Enterovirus Quantitative Real-time RT-PCR
Some specimen types for this assay are reported as qualitative results; please see our Specimen Information section below for more information.
The enteroviruses are well-known etiologic agents of viral meningitis, viral encephalitis, myocarditis, and respiratory tract disease as well as a wide variety of other clinical conditions. Quantitative PCR can be used to detect the presence of the virus as well as track the course of infection.
About Enterovirus
Human enteroviruses are ubiquitous viruses that are transmitted from person to person via direct contact with virus shed from the gastrointestinal tract or respiratory tract. Enteroviruses cause a wide range of infections, ranging from mild illness to clinically significant infection, especially in immunocompromised populations.1-2 Most infections are subclinical, especially in young children, but clinically apparent disease can cause an array of clinical conditions, ranging from rashes and upper respiratory tract infections, to meningitis and other neurological diseases.3
ProcedureExtraction of enterovirus nucleic acid from specimen, followed by reverse transcription of viral RNA, then amplification and detection of cDNA using real-time, quantitative PCR. An internal control is added to ensure the extraction was performed correctly and the PCR reaction was not inhibited. Eurofins Viracor's assay design includes multiple targets to account for viral mutations, which significantly reduces the chance of false negative results. This test has not been cleared or approved for diagnostic use by the U.S. Food and Drug Administration.
SpecificityDetects the entire spectrum of human enteroviruses, including coxsackie A viruses, coxsackie B viruses, echoviruses, polioviruses, and enteroviruses 68 through 71. The assay does not differentiate between serotypes. This assay is designed to specifically detect enteroviruses; however, rhinoviruses are a closely related and highly diverse group of pathogens. Cross-reactivity has been observed with some strains of rhinoviruses. Results should be used in conjunction with clinical findings and should not form the sole basis for a diagnosis or treatment decision.
Same day (within 12 - 24 hours from receipt of specimen), Monday through Saturday.
Specimen Type | Test Code | CPT Code | NY Approved | Volume | Assay Range | Special Instructions |
---|---|---|---|---|---|---|
plasma | 1401 | 87799 | Yes | 2 mL (min. 0.5 mL) |
211 copies/mL to 1x108 copies/mL |
|
CSF | 1403 | 87799 | Yes | 2 mL (min. 0.5 mL) |
83 copies/mL to 1x108 copies/mL |
|
Fresh Frozen Tissue [Qual] | 1405 | 87498 | No | 5 mg fresh tissue (approximately ½ of a pencil eraser size) | Detected/Not Detected |
|
fecal | 1408 | 87498 | No | Size of pea, or 2 mL liquid stool | Detected/Not Detected |
|
BAL | 1409 | 87799 | Yes | 2 mL (min. 0.5 mL) |
224 copies/mL to 1x108 copies/mL |
|
serum | 1410 | 87799 | Yes | 2 mL (min. 0.5 mL) |
211 copies/mL to 1x108 copies/mL |
|
nasal wash | 1413 | 87799 | Yes | 2 mL (min. 0.5 mL) |
150 copies/mL to 1x108 copies/mL |
|
trach asp | 1419 | 87799 | Yes | 2 mL (min. 0.5 mL) |
224 copies/mL to 1x108 copies/mL |
|
throat gargle | 1423 | 87799 | Yes | 2 mL (min. 0.5 mL) |
150 copies/mL to 1x108 copies/mL |
|
NP aspirate | 1424 | 87799 | Yes | 2 mL (min. 0.5 mL) |
150 copies/mL to 1x108 copies/mL |
|
NP swab | 1425 | 87498 | Yes | 2 mL |
Detected/Not Detected |
|
bronch wash | 1426 | 87799 | Yes | 2 mL (min. 0.5 mL) |
224 copies/mL to 1x108 copies/mL |
|
nasal swab | 1430 | 87498 | Yes | 2 mL |
Detected/Not Detected |
|
nasal asp | 1431 | 87799 | Yes | 2 mL (min. 0.5 mL) |
150 copies/mL to 1x108 copies/mL |
|
NP wash | 1447 | 87799 | Yes | 2 mL (min. 0.5 mL) |
150 copies/mL to 1x108 copies/mL |
|
trach wash | 1448 | 87799 | Yes | 2 mL (min. 0.5 mL) |
224 copies/mL to 1x108 copies/mL |
|
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 Eurofins Viracor test requisition form must accompany each specimen. Multiple tests can be run on one specimen. Ship specimens FedEx Priority Overnight® to: Eurofins Viracor, 18000 W 99th St. Ste, #10, Lenexa, KS 66219
Causes for RejectionWhole blood frozen, grossly hemolyzed plasma/serum specimens, specimens beyond their acceptable length of time from collection as listed in the specimen handling, specimens received in trap containers or specimen types other than those listed.
Specimens are approved for testing in New York only when indicated in the Specimen Information field above.
The CPT codes provided are based on Eurofins Viracor's 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. Eurofins Viracor assumes no responsibility for billing errors due to reliance on the CPT codes illustrated in this material.
References1 Chakrabarti S, Osman H, Collingham KE, et al. Enterovirus infections following T-cell depleted allogeneic transplants in adults. Bone Marrow Transplant. Feb; 33(4):425-30.
2 Gonzalez Y, Martino R, Badell I, et al. Pulmonary enterovirus infections in stem cell transplant recipients. Bone Marrow Transplant. 1999 Mar, 23(5):511-3.
3 Pallansch MA, Roos RP: Enteroviruses: polioviruses, coxsackieviruses, echoviruses, and newer enteroviruses. In Fields Virology. 4th edition. Edited by Knippe DM, Howley PM. Philadelphia, PA: Lippincott Williams and Wilkins; 2001:723-75.