Sputum culture

3. Examine colony morphology

White/gray, smooth, raised, beta or gamma, opaque

Think possible GPC in clusters or chains

Gray, smooth, pinpoint, flat/raised, alpha, translucent

Think possible GPC in chains

Gray/tan/bluish-gray/white, small, translucent, raised, convex, smooth, hockey puck

Think possible GNDC

Wide variety of colony morphologies

GNR/GNCB

5. Correlate colony morphology with gram stain results

GPC

Perform catalase

+

Perform coagulase

+

Staph aureus

-

Perform bacitracin or modified oxidase

Bacitracin S/modified oxidase +

Micrococcus species

Baccitracin R/modified oxidase -

(Other) coag neg staph

(Urine) novobiocin

S

Coag neg staph

R

Probable staph saprophyticus

-

Possible streptococci

Beta

Perform PYR

+

Perform bacitracin

S

Group A strep

-

Perform hippurate hydrolysis

+

Group B strep

-

Perform bile esculin

+

Perform 6.5% NaCl

+

Enterococcus species

-

Group D strep

-

Beta strep, not A, B, or D, or Enterococcus species

Alpha

Perform optochin

S

Strep pneumoniae

R

Perform bile esculin

+

Perform 6.5% NaCl

+

Enterococcus species

-

Group D strep

-

Strep viridans

Gamma

Perform bile esculin

+

Perform 6.5% NaCl

+

Enterococcus species

-

Group D strep

-

Non-hemolytic strep

GNR/GNCB (growth on BAP, CHOC, & MAC)

Growth on MAC

+

Perform oxidase

+

G

Glucose fermenter

Correlate with key biochemical reactions

Glucose oxidizer

ADH

+

Growth @ 42 C

+

Pseudo aeruginosa (if green/red/brown pigment, LDC -, ODC - , nitrate +)

-

Additional results needed for definitive ID

-

LDC

+

Perform polymyxim B susceptibility

S

Additional test results needed for definitive ID

R

Burk cepacia complex (if ODC variable, pale yellow colonies)

-

Probable Elizabeth meningoseptica (if ODC -, indole +, yellow pigment)

Glucose asaccharolytic

Additional test results needed for definitive ID

-

(Sterile body source, LF) perform GNR ID panel

(Non-sterile body source, LF) observe lactose fermentation

(Non-GI site) perform spot indole

+

Beta

+

Esch coli

-

Perform PYR

+

Perform GNR ID panel

-

Esch coli

-

Perform GNR ID panel

(GI site) perform GNR ID panel

NLF

Observe swarming on BAP

+

Perform spot indole

+

Prot vulgaris

-

Perform GNR ID panel

Ampicillin S

Prot mirabilis

Ampicillin R

Perform GNR ID panel

ODC +

Prot mirabilis

ODC -

Prot penneri

-

Perform GNR ID panel

Glucose fermenter

Correlate with key biochemical reactions

Glucose oxidizer

LDC

+

Streno maltophilia (if ADH/ODC -, strong maltose oxidizer, pale yellow/lavendar colonies on BAP)

-

Probable Acinetobacter species (if ADH/ODC -, plump GNCB, colorless/pink colonies on MAC)

Glucose asaccharolytic

-

Growth on BAP

+

-

GNR/GNCB (growth with only fastidious organisms)

Perform catalase

+

Perform oxidase

+

Perform XV tests on horse BAP

XV growth

Beta

+

Haem haemolyticus

-

Haem influenzae

X growth

Haem species

V & XV growth

Beta

+

Haem parahaemolyticus

-

Haem parainfluenzae

-

Consider other organisms/repeat testing

-

Perform gram stain

GNCB with school of fish/railroad tracks

+

Suspect Haem ducreyi

Perform XV tests on horse BAP

X & XV growth

Haem ducreyi

-

Consider other organisms

1. First & foremost = always consider source type

May change battery of tests performed

7. Use abbreviated ID if possible

4. Perform gram stain

GPC

GPR

GNCB

GNR

GNDC

GNC

2. Look at different colony types

Multiple colony types

Normal flora

Pathogens

Mixture of normal flora & pathogens

6. For every phase of testing, determine if additional testing is needed

Normal flora

Discontinue testing

Contaminant

Discontinue testing

Pathogen

Continue testing

7. Reporting

Preliminary report

Unable to isolate colonies/subculture/perform gram stain/get colonies to grow

Report as culture ID pending

Normal flora/contaminant isolated

Report as normal flora/possible contaminant & quantitate

Potential pathogen isolated

Report relevant info (i.e. LF GNR) or use abbreviated ID & quantitate

Pathogen ID unknown or pathogen antibiotic susceptibilities unknown = report as antibiotic susceptibility/ID pending

Pathogen ID known or antibiotic susceptibilities known = report as is & do not perform susceptibility testing (i.e. beta hemolytic strep is known to be susceptible to penicillin)

Interim report

Record if there is any additional growth

Run & record any more tests performed (biochemical/susceptibility testing)

Final report

Quantitate growth

Urine/BAL

Quantitate numerically (i.e. >100,000 CFU/ml)

Other

Quantitate qualitatively (i.e. many, few, etc.)

Report pathogen ID/contaminant/normal flora

Note relevant biochemical/susceptibility testing

Date/time/initial

ALWAYS date/time/initial reports, beginning of overnight tests, susceptibility testing, etc.