Authors: Mary A. Williamson Mt(ascp) Phd,L. Michael Snyder Md
Specimens may be collected from sites that are not the primary site of active infection (even though there may be signs of inflammation at the site).
Inadequate site preparation may result in false-positive cultures due to specimen contamination with endogenous flora. Contaminated specimens may also mask the recognition of slow-growing or fastidious pathogens in the culture.
ANAEROBIC CULTURE
Definition and Use
Anaerobic cultures are indicated for evaluation of patient specimens taken from sites with signs and symptoms of bacterial infection (e.g., swelling, redness, heat, pus, or exudate). Infections associated with anaerobic pathogens include surgical and traumatic wounds, sinusitis and pararespiratory infections, pelvic and intra-abdominal infections, osteomyelitis, myositis, gangrene, and necrotic wounds, abscesses, and actinomycosis and infections associated with fistula formation.
Anaerobic cultures are used for the detection of common anaerobic bacterial pathogens from patient specimens. Site-specific aerobic bacterial cultures (e.g., tissue culture, abscess culture, wound culture) are recommended, if available. Specimens are inoculated on several types of anaerobic culture media. (see “Aerobic Culture” for a general discussion about media). Media should be fresh and prereduced. Typical media for aerobic cultures include
Supportive agar media, like Schaedler agar or CDC anaerobic blood agar
Selective/differential agar media:
Phenylethyl alcohol or CNA agar for anaerobic gram-positive pathogens
Kanamycin–vancomycin–laked blood agar, for anaerobic gram-negative bacilli
Bacteroide bile–esculin agar, for
Bacteroides fragilis
group
Egg yolk agar, for characterization of
Clostridium
species
Cycloserine–cefoxitin–egg yolk–fructose agar (CCFA), for
Clostridium difficile