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An IL17RA frameshift variant in a Holstein cattle family with psoriasis-like skin alterations and immunodeficiency.
Häfliger, Irene M; Sickinger, Marlene; Holsteg, Mark; Raeder, Leif M; Henrich, Manfred; Marquardt, Siegfried; Drögemüller, Cord; Lühken, Gesine.
Affiliation
  • Häfliger IM; Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001, Bern, Switzerland.
  • Sickinger M; Clinic for Obstetrics, Gynecology and Andrology of Large and Small Animals with Ambulatory Service, Faculty of Veterinary Medicine, Justus-Liebig University Giessen, 35392, Giessen, Germany.
  • Holsteg M; Bovine Health Service, Chamber of Agriculture of North Rhine-Westphalia, 59505, Bad Sassendorf, Germany.
  • Raeder LM; Institute of Veterinary Pathology, Faculty of Veterinary Medicine, Justus-Liebig-University Giessen, 35392, Giessen, Germany.
  • Henrich M; Institute of Veterinary Pathology, Faculty of Veterinary Medicine, Justus-Liebig-University Giessen, 35392, Giessen, Germany.
  • Marquardt S; Veterinary Sharing Practice, Dr. Siegfried Marquardt and Peter Walter, 47574, Goch, Germany.
  • Drögemüller C; Institute of Genetics, Vetsuisse Faculty, University of Bern, 3001, Bern, Switzerland. cord.droegemueller@vetsuisse.unibe.ch.
  • Lühken G; Institute of Animal Breeding and Genetics, Faculty of Agricultural Sciences, Nutritional Sciences and Environmental Management, Justus-Liebig University Giessen, 35390, Giessen, Germany.
BMC Genet ; 21(1): 55, 2020 05 24.
Article in En | MEDLINE | ID: mdl-32448141
ABSTRACT

BACKGROUND:

Skin lesions and dermatoses in cattle are often associated with infections due to bacteria, fungi or environmental risk factors. Dermatoses with genetic etiology have been described in cattle. Among these rare disorders, there are primary congenital dermatoses that are associated with inherited nutritional deficiencies, such as bovine hereditary zinc deficiency or zinc deficiency-like syndrome. This study presents three cases of Holstein cattle with congenital skin lesions observed on a single farm that resemble zinc deficiency-like syndrome. Close clinical and pathological examinations took place in two cases. Pedigree analysis indicated autosomal recessive inheritance and whole-genome sequencing of both affected calves was performed.

RESULTS:

The two calves showed retarded growth and suffered from severe ulcerative dermatitis with hyperkeratosis, alopecia furunculosis and subcutaneous abscess formation. Blood analysis showed correspondent leukocytosis with neutrophilia whereas minerals, macro- and micronutrients were within the reference ranges. Variant calling and filtering against the 1000 Bull Genomes variant catalogue resulted in the detection of a single homozygous protein-changing variant exclusively present in both sequenced genomes. This single-nucleotide deletion in exon 3 of IL17RA on bovine chromosome 5 was predicted to have a deleterious impact on the encoded protein due to a frameshift leading to a truncated gene product. Genotyping of the affected cattle family confirmed recessive inheritance.

CONCLUSIONS:

A loss-of-function mutation of the IL17RA transmembrane protein could be identified as most likely pathogenic variant for the psoriasis-like skin alterations observed in the two affected Holstein calves. In man, rare recessive diseases associated with IL17RA include immunodeficiency 51 and chronic mucocutaneous candidiasis. This supports the observed immunodeficiency of the presented cases. This study reports the first naturally occurring IL17RA-associated animal model.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Psoriasis / Cattle / Cattle Diseases / Frameshift Mutation / Receptors, Interleukin-17 Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals Language: En Journal: BMC Genet Journal subject: BIOLOGIA MOLECULAR / BIOTECNOLOGIA Year: 2020 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Psoriasis / Cattle / Cattle Diseases / Frameshift Mutation / Receptors, Interleukin-17 Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals Language: En Journal: BMC Genet Journal subject: BIOLOGIA MOLECULAR / BIOTECNOLOGIA Year: 2020 Document type: Article Affiliation country: