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Accurate Diagnosis of Small Ruminant Lentivirus Infection Is Needed for Selection of Resistant Sheep through TMEM154 E35K Genotyping.
Ramírez, Hugo; Echeverría, Irache; Benito, Alfredo A; Glaria, Idoia; Benavides, Julio; Pérez, Valentín; de Andrés, Damián; Reina, Ramsés.
Afiliação
  • Ramírez H; Virology, Genetics and Molecular Biology Laboratory, Faculty of Higher Education, Cuautitlan, Veterinary Medicine, National Autonomous University of Mexico, Campus 4, Km. 2.5 Carretera Cuautitlán-Teoloyucan, San Sebastián Xhala, Cuautitlán Izcalli 54714, Estado de México, Mexico.
  • Echeverría I; Animal Health Department, Institute of Agrobiotechnology (IdAB), CSIC-Government of Navarra, 31192 Navarra, Spain.
  • Benito AA; Molecular and Cell Biology Department, EXOPOL SL, 50840 Zaragoza, Spain.
  • Glaria I; Animal Health Department, Institute of Agrobiotechnology (IdAB), CSIC-Government of Navarra, 31192 Navarra, Spain.
  • Benavides J; Mountain Livestock Institute (IGM), CSIC-University of León, 24346 León, Spain.
  • Pérez V; Department of Animal Health, University of León, 24071 León, Spain.
  • de Andrés D; Animal Health Department, Institute of Agrobiotechnology (IdAB), CSIC-Government of Navarra, 31192 Navarra, Spain.
  • Reina R; Animal Health Department, Institute of Agrobiotechnology (IdAB), CSIC-Government of Navarra, 31192 Navarra, Spain.
Pathogens ; 10(1)2021 Jan 19.
Article em En | MEDLINE | ID: mdl-33478070
Small ruminant lentiviruses (SRLV) cause an incurable multiorganic disease widely spread in sheep and goats that disturbs animal welfare and production. In the absence of a vaccine, control measures have been traditionally based on early diagnosis and breeding with virus-inactivated colostrum with segregation of seropositive animals. However, antigenic heterogeneity, poor antibody production due to low viral load, and single strain design of most available ELISA, pose a threat to SRLV diagnosis. Genome-wide association studies have described TMEM154 E35K polymorphism as a good genetic marker for selection of resistant animals in some American and European breeds. In this study, a multitargeted serological and virological screening of more than 500 animals from four different breeds (latxa, raza Navarra, assaf, and churra) attending to SRLV infection status was performed. Then, animals were genotyped to characterize TMEM154 E35K polymorphism. ELISA procedures, individually considered, only identified a proportion of the seropositive animals, and PCR detected a fraction of seronegative animals, globally offering different animal classifications according to SRLV infection status. TMEM154 allele frequency differed substantially among breeds and a positive association between seroprevalence and TMEM154 genotype was found only in one breed. Selection based on TMEM154 may be suitable for specific ovine breeds or SRLV strains, however generalization to the whole SRLV genetic spectrum, ovine breeds, or epidemiological situation may need further validation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Screening_studies Idioma: En Revista: Pathogens Ano de publicação: 2021 Tipo de documento: Article País de afiliação: México

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Screening_studies Idioma: En Revista: Pathogens Ano de publicação: 2021 Tipo de documento: Article País de afiliação: México