Specimen Collection, Media, and Methods Flashcards
The aseptic collection of blood cultures requires that the skin be cleansed with:
A. 2% iodine and then 70% alcohol solution
B. 70% alcohol and then 2% iodine or an
iodophor
C. 70% alcohol and then 95% alcohol
D. 95% alcohol only
B
In order to attain asepsis of the skin, 70% alcohol followed by 2% iodine is used for obtaining blood cultures.
When cleansing the skin with alcohol and then iodine for the collection of a blood culture, the iodine (or iodophor) should remain intact on the skin for at least:
A. 10 sec
B. 30 sec
C. 60 sec
D. 5 min
C
The iodine should remain on the skin for 1 min because instant antisepsis does not occur when cleansing the skin for a blood culture.
What is the purpose of adding 0.025%–0.050% sodium polyanetholsulfonate (SPS) to nutrient broth media for the collection of blood cultures?
A. It inhibits phagocytosis and complement
B. It promotes formation of a blood clot C. It enhances growth of anaerobes
D. It functions as a preservative
A
SPS is used in most commercial blood culture products because it functions as an anticoagulant and prevents phagocytosis and complement activation. In addition, SPS neutralizes aminoglycoside antibiotics. Addition of SPS may inhibit some Neisseria and Peptostreptococcus, but this can be reversed with 1.2% gelatin.
A flexible calcium alginate nasopharyngeal swab is the collection device of choice for recovery of which organism from the nasopharynx?
A. Staphylococcus aureus
B. Streptococcus pneumoniae
C. Corynebacterium diphtheriae
D. Bacteroides fragilis
C
C. diphtheriae must be recovered from the deep layers of the pseudomembrane that forms in the nasopharyngeal area. A flexible calcium alginate nasopharyngeal swab is the best choice for collecting a specimen from the posterior nares and pharynx.
Semisolid transport media such as Amies, Stuart, or Cary–Blair are suitable for the transport of swabs for culture of most pathogens except:
A. Neisseria gonorrhoeae
B. Enterobacteriaceae
C. Campylobacter fetus
D. Streptococcus pneumoniae
A
Specimens for culture of N. gonorrhoeae are best if plated immediately or transported in a medium containing activated charcoal to absorb inhibitory substances that hinder their recovery.
Select the method of choice for recovery of anaerobic bacteria from a deep abscess.
A. Cotton fiber swab of the abscess area
B. Skin snip of the surface tissue
C. Needle aspirate after surface decontamination
D. Swab of the scalpel used for débridement
C
Anaerobic specimens are easily contaminated with organisms present on the skin or mucosal surfaces when a swab is used. Needle aspiration of an abscess following surface decontamination provides the least exposure to ambient oxygen.
Select the primary and differential media of choice for recovery of most fecal pathogens.
A. MacConkey, blood, birdseed, and Campylobacter
(Campy) agars
B. Hektoen, MacConkey, Campy, colistin–nalidixic
acid (CNA) agars
C. CNA and Christensen urea agars and
thioglycollate media
D. Blood, Campy, Mueller–Hinton agars,
and thioglycollate media
B
Hektoen agar selectively isolates pathogenic coliforms, especially Salmonella and Shigella. MacConkey agar differentiates lactose fermenters from nonfermenters. CNA agar contains antibiotics that prohibit growth of gram-negative coliforms but not gram-positive cocci. Campy agar contains the antibiotics cephalothin, trimethoprim, vancomycin, polymyxin B, and amphotericin B to prevent growth of Enterobacteriaceae, Pseudomonas spp., and fungi.
Select the media of choice for recovery of Vibrio cholerae from a stool specimen.
A. MacConkey agar and thioglycollate media
B. Thiosulfate–citrate–bile–sucrose (TCBS) agar
and alkaline peptone water (APW) broth C. Blood agar and selenite-F (SEL) broth
D. CNA agar
B
TCBS agar is used to grow Vibrio cholerae, which appear as yellow colonies as a result of the use of both citrate and sucrose. APW is used as an enrichment broth and should be subcultured to TCBS agar for further evaluation of Vibrio colonies.
Colistin–nalidixic acid agar (CNA) is used primarily for the recovery of:
A. Neisseria species
B. Enterobacteriaceae
C. Pseudomonas aeruginosa
D. Staphylococcus aureus
D
CNA agar inhibits the growth of gram-negative bacteria and is used to isolate gram-positive cocci from specimens. This medium is especially useful for stool and wound cultures because these may contain large numbers of gram-negative rods.
In the United States, most blood agar plates are prepared with 5% or 10% red blood cells (RBCs) obtained from:
A. Sheep
B. Horses
C. Humans
D. Dogs
A
Sheep RBCs are used in blood agar plates because they are readily available and less inhibitory than cells of other species. The type of hemolysis is determined by the source of RBCs. Sheep RBCs are chosen because of the characteristically clear hemolysis produced by β-hemolytic streptococci, Staphylococcus, and other pathogens producing β-hemolysins. Sheep blood does not support the growth of Haemophilus haemolyticus, eliminating the possibility of confusing it with β-hemolytic streptococci in throat cultures.
All of the following are appropriate when attempting to isolate N. gonorrhoeae from a genital specimen except:
A. Transport the genital swab in charcoal transport
medium
B. Plate the specimen on modified Thayer–Martin
(MTM) medium
C. Plate the specimen on New York City or
Martin–Lewis agar
D. Culture specimens in ambient oxygen at 37°C
D
MTM, New York City, and Martin–Lewis agars contain blood factors needed to support the growth of N. gonorrhoeae as well as antibiotics that prevent growth of normal genital flora. Cultures must be incubated in 3%–7% CO2 at 35°C. Cultures should be held a minimum of 48 hours before being considered negative.
Chocolate agar and modified Thayer–Martin agar are used for the recovery of:
A. Haemophilus spp. and Neisseria spp., respectively
B. Haemophilus spp. and N. gonorrhoeae,
respectively
C. Neisseria spp. and Streptococcus spp., respectively
D. Streptococcus spp. and Staphylococcus spp., respectively
B
Chocolate agar provides X factor (hemin) and
V factor (NAD) required for the growth of Haemophilus spp. Thayer–Martin medium is a chocolate agar containing the antibiotics that permit isolation of N. gonorrhoeae in specimens containing large numbers of gram-negative bacteria, including commensal Neisseria spp.
Cycloserine–cefoxitin-fructose agar (CCFA) is used for the recovery of:
A. Yersinia enterocolitica
B. Yersinia intermedia
C. Clostridium perfringens
D. Clostridium difficile
D
CCFA is used for recovery of C. difficile from stool cultures. Cycloserine and cefoxitin inhibit growth
of gram-negative coliforms in the stool specimen.
C. difficile ferments fructose, forming acid that, in the presence of neutral red, causes the colonies to become yellow.
Deoxycholate agar (DCA) is useful for the isolation of:
A. Enterobacteriaceae
B. Enterococcus spp.
C. Staphylococcus spp.
D. Neisseria spp.
A
DCA inhibits gram-positive organisms. N. gonorrhoeae and Neisseria meningitidis are too fastidious to grow on DCA. Citrate and deoxycholate salts inhibit growth of gram-positive bacteria. The media contain lactose and neutral red, allowing differentiation of lactose fermenters (pink colonies) from nonfermenters (colorless).
Xylose lysine deoxycholate (XLD) agar is a highly selective medium used for the recovery of which bacteria?
A. Staphylococcus spp. from normal flora
B. Yersinia spp. that do not grow on Hektoen agar
C. Enterobacteriaceae from gastrointestinal
specimens
D. Streptococcus spp. from stool cultures
C
XLD agar is selective for gram-negative coliforms because of a high concentration (0.25%) of deoxycholate, which inhibits gram-positive bacteria. In addition, XLD is differential for Shigella and Salmonella spp. The medium contains xylose, lactose, and sucrose, which are fermented by most normal intestinal coliforms producing yellow colonies. Shigella does not ferment the sugars and produces red (or clear) colonies. Salmonella spp. ferment xylose; however, they also decarboxylate lysine in the medium, causing production of ammonia. Therefore, Salmonella first appear yellow but become red.
Some Salmonella produce hydrogen sulfide (H2S) from sodium thiosulfate and therefore appear as red colonies with black centers.
A sheep blood agar plate is used as a primary isolation medium when all of the following organisms are to be recovered from a wound specimen except:
A. β-Hemolytic streptococci and coagulase-positive staphylococci
B. Haemophilus influenzae and Haemophilus parainfluenzae
C. Proteus spp. and Escherichia coli
D. Pseudomonas spp. and Acinetobacter spp.
B
Both gram-positive cocci and gram-negative bacilli will grow on blood agar plates, but the medium is used in conjunction with a selective medium such as CNA agar for gram-positive cocci and MacConkey agar for gram-negative bacilli. H. influenzae requires X and V factors, and H. parainfluenzae requires V factor; the primary isolation medium for Haemophilus is chocolate agar.
Prereduced and vitamin K1-supplemented blood agar plates are recommended isolation media for:
A. Mycobacterium marinum and Mycobacterium avium intracellulare
B. Bacteroides, Peptostreptococcus, and Clostridium spp.
C. Proteus spp.
D. Enterococcus spp.
B
Anaerobic culture media can be prereduced before sterilization by boiling, saturation with oxygen-free gas, and addition of cysteine or other thiol compounds. The final oxidation reduction potential (Eh) of the medium should be approximately –150 mV to minimize the effects of exposure of organisms to oxygen during inoculation.
Which procedure is appropriate for culture of genital specimens in order to recover Chlamydia spp.?
A. Inoculate cycloheximide-treated McCoy cells
B. Plate onto blood and chocolate agar
C. Inoculate into thioglycollate (THIO) broth
D. Plate onto modified Thayer–Martin agar within
24 hours
A
Chlamydiae are strict intracellular organisms and must be cultured using living cells. Direct smears can also be made at the time of culture. Staining cells with iodine may reveal the characteristic reddish-brown inclusions sometimes seen in Chlamydia infections. Fluorescein-conjugated monoclonal antibodies may be used to identify the organisms in infected cells.
Specimens for virus culture should be transported in media containing:
A. Antibiotics and 5% sheep blood
B. Saline and 5% sheep blood
C. 22% bovine albumin
D. Antibiotics and nutrient
D
Media for transporting specimens for virus culture include Hanks balanced salt solution with bovine albumin, Stuart transport media, and Leibovitz–Emory media. Media used for transporting specimens for viral culture are similar to those for bacteria with the addition of a nutrient such as fetal calf serum or albumin and antibiotics. Specimens should be refrigerated after being placed in the transport
media until the culture media can be inoculated.
Cerebrospinal fluid (CSF) should be cultured immediately, but if delayed the specimen should be:
A. Refrigerated at 4°C to 6°C
B. Frozen at –20°C
C. Stored at room temperature for no longer
than 24 hours
D. Incubated at 37°C and cultured as soon as
possible
D
Fastidious organisms such as Neisseria and Haemophilus frequently isolated from the CSF of patients with bacterial meningitis are preserved by placing the fluid in 3%–7% CO2 at 35°C–37°C (or at room temperature for no longer than 30 min), if the specimen cannot be cultured immediately.
The most sensitive method for the detection of β-lactamase in bacteria is by the use of:
A. Chromogenic cephalosporin
B. Penicillin
C. Oxidase
D. Chloramphenicol acetyltransferase
A
β-Lactamase production by bacteria that are resistant to penicillin and cephalosporin is detected using one of these drugs as a substrate. Penicillin is hydrolyzed by β-lactamase into acidic products that can be detected as a color change by a pH indicator. In the iodometric method, a disk containing a penicillin–starch substrate turns blue when a drop of iodine is added. A loop
of β-lactamase–positive organisms applied to the center of the blue spot will reduce the iodine to iodide, causing the area to clear. The most sensitive method of detection is based upon the ability of the organism to hydrolyze the β-lactam ring of a chromogenic cephalosporin.
The breakpoint of an antimicrobial drug refers to:
A. The amount needed to cause bacteriostasis
B. A minimum inhibitory concentration (MIC) of
16 μg/mL or greater
C. A MIC of 64 μg/mL or greater
D. The level of drug that is achievable in serum
D
The breakpoint refers to an antimicrobial concentration in the serum associated with optimal therapy using the customary dosing schedule. An organism is susceptible if the MIC is at or below the breakpoint.
Which of the following variables may change the results of an MIC?
A. Inoculum size
B. Incubation time
C. Growth rate of the bacteria
D. All of these options
D
In vitro testing of drugs is reliable if the method is standardized. In addition to the first three variables, the type of media and the stability of antibiotics affect the results of MIC testing and must be carefully controlled.
According to the Kirby–Bauer standard antimicrobial susceptibility testing method, what should be done when interpreting the zone size of a motile, swarming organism such as a Proteus species?
A. The swarming area should be ignored
B. The results of the disk diffusion method are invalid
C. The swarming area should be measured as the growth boundary
D. The isolate should be retested after diluting to a 0.05 McFarland standard
A
A thin film of growth appearing in the zone area of inhibition around the susceptibility disk should be ignored when swarming Proteus or other organisms are encountered. Discontinuous, poor growth or tiny colonies near the end of the zone should also be ignored.
