Detection of Listeria

Description of the test

• Description: A specific real-time PCR is performed to identify the presence of Listeria monocytogenes.
• Result: Identification of Listeria monocytogenes.

Purpose

Confirmation of presence or absence of Listeria monocytogenes in the sample.

Criteria for performing this test in the context of reference activities

Samples collected from a normal sterile body fluid (lumbar fluid or blood) from patients presenting with symptoms of Listeriosis.

Instructions for samples

•   Type: Samples collected from a normally sterile body fluid (lumbar fluid or whole blood) from patients presenting with symptoms of listeriosis.
•   Minimum quantity: 200µl

Instructions for transport

For safety reasons, samples should be packed in a double protective container and hermetically sealed. If possible, transport should preferably be done refrigerated.

Unacceptable applications

Not applicable

Turnaround time (and frequency of analysis)

• Turnaround time: 15 working days.
• Analysis days: Any weekday (excluding: public holidays, extended weekends and the period between Christmas and New Year).

Reporting of test results

The analysis report is sent in the manner desired by the applicant.