Mucopolysaccharidosis IIID and Beta‐Mannosidosis in Brazilian Anglo‐Nubian Goats: Molecular and Genealogical Insights for the Development and Implementation of a Genetic Disease Eradication Program

Beta mannosidosis and Mucopolysaccharidosis IIID are two autosomal recessive lysosomal storage diseases identified in Anglo-Nubian goats. Even though they are well characterized from the clinical and molecular point of view, there is a gap in studies aiming to understand distribution and dissemination risk in goat populations throughout the world. Considering this, we developed probe-based qPCR tests and combined it with pedigree analysis to deepen the knowledge related to the distribution of both mutations in Brazilian Anglo-Nubian population. This study revealed, for the first time, that the mutation associated with Mucopolysaccharidosis IIID is segregating in our country, expanding the knowledge of the worldwide distribution of this disease-associated allele. Additionally, the combination of genotyping and pedigree analysis enabled the estimation of additional high-confidence putative genotypes, contributing to the reduction of genotyping costs and highlighting a putative pathway associated with the introduction/dissemination of the Mucopolysaccharidosis IIID-associated allele in Brazil. These results can be considered as an initial basis for the proposition of a program to control/eradicate mutations associated with genetic diseases in Brazilian goat populations.

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Publication Details

Journal
Animal Genetics
Published
2026-04-22
DOI
https://doi.org/10.1002/age.70107
Primary Topic
Lysosomal Storage Disorders Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Mucopolysaccharidosis IIID and Beta‐Mannosidosis in Brazilian Anglo‐Nubian Goats: Molecular and Genealogical Insights for the Development and Implementation of a Genetic Disease Eradication Program

Flávia Caroline Moreira Bezerra, Joane Maíra Cavalcante Braga Novais, A. M. G. Ibelli, Gisele Veneroni Gouveia et al.
Animal Genetics
Lysosomal Storage Disorders Research
article

Mucopolysaccharidosis IIID and Beta‐Mannosidosis in Brazilian Anglo‐Nubian Goats: Molecular and Genealogical Insights for the Development and Implementation of a Genetic Disease Eradication Program

Flávia Caroline Moreira Bezerra, Joane Maíra Cavalcante Braga Novais, A. M. G. Ibelli, Gisele Veneroni Gouveia, LIVIA SAMANIELY BATISTA PEREIRA BELLI, João José de Simoni Gouveia, Alexandre Tadeu Mota Macedo, Cássia Regina Oliveira Santos
article en

Abstract

Beta mannosidosis and Mucopolysaccharidosis IIID are two autosomal recessive lysosomal storage diseases identified in Anglo-Nubian goats. Even though they are well characterized from the clinical and molecular point of view, there is a gap in studies aiming to understand distribution and dissemination risk in goat populations throughout the world. Considering this, we developed probe-based qPCR tests and combined it with pedigree analysis to deepen the knowledge related to the distribution of both mutations in Brazilian Anglo-Nubian population. This study revealed, for the first time, that the mutation associated with Mucopolysaccharidosis IIID is segregating in our country, expanding the knowledge of the worldwide distribution of this disease-associated allele. Additionally, the combination of genotyping and pedigree analysis enabled the estimation of additional high-confidence putative genotypes, contributing to the reduction of genotyping costs and highlighting a putative pathway associated with the introduction/dissemination of the Mucopolysaccharidosis IIID-associated allele in Brazil. These results can be considered as an initial basis for the proposition of a program to control/eradicate mutations associated with genetic diseases in Brazilian goat populations.

Animal GeneticsVol. 57(3)
Brazilian Agricultural Research Corporation (BR), Universidade Federal do Vale do São Francisco (BR)
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Fundação de Amparo à Ciência e Tecnologia do Estado de Pernambuco
Openalex Percentile: Top 10%
Lysosomal Storage Disorders Research
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