow as bacterial culture grew (Fig. 1). DSM-ES agar plates were incubated at 35°C until red inhibition zones became apparent. Red inhibition zones around disks containing antibacterials were visually observed and measured. When the disk containing co-amoxiclav extended to any of the other antibiotic disk inhibition zones, ESBL production was inferred [11, 12] (Fig. 2).
Evaluation of the susceptibilities by two methods
Determination of ESBL production using was done by using both DSM-ES and Mueller-Hinton agar. The results of the DDST using the two media were compared.
All the test results were read and interpreted by one of the authors [AAC], who was blinded to the results of microbiological typing.
Among 60 ESBL-producing K. pneumoniae isolates, 59 (98.3%) were identified as ESBL-positive by the DDST on MH agar; and 58 (96.6%), on DSM-ES agar (Table 1). The average incubation period required for detecting ESBL-mediated resistance when using DSM-ES agar was as short as 4 hours.
Of 40 ESBL-producing E. coli isolates, 38 (95%) were positive on MH agar; 37 (92.5%), on DSM-ES agar (Table 1). The average incubation period required for detecting ESBL-mediated resistance by the DDST on DSM-ES agar was 4 hours.
ESBL are encoded on conjugative plasmids, tranposons or integrons. These mobile genetic elements are readily spread under selective antibiotic pressure . Increased clinical use of antibiotics, access to antibiotics without a doctor's prescription in many countries, international travel, and uncontrolled use of antibiotics in the environment and by meat-producers have led to an increase in antibiotic resistance in many bacterial species . Early determination of ESBL-mediated resistance is clinically crucial in cases like meningitis, bacteremia and sepsis in order to start appropriate therapies as early as possible. Even in less emergent situations, early determination of antibacterial susceptibility is important to select the appropriate treatment regimens and increase the success rate of the therapy, lower the rate of side-effects of antibiotics, and decrease health-care costs.
Clinical and financial benefits of early determination of antibacterial susceptibility have been shown in many studies . Barenfarger et al  reported that early reporting of antibacterial susceptibility tests resulted in a decrease in the length of hospital stay by 2.0 days and in the average total cost per patient by US$ 2395. Doern et al  reported a saving of US$ 4194 per patient in addition to a statistically significant lower mortality rate when a rapid antibiotic susceptibility test was used.
The detection of ESBL-mediated resistance in Gram-negative bacilli is one of the major problems in a clinical microbiology laboratory . The techniques recommended for this purpose by the NCCLS guidelines is not easily performed in routine clinical practice. Several automated systems such as Vitek (bioMerieux, NC, USA) and MicroScan Walkaway (Diamond Diagnostics, MA, USA) aimed to provide early results have recently become available and approved by the Food and Drug Administration. Another commercial assay used for ESBL detection, the ε-test is available from two manufacturers (AB Biodisk, Solna, Sweden; and Cambridge Diagnostic Services, Cambridge, UK). These commercial assay kits have a sensitivity of >90% to detect ESBL-mediated resistance.
Published data on the accuracy and the speed of such systems are limited. McGregor et al  evaluated MicroScan to test susceptibility of Gram-negative bacteria, and found major and minor discrepancies in 2% and 8% of the samples assayed, respectively, as compared to a standard test. When testing susceptibility of Gram-positive bacteria, major and minor discrepancies occured in 1% and 7% of the samples assayed, respectively. In this study 93% of the results were available within 7 hours. Ling et al  compared the Vitek 2 AST-No. 12 cards and the broth microdilution method to test susceptibility of 228 isolates, including various members of the Enterobacteriaceae, Pseudomonas aeruginosa and other Gram-negative bacteria. They reported major discrepancies (resistant by the Vitek 2 system but sensitive by the broth microdilution method) in 0.5 %, and very major discrepancies (sensitive by the Vitek 2 system but resistant by the broth microdilution method) in 0.4% of the tests.
A phase-three trial compared the disk diffusion method, which is recommended by the NCCLS guidelines, with an automated growth-monitoring system (Vitek ESBL). In this trial, the two methods were found to be comparable in both sensitivity (98% for disk diffusion vs. 99.7% for Vitek ESBL) and specificity (99.4% for disk diffusion and 100% for Vitek ESBL) . Cormican et al. compared the ε-test with the disk diffusion method. ε-test was found to be more sensitive than the disk diffusion method (100% vs. 87%), whereas both methods were comparable in their specificity .
Although the DDST detected K. pneumoniae more frequently than E. coli, this test was equally efficent to detect ESBL-mediated resistance in both species. The average incubation period required to detect ESBL-mediated resistance in both species was approximately 4 hours. In this study, the DDST on DSM-ES agar proved to be a reliable, rapid and cost-effective test for detecting of ESBL in K. pneumoniae and E. coli. Since the DDST results can be obtained within 4 to 6 hours when DSM-ES agar is used, the use of this media may significantly lower the length of hospital stay, the total cost for patient care and even the mortality rate by fascilitating early treatment.
Shah PW, Stille W: Escherichia coli and Klebsiella pneumoniae strains more susceptible to cefoxitin than to third generation cephalosporins [Letter]. J Antimicrob Chemother. 1983, 11: 597-8.
Jarlier V, Nicolas MH, Fournier G, Philippon A: Extended broad-spectrum beta-lactamases conferring transferable resistance to newer beta-lactam agents in Enterobacteriaceae : Hospital prevalence and susceptibility pattern. Rev Infect Dis. 1988, 10: 867-78.
Jacoby GA, Medeiros AA, O'Brien TF, Pinto ME, Jiang H: Broad-spectrum, transmissible beta-lactamases. N Engl J Med. 1988, 319: 723-4.
Quinn JP, Miyashiro D, Sahm D, Flamm R, Bush K: Novel plasmid-mediated beta-lactamase (TEM-10) conferring selective resistance to ceftazidime and aztreonam in clinical isolates of Klebsiella pneumoniae. Antimicrob Agents Chemother. 1989, 33: 1451-6.
Diekema DJ, Pfaller MA, Jones RN, and the SENTRY participants Group (Americas), et al: Survey of bloodstream infections due to gram-negative bacilli: Frequency of occurence and antimicrobial susceptibility of isolates collected in the United States, Canada, and Latin America for the SENTRY Antimicrobial Surveillance Program 1997. Clin Infect Dis. 1999, 29: 595-607.
Philippon A, Arlet G, Lagrance PH: Origin and impact of plasmid-mediated extended spectrum beta-lactamases. Eur J Clin Microbiol Infect Dis. 1994, 13: 17-29.
Philippon A, Labia R, Jacoby G: Extended-spectrum β-lactamases. Antimicrob Agents Chemother. 1989, 33: 1131-6.
Nordman P, Guibert M: Extended-spectrum β-lactamases in Pseudomonas aeruginosa. J Antimicrob Chemother. 1998, 42: 128-31. 10.1093/jac/42.2.128.
Bush K, Jacoby GA., Medeiros AA: A functional classification scheme for β-lactamases and its correlation with molecular structure. Antimicrob Agents Chemother. 1995, 39: 1211-33.
Jacoby GA, Medeiros AA: More extended spectrum β-lactamases. Antimicrob Agents Chemother. 1991, 35: 1697-1704.
Livermore DM, Brown DF: Detection of β-lactamase-mediated resistance. J Antimicrob Chemother. 2001, 48 (Suppl Sl): 59-64.
Patterson JE: Extended-spectrum β-lactamase-producing Gram-negative bacilli. Seminars in Infect Control. 2001, 1 (3): 184-90.
Nathisuwan S, Burgess DS, Lewis JS: Extended-spectrum β-lactamases: Epidemiology, detection, and treatment. Pharmacotherapy. 2001, 21 (8): 920-8.
Mugnier P, Casin I, Bouthors AT, Collatz E: Novel OXA-10-derived extended-spectrum betalactamases selected in vivo or in vitro. Antimicrob Agents Chemother. 1998, 42: 3113-6.
Paterson DL, Mulazimoglu L, Casellas JM, et al: Epidemiology of ciprofloxacin resistance and its relationship to extended-spectrum beta-lactamase production in Klebsiella pneumoniae isolates causing bacteremia. Clin Infect Dis. 2000, 30: 473-8. 10.1086/313719.
Poutsiaka DD: Antimicrobial resistance in the chronically critically ill patient. Clin Chest Med. 2001, 22: 87-103.
Katsanis GP, Spargo J, Ferraro MJ, Sutton L, Jacoby GA: Detection of Klebsiella pneumoniae and Escherichia coli strains producing extended-spectrum beta-lactamases. J Clin Microbiol. 1994, 32: 691-6.
Sanders CC, Barry AL, Washington JA, et al: Detection of extended-spectrum betalactamase-producing members of the family Enterobacteriaceae with the VITEK ESBL test. J Clin Microbiol. 1996, 34: 2997-3001.
Livermore DM, Struelens M, Amorim J, et al: Multicentre evaluation of the Vitek 2 advanced expert system for interpretive reading of antimicrobial resistance tests. J Antimicrobiol Chemother. 2002, 49: 289-300. 10.1093/jac/49.2.289.
National Committee for Clinical Laboratory Standards: Performance Standards for Antimicrobial Susceptibility Testing; Eleventh Informational Supplement. NCCLS document M100-S11. Wayne Pa: NCCLS. 2001
Jacoby JA, Sutton L: Properties of plasmids responsible for production of extended spectrum β-lactamases. Antimicrob Agents Chemother. 1991, 35: 164-9.
Levy SB, Fitzgerald GB, Macone AB: Changes in intestinal flora of farm personnel after introduction of a tetracycline-supplemented feed on a farm. N Engl J Med. 1976, 295: 583-8.
Barenfanger J, Drake C, Kacich G: Clinical and financial benefits of rapid bacterial identification and antimicrobial susceptibility testing. J Clin Microbiol. 1999, 37: 1415-8.
Doern G, Vautour R, Gaudet M, Levy B: Clinical impact of rapid in vitro susceptibility testing and bacterial identification. J Clin Microbiol. 1994, 32: 1757-62.
McGregor A, Schio F, Beaton S, Boulton V, Perman M, Gilbert G: The MicroScan WalkAway diagnostic microbiology system evaluation. Pathology. 1995, 27: 172-6.
Ling TK, Tam PC, Liu ZK, Cheng AFB: Evaluation of VITEK 2 rapid identification and susceptibility testing system against Gram-negative clinical isolates. J Clin Microbiol. 2001, 39 (8): 2964-6. 10.1128/JCM.39.8.2964-2966.2001.
Cormican MG, Marshall SA, Jones RN: Detection of extended-spectrum β-lactamase (ESBL)-producing strains by the E-test ESBL screen. J Clin Microbiol. 1996, 34 (8): 1880-4.
The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2334/3/22/prepub
This study was carried out at Infectious Diseases and Clinical Microbiology Laboratory of Istanbul Faculty of Medicine with routine expenditures. Only "Diosensimedia-ES" agar was kindly provided as a gift by DIOMED Ltd Co.
The authors wish to thank Dr. Mehmet R. Genç for linguistic help.
A. Atahan Cagatay: None declared.
Tanil Kocagoz is the head of the Research and Development Laboratory at DIOMED Ltd. Co, Istanbul, Turkey.
Haluk Eraksoy: None declared.
About this article
Cite this article
Cagatay, A.A., Kocagoz, T. & Eraksoy, H. Dio-sensimedia: a novel culture medium for rapid detection of extended spectrum β-lactamases. BMC Infect Dis 3, 22 (2003). https://0-doi-org.brum.beds.ac.uk/10.1186/1471-2334-3-22
- Disk Diffusion Method
- Broth Microdilution Method