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Products‎ > ‎PRAS Mono-Plated Media‎ > ‎

Clindamycin Blood Agar (CBA)

Clindamycin Blood Agar (CBA) is an enriched selective medium for the isolation and presumptive identification of Eikenella corrodens.  CBA is a tryptic soy agar base supplemented with clindamycin at a concentration that inhibits most gram-positive and gram-negative anaerobes, with some exceptions.  This medium is prepared, stored and dispensed under oxygen-free conditions to prevent the formation of oxidized products prior to use.
 

Anaerobe Systems PRAS Clindamycin
         Blood Agar (CBA) AS-645


View the full product insertCBA Insert.pdf

Clindamycin Blood Agar Products
 

 Item #

Description 

Size 

Price 

 AS-645

 CBA mono plate

 4 plates

 7.85

 




Formula

Pancreactic Digest of Casein, 15.0 g

Agar, 15.0 g

Soy Peptone, 5.0 g

Sodium Chloride, 5.0 g

Clindamycin, 4.0 mg

Sheep Blood, 50.0 ml

Distilled Water, 1000.0 ml

 

Final pH 7.2 +/- 0.2 at 25 degrees C.

Final weight 16.0 g +/- 1.6.

 

Precautions

For IN VITRO DIAGNOSTIC USE only.  Approved biohazard precautions and aseptic techniques should be observed when using this product.  This product is for use only by properly-trained and qualified personnel.  Sterilize all biohazard waste prior to disposal.

 

Storage and Shelf Life

Storage:  Upon receipt, store at room temperature (13°C - 27°C) in original container until use.  Avoid overheating or freezing.  Do not use medium if there are signs of deterioration (shrinking, cracking or discoloration due to oxidation of media) or contamination.  The expiration date applies to the product in its original packaging and stored as directed.  Do not use product past the expiration date shown on the container.

Shelf Life:  90 days from date of manufacture.

 

Procedure

Specimen Collection:  Specimens for anaerobic culture should be protected from air (oxygen) during collection, transport and processing.  Consult appropriate references for detailed instructions concerning collection and transport of anaerobes.

Methods for Use:  CBA should be inoculated directly with clinical material or a broth that has been previously inoculated from clinical material.  Inoculated plates should be streaked to obtain isolated colonies, immediately placed in an anaerobic atmosphere and incubated at 35-37oC for 24-48 hours.  Additional periods of incubation may be necessary to recover some anaerobes.  Detailed instructions for processing anaerobic cultures can be found in the appropriate references (1, 2, 3, 4, 5, 6).


Materials Required But Not Provided

Standard microbiological supplies and equipment such as loops, saline blanks, slides, staining supplies, microscope, incinerator / autoclave, incubators, anaerobic chamber, other culture media and serological and biochemical reagents.

 

Limitations

CBA will not provide complete information for identification of bacterial isolates.  Additional test procedures and media are required for complete identification.  It is recommended that a non-selective medium such as Anaerobic Brucella Blood Agar also be inoculated from clinical specimens to assure growth of all species present.  Consult reference materials for additional information.

 

Quality Control

CBA should support good growth of Eikenella corrodens found in clinical infections. 

 The following organisms are routinely used for quality control testing at Anaerobe Systems. 

Organism Tested

ATCC #

Results

Time (Hours)

Eikenella corrodens

23834

Growth

24 – 48 h

Escherichia coli

25922

Growth

24 h

Peptostreptococcus anaerobius

27337

No Growth

 

Fusobactrerium nucleatum

25586

No Growth

 

Bacteroides fragilis

25285

No Growth

 

Prevotella melaninogenica

25845

No Growth

 

Propionibacterium acnes

6919

No Growth

 

Clostridium difficile

9689

Inhibited

 

Enterococcus faecalis

29212

Growth

24 h


User Quality Control: The final determination to the extent and quantity of user laboratory quality control must be determined by the end user.

If sterility testing is to be performed on this product, the appropriate percentage of the original shipment amount should be incubated anaerobically and aerobically for 48 – 96 hours.

If the nutritive/inhibitory capacity of this medium is to be tested for performance, it is recommended that the following ATCC organisms be evaluated for growth/inhibition.

 

Organism

Expected Growth

Ek. corrodens

48 hrs

E. coli

24 hrs

E. faecalis

24 hrs

B. fragilis

Inhibited

P. melaninogenica

Inhibited

F. nucleatum

Inhibited

 

Physical Appearance:  CBA should appear opaque and red in color.

 

References

1.        Dowell, V. R., Jr. and T. M. Hawkins.  1974Laboratory Methods in Anaerobic Bacteriology.  CDC Laboratory ManualUSDHEW C. D. C. Atlanta, GA 30333.

 

2.        Engelkirk, P. G., Duben-Engelkirk, J., Dowell, V. R.  1992Principles of Practices of Clinical Anaerobic BacteriologyStar Publishing Co., Belmont, CA 94002.

 

3.        Holdeman, L. V., F. P. Cato and W. E. C. Moore.  1977Anaerobe Laboratory ManualVirginia Polytechnic Institute and State University.  Blacksburg, VA 24061.

 

4.        Jousimies-Somer, H. R., Summanen, P., Citron, D. M., Baron, E. J., Wexler, H. M. and S. M. Finegorld.  2002.  Wadsworth – KTL Anaerobic Bacteriology Manual.  Star Publishing, Co.  Belmont, CA 94002.

 

5.        Walker, C. B., Tanner, A., Smith, C. and S. Socransky.  Selective Medium for Eikenella corrodensJ. Dent. Res1978; 57 (spec iss): 315, Abstract 961.

 

6.        NCCLSQuality Control for Commercially Prepared Microbiological Culture Media; Approved Standard- Third Edition.  (2004).  NCCLS document M22-A3.  NCCLS, 940 West Valley Road, Suite 1400, Wayne, PA 19087-1898.