Ramírez Hugo, Echeverría Irache, Benito Alfredo A, Glaria Idoia, Benavides Julio, Pérez Valentín, de Andrés Damián, Reina Ramsés
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.
Animal Health Department, Institute of Agrobiotechnology (IdAB), CSIC-Government of Navarra, 31192 Navarra, Spain.
Pathogens. 2021 Jan 19;10(1):83. doi: 10.3390/pathogens10010083.
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.
小反刍兽慢病毒(SRLV)引发一种无法治愈的多器官疾病,在绵羊和山羊中广泛传播,影响动物福利和生产。由于缺乏疫苗,传统的控制措施基于早期诊断以及使用病毒灭活初乳进行繁育,并将血清阳性动物隔离。然而,抗原异质性、病毒载量低导致抗体产生不佳,以及大多数现有酶联免疫吸附测定(ELISA)的单菌株设计,对SRLV诊断构成威胁。全基因组关联研究已将跨膜蛋白154(TMEM154)E35K多态性描述为某些美洲和欧洲品种中选择抗性动物的良好遗传标记。在本研究中,对来自四个不同品种(拉查、纳瓦拉品种、阿萨夫和丘拉)的500多头动物进行了针对SRLV感染状况的多靶点血清学和病毒学筛查。然后,对动物进行基因分型以表征TMEM154 E35K多态性。单独考虑ELISA程序时,仅能识别一部分血清阳性动物,而聚合酶链反应(PCR)检测到一部分血清阴性动物,总体上根据SRLV感染状况提供了不同的动物分类。TMEM154等位基因频率在不同品种间差异很大,并且仅在一个品种中发现血清阳性率与TMEM154基因型之间存在正相关。基于TMEM154的选择可能适用于特定的绵羊品种或SRLV毒株,然而推广至整个SRLV基因谱、绵羊品种或流行病学情况可能需要进一步验证。