Tryptose Blood Agar Base w/ Yeast Extract

Intended Use

For the isolation of fastidious organisms and determining the haemolytic reactions.

Composition**

Final pH (at 25°C): 7.3±0.2

**Formula adjusted, standardized to suit performance parameters

# Equivalent to Beef extract

Directions

Suspend 34.0 grams in 950 ml purified/distilled water. Heat to boiling to dissolve the medium completely. Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes. For preparing Blood Agar cool the autoclaved medium to 45-50°C and aseptically add 5% v/v sterile defibrinated blood. Mix thoroughly, avoiding air bubbles and pour into sterile Petri plates.

Principle And Interpretation

Tryptose Blood Agar Base w/Yeast Extract is a tryptose based medium that can be used for the cultivation of fastidious organisms (1, 2), on supplementation with blood. This medium is devoid of dextrose and therefore useful in determining the haemolytic reactions.

Tryptose Blood Agar Base w/Yeast Extract provides additional nutrients (yeast extract) to the fastidious organisms. Tryptose Blood Agar Base w/Yeast Extract can be used as a general-purpose medium without supplementation of blood. This medium can be used to determine the heamolytic reactions of fastidious organisms. The four different types of haemolysis observed are as follows:

a)a-haemolysis: partial lysis of the erythrocytes surrounding a colony, causing a gray green or brownish discolouration in the media. b)ẞ-haemolysis: complete lysis of the red blood cells surrounding a colony, causing a clearing of blood from the medium. c)y- haemolysis: no haemolysis and consequently, no colour change of the medium surrounding a colony. Organisms showing no haemolysis are generally termed non-hemolytic rather than gamma haemolytic. d)a-prime or wide zone alpha: a small zone of intact erythrocytes immediately adjacent to the colony, with a zone of complete red cell haemolysis surrounding the zone of intact erythrocytes. This type of haemolysis may be confused with beta haemolysis (5)

Tryptose, HM Peptone B and yeast extract provide nitrogenous and carbonaceous compounds, sulphur, vitamin B complex and trace elements essential for bacterial metabolism. Blood provides additional nutrients and serves as a base to study haemolytic reactions. This medium not only keeps the blood cells in a good state but also help in forming distinct haemolysis. Tryptose Blood Agar with Yeast Extract favours the good growth of Neisseria meningitides and Streptococcus pneumoniae. However, it can be used with or without blood supplementation.

Type of specimen

Clinical samples: Urine, skin lesions

Specimen Collection and Handling:

For clinical samples follow appropriate techniques for handling specimens as per established guidelines (3,4). After use, contaminated materials must be sterilized by autoclaving before discarding.

Warning and Precautions :

In Vitro diagnostic Use only. For professional use only. Read the label before opening the container. Wear protective gloves/ protective clothing/eye protection/face protection. Follow good microbiological lab practices while handling specimens and culture. Standard precautions as per established guidelines should be followed while handling clinical specimens. Safety guidelines may be referred in individual safety data sheets.

Limitations :

• Individual organisms differ in their growth requirement and may show variable growth patterns on the medium.
• Each lot of the medium has been tested for the organisms specified on the COA. It is recommended to users to validate the medium for any specific microorganism other than mentioned in the COA based on the user's unique requirement.
• Biochemical and serological tests on colonies of pure culture is required for complete identification.

Performance and Evaluation

Performance of the medium is expected when used as per the direction on the label within the expiry period when stored at recommended temperature.

Quality Control

Appearance
Cream to yellow homogeneous free flowing powder

Gelling
Firm, comparable with 1.5% Agar gel

Colour and Clarity of prepared medium
Basal medium: Yellow coloured clear to slightly opalescent gel forms in Petri plates. After addition of 5% v/v sterile defibrinated blood: Cherry red coloured opaque gel forms in Petri plates.

Reaction
Reaction of 3.4% w/v aqueous solution at 25°C. pH: 7.3±0.2

pH
7.10-7.50

Cultural Response
Cultural characteristics observed with added 5% v/v sterile defibrinated blood, after an incubation at 35-37°C for 18-48 hours.

Key: (*) Corresponding WDCM numbers.

Storage and Shelf Life

Store between 10-30°C in a tightly closed container and the prepared medium at 20-30°C. Use before expiry date on the label. On opening, product should be properly stored dry, after tightly capping the bottle in order to prevent lump formation due to the hygroscopic nature of the product. Improper storage of the product may lead to lump formation. Store in dry ventilated area protected from extremes of temperature and sources of ignition. Seal the container tightly after use. Product performance is best if used within stated expiry period.

Disposal

User must ensure safe disposal by autoclaving and/or incineration of used or unusable preparations of this product. Follow established laboratory procedures in disposing of infectious materials and material that comes into contact with clinical sample must be decontaminated and disposed of in accordance with current laboratory techniques (3,4).

Reference

1. Casman E. P., 1942, J. Bacteriol., 43:33.
2. Casman E. P., 1947, Am. J. Clin. Pathol., 17: 281.
3. Isenberg, H.D. Clinical Microbiology Procedures Handbook 2nd Edition.
4. Jorgensen, J.H., Pfaller, M.A., Carroll, K.C., Funke, G., Landry, M.L., Richter, S.S and Warnock., D.W. (2015) Manual of Clinical Microbiology, 11th Edition. Vol. 1.
5. Koneman E. W., Allen S. D., Janda W. M., Schreckenberger P. C. Winn W. C. Jr., 1992, Colour Atlas and Textbook of Diagnostic Microbiology, 4 th Ed., J. B. Lippinccott Company
6. MacFaddin J. F., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria, Vol. 1, Williams and Wilkins, Baltimore.