Hektoen Enteric Agar ISO

Hektoen Enteric Agar ISO

  • Product Details
  • APPLICATIONS
  • SPECIFICATIONS
  • CODE
  • DOCUMENTS

Principles and uses
Hektoen Enteric Agar is a differential and selective medium used for isolating and differentiating enteric pathogens such as Salmonella and Shigella, both of which cause a variety of serious human gastrointestinal diseases; and other Gram-negative Enterobacteriaceae.
It is used particularly in foods where multi-steps are followed to isolate the pathogens of gastroenteritis. The nutrients for growth are provided by the Meat Peptone and Yeast extract. The increased content of the Peptone and the three fermentable carbohydrates (Lactose, Sucrose, Salicin) as sources of carbon and energy reduce the inhibitory action of the Bile salts on Salmonella and Shigella spp. The lactose concentration in this medium is higher than in many other media used for enterics since this helps the visualization of enteric pathogens and minimizes the problem of delayed lactose fermentation. Bromothymol blue and Acid fuchsin are pH indicators. Sodium thiosulfate provides Sulphur, and Ferric ammonium citrate is the indicator for
H2S production. H2S positive colonies are black-centered. Sodium chloride maintains the osmotic balance.
The norma ISO 21567 recommends the Hektoen Agar as a selective solid media for the enumeration of Shigella spp. Although suppressed, partially inhibited E. coli and other organisms which use lactose, sucrose, and/or salicin with the production of acid, give colonies whose tones vary from yellow to orange to salmon. The Salmonella and Shigella are green or green-blue. Proteus is not inhibited but produces a green-yellow colony when it grows. The colonies of Proteus and Salmonella may present a black center and clear edges if they form iron sulfide as a result of H2S production.

Preparation
Suspend 75,6 grams of the medium in one liter of distilled water. Mix well and dissolve by heating with frequent agitation. Boil for one minute until complete dissolution. AVOID OVERHEATING. DO NOT AUTOCLAVE. Cool to 47 ºC and pour into Petri dishes.

For the isolation and differentiation of Gram negative enteric bacteria
Bromthymol blue 0.065 Acid fuchsin 0.1 Bacteriological agar 14 Bile salts N° 3 9 Ferric ammonium citrate 1.5 Lactose 12 Salicin 2 Sodium chloride 5 Sodium thiosulfate 5 Sucrose 12 Yeast extract 3 Enzymatic digest of meat 12
ISO 21567