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SOP

Urine Culture and Colony Count

SOP for quantitative urine culture to diagnose urinary tract infections (UTI) and identify causative organisms.

Last verified 1 month ago 2 min read Microbiology Urinalysis and Body Fluids Bacteriology Quantitative Microbiology #cfu #microbiology #colony-count #Bacteriology #Urine Culture #UTI #Quantitative Culture
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Document Control
Version
1.0
Effective
Aug 28, 2026
Reviewed
Aug 29, 2026
Department
Microbiology
Principle

Quantitative urine culture determines the number of viable bacteria per milliliter of urine. A calibrated loop or pipette delivers a known volume of urine onto solid culture media. After incubation, the number of colonies formed is counted and multiplied by the dilution factor to calculate CFU/mL. This quantification helps distinguish true urinary tract infection from contamination or colonization.

Standard Operating Procedure: Urine Culture

1. Purpose and Scope

To perform quantitative culture of urine specimens to detect and enumerate bacterial pathogens causing urinary tract infections (UTI).

2. Specimen Requirements

  • Type: Mid-stream clean-catch urine, catheterized specimen, or suprapubic aspirate.
  • Volume: Minimum 5-10 mL.
  • Storage/Transport: Process within 2 hours of collection or refrigerate at 2-8°C for up to 24 hours.
  • Rejection Criteria: Improperly labeled, contaminated, or delayed (>24 hours refrigerated) specimens.

3. Safety and Precautions

  • Wear appropriate PPE (lab coat, gloves).
  • Handle all specimens as potentially infectious.
  • Work in a biological safety cabinet if available.

4. Equipment and Reagents

  • Calibrated inoculating loop (1 µL or 10 µL) or calibrated pipette.
  • Culture media: Blood agar, MacConkey agar, CLED (Cystine Lactose Electrolyte Deficient) agar.
  • Incubator (35-37°C), Bunsen burner or incinerator.
  • Colony counter, microscope.

5. Step-by-Step Procedure

  1. Specimen Preparation: Mix urine specimen gently by inversion.
  2. Inoculation:
  • Using a calibrated 1 µL loop: Touch loop to well-mixed urine and streak onto blood agar and MacConkey/CLED agar.
  • Using a calibrated 10 µL loop: Use for specimens with suspected low colony counts.
  • Alternatively, use calibrated pipette to deliver exact volume onto agar surface.
  1. Streaking Pattern: Use quadrant streak method to isolate individual colonies.
  2. Incubation: Incubate plates at 35-37°C for 18-24 hours in ambient air (or 5% CO₂ if required).
  3. Colony Count: After incubation, count colonies on the plate.
  • Calculate CFU/mL: Number of colonies × dilution factor (1000 for 1 µL loop; 100 for 10 µL loop).
  1. Interpretation:
  • ≥10⁵ CFU/mL: Significant bacteriuria (UTI likely).
  • 10⁴-10 CFU/mL: Equivocal (repeat culture if symptomatic).
  • <10⁴ CFU/mL: Usually contamination (unless symptomatic or catheterized specimen).
  1. Identification: Identify organisms based on colony morphology, Gram stain, and biochemical tests.
  2. Antimicrobial Susceptibility Testing: Perform on significant isolates.

6. Quality Control

  • Verify calibrated loop volume monthly by weighing water delivered.
  • Check media sterility and performance with known organisms.
  • Include QC strains (E. coli ATCC 25922) for culture and AST.

7. Reporting Results

  • Report organism(s) identified and colony count in CFU/mL.
  • Report mixed growth if ≥2 organisms present with no predominant organism.
  • Include susceptibility results for significant isolates.

Frequently Asked Questions

≥10⁵ CFU/mL indicates significant bacteriuria in asymptomatic patients; ≥10³ CFU/mL may be significant in symptomatic patients or catheterized specimens.
Blood agar supports growth of Gram-positive and fastidious organisms; MacConkey agar is selective for Gram-negative bacteria and differentiates lactose fermenters.