Fig. Freshly prepared Brain heart infusion (BHI) Broth without inoculation of specimen
Brain Heart Infusion (BHI) broth is a highly nutritive medium and is thus useful for cultivating a wide variety of microorganisms like aerobic and anaerobic bacteria, yeasts, and molds. BHI broth is commonly used in blood culture work and allied pathological investigations.
Composition of BHI Broth
Ingredients
Gms / Litre
HM infusion powder
12.5
BHI powder
5.0
Proteose peptone
10.0
Dextrose (Glucose)
2.0
Sodium chloride
5.0
Disodium hydrogen phosphate
2.5
Final pH (at 25°C)
7.4
Table: Composition of BHI Broth
Principle of BHI Broth
BHI broth constituents like proteose peptone, HM infusion powder, and BHI powder work as sources of carbon, nitrogen, essential growth factors, amino acids, and vitamins. Dextrose is the source of energy. Disodium phosphate (KH2PO4) keeps maintains the buffering action of the medium whereas sodium chloride maintains the osmotic equilibrium of the medium.
Preparation of BHI Broth
Suspend 37.0 grams in 1000 ml purified/distilled or deionized water.
Heat to boiling to dissolve the medium completely.
Desired volumes and containers ( vial or tube or bottle) can be taken according to the nature of the testing purpose.
Sterilize by autoclaving at 15 lbs pressure (121°C) for 15 minutes.
After autoclaving, leave for cooling to room temperature.
Store the plates in a refrigerator at 2-8°C.
Storage and Shelf life of BHI Broth
Store at 2-8ºC and away from direct light.
Media should not be used if there are any signs of deterioration or contamination.
The product is light and temperature-sensitive; protects from light, excessive heat, moisture, and freezing.
Test Requirements
Test specimens ( samples or growth of test organisms)
Allow the medium to warm at 37°C or to room temperature.
Inoculate the specimen as soon as possible after collection.
Incubate aerobically at 35-37ºC for 18-24 hours.
Examine for growth.
Result Interpretation
Organisms
Growth
Escherichia coli ATCC 25922
good-luxuriant
Staphylococcus aureus ATCC 25923)
good-luxuriant
Candida albicans ATCC 10231
good-luxuriant
To say growth nil ( negative)
Subculture into a solid medium and after incubation check the growth that is without colonies.
Table: Result-Interpretation
Fig. BHI broth in Conventional Blood Culture Bottle/BHI broth in McCartney Bottle, 100ml, with Aluminum Screw Cap, and Rubber Liner for Blood culture
Fig. Blood culture bottle without growth of organismsFig. Blood inoculated BHI broth after 4 days of incubation showing bacterial growthFig. Various microbes in blood culture bottles showing their visible growth
Visible signs of growth caused by microbes commonly encountered in blood culture-
Macroscopic observation
Associated microorganisms
Hemolysis
Streptococci, Staphylococci, Listeria species, Clostridium species, Bacillus species
Table: Visible marks of growth caused by microbes commonly seen in blood culture
Modifications and Uses of BHI Broth
BHI Modifications
Uses
BHI broth (Normal)
To prepare inoculum suspensions for antimicrobial sensitivity testing (AST) and a medium for blood culture
BHI broth with Hemin and Vitamin K
Anaerobic bacterial culture and the recovery of fastidious anaerobic organisms
BHI with 10% defibrinated sheep blood
Isolation and cultivation of Histoplasma capsulatum and other fungi
BHI broth with Fildes
cultivating capsular strains of Haemophilus influenzae
BHI broth with 6.5% Sodium Chloride
It is used to differentiate enterococci from non-enterococcal group D streptococci.
Table: BHI modifications and uses
Keynotes on BHI Broth
BHI broth is also the medium for fastidious pathogenic cocci like Streptococcus pneumoniae, Streptococcus pyogenes, Neisseria meningitidis, and other streptococci.
The addition of antibiotics, gentamicin, and/or chloramphenicol is recommended for the selective isolation of fungi.
For the culture of yeasts or mold, a prolonged incubation period may be required to obtain good growth.
For Haemophilus species incubate in a CO2-enriched atmosphere at 35°C with a loose cap.
The original BHI broth was made in 1899 when Edward Rosenow combined dextrose broth with calf brain tissue to grow streptococci and it was modified in 1923 by Russell Haden while working on dental pathogens. Modern BHI broth is different from Rosenow and Haden in which an infusion from porcine brains and hearts rather than calf brain tissue, and uses disodium phosphate as a buffer, rather than the calcium carbonate.
Limitations of BHI Broth
Pure culture needs organism identification. Colony characteristics, biochemical, and/or serological tests should be performed for final identification.
Strains of other catalase-negative gram-positive cocci like Lactococcus, Leuconostoc, Pediococcus, and Vagococcus, have been isolated from clinical specimens. Therefore, the presumptive identification of enterococci based on the bile-esculin reaction and growth in 6.5% sodium chloride broth only cannot be made.
