An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome.

In flat-faced dog breeds, air resistance caused by skull conformation is believed to be a major determinant of Brachycephalic Obstructive Airway Syndrome (BOAS). The clinical presentation of BOAS is heterogeneous, suggesting determinants independent of skull conformation contribute to airway disease...

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Main Authors: Thomas W Marchant, Elisabeth Dietschi, Ulrich Rytz, Peter Schawalder, Vidhya Jagannathan, Sheida Hadji Rasouliha, Corinne Gurtner, Andreas S Waldvogel, Ronan S Harrington, Michaela Drögemüller, Jeffrey Kidd, Elaine A Ostrander, Amanda Warr, Mick Watson, David Argyle, Gert Ter Haar, Dylan N Clements, Tosso Leeb, Jeffrey J Schoenebeck
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-05-01
Series:PLoS Genetics
Online Access:https://doi.org/10.1371/journal.pgen.1008102
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spelling doaj-402f2725caf44336a896c9672964d6392021-04-21T13:48:51ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042019-05-01155e100810210.1371/journal.pgen.1008102An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome.Thomas W MarchantElisabeth DietschiUlrich RytzPeter SchawalderVidhya JagannathanSheida Hadji RasoulihaCorinne GurtnerAndreas S WaldvogelRonan S HarringtonMichaela DrögemüllerJeffrey KiddElaine A OstranderAmanda WarrMick WatsonDavid ArgyleGert Ter HaarDylan N ClementsTosso LeebJeffrey J SchoenebeckIn flat-faced dog breeds, air resistance caused by skull conformation is believed to be a major determinant of Brachycephalic Obstructive Airway Syndrome (BOAS). The clinical presentation of BOAS is heterogeneous, suggesting determinants independent of skull conformation contribute to airway disease. Norwich Terriers, a mesocephalic breed, are predisposed to Upper Airway Syndrome (UAS), a disease whose pathological features overlap with BOAS. Our health screening clinic examined and scored the airways of 401 Norwich terriers by laryngoscopy. Genome-wide association analyses of UAS-related pathologies revealed a genetic association on canine chromosome 13 (rs9043975, p = 7.79x10-16). Whole genome resequencing was used to identify causal variant(s) within a 414 kb critical interval. This approach highlighted an error in the CanFam3.1 dog assembly, which when resolved, led to the discovery of a c.2786G>A missense variant in exon 20 of the positional candidate gene, ADAM metallopeptidase with thrombospondin type 1 motif 3 (ADAMTS3). In addition to segregating with UAS amongst Norwich Terriers, the ADAMTS3 c.2786G>A risk allele frequency was enriched among the BOAS-susceptible French and (English) Bulldogs. Previous studies indicate that ADAMTS3 loss of function results in lymphoedema. Our results suggest a new paradigm in the understanding of canine upper airway disease aetiology: airway oedema caused by disruption of ADAMTS3 predisposes dogs to respiratory obstruction. These findings will enhance breeding practices and could refine the prognostics of surgical interventions that are often used to treat airway obstruction.https://doi.org/10.1371/journal.pgen.1008102
collection DOAJ
language English
format Article
sources DOAJ
author Thomas W Marchant
Elisabeth Dietschi
Ulrich Rytz
Peter Schawalder
Vidhya Jagannathan
Sheida Hadji Rasouliha
Corinne Gurtner
Andreas S Waldvogel
Ronan S Harrington
Michaela Drögemüller
Jeffrey Kidd
Elaine A Ostrander
Amanda Warr
Mick Watson
David Argyle
Gert Ter Haar
Dylan N Clements
Tosso Leeb
Jeffrey J Schoenebeck
spellingShingle Thomas W Marchant
Elisabeth Dietschi
Ulrich Rytz
Peter Schawalder
Vidhya Jagannathan
Sheida Hadji Rasouliha
Corinne Gurtner
Andreas S Waldvogel
Ronan S Harrington
Michaela Drögemüller
Jeffrey Kidd
Elaine A Ostrander
Amanda Warr
Mick Watson
David Argyle
Gert Ter Haar
Dylan N Clements
Tosso Leeb
Jeffrey J Schoenebeck
An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome.
PLoS Genetics
author_facet Thomas W Marchant
Elisabeth Dietschi
Ulrich Rytz
Peter Schawalder
Vidhya Jagannathan
Sheida Hadji Rasouliha
Corinne Gurtner
Andreas S Waldvogel
Ronan S Harrington
Michaela Drögemüller
Jeffrey Kidd
Elaine A Ostrander
Amanda Warr
Mick Watson
David Argyle
Gert Ter Haar
Dylan N Clements
Tosso Leeb
Jeffrey J Schoenebeck
author_sort Thomas W Marchant
title An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome.
title_short An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome.
title_full An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome.
title_fullStr An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome.
title_full_unstemmed An ADAMTS3 missense variant is associated with Norwich Terrier upper airway syndrome.
title_sort adamts3 missense variant is associated with norwich terrier upper airway syndrome.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2019-05-01
description In flat-faced dog breeds, air resistance caused by skull conformation is believed to be a major determinant of Brachycephalic Obstructive Airway Syndrome (BOAS). The clinical presentation of BOAS is heterogeneous, suggesting determinants independent of skull conformation contribute to airway disease. Norwich Terriers, a mesocephalic breed, are predisposed to Upper Airway Syndrome (UAS), a disease whose pathological features overlap with BOAS. Our health screening clinic examined and scored the airways of 401 Norwich terriers by laryngoscopy. Genome-wide association analyses of UAS-related pathologies revealed a genetic association on canine chromosome 13 (rs9043975, p = 7.79x10-16). Whole genome resequencing was used to identify causal variant(s) within a 414 kb critical interval. This approach highlighted an error in the CanFam3.1 dog assembly, which when resolved, led to the discovery of a c.2786G>A missense variant in exon 20 of the positional candidate gene, ADAM metallopeptidase with thrombospondin type 1 motif 3 (ADAMTS3). In addition to segregating with UAS amongst Norwich Terriers, the ADAMTS3 c.2786G>A risk allele frequency was enriched among the BOAS-susceptible French and (English) Bulldogs. Previous studies indicate that ADAMTS3 loss of function results in lymphoedema. Our results suggest a new paradigm in the understanding of canine upper airway disease aetiology: airway oedema caused by disruption of ADAMTS3 predisposes dogs to respiratory obstruction. These findings will enhance breeding practices and could refine the prognostics of surgical interventions that are often used to treat airway obstruction.
url https://doi.org/10.1371/journal.pgen.1008102
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