TDS_BT005_010 _v1

BAIRD-PARKER RPF AGAR
INTENDED USE
Baird Parker RPF (RPF = Rabbit Plasma Fibrinogen) Agar is used for the direct detection and
enumeration of coagulase positive staphylococci. The medium has the advantage of considerably
reducing the number of confirmation tests for the presence of coagulase positive staphylococci
particularly when atypical colonies are observed on other selective media. The medium allows the
simultaneous enumeration and confirmation to be performed in a single operation.
HISTORY
The production of free coagulase considered to be the principal characteristic for recognizing the
pathogenicity of staphylococci, in particular Staphylococcus aureus, was at the origins of the
development of Baird Parker with Rabbit Plasma Fibrinogen. Initial formulations of the incorporation of
plasma in solid culture media revealed inconsistencies between the results obtained by the coagulase
tube test and the formation of a characteristic halo of fibrin around colonies. The differences arose
from the fact that certain strains possessed a coagulase that also activated the plasminogen-plasmin
system as well, resulting in fibrinolysis and the disappearance of the fibrin halo. In order to overcome
this difficulty, it was recommended to add soybean trypsin inhibitor.
In order to favor the detection of coagulase produced by Staphylococcus aureus, Devoyod et al.
studied in 1976, the incorporation of pork plasma into Baird-Parker medium. Hauschild subsequently
improved the performance of Devoyod’s medium through the inclusion of bovine fibrinogen and a
trypsin inhibitor, with a correlative decrease in the amount of plasma. In 1983, Beckers et al. modified
Hauschild's medium, replacing the pork plasma with rabbit plasma, classically used in the coagulase
tube test. These authors also inoculated the medium in depth, rather than the previously used double
layer technique of Devoyod. Finally, the formulation was improved in 1986 by Sawhney, after
completing studies relative to the toxicity of potassium tellurite towards Staphylococcus aureus in a
rabbit plasma fibrinogen medium.
PRINCIPLES
- The growth of staphylococci is favored by sodium pyruvate and glycine.
- Accompanying microflora is inhibited by lithium chloride and potassium tellurite (added
extemporaneously), as well as a high concentration of glycine.
- Rabbit plasma was chosen for its excellent specificity towards staphylococcal coagulase and by its
aptitude to rapidly produce clot formation by forming staphylothrombin from prothrombin. The
rabbit plasma is reinforced with bovine fibrinogen. Staphylothrombin acts by cutting the A and B
fibrinopeptides of fibrinogen, thereby initiating the polymerization process that results in the
appearance of fibrin halos surrounding the colonies.
- Soybean trypsin inhibitor prevents fibrinolysis.
- The black coloration of staphylococcal colonies is due to the reduction of potassium tellurite to
telluride. In addition, the presence of tellurite favors the inhibition of contaminating Gram-positive
microflora.
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RECONSTITUTION OF THE SUPPLEMENTS
Rabbit Plasma Fibrinogen Supplement for 90 mL base: reagent R2 from RPF kit BT005
- Using aseptic techniques, add 10 mL of sterile distilled water at room temperature. The dissolution
may be facilitated by using sterile distilled water preheated to at least 37°C but not more than
44°C.
- Turn end-over-end to dissolve. Avoid frothing the solution. Immediate dissolution is not always
obtained. To accelerate the process, a mechanical agitator (vortex) for tubes can be used to fully
dissolve the lyophilisate. The supplement should be completely dissolved before adding to BairdParker Agar base.
Rabbit Plasma Fibrinogen Supplement for 190 mL base: reagent R2 from RPF kit BT010
- Using aseptic techniques, add 10 mL of sterile distilled water preheated to 37°C at least (44°C
max).
- Turn end-over-end to dissolve. Avoid frothing the solution. Immediate dissolution is not always
obtained. To accelerate the process, a mechanical agitator (vortex) for tubes can be used to fully
dissolve the lyophilisate. The supplement should be completely dissolved before adding to BairdParker Agar base.
INSTRUCTIONS FOR USE
- Melt the medium for the minimum amount of time necessary in order to achieve total liquefaction
RPF kit BT005 or BT010, reagent R1).
- Cool and maintain at 44-47°C.
- For 90 mL of base media (reagent R1 from RPF kit BT005) , add 10 mL of reconstituted Rabbit
Plasma Fibrinogen Supplement (reagent R2 from RPF kit BT005).
- For 190 mL of base media (reagent R1 from RPF kit BT010), add 10 mL of reconstituted Rabbit
Plasma Fibrinogen Supplement (reagent R2 from RPF kit BT010).
- Mix well to insure a proper and complete homogenization. Use immediately.
Enumeration of coagulase positive staphylococci in foods and animal feeding stuffs:
- Transfer 1 mL of the sample to analyze and its tenfold dilution series into sterile Petri dishes.
- Pour 10 to 15 mL of complete medium.
- Homogenize by swirling.
- Let solidify on a cool surface.
- It should be noted that the instructions for certain standards (NF EN ISO 6888-3, NF V 08-057-1,
notably) authorize an alternative surface inoculation.
- Incubate at 37°C for 24 and 48 hours.
Enumeration of pathogenic staphylococci for the bacteriological examination of waters, using
membrane filtration method without confirmation:
- Pour 10 to 15 mL of complete medium.
- Let solidify on a cool surface.
- Place the membrane, filtered side up, on the surface of the agar, insuring a complete contact.
- Return the plate and incubate at 36 ± 2 °C for 21 ± 3 hours and 44 ± 4 hours.
The membrane quality should be validated prior to initiating this application.
Confirmation of pathogenic staphylococci for the bacteriological examination of waters.
- Pour 10 to 15 mL of complete medium.
- Let solidify on a cool surface.
- Transfer the number of characteristic colonies according to the recommendations of the standard
XP T 90-412, or transfer the membrane from Mannitol Salt agar (BK030 or BM085) or from Baird
Parker + Egg Yolk Tellurite [(BK055 + BS060), BM018 or BM091].
- Incubate at 36 ± 2 °C for 21 ± 3 hours.
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RESULTS
Coagulase positive staphylococci are characterized by the formation of gray or black colonies
surrounded by an opaque halo of fibrin that is clearcut, stable and well visible. Count only those plates
containing less than 100 characteristic colonies. Use of the RPF technique eliminates the need for
confirming the results by the coagulase tube test.
For water testing controls, it is necessary to gently raise the membrane in order to verify the presence
(or not) of fibrin halos at 21 ± 3 hours of incubation.
TYPICAL COMPOSITIONS
For 1 L of complete medium :
(can be adjusted to obtained optimal performance)
- Tryptone .........................................................................................10.0 g
- Meat extract .....................................................................................5.0 g
- Yeast extract ....................................................................................1.0 g
- Sodium pyruvate ............................................................................10.0 g
- Glycine ...........................................................................................12.0 g
- Lithium chloride ................................................................................5.0 g
- Bacteriological agar .......................................................................15.0 g
- Rabbit plasma, EDTA .................................................................25.0 mL
- Bovine fibrinogen .............................................................................5.0 g
- Trypsin inhibitor...........................................................................25.0 mg
- Potassium tellurite.......................................................................25.0 mg
pH of the complete medium at 25°C: 7.2 ± 0.2.
QUALITY CONTROL
- Complete prepared medium : amber agar.
- Typical culture response after 48 hours of incubation at 37°C :
Characteristics
Growth
(Productivity Ratio : PR)
Microorganisms
PR ≥ 50%
PR ≥ 50%
limited, score 0-1
inhibited, score 0
Staphylococcus aureus
DSM 799
Staphylococcus aureus
ATCC® 25923
Staphylococcus epidermidis ATCC 12228
Escherichia coli
ATCC 25922
Colony
color
Fibrin halo
black
black
black
presence
presence
absence
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- Typical cultural
NF T 90-461)
response
after
Microorganisms
Staphylococcus aureus
Enterococcus faecalis
CIP 53.154
CCM 2541
44
hours
of
incubation
Growth
(Productivity Ratio : R3)
66% ≤ R3 ≤ 150%
inhibited
at
36°C
(XP
T
Characteristics
Colony color
Fibrin halo
black
presence
STORAGE / SHELF LIFE
Ready-to-melt media in vials :
- Store between 2-8°C, shielded from light.
- The expiration date is indicated on the label.
PACKAGING
Code
RPF kit :
- Composed of 6 x 90 mL vials of base media (R1) and
6 freeze-dried RPF supplement vials (R2)
- Composed of 6 x 190 mL vials of base media (R1) and
6 freeze-dried RPF supplement vials (R2)
90-412 ;
BT00508
BT01008
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PHOTO SUPPORT
Product Reference : BT00508, BT01008
Media used for : Detection / enumeration / confirmation of coagulase positive Staphylococci.
Staphylococcus aureus
Baird Parker RPF agar
Ref : BT00508
Incubation : 24 hours / 37°C
Characteristics : Coagulase positive staphylococci are gray to black surrounded by a halo of fibrin.
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BIBLIOGRAPHY
LOEB, L.. 1903. The influence of certain bacteria on the coagulation of blood. Journal of Medical Research, 10 : 407-419.
DUTHIE, E.S.. 1954. Evidence of two forms of staphylococcal coagulase. Journal of General Microbiology, 10 : 427-436.
BAIRD-PARKER, A.C.. 1962. An improved diagnostic and selective medium for isolating coagulase positive staphylococci.
Journal of Applied Bacteriology, 25 : 12-19.
DEVOYOD, J.J., MILLET, L. et MOCQUOT G.. 1976. Un milieu gélosé pour le dénombrement direct de Staphylococcus
aureus : milieu au plasma de porc pour S. aureus (PPSA). Canadian Journal of Microbiology, 22 (11) : 1603-1611.
STADHOUDERS, J., HASSING, F. and van AALST-van MAREN, N.O.. 1976. A pour-plate method for the detection and
enumeration of coagulase-positive Staphylococcus aureus in the Baird-Parker medium without egg yolk. Netherland Milk
Dairy Journal, 30 : 222-229.
HAUSCHILD, A.H., PARK, C.E. and HILSHEIMER, R.. 1979. A modified pork plasma agar for the enumeration of
Staphylococcus aureus in foods. Canadian Journal of Microbiology, 25 : 1052-1057.
BECKERS, H.J., van LEUSDEN, F.M., BINDSCHEDLER, O. and GUERRAZ, D.. 1984. Evaluation of a pour-plate system
with a rabbit plasma-bovine fibrinogen agar for the enumeration of Staphylococcus aureus in food. Canadian Journal of
Microbiology, 30 : 470-474.
SAWHNEY, D.. 1986. The toxicity of potassium tellurite to Staphylococcus aureus in rabbit plasma fibrinogen agar. Journal
of Applied Bacteriology, 149 : 149-155.
FIL provisoire 145A . Novembre 1997. Lait et produits à base de lait. Dénombrement des staphylocoques coagulase-positifs.
Techniques de comptage des colonies.
De BUYSER, M.L., AUDINET, N., DELBART, M.O., MAIRE, M. and FRANCOISE, F.. 1998. Comparison of selective culture
media to enumerate coagulase-positive staphylococci in cheeses made from raw milk. Food microbiology, 15 : 339-346.
NF EN ISO 6888-2 (V 08-014-2). Octobre 1999. Microbiologie des aliments. Méthode horizontale pour le dénombrement des
staphylocoques à coagulase positive (Staphylococcus aureus et autres espèces). Partie 2 : Technique utilisant le milieu
gélosé au plasma de lapin et au fibrinogène.
NF EN ISO 6888-2/A1 (V 08-014-2/A1). Décembre 2003. Microbiologie des aliments. Méthode horizontale pour le
dénombrement des staphylocoques à coagulase positive (Staphylococcus aureus et autres espèces). Partie 2 : Technique
utilisant le milieu gélosé au plasma de lapin et au fibrinogène. Amendement 1 : Inclusion des données de fidélité.
XP CEN ISO/TS 11133-2 (V 08-104-2). Janvier 2004. Microbiologie des aliments. Guide pour la préparation et la production
des milieux de culture. Partie 2 : Guide général pour les essais de performance des milieux de culture.
NF V 08-057-1. Janvier 2004 (2e tirage de Décembre 2004). Microbiologie des aliments. Méthode de routine pour le
dénombrement des staphylocoques à coagulase positive par comptage des colonies à 37 °C. Partie 1 : Technique avec
confirmation des colonies.
NF EN ISO 6888-3 (V 08-014-3). Juin 2003 (3e tirage d’Avril 2005). Microbiologie des aliments. Méthode horizontale pour le
dénombrement des staphylocoques à coagulase positive (Staphylococcus aureus et autres espèces). Partie 3 : Recherche
et méthode NPP pour les faibles nombres.
XP T 90-412. Juin 2006. Qualité de l’eau. Recherche et dénombrement des staphylocoques pathogènes. Méthode par
filtration sur membrane.
NF T 90-421. Août 2006. Essais des eaux. Examens bactériologiques des eaux de piscines.
*Benchmark value refers to the expected shelf life when prepared under standard laboratory conditions following manufacturer’s instructions. It is provided as a
guide only and no warranty, implied or otherwise is associated with this information.
The information provided on the package take precedence over the formulations or instructions described in this document.
The information and specifications contained in this technical data sheet date from 2011-03-08.
They are susceptible to modification at any time, without warning.
Code document : BT005 RPF/E/2011-03 : 1.
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Biokar Diagnostics – Rue des Quarante Mines – ZAC de Ther – Allonne – B.P. 10245 – F60002 Beauvais Cedex – France
Tél : + 33 (0)3 44 14 33 33 – Fax : + 33 (0)3 44 14 33 34 – www.biokar-diagnostics.com