Progressive Retinal Atrophy (PRA-b) (Bengal)Quick Summary
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Phenotype: Bengal progressive retinal atrophy is characterized by progressive blindness. The loss of the cells begins around 7 weeks of age and slowly progresses until the cat has very compromised vision by approximately 2 years of age. Blind cats tend to have more difficulty at night, sometimes becoming more vocal and more attached to their owners. The pupils are usually more dilated for affected cats than for cats with normal vision in the same lighting conditions. Affected cats also tend to carry their whiskers in a more forward position.
Mode of Inheritance: Autosomal recessive
Alleles: N = Normal/Unaffected, PRA = Progressive retinal atrophy
Breeds appropriate for testing: Bengal, Savannah Cat, Toyger, Highlander
Explanation of Results:
- Cats with N/N genoytpe will not have Bengal progressive retinal atrophy and cannot transmit this PRA-b variant to their offspring.
- Cats with N/PRA genotype will not have Bengal progressive retinal atrophy, but are carriers. Matings between two carriers are predicted to produce 25% kittens affected by PRA-b.
- Cats with PRA/PRA genotype will have Bengal progressive retinal atrophy, a condition leading to blindness in Bengal cats, and will transmit this PRA-b variant to all of their offspring.
$44 one test per animal
$66 this test + PK Deficiency test
Sample Collection:
Cat DNA tests are carried out using cells collected from your cat's cheeks and gums using household cotton swabs.
The cat DNA submission form with instructions and a place to tape the cotton swabs is sent to you via email after you place an order, and can be printed from your home computer. Test kits are not mailed.
Step-By-Step Instructions:
1.
Purchase regular household cotton swabs for cat DNA collection (the cotton swabs can be purchased at a pharmacy or drug store)
2.
Use both ends of the two cotton swabs for a total of four swabs.
3.
Collect the DNA sample by swabbing the cheek and gums of the cat. Wave the swab in the air for 10-15 seconds to air dry it before attaching it to the submission form. We recommend swabbing different areas of the cat's cheeks.
4.
After swabbing the cheek and gums, tape the cotton swabs to the bar-coded submission form printed from your MyVGL account.
The Veterinary Genetics Laboratory at the University of California, Davis in collaboration with the Lyons Feline Genetics and Comparative Medicine Laboratory at the University of Missouri discovered the genetic test for progressive retinal atrophy (PRA), which causes an autosomal recessive blindness in Bengal cats. The disease causes the destruction of the cells that register light (photoreceptors) in the back of the eye (the retina). The loss of the cells begins around 7 weeks of age and slowly progresses until the cat has very compromised vision by approximately 2 years of age. However, blindness develops at different rates in different cats. We have examples of cats over 2 years of age chasing a laser pointer; however vision testing by an ophthalmologist indicated that the cats should be blind. Blind cats tend to have more difficulty at night, sometimes becoming more vocal and more attached to their owners. The pupils are usually more dilated for affected cats than for cats with normal vision in the same lighting conditions. Affected cats also tend to carry their whiskers in a more forward position. Once affected cats know their surroundings, they are very mobile and active. Our thanks to the breeders who came forward and helped us establish a colony so that we could define the condition and find the gene responsible for this defect.
The causative DNA variant appears to be novel to the Bengal breed and occurred early in a popular lineage of the Bengals. We expect Bengal cats worldwide to have the condition and we have had reports of affected cats in the United Kingdom, Europe, and the USA. Bengal PRA is autosomal recessive, thus two copies of the mutant DNA variant are required for the cats to be blind. The blindness can be detected either by the DNA test or by an eye exam prior breeding age. Carriers, cats with one copy of the mutation, can only be detected by the DNA test.