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6-2 The antibiotic disk sensitivity test

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One of the most widely used methods to determine the susceptibility of microorganisms to antimicrobial agents is the disc agar-diffusion method. The principle of this method is dependent upon the inhibition of reproduction of a microorganism on the surface of a solid medium by an antimicrobial agent which diffuses into the medium from a filter paper disc. Thus, for an organism which is truly sensitive (susceptible) to an antimicrobial agent (i.e., affected at the target site as explained above), we expect to see a zone of inhibition around the disc impregnated with the agent; beyond this zone an unaffected, area of normal growth (lawn) of the organism is present. However, the degree of inhibition necessary to make each antibiotic effective during use is unique, hence each resistance zone size cutoff is specific to the antibiotic. Accurate measurement of zone diameter is necessary to properly interpret this test.

Period 1

Materials

12 to 18-hour cultures of Staphylococcus epidermidis, Pseudomonas fluorescens, Escherichia coli, Enterococcus faecalis and Bacillus subtilis (all grown in Trypticase Soy Broth). Each person will choose one culture from this list.

1 sterile cotton swab

2 plates of Penassay Agar

2 antibiotic disc dispensers, each dispensing four antibiotic discs

  1. Dip the sterile cotton swab into the culture to be tested. With the swab, cover the entire surface of each of the Penassay Agar plates such that a confluent lawn of growth would result if nothing more were to be done on the plates. Let the plates dry at room temperature for several minutes.
  2. With the disc dispensers, apply four antibiotic discs to each of the plates, making sure that all eight antibiotics are represented on your plates. The instructor will demonstrate the use of the dispenser.
  3. Incubate the plates for 1-2 days at 37°C.

Period 2

Materials

1 ruler with millimeter (mm) divisions

Disk sensitivity test

Figure 10.1. Disk sensitivity test. The results of the disk sensitivity test for P. fluorescens, E. coli, B. subtilis, and S. epidermidis. Notice that the gram-positive bacteria are more sensitive to the antibiotics that we used here. To make your measurements, take a ruler, measure the diameter of the zones of clearing on the screen. Compare the diameters you measure to the table in Figure 10-2.

  1. With the ruler, measure the zones of inhibition in millimeters from the underside of the plate. Measure the entire diameter of the zone, including the disc. For any zone which contains one or more isolated colonies, what do these colonies represent? Would you choose to ignore their presence? Is this a zone of inhibition after all?
  2. Interpret your findings with the aid of the table below. (The instructor may substitute other antibiotics and indicate their zone diameter data.) Compare the patterns of susceptibility and resistance with respect to gram reaction, potential pathogenicity and natural habitat of each organism.

Figure 10-2 lists many common antibiotics that are used in the disk sensitivity test and their zones of clearing.

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Figure 10.2. Zones of clearing for various antibiotics. The zone of clearing varies depending upon the antibiotic and its chemical properties. The medical effectiveness of antibiotics in patients has been correleated with a certain zone size and this is used to decide whether an antibiotic will be useful for treating a test pathogen.
*For this agent, the zone is measured at the margin of heavy growth. Sulfonamides may not inhibit the tested culture until after several generations. Therefore, a band of slight, hazy growth just inside the margin of the heavy growth may be ignored.