Dr Simon Petersen-Jones DVetMed PhD DipECVO MRCVS
Department of Small Animal Clinical Sciences
College of Veterinary Medicine
Michigan State University
D-208 Veterinary Medical Center
East Lansing, MI 48824-1314
Tel: (517) 353-3278
Fax: (517) 355-5164 Email: peter315@cvm.msu.edu
Progressive retinal atrophy – PRA- was a term that used to strike
terror into the hearts of many dog breeders. How distressing it must have
been to know that a beautiful puppy that you had bred was going to go
blind, to say nothing of the anguish felt by the new owners of the pup.
Until recently the only options available to breeders with PRA in their
lines was to either do a test mating to check that a dog that might have
PRA in its background was not a carrier of the disease, or to completely
avoid lines with any hint of PRA in the background. Neither approach was
ideal, test mating is time consuming and expensive and potentially results
in PRA-affected animals. Avoiding affected lines could mean that some
outstanding animals could not be used and that the available “gene
pool” was narrowed, this itself could lead to a different set of
problems.
Cardis from across the world suffered from PRA. The problem was first
reported in the veterinary press in the early 1970s and we know now that
cases occurred in Europe, North America and Australasia. Thanks to the
co-operation of breeders from across the world we were able to collect
enough blood samples from affected dogs and carriers to allow us to
identify the gene mutation that causes PRA in Cardis. We know that PRA in
the breed results in a progressive loss of the cells in the retina that
register light (photoreceptors). There are two sorts of photoreceptor,
called rods and cones. They convert light into electrical messages that
are sent to the brain via the optic nerve. The rod photoreceptors are
designed to function in dim light and do not register colors. In contrast
the cone photoreceptors work in brighter light and are responsible for
color vision (and yes, dogs do see in color, although not quite in the
same way as humans). PRA in the Cardis affects a gene that works in the
rods. The gene defect leads to an abnormal accumulation of material in the
rod photoreceptor causing it to die. This affects the rods very early in
life, indeed we suspect that they may not even form correctly. The result
of this is that affected puppies can be shown to have defective nighttime
vision from as early as 6 weeks of age (testing vision at this young age
is not easy!). The PRA gene is not normally functional in the cone
photoreceptors, so it is surprising that these cells also die. Their death
is probably a result of the mass death of the surrounding rod cells. As
the cones die the affected dogs also lose their daytime color vision. It
takes a while for this to occur and the affected dog is 2 to 3 years of
age before he/she has severe problems seeing in bright light. Currently
there is no treatment for PRA.
Once we had identified the gene defect that caused PRA in Cardis it was a
relatively easy matter to come up with a diagnostic test. This test is
capable of distinguishing between affected dogs, carrier dogs and
genetically unaffected (normal) dogs. All that is needed is a small DNA
sample from a blood sample or a cheek swab, so the test can even be
performed on young puppies. We have recently altered our PRA test so that
it can be run at a lower cost and can be performed on cheek swabs. We can
therefore reduce the price of the test to $35/test. We can send out cheek
swab collection packs at a charge of $4/kit (contact details at end of
article). The most important time, however, to test dogs is when planning
to breed. To ensure that no PRA-affected puppies are born one has to
ensure that both parents are tested and that two carriers are not mated. A
litter from a carrier x carrier mating will on average have 25% of puppies
affected and 50% carriers. Now that a test is available, carriers can be
used for breeding, so long as they are not mated to another carrier. This
enables those breeders with PRA in their lines to eradicate the problem
from their lines over a few generations without losing the good features
that their line exhibits. The concept is that by testing prior to breeding
they can separate the “good” genes that their dogs have from the
“bad” gene (i.e. the PRA gene). We have currently tested nearly 600
dogs and are finding a carrier rate of about 8.5%.
Here at Michigan State we are continuing to study PRA and search for the
gene defects that cause the disease in many other breeds of dog. The work
is laborious and expensive, but we are confident that we will be able to
identify the cause of PRA in other breeds and develop further tests for
this distressing disease. If you would like to support the gene searching
in other breeds we would welcome any donations to this work and we are
currently fundraising to develop a major center for eye research at
Michigan State which will look into many other hereditary eye diseases in
dogs as well as PRA. If you would like to support the PRA research please
send checks made out to Michigan State University and marked PRA research
to Dr Petersen-Jones. If you would like to discuss contributing towards
the major animal eye research center please contact Dr Petersen-Jones in
the first instance.
People wishing to submit samples from Cardigan Welsh corgis for PRA
testing can obtain the submission
forms via the web page of the CWCCA or by contacting Dr
Petersen-Jones.
Test kit for collecting cheek swabs – send check for $4.00 (payable to
Michigan State University) to:
Dr Petersen-Jones (Corgi test)
Dept. Small Anim. Clin. Sci., Michigan State University, D-208 VMC,
East Lansing MI 48824-1314
Cheek swab PRA test for corgis - $35.00/test.
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