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B.G. Sulpha HiVeg™ Agar (Brilliant Green Sulpha HiVeg™ Agar)
Composition**
| Ingredients | Gms/Litre |
|---|---|
| Yeast extract | 3.000 |
| HiVeg peptone No. 3 | 10.000 |
| Lactose | 10.000 |
| Sucrose | 10.000 |
| Sodium sulphapyridine | 1.000 |
| Sodium chloride | 5.000 |
| Brilliant green | 0.0125 |
| Phenol red | 0.080 |
| Agar | 20.000 |
Final pH (at 25°C): 6.9±0.2
**Formula adjusted, standardized to suit performance parameters
Directions
Suspend 59.09 grams in 1000 ml distilled water. Heat to boiling to dissolve the medium completely. Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes. To maintain selectivity of the medium, DO NOT OVER STERILIZE OR OVERHEAT the medium. Cool to 45-50°C. Mix well and pour into sterile Petri plates.
Principle And Interpretation
Brilliant Green Sulpha HiVeg Agar is prepared by replacing proteose peptone with HiVeg peptone No. 3 which makes the medium BSE/TSE risks free.
Salmonella species are ubiquitous in the environment. They enter the gastrointestinal tract of animals due to the consumption of contaminated feed. Meat and meat products, eggshell and its contents from these infected animals stands to be the major cause of salmonella pathogenesis (1-5).
Salmonella species are usually the causative agents of a self-limiting gastroenteritis. In some cases they may also cause typhoid fever. Contamination with Salmonella is most frequently encountered in the poultry industry.
Brilliant Green Sulpha Agar is used for the selective isolation and detection of Salmonella species in foods especially from eggs and egg products. It was first formulated by Kristensen, Lester and Jargens (6). This was further modified by Osborne and Stokes (7) by the addition of 0.1% sodium sulphapyridine. Addition of this helped to increase the selectivity of the medium. B. G. Sulpha HiVeg Agar is the modification of B. G. Sulpha Agar recommended for same purpose. Colonies of Salmonella may sometimes vary from red to pink to white depending upon the strain and time of incubation. Do not autoclave the medium for more than 15 minutes as it decreases the selectivity of the medium (8).
Yeast extract and HiVeg peptone No. 3 provides essential growth nutrients, amino acids and vitamins. Brilliant green used in the medium is inhibitory to gram-positive and most gram-negative lactose/sucrose fermenting bacilli. Sulphapyridine enhances the selectivity of the medium. The medium does not support the growth of Salmonella Typhi as well as Shigella. Since Brilliant Green Sulpha HiVeg Agar is highly selective, a less inhibitory medium should be simultaneously used to recover organisms from the pre-enriched culture (Selenite Cystine HiVeg Medium).
Quality Control
Appearance: Light yellow to pinkish purple Homogeneous Free flowing powder
Gelling: Firm, comparable with 2.0% agar gel.
Colour and Clarity of Prepared Medium: Greenish brown clear to slightly opalescent
Reaction: Reaction of 5.91% w/v aqueous solution at 25°C. pH: 6.9±0.2
pH: 6.70-7.10
Cultural Response
Cultural characteristics observed after an incubation at 35-37°C for 24-48 hours.
Cultural Response
| Organism | Inoculum (CFU) | Growth | Recovery | Colour of colony |
|---|---|---|---|---|
| Enterococcus faecalis ATCC 29212 | 100-1000 | inhibited | 0% | |
| Escherichia coli ATCC 25922 | 100-1000 | none-poor | <20% | yellow green surrounded by intense yellow-green zone |
| Proteus vulgaris ATCC 13315 | 100-1000 | inhibited | 0% | |
| Salmonella Enteritidis ATCC 13076 | 100-1000 | good | >50% | pink - white, surrounded by brilliant red zone. |
| Salmonella Typhimurium ATCC 14028 | 100-1000 | good | >50% | pink - white |
| Staphylococcus aureus ATCC 25923 | 100-1000 | inhibited | 0% |
Storage and Shelf Life
Store below 30°C in tightly closed container and the prepared medium at 2 - 8°C. Use before expiry date on the label.
| Product Name | B.G. Sulpha HiVeg™ Agar (Brilliant Green Sulpha HiVeg™ Agar) |
|---|---|
| SKU | MV492 |
| Product Type | HiVeg™ |
| Physical Form | Powder |
| Origin | Animal Free (Veg) |
| Packaging type | HDPE |
| References | 1. Doyle M. P., (Ed.), 1989, Foodborne Bacterial Pathogens, Marcel Dekker, Inc., New York. 327- 445 2.DAoust J. Y., 1994, Int. J. Food Microbiol. 24: 11-31. 3.Kristensen M., Lester V., and Jargens A., 1925, Brit. J. Exp. Pathol. , 6:291. 4.Osborne W. W. and Stokes J. L., 1955, Ottawa; Food and Drug Laboratories, 1962. 5.Brooks and Taylor, 1955, Rep. Rd. Invest. Bd. 60, H. M. S. O., London, England. 6.Forsythe, Ayres and Radlo, 1953, Food Technol., 7:49. 7.Stadelman, Ikeme, Roop and Simmons, 1982, Poultry Sci., 61:388. 8.MacFaddin J. F., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria, Vol. I, Williams& Wilkins, Baltimore, MD. |
| Customized Product Available | No |










