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Witness FeLV-FIV

This page contains information on Witness FeLV-FIV for veterinary use.
The information provided typically includes the following:
  • Witness FeLV-FIV Indications
  • Warnings and cautions for Witness FeLV-FIV
  • Direction and dosage information for Witness FeLV-FIV

Witness FeLV-FIV

This treatment applies to the following species:
Manufacturer: Zoetis

FELINE LEUKEMIA VIRUS ANTIGEN - FELINE IMMUNODEFICIENCY VIRUS ANTIBODY TEST KIT

I. General Information

WITNESS™ FeLV-FIV test is indicated for use when history and/or clinical signs may suggest an infection by feline retroviruses. It will also be particularly recommended prior to an FeLV vaccination, especially in cats belonging to an at risk population.

Ii. Test Principles

The WITNESS™ FeLV-FIV is a simple test based on Rapid Immuno Migration (RIM™) technology. FeLV antigen is detected using antibodies directed against the circulating p27 capside protein.

The detection of FIV is based on the presence of antibodies against the transmembrane region of the virus, using a synthetic peptide from the gp40 protein.

In both cases, sensitized colloidal gold particles will form a complex with either the p27 antigen (FeLV) or antibodies (FIV) present in the sample.

The formed complexes migrate along the strips. The complexes are then captured on a sensitized reaction line where their accumulation causes the formation of a clearly visible pink/red band.

Control bands located at the end of the reading windows (3) ensure that the test was performed correctly.

III. SAMPLE COLLECTION

● The test can be performed on unclotted whole blood anticoagulated with EDTA or heparin, serum or plasma.

● Samples should always be collected with a sterile needle and syringe.

● Haemolysis does not significantly interfere with the test, but strongly haemolysed samples may partly obscure a weak positive band.

IV. SAMPLE STORAGE

Anticoagulated whole blood samples should preferably be tested immediately after collection but not longer than 4 hours after collection, if stored at room temperature.

If testing is further delayed, samples should be kept refrigerated (+2°C and 8°C) for up to 4 days.

For prolonged storage, samples (serum and plasma only) should be kept frozen (-20°C).

V. KIT CONTENTS

● 10 or 25 Pouches, each containing 1 test device and desiccant.

● 10 or 25 Pipettes.

● 1 or 2 Saline Buffer dropper bottles (5.4 mL).

● Instructions for use.

VI. PRECAUTIONS

● Do not use this kit or any of its components after expiration date.

● Kit should be stored at +2 °C - 25 °C (35 °F - 77 °F). Kit should not be frozen.

● Use the test immediately after opening the sealed pouch (within 10 minutes).

● Avoid touching or damaging the membrane in the sample wells or the results windows.

● The WITNESS™ device should be placed on a flat, horizontal surface while performing the test.

● Use a separate pipette for each sample.

● Hold pipette and buffer bottle vertically when dispensing sample and buffer respectively.

● Handle all reagents and samples as biohazardous material.

● Saline Buffer contains sodium azide as a preservative.

● For veterinary use only.

VII. TEST PROCEDURE

Important: Allow samples and buffer drops to fall onto the membrane in each sample window. Do not touch pipette tip, sample or buffer drops, or buffer bottle tip directly to the membrane.

1. SAMPLE APPLICATION

● Tear open a pouch provided and place the test device on a flat horizontal surface.

● Holding the provided pipette vertically, add one drop of sample to each test well (1).

2. BUFFER DISPENSING

● Check that the sample has fully absorbed into the membrane.

● Remove the cap from the buffer bottle, hold it vertically and add two drops of buffer to each sample well (1).

● Leave the test device flat during migration of sample/reagent complex through the reading windows.

3. READING TEST

After 10 minutes, observe the presence or absence of pink/red bands in the reading windows (2) and (3).

Note:

It is possible to read the test before 10 minutes if two pink/red bands are clearly visible in the results windows (2) and (3).

The presence of only one band in reading window (3), prior to the end of the development time (10 minutes), does not mean that the test is complete, as a test band may appear more slowly than the control band.

VIII. RESULTS

Valid Results

● Test is valid if a pink/red band is present in reading window (3).

Interpretation of Results

● Positive. One band in reading window (2), with one band in window (3): sample is positive for FeLV antigen and/or FIV antibodies.

● Negative. No band in reading window (2), with one band in window (3): sample is negative for FeLV antigen and/or FIV antibodies.

Note:

No band in control window (3): invalid test.

A test result should always be interpreted in the context of all available clinical information and history for the cat being tested.

SYMBOL DESCRIPTIONS

Zoetis Inc., Kalamazoo, MI 49007, USA

U.S. Vet. License No. 190

1-888-963-8471

www.zoetis.com

SYNBIOTICS EUROPE SAS, a wholly-owned subsidiary of Zoetis, Gerland Plaza, BAT. E, 23 Rue Pierre Gilles de Gennes, 69007 Lyon, FRANCE

50167100

CPN: 1115058.0

ZOETIS INC.
333 PORTAGE STREET, KALAMAZOO, MI, 49007
Telephone:   269-359-4414
Customer Service:   888-963-8471
Website:   www.zoetis.com
Every effort has been made to ensure the accuracy of the Witness FeLV-FIV information published above. However, it remains the responsibility of the readers to familiarize themselves with the product information contained on the US product label or package insert.

Copyright © 2018 Animalytix LLC. Updated: 2018-10-31

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