Buffered Glucose HiVeg™ Broth (Glucose Phosphate HiVeg™ Broth) (MR-VP HiVeg™ Medium)

Principle And Interpretation

Methyl Red and Voges-Proskauer test are among the two various tests used in the biochemical identification of bacterial species. These tests were originally studied by Voges, Proskauer (1) and subsequently by Clark and Lubs (2) to differentiate between members of the coli- aerogens group. Both the tests are based on the detection of specific breakdown products of carbohydrate metabolism. All members of Enterobacteriaceae are, by definition, glucose fermenters. In MR-VP Broth, after 18-24 hours of incubation, fermentation produces acidic metabolic by products. Therefore initially all enterics will give a positive MR reaction if tested (3,4,5). However, after further incubation, required by the test procedure (2-5 days), MR positive organisms continue to produce acids, resulting in a low pH (acidic) that overcomes the phosphate buffering system and maintains an acidic environment in the medium (pH 4.2 or less). MR-negative organisms further metabolize the initial fermentation products by decarboxylation to produce neutral acetyl methyl carbinol (acetoin), which results in decreased acidity in the medium and raises the pH towards neutrality (pH 6.0 or above) (6). In the presence of atmospheric oxygen and alkali, the neutral end products, acetoin and 2, 3-butanediol, are oxidized to diacetyl, which react with creatine to produce a red colour. MR-VP HiVeg® Medium is prepared by completely replacing animal based peptones with vegetable peptones to avoid BSE/TSE risks associated with animal peptones. The Methyl Red (MR) test is performed after 5 days of incubation at 30°C (7). The Voges-Proskauer test (VP) cultures are incubated at 30°C for 24-48 hours (8). Various test procedures have been suggested for performing the VP test by Werkman (9), OMeara (10) Levine, et al (11) and Voughn et al (7). Werkmans Test (9): Add 2 drops of a 2% solution of ferric chloride to 50 ml culture and 5 ml of 10% sodium hydroxide. Shake the tube to mix well. Stable copper colour developing in a few minutes is positive reaction. OMeara Test (10): Add 25 mg of solid creatine to 5 ml culture and then add 5 ml concentrated (40%) sodium hydroxide. Red colour development in a few minutes after shaking the tube well is a positive reaction. Levine, Epstein and Voughn (11) modified OMeara technique by dissolving the creatine in a concentrated solution of potassium hydroxide (R031, OMeara Reagent). Voughn, Mitchell and Levine (7) recommended the method of Barritt (5) as, addition of 1 ml of Barritt Reagent B (R030 - 40% potassium hydroxide) and 3 ml of Barritt Reagent A (R029 - 5% a-naphthol in absolute ethanol) to 5 ml culture. Positive test is indicated by eosin pink colour within 2-5 minutes.