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Fungitell® ß-D-Glucan Assay

Test Code: 1700
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Clinical Utility

The Fungitell ß-D Glucan assay is indicated for the presumptive diagnosis of invasive fungal disease through detection of elevated levels of (1,3)- ß-D-glucan in serum. Normal human serum contains low levels of (1,3)- ß-D glucan, typically 10 to 40 pg/mL, presumably from commensal yeasts present in the alimentary canal and gastrointestinal tract. However, (1,3)- ß-D-glucan is sloughed from the cell walls during the life cycle of most pathogenic fungi. Thus, monitoring serum for evidence of elevated and rising levels of (1,3)- ß-D-glucan provides a convenient surrogate marker for invasive fungal disease.

The Fungitell ß-D Glucan assay detects (1,3)- ß-D-glucan from the following pathogens: Candida spp., Acremonium, Aspergillus spp., Coccidioides immitis, Fusarium spp., Histoplasma capsulatum, Trichosporon spp., Sporothrix schenckii, Saccharomyces cerevisiae, and Pneumocystis jiroveci.

The Fungitell ß-D Glucan assay does not detect certain fungal species such as the genus Cryptococcus, which produces very low levels of (1,3)- ß-D-glucan, nor the Zygomycetes, such as Absidia, Mucor, and Rhizopus, which are not known to produce (1,3)- ß-D-glucan. Studies indicate Blastomyces dermatitidis is usually not detected due to little (1,3)- ß-D-glucan produced in the yeast phase.

Procedure

The assay is based upon a modification of the Limulus Amebocyte Lysate (LAL) pathway. The key assay reagent is modified to eliminate Factor C, and is therefore specific for (1,3)- ß-D-glucan and does not react to other polysaccharides, including beta-glucans with different glycosidic linkages. Similar to enzyme immunoassays, the Fungitell ß-D Glucan assay is performed in microplates and read in an incubating reader. This test has been cleared or approved for diagnostic use by the U.S. Food and Drug Administration.

Same day (within 8 - 12 hours from receipt of specimen), Monday through Saturday.

Specimen Type Order Code CPT Code NY Approved Volume Assay Range Special Instructions
BAL 1709 87449 Yes

2 mL (min. 0.1 mL)

  • Negative: Less than 60 pg/mL.
  • Indeterminate: 60 to 79 pg/mL.
  • Positive: Greater than or equal to 80 pg/mL
  • Collect 1-3 mL in a sterile, screw top tube.
  • Ship on dry ice for overnight delivery Monday through Friday.
bronch wash 1726 87449 Yes

2 mL (min. 0.1 mL)

  • Negative: Less than 60 pg/mL.
  • Indeterminate: 60 to 79 pg/mL.
  • Positive: Greater than or equal to 80 pg/mL
  • Collect 1-3 mL in a sterile, screw top tube.
  • Ship on dry ice for overnight delivery Monday through Friday.
CSF 1703 87449 Yes

2 mL (min. 0.1 mL)

  • Negative: Less than 60 pg/mL.
  • Indeterminate: 60 to 79 pg/mL.
  • Positive: Greater than or equal to 80 pg/mL
  • Collect 2 mL in a sterile, screw top tube.
  • Freeze and ship on dry ice for overnight delivery Monday through Friday.
serum 1710 87449 Yes

2 mL (min. 0.1 mL)

  • Negative: Less than 60 pg/mL.
  • Indeterminate: 60 to 79 pg/mL.
  • Positive: Greater than or equal to 80 pg/mL
  • Collect 3-5 mL whole blood in a gel separator tube (SST).
  • Centrifuge specimen within 2 hours of draw to pellet cells below the gel.
  • Minimum volume of 0.5 mL serum for adults and 0.2 mL for infant (see assay limitations) and pediatric samples following centrifugation.
  • Specimen can be stored refrigerated at 2 to 8°C or preferably stored frozen and shipped for overnight delivery.
  • The serum can be decanted into a suitable container that is free of interfering levels of (1-3)-B-D-glucan; however, the use of pour-off tubes is not recommended due to the potential for environmental contamination of the sample that can lead to false positive results.  Serum samples which are transferred to sterile, leak-proof containers should be handled in a sterile cabinet.  Interpret results from samples provided in pour-off tubes with caution.
  • Ship on dry ice for overnight delivery Monday through Friday.

Serum Reference Range:

Negative: Less than 60 pg/mL. Indeterminate: 60 to 79 pg/mL. Positive: Greater than or equal to 80 pg/mL

A reference range for specimens other than serum has not been established by the USFDA or Viracor Eurofins. The Fungitell ß-D Glucan assay is indicated for presumptive diagnosis of fungal infection. It should be used in conjunction with other diagnostic procedures. The Fungitell ß-D Glucan assay does not detect certain fungal species such as the genus Cryptococcus, which produces very low levels of (1,3)- ß-D-glucan. This assay also does not detect the Zygomycetes, such as Absidia, Mucor and Rhizopus, which are not known to produce (1,3)- ß-D-glucan.

Assay Limitations

There are reports in the peer reviewed literature of lowered assay specificity in patients with gram positive bacteremia.

Patients with renal failure on hemodialysis utilizing cellulose membranes may have false positive results.

Patients treated with fractionated blood products such as albumin and immunoglobulin and in specimens and subjects exposed to glucancontaining gauze. Patients require 3 to 4 days for the restoration of baseline levels of serum (1,3)- ß-D-glucan, after surgical exposure to (1,3)- ß-D-glucan-containing sponges and gauze. Accordingly, the timing of sampling of surgical patients should take this into account.

Samples obtained by heel or finger stick methods are unacceptable as the alcohol-soaked gauze used to prepare the site (and potentially, the skin surface-pooling of blood) has been shown to contaminate the specimens.

A negative test result cannot rule out the diagnosis of invasive fungal disease. Patients at risk for invasive fungal disease should be tested twice per week.

The performance of the Fungitell ß-D Glucan assay has not been evaluated with specimens from neonates and infants <6 months of age.

Patients whose GI tract is colonized with Candida and have mucositis may have a positive Fungitell ß-D Glucan assay result without invasive fungal disease.

Shipping

Ship Monday through Friday. Friday shipments must be labeled for Saturday delivery. All specimens must be labeled with patient's name and collection date. A Viracor Eurofins test requisition form must accompany each specimen. Multiple tests can be run on one specimen. Ship specimens FedEx Priority Overnight® to: Viracor Eurofins, 1001 NW Technology Dr, Lee's Summit, MO 64086.

Causes for Rejection

Lipemic, icteric, or hemolyzed specimens. Specimens that have been stored at ambient temperature. Specimens that have been stored at 2 to 8°C for >5 days. If storage longer than 5 days is needed, samples should be frozen at -20°C or colder. Unless indicated as stored frozen, the specimen will be rejected if the draw date is >5 days from receipt at Viracor Eurofins. Specimens other than those listed in the specimen information.

Specimens are approved for testing in New York only when indicated in the Specimen Information field above.

The CPT codes provided are based on Viracor Eurofins' interpretation of the American Medical Association's Current Procedural Terminology (CPT) codes and are provided for informational purposes only. CPT coding is the sole responsibility of the billing party. Questions regarding coding should be addressed to your local Medicare carrier. Viracor Eurofins assumes no responsibility for billing errors due to reliance on the CPT codes illustrated in this material.

Information derived from the Fungitell package insert (Associates of Cape Cod, Inc.). Fungitell is a product and registered trademark of Associates of Cape Cod, Inc.

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