Legionella Culture
Test Code
CXLEG
Description
Legionella culture is used when atypical respiratory illness is suspected such as Legionnaire's Disease (a type of pneumonia) and Pontiac disease (a flu-like infection). Note that Legionella may be better detected using PCR instead of culture.
Collect
Appropriate specimens for testing:
- Expectorated sputum
- Bronchoscopy samples: brushes, washes, and lavages
- Needle aspirates of lung tissue
- Sterile fluids (pleural, pericardial, and peritoneal)
- Tissue
Submit specimen in a sterile container or a syringe capped without the needle.
Saline may be inhibiting to Legionella.
Preferred volume: 3 mL
Minimum Volume: 0.25 mL
Patient Prep
Avoid antibiotic administration prior to sample collection.
Unacceptable Conditions
- Specimens received outside of temperature storage requirements
- Specimens received outside of stability time frame
- Specimens that do not meet the minimum volume requirement
- Specimens in non-sterile containers
- Specimens from a source not acceptable for this testing
- Specimens that are excessively leaking
- Mislabeled or unlabeled specimen
Stability
Source of Specimen |
Temperature |
Recommended Stability |
Maximum Stability |
Note |
Sterile fluids: pleural, peritoneal, pericardial, ascites, amniotic, culdocentesis, synovial fluids, and cerebrospinal fluid Deep Wounds: Tissue/biopsies, abscess aspirates, fine needle aspirates |
Room temperature (20-25°C)
|
ASAP |
≤24 hours |
Do not refrigerate |
Expectorated/ Induced Sputum Bronchoscopy (Bronchial Wash, BAL) |
Room temperature (20-25°C)
|
≤2 hours |
≤2 hours |
Sputum mailers are accepted ≤ 5 days |
Refrigerated (2-8°C)
|
-- |
≤ 24 hours |
|
Performed
7 days a week from 8 am to 6pm
Methodology
Bacterial culture using media specific for Legionella
Turnaround Time
14 days
Department
Microbiology Lab
Study Offerings
CAP/CLIA
Reference Interval
No Legionella sp. isolated
Interpretation
- Legionella spp. - will be sent to the state health department for confirmation
- No Legionella spp. isolated
CPT Code
87081
New York Approved
Standard
FDA
Standard Method