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Overview of Bacterial Identification Methods and Strategies (Bailey and Scott's Diagnostic Microbiology)

This document provides an overview of various bacterial identification tests, including the expected results for positive and negative controls. It lists the test name, incubation details, what a positive result would look like, example positive and negative control bacteria, and any additional comments. Some of the more commonly used identification tests mentioned include catalase, coagulase, citrate, triple sugar iron, urease, indole, motility, and lactose fermentation. The tests can help identify bacteria by their metabolic activities or presence of certain enzymes.

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Aj Brigente
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0% found this document useful (0 votes)
159 views7 pages

Overview of Bacterial Identification Methods and Strategies (Bailey and Scott's Diagnostic Microbiology)

This document provides an overview of various bacterial identification tests, including the expected results for positive and negative controls. It lists the test name, incubation details, what a positive result would look like, example positive and negative control bacteria, and any additional comments. Some of the more commonly used identification tests mentioned include catalase, coagulase, citrate, triple sugar iron, urease, indole, motility, and lactose fermentation. The tests can help identify bacteria by their metabolic activities or presence of certain enzymes.

Uploaded by

Aj Brigente
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as DOCX, PDF, TXT or read online on Scribd
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Overview of Bacterial Identification Methods and Strategies

(Bailey and Scott’s Diagnostic Microbiology)


Test Incubation Expected Results (+) Control (-) Control Comments
Acetamide utilization 35’C for up (+) Blue Pseudomonas Stenotrophomonas
to 7 days (-) Green aeruginosa maltophilia
Acetate utilization 35’C for up (+) Blue Escherichia coli Shigella flexneri
to 7 days (-) Green
Bacitracin test 35’C for (+) Any zone of Streptococcus Streptococcus Amount of Bacitracin:
18-24 hrs inhibition pyogenes agalactiae 0.04 U
(-) No zone
Bile Esculin agar 35’C for (+) Blackening of agar Enterococcus Streptococcus mitis Conc.: 40% Bile
48 hrs (-) No blackening faecalis Indicator:
Ferric ammonium citrate
Bile Solubility test 35’C for (+) Colony disintegrates Streptococcus Enterococcus Rgt: 10% Sodium desoxycholate
30 mins (-) Intact colonies pneumoniae faecalis
Butyrate disk Room temp (+) Blue color Moraxella Neisseria Rgt: Bromo-chloro-indolyl
for 5 mins (-) No color change catarrhalis gonorrhoeae butyrate
CAMP test 35’C (+) Arrowhead zone of Streptococcus Streptococcus CAMP:
overnight beta-hemolysis agalactiae pyogenes Christie
(-) No enhancement of Atkins
hemolysis Munch
Peterson
Catalase test (+) Bubble formation Staphylococcus Streptococcus Rgt: 30% H2O2
(-) No or few bubbles aureus pyogenes BAP contains blood
(Hgb  false positive)
Cetrimide 35’C for up (+) Growth Pseudomonas Escherichia coli
to 7 days (-) No growth aeruginosa
Citrate utilization 35-37’C for (+) Growth w/ or w/o Klebsiella Escherichia coli Indicator: Bromthymol blue
up to 7days change in color from pneumoniae Medium: Simmon’s citrate agar
green to blue
(-) No growth
Coagulase test b. tube test: a. Slide test Staphylococcus Staphylococcus Slide test: detects clumping
a. Slide test 35’C for (+) Clumping aureus epidermidis factor (bound coagulase)
b. Tube test 4 hours (-) No clumping Tube test: detects free coagulase
b. Tube test Rgt: Rabbit EDTA plasma
(+) Clot formation
(-) No clot

lec.mt 04 |Page | 89
Test Incubation Expected Results (+) Control (-) Control Comments
Decarboxylase test Glucose non (+) Alkaline (purple Lysine Lysine
(Moeller’s method) fermenters: color) Klebsiella Enterobacter
35’C for 7d (-) Acid (yellow color) pneumoniae cloacae
Glucose Ornithine Ornithine
fermenters: Enterobacter Klebsiella
35’C for 4d cloacae pneumoniae
Arginine Arginine
Enterobacter Klebsiella
cloacae pneumoniae
DNA Hydrolysis 35’C for (+) Colorless Staphylococcus Staphylococcus Medium: DNase agar (DNA-
(DNase) 13-24 hours (-) Green aureus epidermidis methyl green complex)
Serratia
marcescens
Esculin Hydrolysis 35’C for (+) Blackened medium Klebsiella Shigella flexneri
7 days and loss of fluorescence pneumoniae
under Wood’s lamp
(-) No blackening and no
loss of fluorescence
under Wood’s lamp
Fermentation Media a. Peptone: a. Peptone medium a. Peptone a. Peptone medium a. Peptone medium:
a. Peptone medium 35’C for up (+) Pink w/ or w/o gas medium Pseudomonas Indicator: Andrade’s indicator
b. Heart Infusion to 7 days formation in Durham w/ gas: aeruginosa b. Heart infusion broth:
b. Heart tube Escherichia coli b. Heart infusion Indicator: Bromcresol purple
infusion: (-) Growth but no change w/o gas: broth
35’C for in color Shigella flexneri Sorbitol:
4 days b. Heart infusion broth b. Heart infusion Streptococcus mitis
(+) Yellow broth
(-) Growth but no change Sorbitol:
in color (purple) Streptococcus
mutans

Flagella Stain (+) Flagella Peritrichous: Klebsiella Rgt: RYU flagella stain
(Wet-Mount technique) a. Peritrichous Escherichia coli pneumoniae
b. Lophotrichous Polar:
c. Polar Pseudomonas
d. Tufted aeruginosa

lec.mt 04 |Page | 90
Test Incubation Expected Results (+) Control (-) Control Comments
Gelatin Hydrolysis 35’C (+) Partial or total Proteus vulgaris Enterobacter
(Gelatinase) (or 25’C) liquefaction at 4’C aerogenes
for up to 14 (-) Complete
days solidification at 4’C
Growth at 42’C 35’C and (+) Good growth at both Pseudomonas Pseudomonas
42’C for 35’C and 24’C aeruginosa fluorescens
18-24 hrs (-) No growth at 42’C but
good growth at 35’C
Hippurate test 35’C for (+) Deep purple color Streptococcus Streptococcus
2 hrs (-) Colorless or slightly agalactiae pyogenes
yellow pink color
Indole production 35’C for (+) Pink- to wine-colored a. Kovac’s method a. Kovac’s method
a. Kovac’s method 48 hours ring Escherichia coli Klebsiella
b. Ehrlich’s method (-) No color change b. Ehrlich’s pneumoniae
method b. Ehrlich’s method
Elizabethkingia CDC group EO-2
meningoseptica
LAP test Room temp (+) Red color Enterococcus Leuconostoc sp Rgt: cinnamaldehyde
for 5 mins (-) No color change or faecalis
dev’t of slight yellow
color
Litmus milk 35-37’C Color of Indicator: Alkaline: Indicator: Litmus paper
Acid: Pink, mauve Alcaligenes faecalis
Alkaline: Blue Acid:
No change: Purple Enterococcus
White: Reduction of faecium
indicator Peptonization:
Consistency of Milk Burkholderia
Clot/Coagulation: Acid or cepacia
Alkaline pH
Digestion: Dissolution of
clot w/ shrunken,
insoluble pink clot (acid)
Peptonization:
Dissolution of clot w/
shrunken, insoluble blue
clot (alk)

lec.mt 04 |Page | 91
Test Incubation Expected Results (+) Control (-) Control Comments
Lysine Iron Agar 35’C for K/K: K/K w/ H2S: K/A: Decarboxylation: Butt (Purple)
18-24 hrs (+) Decarboxylation Salmonella Shigella flexneri Deamination: Slant (Red)
(-) Glucose fermentation typhimurium H2S indicator: Ferric ammonium
K/A: R/A: citrate
(+) Glucose fermentation Proteus vulgaris
(-) Decarboxylation
K/A or K/K w/ H2S:
(+) Black precipitate
(FeS)
R/A:
(+)Deamination
(+) Glucose fermentation
Methyl Red test 35-37’C for (+) Bright red color Escherichia coli Enterobacter MR detects mixed acid
48 hrs (W+) Red-orange color cloacae fermentation
(-) Yellow Indicator: Methyl red
Voges-Proskauer b. Coblentz (+) Red color a. Barritt’s method a. Barritt’s method VP detects acetoin
a. Barritt’s method (For method: (-) Yellow color Enterobacter Escherichia coli (acetylmethylcarbinol) formation
Gram-negative rods) Room temp cloacae b. Coblentz method Rgts:
b. Coblentz method (For for 30 mins b. Coblentz Streptococcus mitis a. Barritt’s mtd: α-naphthol +
Streptococci) method KOH
Streptococcus b. Coblentz mtd: α-naphthol +
mutans 40% KOH w/ creatine
Microdase test Room temp (+) Blue to purple-blue Micrococcus luteus Staphylococcus Modified oxidase rgt:
for 2 mins color aureus Tetramethyl-p-
(-) No color change phenylenediamine
dihydrochloride in
dimethylsulfoxide
Motility testing b. Semisolid a. Hanging drop Escherichia coli Klebsiella Coverslip size: 22 x 22 mm
a. Hanging drop agar deep: (+) True motility pneumoniae In Brownian movement, the
b. Semisolid agar deep 35-37’C for (-) Brownian movement organisms may appear quite
up to 7days b. Semisolid agar deep active, but they remain in the
(+) Motile: spread out same relative position to other
into the medium from organisms or debris in the field
the site of inoculation
(-) Nonmotile: remain at
the site of inoculation

lec.mt 04 |Page | 92
Test Incubation Expected Results (+) Control (-) Control Comments
MRS Broth 35’C for (+) Gas production Leuconostoc Pediococcus Durham tube detects gas
24-48 hours (-) No gas production formation (bubbles)
MUG test 35’C for (+) Electric blue Escherichia coli Pseudomonas MUG: 4-methylumbelliferyl-beta-
up to 2 hrs fluorescence aeruginosa D-glucuronide
(-) Lack of fluorescence Uses 366nm UV light
Nitrate reduction 35’C for 48 After addition of the rgts: NO3+, no gas: Acinetobacter spp. Reagents:
(NO3NO2) hours or (+) Red color Escherichia coli Sulfanilic acid
max. of 7d (-) Colorless NO3+, w/ gas: Alpha-naphthylamine
If colorless, add Zinc Pseudomonas Zinc dust: to make sure the
dust: aeruginosa nitrite has not been oxidized to
(+) Colorless nitrate
(-) Red color
Nitrite reduction 35’C for (+) Colorless w/ gas Alcaligenes faecalis Alcaligenes Durham tube detects nitrogen
(NO2N2) 48 hours (-) Red w/o gas piechaudii gas formation
Zinc dust: to make sure the
nitrite has not been oxidized to
nitrate
ONPG 37’C for (+) Yellow Escherichia coli Salmonella ONPG: O-Nitrophenyl-beta-D-
4 hours (-) Colorless typhimurium galactopyranoside
Optochin test 35’C for (+) Zone of inhibition Streptococcus Streptococcus mitis Optochin (P disk):
18-24 hrs >14mm pneumoniae Ethylhydrocupreine
w/ 5% CO2 (-) No zone of inhibition hydrochloride
Equivocal: <14 mm zone Medium: 5% sheep BAP
of inhibition (perform
bile solubility test)
Oxidase test (+) Dark purple color Neisseria Escherichia coli Oxidase rgt:
(Kovac’s method) (-) Absence of color gonorrhoeae Tetramethyl-p-
phenylenediamine
dihydrochloride
Oxidation/Fermentation 35’C for up (+) Yellow (Acid deep) Fermenter: Nonutilizer: Stab agar deeps using a needle 4-
(OF) medium to 7 days (W+) Deeper red (Alk) Escherichia coli Alcaligenes faecalis 5x to a depth of 1 cm
(CDC method) (-) Red (alkaline deep) Oxidizer:
(NC or N): No change or Pseudomonas
Neutral, there is growth aeruginosa
in the media
(NG): No growth

lec.mt 04 |Page | 93
Test Incubation Expected Results (+) Control (-) Control Comments
Phenylalanine 35’C for (+) Green color Proteus vulgaris Escherichia coli Rgt: 10% Ferric chloride
Deaminase 18-24 hrs (-) No color change
PYR test Room temp (+) Bright red color Enterococcus Streptococcus mitis PYR: L-pyrrolidonyl-beta-
(PYRase) for 2 mins (-) No color or an orange faecalis naphthylamide
color Rgt: N,N-
Methylaminocinnamaldehyde
Pyruvate broth 35’C for (+) Yellow Enterococcus Enterococcus
24-48 hours (-) No color change or faecalis faecium
yellow-Green
Salt Tolerance test 35’C for (+) Visible turbidity w/ Enterococcus Streptococcus mitis Conc.: 6.5% NaCl
48 hours or w/o color change faecalis Indicator: Bromcresol purple
from purple to yellow
(-) No turbidity and no
color change
Spot Indole test (+) Blue color Escherichia coli Enterobacter Rgt: 1% paradimethylamino-
(-) No color or slightly cloacae cinnamaldehyde
pink color Inoculum should not be selected
from MAC because the color of
lactose-fermenting colonies can
interfere w/ test interpretation
Triple Sugar Iron agar 35’C for K/K: A/A w/ gas: K/K: TSI contains:
(TSI) 18-24 hrs Glucose, lactose and Escherichia coli Pseudomonas 1 part glucose
sucrose nonutilizer K/A w/ H2S: aeruginosa 10 parts lactose
K/A: Salmonella typhi 10 parts sucrose
Glucose fermentation Peptone
only Indicators:
A/A: pH: phenol red
Glucose, sucrose, and/or H2S: ferrous sulfate
lactose fermenter
Black ppt (butt):
H2S production
Bubbles/cracks:
CO2 or H2 (gas)
production
Urea Hydrolysis 35’C for (+) Magenta color Proteus vulgaris Escherichia coli Indicator: phenol red
(Christensen’s method) 48 hrs up to (-) Light orange Ammonia alkalinizes the medium
7 days pH 6.8: light orange
pH 8.1: magenta

lec.mt 04 |Page | 94
Test Incubation Expected Results (+) Control (-) Control Comments
X and V factor test Overnight (+) Growth: Around XV disk: Haemophilus X factor: hemin/hematin
at 35’C Growth around XV disk: Haemophilus aphrophilus (does V factor: NAD
Shows a requirement for influenzae not need X, V, or XV Medium: TSB
both factors Around XV and V factors for growth) Avoid carrying over of any X-
Growth around V disk, disks: factor contained in the medium
no growth around X disk, Haemophilus the organism is taken from
and light growth around parainfluenzae A loop, not a swab, should be
XV disk: used to make a suspension
Shows a V factor
requirement
(-) Growth over entire
surface of the agar

lec.mt 04 |Page | 95

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