Wisconsin Lab Testing Services

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Test Pricing Information


List of Diagnostic Tests Performed

2000             Rapid Human Herpesvirus Six (HHV-6) Culture andAntigenemia                 

Methodology:

Shell vial culture. Detects both active HHV-6 A and HHV-6 B infection, but does not differentiate between them.

Performed: Tuesday, Wednesday, Thursday, Friday
Reported: Within 5 days after receipt in lab
Specimen Required:

Collect: Whole blood: 7-10 ml in ACD (acid citrate dextrose). Bone marrow: 2-3 ml in sodium heparin.
Bronchoalveolar lavage: 2-3 ml in sterile, leak-proof container.
Transport: ACD tube and bone marrow at room temperature.
Bronchoalveolar lavage refrigerated (wet ice).
Ship Monday-Thursday.

Unacceptable Conditions:

Specimen received frozen.
Specimen received greater than 48 hours from collection.
Serum or plasma received instead of whole blood.
Stability: Whole blood and bone marrow: Room temperature, 48 hours.
Bronchoalveolar lavage: Refrigerated, 48 hours.

Remarks:

Only one ACD tube necessary for the Rapid HHV-6 Culture and PCR testing.
Transport as whole blood.

Reference Value: Negative.

Result is qualitative. Negative or Positive.

Interpretive Data:

Negative result suggests, but does not prove, the absence of active HHV-6 infection. Positive result is consistent with active HHV-6 infection.


1100                           Human Herpesvirus Six (HHV-6) DNA Nested PCR                                        

Methodology:

Polymerase Chain Reaction. Enhanced sensitivity of nested PCR for the detection of active infection. Detects and differentiates HHV-6 A and HHV-6 B.

Performed: Monday - Friday
Reported: Within 4 days of receipt in lab.
Specimen Required:

Collect: CSF or one 7 to 10 ml ACD (acid citrate dextrose) tube.
Transport: 1 ml CSF or plasma (ACD) in a sterile, leak-proof container, frozen (dry ice).
Or ship ACD tube as whole blood at room temperature.

Unacceptable Conditions:

Whole blood received frozen.
Whole blood received greater than 48 hours from collection.

Stability:

Plasma and CSF: Room temperature, 4 hours. Refrigerator, 3 days. Frozen, 1 year.
Whole blood: Room temperature, 48 hours.

Reference Value: Negative


1200                               Epstein-Barr Virus (EBV) DNA Nested PCR                                                     

Methodology:

Polymerase Chain Reaction. Enhanced sensitivity of nested PCR for the detection of active infection.

Performed: Monday - Friday
Reported: Within 4 days of receipt in lab.
Specimen Required:

Collect: One 7 to 10 ml ACD (acid citrate dextrose) tube.
Transport: Plasma (ACD) in a sterile, leak-proof container, frozen (dry ice).
Or ship ACD tube as whole blood at room temperature.

Unacceptable Conditions:

Whole blood received frozen.
Whole blood received greater than 48 hours from collection.

Stability:

Plasma: Room temperature, 4 hours. Refrigerator, 3 days. Frozen, 1 year.

Reference Value: Negative


3000         Rapid Human Cytomegalovirus (HCMV) Culture and Antigenemia              

Methodology:

Shell vial culture. Detects active HCMV infections by immunofluorescent staining with a HCMV specific monoclonal antibody.

Performed: Tuesday, Wednesday, Thursday, Friday
Reported: Within 5 days upon receipt in lab
Specimen Required:

Collect: Whole blood: 7-10 ml in ACD (acid citrate dextrose).
Bone marrow: 2-3 ml in sodium heparin.
Bronchoalveolar lavage: 2-3 ml in sterile, leak-proof container.
Transport: ACD tube and bone marrow at room temperature.
Bronchoalveolar lavage refrigerated (wet ice).
Ship Monday - Thursday.

Unacceptable Conditions:

Specimen received frozen.
Specimen received greater than 48 hours from collection.
Serum or plasma received instead of whole blood.

Stability:

Whole blood and bone marrow: Room temperature, 48 hours.
Bronchoalveolar lavage: Refrigerated, 48 hours.

Remarks:

Only one ACD tube necessary for the Rapid HCMV Culture, Rapid HHV-6 Culture and PCR testing. Transport as whole blood.

Reference Value: Negative

Result is qualitative. Negative or Positive.

Interpretive Data:

Negative result suggests but does not prove the absence of active HCMV infection.
Positive result is consistent with active HCMV infection.


1400                         Human Cytomegalovirus (HCMV) DNA Nested PCR                                   

Methodology:

Polymerase Chain Reaction. Enhanced sensitivity of nested PCR for the detection of active infection.

Performed: Monday - Friday
Reported: Within 4 days upon receipt in lab.
Specimen Required:

Collect: CSF or one 7 to 10 ml ACD (acid citrate dextrose) tube.
Transport: 1 ml CSF or plasma (ACD) in a sterile, leak-proof container, frozen (dry ice).
Or ship ACD tube as whole blood at room temperature.

Unacceptable Conditions:

Whole blood received frozen.
Whole blood received greater than 48 hours from collection.

Stability:

Plasma and CSF: Room temperature, 4 hours. Refrigerator, 3 days. Frozen, 1 year.
Whole blood: Room temperature, 48 hours.

Reference Value: Negative


1300                      Human Herpesvirus Seven (HHV-7) DNA PCR                                                     

Methodology:

Polymerase Chain Reaction. Enhanced sensitivity of nested PCR for the detection of active infection.

Performed: Monday - Friday
Reported: Within 4 days upon receipt in lab.
Specimen Required:

Collect: One 7 to 10 ml ACD (acid citrate dextrose) tube.
Transport: Plasma (ACD) in a sterile, leak-proof container, frozen (dry ice). Or ship ACD tube as whole blood at room temperature.

Unacceptable Conditions:

Whole blood received frozen. Whole blood received greater than 48 hours from collection.

Stability:

 Plasma: Room temperature, 4 hours. Refrigerator, 3 days. Frozen, 1 year.

Reference Value: Negative


Additional instructions

All specimens should be labeled with the patient's name and collection date.
Ship specimen with a completed WVRG Test Request Form.
Ship specimens for testing, Monday through Thursday, to the following address:

Wisconsin Viral Research Group
10437 Innovation Drive
Suite 321
Milwaukee, WI 53226

Call (414) 774-8612 for a specimen kit with instructions for the submission of blood samples.

PCR tests use a commercial kit or reagent that has not been approved or cleared by the FDA.
The performance characteristics were determined by WVRG.


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