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References in periodicals archive ?
(4) (3) characters Indol + NA - MR + NA - VP - NA + Citrate - NA - Urease - + + Oxidase - - + Catalase + + - Haemolysis on V + - blood agar Growth on MCA LF - - Growth on BHI + + - Growth on EMB + - - Growth on BA + + + Table 2.
A 0.5 McFarland turbidity standard suspension prepared from well isolated colonies of the bacterial isolates was swabbed onto the surface of Mueller-Hinton blood agar plates.
Isolation and identification of causative agent: Bone marrow, heart blood and liver was inoculated on Brain Heart Infusion (BHI) blood agar and incubated at 37oC for 24 hours.
Traditionally conventional media like Blood agar (BA) and MacConkey agar (MAC) are being used in combination by most of the laboratories especially in the developing countries for long and Cystine lactose electrolyte-deficient (CLED) agar has been added later on but none of these media singly or in combination can support the growth and/or identification of possible uropathogens.6 As a result there is continuous strive by the laboratories to streamline and improve urine culture algorithms.
Were confirmed with blood agar culture and bacitracin (0.04 U) disc sensitivity test, which is used in the presumptive identification of group A, beta-haemolytic Streptococci.
Hair sheep blood, citrated or defibrinated, fulfills all requirements of blood agar for diagnostic microbiology laboratory tests.
The three positive samples, which were not treated with antibiotics prior to sample collection, showed growth of Pasteurella multocida on blood agar. On blood agar colonies were small, pin point, grey, translucent, dew drop like and non-hemolytic.
A high inoculum of each strain on blood agar was suspended in sterile normal saline by using a sterile cotton swab.
After the organism was identified, we found that it was able to grow on blood agar at 4[degrees]C after 6 days of incubation.
The causative bacterium is gram positive, pleomorphic, intracellular, non-motile, aerobic to facultative anaerobe which grows well on blood agar, forming small, whitish and opaque colonies (Coyle and Lipsky, 1990).
The samples were transported to the laboratory and streaked on Blood Agar medium and plate of Sabouraud Dextrose Agar (SDA) with chloramphenicol and gentamicin.