BBL™ Middlebrook 7H11//7H11 Selective Agar  8801671 • Rev

BBL™ Middlebrook 7H11//7H11 Selective Agar  8801671 • Rev

BBL™ Middlebrook 7H11//7H11 Selective Agar 8801671 • Rev. 03 • Nov 2014 QUALITY CONTROL PROCEDURES I INTRODUCTION Middlebrook 7H11//7H11 Selective Agar, when supplemented with Middlebrook OADC Enrichment, is used in qualitative procedures for the isolation and cultivation of mycobacteria. II PERFORMANCE TEST PROCEDURE A. Middlebrook 7H11 Agar 1. Inoculate representative samples with the cultures listed below. a. For mycobacterial organisms, spread plate inoculate a 7H9 broth suspension diluted to yield 103 - 104 CFU/plate using a sterile glass spreader. b. Incubate plates at 35 ± 2 °C in a CO2-enriched atmosphere. c. Include plates of a previously tested lot of Middlebrook 7H11 Agar as controls for the mycobacterial strains. 2. Examine plates after 7 - 21 days for growth and pigmentation. 3. Expected Results Organisms ATCC™ Recovery Pigmentation *Mycobacterium tuberculosis H37Ra 25177 Moderate to heavy growth Cream *Mycobacterium kansasii, Group I 12478 Moderate to heavy growth White/cream yellow *Mycobacterium scrofulaceum, Group II 19981 Moderate to heavy growth Orange *Mycobacterium intracellulare, Group III 13950 Moderate to heavy growth Cream *Mycobacterium fortuitum, Group IV 6841 Moderate to heavy growth Cream *Recommended organism strain for User Quality Control. B. Middlebrook 7H11 Selective Agar 1. Inoculate representative samples with the cultures listed below. a. Use inoculum preparation and spread plate testing as outlined above for all mycobacterial organisms. b. For E. coli, C. albicans, P. mirabilis and P. aeruginosa streak inoculate culture diluete 103 - 104 CFU/plate. c. Incubate plates at 35 ± 2 °C in a CO2-enriched atmosphere. d. Include plates of a previously tested lot of Middlebrook 7H11 as controls for the mycobacterial strains. Include plates of a previously tested lot of TSA with 5% Sheep Blood as controls for non-mycobacterial organisms. 2. Examine plates after 7 - 21 days for growth and pigmentation. 3. Expected Results Organisms ATCC Recovery Pigmentation *Mycobacterium tuberculosis H37Ra 25177 Fair to heavy growth Cream *Mycobacterium kansasii, Group I 12478 Fair to heavy growth White/cream yellow *Mycobacterium scrofulaceum, Group II 19981 Fair to heavy growth Orange *Mycobacterium intracellulare, Group III 13950 Inhibition (partial to complete) Cream *Mycobacterium fortuitum, Group IV 6841 Fair to heavy growth Cream *Escherichia coli 25922 Inhibition (partial to complete) N/A *Candida albicans 10231 Inhibition (partial to complete) N/A Proteus mirabilis 12453 Inhibition (partial to complete) N/A Pseudomonas aeruginosa 27853 Inhibition (partial to complete) N/A *Recommended organism strain for User Quality Control. III ADDITIONAL QUALITY CONTROL 1. Examine plates as described under "Product Deterioration." 2. Visually examine representative plates to assure that any existing physical defects will not interfere with use. 3. Determine the pH potentiometrically at room temperature for adherence to the specification of 6.6 ± 0.2. 4. Note the firmness of plates during the inoculation procedure. 5. Incubate uninoculated representative plates at 35 ± 2 °C for 72 h and examine for microbial contamination. PRODUCT INFORMATION IV INTENDED USE These media are used in qualitative procedures for isolation and cultivation of mycobacteria, especially Mycobacterium tuberculosis, from clinical and nonclinical specimens. Middlebrook 7H11//7H11 Selective Agar bi-plates provide two media, one moderately selective and one highly selective, for the recovery of mycobacteria from specimens containing mixed flora. The Middlebrook 7H11 Agar is contained in the sector differentiated by the Roman numeral "I" molded into the bottom of the sector. The 7H11 Selective Agar is contained in the sector marked "II." 8801671 1 of 4 V SUMMARY AND EXPLANATION Middlebrook 7H10 Agar is based on an improved formulation for the oleic acid-albumin agar that Middlebrook and Cohn developed to promote early growth of tubercle bacilli in vitro and to facilitate wider application of drug-susceptibility testing.1-3 Because of its relatively simple chemical formulation, it is less likely to support contaminants than the egg-based media commonly used for the cultivation of mycobacterial species.4 Middlebrook 7H11 Agar was developed by Cohn et al. by the addition of casein hydrolysate to 7H10 Agar.5 7H11 Agar provides enhanced growth of fastidious, drug-resistant strains of M. tuberculosis that grow poorly (or not at all) on 7H10 Agar or other widely- used media.5,6 The 7H11 Selective Agar is 7H11 Agar modified by the addition of four antimicrobial agents: polymyxin B, carbenicillin, amphotericin B and trimethoprim lactate. Mitchison et al. initially developed the medium to reduce the need for decontamination procedures.7 They found that the alkaline agents used to reduce the growth of contaminating organisms inhibited some species of mycobacteria. McClatchy recommended reducing the concentration of carbenicillin used by Mitchinson et al. to make the medium less inhibitory to mycobacteria.8 VI PRINCIPLES OF THE PROCEDURE Middlebrook 7H10 Agar is a defined medium consisting of oleic acid-albumin enrichment, glycerol, dextrose and inorganic compounds to supply the nutrients necessary to support the growth of mycobacterial species. Catalase destroys toxic peroxides that may be present in the medium. Malachite green acts as an inhibitory agent to provide partial inhibition of contaminating bacteria. Middlebrook 7H11 Agar consists of 7H10 Agar supplemented with pancreatic digest of casein to enhance the growth of fastidious strains of M. tuberculosis. The addition of antimicrobial agents to 7H11 Agar improves the recovery of mycobacteria from specimens containing mixed flora.6 Polymyxin B is a polypeptide antibiotic that selectively inhibits most species of gram-negative bacilli, including Pseudomonas, but not Proteus species.9 Carbenicillin is a semi-synthetic penicillin effective against gram-positive and gram-negative bacteria, including strains of Escherichia coli resistant to other antimicrobial agents.9 Amphotericin B is an antifungal antibiotic, and trimethoprim lactate is a synthetic antimicrobial agent that inhibits both gram-positive and gram-negative bacteria, including Proteus species. VII REAGENTS Middlebrook 7H11 Agar Approximate Formula* Per Liter Purified Water Magnesium Sulfate............................................................... 0.05 g Zinc Sulfate ....................................................................1.0 mg Ferric Ammonium Citrate ..................................................... 0.04 g Copper Sulfate ...............................................................1.0 mg Sodium Citrate...................................................................... 0.4 g Biotin...............................................................................0.5 mg Ammonium Sulfate ............................................................... 0.5 g Calcium Chloride ............................................................0.5 mg Monosodium Glutamate ....................................................... 0.5 g Malachite Green .............................................................0.25 mg Disodium Phosphate ............................................................ 1.5 g OADC Enrichment ......................................................100.0 mL Monopotassium Phosphate .................................................. 1.5 g Glycerol ..........................................................................5.0 mL Agar .................................................................................... 13.5 g Pancreatic Digest of Casein ...........................................1.0 g Pyridoxine ............................................................................. 1.0 mg *Adjusted and/or supplemented as required to meet performance criteria. OADC Enrichment Approximate Formula* Per Liter Purified Water Sodium Chloride................................................................... 8.5 g Bovine Albumin (Fraction V) .............................................. 50.0 g Dextrose ............................................................................. 20.0 g Catalase ............................................................................... 0.03 g Oleic Acid ............................................................................. 0.6 mL *Adjusted and/or supplemented as required to meet performance criteria. 7H11 Selective Agar is Middlebrook 7H11 Agar with the following antimicrobial agents added per liter: Polymyxin B .......................................................................200,000 units Carbenicillin .........................................................................50.0 mg Amphotericin B ....................................................................10.0 mg Trimethoprim Lactate .......................................................... 20.0 mg Warnings and Precautions: For in vitro Diagnostic Use. If excessive moisture is observed, invert the bottom over an off-set lid and allow to air dry in order to prevent formation of a seal between the top and bottom of the plate during incubation. Pathogenic microorganisms, including hepatitis viruses and Human Immunodeficiency Virus, may be present in clinical specimens. "Standard Precautions"10-13 and institutional guidelines should be followed in handling all items contaminated with blood and other body fluids. Prior to discarding, sterilize prepared plates, specimen containers and other contaminated materials

View Full Text

Details

  • File Type
    pdf
  • Upload Time
    -
  • Content Languages
    English
  • Upload User
    Anonymous/Not logged-in
  • File Pages
    4 Page
  • File Size
    -

Download

Channel Download Status
Express Download Enable

Copyright

We respect the copyrights and intellectual property rights of all users. All uploaded documents are either original works of the uploader or authorized works of the rightful owners.

  • Not to be reproduced or distributed without explicit permission.
  • Not used for commercial purposes outside of approved use cases.
  • Not used to infringe on the rights of the original creators.
  • If you believe any content infringes your copyright, please contact us immediately.

Support

For help with questions, suggestions, or problems, please contact us