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Ready-to-use media

XLD Agar EP/USP

Solid medium for the isolation of enteropathogenic species, especially Salmonella and Shigella, according to Pharmacopoeial Harmonised Method and ISO Standard.

Cat. No.
LC-794
Format
20 plates, 90 mm
Storage
15 to 25 °C
Minimum guaranteed shelf life
1 month
Standards
European Pharmacopoeia

Xylose Lysine Deoxycholate Agar is a selective differential medium, suitable for the detection of pathogenic enterobacteria, especially Shigella. Gram-positive microbiota are inhibited by the low amount of deoxycholate, whilst Shigella grows.

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Cat. No.FormatPrice
LC-79420 plates, 90 mm

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Key features

Applications

Selective isolation of Salmonella and Shigella.

Industry

Clinical, final product quality control, food, pharmaceutical/veterinary.

Standards

European Pharmacopoeia.

Presentation

20 prepared plates, 90 mm, with 21 ± 2 mL.

Description and technique

Xylose, lactose or sucrose fermentation produces the acidification of the medium, and this is seen by the indicator turning yellow around the colonies. This colour disappears after 24 hours, so observations must be carried out between 18 and 24 hours.

Hydrogen sulfide production from thiosulfate is easily detected because colonies become darker, due to the ferric sulfide precipitate. Lysine decarboxylation to cadaverine may also be observed in the medium, since it produces alkalinization and consequently the indicator turns red.

All these reactions allow a good differentiation of Shigella. Edwardsiella and Proteus inconstans are the only enterobacteria other than Shigella which do not ferment xylose and therefore show a negative fermentation reaction. Salmonella ferments xylose, but it is consumed quickly and alkalinization of the medium due to lysine decarboxylation may mask the reaction. Salmonella colonies become darker due to ferrous sulfide precipitates, which is also a common property with Edwardsiella.

Other types of enterobacteria do not suffer this phenomenon, since acid accumulation due to lactose and sucrose fermentation is so high that it prevents pH reversion by decarboxylation and even ferrous sulfide precipitate in the first 24 hours.

In the quality control, typical colonial appearances on XLD medium after 18-48 hours of incubation at 30-35 °C are described.

Presentation

Presentation20 prepared plates, 90 mm
Filling21 ± 2 mL
Packaging1 box with 2 packs of 10 plates/pack. Single BOPP film. With desiccant. Lateral labelling.

Composition

Ingredientg/L
Xylose3.50
L-Lysine HCl5.00
Lactose7.50
Sucrose7.50
Sodium chloride5.00
Yeast extract3.00
Phenol red0.08
Sodium deoxycholate2.50
Sodium thiosulfate6.80
Ammonium ferric citrate0.80
Agar13.5

Quality control

Physical/chemical control

ColorRed
pH7.4 ± 0.2 at 25 °C

Microbiological control

According to USP and European Pharmacopoeia.

Inoculate with 10-100 CFU according to the harmonized Pharmacopoeias or with 100-1000 CFU for selectivity.

Analytical methodology according to ISO 11133:2014/Amd 1:2018; A2:2020.

Aerobiosis. Incubation at 30-35 °C. Reading at 18-24/48 h.

MicroorganismGrowth
Salmonella typhimuriumATCC 14028, WDCM 00031Good - culture medium and red colonies, black center (H₂S +)
Salmonella abonyNCTC 6017Good - culture medium and red colonies, black center (H₂S +)
Staphylococcus aureusATCC 6538, WDCM 00032Inhibited

Sterility control

Incubation 48 h at 30-35 °C and 48 h at 20-25 °C: NO GROWTH.

Check at 7 days after incubation in same conditions.

Bibliography

  • ATLAS, R.M., L.C. PARK (1993) Handbook of Microbiological Media for the examination of Food. CRC Press Inc. Boca Raton.
  • DOWNES, F.P. & K. ITO (2001) Compendium of Methods for the Microbiological Examination of Foods. 4th ed. APHA. Washington DC. USA.
  • EUROPEAN PHARMACOPOEIA 11.0 (2023) 11th ed. § 2.6.13. Microbiological examination of non-sterile products: Test for specified microorganisms. Harmonised Method. EDQM. Council of Europe. Strasbourg.
  • HORWITZ, W. (2000). Official Methods of Analysis of the AOAC International. 17th ed. Gaithersburg Md. USA.
  • ICMSF (1978) Microorganisms in Foods 1. University of Toronto Press.
  • PASCUAL ANDERSON, Mª R. (1992) Microbiología Alimentaria. Díaz de Santos, S.A. Madrid.
  • TAYLOR, W.J. (1965) Isolation of Shigella. I. Xylose Lysine Agars: New media for isolation of enteric pathogens. Am. J. Clin. Path 44:471-475.
  • US FDA (Food and Drug Administration). (1998) Bacteriological Analytical Manual. 8th ed. Rev. A. AOAC International. Gaithersburg, Md. USA.
  • USP 33 - NF 28 (2011) <62> Microbiological examination of non-sterile products: Test for specified microorganisms. Harmonised Method. USP Corp. Inc. Rockville. MD. USA.

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