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Identification of Pathogenic Bacteria by Laboratory Methods M. Kent Froberg, MD
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Laboratory Methods ID of pathogenic bacteria using series of differential tests differential & selective media morphology & staining biochemical properties antibiotic resistance or susceptibility plasmid, ribosomal or DNA analysis
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Gram Positive Cocci Staphylococci vs Streptococci –Staph aureus catalase +, coagulase +, & -hemolytic –Strep , , or non-hemolytic, catalase -
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Catalase Enzyme that converts H 2 O 2 H 2 O and O 2 Visible bubbles when drop of 3% H 2 O 2 is added to culture of catalase + bacteria
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Catalse +Catalse -
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Catalase - Catalase +
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Between Staph Species S aureus coagulase + (clots plasma) S epidermidis & saprophyticus coagulase neg –S saprophyticus novobiocin resistant –S epidermidis novobiocin sensitive
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Lower tube shows fibrin clot following addition of plasma to culture of Stap aureus. Top tube is negative indicating non-pathogenic Staph.
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Left: novobiocin resistant Staph saprophyticus Right: novobiocin senstitive Staph epidermidis
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Between Strep Species Hemolysis: –Strep pyogenes & agalactiae hemolytic –Enterococcus variable hemolysis –Strep viridans & pneumoniae hemolytic
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Beta-hemolysis with clearing of blood agar
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Green discloloration of alpha-hemolysis
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No hemolysis on blood agar
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More Strep Tests Strep pyogenes bacitracin sensitive Strep agalactiae & Enterococcus bacitracin resistant Strep viridans resistant to optochin Strep pneumoniae sensitive to optochin
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Zone of inhibition around optochin disk - presumptive identification of Strep pneumoniae
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Motility Tests Many bacteria show motility in media Agar tube inoculated with needle stab Media contains tetrazolium bacteria reduces to formazan (red color) Location of bacteria determined by location of red color Useful for Borrelia, Vibrio, Salmonella, E coli, etc.
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2,3,5-Triphenyltetrazolium chloride (TTC)Formazan (red color)
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Left tube: motileCenter: nonmotileRight: control
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Oxidase Tests Presence of cytochrome oxidase Neisseria & Pseudomonas + Enterobacteriaceae neg Test converts colorless tetramethyl-p- phenylenediamine to oxidized form (deep purple/blue)
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Oxidase + colony at 12 o’clock, 3 & 9 o’clock cultures are negative
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Oxidase test done on paper saturated with oxidase reagent. Pseudomonas on left (+), Staph aureus on right (-).
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Enterobacteriaceae API 20 E series of substrates and indicators that are inoculated with unknown and media Tests for enzymes and carbohydrate utilization Pattern of + and - results compared to a table of known results to identify unknown
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Oxidation-Fermentation Tests Mostly used to distinguish fermentative Enterobacteriaceae from oxidative Pseudomonas & Bordetella Grow isolate in low agar content media in presence of different sugar substrates and pH indicator Stab media: one tube sealed with mineral oil to promote anaerobic growth/ other tube unsealed Indicator yellow at pH 6.0/ green at pH 7.1, blue at pH 7.6
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Mineral oil covers media in tubes 1 & 3. Pseudomonas in tubes 1 & 2, Shigella in tubes 3 & 4.
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Enterobacteriaceae Enterotube II 12 compartments of various media allows determination of 15 different characteristics of organism Positive results given a number, added in groups and sums combined to create unique 5-digit identifier in computer databank
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Question #1 1.The laboratory obtains a surgical wound swab from a 56 year old male four days after undergoing a colectomy for colon cancer. The isolate is gram +, catalase +, coagulase + and hemolytic. It is most likely a.Streptococcus pyogenes b.Enterococcus faecalis c.Staphylococcus aureus d.Staphylococcus saphrophyticus e.Streptococcus viridans
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Question #2 2.The initial data necessary to adequately identify a bacterial unknown are its a.Ribosomal sequence b.Antibiotic resistance pattern c.Motility d.Ability to ferment glucose e.Morphology and gram staining
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Question #3 3.Streptococcus viridans and pneumoniae are both hemolytic, catalase -, gram + cocci. Which test may readily distinguish them? a.Enterotube II b.Novobiocin resistance c.Motility test d.Oxidase test e.Resistance to optochin
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