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Mutations in Ovis aries TMEM154 are associated with lower small ruminant lentivirus proviral concentration in one sheep flock

机译:绵羊TMEM154中的突变与一只绵羊群中较低的小反刍动物慢病毒原病毒浓度相关

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Small ruminant lentivirus (SRLV), also called ovine progressive pneumonia virus or maedi-visna, is present in 24% of US sheep. Like human immunodeficiency virus, SRLV is a macrophage-tropic lentivirus that causes lifelong infection. The production impacts from SRLV are due to a range of disease symptoms, including pneumonia, arthritis, mastitis, body condition wasting and encephalitis. There is no cure and no effective vaccine for preventing SRLV infection. However, breed differences in prevalence and proviral concentration indicate a genetic basis for susceptibility to SRLV. Animals with high blood proviral concentration show increased tissue lesion severity, so proviral concentration represents a live animal test for control post-infection in terms of proviral replication and disease severity. Recently, it was found that sheep with two copies of TMEM154 haplotype 1 (encoding lysine at position 35) had lower odds of SRLV infection. In this study, we examined the relationship between SRLV control post-infection and variants in two genes, TMEM154 and CCR5, in four flocks containing 1403 SRLV-positive sheep. We found two copies of TMEM154 haplotype 1 were associated with lower SRLV proviral concentration in one flock (P < 0.02). This identified the same favorable diplotype for SRLV control post-infection as for odds of infection. However, frequencies of haplotypes 2 and 3 were too low in the other three flocks to test. The CCR5 promoter deletion did not have consistent association with SRLV proviral concentration. Future work in flocks with more balanced allele frequencies is needed to confirm or refute TMEM154 association with control of SRLV post-infection
机译:小反刍动物慢病毒(SRLV),也称为绵羊进行性肺炎病毒或马代-维斯纳病毒,存在于美国24%的绵羊中。像人类免疫缺陷病毒一样,SRLV是一种嗜巨噬细胞性慢病毒,会引起终身感染。 SRLV对生产的影响是由于一系列疾病症状引起的,包括肺炎,关节炎,乳腺炎,身体状况消瘦和脑炎。没有治愈方法,也没有有效的疫苗来预防SRLV感染。但是,流行和原病毒浓度的品种差异表明对SRLV易感性的遗传基础。具有高血液原病毒浓度的动物显示出增加的组织病变严重程度,因此就原病毒复制和疾病严重程度而言,原病毒浓度代表了活体动物测试,以控制感染后。最近,发现具有两个拷贝的TMEM154单倍型1(在位置35处编码赖氨酸)的绵羊的SRLV感染几率较低。在这项研究中,我们检查了四个含有1403 SRLV阳性绵羊的羊群中SRLV感染后控制与两个基因TMEM154和CCR5变异之间的关系。我们发现两份TMEM154单倍型1与一组鸡群中较低的SRLV原病毒浓度相关(P <0.02)。这为感染后的SRLV控制确定了与感染几率相同的有利双倍型。但是,在其他三个鸡群中单倍型2和3的频率过低,无法进行测试。 CCR5启动子的缺失与SRLV前病毒浓度没有一致的关联。需要在等位基因频率更均衡的鸡群中开展未来工作,以确认或反驳TMEM154与控制SRLV感染后的关联

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