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Dehydrated culture media

Bolton Selective Enrichment Broth Base ISO

For the selective pre-enrichment of Campylobacter in food samples.

Cat. No.
LC-1441
Format
500 g
Storage
2 to 25 °C
Minimum guaranteed shelf life
15 months
Standards
BAMISO 10272ISO 11133

Bolton Selective Enrichment Broth is used for the selective pre-enrichment of Campylobacter in food samples with low numbers of campylobacters and low level of background microflora and/or with stressed campylobacters. It is recommended by ISO 10272.

Supplement to be added: Bolton Selective Supplement LC-6070

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Cat. No.FormatPrice
LC-1441500 g

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Key features

Applications

Selective enrichment of Campylobacter.

Industry

Food.

Standards

BAM, ISO 10272, ISO 11133.

Preparation

13.8 g in 475 mL of distilled water; boil for one minute, sterilize in autoclave at 121 °C for 15 minutes.

Principles and uses

Campylobacter genus are Gram-negative, microaerophilic bacteria that can be present in milk, untreated water or undercooked food.

Injured organisms are not generally detected and therefore a recovery step must be included in examination procedures. This is of importance, particularly in the food industry as various processes such as heat, desiccation, preservation processes, pH changes, etc., cause sublethal injuries to Campylobacter. The broth is rich in nutrients and produces high resuscitation rates for sublethally injured bacteria and intense growth.

Meat peptone provides nitrogen, vitamins, minerals and amino acids essential for growth. Lactalbumin hydrolysate provides nitrogen, amino acids, vitamins, and carbon and is specially indicated for culture media for Campylobacter growth. Yeast extract is a source of vitamins, particularly the B-group. Sodium chloride supplies essential electrolytes for transport. Alpha-ketoglutaric acid is incorporated to satisfy the specific nutritional requirements of Campylobacter species. Sodium pyruvate is a source of energy for bacterial metabolism and aids in resuscitation of stressed organisms. Sodium carbonate is a pH regulator. Hemin provides X factor, which stimulates the growth of many microorganisms. The addition of Bolton Broth Selective Supplement inhibits the accompanying Gram-positive bacteria due to trimethoprim, Gram-negative bacteria due to vancomycin, cefoperazone and trimethoprim as well as yeasts and moulds due to cycloheximide.

Technical specifications

SolubilityWithout residues
AppearanceFine powder
Color of the dehydrated mediumBeige
Color of the prepared mediumDark amber. With blood: cherry red
Final pH (25 °C)7.4 ± 0.2
Amount13.8 g in 475 mL
Storage2 to 25 °C

Formula

Ingredientg/L
Alpha-ketoglutaric acid1
Hemin0.01
Sodium carbonate0.6
Sodium chloride5
Sodium metabisulfite0.5
Sodium pyruvate0.5
Yeast extract5
Enzymatic digest of animal tissues10
Lactalbumin hydrolysate5

Typical formula in g/L, adjusted and/or supplemented as required to meet performance criteria.

Preparation and use

Preparation

Suspend 13.8 grams of the medium in 475 mL of distilled water. Mix well and dissolve by heating with frequent agitation. Boil for one minute until complete dissolution. Sterilize in autoclave at 121 °C for 15 minutes. Cool to < 47 °C and aseptically add one vial of the Bolton Selective Supplement (LC-6070) and 25 mL of sterile lysed horse blood. Homogenize gently and dispense into tubes.

According to ISO 10272

For the detection and enumeration of Campylobacter spp. for samples with low numbers of campylobacters and low level of background microflora and/or stressed campylobacters according to ISO 10272:

  1. Add the test portion to the liquid enrichment medium Bolton Broth. In general, for preparing the initial suspension, combine a quantity of 10 g or 10 mL of the test portion with 90 mL of the Bolton Broth.
  2. Incubate in a microaerobic atmosphere at 37 °C for 4 to 6 h, then at 41.5 °C for 44 ± 4 h.
  3. From the enrichment culture obtained, inoculate two selective media, CCDA agar (LC-1129) and any other selective medium using different selective principles.
  4. Incubate the selective solid media at 41.5 °C in a microaerobic atmosphere for 44 h to detect the presence of suspect Campylobacter colonies.
  5. Examine the suspect Campylobacter colonies for morphology and motility using a microscope, subculture on a non-selective blood agar, and then confirm by detection of oxidase activity and an aerobic growth test at 25 °C.

Quality control

According to ISO 11133

Incubation conditions: 37 ± 1 °C / 5 ± 1 h, then 41.5 ± 1 °C / 44 ± 4 h, microaerobic atmosphere.

Inoculation conditions: target microorganisms (< 100 CFU) / non-target microorganism (> 1000 CFU) / selectivity (10⁴-10⁶ CFU).

MicroorganismSpecificationCharacteristic reaction
Escherichia coliATCC 25922< 10 colonies on TSA
Staphylococcus aureusATCC 25923< 10 colonies on TSA
Campylobacter jejuniATCC 29428 + Escherichia coli ATCC 25922 + Staphylococcus aureus ATCC 25923> 10 characteristic colonies in mCCD agarGreyish, flat and moist, sometimes with metallic sheen
Campylobacter coliATCC 43478 + Escherichia coli ATCC 25922 + Staphylococcus aureus ATCC 25923> 10 characteristic colonies on mCCDA agarGreyish, flat and moist, sometimes with metallic sheen

Bibliography

  • ISO 10272-1:2017 Microbiology of the food chain. Horizontal method for detection and enumeration of Campylobacter spp. Part 1: Detection method.
  • Post, D. E. (1995). Food-Borne Pathogens Monograph Number 3 Campylobacter.
  • Bolton, F.J. (1995) Personal communication.
  • Hunt, J.M. (1998) Campylobacter. In: F.D.A. Bacteriological Analytical Manual, 8th Edition (Rev. A) 7.01-7.27. AOAC, Arlington Va.

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