C.L.E.D. HiVeg™ Agar w/ Bromo Thymol Blue

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SKU:
MV792
Used for isolation and differentiation of urinary pathogens on the basis of lactose fermentation.


Intended use

Recommended for isolation and differentiation of urinary pathogens on the basis of lactose fermentation.

Composition**

Ingredients g/L
HiVeg® peptone 4.000
HiVeg® hydrolysate 4.000
HiVeg® extract 3.000
Lactose 10.000
L-Cystine 0.128
Bromothymol blue 0.020
Agar 15.000
Final pH (at 25°C) 7.3±0.2

**Formula adjusted, standardized to suit performance parameters

Directions

Suspend 36.15 grams in 1000 ml purified / distilled water. Heat to boiling to dissolve the medium completely. Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes. Cool to 45-50°C. Mix well and pour into sterile Petri plates.

Principle And Interpretation

On a solid medium, Sandys reported that swarming of Proteus species can be controlled by restricting the electrolytes (1). Formerly swarming of Proteus was controlled by adding alcohol, surface-active agent, sodium azide, boric acid etc. to the medium (1). Later on Sandy's medium was modified by Mackey and Sandys (2), by replacing mannitol by lactose and sucrose and elevating concentration of agar and bromothymol blue. This formulation was further modified by the same authors, called C.L.E.D. (Cystine-Lactose-Electrolyte-Deficient) by deleting the sucrose and by including L-cystine for promoting the growth of cystine dependent dwarf colony coliforms (3). This medium is recommended for use in urinary bacteriology, promoting the growth of all urinary pathogens. C.L.E.D. Medium is also recommended for dip stick procedures and as dip inoculum transport medium for urine specimens (2,3,4). C.L.E.D. HiVeg® Agar w/ Bromo Thymol Blue is prepared by using vegetable peptones in place of animal based peptones which make the media free of BSE/TSE risks. HiVeg® peptone, HiVeg® hydrolysate and HiVeg® extract provides nitrogenous and carbonaceous compounds, long chain amino acids, vitamins and other essential growth nutrients. Lactose is the fermentable sugar. L-cystine supports the growth of dwarf coliform colony. Bromo thymol blue is the pH indicator which turns yellow at acidic pH. Bacteriuria may be quantitated by inoculating the surface of an agar medium by proper dilution. Inoculate the medium immediately after urine collection. It can also be inoculated by calibrated loop or duplicate dilution pour plate methods (5,6)

Type of specimen

Clinical samples

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 :

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 specimens. Safety guidelines may be referred in individual safety data sheets.

Limitations :

  • Initiation of antibiotic therapy, before collection of sample, low urine pH (less than 5) etc. may result in low bacterial count from infected patients.
  • Shigella species may not grow on this medium.

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
Green coloured, clear to slightly opalescent gel forms in Petri plates.

Reaction
Reaction of 3.61% w/v aqueous solution at 25°C. pH: 7.3±0.2

pH
7.10-7.50

Cultural Response
Cultural characteristics observed after an incubation at 35-37°C for 18-24 hours.

Organism Inoculum (CFU) Growth Recovery Colour of Colony
Enterococcus faecalis ATCC 29212 (00087*) 50-100 good-luxuriant >=70% slight yellowish or greenish
Escherichia coli ATCC 25922 (00013*) 50-100 good-luxuriant >=70% yellow, opaque, centre slightly deeper yellow
Klebsiella pneumoniae ATCC 13883 (00097*) 50-100 good-luxuriant >=70% yellow to whitish blue
$ Proteus hauseri ATCC 13315 50-100 good-luxuriant >=70% blue
Salmonella Typhi ATCC 6539 50-100 good-luxuriant >=70% bluish
Staphylococcus aureus subsp. aureus ATCC 25923 (00034*) 50-100 good-luxuriant >=70% deep yellow

Key: *Corresponding WDCM numbers. $ Formerly known as Proteus vulgaris

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 sample must be decontaminated and disposed of in accordance with current laboratory techniques (5,6).

More Information
Product Name C.L.E.D. HiVeg™ Agar w/ Bromo Thymol Blue
SKU MV792
Product Type HiVeg™
Physical Form Powder
Origin Animal Free (Veg)
Packaging type HDPE
References 1. Sandys, 1960, J. Med. Lab. Technol., 17:224.2.Mackey and Sandys, 1965, Br. Med. J., 2:1286.3.MacKey and Sandys, 1966, Br. Med. J., 1:1173.4.Dixson J. M. S. and Clark M. A., 1968, Conc. Med. Assoc. J., 99 (15)5.Benner E. J., 1970, , Appl. Microbiol., 19(3), 4096.MacFaddin J. F., 1985, Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria, Vol. I, Williamsand Wilkins, Baltimore7.Isenberg, H.D. Clinical Microbiology Procedures Handbook. 2nd Edition.8.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.
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