Quick Summary
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Phenotype: NME is an inflammatory disease of the central nervous system that is usually progressive and fatal. Symptoms of NME include seizures, depression, ataxia, abnormal gait, and blindness. Female, fawn-colored Pugs younger than 7 years of age are more apt to develop NME than older, male, and non-fawn colored individuals.
Haplotype: N = Normal, S = NME-associated susceptibility variants
Breeds appropriate for testing: Pug
Explanation of Results:
- Dogs with N/N haplotype have no copies of the NME-associated risk variants and are at low risk of developing necrotizing meningoencephalitis. They cannot transmit these NME risk variants to their offspring.
- Dogs with N/S haplotype have one copy of the NME-associated risk variants and are at low risk of developing necrotizing meningoencephalitis. They may transmit these NME risk variants to 50% of their offspring.
- Dogs with S/S haplotype have two copies of the NME-associated risk variants and are 12.75 times more likely to develop necrotizing meningoencephalitis in their lifetimes. They will transmit these NME risk variants to all of their offspring.
Results of this test can be submitted to the OFA (Orthopedic Foundation for Animals)
$55 single test per animal ($5 discount on 3 or more dogs)
$25 as additional health test on same animal
$80 Susceptibility to Pug Dog Encephalitis (PDE) + Pyruvate Kinase Deficiency (PKDef) (same animal)
Sample Collection
Dog DNA tests are carried out using cells brushed from your dog's cheeks and gums. The preferred cytology brushes are sent to you by mail, or you may provide your own brushes. For accepted alternative brushes, click here
We recommend waiting until puppies are at least three weeks old before testing.
Step-By-Step:
- Make sure the dog has not had anything to eat or drink for at least 1 hour prior to collecting sample.
- When swabbing puppies, isolate each puppy from the mother, littermates and any shared toys for 1 hour prior to swabbing. Puppies should not have nursed or eaten for 1 hour prior to collecting sample.
- If collecting samples from more than one dog, make sure to sample one dog at a time and wash your hands before swabbing another dog.
- Label brush sleeve with name or ID of dog to be sampled.
- Open brush sleeve by arrow and remove one brush by its handle.
- Place bristle head between the dog’s gums and cheek and press lightly on the outside of the cheek while rubbing or rotating the brush back and forth for 15 seconds.
- Wave the brush in the air for 20 seconds to air dry.
- Insert brush back into sleeve.
- Repeat steps 5 - 8 for each unused brush in sleeve on a fresh area of cheek and gums. Make sure to use and return all brushes sent by the VGL. In most cases, it will be 3 brushes per dog. If using interdental gum brushes, please note that the VGL requires 4 brushes per dog and only moderate or wide interdental gum brushes are accepted.
- Do not seal brushes in sleeve.
- Place all samples in an envelope and return to the address provided.
ATTENTION:
- Do not collect saliva/drool – the key to obtaining a good sample is getting cheek cells on the swab
- Do not rub swab on the dog’s tongue or teeth – this will result in poor quality sample
- Do not collect a sample from a puppy that has recently nursed – the mother’s genetic material can rub off on the puppy’s mouth and contaminate the sample
Approximately 1.2% of Pug dogs die of necrotizing meningoencephalitis (NME), also known as Pug dog encephalitis (PDE). NME is an inflammatory disease of the central nervous system that is usually progressive and fatal. Symptoms of NME include seizures, depression, ataxia, abnormal gait, and blindness. Female, fawn-colored Pugs younger than 7 years of age are more apt to develop NME than older, male, and non-fawn colored individuals.
Recent research has revealed that susceptibility to NME is associated with the dog leukocyte antigen (DLA) region of dog chromosome 12. The association is at or near the region containing the DLA class II genes. Dogs that are homozygous for the NME-susceptibility haplotype, ie, those with two identical copies of the NME-associated markers (denoted S/S) have an observed risk of 12.75 for NME in their lifetime over Pugs that have only one (N/S) or no (N/N) copies of these markers (observed risk of 0-1.08).