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HelpTest Code CCMVS Congenital Cytomegalovirus (cCMV), Molecular Detection, PCR, Saliva
Ordering Guidance
This test should be ordered to test saliva specimens from patients 21 days old or younger. To test saliva from patients older than 21 days, order CMVPV / Cytomegalovirus (CMV) Molecular Detection, PCR, Varies.
To test urine specimens from patients 21 days or younger, order CCMVU / Congenital Cytomegalovirus (cCMV), Molecular Detection, PCR, Urine. To test urine from patients older than 21 days, order CMVPV / Cytomegalovirus (CMV) Molecular Detection, PCR, Varies.
For CMV testing on plasma specimens, order CMVQN / Cytomegalovirus (CMV) DNA Detection and Quantification by Real-Time PCR, Plasma.
Specimen Required
Supplies: BD UVT with minitip flocked swab (T971)
Collection Container/Tube: Flocked swab
Submission Container/Tube: Sterile, screw-capped, tube containing viral transport media with flocked swab containing saliva
Specimen Volume: 1 Swab in viral transport media
Collection Instructions: Collect and send specimen per swab manufacturer instructions.
Secondary ID
620659Useful For
Aiding in the rapid diagnosis of cytomegalovirus (CMV) infections in neonates 21 days of age or younger using saliva specimens
Method Name
Real-Time Polymerase Chain Reaction (PCR)
Reporting Name
Congenital CMV, PCR, SalivaSpecimen Type
SwabSpecimen Minimum Volume
Saliva swab submitted in minimum volume of 0.3 mL of viral transport media.
Specimen Stability Information
| Specimen Type | Temperature | Time | Special Container |
|---|---|---|---|
| Swab | Frozen | 7 days |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.Clinical Information
Cytomegalovirus (CMV) is a double-stranded DNA virus of the Herpesviridae family. CMV is transmitted through direct contact from a variety of infected body fluids, as well as through sexual contact, organ transplantation, and intrauterine transmission during pregnancy.(1) CMV infection may be asymptomatic but can cause a wide range of symptoms in immunocompromised individuals. Congenitally acquired CMV (cCMV) may lead to long-term sequelae, including visual and hearing impairments, and cognitive and motor deficits.(2) Current recommendations indicate testing urine and saliva swabs for cCMV using a nucleic acid amplification detection method.(3)
Reference Values
Negative
Interpretation
A positive result indicates the presence of cytomegalovirus (CMV) DNA in the patient sample.
A negative result indicates the absence of CMV DNA in the patient sample.
An invalid result indicates inability to conclusively determine presence or absence of CMV DNA in the patient sample.
Cautions
This test is not validated for sample types other than saliva swab and urine specimens from infants 21 days of age or younger.
Negative results do not preclude cytomegalovirus (CMV) infection and should not be used as the sole basis for treatment or other patient management decisions.
False-negative results may occur if the viral nucleic acid is present at a level below the analytical sensitivity of the assay, if the virus has genomic mutations, insertions, deletions, or rearrangements, or if the assay is performed very early in the course of illness.
The performance of this test has not been established for monitoring treatment of CMV infection.
Supportive Data
Accuracy:
To assess the accuracy of the Simplexa Congenital CMV (cytomegalovirus) Direct assay, clinical saliva swab specimens (n=47) and contrived saliva samples (n=8) were tested, and the results compared to those of a routine, lab-developed (LDT) CMV PCR assay.(4) Results are summarized in the Table:
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Table. Saliva Accuracy
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a. There were three initial Simplexa internal control failures; all saliva swab samples were retested by Simplexa in singlet. Two samples returned valid results and one repeated as invalid.
Simplexa cCMV Direct assay accuracy results for saliva samples produced 100% positive agreement, 96% negative agreement, and 98% overall agreement.
Clinical Reference
1. Manicklal S, Emery VC, Lazzarotto T, Boppana SB, Gupta RK. The "silent" global burden of congenital cytomegalovirus. Clin Microbiol Rev. 2013;26(1):86-102. doi:10.1128/CMR.00062-12
2. Cannon MJ, Griffiths PD, Aston V, Rawlinson WD. Universal newborn screening for congenital CMV infection: what is the evidence of potential benefit?. Rev Med Virol. 2014;24(5):291-307. doi:10.1002/rmv.1790
3. Rawlinson WD, Boppana SB, Fowler KB, et al. Congenital cytomegalovirus infection in pregnancy and the neonate: consensus recommendations for prevention, diagnosis, and therapy. Lancet Infect Dis. 2017;17(6):e177-e188. doi:10.1016/S1473-3099(17)30143-3
4. Binnicker MJ, Espy ME. Comparison of six real-time PCR assays for qualitative detection of cytomegalovirus in clinical specimens. J Clin Microbiol. 2013;51(11):3749-3752. doi:10.1128/JCM.02005-13
5. Fernholz EC, Vidal-Folch N, Hasadsri L. Rapid and direct detection of congenital cytomegalovirus using a commercial real-time PCR assay. J Clin Microbiol. 2023;61(3):e0178122. doi:10.1128/jcm.01781-22
Method Description
The Simplexa Congenital CMV Direct assay is a real-time polymerase chain reaction (PCR) system that enables the direct amplification and detection of CMV DNA from either saliva swab or urine specimens without nucleic acid extraction. The system consists of the Simplexa Congenital CMV Direct Reaction Mix, the LIAISON MDX (with LIAISON MDX Studio Software), the direct amplification disc, and associated accessories.
In the Simplexa Congenital CMV Direct assay, bifunctional fluorescent probe-primers are used together with corresponding reverse primers to amplify CMV DNA. A well-conserved region of the CMV UL83 gene is targeted to identify CMV DNA. An internal control is used to detect PCR failure or inhibition.(Package insert: Simplexa Congenital CMV Direct. Diasorin; REF MOL2255. Rev. 01, 011/2022)
Day(s) Performed
Monday through Sunday
Report Available
Same day/1 to 2 daysSpecimen Retention Time
7 daysPerforming Laboratory
Mayo Clinic Laboratories in Rochester
Test Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
87496
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| CCMVS | Congenital CMV, PCR, Saliva | 83065-3 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| 620659 | Congenital CMV, PCR, Saliva | 83065-3 |