First Identification and Characterization of Burkholderia spp. Isolates (UZ Brussel)

Last updated on 14-2-2025 by Amber Van Laer

Test Description

Identification (First Step)

After culture on agar, an analysis using MALDI-TOF mass spectrometry is performed. The result of this initial analysis is reported immediately. Depending on the microorganism’s nature, identification may be at the genus, complex, or species level (e.g., Achromobacter spp. are reported at the genus level, while Stenotrophomonas maltophilia is reported at the species level). Members of the Burkholderia cepacia complex, except B. multivorans, cannot be reliably differentiated and are reported as a complex.

Randomly Amplified Polymorphic DNA Typing (RAPD)

Strains are typed using the RAPD technique to quickly assess whether there is similarity with previous isolates of the same species from the same patient.

Antibiotic Susceptibility Testing

Microdilution is used to determine the isolate’s susceptibility to the following antibiotics:
Temocillin, piperacillin, piperacillin/tazobactam, aztreonam, ceftazidime, ceftazidime/avibactam, ceftolozane/tazobactam, cefiderocol, meropenem, ciprofloxacin, levofloxacin, tobramycin, amikacin, tigecycline, eravacycline, trimethoprim/sulfamethoxazole, colistin.

Since EUCAST does not provide critical concentrations for the Burkholderia cepacia group, the PK/PD table values, Pseudomonas spp. breakpoints, or CLSI values are used for a provisional interpretation.
Antibiotics with known intrinsic resistance are always reported as resistant (e.g., colistin for B. gladioli).

Purpose of the Test

The objective of these tests is to rapidly obtain a preliminary identification of the Burkholderia cepacia complex. Antibiotic susceptibility testing aims to help guide antimicrobial therapy. It should be noted that there are few guidelines for the clinical interpretation of these bacteria’s susceptibility, and results should be interpreted with caution.

Criteria for Performing This Test in the Context of Reference Activities

  • Patients with Cystic Fibrosis: Laboratories are advised to refer up to two respiratory isolates per patient per year per bacterial species to the National Reference Center (NRC).
  • Other Patients: Only with well-documented justification (e.g., outbreak investigation, unusual clinical presentation).

Sample Collection

Specimen

Bacterial isolates from cultures of respiratory secretions of a cystic fibrosis patient or relevant specimens from other patients.

Storage

Not applicable.

Transport

Isolates are transported to the NRC without refrigeration. The NRC does not provide transport materials; the referring laboratory uses its own (e.g., tubes with nutrient medium or Petri dishes) for transport according to UN3373 standards.

Unacceptable Requests

Indications

  • Isolates without clinical relevance.
  • Isolates of Pseudomonas aeruginosa or Acinetobacter spp.
  • Environmental isolates (unless under a specific agreement for exceptional circumstances, such as an outbreak investigation).
  • Isolates without a completed request form.
  • A maximum of two isolates per species per patient per calendar year are accepted.

Sample Collection

The NRC does not accept primary clinical samples.

Turnaround Time

  • Preliminary Identification: 2 working days. A first MALDI-TOF MS analysis is generally possible after overnight incubation, with results reported the following day.
  • Antibiotic Susceptibility Testing: 5 days.
  • RAPD Typing: 14 days.

Result Transmission

  • By mail.
  • Via Medibridge for laboratories and prescribers registered with UZ Brussel.

Accreditation

Is the analysis accredited?
INAMI-RIZIV code: 
ISO 15189 | Kwaliteit en competentie van medische laboratoria

Materials and methods

Material(s): 
Method reference: 
Identificatie en bepaling van antibioticagevoeligheid

Turnaround time and time slots

Turnaround time: 
14 days

Analysis categories

Medical

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