Last updated on 6-2-2025 by Amber Van Laer
Test description
Extraction M. pneumoniae/C. pneumoniae DNA from matrix. Amplification DNA by real-time PCR.
Purpose of the PCR test
- Confirmation of diagnosis
- Surveillance
Criteria
Criteria for PCR detection of Mycoplasma pneumoniae
- Children or adults diagnosed as ambulatory or hospitalised patients with pneumonia not considered nosocomial: documented by an RX thorax, not suspected to be caused by pneumococci based on gram staining of sputum or culture results if available.
- Children or adults with persistent cough for at least 2 weeks (= patients who may be considered sporadic cases of Bordetella pertussis infections).
- Outbreaks: several linked patients with unexplained respiratory tract infection
- Children or adults with meningitis/encephalitis not suspected to be caused by meningococcal disease, S. pneumoniae or HSV
Criteria for PCR detection of Chlamydophila pneumoniae
- Children or adults diagnosed as outpatients or hospitalised patients with pneumonia not considered nosocomial: documented by an RX thorax, not suspected to be caused by pneumococci based on gram staining of sputum or culture results if available
- Children or adults with persistent cough for at least 2 weeks (= patients who may be considered sporadic cases of Bordetella pertussis infections).
- Outbreaks: several linked patients with unexplained respiratory tract infection
Suitable samples for PCR diagnostics of Mycoplasma pneumoniae, Chlamydophila pneumoniae
- Respiratory sample (sputum if available or throat swab), biopsy (unfixed), CSV (M. pneumoniae detection only)
- Swabs: cotton, Dacron or Flocked; dry in sterile container or preferably in universal or virus transport medium
- Minimum sample volume: 0.25 ml
- In a sterile container.
Transport instructions
University Hospital Antwerp:
All practical info related to sending samples is available via our website.http://labogids.uza.be/?_ga=2.216276886.125138701.1627394894-1313601540.1609427347
University Hospital Leuven:
All practical info related to sending samples is available through our website.http://www.uzleuven.be/lag/
Unacceptable requests
- Insufficient volume
- Sample not suitable for analysis
- Incorrect transport/storageIncomplete application form
- Application does not meet the criteria
Turn around time and analysis frequency
Analysis frequency:
- PCR detection M. pneumoniae in CSV: daily
- PCR detection M. pneumoniae, C. pneumoniae in respiratory sample:
- UZA: 3x per week
- UZ Leuven: 2x per week
Turn around time:
- PCR detection M. pneumoniae in CSV: 2 working days
- PCR detection M. pneumoniae, C. pneumoniae in respiratory sample: 2 working days
Response time: less than 1 working day
Reporting of test results
How: mail or fax at applicant’s discretion.
Accreditation
Is the analysis accredited?
Materials and methods
Material(s):
Method reference:
-
Turnaround time and time slots
Turnaround time:
3 days
Analysis categories
Medical