Burkholderia Cepacia Selective Agar

$45.00$95.00

250 mL, 500 mL
Number of sizes: 2
Type: Agar Gel

Prepared Media – Ready to Dissolve

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SKU: BCSA-ML Category:

Description

Intended Use and Principle of Procedure
PC Agar and OFPBL Agar are used in the selective isolation and detection of Burkholderia (formerly Pseudomonas) cepacia from clinical and nonclinical specimens.

These media provide a variety of enzymatic digests of proteinaceous substrates, inorganic salts and other nutrients to satisfy the nutritional requirements of these organisms. Selective agents are incorporated to improve the recovery of Burkholderia Cepacia by inhibiting common contaminants. PC agar incorporates crystal violet to inhibit gram-positive cocci, especially enterococci and staphylococci, bile salts to inhibit most gram-positive cocci other than enterococci, and ticarcillin and polymyxin B to inhibit gram-negative bacilli. OFPBL Agar incorporates polymyxin B to inhibit gram-negative flora, while bacitracin inhibits the gram-positive organisms and Neisseria. 4 PC Agar contains the pH indicator phenol red to facilitate detection of Burkholderia Cepacia. Alkaline end products from the metabolism of pyruvate raise the pH of the medium, causing the color of the indicator to change from light orange to pink or pink-red in the area of growth. In areas of heavy growth of Burkholderia Cepacia, the pink color intensifies. OFPBL Agar contains the pH indicator bromthymol blue to facilitate detection of Burkholderia Cepacia. Acid end products from the metabolism of lactose lower the pH of the medium resulting in a yellow color change. Burkholderia Cepacia colonies will also have a yellow color.

 

Summary and Explanation
Burkholderia cepacia is an opportunistic pathogen generally associated with nosocomial infections.1 Studies indicate that Burkholderia Cepacia may be an important pulmonary pathogen for patients with cystic fibrosis (CF).1,2 The incidence of this organism in the respiratory tract of CF patients is often accompanied by rapid deterioration in pulmonary status and death.3 Recovery of this organism on commonly used media, such as blood agar or MacConkey Agar, is difficult because common isolates, such as Pseudomonas aeruginosa, Escherichia coli and Staphylococcus aureus, overgrow the slower-growing colonies of Burkholderia Cepacia and mask its presence.

Gillian et al. developed PC Agar for improved recovery of Burkholderia Cepacia. 2 Crystal violet, bile salts and two antimicrobial agents are used as selective agents. Phenol red facilitates detection of Burkholderia Cepacia by a color change in the medium. They reported isolating Burkholderia Cepacia on PC Agar from respiratory secretions of 35 CF patients, but isolated the organism from only 21 patients on MacConkey Agar.2 Welch et al. developed a differential but less selective medium for the recovery of Burkholderia Cepacia. 4,5 This medium, OFPBL Agar, is OF (oxidation-fermentation) basal medium supplemented with polymyxin B, bacitracin, lactose and agar. The indicator, bromthymol blue, aids in the detection of Burkholderia Cepacia isolates through a color change in the medium. These investigators reported isolating Burkholderia Cepacia on OFPBL Agar from 58 CF patients, while only isolating this organism from 19 patients on MacConkey Agar.

 

Expected Results
Typical colonies of Burkholderia Cepacia on PC Agar are grayish-white with a pink-red zone in the surrounding medium.2 Typical colonies of Burkholderia Cepacia on OFPBL Agar are yellow with yellow zones in the surrounding medium.

 

Procedure
Use standard procedures to obtain isolated colonies from specimens. Incubate the plates in an inverted position (agarside up) at 30-35°C for a minimum of 4 days to allow sufficient time for colony development and for the color of the indicator change.

 

Limitation of the Procedure
Organisms other than Burkholderia Cepacia may also grow on PC Agar and produce alkaline end products that cause the medium to become pink. Other organisms, e.g., B. gladioli, may also grow on OFPBL Agar and resemble Burkholderia Cepacia (yellow colonies). Therefore, these media should not be used as the sole method of identification of Burkholderia Cepacia.

 

References
1. Gilligan and Whittier. 1999. In Murray, Baron, Pfaller, Tenover and Yolken (ed.), Manual of clinical microbiology, 7th ed. American Society for Microbiology, Washington, D.C.

2. Gilligan, Gage, Bradshaw, Schidlow and DeCicco. 1985. J. Clin. Microbiol. 22:5.

3. Gilligan and Schidlow. 1984. Clin. Microbiol. Newsl. 6:42.

4. Welch, Muszynski, Pai, Marcon, Hribar, Gilligan, Matsen, Ahlin, Hilman and Chartrand. 1987. J. Clin. Microbiol. 25:1730.

5. Carson, Tablan, Cusick, Jarvis, Favero and Bland. 1988. J. Clin. Microbiol. 26:2096.

6. MacDonald, Gilligan, Welch, Reller and Menegus. 1994. In Consensus conference: microbiology and infectious disease in cystic fibrosis, vol. 5:1. Cystic Fibrosis Foundation, Washington, D.C.

7. Gilligan. 1996. Clin. Microbiol. Newsl. 18:83.

8. Christenson, Welch, Mukwaya, Muszynski, Weaver and Brenner. 1989. J. Clin. Microbiol. 27:270.

Additional information

Size

250mL, 500mL

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