Literature DB >> 19751487

Retinal degeneration in the Abyssinian and Somali cat (rdAc): correlation between genotype and phenotype and rdAc allele frequency in two continents.

Kristina Narfström1, Victor David, Oswald Jarret, Julia Beatty, Vanessa Barrs, David Wilkie, Stephen O'Brien, Marilyn Menotti-Raymond.   

Abstract

OBJECTIVE: To characterize hereditary retinal degeneration in the Abyssinian cat (rdAc) in a recently established closed colony segregating for the rdAc mutation, and evaluate possible differences in the age of onset and progression of disease phenotype since the initial description of rdAc 25 years ago. The sample size of an earlier study was increased in order to determine the allele frequency in Abyssinian and Somali cats on a worldwide basis. ANIMALS STUDIED: Twenty rdAc affected cats from the closed animal facility, 87 Abyssinian and Somali cats for study of genotype-phenotype concordance, and DNA from 131 Abyssinian and Somali cats from Scandinavia, the UK and Australia for evaluation of the rdAc allele frequency. PROCEDURES: DNA was extracted from blood and buccal swabs using commercially available kits, followed by genotyping. Ophthalmic examinations were performed in the USA and Sweden by two board-certified veterinary ophthalmologists.
RESULTS: A greater variation in the age of onset and progression of the disease was observed compared to that previously described. An excellent correlation between genotype and phenotype was observed. A population genetic survey revealed that the rdAc allele is in moderate abundance in the Abyssinian breed in Europe and Australia. Surprisingly, homozygosity for the mutant allele was observed in a Siamese cat with ophthalmoscopic findings similar to those originally described for affected rdAc individuals.
CONCLUSIONS: Alertness to the potential of rdAc is needed on the part of the veterinary ophthalmology community, not only in Abyssinian and Somali cats but possibly also in other related cat breeds.

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Year:  2009        PMID: 19751487     DOI: 10.1111/j.1463-5224.2009.00710.x

Source DB:  PubMed          Journal:  Vet Ophthalmol        ISSN: 1463-5216            Impact factor:   1.644


  6 in total

1.  Mutation discovered in a feline model of human congenital retinal blinding disease.

Authors:  Marilyn Menotti-Raymond; Koren Holland Deckman; Victor David; Jaimie Myrkalo; Stephen J O'Brien; Kristina Narfström
Journal:  Invest Ophthalmol Vis Sci       Date:  2010-01-06       Impact factor: 4.799

2.  Widespread retinal degenerative disease mutation (rdAc) discovered among a large number of popular cat breeds.

Authors:  M Menotti-Raymond; V A David; S Pflueger; M E Roelke; J Kehler; S J O'Brien; K Narfström
Journal:  Vet J       Date:  2009-09-10       Impact factor: 2.688

3.  The domestic cat as a large animal model for characterization of disease and therapeutic intervention in hereditary retinal blindness.

Authors:  Kristina Narfström; Koren Holland Deckman; Marilyn Menotti-Raymond
Journal:  J Ophthalmol       Date:  2011-04-14       Impact factor: 1.909

4.  Animals Models of Inherited Retinal Disease.

Authors:  Ala Moshiri
Journal:  Int Ophthalmol Clin       Date:  2021-07-01

Review 5.  Assessment of Safety and Functional Efficacy of Stem Cell-Based Therapeutic Approaches Using Retinal Degenerative Animal Models.

Authors:  Tai-Chi Lin; Magdalene J Seiler; Danhong Zhu; Paulo Falabella; David R Hinton; Dennis O Clegg; Mark S Humayun; Biju B Thomas
Journal:  Stem Cells Int       Date:  2017-08-27       Impact factor: 5.443

6.  Retrospective and prospective study of progressive retinal atrophy in dogs presented to the veterinary hospital of the Federal University of Parana, Brazil.

Authors:  Henrique M Freitas; André T Somma; Bret A Moore; Fabiano Montiani-Ferreira
Journal:  Open Vet J       Date:  2021-07-22
  6 in total

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