HiCrome™ Enterococcus faecium HiCynth™ Agar Base

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SKU:
MCD1580
For the chromogenic identification of Enterococcus faecium from faeces, sewage and water supplies.


Intended use

Recommended for chromogenic identification of Enterococcus faecium from faeces, sewage and water supplies.

Composition

Ingredients g/L
HiCynth™ Peptone No.2* 23.000
Corn starch 1.000
Sodium chloride 5.000
Arabinose 10.000
Phenol red 0.100
Chromogenic substrate 0.100
Agar 15.000
Final pH (at 25°C) 7.8±0.2

**Formula adjusted, standardized to suit performance parameters

* Chemically defined peptone

Directions

Suspend 27.1 gram in 500 ml purified/distilled water. Heat to boiling to dissolve the medium completely. DO NOT AUTOCLAVE. Cool to 45-50°C and aseptically add sterile rehydrated contents of 1 vial of AzCe Selective Supplement (FD226). Mix well and pour into sterile Petri plates.

Principle And Interpretation

HiCrome™ Enterococcus faecium HiCynth™ Agar Base is recommended for the chromogenic detection of Enterococcus faecium from urine, faeces, soil, food, water, plants and animals. E.faecium is commonly found in the gastrointestinal tracts of humans (1). The resistance exhibited by Enterococcus species to various antimicrobials has led them to being a major cause of human infections including nosocomial infections (2). E.faecalis causes 80-90% of infection while E.faecium causes the majority of the remainder (3). The use of selective media for the isolation of Enterococci has been previously reviewed, including those containing chromogenic substrates (4) and media containing cephalexin-aztreonam supplements. Enterococcus species possess the enzyme β-glucosidase, which specifically cleaves the chromogenic substrate to produce blue coloured colonies. E.faecium ferment arabinose; and cleaves the chromogenic substrate present in the media to produce green coloured colonies along with yellow colouration to the medium. E.faecalis does not ferment arabinose and therefore retains the blue colour.

HiCrome™ Enterococcus faecium HiCynth™ Agar Base is prepared by replacing animal and vegetable peptones with chemically defined peptones to avoid BSE/TSE risks associated with animal peptones. HiCynth™ Peptone No.2 serves as a source of carbon, nitrogen and essential growth nutrients. Corn starch neutralizes the toxic metabolites while sodium chloride maintains the osmotic equilibrium. Phenol red serves as a pH indicator with arabinose being the fermentable carbohydrate.

Type of specimen

Food samples: fermented foods, meat products; Water samples.

Specimen Collection and Handling

For food samples, follow appropriate techniques for sample collection and processing as per guidelines (5). For water samples, follow appropriate techniques for sample collection, processing as per guidelines and local standards (6). After use, contaminated materials must be sterilized by autoclaving before discarding.

Warning and Precaution

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

  1. Some species may show poor growth due to nutritional variations
  2. Slight colour variations may be observed depending upon the utilization of the substrate by the organism.

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:
Light yellow to pinkish beige homogeneous free flowing powder

Gelling:
Firm, comparable with 1.5% Agar gel

Colour and Clarity of prepared medium:
Red coloured, clear to slightly opalescent gel forms in Petri plates

Reaction:
Reaction of 5.42% w/v aqueous solution at 25°C. pH: 7.8±0.2

pH:
7.60-8.00

Cultural Response

Cultural characteristics observed with added AzCe Selective Supplement (FD226) after an incubation at 35-37°C for 24-48 hours.

Organism Inoculum (CFU) Growth Recovery Colour of Colony
Escherichia coli ATCC 25922 (00013*) >=104 inhibited 0%
Enterococcus faecalis ATCC 29212 (00087*) 50-100 luxuriant >=50% blue
Enterococcus faecium ATCC 19434 (00010*) 50-100 luxuriant >=50% green
Enterococcus hirae ATCC 10541 (00011*) 50-100 luxuriant >=50% blue
Pseudomonas aeruginosa ATCC 27853 (00026*) >=104 inhibited 0%
Staphylococcus aureus subsp.aureus ATCC 25923 (00034*) >=104 inhibited 0%

Key: (*) Corresponding WDCM numbers.

Storage and Shelf Life

Store between 15-25°C in a tightly closed container and the prepared medium at 2-8°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 (7,8).

More Information
Product Name HiCrome™ Enterococcus faecium HiCynth™ Agar Base
SKU MCD1580
Product Type HiCynth™, HiCrome™
Physical Form Powder
Origin Chemically defined (HiCynth™)
Packaging type HDPE
References 1.Skinner F. A. and Quesnel L. B., (Ed.), 1978, Streptococci. Academic Press, Inc. (London) Ltd., London, United Kingdom,p. 245-2612.Chenoweth C., Schaberg D., The Epidemiology of Enterococci, Eur. J.Clin. Micorbiol. Infect. Dis., 9:80-89, 1990.3.Moellering R. C., 1992, Clin. Infect. Dis. 14:1173.4.Willinger B. and Manafi M., 1995, Lett. Appl. Microbiol., 20:300-302.5.Baird R.B., Eaton A.D., and Rice E.W., (Eds.), 2015, Standard Methods for the Examination of Water and Wastewater, 23rd ed., APHA, Washington, D.C. 6.Isenberg, H.D. Clinical Microbiology Procedures Handbook 2nd Edition.7.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. 1.8.Salfinger Y., and Tortorello M.L., 2015, Compendium of Methods for the Microbiological Examination of Foods,5th Ed., American Public Health Association, Washington, D.C.
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