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Supplements and additives

Legionella AB Supplement ISO

Sterile selective supplement for the isolation of Legionella spp. from environmental water samples.

Cat. No.
LC-6093
Format
10 vials
Storage
2 to 25 °C
Minimum guaranteed shelf life
15 months
Standards
ISO 11133ISO 11731

The discovery of the causative organism of Legionnaires' disease has permitted big progress in the studies around it. New media for the culture and the enumeration of Legionella spp. have been developed in the last years.

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LC-609310 vials

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Key features

Applications

Selective isolation of Legionella.

Industry

Water.

Standards

ISO 11133, ISO 11731.

Presentation

10 freeze-dried vials with 3 ± 0.1 g.

Description and technique

Description

Legionella BCYE + AB selective supplement, when added to the agar base, gives the antibiotic support in order to obtain a selective final medium.

The selectivity is raised by the addition of sodium cefazolin that acts against Gram-positive bacteria, polymyxin B that inhibits Gram-negative bacteria and natamycin that is an antifungal agent and inhibits the yeast growth.

Technique

Collect, dilute and prepare samples and volumes as required according to specifications, directives, official standard regulations and/or expected results.

Reconstitute 1 vial of Legionella BCYE + AB Selective Supplement with 9 mL of sterile distilled water, in aseptic conditions, and add it to 500 mL of melted Legionella BCYE Agar Base cooled to 47-50 °C, supplemented before with Legionella BCYE growth supplement. Do not overheat once supplemented.

Pour the complete medium into Petri dishes and, once solidified on a flat surface, spread the plates by streaking methodology or by MF method.

Allow the inoculated plates to stand until the inocula have been absorbed. Invert the plates and incubate at 36 ± 2 °C for up to 2, 3, 5-10 days. To ensure the atmosphere in the incubator is humid, place a tray of water in the bottom of the incubator. Top up this tray with fresh water (if necessary) each time the plates are examined. Incubation in an atmosphere of air with 2.5% (volume fraction) CO₂ may be beneficial for the growth of some Legionella, but it is not essential.

Examine the plates with a plate microscope on at least three occasions at intervals of 2, 3 to 5 days during the 10-day incubation period, as Legionella grow slowly and can be masked by the growth of other organisms. Record the number of each type of colony present.

Colonies of Legionella are often white-grey-blue-purple in colour, but may be brown, pink, lime-green or deep-red. They are smooth with smooth edges and exhibit a characteristic ground-glass appearance. Under ultraviolet light colonies of several species autofluoresce brilliant white, but others are red and L. pneumophila appears dull green often tinged with yellow. All presumptive colonies must be confirmed by cultural, biochemical, serological or genetic methods.

Presentation

Presentation10 freeze-dried vials
Filling3 ± 0.1 g
Packaging22 ± 0.25 x 55 ± 0.5 mm glass vials, tag labelled, white plastic cap - 10 vials per box.

Composition

IngredientAmount per vial
Polymyxin B sulfate40,000.00 IU
Sodium cefazolin4.50 mg
Pimaricin (syn. natamycin)35.00 mg

Reconstitute the original freeze-dried vial by adding 9 mL of sterile distilled water.

Quality control

Physical/chemical control

ColorWhite

Microbiological control

Reconstitute 1 vial as indicated in Composition; shake and dissolve completely.

Add 1 vial to 500 mL of medium base. DO NOT HEAT once supplemented.

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

Aerobiosis. Incubation at 36 ± 2 °C. Reading 3-5 days, up to 10 days.

MicroorganismGrowth
Escherichia coliATCC 8739, WDCM 00012Inhibited
Enterococcus faecalisATCC 19433Inhibited
Legionella anisaATCC 35292, WDCM 00106 (by MF)Good (≥ 50%), grey-blue colonies
Legionella pneumophilaATCC 33152, WDCM 00107 (by MF)Good (≥ 50%), grey-blue colonies

The reference medium is validated GVPC.

Sterility control

Add 5 mL of the sample to 100 mL of TSB and to 100 mL of Thioglycollate.

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

Bibliography

  • ATLAS, R.M. & L.C. PARKS (1993) Handbook of Microbiological Media. CRC Press. Boca Raton. Fla. USA.
  • CLESCERI, L.S., A.E. GREENBERG & A.D. EATON (1998) Standard methods for the examination of water and wastewater. 9-106. 20th edition. APHA-AWWA-WEF. Washington DC, USA.
  • EDELSTEIN, P.H. (1981) Improved semiselective medium for the isolation of Legionella pneumoniae from contaminated clinical and environmental specimens. J. Clin. Microbiol. 14(3):298.
  • FEELEY, J.C., R.J. GIBSON, G.W. GORMAN, N.C. LANGFORD, J.K. RASHEED, C.D. MACKEL & W.B. BAINE (1979) Charcoal-Yeast Extract Agar: Primary isolation medium for Legionella pneumophila. J. Clin. Microbiol. 10(4) 437.
  • ISO 11731 Standard (2017) Water Quality - Enumeration of Legionella.
  • ISO 11133:2014/Amd 1:2018. Microbiology of food, animal feed and water. Preparation, production, storage and performance testing of culture media.
  • MacFADDIN, J.F. (1985) Media for Isolation-Cultivation-Identification-Maintenance of Medical Bacteria.
  • PASCULLE, A.W., J.C. FEELEY, R.J. GIBSON, L.G. CORDES, R.L. MYEROWITZ, C.M. PATTON, G.W. GORMAN, C.L. CARMACK, J.W. EZZELL & J.N. DOWLING (1980) Pittsburgh pneumonia agent: Direct isolation from human lung tissue. J. Infect. Dis., 141:727.
  • UNE-EN ISO 11133 (2014). Microbiología de los alimentos para consumo humano, alimentación animal y agua - Preparación, producción, conservación y ensayos de rendimiento de los medios de cultivo.
  • WARD, K.W. (1995) Processing and interpretation of specimens for Legionella spp. In "Clinical Microbiology Procedures Handbook" Chap. 12.1 edited by H.D. Isenberg. ASM Press. Washington DC, USA.

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