B.G. Sulpha HiVeg™ Agar (Brilliant Green Sulpha HiVeg™ Agar)

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SKU:
MV492
This is a highly selective medium for isolation and detection of Salmonella species in food, especially eggs and egg products.


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.

More Information
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.
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